Tag | Content |
---|
EnhancerAtlas ID | HS118-19845 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr9:139531740-139533160 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr9:139531803-139531818 | GAGGTCAAGAGATCG | + | 6 | ZNF263 | MA0528.1 | chr9:139532885-139532906 | AGAGGAGGGGGAAGATGAGTG | + | 6.4 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGCAAATTAA AATTACAGTG AGATGCAGCC GGGCGCAGTG GGAGGCCGAA GCAGGCGGAT 60 CATGAGGTCA AGAGATCGAG ACCATCCTGG CCAACATGGT GAAACCCATC TCTAAAAATA 120 CAAAAATTAG CCGGGTGTGG TGGTGCGTGC TTGTAGTCCC AGCTACTAGG GAGGCTGAAG 180 CAGGAGAATC GCTTGAACCC AGGAGGTTCC CAGGTTGAAC CCAGCCTGGC AAAAGAGCAA 240 GACTCCATCT CAAAAAAAAA AAAAAAAAGA AAAATTACAG AGAGTTGCCG GTACATACCA 300 GTTCATCAAT GGTAGCAAAC ACATCTCACG AATGTAAGAC GTTAAATAAT CAGAGAAACT 360 GTGTGCAGGC TGTATGGAAC TGTCACGAGA CAACATTGCA ACAAATTCAA CTTAAAAATC 420 TTAATTGGCT TTCATTCACA ATTCTGAAAT TGGCTTAGAA CCAGGACAAA TTCAGACCTG 480 GAGCTGCACA ACGTTCATGG AAACGGAAGT GATGCGCAGA GGCAGTTTTG GTGGTGGCCG 540 CTGGGCACTT TGCCTTGAAA TCAGCGGCCA CTGGCAACTG ACAGCTGGCA GCTGCGGTGA 600 CCTGGACCCA GTCCCTGTGA CAAGAGGCCA GCCTTCTGTG GCCTTCAGGC CATGCCAGGC 660 TGCAGTTTGC TGTATGGACT CATGCCCCAG GCCTCCTCGG TGAAAACTTA ACAGGACTCT 720 CGGGTTCATT TTGAAACCTT TATGTAAGTC TTAGCCGGGC ACGGTGGCTC ATGCCTGTAA 780 TCCCAGCACT TTGGGAGGCT GAGGCAGGTG GATCATGACG TCAGGAGTTT GAGACTAGCC 840 TGACCAACAT GGTGAAACCC CGTCTCTACT AAAAGTACAA AAACTGGAGG CCGGGCACAG 900 TGGCACATGC TTGTAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC ACTTGAACCC 960 AGGAGATGGA GGTTGCAGTG AGCTGAGATC GCGCCATTGT ACTCCAGCCT GGGCAACAGA 1020 GCAAGACTCC ATCTCAGGAA AAAAAAAAAG AAGAGAAACC TTTATGTAAG TCTAAATCTA 1080 TTCTGAAATT AAAAGTTGAT GTAAAAATCT TTAAAACGTA GGCTGCAGTC ACATGGGGGG 1140 AAGCCAGAGG AGGGGGAAGA TGAGTGAAGC CCAGCTCTGC TCCTGGGAGC TGAAAGCACA 1200 GGTGTCAAAA CACCAGCCGG GAGTGCGGCA GTGCAAGGCC TGGCCCTGCC TTCCCCAAGT 1260 GCTCAGGACA GAATTTTCCA TCTGTTTTAT TTTTTAAATT TTTATTGATT GATTCATTCA 1320 TTCATTTATT GAGATGAAAT CTCGCCCTGT CGCCCAGGCT GGAGTGCAAT GGCATGATCT 1380 CGGCTCACTG CAACCTCCAC CTCCCGGGTT CAAGCAATTC 1420
|
| |
|
|
|