Tag | Content |
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EnhancerAtlas ID | HS176-05589 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:79708540-79709920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr10:79709136-79709150 | CTGAGTCACTTCCT | - | 6.23 | ZNF263 | MA0528.1 | chr10:79709423-79709444 | GGTGGAGGATGGAGCAGAGGA | + | 6.27 |
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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 |
GH10I077948 | chr10 | 79708014 | 79710279 |
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Enhancer Sequence | TCCTCCCGCC TTGGCTTCCC AAAGTGCTGG GATTACAGGC ATGAGCCACC GCGCCCAGCC 60 AGATAGTAGC CATCTTAATG GAGTGAGATG GCTTACTTTT AAACATTATT TCTAAACTGA 120 ACCCAGACCC TGGCATATTA GAGGTGGTTA CACAGTGAAC GCATTTGACG AACAGTCAAG 180 GTAATTTTGT TTTCCAGGGT TTGCTCCATG AATAAACAAT CTCTGAGAGG CTAGTATCTT 240 GTCCAAGGTC AAGAGCCTGA ATTTGAATTG TCTGACTGAA AGGCAGCATG TTCTCTACTA 300 GTCACCTCTC TACCTGGTTC CACCCTATGC AAGGCAAACA AACGCAGAAG AAAGAAACCC 360 ATTGCCGTGC AAAATCCAGT GATTCCAAAC CCAACCAGCC CACCAGGGAT GTTCTGGGAG 420 TCCGAGCTGG GGACAGGAGC ACAGCCAGCC CTAGCCAGCC CTCCCCCCAC CACACTCAGT 480 GCCTGGCGGG GCAGAGCGAG TCACATTTCA GCCTCACTCA CAGGCCAGCT TGAAATTCGG 540 CCCAGCCGCC ACTGCCTCCT GAGAACTCCT CCGGATGCCT GCAGGCTTAT GCGGGGCTGA 600 GTCACTTCCT CACCTTAATT CTCCCCTAAT ACCTTCCCTT TCTCTGCTGC TTTACTCCTG 660 GCACCACTGT CTGGGTGTGG AATGTCTGGG GAAGCTGTGC AGGTGGGTTG GCTGAGCTGT 720 CTGCCCAGAT ACCACAAACA TGGCTGGGGA GAGAGGATGC AGGGGTAAAA GTAAAGCCAG 780 ATTTGTCTGC TGGCTCTTAA GCGCATCCTA ATCCCCTCAG TCAGTTTGAT CTTCGCAAAC 840 ATGAGCACAG GTCAATATCT CTAAGCTTGG GTCCTGAGGG GCTGGTGGAG GATGGAGCAG 900 AGGATGGATG AAGAGGAACA GGAAGTGAGG GGAGAGTGAT GGCTGCTTTG GCTTTTAGAA 960 ACTTCCATCC CACATTACTT TCCCTAGGGA AGCTCCCACC TCCCATCCCT GGGAGAACAG 1020 ACTGCATCCT GGAAGGTCAA GTTCCAGGTC ATGTTAAATA TGATGGTTTC CTGGATGAGT 1080 CTAAGGACAT ATCATTAATA TCTTCAGCCT ATTTCCAGAA GTCCTGCTGT TCCTCTTACC 1140 TACATGTATG CTGTTCTTCC CTGTGTACAA CTTAACTTTC CTTTTCAGGT TTCGGATGCT 1200 TTGTCTGTAC ATTGCTTTGT GTGTTTGCCT GCCTCAGCTT GTACTTTCGG AGATAGAAAT 1260 TGGGTCAAAG TTTTAATTTT TATTTAAGTT ATTCATTTAT ATAGTTTAAA AAGTCAAGGG 1320 ATGGTGCAAG ATTTATGAAA AAGAGCCCTC TCCCTTCCCC TTAGCAGAGA TAATCATCTT 1380
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