Tag | Content |
---|
EnhancerAtlas ID | HS060-32297 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr7:102502050-102503470 | 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 | ACCCAGAATA TTCTGCAAAC ATGAGAAGTG TTTGTTATAA AGAATATATA GTAACATACT 60 TAGGTTCAAA AAGCAGTACA CAAAATTATA TCTGCAGGCC GGGCGCGGTG GCTCATGCCT 120 GTAATCCCAG CACTTTGGGA GGCCAAGGCA GGTGGATCAC CTGAGGTCAG GAGTTCACGA 180 CCAGCCTGGC CAGCATGGCA AAACCCCATC TCTACTAAAA ATACAAAAAT TATCCGGGCA 240 TGGTGGCAGG TGCTTGTAAT CCCGGCTACT CGGGAGGATG AGGCAGGAGA ATCGCTTTAA 300 CCCAGGAGGC AGAAGCTGTA GTGAGCCAAG ATCGTGCCAC TGCACTCCAG CCTGGATGAC 360 AGAGTGAGAC TGTGTCTCCA AAAAAAAAAA AAAAATTCAC ATCTGCATAT GTGTGTGTAT 420 AGTGTATGTA TATGTGTATT AAAAGAAACA GACGTTTTGG GCAGGGCGCA GTGGCTCACG 480 CCTGTAATCC CAGCACTTTT GGAGGCCAAG GCGGGTGGAT CATGAGGTCA GGAGTTCGAG 540 ACCAGCCTGG TCAATGTGGT GAAACCCCGT CTCTACTAAG AATACAAAAA TTAGCCAGGC 600 GTGTAGTCCC CGCTACTCGG TAGGCTGAGG CAGAAGAATT GCTTGAACCC AGGAGGCGGA 660 GGTTGCAGTG AGCTGAGATT GCACTACTGT ACTCCAGTCT GGGCGACAGA GGGAGAATCT 720 GTCTCAAAAA AAAAAAAAAA AAGAAAAGAA ATGGACGTTT TGGAGGGTGC GCAATGATAT 780 GAATATGTTT TTTCATTATT CATATTTCTT TTTGTATTAC TAGTGTTTGT GAAAATAGCA 840 TAATTTGGAG GAAAAACCCA ATATGTGTCT GTTATTGAAT ATTTTTGTGT ATCAACAAAG 900 AATTATATAA AATATTTACA CTAGGCTTTA TTTCTTTATA CAAAGCAACA CAGTTCTGGT 960 TAGTTTACTT TCTATTCTAA ACAAACCATC AGCACAAATG TGCTAATATT CAAGCAAAGT 1020 ACTCAGCTAT GAATGTTAAC ATGTACAAGT ATTATATACA TAGATGAACA GTTTTACTTT 1080 ACAAAAATTG ATGGATACTG CTCTATCTTC ATATTACTTG ACCCAGCTTT GAAGCCTGAC 1140 TCTGCTGACC ATCCCCTGCT TTTTGAAATA GCATCTTCCT TGTTTCTCAT GATATTACTC 1200 TGACCTCTGT CTCCACCTAC TTCTCTGGAT GTTCGTTTTC AGTTTCCTTT GTAGGTTCAT 1260 CTTCCAAATC TATTCAATAC ATACTGATGT TCCCTGGAGC TTGGAACTTG ACCTTCTCTT 1320 CTCTTTGTGA CTCTCATCCA TGGCTTTGAC CACTTCAGCC ATCTCTAGAT CTAGCCCAGA 1380 TCTCCCTCCT GAGATACAGA TCTTGTTCTC TAACTGATAA 1420
|
| |
|
|
|