UCSC Genome Browser on Human (GRCh37/hg19)
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chr1:42,844,193-42,844,315 123 bp.
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  Click on a feature for details. Shift+click+drag to zoom in. Click grey side bars for track options. Drag side bars or labels up or down to reorder tracks. Drag tracks left or right to new position. Press "?" for keyboard shortcuts. Use drop-down controls below and press refresh to alter tracks displayed.   move end
  
-   Custom Tracks
CHP2_Designed
MDsanger
IAD105428_Designed
-   Mapping and Sequencing
Base Position
p14 Fix Patches
p14 Alt Haplotypes
Assembly
BAC End Pairs
BU ORChID
Chromosome Band
deCODE Recomb
ENCODE Pilot
Exome Probesets
FISH Clones
Fosmid End Pairs
Gap
GC Percent
GRC Incident
GRC Map Contigs
Hg18 Diff
Hg38 Diff
Hi Seq Depth
INSDC
liftOver & ReMap
LRG Regions
Map Contigs
Mappability
Problematic Regions
Recomb Rate
RefSeq Acc
Restr Enzymes
Short Match
STS Markers
-   Genes and Gene Predictions
UCSC Genes
NCBI RefSeq
CCDS
CRISPR Targets
Ensembl Genes
EvoFold
Exoniphy
updated GENCODE Versions
H-Inv 7.0
HGNC
IKMC Genes Mapped
lincRNAs
LRG Transcripts
MGC Genes
Old UCSC Genes
ORFeome Clones
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
Publications
COVID Rare Harmful Var
CADD
ClinGen
ClinGen CNVs
ClinVar Variants
Constraint scores
Coriell CNVs
COSMIC Regions
DECIPHER CNVs
DECIPHER SNVs
Development Delay
new Dosage Sensitivity
GAD View
GenCC
Gene Interactions
GeneReviews
GWAS Catalog
Haploinsufficiency
HGMD public
Lens Patents
LOVD Variants
MGI Mouse QTL
OMIM Alleles
OMIM Cyto Loci
OMIM Genes
Orphanet
PanelApp
Polygenic Risk Scores
new Prediction Scores
REVEL Scores
RGD Human QTL
RGD Rat QTL
SNPedia
UniProt Variants
Variants in Papers
Web Sequences
+   mRNA and EST
+   Expression
+   Regulation
+   Comparative Genomics
+   Neandertal Assembly and Analysis
+   Denisova Assembly and Analysis
-   Variation
dbSNP 155
COVID GWAS v4
COVID GWAS v3
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 Chain
Simple Repeats
WM + SDust
Invisible link