EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS050-44579 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr22:30129070-30130210 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr22:30129076-30129086GTCACGTGAC+6.02
BHLHE41MA0636.1chr22:30129076-30129086GTCACGTGAC-6.02
MITFMA0620.2chr22:30129072-30129090GTCAGTCACGTGACCAAG+6.34
MITFMA0620.2chr22:30129072-30129090GTCAGTCACGTGACCAAG-6.34
USF1MA0093.2chr22:30129076-30129087GTCACGTGACC+6.14
USF2MA0526.2chr22:30129074-30129090CAGTCACGTGACCAAG-6.5
USF2MA0526.2chr22:30129072-30129088GTCAGTCACGTGACCA+6
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_65901chr22:30128976-30130779Pancreatic_islets
SE_66883chr22:30127747-30132023H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223012952830129628
chr223012920030129400
Number: 1             
IDChromosomeStartEnd
GH22I029733chr223012914930130450
Enhancer Sequence
GAGTCAGTCA CGTGACCAAG TGACACCCTC GGGATGAGGC CTGAGGGCCT GGAATACCAG 60
CCCCACATCG GCTGCAGACA CGGCCTTCCC ACTTCAGCTC CCTCTGCTCT GGCACACTCC 120
CACACCCCAA CATCCAGCCT TCAGGCAAGG TGAGGCCCTG GCAGCTCCTG GCAGGCTCAG 180
GGGCCCAGTG GCCAGCCCTC TGCAGAGAGA GAAGGGCTTG GGCCTGCGGA GAGGGGTTTG 240
GAGAGGCCTC TGACCTCCGA GGGGGAGGTG GAGAGCCGGG GTCAGGAGCC CTGGGAGTTT 300
CCCCTGCTGC ACCCACCCAA CCTGCCCCTC TCTGGACCAG ACCTGCCATG CAGAGTCAAG 360
GACTCCGGGG AGCTCTGGGT GCAGCCTCCA GGACCCCCAG GTGTGAGAGG ACAGGGACAT 420
CCCCTGCTTC ATGGCTCACT GCCTGCTAGA AAGTGCAGAA GGCAGCTCTT GACATGATTT 480
ATGGCACTGG GGAGATTTCA TAAACTCCAC CAGCCGCAGA GAAGGCGGGG AGGCTCCGCA 540
GTTGCTGGAA GGGAGTGCCC TAGCTGCCAG CCAAGCCTGG GCTCCCTGCA GGGCCACAGG 600
GACAGTGGGG ATCCCCAGGG AGGGTGTGAT CCTGGGGAGC CCCTTCCCCT GAGCCTCAGG 660
CCCTTCCTCT AGAAAATGGG GCAGATTCCT GGGAACCTGG GACCTCCTGG GTCCAAGTCT 720
CAGCCCCGTG CCCCTGCCTG CCCTGAGGTC CCGCCAGTAG ACAGGCATAC CCAGTGCCTG 780
CTCACACACA CTGGCACACT GCCAGGGCCC CAGACACGTG AGCCAAAGCC TTGGGGACAT 840
TGAGGTGCGT GTCTGGCACA ACTCTGCTCG TAGCTTCTCT GGTGACCTGT TTGTCCTGTG 900
CGTGAGGACA GGAGCCACTC TCTTGCATTT TCCCAGCCGC GGTCCTAATC AGAGGAAACA 960
GAGTCGAGGA GGAGGATGGG CCAGGATGGC AGCGCCCGCC CAGAGAGGGG TGCAAAGGAG 1020
AGATTAAGAG GGATAGAGTC GCAAACTGAA GAGCCAACAA TGGGCAGCAG GGCCAGGCCT 1080
GGCCTTGCCG AGGGATTAGT CTGTGTGTCT GAGGCCGCCG CTGCTCTTGA CAGATCCCTC 1140