Tag | Content |
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EnhancerAtlas ID | HS112-01022 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr1:160390980-160392460 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:160390987-160391008 | GGGGGAGAAGAGGAGAGGAGG | + | 6.12 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTCCCTGGG GGAGAAGAGG AGAGGAGGTG CTTGTTGGGT GAATGGGGAG AGGAAGACCA 60 AGGAACTTCT GTAACTGCTG GAAATATAGG GCAATGATGA CATGAGTTGG GGGTGTGTGC 120 TTGTTTTCCG TTGCTGCCCT AACAGATTAC CATAAACTTA GCAGCTGTGA AACAGCACAC 180 ATTTATTATC TCCCAGTTCC ATGGGTCAGG TGCAGGCTGG CTGGAGGCTG TGCTCAGGCC 240 TCACAGGCTG AAATCAAGAG GACTCTCATC TGAGCCTATG CTTTCTCTTT CAAGCTCATT 300 ATTATGGGGA GAATTCAGTG CCTTGTCACA TAGCCCCATA GGCAGTTTAC ATGATGGTAG 360 TGCACTTTTT TTTCCAGCAG AAACAGGTCT CTGACCTCTG CCACCAGCTG GAGATAATGC 420 TGATTTTAAA GAGCTCATGT GATGAGATCA GGCCCTAAAG GACAGTCTTC TTTTAAGGCC 480 ACTGACTTGG CACATTAATT ACATCTGCAA AATGTACCAA GATTGTTGTC TAATGAGGGG 540 ATGGGAGTCT GGTAGAAGTG GAGGGTATCT TTGAATTCTG CCTGCCACAG TGGGGTAGGG 600 ACCCAATAAA GGGATGTGAG CTTTACCTGC AACAGCATGG ACTCAGGCTA GACTAGCCTG 660 CCTGCCAGTA GATCTTGAGA GGACTCACCA GATGGTGCTT TTGTTGCCTT CAAAAAATGA 720 CGTTTTATTG CCTATATTTT GGTAAATTCT TAAATGCCAT CCTAGCTTCT CCCTTTCCCT 780 ATTCATATTA TTAAGTGAAT TTAGTCAACC CTGAAGAATC TTACTTGGTG CCTACTCTGC 840 CGGGTTCCAT CTTGGTCTGT CGGGAGTTCC CTGAGGGAGG AGCAGAGTGC CTCAGGACTT 900 GACCACGCAC CTGGCCTCCG CCCCATCTCC CACATGAACT CCAGGCTTCA AGGGCAAGAG 960 GTAGCCCTTA CCTTGTTCCT ATTTGAGGCT GGCATCCCCT GTAGTAGAAC AAAGATCACC 1020 AACTCCATTT CTGTGGCATT CCAACCTGTC TCTAATTGTC TTGGAAATGG CCTGAGACTT 1080 GGGAAGGAAA CCAGTGATGT CCCTACCCCT TTATCTTCTG CCCTGACCAG GGTCATCCAA 1140 TCTCCTGTAC TGCCACCACC ATTTTTGGCA CATAGAGGAC TCTTTCCTTT CCCCATTACC 1200 TTGCTTTTAA CCAGGAGCAA ACTTTTTCCT TTGTTTACCT GAGATAAAAG GATCTTTTCA 1260 AAGGGAATTT ACTGAGAAAT GTAGGGGAAG CAAGAGAATA AAGGAAGAAA TGATAGACAT 1320 ACACAGATCC ACACCTATAT ACCCAGAGTC CCATCTGAAA TGACTCAGGT TCCTGGGTTC 1380 TGCATAGAAG GCCTCACTTT CTTTCTTTGT CCTGTCACTT CAGGCTGGTC CTGCTCTTAG 1440 GCCAGGGGGC TTTTATTTTG GTTTTTGGAC TTGAAGTGCA 1480
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