Tag | Content |
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EnhancerAtlas ID | HS101-36856 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr6:18042600-18044090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:18043725-18043746 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Klf1 | MA0493.1 | chr6:18043031-18043042 | AGGGTGTGGCT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64611 | chr6:18042943-18043865 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I018042 | chr6 | 18042656 | 18044230 |
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Enhancer Sequence | TCCTGCAACA AAGAGAGCAC TTCTCTTCCT TTGTCATTTT CCCTGTGGTC TCTTAGGACA 60 CGCTAGGTCC CCTGCTTCTC TTCTTATATC CTCTCCTCTC CCCAAGGGGA GTTTCTTCTG 120 CATATTCATA GTTTCTGCTC CTTCTTTTCC TTGGCTTGGC CATCCTGGAC ACAAACCTAG 180 TTGTGATGGC AGCACACTCC ATGGAGCTGG TGAGAGCCCC ACCCCTTCTG AGTTGGGACA 240 GGAGCTCCCC GGGTGCTGCT ATAGCCGCCC AATGCAGCTG CAGACCCAGG CCTCCTGCTC 300 TACAGAGCAG GCAGGAACCC CACTCTCCTG GGTGGGGCTA CAGGAACCCA AACTGTAGCT 360 GTGGATTCAT CTGAGCCTCC CTGTGCTCTT GGGGGAGGGC TGGCAGCAGG CAGGATCTGC 420 CTTTCTGGGT GAGGGTGTGG CTGCAGCCAC CCTCCTAGAT GCGGGAGCCA GGTGTCTCTG 480 CAGCCTGCAC CCTCAGCAGC CCCAGGAAGG ACCCCCTCCG CTGCCCTGAG CCACCCACTC 540 CTCTGAGCTG TTCTAACACT AAATAAAACT CTTCTTCTCC ACCCTGCGCT TGTCTGTGTA 600 CCTCATTCTT CCTAGATGCA GGGTGAGAAC TCGGGCAAAG GTGCTTCGGC CGCAGAGGTT 660 TCCCACCAGA AAAATTGACA CCCCAGAGAT CCTGTAACAC TTGGACATCA GTGTCTGCAT 720 CCTTTTGTTT TCTGTTCTTT CTCCTGCTAA GTGACCCCTT TTCTTGTTAC TTTTCCATTC 780 AAGCTGCTGG CAGAAAGAAG CTGTCTGGCC ATGTTCAGGC TAGAAGTCAC AGTCAGCTCA 840 TACCTGCCTA GGTCAGAGGC TCCATCCGGT CCCACATCCA TAAGAGGCTG GTGGAAAACA 900 TGCTGCCTAA CCCCACCACT TTGACAAGTG GATGTCAGTG GGCAGGGCCC ATGGAGCCTG 960 CTCAGCAGAG CACTGTTGTT CCTGGAGGCC ATGCTGACTG CAGCAGTCAA GGCTTTAGCT 1020 GCTTTACCAG TGCTCCCCTC CAGAGCTCCG TGGCAGGGTG AGTCATGCTG TGGGAATCTC 1080 ACACTGGAAA TGGCCAAAAA GCTTCTATTT GCTTCAGTGT TAGTTTCTTT CTTTCTTTTT 1140 TTTTTTTTTT GAGATGGAAT CTTACTATGT CACCCAGGCT GGAGTGTAAT GACTCGATCT 1200 TGGCTCACTG CAACCTCCGT CTCCTGGGTT CAAGCAATTC TCCTGTCTCA GCCTCCTGAG 1260 TAGCTGGGAC TACAGGAGCC TGCCACCACA CCCAGCTAAT TTTTTGTATT TTTAGTAGAG 1320 ACGGGGTTTC GCCTTGTTGG TCAGGCTGGT CTCGAACTCC TGACCTCAGA TGATCCACCT 1380 GACTCGGCCT CTCAAAGTTC TGGGATTATA AGCATGAGCC ACCACGCCTG GCAATGTTAG 1440 TTGGTTAGCC TGAGGAAACT GACACTTTTC TGAGGGGTAG CTAGCATGGC 1490
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