Tag | Content |
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EnhancerAtlas ID | HS078-01272 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:112780430-112781740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG2 | MA0669.1 | chr1:112781338-112781348 | AACATATGTC | + | 6.02 | ZNF263 | MA0528.1 | chr1:112781253-112781274 | TCCTTCTCCTCTCCATCTTCC | - | 6.31 | ZNF263 | MA0528.1 | chr1:112781271-112781292 | TCCTCCTCATTTCCTTCCTCT | - | 6.44 | ZNF263 | MA0528.1 | chr1:112781259-112781280 | TCCTCTCCATCTTCCTCCTCA | - | 7.29 | ZNF263 | MA0528.1 | chr1:112781256-112781277 | TTCTCCTCTCCATCTTCCTCC | - | 7.52 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCACATTTT ACATTCCAAC CCATCAATGA ATCCTGCAGG TTTTCCCTTC AAAATACATC 60 TAGAATCTAA CCACTTCTCA CCACCTCCAC CCACTGTCTC CCTGCCCCAA GCCACCACCA 120 TCACTTGCCT GAATTATAGC AATAGCTTCT GAAAAATTGT CCCTGATTAA CCCTTGCCCC 180 TTGCAGACTT TTCTTCACAT AGCAGCCAGA GTAATTTTTA AAAACATAAG TCAAATTACA 240 CCACTTATCT GTAAAACTTA CAGTGTCTTC CAATCTCACT CAGAGTATGA TGTGCCAGTT 300 TGACTGAGCC ATGGAGAGCC CGGATGTTTG CTCAAACATT ATTCTGGGTG TGTCAGTCAA 360 GGTGTTTCTC AATGACATTA ACATTTGGAT CTGTTGATAG TAAAGCAAAT TGCCCTTCTC 420 AGTGTGGGTG GCCTCATCCA ATCAGTTGAA AGCTGACTAG AACAAAAGGG CTGATCCTTC 480 CACAAGTAAG GGGGACTCCT CCTTCCTGAC TGCCTTTGAG CTGAAACACT GGCTTTTTTC 540 CACCCCTCAG GCTTAAACTA AAATATTGGT TCTTCCCAGG TCTCCAGCCT GCCAGTATGC 600 AAACTAGAAC TACACCACTG AGTCTCCTGG GTCTCTAGGG TGCCAACAGC AGATCTTGGG 660 ACTTGTCAAA CCGCATAATT GCATGAGCTA ATTCCTTACA ATAAGTCTGT TTATATATAC 720 ACCCTGTTGA TTCTGTTTCT CTGCAGAACC CTGACTAACA CACAGATCCA AAGTCTTTAC 780 CAAGACCTCC AGGGTCTTAT ATAATCAGAC CTCCTATTAC CTCTCCTTCT CCTCTCCATC 840 TTCCTCCTCA TTTCCTTCCT CTCCCCTTCA AATGCTGTGC TCCCACAATG TTAGCCTCAA 900 ATGAGTCAAA CATATGTCCC CCTTGGGACT TTTGCACCTG CTGTTCCTTC TGCCTGGAAA 960 GCTCTTCTGC ACAGCTCACT CCTTCACTTG CTAAAGGTCT CTCCCAGCTC ACTGATGTCT 1020 TATTGGAGAG GACAACCTTG ACACACGCCT CTGTCCCATA TAAAATAGCA ATCCATCCCC 1080 ATATGACATT CCTAAGTCTT CTTCTCCTGC TTTAATTTTC TCTGTCATGC CCTTGACTGC 1140 CTGATATATT AAATATTTGT CTGCTTACTG TCTTTTCCCA CACTAAAATG ACTCAGACAA 1200 AAAAACACAC AGATAGAAAA ACAAGCAGTA AAGGAGGATA AAGCATGAGA AGGCATTGTC 1260 TCAAATAGGG GAGTTAGGAA AGGCCTCCTT GAGGAAATGA AATGGATACA 1310
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