Tag | Content |
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EnhancerAtlas ID | HS195-01381 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr11:133797440-133799320 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr11:133797663-133797677 | CTGCCACGTCACCA | + | 7.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 133797860 | 133798306 | chr11 | 133798392 | 133798947 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I133927 | chr11 | 133797236 | 133799251 |
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Enhancer Sequence | CCACAGGGCT CATTCATCCA ATCAGACTGG AGTCACCTGA GATGTCCAGG GTATAAGACC 60 ATAATGACCA GGGGTTTCCC CACAGTGGGG CCAGGATCCC TAAGGCCGTA AGGGTTGGAA 120 GAAGGTCACG CTATGCATGG AGAGTAGGAA GACGGGCCGA GGGTGTTCCC TTGTTCCACA 180 GGCTCCCAAC TCCCAGCAAA GCCGGAGGGC TATGGGTGCA GTGCTGCCAC GTCACCACAG 240 GGAGGAGACA TGGTCCTGTG GGACTGGCCC TCTCCTTGCA GCCCTGAGCT GTAACCTGGT 300 GGGTGCCCTC CAGGATCCAC TCCCGGGTCC CGGCTCACTA CCGTGCACGC CCAGGAGGGT 360 GAGATGAGGC AGCGGAAAGC AGTACAAAAA GAAGCCGGCG CCAAACGTCG GAGTCAGTGC 420 ACAGAGTTAG AGGCAGGCAG AAAGAAAGGA GACCTCCCCA ACCTCGGCCC CGCCCTTCCC 480 TGGCCCAGGC AACAAAGCAG CGAGGAGCCA CGTGTGGAAA AGCAGTGCAG ATGAGCAGCA 540 GCGTGGAGCA GCAGCGTGAA GCAGCACCGC AAGCAGCAGG GGAGCCCCAA TCTACACCTG 600 AGCCCCCCAT CGTATGCCCA GACCTCCCAC CCAGGCATCT CCAAAGACAG CTTGACCACA 660 CCAAATGTCC CACCCTGGAC ACCTAGGCGC TGAGCAGCAC CGGTCTCCCA GCAGCCACCG 720 GGCAGGCTGG TTAGGGCCCC CACGCTGCTG CGGGAGGAAC AGAGTAAGGG GACGGGAGGT 780 GAGCTGCGGC AACTCCCATC ATCCAGGTGC AGTTCTCCAA TCAGAATCAA GACACCCAGG 840 ACACTCCGCC CGGGAAGCAG CCACCGAACC ACCATGATGG GAGACAGAGC GGGTGCCCCT 900 CTCAACTTCC CTCGCTGCTG AGAAGTGGAT AAAGGGGTCT CCCTGAACCC CCTGAGCTGC 960 CCCAGGTGCC TGCCTTTTCC CCCTCCCCTC GAGCTCCCCC TCCTCGAGTT GAGCCTGGCT 1020 AGAGAGACAC CTGCAGGTGA GACAGGTCTA AAAGAAGGCA CTGAGGGGCT CGCCCTCCCA 1080 GCTCAAGGTT GTCACCCCCG GGGCAGGGCA GGTGGCTGCC ACTCTTACTC AAACAGGAGT 1140 GTAGGGAGGG GCAGCCCTTG GGGGTGGGAG GAGTCAGCTA GGCTTCCTTC TCCTCCCTTC 1200 CTGTGCCTCC TGCCCTCACC CCGCTTGGCA CATTTTTGAG ATCTGTATCT ACCCTAAGGT 1260 TTGCGCAAAG ACCTCATATG ACTGCATCTG GCTAAACTGA CAACAGAGGA ATGAAAACAA 1320 TCGAGAAACA CATGGTCCTA GAGAGAAAAT GCAGGGGCTG ACCCCAAGGC TGGGAAGTGA 1380 GCATCACCTC TCCACACCAG TTTCTGTGGC CTCTGGGGAA AAGACAGAAT AAAAACTAGA 1440 CTACAGGAGG TGGGGAGGGT GAACACGTAC AAATCATAGT GAGAAAGAAC CAGTAAGACC 1500 TGGTGTTTGC CAGCACAACA GGATTACAAG CAACAATAAT GTATCATACA TTCTTAAACC 1560 ACTATGAGTA TAATTGGATT GTTGGAACAC AAAGGACAAA TGTTTGAGGG GTGGATACCC 1620 CTTTACCCTG ATGCGATTAT TACACACTGC ATGCCTATAT CAAAATATCT CACGTACCCC 1680 ATACCTACAA ACGTATGTAC CATGTACCCA CAAAAATTAC AAATACAAAA ATACAAAAAA 1740 AATTAGTCTA AAAACTAGAC TCTACACTTA AGGCTGGGCA ATTTCACAAA GCCCTTGAAG 1800 GGCAGGAGTC TCTTCCAGGC TCCAGAGGAA TCCAGAGGAT GAAGCAGGAC GCAAAACGAG 1860 GCAGCACGTG AGCAGGGAGA 1880
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