Tag | Content |
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EnhancerAtlas ID | HS188-12122 | Organism | Homo sapiens | Tissue/cell | Th2 | Coordinate | chr7:148676260-148677660 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:148676430-148676445 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTAGAAATCA ATAACAGAAC AATATCTGGA AAATCCCCAA ATATTTGAGG GTTAAACAAT 60 AAACTTGTAT TAGTCCGTTC TCACACTGCT ATAATGAATT TCCCCACCAG GTGCAGTGGC 120 TCAAGCCTGT AATCACAGCT CTTTGGGAGG CCAAGGAGGG CAGATCACCT GAGGTCAGGA 180 GTTCAAGACC AACCTGGCCA ACACGGTGAA ACCCCATCTC TACTAAAAAT TACAAAAAAT 240 TAGCCGGGTG TGGCGGCAGG CACCTGTAAT CCCAGCTACT TGGGAGGTTG AGGCAGGAGA 300 ATCGTTTGAA CTTGGGAGGC AGAGGTTGCA GTGAGCCGAG ACTGTGCCAT TGCACTCTAG 360 CTTGGGCAAC AAGAGCAAAA CTCCATCTCA AAAAAAAAAG AGACCAGGCA CTGTGGCTCA 420 TGCCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCAAGCAG ATCACTGGAG GTCAGGACTT 480 CCTGACCAAC GTGGTGAAAA CCCATCTCTA CTAAAAATAC AAAAATTAGC TGGTCGTGGT 540 GGTGCATGCC TGTAATCCCA GCTACTTGGG AAGCTGAGGC AGGAGAATCG CTTGAACCTG 600 GGAGGCAGAG GTTGCAGTGA GCTGAGATCG CTCCATTGCA CTCCAGCCTG GGCAACAAAA 660 GCAAAAAAAC TCTGTCCCAA AACTGGGTAA TTTATAAAGG AAAGAGGTTT AATTGACTCA 720 CAGTTCTCAT GGCTGAGGAG GCCTCAGGAA ATTTATAATC ACGGCGGAAG AAGCAGCAAG 780 CACCTTCTTC ATAAAACAGC ACTAGAGAGA CCACAACAAG CAGGAGAGGA ACTACCAAAG 840 AAACACTTAT AAAACCATCA GATCTCGTGA AACTCACTCA CTATCACGAG AATAGCACGC 900 GGGAAACCAC CTCCATGTTT CAATTACCTC TCACCAGGTT CCTTCCTCAA CACCTGAGGA 960 TTACAATTCA AAGCTGGGTG CGGTGGCTTA TGTCTGTATT CCCAGCACTT TGGGAGGCTG 1020 AGGCGGGTGG ACCACCTGAG GTCAGGAGCT CGAGACCAGC CTGGCCAACA CAGTGAAACC 1080 CCATCACTAC TAAAAATACA AAAATTAGCT GGGCACGGTG GTGGGCACCT GTAATCCCAG 1140 CTACAGGGGA GGCTGAGGCA GGAGAATCAC TTGAATCCAG GAGAAGGAGG TTGCAGATCA 1200 CACCATTGCA CTCCAGCCTG GGCAACAAGA GCAAAACTCC GTCTCAAAAA AAAAGAAAAA 1260 AAATTTTTTT CAAGATGAAA TTTGGGTGGG AACGCAAAGC CAAACCATAT ATATATAATT 1320 TTTTTTTAAG ACAGTCTTGC TCTGTCGCCC AGGCTGGAGT GCAGTGGAGT GATCTCGGAT 1380 CACTGCAACC TCCATCTCCC 1400
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