Tag | Content |
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EnhancerAtlas ID | HS012-15788 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr2:3328370-3329550 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr2:3329380-3329398 | GGAAAGAGAAAGCATATC | + | 7.19 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 3328429 | 3328567 | chr2 | 3328864 | 3329518 |
| Enhancer Sequence | AAAGCCGACC CTGCCCAGGG CACCACTTGT TTGTGAAGCA TTTCGTGACC ACTCGTCACT 60 CTAATAATCA GTCTCTCAGG ACGTCCTCAA CTCTGGTCAG TGGGATGATG CAGTAGGCAG 120 GAGGCCCGCT GGAAGATCCC CAGGATCCAG CCTCGTGGGC CCCGGTCACG CCGGGGGGAG 180 TGCAGGCGGC CTGCGCGCTC AGACTTCCGA AGTGGCCGCT GCCGCGCCTC CAGCACCTCG 240 GGGGGAGGGC CTGACCCTCA CCAGGCTGGG GTCAGTGGCG CCTTGGTTTT AGGGCCTCAC 300 GCCTCACAGG AGCTGTAACA ACCTGAAAAG CAGCGCTTCC AGGTTCCCAC AATCTGGCAG 360 GACCGCCACC CTCAGCAAGG CCAAAGAACG GCCTCCAGGG GTTTAGGGTC AGAGTCCTAA 420 GTCCAGACAC AACTGCCTGA TCAGTTCTGT CTTTTATCAT AAGCAACCCT GCCTAGTGAC 480 CTGCTAGAGC ACTGCCCCTC TCTGGTTCCC AGGGAGACAG AGCTACAACT GGGCCCAAAA 540 AGGAAAGTTG ACGAGAAGGC CAAGCTCTGG GCTCCCTGCA AGGGCCGGCG GTCAGGACCA 600 CCCCAAATAT CATCCTGCAT CACTGAGCAG CCCCAAGAGG TGTCCCCAGC GTGGGGCCCT 660 GTGCAGCGAG CCTGTGCAGA GCACGCCTGA TGCTCACAGG TACAGTGGGA GGTGCATCTC 720 CAGGTTGTGA GAATGGGAAT TCTCCCACTG CGGAGGAGAT GAGGTGAAAA GGAGGTGGGG 780 TCTTCAGAGA GGACCAGCAT CCTGTCCACT GTGGCCCTTT GGATTTGGCA AAGGAAAGTC 840 AAGACAGTGA AGCGGTGACA GGAAGCTGGG GCGGGCCACC TTCCACTCGA GGGCCGCCCA 900 GTGAAAGGGC CCATTTCAGC ACAAAACCTT CCCTGTGCCA CCCTCCCTAC TCCCAACCCC 960 CGAAAACAGA GCTTCTGTCC TTGTCTTCAG GGAGCCACAC CAATGGCAGA GGAAAGAGAA 1020 AGCATATCCT ACTGTGACAG CATCCTTTAC ACACTGCTAC GTGTTTGCAT AACAGGGCCT 1080 GGGGACCTTC TCTGAAGGGA CCCTCCACAA GCCTCATGTT TCACTTGAGA GATTACCGCA 1140 CAGTTTGCAT TCTACTTTGT AACATATCTA CATTCATTTC 1180
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