Tag | Content |
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EnhancerAtlas ID | HS133-11524 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:58298720-58300010 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:58299789-58299807 | CCTGCATTCCTTCCTGCC | - | 6.76 | FOSL1 | MA0477.1 | chr16:58298986-58298997 | GATGAGTCACT | - | 6.02 | JUND | MA0491.1 | chr16:58298986-58298997 | GATGAGTCACT | - | 6.32 | Klf1 | MA0493.1 | chr16:58299597-58299608 | TGGGTGTGGCT | - | 6.14 | Stat6 | MA0520.1 | chr16:58299242-58299257 | GTTTCTCTGGAAGAG | - | 6.54 | ZNF263 | MA0528.1 | chr16:58299837-58299858 | TCCCTCCACTCTCCTTCCTCC | - | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I058264 | chr16 | 58298089 | 58300236 |
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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
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