Tag | Content |
---|
EnhancerAtlas ID | HS053-38896 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr8:81211880-81213990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr8:81213233-81213244 | TATGCCAAGTA | - | 6.14 | RARA(var.2) | MA0730.1 | chr8:81213093-81213110 | TGCCCTCAGGATGACCT | - | 6.48 | RREB1 | MA0073.1 | chr8:81213777-81213797 | CCCCCCACCACCACACACAC | + | 6.25 | RREB1 | MA0073.1 | chr8:81213784-81213804 | CCACCACACACACACACACA | + | 6.41 | RREB1 | MA0073.1 | chr8:81213767-81213787 | CCCCCCCTCACCCCCCACCA | + | 7.13 | ZNF263 | MA0528.1 | chr8:81213768-81213789 | CCCCCCTCACCCCCCACCACC | - | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH08I080301 | chr8 | 81212261 | 81212430 | GH08I080300 | chr8 | 81212434 | 81214170 |
|
Enhancer Sequence | CACTGCAAGC TCCGCATCCC GGGTTCATGC CATTCTCCTG CCTCAGCCTC CCGAGTAGCT 60 GGGACTACAG GCACCCACCA CCACGTCTGG CTAATTTTTT GTATTTTTAG TAGAGACAAG 120 GTTTTACCAT GTTAGCCGGG ATGGTCTCGA TCTTCTGACC TCGTGATCCG CCCACCTCGG 180 CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCTGCGCCC GGCCAGTAGC TTTTATTTTT 240 TTAAGCATTG GCAAAATATT TCTATAAATA AATACCTGCC CTTGTCAATT TTATTTCTAT 300 AAAACTTCTC CAAATATCAT TTGGTAATTG AGCTTCTAAA TAAGATGCCC TCCTAAAAAT 360 TGTAAACTGT GTTTGCTAAC TAATAAGAGG CATGAAGTGT TCCATGACTG TATTATTCTT 420 GGGGATTCAG GCTGTGGTGA TGTGAGCAGC CACCCCCTTG GGACACATCA TGCTGGTAAA 480 CCACTGATTC ATGACACACT GCCAGGAATG GCTGTCATCC AAGTCCCGGG GCAAGTTCAG 540 CCAGCGCCAG AAATCACCCA AGAAGGGCTA GTCAGATGTT TAAATTCCTG CCTTTGTCAG 600 AATCCTAAGA ATTATTTTTG ATACCTCCTT TTCCCCTCCC ATCTTTATCC AATCAATTAC 660 CAACATCTCT CAACTGGTTT CACTTCCTAA ATGCCTCTCC AATCTGTCCA CTCCTCTTTT 720 ACTCTACCAC CGCTTTCCTA GGCCAAACTG CCTGGATTAT TACAAAATCT TTCCAACTAG 780 GTTACCCCAT CCACTTTTGT CCCCCTCCAA TCAAGTCCCC ACACAGTGGC CAGGTTGATT 840 GAAAAGCAAG CATAGATCTG AGTGGTCTTT CCTCTCCCTC CCAGACTCCG GTGGCTTCCC 900 CTTGCTCTCA GATGGAAGAT CAATATCTGC ACCTGCCCAG GGGCCATGAA TGAACTGGCC 960 TCTCTCCAAC TGGCCAGTCT CATCCTGTAC TTCACATCAC TATTCTCCCA CTTTCTCCAC 1020 GACATTAATC TGCTCATGGC TCCTCGTATC TCACGAAATT TGGGGAAGAC CCACGTACCT 1080 GAATTTTCCC AAAAGTTCCT TAGGTGGTTC TGAACCACTA CTATGGTTGA AAGTTTTAAT 1140 AGCTAGACTG GCTCTTCCTG TCTGTGCCAG GGCGGCATGT GGTGCATGCC AAGCCACAGA 1200 GATGCTCAGG CTGTGCCCTC AGGATGACCT AGTGGGAGAC AGCAGCACCA CTGGTGGCAG 1260 AGAACCCTGG CATCAAGCTC TTTGGGAAGT GGAGCTCCGA TGATGTGCAG ATCTGGCACT 1320 TGCTTGCAGG ATTACACTGC AGTGAAGGAG AAGTATGCCA AGTACCTGCC TCACAGTGCA 1380 GAGCGGTATG CCGCCAAACG CTTCCGCAAA GCTCAGTGCC CCATCGTGGA GTGCCTCACT 1440 TACTCCATGA TGACGCACGG CCGCAACAAC CGCAAGAAGC TCATGATCAT GCGCATCGTC 1500 AAGCACGCCT TCGAGATCAT CCAGCTGCTC ACAGGCGACA ACCCTCTGCA GGTCCTGGTG 1560 AACGCCATCA TCAACAGTGG TCCCCGGGAG GACTCCACAC TCACTGGGCG AGCCAGGATC 1620 GTGAGACGAC AGGCTGTGGC CGTGTCCCCA TTAAGCCGTG TGAATCAGGC CATCTGGCCG 1680 CAGTGCACAG GAGCTCTTGA GGCTGCCTTC CGGAACATCA AGACCATTGC TGAGTTCCTG 1740 GCAGATGAGC TCATCAGTGC TGTCAAGGGC TCCTCCAACT CCTATGCTAG CAAGAAGAAG 1800 GACGAGCTTG AGTGTGTGGC CAAGTCCAAC CGCTGATTTT CCCGGTTGCT GCCCAATAAA 1860 CCTGTCTGCC TTCTGCCTTT TGGGACGCCC CCCCTCACCC CCCACCACCA CACACACACA 1920 CACACACACA CACACACACA CACACACACA CACACACGAA GTAGCTAGAC TGAAGATGGA 1980 GCCAAGTTGA AACTTGCGTC CCAGGCTCTT ATGATAGCAT CAGAGTTTGA CTTAGGTTTA 2040 AAAAGCAGGC CAGGAAAAAT TTCAAAGTGG CAAGTCATGG GGCAGGCTTT GCAGAGCAGT 2100 CACTGCTGTT 2110
|