Tag | Content |
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EnhancerAtlas ID | HS184-30478 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr8:135490960-135492040 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr8:135491755-135491769 | TGTCTTTGATCTTG | - | 6.03 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGACCTGCGG GAGGAGGGCA AGAGAAAGGT CACCCAGCGC CTACTTCCCG GTCCAGCGTA 60 ACAACAAAGT CACAACTACA GTTTAGGAGG CACCAGTGCG CTGCGGGAGC ACGTCCATTC 120 TCCACGGATC CTCTCTACCA GGCTGTGCTT GCTCTCATGC CCATTTTACA GCTGAACAGA 180 ATGAGGTTCA GCAATGTAGG GCAACGTGGT CAGGGTCCCC AGCCGTGGCA AATGGTGGAA 240 CCTAAGTTCA AACCCAGAGT CCGAGGTTGT TTCTGATGCC GAGCTGCTTC CCGGGGCTTC 300 CAGGAGGTGT GGGGTTACCT AGAGAATGAG GGCTGGAAGG CATGGTGGGG GTTAGTTACT 360 GCAGGTGTCA GTGGTAGGGG TTGGCGGTGC TCCTGGAAAT TTATAGCTGG TCCATCTGGC 420 AGTGATAAAG GCACTACGTC TATCCTGGGC TCTCTGTGTT TCCACACTCA GGGAGCTTGC 480 CTCTGTGTGA AGATCTGTAT CACACTAGGA AGGAGCAGAC GCCTGGCAGG CCTGATTTTC 540 CCCAGGTGTC GTCCGTCCAG CAACACTAAT GCCTTAACTA TTTGGGGGAA GGCCTGCTGG 600 TGGAAACTCA CTGCCACAGG GCTGGACAGG AGAGCCTTCT GGGTATCCGT CAGGGGATGG 660 GACCTCATGG ATTCTATGGC CAGGCCTTTC TCTGAAGCTC CAAGCTGCCA GATTCCAGGC 720 AAGACCAAAT GCCAGCTGGT GCTAATATCC CACATCCCTC ATGCTGCCAG CTCTGGGCTG 780 TTTTTAAATA ACAACTGTCT TTGATCTTGA GATGAGAAAC AAAAGACATG GAGTTGAGAC 840 CTTAGAGCTG CAAAAATGAG TGAAGGATTA GAAAACAGGC ACAAGAGGAA AGCAAAGGGG 900 CCTGGAATTA TCTAGCTGGA GGATAAGAGA GTCTTCAGAC TTACAGAGGG GTGTCAGGGA 960 CACCCATTCA TTTCCAGGTG AGTCTGAATG GCAAGGTGGG GAGAGCACGT GCTTTGTCCT 1020 GCACTGACCG GGCTTTGAGC ATCAATTCCA CCATTTATAA GCTACGAGGC CTGGGCAAGA 1080
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