Tag | Content |
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EnhancerAtlas ID | HS136-14173 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:169582570-169583740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr3:169582648-169582663 | GAGGTCAGGAGTTCA | + | 6.22 | Znf423 | MA0116.1 | chr3:169583157-169583172 | GCACCCATGGGGGGC | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I169864 | chr3 | 169582671 | 169583930 |
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Enhancer Sequence | ATCTGTGAAA CCGGCCAGGT GCAGTGGCTC ATGCCTGTGA TCCCAGCACT TAGGAAGGCT 60 GAGGCAGGTG GATCACCTGA GGTCAGGAGT TCAAAACCAG GCTGGCCAAC ATGGCAAAAC 120 ACCGTCTCTA TTAAAAATAC AAAAATTTGC CAGGCGTACT GGCATGCACC TGTAATCCCA 180 GCTACTTGGG AGGCTGAGGC AGGAGAATTG CTTGAACCCA GAAGGCAGAG GTTGCGTGAG 240 CCGAGATTGT CCCACTGCAC TCCAGCCTGG GCAACAGAGC AAGACTCCAT CTCAAAAAAA 300 AAAAAACCTA TGAAACCAAA TTAGCCCAGT GTAGTGGCGG GTGCCTGTAG TCCCAGCTAG 360 TAGGGGGCTG AGGCACAAGA ATCTCTTGAA CCCGGGAGGT GGAGTTGCAG TGAGCCGAGA 420 TTGCGCCACT GTAGTCCAGC CTGGGCGACA GAGTAAGGCT CTATCTCAAA AAAAAAAAAA 480 AGAAAAATTA TATGAAGCCT TCTCTTCACA GGATACCTTA TGTCACAGCT CAGTGTGTAG 540 AACAAGTGAG TCAGGGCTGC TACAGCTAGG CTGGAGTGGG GTGGGAGGCA CCCATGGGGG 600 GCGCATTAGT AACCACACAG GAGCCGCTCT GTGGAGATTG AGGCCTTTTC CTAGCTGTGT 660 TAGCTCTGAA CAAAGCTCTC GGTTCTTAGT GCTCTCACTA AGTTCCTTTC CGACTGAAAT 720 CTGTCAAGGT TTGTCAACCA AAACTCTCGA CACTCATAAA ACATTATTAC ACATTGGTAA 780 CATGGGTGGT ACTGTACCAG GAACCAACAT AACAAGTTCC TGTTTTCAAA GAGCTGCCTG 840 TTTAATGAAA GAGACAGCAA GAAAGCCACC GTTACCGTAT AGATGAGAAG TGGAGGCACG 900 CAGGGGTGTG TGGTTCCACA CTTCAGTGAC AATAAGTACC TCAAGTCTGG TGATTCCAGG 960 TCGGGGAGGA GGGTCTTGGG AAGTTTCCAA GAGAAACTGG TGCCTGGATT GCACCTTAAA 1020 GGAAGAGTGG GAGTCATCCA GGTGGGTGGA CATGAGGGAG GGATAAGTCG GGGGGTTGCA 1080 GGGGAGGATG GTGACACGAG GGAACATCTT TCTAGCCACA AAGAACCACT TGCTGGGGAT 1140 GGGAGAAGAA TGTGGCCAGT CCAGGGAATT 1170
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