Tag | Content |
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EnhancerAtlas ID | HS058-07352 | Organism | Homo sapiens | Tissue/cell | GM10847 | Coordinate | chr7:102502080-102503550 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:102502212-102502227 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTGTTATAA AGAATATATA GTAACATACT TAGGTTCAAA AAGCAGTACA CAAAATTATA 60 TCTGCAGGCC GGGCGCGGTG GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA 120 GGTGGATCAC CTGAGGTCAG GAGTTCACGA CCAGCCTGGC CAGCATGGCA AAACCCCATC 180 TCTACTAAAA ATACAAAAAT TATCCGGGCA TGGTGGCAGG TGCTTGTAAT CCCGGCTACT 240 CGGGAGGATG AGGCAGGAGA ATCGCTTTAA CCCAGGAGGC AGAAGCTGTA GTGAGCCAAG 300 ATCGTGCCAC TGCACTCCAG CCTGGATGAC AGAGTGAGAC TGTGTCTCCA AAAAAAAAAA 360 AAAAATTCAC ATCTGCATAT GTGTGTGTAT AGTGTATGTA TATGTGTATT AAAAGAAACA 420 GACGTTTTGG GCAGGGCGCA GTGGCTCACG CCTGTAATCC CAGCACTTTT GGAGGCCAAG 480 GCGGGTGGAT CATGAGGTCA GGAGTTCGAG ACCAGCCTGG TCAATGTGGT GAAACCCCGT 540 CTCTACTAAG AATACAAAAA TTAGCCAGGC GTGTAGTCCC CGCTACTCGG TAGGCTGAGG 600 CAGAAGAATT GCTTGAACCC AGGAGGCGGA GGTTGCAGTG AGCTGAGATT GCACTACTGT 660 ACTCCAGTCT GGGCGACAGA GGGAGAATCT GTCTCAAAAA AAAAAAAAAA AAGAAAAGAA 720 ATGGACGTTT TGGAGGGTGC GCAATGATAT GAATATGTTT TTTCATTATT CATATTTCTT 780 TTTGTATTAC TAGTGTTTGT GAAAATAGCA TAATTTGGAG GAAAAACCCA ATATGTGTCT 840 GTTATTGAAT ATTTTTGTGT ATCAACAAAG AATTATATAA AATATTTACA CTAGGCTTTA 900 TTTCTTTATA CAAAGCAACA CAGTTCTGGT TAGTTTACTT TCTATTCTAA ACAAACCATC 960 AGCACAAATG TGCTAATATT CAAGCAAAGT ACTCAGCTAT GAATGTTAAC ATGTACAAGT 1020 ATTATATACA TAGATGAACA GTTTTACTTT ACAAAAATTG ATGGATACTG CTCTATCTTC 1080 ATATTACTTG ACCCAGCTTT GAAGCCTGAC TCTGCTGACC ATCCCCTGCT TTTTGAAATA 1140 GCATCTTCCT TGTTTCTCAT GATATTACTC TGACCTCTGT CTCCACCTAC TTCTCTGGAT 1200 GTTCGTTTTC AGTTTCCTTT GTAGGTTCAT CTTCCAAATC TATTCAATAC ATACTGATGT 1260 TCCCTGGAGC TTGGAACTTG ACCTTCTCTT CTCTTTGTGA CTCTCATCCA TGGCTTTGAC 1320 CACTTCAGCC ATCTCTAGAT CTAGCCCAGA TCTCCCTCCT GAGATACAGA TCTTGTTCTC 1380 TAACTGATAA CTAGACATCT GAATGTGTCA TAGGCACCTC TAACTCAGCA CTGTTACTTT 1440 CAGAGAACTA GAATTCAAAC TGGAAGCCAT 1470
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