Tag | Content |
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EnhancerAtlas ID | HS180-44107 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr7:7173240-7174680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr7:7173966-7173979 | TACATTTGCATAA | + | 6.18 | RARA(var.2) | MA0730.1 | chr7:7174575-7174592 | TGACCCCTTACTGACCC | - | 6.03 | RELA | MA0107.1 | chr7:7173280-7173290 | GGAAATTCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTAAAATTA AATGCTGCTC AAGAGATCCC TATTTCTTCT GGAAATTCCC AAAGTAGTGG 60 CTCATATGTG ACCTCCCCAC AAAAAAGCTA AACTGTTCCA CATACAAAAC AAAAAGGAAC 120 TCAAGAGTTT CCAGGGCAGC CTGGAAGCAA GGAGATAGCA GTAAGAGAAT GCCAGGACTT 180 GGAAGTGAAG TAAAAAGATG GAGGAGAGGT TCTCACCAGA GGGCAGGGGG CCCAGTCAGA 240 TGGCAGCAGG GAGGAGCCCT TGAGAGAAGG GTGGACAGCG ATACATCCCC CATGTCAAGA 300 CAGTGATGTC TAATGTTCAA GTTTAAATCA TTGTCAATTC TTTCATGAGC TTTCGTACTG 360 TCTGTTAGTT TAAACAATAC AAAAAGTCTA CTATCCCTGA GTAAGAGTCT GACCTTCAGG 420 GTCAGGGAAG TTTGGAGTAG CTGCAGAGAC TTTAGTCCTA CATTCTCCTG GGTAAGGCCA 480 TCATCTGGTC CCACATTCTA CAAAAAGTCC ACTTCCCAGA CCTTGTGTCC CAATTTTGTC 540 TTCAAAAAAT ATTGTCGTTG TGAAATCATC CCTGTGGAAA AACTGGAAAG AAAGATTTTT 600 CTGTGCTGCA GGGAGGGCCC CATAGAGAGC AGATGACAGC ACAGATTTGA AAGTAGAACC 660 AGGCAGCATA GCTTTTGCCA ACAGTGTTCA ACAGAAAGAA AAGAAAGATC TATATTTTTA 720 TTGTATTACA TTTGCATAAG TAAACCCTAG AGGGATATCA AAGAAGCTAA TCAAGTAAGT 780 ACTTAGGGTG GGGCGAGGTG GGTGATAAGG CAGATGAGGG CAGAGGTGGG AGTGATAATT 840 TTTACTATGC ATACTTTTAT ATTATTTGAT TTTTGAACTA TGTGAATATA TTATATATTC 900 AAAACGTTGA AAGAAATTGA AAAAGAAAAA AGTCTTCCAA GCATCACAGA TTTTGTTCAA 960 GCTGTTTTGG GAGAACAAAG GAGTAGGACA GAATCCATCA AGAGGGAAGC AACATAGACA 1020 GAGGACAGTA GTCAAAGAAA GAATTACAAT GTCAAGATAA GCAGGAAATG TGAACATGAG 1080 GGAATCAAGG GAACTAGGAG TCCCTGACTC AAATCCCCCT TCCTTGAAGT TCCAGAAATA 1140 CTTAGGGGGA GAGGCTTAGG ATGAGGAGGA GGATGTTGGG CTTTCCAGAG AATGTGGAAT 1200 AGGAGCTGGA GACTTTGCAA CTTTGAATAT TAGAAGAAAG GGTGGCCCCA GAAGGATGGT 1260 GTGACTTGAG GACATCCAGG TGGCAGATAC TTAGATTATA TTAGCATGGC ATCCAACGCC 1320 CTTGACAATT TGATCTGACC CCTTACTGAC CCTCACTTCT TTCCTGCAGC ACTTTTCTCA 1380 TTAAGGACCA GTCCAGGCTA AGTGTTGGGG ACACAGGATG AATGCAAGAT TAAGGAGCAC 1440
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