Tag | Content |
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EnhancerAtlas ID | HS101-14287 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr14:103533740-103535660 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr14:103534921-103534936 | GGAGACCAAAGGTCA | + | 6.2 | Nr2f6(var.2) | MA0728.1 | chr14:103534414-103534429 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr14:103535081-103535102 | GGAGCTGGGGGAGAGGGAGGG | + | 6.6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27372 | chr14:103531251-103535619 | Esophagus | SE_34836 | chr14:103530923-103535742 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103065 | chr14 | 103532068 | 103535052 |
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Enhancer Sequence | AGTGACGCAT GACTAATTTT TTTTTTTTTT TTTTGATACA GGTCTTGCTC TGCCGCCCAG 60 GCTGGAGTAC AGTGGCACAA TCTTGGCTCA CTGCATCCCT GACCTTCCGC ACTCAAGTGA 120 TCCTCCCACC TTGGCACCAA CACCCCACCC CCTGCCCCTT CTCACGTAGC TGGGACTACT 180 GGTATACACC ACCATACTTG GCTTTTTTTT TTTTTTTTTT GCATTTTTTT GCAGAGTTAG 240 AGTTTCATCA TTTTGCCCAG GCTGGTCCCA AACTCCCAGG CTCAAGTGAT CTGCCTGCCT 300 TGGTCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCA CACCCAGCTG TGACTGTACT 360 TCTTGCTCAA TGTTTTTTAT TATCAGGAAA AGGGAAGGGA GCTCATTAAA GACAAGTCAT 420 AAAGGAATCA GATTCTGAAG GAACAAAAGT TTGGGTTATC TCACTAAGGC TGTAAAAAAA 480 CAAAAAGGGC TGGCCAGGCG CGGTGGCCAG CACTTTGGGA GGCCGAGGCA GGCAGATCAC 540 TTGAGCCCAG GAGCTAGAGA CCAGCCTGAA CAACCTAGTG AGACCCCCCT CTCAAAAAAA 600 TACAAAAGCT AGCCAGGTGC ACTGGCTCAT GCCTATAATC CCAGCACTTT GGGAGGCCGA 660 GGCAGGCAGA TCATGAGGTC AGGAGTTCAA GAACAGCCTG GCCAACATAG TGAAACCCCA 720 TCTCTACTAA AAATACAAAA ATTAGCCAGG CGTGGTGATG AGTGTCTGTA GTCCCAGCTA 780 CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AACCCGGGAA GGCTGAGGTG GGAGGATCAC 840 CTGAGCCTGG GAGGTGGAGG CTGCAGTGAG CCGTGATTAC ACCACTGCAC TGCAGCCTGG 900 GCGACAGAGT AAGACCCTGT CTCAAAAGAG AGAGAAAAAA AGTGTTGCTG CGGAGCCAGC 960 CGAGGGGAGG GGCCATAGGA TGGCGGCTGA GGAGCGCTGC CTAGGCAGCA TGGCTGGGGG 1020 GCATCCGTCA GCGGGCTGCT TCCCTCCTGC CCATTCCCAC CCCCTCCCAC CTTAGTGAAG 1080 AGGCTGGCAG TGCCGGGCTC TCAGCCTTCA GGTTGGTGCA CACACAGTCG AGGGTGATGG 1140 GACGTCATTT GCCCTGGGTG CTGAAGACAC AGGGCAAGGG TGGAGACCAA AGGTCAGCAG 1200 GGTGGATAGC TGCTGGATAG CTGCCTCTGC CCCTCCAGAC CCACTCTCCA TCCTGCTCTG 1260 TACCCCAGGT GGGCTGCGCC CACAGGCCAC CTGGCCCCCT GACTGCTGGG TTTGGCCAAT 1320 GGGGCCTCTG GCATGTGGCT GGGAGCTGGG GGAGAGGGAG GGAATACTCG TTCCCCACGT 1380 TCCCCAGGAG CTGCGCCTTG GCCACATCTT TCTTCTGAAG TCTGGGGTCC CTCTCCTCGG 1440 AGCTCCTCTC TCCAGGATCC GGCCACTCCT CCCTCTTGCC GTCCTCAGAG GACCCAAAGG 1500 TGGAAACAGC TCCCACCCCT GCCTGACTTG CTGGCACCCT GCCCACACCT CGGTAAGGTG 1560 GCCTCTCTCA TCCTCTCCTC CATCCCCTGC GTCAGTGTGA CCCCTTCTGG GACTGCCTAA 1620 GACGCGACAT GCACAGTGAC ACTCATAGCG GTGCTCCTCG TTTTAAAAAC GAAAGCTTAG 1680 GCCAGGCACG GTGGCTCACG CCTGTAATCC CAGCAATTCA GGAGGCTGAG GCAGGCAGAT 1740 CACGAGGTCA GGAGTTCGAG ACCAGCCTGG CCAATATAGT GAAACCCCAT CTCTACTAAA 1800 AAATATGTAA AAATTAGCCA GGCATGGTGG CATGCTCCTG CAGTCCTAGC TATGCGGGAG 1860 GCTGAGACAG AAGAATCGCT TGAACTCGGG AGGCGGAGGT TGCAGTGAGC TGAGATGGAG 1920
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