Tag | Content |
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EnhancerAtlas ID | HS179-10053 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr12:130091370-130093280 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:130091606-130091627 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | IRF1 | MA0050.2 | chr12:130091584-130091605 | GCTTAGTTTCTTTTTCTTTCT | + | 6.36 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I129607 | chr12 | 130091623 | 130093048 |
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Enhancer Sequence | AACTCTCTAC CAAAATGCTT GTTATATGAT GTAACTCTCA AAATGCTACC TGATTCTAAA 60 GAATGCATTT GCTCATAGAA CAGTGAGAGG TGGCAGGTGC ATTGTTCATT CTCTTGGATT 120 TCCAACGAAC ATTTATTATG CTTTTCTGCA ATTGTTACTT TCCTTGTCTA TCTTGGAAAT 180 GAAGAAACTG TGTTCTCATC TCTGTGTCTC CACTGCTTAG TTTCTTTTTC TTTCTTTCTT 240 TCTTTCTTTT TTTTTTTTGA ATAGTCACTC TGCAATTGGG GAGGGTCGCA AGATTACCTT 300 GTTCAACAAT TTGTTAGAAG AACTCACAGA ATGTGGCAAA GCTGGTATCC TCACCATCAC 360 AGTTTATTAT AGCGAAATGA TACCGATTAA AATCAGCAAC AAGAAAGAAA AGGTGCTTAG 420 GGTAGGATCT CTGGGAGCCT GGGTGTAGAA CTTCCAGTTC TCTCCCAGTG GGTCACGCAG 480 AGTGGGCTCA TTCCTCGCAG CAAAAACCTG CGATCGCATG CACAGAGTAC TGCTAACTGG 540 GGAAACCCCT CTGGAGCTTG GCATGCAGAA TTCCTACGAA GGGTTGCTCC CACGGTCAGG 600 GCTGACCACC TGCAAGGCTG ACCTCAACCT CTAGCTCCTC CAGAGATGAG TCAATGTTGG 660 GTGGATCAAG CCTCCACTAT AAATTCATTT TTAGCATAGA CTATCTGTCT TGGCCCAAGG 720 TCTCCAGATA AACAAAGACA CTCTTACAGG CAGGAAATTC CAAGGGCTTA GAGGCTACCA 780 CCCAGGAGGC CAGACAAAGG GCCAAGCCTT TTTCTGGTGC AGTTAACCCT TGACTGCACA 840 CACTGAGTGT TCATTCAATA AATAGAATGA CCGACTACAG GATGAATAGA TGAACAGAGA 900 CCAATTCCAA AATGAAGACG TATTTTTAAA TGCCTTTTTC TGTGTTTTGG AGTACCTGTA 960 GATTTCATAC CAGCTTTCCC CCACTACCCT CTAAGATATA GAGGCTGCTT GCTGAGTTTC 1020 TCATGGCATA AATCCAGCTT TTAATTCCAC CCATCAACTT ATAGCATACT TTTCAAGCCC 1080 AGAATCACTA TTGCTCAAGT GTATTGTACC AGATAATCAC ACTCAGCCCC CAGTGAATGT 1140 GCTGACTGCG GCGGGGGAGG AGCCGACAGA TCAGCGTTGT TTCTGTGGAG TCTGTGAAAT 1200 ATTGATTGCT GTGGGGGAAA AACAGATAAC ACATTGCAAG AAGAATAGAA TAATCACCCA 1260 CAAACCCCTG GCTTTTAAAC TAAAATCACT GTGAAGGAAC AGCGAAGTGT GTTTTAAGGA 1320 GTTTTATCTA CCCCTCTTCA TCCTGAAGCA GCAGAAATAA GAACTCTGAT GTTTACTCAC 1380 TTGAAGTGCA CTGGCTTTTC AATTAACGGA CCAGAAGAGT TTGCAAAGAC TATCAAAATA 1440 CCAACTTTTC TGCAGGGAGT GAGCTGTGAT GCCCAGACTA GGAGACAGAC ACTCTCCCTT 1500 TAGAAGCCCA ACCTAATTTC AGTCTGGACT AGGACTTGTT GCTGTTTTCA GTCTGCAAAA 1560 ATGAGGCCTA ACTATGTAGA TGATGAATGA AGGTTCGGTT GTCACTAAAA AGGGTACCAA 1620 GGCTCTGAGA CAGGTCAGAG CTTAGACAAC CAAAGCTCCT ATTTGGCAAA TATCTGACAC 1680 TGTTGATGAG AGACTGGCTT GCTCGCTGGA TGGAAATGCA GTCAATTTTC TTCTGAAACC 1740 TCTAAGCATT CTCCTTGATA TCCACTGTTT CTGAAAAAAT CATGTCGCGT TTACAGCTAA 1800 GAAAGAACCT ACATATTCCG TAGAAAAGCA GGTAGCCTCT TTTAATGGGT AAGCCCAAAA 1860 TATCAAAGTT GATGAAGCCA TCAGCTCCGG CCTTTCTCCG TCTGTCATGC 1910
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