Tag | Content |
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EnhancerAtlas ID | HS133-01544 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:44508720-44510080 |
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) |
ESR2 | MA0258.2 | chr1:44509526-44509541 | AGGGCTTTGTGACCT | - | 6.3 | FOSL2 | MA0478.1 | chr1:44510016-44510027 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:44510016-44510027 | GGGTGACTCAG | + | 6.02 | NR2C2 | MA0504.1 | chr1:44509003-44509018 | TGACCTTTCACCCCC | - | 6.86 | Nr2f6 | MA0677.1 | chr1:44509003-44509017 | TGACCTTTCACCCC | - | 6.42 | PPARG | MA0066.1 | chr1:44509683-44509703 | GTAGGTGCCAGTGACCCATT | + | 6.95 | Rxra | MA0512.2 | chr1:44509003-44509017 | TGACCTTTCACCCC | - | 6.91 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59695 | chr1:44488673-44541066 | Ly4 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I044044 | chr1 | 44509981 | 44510130 |
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Enhancer Sequence | AACCTCCCTG AGCCCTTACT TGAGGCAACA TGTGTGAGCT CTTCACCTGT CTACATGTCT 60 GACCTGCTGG TCAGCCCTGA CACCAGAACC CCACGCTTGA GTCACTTAAC TAGCAGCAGA 120 GTCAGACTCT GAGACCATCC CTTTAGAGGG AGCAGCAGAG GAAATGGGAG CTGGAGGGGA 180 AGGGAGTGGT GGAGATGGGG GTGTGAACTG GGAGAAGCAG GCATGGGGGA AAACTCTGGG 240 CTGTCAGCCC CTAGCTATGG TCGGGAATGT TCCCAGGCAG CACTGACCTT TCACCCCCAC 300 CCGCCTCGGT GCGATGATTG GCTGTCTCTG CCATCCCCGC TTCCGGGACC AGAAGCCACC 360 TCTGGAGCAA CTGGGGCATC CCCATGGCAA CCATGCCAGG CCAGGTTGGG AGAGGTGTGG 420 GGCTCCTTCA CAGCCTTTTA TTGCCCCAAA ACAGGTTGAC ACTCTCGTCC TGGTAACCCT 480 CAGGGCCCTG CAGATCACAG TGTCCAGAGA GGAGGGGCTG TTGCTCCTAG CAGGTCTCTT 540 GATTCAGGAA AAAGCGTTTC TCTGGTCTCA GCCAGATCCT TCCTGGGCTG ATCTGTTGGG 600 AAACCCAAGC TCTCTGTCCT TGGGCCCCTA GCCCCTACCA ACACCCTCCT AGCGCATTCT 660 AGCAGGAGAG CGAGAGGGAG TGGAGACAGT CTGAACTCTT CCCTCTGCCC ACCTGGGTGT 720 GGGCTTGGTG AGATACTGAG GCTGGGGTGT CCACCTGAGT CCGTGGAGGG AGGAGCGACT 780 ACGGTGCGGT GGGGGCGAGG CCACTCAGGG CTTTGTGACC TAGACAGAGG ATTTATGTGG 840 GTGATTAGCT GTCACGTTGG GTCTAAGCTC CTTACCCTCA GAACCTAGCT TTCCTGCCTG 900 CCCCCAGGGC TAATCCAGAG GTGGGGGAGG GGCTAAAGAC ACTGGGCTCT GCCAGGGGCC 960 TTGGTAGGTG CCAGTGACCC ATTCTGTGTA ACCAGCTGTG GCCTGTTCTC TGTGTATTTC 1020 TGCTTTTGTG GGTTTCTCTG GCTCTTCCTG CCTTTGAATA TGTGCACCTG GGTTTCCTTC 1080 TATCCCTCTC TCCATGTATG CCTTCTGTGC TGTGAACAGC TCTGTGACCC TGACTCTGGG 1140 AAGCTGTGGT TGTTGGCAGA AGGCAGGGAC ACCACTGGGT AATGGGTCAC ACAAGTCTCA 1200 ATGACCGGAC TGTGGTTGAC AGAAAGTCTT GGGGACACAG ATTTGTAGCT GGCGTGGGGT 1260 TTTCGATAAC ACAGGGTCCA GGTGGCAATG TATTGGGGGT GACTCAGGGT TTGAGGGACA 1320 TGGGGTTATT TGTAGTTGAC ACACAGATTA GGTGAGCCTG 1360
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