Tag | Content |
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EnhancerAtlas ID | HS121-37548 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr9:130167840-130169390 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf12 | MA0742.1 | chr9:130169255-130169270 | AAAATGGGTGTGGCC | - | 6.26 | Klf1 | MA0493.1 | chr9:130169259-130169270 | TGGGTGTGGCC | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATGGTGAGG GCAGGCTCCA CCAGCACCGC GTTCGTGCAG TCAGCCGAGA AGCACTTTCT 60 AAAACCACTT GTATTGCAGA AGACCCAGGG TCGTGGCCTT ACATGCAGCC TGAGCCCCAC 120 CATGCCTGGG CCACTGGCCA TCTTGGGCAA GGCGACGTGG AGGCAGATGG GCTAGGCCAG 180 ATGGGGAACC CAGGCTGTGA CCCCTTGGGA GTCCTCTGCC TGTCTTGGCA GTCAGACAGC 240 ACAGCTGGCC TCTCCCCTTA GTGAACGTCA GGAAAGCGGG CCTTGAGCCT AAGGTCTTAC 300 ATGGGAAGAG TTGACAGGGC TGGGCTGCAG CCCCACCCTG GCTACTTCCT TGCTGTGTGA 360 CCTTGGGTAT GATGCTTACC TTCTCTGAGC CCGCTTCTTT GGCTGAAACT GGAGGAGAGT 420 AACAGCAGCT TGCTCTTAAG ACGGATGGGA GCATTAATTC AGTTCATCCT GTTGCTGCCT 480 TCTCACGGAT GGACTGGCAC AGGTGTGGCC CCTGTCCCGG GGCTTCCCAG CCAACAGAGA 540 GACAGTTCTG GGGTAGATGA TCTGGTTGTT TGTTCAGTCA TTTGTGCCCT CCAGGTCTCC 600 TGGCATGTGC CATGTCCAGG CCCATTCAAG GCGCCAGGGA GAGCAATGAA CAAGATGGAC 660 AGGGTCCCCT TTATGACAAG GACGGGAAAG GCCATGGCAG TGGTGGGAGA ATGAACCCCA 720 GTGGGGCTGG GTTAGGATGT GGTGGGGCGG GTCATGAGGG GCCAGCCTGG AGTCTGTGCA 780 GAGCTTGGGA CCCGCTTAGG CAGGACTGCC CGGGGAGCAC ATCGAGGGGG CCAGGCCGAT 840 GCCTGGGGGT GGAGATTACT TGCTGCAGCT GGGAGGGGAT GCGCAGCAAA GGAAGGAGGA 900 AAAGAAGCCA AGAAGGAGGT GACAAAGGAC CTAACAGTCC TTTTTTAGGA GAGAAAATGT 960 CCAAGAGGCC AAGAGAAGGC CTTCGAGGAG GGAGAGATCG CCAGGTCCCA GAGGACCAGG 1020 AGCTGAGAAG CACCTTTTTA GTTCTGGCAC GTGGGAGGTC ACAGTGGTGG TGGATGGCAG 1080 GGACAGGTTC TGACTGAAGG CCCCATGTGC TCCTGGGGCC ATGCTCGCTT TGCCCTGTCT 1140 CACCCATTTC CACCACACTA TGAAAGAACC CACCGGGGGC CTCAGGGTGG GGCCAAAGCT 1200 GAGGGTGGAG GGTTGGTCTG TGGGCCCTGG AGTCAGACCT GGAACAGGAG CCCAGCTGTC 1260 ACTGGATAGC GGGTCTCTGG CCTTGAGGCA GTCACTTCAT TGCTGTGAGC CTCAGTTTCC 1320 CCAGCCATAC GACCTCGGTA TCTTGGACAG TGCTCGGCCC AAGCCACCAG ACTGGATGCC 1380 AGACTATCCT CCATGTCCCA GAGCTGGGTG GAGATAAAAT GGGTGTGGCC TTGGGCAGGG 1440 CAGGCTGGGG TCAGGGGACT GGACCCCCTG GTGGCAGAGC TGTCTCAGTG ATCGCGTGGG 1500 GCTTCCTGAT CTCTCCCCGC GTCCACCCAT GGCCTTTCCT CTCTCTGCAG 1550
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