Tag | Content |
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EnhancerAtlas ID | HS113-19022 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr2:33347850-33349280 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr2:33348393-33348404 | TGTGGATTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr2:33348808-33348829 | CCACCCTCCTCCTCCTCATCT | - | 6.47 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01563 | chr2:33346961-33348621 | Aorta |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I033123 | chr2 | 33348521 | 33348531 |
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Enhancer Sequence | CTCCATGAGG TTTGGCTTAT ATGGCCAGCT GGTTCTGCGT TCTGGGTTCT CTTGAGACGT 60 CTATCTCCTT CTTGCTGTAC ACAACCGCAG TTGAACATCC TGTTGCTTGA GATAATGTGC 120 ACCCCCTTGT TTTGTAGGCA AGAGACCTCA GCTAATACAA GTTCTATTTC TACTCTGCTC 180 TCTAACAGCT GCATGTCCTG ATTACACAAA GCACCAAAGC TTGACTTCTA GAGAGGGAAA 240 ACCCAGCTGC TCAACTTTTC CTCACTCTCT TTATAGCTTT TCCTCACTCC CTTTATAGCT 300 CTTAGTCCTG TCCACATTCC CTCTTTCCAC ATAGAAAGAG GAGTGGGTGG GTCAGTTCCA 360 TCAGTTCCCT GAGACCCCTG CAACACTTGG AGAATTGTTC TGCCTGGCCT GCGGGTTACT 420 AGGACCTGAT GGTATTGCTG TATTCATGTC TAAGCTTCCA CTGGAATTTT TAACAGAAAC 480 ATTCTCAGGT CTGGGGGATT CTTGCCCACA TGGAATGGAG AATGTTCACC TTCAGTCAGT 540 GAGTGTGGAT TGGGAAACCT TTTCAGTAAG ATTCCTGGAA TCCTATCATG CCTCCTGTTC 600 ATTCATCTTT TTTTTTTTTG GTATGGGTTT TCTGGCAACC ACAATGCAGT ATGTGTGTAA 660 GTACATAGCA GGCATGCTCT GCCATGTCTT GAACATGGAA ATCTAGCAAA ATTAGATGCC 720 TCTCTTTGAA AGGGTTTTTC AAAGACTATT AATGGAGAAA GTGATTCATG GTGTTTCTTG 780 TCAGAGATCC CAGTTTCCAA ACCACATCTT AATATACCTT AAGAACATAT ACTCTGAGCA 840 AGAAAATACA AACAGATGTG CTGAAGGCAT TGTGAATTGT ATTCTTGTTA TCAAAGATCA 900 GGTAGTTAGG AAATTTGGAC ATAGGCTTCT TTGTCCCAGC AAAGACATGA GGTAAGTTCC 960 ACCCTCCTCC TCCTCATCTA TTTAGCACTT TCTGCATGCC AACCATGGTA CTAAGCACTT 1020 TATATGCATT AATTAAGTAT GTTACATTAT AATACTTGTA TATTACTTGA TTACTACTTA 1080 AAATGCATTC CTTAAGTTAG GAACCAAAAA TTGAATTTAA AATTACAGAA ATCAATCTTA 1140 TTCATTGAAA AAAAGTACCA CTTTAGCTCT TTGTGTAAGT TATCTTTAGG CAAGTGCAAA 1200 GTCAAGATTT GACTATATTT TAGATATTTT AAAATTGTAT TATATTTTAG ACTTTTAACA 1260 CAATAACATG TTTTAAAAAT TTGTTATGTG ACTATAGAGC TGCTAACAAG AGGTGTTTAG 1320 CTTAACAAAA ATTACTCAAA TGCGGCCAGG TACGGTGGCT CACGCCTGTA ATCCAGGCAC 1380 TTTAGGAGGC CAAGGCGGGC AGATCACTTC AGGTCAGGAG TTCAAGACCA 1430
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