Tag | Content |
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EnhancerAtlas ID | HS019-06769 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr17:8964850-8966300 | 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 | chr17:8965240-8965255 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGGCCCTT CCTCAAAGAT AGGTTTGGAG TGGGGCCCTA GGATTTGATA TCTAACAAGT 60 GCCCAGGTGG TGTTGATATT GCTAGTCTGT CCACATTTGG AGAACCACTG GTAAGCGATG 120 GGCATCCAGG AGCAGTTTTT TTGTTGTTGT TGTTGTTTTT GTTTTATTTT GTTTTGTTTT 180 GTTTTTTTGA GACGGATTCT CGCTCTGTCG CCCAGACCAG AGTCCAGTGG CGTGGTCTTG 240 GCTCACTGAA ACCTCCACCT CCCGGGTTCA AGCAATTCTC CTGCCTCAGC CTCCCAAGTG 300 GCTGGGATTA CAGGTGCCTG CCACCACGCT GAGCTAATTT TTTGTATTTT TAGTAAAGAC 360 GGTGTTTCAC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACCTCGTGAT GCGCCTGCCT 420 CGGTCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA CAGCCAGCCA GGAGCAGTTT 480 TTAGCAGGGG ACAAGCCTGA TGAAATGGCG TAAACGATGG CCACTGGATA TGGCTGTGAG 540 AGCAATCACT CATTAAATCA GGTGGTTTTG TTCCTGAATC AATCTTGCAT CTCAGTAGAT 600 TTTTAGTCCC CGAGGCTCAG ACTGCCAACA AAAAATCTTT CAGGGCATTG TAATATTTTG 660 ATGACCACAG ACTTCCTTGG AATGAAGTTG TCCCAATTCC GAATGAGGGG CCACGGCCTC 720 ATAAAAGGTT TTTATTCCCC TTTCTGGGCT GGAGAAGCCA TCTAGGAAAA TGCTGTTTCT 780 GTACCTAAAG TGTTGGGATT TTCAGATTGT TTTCATGAGT TACAGACACA CGGAGCAGCA 840 TGCTTGAACT TAGACCCTTT CTGCAAATGT CAGGCTGTAT GATAATTGAG CCAGAATGTT 900 ACTCGAGCTT TCTGACACAT TTTTTGAGAC CTCCCATCCA GTATTCTCAT ACAGAAATAT 960 GGCTCCTCCA GGTGTGCACT TAACACTCGC TTCTTTGCAG CCAGGGGAAC CTTTAGCTAA 1020 GGAAAAAAAA GCCCTCCTAC CCTTGGTTTC AAAAGGTTTT GAAATGCTAA TTCACAACCA 1080 TGAAGTATTC TGACAGCCTG GAATGTTATT CAGGGCAATC AGGCACCTTG ATTATTACAG 1140 AAGTGTGAAA GGTAAATTGC TGCTACCCAA GAAGTCACCC AGCTTTTCAA GAGAAAGCTC 1200 AGAAAAATAG CACATAAAAT TATGTTCGGG GATTACACTT CATGTATCGT GTGATGGGGT 1260 GCTCTGACAC CCAGCGTGTC TGTAGGTGTC ACAACGTCAG CTCGTAGTAG AAATGTAACA 1320 GCATTTGCCA GCGTCGCCCT TAAGTAAAAA AAAATAATAA TAATACAGGA TTGTGGGAAA 1380 CATTTTCAGA ATGTGTTGTA TGCCTATCTA AAATCTGAAA GTACATCTTT TTTGAGCTTC 1440 TGCTTTTCCT 1450
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