Tag | Content |
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EnhancerAtlas ID | HS184-07928 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr12:69811490-69812550 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr12:69811654-69811665 | AAGCAATAAAA | + | 6.32 | Foxq1 | MA0040.1 | chr12:69812239-69812250 | CATTGTTTATT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTTGTTGGT GTTTCTGTGA AAACAACAGC AGCCGCTTGT TACTGCAGAA ATGGTCCCTT 60 TGGAAATCAG CAGCACTTCG TTTAACGCTG GCATTTTTGT TGCGTGTCTC CCCAGAAATG 120 CTTGGCTTAA TATTCTTACA ATAGGGAAAA AAAAAAAAAA AAAAAAGCAA TAAAAGCTTT 180 TGAAGCCAAA TGCCCCTTAA AAAAACTGCT GATGGGGAAA TCTTTTCTCA CACAGAAAGA 240 GATTTCAGTT AAGATGATCA AATAAAATAA GCTATATTTA AAGTTTCTGG CTCTTTCGTT 300 TACCTTAGTC AAATAAAGCT TGTGTATTTT AGAGATGAAA TCAAAGGTCA TTCTTCTGAT 360 AGAGACAGAT TCTGGGGATT GTCTCCTATT TGGGAAGCCA TTTTAGCAGT GACTTCAGCC 420 TTGGCAGGTG ATAATGCTGT TCAAGTCATA TTCAGTAAAG GGAAGAGTTC CAAAATCTTT 480 CATTTCTGTA CTGAAGATCC TATGCTTGCA ATATGTATAA GGCATTATTT ACTAGCCAGC 540 CTGGCCCATA AAGTAATGTG GTGAAACCCT GTCTCTACTA AAAATACAAA AATTAGCGGG 600 GTAGGATGGC ACACGTCTGT AATCCCAGCT ACCAGGGAGG CTGAGGCACA AGAATTGCCT 660 GAATCCGGGA GGTGGAGGTT GCAGTGAGCC AAGATCTTGC CACTGCACTC CAGCCTGGGT 720 GACAGAGTGA GACTCTGTCT CAAAAAAAAC ATTGTTTATT GGTTTTCTGA TCTGCACCAA 780 ATCTTGATTG TCAGTTTGCT CTCCTTCTTT GTTAAATGTC TGTGATAAAC AAATGCTCAT 840 CTAAAACATT CATTTGTCAA CAAAGGAATG TATGTGTTGG AGGGAGTCAA CAACCAAGAA 900 TTAGAGTAAT TGAAGTTGGT TTTTTTCTTC CACATATTTC CCTTGGTAGA ATCTATCCCT 960 GTGTGATAGC ATTAACTCTC ATCTGTTTCA TACCAAACTA AAGCCTACAT AATCTAAATG 1020 CATTTGAGCT AATCCTTCAA CTTTGCTACC TTCATCATAA 1060
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