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

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EnhancerAtlas ID
HS133-11524 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr16:58298720-58300010 
Target genes
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:58299789-58299807CCTGCATTCCTTCCTGCC-6.76
FOSL1MA0477.1chr16:58298986-58298997GATGAGTCACT-6.02
JUNDMA0491.1chr16:58298986-58298997GATGAGTCACT-6.32
Klf1MA0493.1chr16:58299597-58299608TGGGTGTGGCT-6.14
Stat6MA0520.1chr16:58299242-58299257GTTTCTCTGGAAGAG-6.54
ZNF263MA0528.1chr16:58299837-58299858TCCCTCCACTCTCCTTCCTCC-6.12
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr165829949058299730
Number: 1             
IDChromosomeStartEnd
GH16I058264chr165829808958300236
Enhancer Sequence
TATCAAACAC TGAAGTGTGA AACCTTGTTA AAGACATGCA GAATAATTGT CCTCTATACC 60
AAAAGTACCA ATACCTCCAC AAGGGTAGGC ACTGGGCTGA GTGCTAAGGG TACAGCATTT 120
AGACAGCACC AGGCAGAAAT GGGCTCTTCT CTTCTGTGAG TTTCATGTGT GAGCCTGAGT 180
CAAGGTGGCA GCTTTTTCTC TGACTTTATG CCCTCAAGCC CTGCCTGCTG GAGTCTGGTA 240
AAATGTAAGC ATGTGACTAC AGCTGCGATG AGTCACTCCA GACTGCCTGT AAACTAGTGA 300
TCTGGGGCCT TGTAGGTAGA ATTCTAAGAT GTCCCCAAGA ATCCCTGGCC CTTGGTGTCT 360
ACACCCTGTA TAATCTCTGG CCAGGACTGT GAATATGATG GATTCAGTTA AGTTCTGTTC 420
TGTTCAATGA TTCGGTTATA CTGTATGGCA CAGTTGATCT AAAGACAGGG AGATCACCCA 480
CTTGGGCCTG ATCTAATCAC ACGAGTCCTT TGAAAGAACA GAGTTTCTCT GGAAGAGGAA 540
GTCATAGATG TGAAGCATGA GGAGAAATGG CTGGAGGAGG TCTTCTCCAT TGTGGGCTAG 600
AAGACAGAGG GGCCACATGG AAGGGATTCA AGAGGGGCCT CTGGGAGCTG AGAGCGACCT 660
CCTGCTGACA GCCCAAAAGA AAACAAGGGC CTTGGTCCTA CAGCTTCAAG GAAGTGCCTT 720
CTGCCAACAA TAAGTGAGCT TGGAAGAGGA CCCTGAGCCC TTGACAAGAA CCACAGCTCT 780
GGGCGGACAC CTTGATTTCA GCCAGATGTG ACCATGGGGG AGAGTCCAGC CACACTGTGC 840
GCAGACTTCC GGCCTATGGA AGCTGTGAGA TAATAAATGG GTGTGGCTCT AAGCCACAAA 900
AGTCTGTGGT AATTTGTTAT GTAGCGATAG GAAGTGAATG CAGTCCTTTA CAGAAGTGGC 960
CTCCTCAAGG GACCCACATC TTGACTCAGC ATCACCAATT TCGCTCTCAT CAGCCTTCGT 1020
GGATACCTGC CCCGGCAGAG CCAGTGATGG CCTCGCTGCT GCTCTTGTAC CTGCATTCCT 1080
TCCTGCCCTG CCGCTCTAAG TTGGTGACCG CTTGTCTTCC CTCCACTCTC CTTCCTCCCA 1140
CCTGAATTGC TGGACTTGCG GCAAAGTCCT GCCCCATCTC CCCGGCCCCA CGTCTGACCC 1200
CATCAGTGTG GTCTCATTCA CTTTTGCTTT CCTTAGCAGA GCAACTTTCA TGCAGGACAT 1260
GGAACAGGAA ATGAGCCTTA AAGAAGTGAG 1290