Tag | Content |
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EnhancerAtlas ID | HS098-22384 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr16:75254110-75255280 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:75254874-75254889 | TGAACTCCTGACCTT | - | 6.04 |
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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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Enhancer Sequence | CACTCTTGTC ACCCAGGCTG GAGTGCAGTG GCGTGATCTT GGCTCACTGC AACCTCCGCC 60 TCCTGGGTTC AAGCATTTCT CCTGCCTCAG CCTACTGAGT AGCTGGGATT ACAGGCATGC 120 ATCACCACAC CTGGCTAATT TTTGTATTTT TAATAGAGAT GGGGTTTCAC CATATTGGTC 180 AGGCTGGTCT TGAACTCCTA ACCTCCAGTG ATCCGCCCAC CTCAGCCTCC CAAAGTGATG 240 GGATTACAGG CGTGAGCCCC CATGCCCGAC CTGGGGTCTT ATTATGTTGT CCAGGCTGGT 300 CTCGAAATCC TGTGCTCGAG TGATCTGCTC ACCTCAACCT CCCAGGGTGC TGGATTACAG 360 GTGTGAGCCA CTGTGCCTGG CTGATGTAAC TAATACTCCA TTCTACCTCC ATTCTACAAC 420 AATGTGCTTT TTCCCTACTC AAATCTTCTC ACTTCCTGCA TGTTGACGTG GAGTTTCAGC 480 TCATTCACCT GCATTTTTAT AATGCGTGCT CTGTTGTGTG AGTATGCCAC CATCTAGTTC 540 TCTTATTTAT TTATTTATTT TTTTAGATGG AGTTTCACAC TTGTCGCCCT GGCTGGAGTG 600 CAGTGGCATG ATTTCGGCTC ACTGCAACCT CCACCTCCCA GGTTCAAGCA TTTCTCCTGC 660 CTCAGCCTCC TGAGTAGCTG GAACTACAGG CATGAGCCAC CACCCCAGCT AATTTTTGTA 720 TTTTTAGTAG AGACAGGGTT TCATCATATT GGCCAGGCTG GTCTTGAACT CCTGACCTTG 780 TGATCCACCT GCCTCGGCCT TCCAACGTGC TCTTTCTCAT TTTTTTGCTA TTACAATACC 840 AGTTTTTGAT GCTCTGAAAC GTCAGGGAGG CACCTTGCCT GCCTGTGTTC CTGTGGGCAG 900 GAGACGCAGG GGCTGCCTTG TAAGCAGGCG AATATGACCC CAGAAGGGGA CAGCTGGTCT 960 GAGGGACGCG GGTGTGCTCA AATGTAAAGC CCAGTTTGTT GGGTTGGCCC GCGCACAGGA 1020 GTCGAGAATC TGGTCCTGAC ATAGCAGAGG CATGGTGGGC GTGTGTGGAA CACCTGACTA 1080 TTTTCATTGT TTTGTTTTCT GCTTCCAATG TGCCATTTTA TGGTGTGGAA GTAAAGTCCA 1140 GCTGTGTTTG TTTTGATTTT TTCTTGAGAT 1170
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