UCSC Genome Browser on Human (GRCh37/hg19)
Move Zoom in Zoom out
chr19:44,114,229-44,121,850 7,622 bp.
  
-   Hub: LongRange Test Hub Info  
short1000
short1018
short1036
short1050
short1068
short1090
short1108
short1127
short1145
short1163
short1181
short1195
short1213
short1231
short1250
short1270
short1286
short1300
short1314
short1332
short134
short1380
short1428
short1446
short1460
short1476
short1495
short1514
short152
short1530
short1548
short1562
short1582
short1598
short1616
short1634
short1652
short1670
short1685
short1700
short1715
short1730
short1745
short1760
short1775
short1790
short1805
short1820
short1835
short1850
short1865
short1880
short1895
short1910
short1925
short1940
short1955
short1970
short1985
short200
short2000
short2015
short2033
short2051
short2069
short2087
short2105
short2123
short2141
short2159
short216
short2177
short2195
short2213
short2231
short2249
short2267
short2285
short2303
short2321
short2339
short234
short282
short298
short312
short326
short345
short363
short383
short397
short413
short431
short453
short473
short489
short508
short527
short541
short560
short576
short594
short616
short636
short654
short668
short686
short704
short722
short770
short816
short832
short848
short866
short914
short958
short972
short986
+   Mapping and Sequencing
-   Genes and Gene Predictions
updated GENCODE V47lift37
NCBI RefSeq
Genes Archive
CCDS
CRISPR Targets
Ensembl Genes
EvoFold
Exoniphy
updated GENCODE Versions
H-Inv 7.0
HGNC
IKMC Genes Mapped
lincRNAs
LRG Transcripts
MGC/ORFeome Genes
Old UCSC Genes
Other RefSeq
Pfam in UCSC Gene
Prediction Archive
Retroposed Genes
sno/miRNA
TransMap V5
tRNA Genes
UCSC Alt Events
UniProt
Vega Genes
Yale Pseudo60
-   Phenotype and Literature
OMIM
Publications
AbSplice Scores
CADD 1.6
new CADD 1.7
new ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC Regions
COVID Data
DECIPHER CNVs
DECIPHER SNVs
Development Delay
Dosage Sensitivity
GAD View
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
Haploinsufficiency
HGMD public
Lens Patents
LOVD Variants
MGI Mouse QTL
Orphanet
PanelApp
Polygenic Risk Scores
Prediction Scores
REVEL Scores
RGD Human QTL
RGD Rat QTL
SNPedia
new SpliceAI
UniProt Variants
Variants in Papers
Web Sequences
-   mRNA and EST
CGAP SAGE
Gene Bounds
H-Inv
Human ESTs
Human mRNAs
Human RNA Editing
Other ESTs
Other mRNAs
Poly(A)
PolyA-Seq
SIB Alt-Splicing
Spliced ESTs
UniGene
-   Expression
GTEx Gene V8
Allen Brain
Burge RNA-seq
CSHL Small RNA-seq
ENC Exon Array
ENC ProtGeno
ENC RNA-seq
EPDnew Promoters
Affy Archive
GIS RNA PET
GNF Atlas 2
GTEx Gene
GTEx Transcript
GWIPS-viz Riboseq
Illumina WG-6
PeptideAtlas
qPCR Primers
RIKEN CAGE Loc
Sestan Brain
-   Regulation
ENCODE Regulation
CD34 DnaseI
CpG Islands
ENC Chromatin
ENC DNA Methyl
ENC DNase/FAIRE
ENC Histone
ENC RNA Binding
ENC TF Binding
FANTOM5
FSU Repli-chip
GeneHancer
Genome Segments
GTEx Combined eQTL
GTEx Tissue eQTL
JASPAR Transcription Factors
NKI Nuc Lamina
ORegAnno
Rao 2014 Hi-C
ReMap ChIP-seq
Stanf Nucleosome
SUNY SwitchGear
SwitchGear TSS
TFBS Conserved
TS miRNA Targets
UCSF Brain Methyl
UMMS Brain Hist
UW Repli-seq
VISTA Enhancers
-   Comparative Genomics
Conservation
Cons 46-Way
Cons Indels MmCf
Evo Cpg
GERP
phastBias gBGC
Primate Chain/Net
Placental Chain/Net
Vertebrate Chain/Net
CHM13 alignments
+   Neandertal Assembly and Analysis
+   Denisova Assembly and Analysis
-   Variation
dbSNP 155
1000G Archive
Array Probesets
dbSNP Archive
dbVar Common Struct Var
DGV Struct Var
EVS Variants
ExAC
Genome In a Bottle
Genome Variants
GIS DNA PET
gnomAD
HAIB Genotype
HapMap SNPs
HGDP Allele Freq
Platinum Genomes
-   Repeats
RepeatMasker
Interrupted Rpts
Microsatellite
NumtS Sequence
Segmental Dups
Self Alignment
Simple Repeats
WM + SDust
Invisible link