Tag | Content |
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EnhancerAtlas ID | HS101-39160 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:569480-570720 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:570099-570120 | TTTTTGTTTCTGTTTTTGTTT | + | 6.46 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24737 | chr7:569479-570097 | Colon_Crypt_3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I000529 | chr7 | 569480 | 570097 |
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Enhancer Sequence | AACACAGGAG GACCTTTTCC TTCATCACCA ACCATGCCCC CCCCCAGCCT CCACCCCCGC 60 CCCGAGGGAG AGGCCTGGGG AGCACAGGCT ACTTTCTGAG CTTCCGGAAG TTGCAGGTCA 120 ACCTGGCGGC AATTTGGCAC CAGGAGCCAC CAGTGTGGCC GCGGCCCCTG ACCCTGTAAT 180 CCCACATCGG GCACCCAGCC TAAGAAAACG ACACGTTTGC TTCAAGGGCT CAGAGCACCA 240 GGATTTAAAA CAGCAACTAG GAACAACCTA AGATCCTAGG TGCTCCGAGA TCAAGATGCC 300 AGAAAATAAA TCAAATCAAA TCAAATCCCA GGCGCAAACG GCCCTCGTGT TCTTACCCCT 360 CCTCTCGCTG TTGGAAATCG CGGCTCCATT TATGGGTGGA CAGAAAGACA GCCTCCTAGC 420 ACCGGGCTTA TAGCTTCCAC GCCCTGTTCT TCTCCAAGCC CTCGCCCGGC GCTGCCCGGT 480 CCTCAGGGCG CGACACGACG CTGCCCGCTG AGGCGTCAGA GCTTGGGGCT GCTTGTCACG 540 TTTCCTCCAC ACCCAGCGTC CGGATGCTCT GTGATGTGTT AATGTTACTT CTCTAAGAAT 600 CACTGTTGCT TCTGGGGTTT TTTTGTTTCT GTTTTTGTTT TGAGACGCAG TCTCGCTCTG 660 TCACCCAGGC TGGAGTGCAG TGGTGCAATC TCGGCTCACT GCAACCTCTA CCTCCCGGGT 720 TCACGCCATT CTCCTGCCTC AGCCTCCCGA GTAGCTGGGA CTACAGGCGT CCGCCACCAC 780 GCCCGGCTAA TTTTTTTGTG TTTTTCAGTA GAGACAGGGT TTCACCATGT TAGCCAGGAT 840 GGTCTCGAAC TCCTGACCTA ATGATCTGCC CGCCTCAGCC TCCTGAAGTG TTGGGATTAC 900 AGGCGTGAGT CACGGCGCCT GGCCCCAGAA ATGCTGTTGC TTCTGTTTTA TAAGAGGCAC 960 TGGGGCATGA AAAGCTATAT CTCTGATGGG GCTGTGTGCC TGGCGGGTCC TGCCTGGCTC 1020 TGGCCCCCAG GTGCCCTCTG AACGGACAGT GCTGCCTGGG GACGCCCCTG GCCACACAGG 1080 CCAGCCCCCG CCACTGGGCC AGCAGAGCTG GGCTTTAGAG TTGACCTCCT GCCGACTGTG 1140 TGACCTCAAG CAACTCACGC TGACGCCCTG AGCCTCAGTT TACCCGTCTG GGATGCGATG 1200 ACTGCCACTC CAGTGCTGCT GTGATGGGAA AAACAGAAGC 1240
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