Tag | Content |
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EnhancerAtlas ID | HS184-07418 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr12:45342330-45342960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr12:45342713-45342732 | GGCTGCCCTCTGGAGGCCG | - | 6.64 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I044948 | chr12 | 45342581 | 45342730 |
| Enhancer Sequence | GAGCTGCTTC TGGGAGATAA TTTAAATAAG CCACCCTGTG CATTTTGAGG GACGTACAAA 60 AATAAAGTTT GGACTTGCTG CCACATCCTC TAGATACCTG TTATATTCTT CCTGAAATTT 120 AGTGACAGAA TCTACCCTGT AGTATCCAAC ACTGTACAAC TGGCAGGTTT GAGAAGTCAT 180 CTTGAGTTGG GGTGGTGCTA ATGGACATTC CCCAGGAGCA CCTAAAGGGA AGCTATGAAG 240 GCGACTCTAG GTGGTGTCAC ACACCCTTGC TTCCCTGGGC AACATCCGCG GGGCTTTGAG 300 AATGTTCCTG GGAACGTTGA TCTCCGAGTG AAGGTTGGAG CTTCCTAGTG ACCACTAGGG 360 GGATCGGGAG CACCGTTGCG GCAGGCTGCC CTCTGGAGGC CGTGAAAGGA AAGGGCTCCA 420 GGGATGTTCT GAGGTTTACA GGCTGCACAC ACCAAACAGC AGTGGATGCT GACGCTAAAA 480 GACTATTAAT GGGCCAGGAG TGGCGGCTCA CGCCTGTAAT CCCAGCACTT TGGAAGGCCG 540 AGGCGGATGG ATCACGAGGT CAACAGATCG AGACCATCCC GGCCCACATG GTGAAACCCC 600 GTCTCTACTA AAAATACAAA AATTAGCTGA 630
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