Tag | Content |
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EnhancerAtlas ID | HS133-20585 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:40297460-40298450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr21:40297638-40297648 | TTTAATTAGA | - | 6.02 | REST | MA0138.2 | chr21:40297784-40297805 | TGCAGCACTGGGGACAGCCCC | + | 6.22 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_02217 | chr21:40296549-40299270 | Aorta | SE_03066 | chr21:40297453-40297905 | Bladder | SE_03066 | chr21:40297922-40298364 | Bladder | SE_24315 | chr21:40297520-40297888 | Colon_Crypt_2 | SE_24315 | chr21:40297948-40298367 | Colon_Crypt_2 | SE_26446 | chr21:40297106-40298938 | Duodenum_Smooth_Muscle | SE_26838 | chr21:40296860-40298551 | Esophagus | SE_32103 | chr21:40297462-40298468 | Gastric | SE_50281 | chr21:40296792-40299484 | Sigmoid_Colon | SE_51455 | chr21:40297003-40298933 | Skeletal_Muscle | SE_52609 | chr21:40297095-40299117 | Small_Intestine | SE_56762 | chr21:40297467-40298333 | VACO_400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I038925 | chr21 | 40297200 | 40298763 |
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Enhancer Sequence | AATCAACCAT GCACTGCTGT CCTCCTTGCA CACCACTGAA GAGGCTCCTG CCTTCTTTGG 60 CGGTCCCTCC ATTCATATCC AGCATCATAA GATGTCAGGC ACACATCTCA GCCTGCTGTA 120 TTCCCAGCAG AGGAGGCAGA GCCAGGACAC CAGCCCATTC TTCCTAACTA ATCTGCCGTT 180 TAATTAGACC AGTTCTTCTC AACAACGGGG TGCTGTTTCA CCCAGGGGAC ACTGGCAACC 240 TCTGGAGGCA TTTTTGGTTG GCACAAATGG GGCAGGGGTG CTTCTGGCAT CTGGCAGGTA 300 GGAACAGGGG TGCTGCTAAC ATCCTGCAGC ACTGGGGACA GCCCCCCACA CCAGAAAACC 360 ATCCCATCCA AAATGCTAAC CCATAGATCA GAAGGAAGAT GAGCCTGGGG AGAAAACTAG 420 AGAGGATTTT GCTCCAGAAA AAAATGACCC ACAATAAAGC TGGCTCAGCT CCTTTCAAAA 480 TTAAATACCT TCCTTCTTTG TCACACACTG GAAAACGAGC GAGTTTCTAT TTCAGGCTGT 540 GGGGTGAGTT AGCGTCGGCT TGGCCGGCTG TCTGGCAGAG GCTCCGATTC ATCAATGACA 600 GCTAAGTGTG GTTTGCTGTG TGTCAGGAGA AGGTCCAGGA TGGGCTGGGG CAGGGAGTGT 660 GGGGGGCAGA CCACCCTCAT CTCTGGGGCT GCTGGAGCTT CCGGAGCCTG GAGCACACCC 720 AGCCTGCTTC TCCTTGTGGG AAGTGATTAA ATGTGAAGCT TAAAGCTGTA AGGACTTCCT 780 GGCATCGCGG GTTTTTACTT CTGAACTTGT TCCCCCCTCT CTTTACTTGC CCTCTGAAGC 840 TCCCAAATTC AGGGCCAGGC ACAGTGGCTC ATGCCTATAA TCCCAGCACT TTGGGAGGCC 900 AAGGCAGGTG GACTGCTTGA GGCCAGGAGT TGGAGACCAG CCTGGCAATA TAGCAAGACC 960 CCATCTCTAT AAAATAAATT AATTAAGCTC 990
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