Tag | Content |
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EnhancerAtlas ID | HS101-11265 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:104547580-104549010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:104548113-104548134 | ATATGAAAAATGAAAGAAAAA | - | 6.25 | IRF1 | MA0050.2 | chr12:104548070-104548091 | AAAAAAAAAAAGAAAGAAAAC | - | 6.33 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 104548642 | 104548712 | chr12 | 104548117 | 104548490 |
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Enhancer Sequence | TTTATGGCAC TAAAATAGAG CTTTTACAGG ACACCTGATC ATTTAGAAAA CTATTAGGTA 60 GGTGGGGCAT GGTAGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCAT GGTGGGAGGA 120 TTTCTTGAGC CCAAGAGGTC GAGGCCACAG TGAGCCAAGA TTGTGCCACT GCACTCCAGC 180 CTTGGCAACC AGAGTGAGAC CCTGTCTCAA AAAAATCAAA AAAGGCCAGG TGTGGTGGCT 240 CATGCCTGTA ATCCCAGCAC TTTGGGAGGT TGAGGCAGGC AGATCAAATG AGGCCAGGAG 300 TTCAAGACCA GCCTGGCCAA CACAGTGAAA CTCCATCTCT ACTAAAAATA CAAAAATTAG 360 GTGGGTGTGA TGGCACATGT TTGTAGTCCC AGCTACTCGG GAGGCTGAGG CACAGGAATC 420 TCTTGAGCCT GGGAGATGGA GGTTGCAGTG AGCTGAGATC ACGCCACTGG TGACAGAGGG 480 AAACTGTCTC AAAAAAAAAA AGAAAGAAAA CTATTATGTA GAAACCCTAC CTAATATGAA 540 AAATGAAAGA AAAATGAAGG TGAGTAGCAG GGCAAGAGCA GGAAATGCTG GGTGGGGAAC 600 AAGAAGGACT GTGATTTGGA CCACGATAAG GTTGCTCACT GAGCAGCGGA AAGTTCTCTA 660 ATGGGCAGAT CCAAGGGGCG GTTCAGCTTG GAAGGGCTTC TATGAGCAGA AGTGGCCTAA 720 AGACTGTTGT GCTGGCTCTC CACTTCCTCA TATTTCAATT GTTGCTCTAG ACCAGAGGGC 780 AGCAAACCTT CTTTCAGGGG CAGATAGTAA ATACTGTAAA CTTTGCATTG CGACAACTCT 840 GGGCATGGTG GTGTGCACCT GTATTCCCAC ATCTTACACT AAATTGATTC CAAATGCCCT 900 ATTCATGGCC CTCTTGCCTG ACAGCTGCCT CCACTACCTC CAACAGTGGC AGAAGTCAGT 960 GGCCATGTTT GTTTAAGGAT CTTAGCACTG TAATCATAGC AGGCACTTAT AAAAATAATT 1020 GTCAATATAG TCAATAGAGT AGAATTCTCT TGTGAATACA GCACACACCT GTCTGCCCAG 1080 CATGCCTTTT CACTCTTCTT TCGGTGACAT TGCTCTCCTT CTTTGGGGAT AATTGCTTTT 1140 CCCCCACCTC CAACTACATG ATCCTAGAGG GTGCAGCCAA TCCTATTACA CGGTACTTGA 1200 CACAAGCCAG GCTGATTACA GTACCTCACC TCCCCCAGCC ACAGGGATTA GCTTGAGGAG 1260 TGGGCCAAAT CAGGCCAAAT AGGATCATTC TATTGGGTTT TAAAATCTAG ATCTAGTGGA 1320 AGAAAAAGCA AACATTTACT TTGCTCCTAG GTGACAAAGT CATGATGTGA CCCAGAATTC 1380 CCAACAGATA CCTCCCTTGA GATATAGAAA ATACTTGTCT ACATAGGAAA 1430
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