Tag | Content |
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EnhancerAtlas ID | HS121-27177 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr3:52731950-52734270 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:52732785-52732806 | CTTGCCTTTCATTTTTTTTTT | + | 6.29 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I052696 | chr3 | 52730424 | 52732011 |
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Enhancer Sequence | CTGAAAACAC AAGGAAGGCA CTGTGATTAC AATCTCATGG GCTTTTGATA TAGAGTCCAA 60 GACATGGAAA AAGGGAAGGT AAGGATTATG GTACTGATCT ACCTCATTCT CCCCCATTAA 120 ACTGAAGCAT ATAGCCCTGA AACTTTCCCT GTATGTAAAT AAGCTTTTGG AAAAGTGGAG 180 GAAGCATTTT TTAAAATACA CTGACAGCAC TTTGGTACAC TACTGGTAGG AAAATAACAG 240 AACCTGTTAG AATGTATTAT GGCAATTTGT ATCAAGAGTT TCCTAAGGAC AAAATCTGAA 300 ATATAATCAA AAGAAAGAAT TTTATTTAAA TTGTGAAAAC TTAGCAGCAA ACTAAATCAA 360 TGTTTTTCAA GTCACGAATC ACAAGTAGGC ATGAAACCAA TTGAGTGAGT CACAATCAAT 420 TTATACAGAA AAAGTTTCTG GATTGCAATA GAAAACTGAA ATAGAGGCCG GGCATGGTAG 480 GTCACGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCGG GTGGATCACT TGAGGTCAGG 540 AATTTGAGAC CAGCCTGACC AACATGGTGA AACCTCATCT CTACTAAAAA TACAAAATGA 600 GCCAGGTGTA GTGGTGAACA CCTGTAATCC CAGCTACTTG GGAGACTGAG GCAGGAGAAT 660 CGCTTGAACT CGGGAGGTGG AGGTTGCAGT GAGCCAAGAC TGTACCACTG CACTCCAGCC 720 TGGGCAGCAA TAGGAAAACT CCATCTCAAA AAAAAAAAAA GAAAACTGAA TTAGAATACC 780 AAAGAAAACA TAGTGTATCA CACAAGGAAA CTGCAATTAC TGTCCTGTAT GCATTCTTGC 840 CTTTCATTTT TTTTTTTTTA TTCCTCATTG AACCCTGGTA TTTACTATGT GCCAGGCAAT 900 ATCTAGGCAC TGGGGTTACA GCCATGAATA AAACATCCCT AACTTTCTGA GGATAGACAG 960 CCAATAAGCA AATACACATG TATGTACATG TGCTACATGT AATGTATTTC CTATTGTAGG 1020 GCTGCCATCA AAAAGTCTGA AAGCTGTTGT AGCAAAAGAT GTTATCCTGT GGAAACAAAT 1080 TAATAGACAT TAAGATTATG TATGAAGAGT TTCTACCATC ACAGTGACAT GATATACAGA 1140 AAAACATGTC ATGTACAGTT TATATATAGT ACAATCTCAA CTGTACAGAA AAAAAGATGT 1200 GTAGGAAAAA ACTGGAAGGT ACTAAGCCAA AATTGTAAAT GAAATCATTC AACCAACTAA 1260 TATTTATTGA ACAGCTAGTA TCAGCCATCA TCCATAGGCA CAGAAGATAA AACAGTACAC 1320 AAATTGCCTT CATGGAGCTT AAATACTGTT GTCTCTTTTT TTTTTTCTTG AGACGAAGAC 1380 TCACTCTGTC ACCAGGCTGG AGTGCAGTGG CGTGATCTTG GCTCACTGCA ACCTCCGCCT 1440 CCTGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGACTA CAGGCGCATA 1500 CCACCACGCC CAGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGGCCA 1560 GGCTGGTCTT GTACTCCTGA CCTCGTGATC TGCCCACCTC AGCCTCCCAA AGTGCTGAGA 1620 TGGTCTCGAT CTCTGACCTT GTGAGACGCC CACCTTGGCC TACCAAAGTT TTGGGATTAC 1680 AGGCATGAGC CACTGCTCCC GGCCGCTGTT CTCTTTTTTA TAAACTTTCC TACCAGGAAC 1740 ATGCATTACT TTATATGTAT CATACATATA TACACGTGAT AAAACATGCT ATCAGAGCAC 1800 TCCGTGAAAG TCAGGGGAAA GCTATTACAG TCTCTCACTC TGGTCAGCTA TGGTGGGTGG 1860 CAATCCAAAA ATGATTTTTG ACAAACACTC AAGCCTCAAA CATTTCTCAG TACCAAGGGA 1920 GAACAGTATG AACGACTAAT TCAATATACT GTGCGATATA TTATACAACA CAGTGATTTT 1980 TAAAAATCAC TTGACAAACT TTTATTGCTA CAGTCCCACT GATGCAGCTG CACAGCTGAA 2040 GGAAAGTAAC TAGACTGACA CTCTAGTGAC TAGAGCAGGC ATCAAACACC AAGGACACTG 2100 GTATGCCCTC ACTTTCTGAA GCCCTGTCCT GCTGACATGT GAACAGATGG CAGCCCTCAG 2160 AGGCTCTCCT AAGGCCTCTG ATTTGGTGAA AAGGAATATT CTGTCAGATC AAACCCTTAA 2220 CAAACAACTG CTAGTACTAC CGGAAGAAGA ACAACTTAGG ATGTGTGACA CAGAGAATAC 2280 CAGGTCCGCA ACAGATTCTA AGGCATTATT AATAAGTGCT 2320
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