Tag | Content |
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EnhancerAtlas ID | HS195-01724 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr12:122191340-122193840 |
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) |
SRF | MA0083.3 | chr12:122192648-122192664 | TTTCCAAATAAGGTCA | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122191696 | 122192222 | chr12 | 122192415 | 122192568 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121753 | chr12 | 122191888 | 122192630 |
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Enhancer Sequence | GTGGTGGGTG CCTGTAATCC CAGCTACCCA AGAGGTTGAG GCAGGAGAAT CACTTGAACC 60 TGGGAGGCAG AGGTTGCAAT GAGCCAAGAT TGTGCCACTG CACTCCAGCC TGGACAACAG 120 AGCGAGACCT TGTCTCAAAA ACAAACAAAA AAAAAAAGAA TGTTCTGGAG TTAGGTAATG 180 GTTGTACAAC TCTGAATATA CTAAAAATCA CTAAATTATA TACTTTAAAA GAACAAGTTT 240 TATGGTATGT GAATTATATC CCAATTATAT TTAAAAAAAA AAAGAGAAAA AGAGAAAAGA 300 AAATGGTTTT GAGACCAACT GGCTGTTACT ATGGGCAGGT TCCCTCTGGG AGCCTCAGTC 360 TCCCCATCTG TAAAACAAGG GTGACGGCAG TCCCTGCCTC ACAGGGCTGT GACAATTCAG 420 GGAGCTGGCA CCGTGTGTGG AAGCTCCACC CTGGCTGGCA CGTGGAGGCG CTGCTGGGGG 480 TGCTCCCCAG CTGCTGGTAC CGTCCAAGTG CAGCACAGCC ATGCCGTGAG GCTGTGGGCT 540 GCTGCTGCCC TGCCTGGGCT GCTGTTCCTT TCTCTGGCCC TGGGTTCTCT GTCCCCAGGG 600 GAAGCGGTCA AGTACGGTTT GGGCATTTGG CCTATGTGCC AAGCGTTTAT TGCCTGGCAG 660 GCACTTGGCT GGGCATCCGG CTGCTGGTCT GGCCACTTGA ATGCCCAAAC AAAGGCTCTT 720 TCAGGCCCTG GGCCCGTGCT CGCCTGCTGC CCAGAGCCTG GCCTGTTTCC ACGAGGGCAA 780 AGGCTGCACA CATCTGTACT ACTCCTCATG TGCCTCCCTC AAAGAGGGTA AAAGTTGTCA 840 ATGTGCAGCC ACAGTCCCTT GCACAGGGAC CTCCAGGGCC CTCCGAAGGC AAACCCTTGC 900 TGTCCTGAGG CCCAAGGTTC CCCGAGGGCC TGGGCGTCTC TTTTTCTCCT ACCTGCTTCT 960 GTGTTCATCT CCTAGGGCCA CTGTAACTAA GTACCATAGA CTGGGGGCTT AAAACGACAG 1020 ACACATTTTC CCACAGTTCT GGAAGCCGGC GGTCTGAAAG CAGGGCGTGG CAGGGCCATG 1080 CCGCTCCACA GGCTTCGGGG AGGGAGGACC CTTCCTCGCC TCTCCAGCTT CTGGGAATTG 1140 CCAGCAAGCC CGTATTGCCT GGCTTAAAGC TGTGTTTCAC TCGCCTCTGT CTCTGTCACC 1200 ACGCCACACG GCCTCCTTCC CTAGTGTAAG GACACTAGAC ACTGGATTTA GAGCCCACCC 1260 TAACACAGTA TGACCTCATT TGAACTAATT CCATCTACAA AGACCCTGTT TCCAAATAAG 1320 GTCACATTCT GAGGTCCCAG TGGACGTGAA TTTTGGAAGG ATGCTATTCA ACCCAGTACA 1380 CCTTCTATAG GCTAAAAACG GGGCAGAGGA GGGGGATTGG ACGGGCCGTT CATCTCTGTG 1440 CCGGTGCCCC CGGGAAGCCT GCCCTGCTGT TTAACCTTAG GCAAATGACG AACCTCTCCC 1500 AGCCTCAGTT TCTTGACAGA TACAGTGAGC GTGACAGGAG CTACTTGGCA GGGCAGCTTG 1560 GAGGGCAGGA GAAGCTGTGT CTGGAGACTG GTTAGACTGG TGCCTGTTTA AATATTAGCA 1620 CCGGTTAGCA TCACCGTTGT TTTGGGCTAA GACTGGGCAT ACGGGAAAAA GGCTCACAGC 1680 TTCATAGCTA GTGCGTCCAC AGAGCAGGAT TCTCTTTTCT TCCTCTTGCC CCTCTTGGGA 1740 TGGTTTCCTG GCTAGGCTCC CCACCCGGAG GCCCTTCTTG GTACCACTAA GCCTGCAGCT 1800 GGGCATGGCC AGCATCCTCT AGGGTTCTGG GTCCAGCTCT GCCACTCACG GGCTTTGTGA 1860 CCTGAAGTGG ATCCCTGGGC CTCTCTGTCT GTCTCCTCAC CTTTTCCACA GGCTCCAGGA 1920 CATCTACTCC ACCAGTACTC CTTGGGCGTT TGGAGGCTTT GGTGAGGCAG CAGGAGAGTT 1980 GGAAGCCTCC TTCTGCTGCC TTCAGGCCAA GAGGCTGTGC CTGGTTAGGA CTGTCCTCTA 2040 TCAGGTTTGA ACCAGGCTAG GAAAGAGGTA GTCAGAGTTA ATTTTGGCTC GAGTGGGCTT 2100 GGGTTTGGAC CTCACTCCAG TGCTTGCCGT CTGTGTGATC TGTAAAATGG GAAGTGGTAC 2160 TGTCTTAGTG TGGGTTGGCC CAGAAGAGAC CCCCAAGACA AGCATTTTAG TGCCAGTAGT 2220 TTATTTAGGA GGTGATCCCA GGAGACACTG GTAGTGGAAT GGGAAGTGAG GCAAGAAAGC 2280 ATTATCCTGT GGGTAGTTGG AGCTCAATAC TGCTAGGGAA TGAGGGGACA GCGTAGAACA 2340 TGCCTCAGAG TTATCCCACC TGAGGGTGAG GGAGCTGGGG TATTTATCCA CCATTTGCTA 2400 TCAGTTGGGG CAGTTGAGGA CTGACCCCAG AGGGTGTTAA TTGCTCCACC CTTCTGATCT 2460 GCACCTTGCA CCAGCAGAGT AGATGCTGGT GGCTTGATAA 2500
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