Tag | Content |
---|
EnhancerAtlas ID | HS184-17061 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr2:171829750-171831250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:171830100-171830119 | GGGCCACCAGGTGGCGCCG | + | 7.85 |
| | 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 |
GH02I170973 | chr2 | 171829415 | 171831716 |
| Enhancer Sequence | AAAAATAATA GTTGCATTGG ATATGGCTAA TTTTACGAAT TAACTTCAGT GAAAAAAGGG 60 AATGGTTTTA AAGAGAAGTG ATGGGTGAGT TCTTGAGTTA ATTCCCTCAG GGGAAGCAGG 120 TGCGCCTGGA GAGCTCAAAC CGAGGCCCCT GCTTCACAGG CGGGCGGGCT TTGGGGTAGG 180 AGCTGAATCC ACGTAGGTCT GCCCGGTCCC ACGCCTCAGT TCTGTCCCCA CGCGGCAGGT 240 TCCTGGAACG ACATTCACCT TTGTTCAGGA ACTCCGGTCT TACCGCCGCC CACGTGGAGT 300 GGGATCCGAG CCAAGGGGGC CTCCCGAGCG GGGACTACAG TGCGCGCCAC GGGCCACCAG 360 GTGGCGCCGG GAGCCTGGGA AAGCCGCGCC CCGCCAGCGG CCGCGGGGTC TCCGGGCCGC 420 CCTCGCAGGG CCCCTGGGCG GGGCCGGGGC GTCGCGGTGG GGCGCTTTCC GTTCTTTGGA 480 AGAAGGGCTC TGGTCCCCCG CTTTCTTTCC ATCTCAGACC CAGTGCGGAA ACGTGGGGGA 540 TGAGCCTGGG CGCCTTCACC AAACGGAACC CCCTTTAATC TGATGTGAAG GCAAATCTCT 600 CCACCGGGGG ACCCGTTGGG TGCGGCGGAG ACACCCTTCG GTGGCTGAGA AACCCTCAGA 660 CGCCGTGGAA GCACCAGGGG TCTGAGCGCC CAGTGCGGGA GGTGCGGGGC CGGCTTCCCT 720 CCCCGGGGCT GGAGCCTTCA GGAGCGCCGC CCCCACCCGG CTTCCTCCGA GGGCAGTGCT 780 GGACTCTGGC CTGGCCCCTG GCCGGCCGCT GCCCTTGGCC TCGTCCAACC CACACCCGCG 840 GGGCGGAGGC TCCTGCTGTG CACAAGCCCG GGGCGCCGGG GTGGGGCGGC TGGGTCTGGG 900 CCCAGGTGTC CCGAATCCAA AAGCATCCCA CTGCGCTGCC TGTAAATTAG CGATTTCGGA 960 TCTAGTGATG AGCAGAGGGG ACAGAATAGC CCAGAGGCCG GGTAACTAAC ATGTGCGGGA 1020 TCAAGGAAGG CGTTCGTGGG CAGCTACTAT TAGGGCTTTG AAGAATGCAT AGAGGTTCTC 1080 TTAGGTGGTC AAAGTGGAAG GAAGAGGTTC TCTTAGGCAG AGGGAACAGC GTCTGCAAGG 1140 ACACACAGGA ATGTGGCACG TGGTGTGTCC CGGAACTACA AACAGCTCTG GTTGCTGGAA 1200 TGTGAAAAGT CAAGTATGGA GTGGTAGCAG TTGCCACAGA AGGGGGAGCG GGGCCAGATC 1260 GCCGAAGGCC TTGAATGCCA TGCTCAGGGG CTTAGACTGC ACTGCCCTGG GGAGTTTATA 1320 AGGGGGATGG ATGTTTTTTG TTCTTGGCAG TGAAGTACCC AGGGAGCTTG CCCCTTACAT 1380 AGGTCAGTGG TCTGAAAAAC CTCCTTTTTG GCAAGCAGGG GCCTTTCGTG AAAGAAAAAA 1440 AAAATCATAT GGCACATAGA TTCAAAAGCC AGGCCAGTGT GGAGCTGCCG GCAGTTTCCC 1500
|
| |
|
|
|