Tag | Content |
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EnhancerAtlas ID | HS133-07061 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:12713410-12715050 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SCRT1 | MA0743.1 | chr12:12714132-12714147 | ATGCAACAGGTTTTT | + | 6.41 | SCRT2 | MA0744.1 | chr12:12714132-12714145 | ATGCAACAGGTTT | + | 6.2 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_24918 | chr12:12711501-12716377 | Colon_Crypt_3 | SE_27729 | chr12:12710555-12717588 | Fetal_Intestine | SE_28607 | chr12:12710484-12717502 | Fetal_Intestine_Large |
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Enhancer Sequence | ATTAAAAAAA ATTTTAATGC AACTTTCCAC ATTGTCTTCA AACTCAGTAA ATTCCACAAT 60 TTTAAAAAAC AAAAACCTTT CACCGTGCCT ACTCACATTT TTACTAAAAT CCCTACACAG 120 AGCCATACAT TCTGCTTTTC ATTTTACTTC TCCAAGCTGC TGCCTTCACC AAATAGACTC 180 CACGAGCCTC CCAAGTGGTA TCCACCAATA TATGTGATAC TCAAGGAAAA GTAGGTATTA 240 AAGAGTAATT AATTCAATTG GTACGAAATC TTTTCTTTTA AAATTTTACC TTAACTTTAA 300 AAAGCCCTTT TCTTGATGGA GGTGAAACAG CATAAATCCT TTGAGGAAAC GGTTATCCTT 360 TACGTGGACT CTCCATCAGC CCCATAAGGT GAGTGGCATA AAGAGGCATT TTTCTGACAG 420 TCTCAGTTCC CCAAACACTA GTCCTAAACT TTTGCATGGA TGGTAAATTT CACACACACA 480 CACACACACA GAGGCGGAAA AGAAAGAAGA GAAAGAAACA TACCTGGTTT ATTTTCTAAA 540 CAGGTTTGAT AGGTTTGGTT CACTTGAAAG AGCAGAGTAT TTACTTATAA TCTTTTAAAA 600 CAGAAGTGGG AGCCAGAGCG CTGGGTAAAT AAAAACTTCA GAGAGTTTTA AAACCCTGCA 660 TCTTAACTCA CTTCCCTTTG GTTCAAGGGG ATGGCACAGC AAACCCCACG GCAAATGAGA 720 TTATGCAACA GGTTTTTTTC CTCCCCAGCT TATTCATCAC AGGCTGGTTA GAGGTGTGCT 780 TTCTCCAATC TGAGACACCC ACGACTTCAA AACGCCAAGA ATCCTTGCAG TTGATGTTTC 840 CTAAACTTCT TTAGGATTTT GCAGTATCCA TTCATTTTCA GATCTACTTG CCTTTTCTCT 900 GGTTCATTAT TGGTATTCTT TAGGAAATAA ACCCAGCATC TGAAAATATT TCCCTCTGTG 960 GTGTTTCATT ACATGAAACT ACACGTGATA CACAGACCCT GGGCTTTTTT ATTTCTCACG 1020 TTTTGCAGCT AGTGTAAATA AAGAAGTCAC TAGGCGTCGG GCCCCCCAAC GCCAAGACCC 1080 GAGCCCCTGT CCGAAAATTG AGGGCTTTTT CGGTTGGTTG GTTGAAGAAA GCAGCACCGT 1140 CACCACCCAG GTGGCCTCGC TGCTTACACC AAAGGCGAAC TGGGGATAAT GGGAACAGTC 1200 AGGCCAGGGC CCCACTTGGC AGGCGTGTTG TGTAACAGTC GCGCCTGGAA GTGAGCAGCT 1260 TCGCCCGCAA AGGTGCCGCG TCCCGCGGCG GCCGCTCCTC TCGGCGGGGC CCGGTCCAAG 1320 CGCCGCGCAG CGGCCGGGAG CGCACCCACT GCGACCCCGC GCCCGGCCGC ACGCCCCCTT 1380 CCCGCTCCGG CCAGCCTCCG GCCAGGCCTA CACCCCCGCT TCAAACGCTC CTGCGGCCCC 1440 CGGCCGCGGT CGCCCCCACG CCGCCTCCCG AAAGGGTGGC CGGTACGCCC GGGAAGGCAG 1500 AGACGGCGGG GCTGGAGCGC GGCGCCCGGC ACCGGGAGTC GGGGCGCGCT GCGGAGCGTC 1560 CATGCGGCCG GGCGGGAGGG CGCCCCGGGC CCCGCACCCT CCCGCCCGCA CACCCCGCGC 1620 GGCCCGCCAA GGCCACTTAC 1640
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