Tag | Content |
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EnhancerAtlas ID | HS121-34557 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr7:127714740-127716910 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr7:127715299-127715311 | TGCAGTGATTTG | - | 7.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGTACATGT GGCAGCCCAG CTGTGCTCTC CCTGCCCTCC CGTCCTCCTC ACACACTAAT 60 GCTGCTGCCT CCAGAGAACA GGAGGAAGTT CTCTCATCCC CACAGAGTAG CCCAGGAAGG 120 TGTTGGTCTC AGACCCCACA CCAAGGCCAC ACACAGGCGA GGAGAGGCTG CCAGCTGAGG 180 TGTCCTCGGC CACAGCCTGT TGCAGACCTG AGGTGGGCCT GGGCTGCCAG CCCAGAATGT 240 CATCAGTGAT CCCAGGCCTG CTCAGGTGGT CCTGAAGCAG AAATCTGTCT AGGTGACTGT 300 GGAGCCATGG GACAAAATGC CCGGGGCGCC CCTCCCTCCC CAGCCCTGAC CCTTCTCTGT 360 CAGTGCCCTC AGGACTGGGC GGCCCAAGCC CACATCTGAA TTTCCTTCAC ATTGCCCCGT 420 GGGGAAACAA CCCTAGGAGA GGCCTCTAGC TGTTAGGACA AGAGATTTAT AGCCCATCAG 480 TCTCTGTGGG CACCGCATTG AAGAGACAAG GGGGATGGGG TGGAAAGTGG CTTTTGGAAA 540 CCAATTGACA ATTGAGGAAT GCAGTGATTT GGAGGTGGGA GCCGGGCTCA CCCAGCCTGT 600 TGCTTTTGAC TTATAGCCCG GCCCTGATAA TGGGGATAAA TCAGCTGGCC ACCAATTTGT 660 CAGGGCTTCT CTGAGCTTGA GGAGGATTCG TGGGACAGCC GTGCTGAGCT ATAAATTTGT 720 TCCAGGAATA AATGCTTCCT TCCCCATGGG GCAGCCATCT GGCTCAAAAC TCACTTCCCA 780 GAGCTAAGGC CCGGACACCT GCCAAAAAGA GTCGGGGGCT TTGAGGCCCC AGAAGCACCA 840 GATTCTTCAC CAGCCCCAAG CAGCTGCCTC CTCATTCAGG GCATCTCTTG TCCCCTTGGG 900 ACTGTCCTCC TGGGTCTCTC TCTATCTATT CTTCCCTTCC CCTGGGGATT GGGGCAGGCA 960 ACCAGCCCCT TGGTGGTAGA GGAGAGTGGA GGTGGAAAGA CTCCAGGGAA AGGTGGACCA 1020 CAAAGCTAGC ACAGATGAAA GGGACGGTCA GTGCCCTGCA GGAGGCAGCC ACCATCAGAC 1080 CTCAGAGGAG ATTCCCACCT CCTGCTCACA TCAAGCCTCC TCCTCCCAGA ATGAGGGGGA 1140 AGCAGGCAGC CTCAGCTCCT ATAGGAAAGG AGTCACACGG CTTCTTCCTG GATTTCCTGC 1200 TTGTGACAGC TGAACTTAAG ACTGCCACCC CCATGTCCTC TGCCTGCTGC AGGGAGAGGG 1260 GGGGAGGGGC AGCGCTGGGG CCTCCTGTTT AAAGGTTGGC ACTTTCACAG AAGAGTTAGC 1320 AGCTGGGGGT AGAGCGGCAA GCCCCAGAGT CTAACGCCCA GAGGCCAAAA GCATCTTCGT 1380 CCTTGCCCTG CTTCCTGGCT TTTCAGCAGT GAACCTGGAA GCCACCTTTT CAGAGCTGGG 1440 CGATCCTCTA CCCTCTAAGA GTAGAGACTC TAGAGGAACC CAGGGGAGCA CAGGGAGGGG 1500 ACTCTGGCCT GAGATGGAAG GGTGGGTTCC CTGCCAGGGG CTGTGCTGAA CTCAGCATCG 1560 TTATTTACTG CACAGTGGGT TTGTCTGAAA GAGCCCAAGT CACCATTTTG CTGGTGCCAC 1620 TTGATGACGC TGAGGAGTAA TTACCAGTGA TTAATTACTT ACACGGCCTG CGTGTTTTTA 1680 TTCCAGTCCA ATTAAAATGC AGTGCACAAC TCTCAGTGCT AGGGCCTGCC GCCTCCTGGG 1740 TCCCTCTCCT GCAAATCCCA GTCTGCTCGT CAAGGATCCT GAGGAACCGA GGCTGGCTTT 1800 CTTCCTCCTG GAGGGGCTGT TTCCCAGGAG CAGCACTAGC AGAGCTTTGT AGCAGCTCTA 1860 AGAGTTGGCT GAACCCTGAT AAGAGCATCT GGTGGCCGGC TGGGGGACAG TAACCTGAGT 1920 ATCTGGGGTG TACCCAGCCT TGTCCCACTT GATCCCACAA GGGCTGCCTT ACCTGTCAAG 1980 AGACAGTGGT TACAAGATCC TGTTAGCATC AGGATGCAGG AATGTTTGTG CCTGTAGCTA 2040 ACCAAGGAAA GGTAATGCTG AGGGATTCTG TGAGACCAGG AAGTGCAGAA GGCTTTAGGG 2100 AGTGTGATTG TGTGTGCATG CATTCGTGAG TGTGTCTGTC TGGGGGAATC TGAGAATGCT 2160 GGTTTCCCAG 2170
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