Tag | Content |
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EnhancerAtlas ID | HS053-10555 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr12:122310330-122311410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:122310355-122310370 | TGAACTACTGACCTC | - | 6.07 | RARA | MA0729.1 | chr12:122310352-122310370 | TCTTGAACTACTGACCTC | - | 6.1 | ZNF263 | MA0528.1 | chr12:122310490-122310511 | TCTCCATCCTTTCCCTGCTCC | - | 6.81 |
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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 |
GH12I121871 | chr12 | 122309456 | 122312164 |
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Enhancer Sequence | TTCACCATGT TGGCCAGTCT AGTCTTGAAC TACTGACCTC AAGTGATCCA CCTGCCTCAG 60 CCTCCCAAAG CATTGGGATT GCAGGCATGA GCCACCGTGC CTGGCCTAAA ATTTCTTGTC 120 TCTCCAGCAT CCACTCCTGT TCTCATAACA GCGTCTCCCT TCTCCATCCT TTCCCTGCTC 180 CGTTCATGTC GTTTGGGTGG GGCATGTGAG CCAGGACTGG GCAGTGAGAA TCCCTGTGAT 240 TGGTTCAGGG CTGGGCACCT GGCCAGAACT GGCCATATGG ATTTGCTCTG GATCTTCTGC 300 TTGAGAAAAG AGGCTCACTC TGAGCTCTGA GTATGCTGCA CTGATCCAGT GGTGCTGCGG 360 GGGCCAACCC TGAGTCAGCT GAAGGAAAAC ATGCTTGTAT ATAAAGCCAG AACAGAGAAA 420 CCAGAGCTGA GAGAAGATAG GCTGATTCCT GATGTCTGAG CAACTTGTTC CAGGCAGAAA 480 CAAGCTCCTG GATGAGTCAA ACCTTTTTCC CTTTTGCTTA AGCTAGTTTG AGTTGGGTTT 540 CTGGCATTTA CAACCACTGG TGCTGACAAA CACAAAGAAA GAAACAATAA CACCACCACC 600 ATCTGTGAGC ATGTATTCAC TGTCAAGCAC CGAGGTAGGG ATCATGGGGA TTGTCTGTTC 660 CACAGGGAGG TAGTACTTGA TCATTTTGTT TGCATTTGCT GGCACACATA AAATAAAGTT 720 GACTGATTTT AGCAGTTTTT ATTATTATTT TAAAACTCTC TGCAGACATT GCATCCCTGT 780 GGTAGATTCT ACTGTCCATA ACCCTTCAAG GAAGGCCTCA ATGCCCAGCT GTAGGGAGAC 840 TGGTTGGCTG TCACCTCCTA TCGGATCTGC CTCAGCTGTA GAGACTTGGC CACAGCTTTC 900 CCAGAGCAGC CCACTTTTTG TGATTGAGCA AGGGAGTAGA GAGGCTGGTC CCTTTCAGCC 960 CAATGGGGGT GACTCTGACC AGTGAGTCTG TCTCCAGGGC CCCGGTAGGG CTGGCCAAGG 1020 CCTTGTGGAG TCTCCACCAC TGAGTTCTCC TTCTCCCCAG TCCAGCCTCC TCTGCTTCCT 1080
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