Tag | Content |
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EnhancerAtlas ID | HS118-13595 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr3:183182060-183183120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr3:183182611-183182623 | GTCTGTTTACAT | - | 6.44 | FOXP2 | MA0593.1 | chr3:183182612-183182623 | TCTGTTTACAT | - | 6.02 | Foxo1 | MA0480.1 | chr3:183182870-183182881 | TCTTGTTTACA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr3:183183070-183183085 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCCGTGCCT CAGCCTCCCG AGTAGCTAGG ACTACAGGTG CATGCCACCA TGCCCAACTA 60 ATTTTTGTAT TATATTAGTA AAGACGGGGT TTCACTATGT TGGCCAGGCT TGTCTCAAAC 120 TCCTGACCTC GTGATCCACC TGCCTTAGCC TCCCAAAGTG CTGGGATTAC AGGTGTGAGC 180 CACCGCGCCC GGCTCTCTCC ACACTCTTCT TAGATGTCCC ATCTGCTCCT CCAAGCATCA 240 GACCAGTGTT CCCCAGGTGT GTTCAGTCAG ATGACCTGTT GGCACCTCAA CATGTTCAAA 300 GCTGAACTTA CCATCTTGCC ACATTGCTAC TAACCTCATT ACCTTGAACC TCTTCCCTAA 360 TCTAGACTTC AGCAAACATA TCCAACTTTT CCTACCTTTG GTCTTGTTTT ATCTAATCCA 420 TTTACTGTGC AGCCCCCAGG GTACAGAAAC AGCTGGATTG TTACATCATA GTGTTTGCCT 480 TATTTGAACA CAGTTCGAAC AGTTGGCCAC CTTTGGCCGA AACTCAGTGA TTGGTACAAG 540 ACTAGATTAC AGTCTGTTTA CATATCCAGT TAGGTGACAC TTCACTATGT ATGGAGAAAC 600 CTTTAGGCTG AACTTAAAAT ATGTAAGGAG GCAGCTTTAG CCTAAACTTA ATTTAACAGG 660 TGGTAGCAAA GGTTCTAAGG AGGGAGATTC TTCATTCAAC AAGCAGGGAA CCCTACCCGA 720 GAGGGGCAAC ATGAAGGCAC GCAGGCTTGG GCTCACTCCT GTTTCCCAGC TCATCCTTGT 780 AATAAATGTT TTTCACCATC AGGACATACT TCTTGTTTAC ATATGACCTT TAGCAGAATA 840 CGTATACATG ATATAAAACA GGATGATTGC CAAGTAGCAA TTTTAACTGC TACAATACAC 900 TTTATCAGCT CTCATATATC TACCTGTTTG AAAATGCTTA TCTGGGCCAA GCGCAGTGGC 960 TCACACCTGT AATCCCAACA CTTTGGGAAG CCAAGGCAGG TGGATCATCT GAGGTCAGGA 1020 GTTCAAGACC AGCCTGGCCA ACATGCTGAA ACCCCATATC 1060
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