Tag | Content |
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EnhancerAtlas ID | HS161-14607 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr8:29512460-29513910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr8:29512681-29512691 | ACCACGTGCT | + | 6.02 | SOX10 | MA0442.2 | chr8:29512901-29512912 | GTCTTTGTTTT | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36200 | chr8:29512144-29514863 | HMEC | SE_56175 | chr8:29510734-29517401 | u87 | SE_64743 | chr8:29512106-29514610 | NHEK |
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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 |
GH08I029654 | chr8 | 29511014 | 29515485 |
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Enhancer Sequence | CCTGGGCTTT AATTTCCTCA TCTGTACAAA GAGAAGACTG GCTGAGAACA GAGGCAAAAT 60 GGTTGTCACG CTTTGGCAAT CAAACAGCCG TACATGTTTC AGGTGTTAAG GAAGATAGAT 120 GCTCTAACAC AAAATTCTGT CTTCTCTTAC TCTCTTGAAA AACAAACAAG ACAAAACATT 180 CGCAGAGCTG GAGACAGGAA GAATGAGCTT GGAAGATCAG GACCACGTGC TGGTTTCACT 240 ACCTCTGGTC ACCCCAGCTC ATTCTTCTGC TGAAAAGAGG CAGGAGAACA GTGAGAACAG 300 GGTGGTGGTC CCCAAGGGAA GAATGATCAA TGGAGACAGT TTCATGATGC CATTCATGAA 360 ATTCATCAGA ATTTCATGAT GCCCCTTGGG GTGACTATCA GGGTTTTAAG TTATTCTTGA 420 GAGTTTCTCG AACGCTTTTC TGTCTTTGTT TTCTAAAAGA CTTTGATGAT GGCAGTGGGA 480 GCTCAGATTC ATGTTGGAGT TACCATTCTG GTTTGCCAAG GTAGTGGAGG AATGTGGAAA 540 GACGTCGCTG CACTTTAGTC CTGTACTTCT GACCTGTACT CAAAGGCCTT TCCCTTCCTA 600 CCCTGGGGCA TCTCCCCACA CAGGAGCTTC ATGCCAGCTT CCCCTCTGCT GGGGTTGCCA 660 ACTCATGACT CCCTGGGGGA GGCCTCCGCA CTAGCCTGCC AGCACCTTCT TCTTTCCTTG 720 AAGGCTTGTG ACTCATAGCT GCTGTGTAAC GTGTGGCACC CCCAGACAGG AACACATCTT 780 GCAAATTGCA TCGGGGGCTG CTTCTCTGGT CTTCCTTCTG GATACCAGAT TTGGAGGTGC 840 CAAATGGAAT TGAATTCTTT ATAGGTTAGA GAGCATTTAA CTATACCTGG CAGGGCTCTT 900 TAACTCAGAC TTTAGAGTTT TTTTTTCATA TCTATACACA CACACAGATA TATTTCATAA 960 TAGGCAACAT GACTAATATT TGCAGTATTG TTTTGATTCT ATCAGTGCAA CTGGTTCACT 1020 CATTCCTGAG TGTCTAAACA TCATTAAGAT TCTAAAGGTT TGCTCTGAAG AACATACTCA 1080 GAATAAGTTC TGGTATTTTT CTCTGGACAT GTTGTTTTCC AACTACTTAG AGAAAACAAC 1140 AAAGTGGGAT AAGACTGGAT AGGCAAATAG GTTTGATTTT ATTTGCCAGT GCCAGTTGAT 1200 GTATCATGGC TTCCTCGTGG CTGTGTTGAA AGGGATCGTG AGACACTGAC TTGGCAGGAA 1260 GAGGTGCCTT GGCAGGAAGA AGTGCCTAGT GGATGAGCAA TGCCTGCTCT GGGCAAGGAG 1320 GGGACCAAAT AGCATGTGTG CCACTTTTAG ACCCTCCCTG GACAATATCT TTCCAGCCAC 1380 TGCCTGCCTC ATCCTCCTCC TTGAAACCAG AGGGCAAGGC ATGATGTTCC ACCGATAGGA 1440 TTATTGTCTA 1450
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