Tag | Content |
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EnhancerAtlas ID | HS133-06538 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:110207730-110209270 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr11:110208625-110208642 | AAGGTCTTTGTGACCTA | - | 6.19 | ESR2 | MA0258.2 | chr11:110208626-110208641 | AGGTCTTTGTGACCT | - | 6.63 | NFAT5 | MA0606.1 | chr11:110209237-110209247 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr11:110209237-110209247 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr11:110209237-110209247 | AATGGAAAAT | - | 6.02 | STAT1 | MA0137.3 | chr11:110208376-110208387 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr11:110208376-110208390 | TTTCCAGGAAAGAG | + | 6.67 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I110336 | chr11 | 110207164 | 110211759 |
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Enhancer Sequence | GTGCCCGGCC TAAAGATAAC TGATTTTCTT AAACAAAGTC AATCGTATAA ATGCATTTGT 60 TTTTATAGCA TATATGAAAG TGTTCATGGA AAGGGATACC GATCCAGACC CCATTCTTTC 120 TTGCATGGAC CTCATGCAAG AAAGAATTCA GGGCCAGGCG CGGTGGCTCA TGCCTGTAAT 180 CCCAGCACTT TGGGAGGCCG AAGCGGGCGG ATCACAAGGT CAGGAGATGG AGACCATCCT 240 GGCTAACAGG GTGAAACCCC GTCTCTACTG AAAATACAGA AAATTAGCCG GGCGTGGTGG 300 CACGAGCCTG TAGTCCCAGC TACCTGGGGG GGCTGAGGCA GGAGAATGGC GTGAACCTGG 360 CAGGCGGAGC TTTCAGTGAG CCGAGATCCC GCCACTGCAC TCCAGCCTGG GCGACAGAGC 420 CAGACTCCGT CTCAAAAAAA AAAAAAAAAA AAAAAAAAGA AAAAAGAAAA GAGAAAGAAT 480 TCAAGGTGAC CCCATAGAGT AAAGTGAAAG CAAGTTTATT AAGAAAGTAA AGAAACAAAA 540 GAATGGCTCT TCCATAGGCA GAGCAGCAGC ATAGGCTGCT CAACTAATTA CACTTAACAG 600 TTGTTTCTTT ATTATATGCT AAACAAGGAG TGAGTTATTC ATGAGTTTTC CAGGAAAGAG 660 GTGGGCAATC CCCGGAGCTG AGGGTTTCTC CCCTTTTTAC ACCACACAGG GTAACTTCCT 720 GACGTTGCCA TGGCATTTGT AAACTGTCAT GGTGCTGCTG GGAGTGTCTC TTAGCATGCT 780 AATGCCTTAT AATTAGAGTA TAATGAACAG TCAGAATGAC CAGAGGTCAC TTTCGGCACC 840 ATCTTGGTTT TAGTGGGATT TGGCCAGCTT CTTTATCACA TGCTGTTTTA TCAGCAAGGT 900 CTTTGTGACC TATATCTTGT GCTGACCTCC TGTCTTATCC TGTGACGAAG AATGACTAAC 960 CTCTTGGGAA TGCAGCCTAG TAGGTTTCAG CCTTATTTTA CCCAGCCCCT GTTCACTATG 1020 GAGTCACTGT GATTCCAATG CCTCTGACAG AAGTAAAATA TATGATAACA TAACACAGAG 1080 GCTGAAAGGC CTATACTGTT ACAAGGTTCT CATGCAACAC ATGAAGTGGT ATAATATTAT 1140 TTGAAGATAG ACTGTGATGG ATTAAAGATG TATATTTTAA ACCCTAGGTT AAGCACTAAA 1200 AATGTATGTG AATGAAGTAC AAATAGTGAG CCAATAATAA AGATGAAATG GACTCATTAA 1260 AAATACCCAA ATAATCCAAA ACAATATAGA AATAGAGGAA AGAGGAATCA CAGAACCAAA 1320 AAGAAAAAAA AAACTACAAA AAATTAAGGC TGAGCACAGT GGCTCATGCC TGTAATCCCA 1380 ACAATTTGGG AGGCTGAGGT GGGAGGATCA CTGATGCCAG GGTTTGAGAC CAACTTCAGC 1440 AACATAGGAA AATCCCATCT CTACCAAAAA CAAAAACAAG TAAAAGAATC AAAGAACAGA 1500 TGGAATAAAT GGAAAATGAC TACGAGATGG AAGATTTTAA 1540
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