Tag | Content |
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EnhancerAtlas ID | HS059-14566 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:90107460-90108890 |
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) |
IRF8 | MA0652.1 | chr14:90108039-90108053 | TTGAAACCGATACT | + | 6.08 | ONECUT3 | MA0757.1 | chr14:90108429-90108443 | CCAAAATCAATAAA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_18566 | chr14:90104619-90109188 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I089641 | chr14 | 90107421 | 90108736 |
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Enhancer Sequence | TTTCAGTGCA TTTTCATTAC CTTCGGCCTC TGAAAGAGTT GAGAGAGTAC AACTTAGCTT 60 CAAAGTTATG GTAAATATTT GTTGAAAGAA ATAATTATAC TCTGTGCAAT ATTGGATTTT 120 AAATGATCAA AAAATTAAAA AAACCACAAA TTCATTGCTT AAAAATATTT CACTATCAAT 180 CTGAATTCAA ATAAAGAAGC AGCTTCGTTG GCAGACTAGT TGGCTCAGTG AAAAATGAAT 240 GAGCAGAAAT ATTTTTATCC AAATTATTGT AGCTGATGCA ACCTTCTTTT TAAAAGAGTG 300 TTTTAAATTA AAAGACCAAT CATTTCTTCA TCATCTAGAG GGGGAAGAAA CTTGTAATGT 360 AAAATCCTAT TTACTGAGTT GTTGGATAGG ATAGTAAAAT TCCACAGATC TGGGTTTACA 420 CACACACACA TATGCACACA CATTTACAAT TGTATTGCAC AGACAGCAAG TGTGAGTCTT 480 GCTTCTACCA ACGCAGTACA AAAGGAAGCT GAGAGAGTCA AGGGAAAACC CTGTCCACGT 540 TGTGTTGACA CAGTTAGAGT AAAGTGAAAG AGTCAAAGGT TGAAACCGAT ACTAAGACTA 600 CTATCAGATT TCGCAGAAAA GAGCTCTTCT AGGTACTGCA GATAAAATAA TACTCCAATA 660 ACTGATCGAT CATTCCTTTT ATGAAAGTAC CACTGAGTTG TTTGTGAAAC CCTCAGTAGC 720 TTTAAAAGAT ACTCCAAATA TCATATCCCA GATATTGTTC CACCTGTCTT TTCAGAAAAA 780 GAAGCAGAAA AAGAACTGTA CCTTTCTCCA TTGCCTGTGT CCGGTAAACT CTTGGCAACA 840 ACATGATAGA CAACCACTAG CACTATTTAA CCTCTTTGAG CCTCCATTTC CTGATCAGTA 900 AAATGAAGCA GGTGATCACT TGGGAATCCC CTGGAGTCTT TGAAATCATA ATTCTAAGCT 960 TTGTCAAAGC CAAAATCAAT AAAAAGAAGA AAATAGGTTC TAAGATAACG CGAGACTAGC 1020 TTTATTTTTT TCTGTGCTTG GGCAGAGCTG TGACCAGCCA CCTGGAACAT CATATTGGAT 1080 TCTGACTCCC TTTCTTTCTG CCCCAAATTA AAGTACCTTT TCTTTGGTAT TTCACTGAAT 1140 CTTTAAAGTA GTCAATAGTA AACACCATTT TGTAAATAAA GTTGTCTCAT CTGGTAACTA 1200 CAAAATACAA ATATATCTTT CAGACACGAT TTCAGATGAA TTCTTCAATG CAAATGGAAA 1260 TGACTTTTTT CAATGTATTA TTAAGAGATG GTAGATAACT AGCCTAATGC AAAGACTTGA 1320 TCTAGTGTAA GGTCAGTAGA CAAAAGACCA CCTGTGAAAA CCAAGGGTTG TACCCTTTTA 1380 GTACGGGGAA CTTTGTCTCC TGTTGGCCTA AAACCAGTTT ATGAGGTCTT 1430
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