Tag | Content |
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EnhancerAtlas ID | HS101-14303 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr14:103711630-103713050 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:103712923-103712944 | GTGTACTTTCATTTTCAATAA | + | 6.41 | JUND(var.2) | MA0492.1 | chr14:103712191-103712206 | CATGACCTCATTCTT | - | 6.25 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103245 | chr14 | 103711808 | 103713700 |
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Enhancer Sequence | CTCGAACACC TGACCTCAAG GGATCCACCA GCCTTGGCCT CCCAAAGTGC TGGGATTACA 60 GGTGTGAGCC ACCGCACCCA GCCCATTTAA CTTTTTGAGT GATTTCTAAT TAATTTCCCA 120 CTTCTCGTCC TGGTCTGAAG AATAAGGTAA CTGGCTGCAG ATCAGCTTCA GCTGGGGATC 180 TCCAGGTGGA AGGTACCCAT GCATGCAGGA CTGCCTTTTT ATTTATTTTT TTTAATTTTA 240 CGTTAAGTTC TGGGATACAC ATGCAGAACG TGCAGGTTTG TCGCATAGTA TACATGTGCC 300 GTGGTGGTTT GCTGCACCTA TCAACCCAGC ATCTAGGTTT TAAGCCCCAC ATGTATTAGG 360 TATTTGTCCT AGTGCTCTCC CTCCCCTTGC CCTTTACCCC CTAACAGGGC CACGGTGTGT 420 GTTTTTCCCC TCCCTGTGTC CTTGTGTTCT TATTGTTCAG CTCCCACTTA TGAGTGAGAA 480 CATGCGGTGT TTGGTTTTCT GTTCCTGTGT TAGTTTGCTG AGAATGATGC CTTCCAGCTT 540 CATCCATGTC CCTGCAAAGG ACATGACCTC ATTCTTTTTT ATGGCTGCGA GGACTGCCTT 600 TTTAAAATGA GAAATGTGAA TGCATGAGTC AGTGCCTTTG AGTTTAGCTG CACAAGGAAT 660 TGGTAAACAA TCCCCAACAT GGGCCCTTCT GGTGAGCTGG AGGGAGTCCC TTATTTGATA 720 GAAAGAGTCC TTGATTTGAT GTCTTTTCCA AGAATCAAAA CCTCCTAGTT GCAGGCCATG 780 ACCTCTGATG TCTTCGTCTC CTGGGTGCTG ACTCTTCAAA GAATCTTTAA TTTAGAGTTT 840 TTAGTGAGAA GCTGTATAAG GCCTTGCAAT CATGAAGAAT GTCACCTTTA GGGTGAGCTG 900 GTTCACTGGG CTCCTTCCTC CAGGCACATG GGGCTTCCTG CAGTTATTTC AAAGGGAGAA 960 AGCTGAGGTT TTCCAAACAG GTAGAAGGTA ATTTAAGCAA TACCAATGGA AGAGCCTTAG 1020 GCAAGACAAG GTTCAAAGTT TCTGTAAACT TTGCCATTTG TTCTTGTATC CATTGTGGCA 1080 GGAAAATAAG GTCTGGAGGC AGGGAACATA AGGCCAATTC ACACTTCAGC TATAACAGGA 1140 AATATCCTCT CCATATGGCA TCACTTTACG TCATCCTCTT CATTTACACA GGGTGTACCC 1200 CAAGTAGAGG GTATTTAAAC TCACATAAAC TCACAAAAAC TCTGTAACAG GGCCTTTGAG 1260 CCCCTATGCT CAGGCCCACT ACCACACTGT GGAGTGTACT TTCATTTTCA ATAAAACCCT 1320 TCATTCGGCT GGGTGCAGTG GCTCACGCCT GTAATCCTAG CACTTTGGGA GACGAGGCAG 1380 GTGGATCACC TAAGGTCAGG AGTTCGAGAC CAGCCTGGTC 1420
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