Tag | Content |
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EnhancerAtlas ID | HS176-16506 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:44341280-44342720 |
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) |
ZNF263 | MA0528.1 | chr17:44342661-44342682 | TCTTCTTCTTCTTCTTCTTCC | - | 6.05 | ZNF263 | MA0528.1 | chr17:44342667-44342688 | TCTTCTTCTTCTTCCTCTTCT | - | 6.25 | ZNF263 | MA0528.1 | chr17:44342664-44342685 | TCTTCTTCTTCTTCTTCCTCT | - | 6.98 |
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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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Enhancer Sequence | TTGGACTCCT GACCTCAAGT GATCTGCCCG CCTCAGCCTC CCAAAGTGCT GGGATTACTG 60 GTGTGGGCCA CTGCATCTGG CTCCCACCAT CTCTATTAAA ATAAGATAAA ATAAACATAA 120 AATAATGAAC CGACAAAATA ATAATACAAT TCATTGTAAG TAAAATGCTA TCCTGAGTTC 180 TGTGAGTCAT TCTGGATAAT TCAAATTCTC TAGAATTACC ACCTCAGCTG ACTTTTTTTT 240 TTTTTTTTTG TAGAGACCAG GCTGGTCTTG AATTCTTGAG CTCAAGTGAT CCGCTTCCCT 300 CAGTCTCCCA AAGTGCTGGA ATTACATGTG TGAGCCACTG AGCCTGGCCT ACAAATTCTT 360 TATTATACAA CACACAGTAG ATGCTCAATA AATATTTGCT AAGCAGAAAC ATACACTCAA 420 AATACCAGAA ATTATCAAGG AAGTTGCCAG TTGGTCTCTT GGGTTCTTCC TCCCGACAGG 480 TATACACACC TATTGTAAAG ATGAACACAT TAGGCTGTGA GAAACCAATA CTGTTAAACA 540 TTCCAATCAG GTGACAAACT CCCTGGGCTC TGGTTTATAT TACCAAGCAA CCTGATGATA 600 ACTTGGCTTC CTGTGTGGCT TGTTTATAGA AAGAGAATGC TACCCAGGCT GACGTGAGTT 660 GCATTTCTGA GTTGATTTCT CACTGTAAAT TAATAAACTG GCATTCTGGC TACATAGATC 720 AGTCTCTTTG AACTCTTTGT ACCTTCCACC ATTAGTGTGA TTTCTAAGGC TGCAAGCCAG 780 ACACTGCCCA AGACCCAGCA CTGGACTCTG GTGAGTTCTT CCAGCTGTTG CCACCCCAGG 840 AGGCTCTGGG AGCCCCTGGG AACCATCCAG CTTGCTCTCT GTCTCTACAT TTCAGGGTGT 900 GGGTTTCAGG GCATTCACAA CATTCCTGCA ACAGAAGAGT TTTGGGAACA CCCCCAGCAG 960 GATGTGGGTG ATTTGAATGT ATGTCAGAGA TGTGGTTGTA ACTGAGAAAT CTTAAGCCTA 1020 GTGAATTTTA TTCCACTTGA CTTAAATAAA GAGCACGTGA AAGAAGGGGA TCTGAGGACA 1080 TCTATGAACA GGGCCCCGAG GGCATGAACT TACTAGTGTT TATATGACTA GTGTTTATCT 1140 GGGCCTGTCT AGTCTGGAGA ACCTGACTCT GGTGTACCCA AGCTTTGCAG TGGCTGTAGA 1200 GGTTTGCTCT TTTGGAGGGA GAAGATAATT CATTCCTCCA ACACCTGAAT GAGGGTAGAT 1260 TAACCCACCT CCTTCAGCTG CAATTTGGCA AATTTCTCTT CTTTGATTTA ATGCTCAACG 1320 GACAAATTTC CTTTCTTCTT CTTCTTCTTC TTCTTCTTCT TCTTCTTCTT CTTCTTCTTC 1380 TTCTTCTTCT TCTTCTTCTT CCTCTTCTTC TTTTTTTCTC CTCTTCTTCT TCTTCTTCTC 1440
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