Tag | Content |
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EnhancerAtlas ID | HS120-04852 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr4:24974620-24976090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr4:24975154-24975165 | TGCCTGAGGCT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 24975200 | 24975985 | chr4 | 24975738 | 24976056 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I024973 | chr4 | 24974653 | 24976822 |
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Enhancer Sequence | AACAAGAACC TTGGTTTCCA CAACCCCTCA TCTTGACCTA GACACTCTTC TATTGATTCC 60 AGGTCTTTAG ATAATAACTT AATTCTTTTA ATCAATTGCC AATCAGAAGA TCTTGGAATC 120 CCCCTATGAC CTGTAACCCT CCCCTTCAAG TTGTCCCACC TTTTCAGACC AAACCAATAT 180 ATACCTCACA TGTATTGACT GAAGTCTTAT GTCTCCCTAA CACATATAAA AACCAAGCTG 240 TAACCCAACC ACCTTGGGCA CATATTCTCA GCACCTCTTG GGACTGTGCC TCAGGCCTTA 300 GTCACTCATA TTTGGCTCAG AATAAACCTG TTTAAAAATT TTATGGAGTC TGACTCTTTG 360 TGTCGACATG GTGGTGGTCC CATGGGTGTA CACATATGTC AAAACTTATC CAATTGTACA 420 CTTTAAGTAT ATGGAGTTTA CTGTATATCA ACTGTACCTC AATAAAGTGC ATTTAAAAAA 480 AGTCTGGAGA AAAAGAAGTC CCCTTTTGTT TGCACTTGGA GCTGTGATTA AGCATGCCTG 540 AGGCTACTGG CAGCTATCTT GACATTGTGA GGAGAAAACA TGCTTGAGAG TGAGGCCAAC 600 CCAGAGGATA AAAAGAACTG AAAAAGGCCA GAGTTAGACC AGATTCCAGC CATCCATCGG 660 TACTGGATCC AGCTGTGCCT ACAGCAGTCT CTGGAATTTT TGCTCATTGA GACAATACGT 720 GTGTGTGAGT GTATGATTAA CCCGGTCTGA ACTGAGTTTT GTTGGTTACA ACTGAGGAGT 780 TCTGTGCAAC GTTATCCACA GTCCACCAGG CAGGCTGAGA GCTGCTTCTT AACCAGCAAG 840 TGCCTCATGG AGGGATTGGG TTTGGGGTTA TGGAAGTGAA CAGAGCTGCC TGCCTTAAGG 900 CAAGTAGGCC TTGCTCTGTT CCCCTTGCAG TCCCCGAGCC CGGGAAGCCC GAGAGGGAGC 960 CCTTCAGTGC TTGTGCACTC GGCTGTTTCG CAAGAGTCAC GGTCAGTTGC GCCTCTGCTT 1020 CGGAAGAGTA TTTTTAGTGG CAAATAAAGT GGTGCGCAAA TAAACAAACG CCTGGAACAA 1080 ATCCTGCAAA GGAGAGCGCC TGTGTGCGGC CCACTGTCTA ACTAGGTCAG CCTCGGGCAC 1140 AGCTCCTTTT GACAGTTTGC TCCCCAGGGC GGAAGGTGAC CCGCAGGTGC CGGCTGCTTT 1200 CCCCACCAAT CAGCCATCTG TGGTTTGAGA CTCACAAGCT TAGGAGAGAC TCGGGAGGCA 1260 TCAGTTCCGC ATCCCGCACT CCCACGTGAA TTTGCCCCCG CCCTGAGTCA GAACCCTAGA 1320 GGGGTGAAAT CCCTGAATTC TGCAGAGGAA ACCCATACTT CTTTGCTTTT TCAGCAATTC 1380 CAGGAGATGT CGTTTTTCAA GTGGCAAATG TGTGGCTCTA GAGGACAGAG TAACCACCTT 1440 GCAGCCAAGA AGCCCTGATG TCAACTCCCA 1470
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