Tag | Content |
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EnhancerAtlas ID | HS052-01246 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr1:47087560-47088990 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:47088736-47088751 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I046622 | chr1 | 47087744 | 47088850 |
| Enhancer Sequence | GTTGCAGACC TTCCCCTTGC TTTGTGGGTG GTGACAAAGG CCTCGGTCTT CTAAGGAACT 60 TCCACTGGGC CCACGAGTCC CACTGGCTAC AAAGGAATAT TATTGAACAA CAGGTCAGGG 120 AGGAGTGGCT TGTAAAAGGG AAAGGTTCTT GGATATCATT TAGTCTAATC TCCTCGAAGT 180 ATGTGGAAAA CTGAGACATA GGGAGAGGAA GAGATCAGCC CAATGATGAA TCATGACAAT 240 AAAAACCATT CAGTGAACCT TACGTATGCC TCTCCCTGAG AGGCATATTC TCATTTCTTC 300 TTCTCAGCAA CCCTGGGAGA GAGGGAGGTT TATCTTTCTA GAGCTTTTAA GTTGTTCTTC 360 CCTTCAGAGA GGGACGGAGG GGCTGGAAAG AAAGTTCCAC TAAGTAGAGA GAAGGGATTG 420 GCCGTGTTTA GATGACGTTC CAAACTCTAC ACTGCAGCTC TCTTTGGGTC CCATCTTGGC 480 TTCATGTCCA GGAGATGGGA GAGCTGTGTC TGCTGCAGCG GGAAGCAGCA ATTCAGTGGG 540 TGGAGTCCAC TTCTTATTGG AGACTCATGC TGCACCCCGT AGAGTCTGGA TTCCACACAA 600 GTACAGCTTG TGACTTCCTG CAGAATGTCA TCAAATTGCA TTTGGGGCCT TTTCAAGAAG 660 TAGCTGTAGG AGCTCCGCTT TGCCTAAGGC TAAGCAGACT AAGGGTATGC TCTTGGCTTT 720 CCCAGGAAGT TTTCCTAAAT TACACCAGCT GCCTGGAACC AACCCTCCTC AGGGGGGAGC 780 CCTTGACACA AAAAGTTCTC AGTGGTTTGC AGATGCACTC CTTGGTTAAG CCCATGGAGG 840 TTGTGTCTTC CCTTTTGGAC TATAAGCCCT TAGAATTGGG TTTTTATTTA TTTTGCCTCC 900 TCCCATGTTA CCTTGTAGCA GCAACTGACA GTTGTAAGGA ATGTTCTGGT TTACAAAGTG 960 CTTTTACTAC TCTTTTTTTT TTTGAGATGG AGTCTCGCTC TGTCACCTAG GCTGGAGTAC 1020 AATGGCGTGA TCTCGGCTTA CTGCAACCTC CGCCTCCCAG GTTCAAGTGA TTCTCCTTCC 1080 TCAGCCTCCT GAGTAGCTGG GATTACAGGC ACACACCATC ACGCCCAGCT AATTTTTGTA 1140 GAGACAGGGT TTCGCCATTG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCT 1200 TTCCGCCTCA GCCTCCCAAA GTGCTGGGAT TACATGCGTG AGCCACCGTG CCCGGCCTAC 1260 TCTGGTCATT TTTGAGCCCT GTAACAACCT TGGAATGTGA GTATTGGCTC CAAAAGGTGA 1320 AATGACTTGG CCAAGAAGCA CAGCTTGAAA TGGCAGAGCA GGGCCGGGTG GGGTGGCTCA 1380 TGCCTGTAAT CCTAGCACTT TGGGAGGCTG AGGTGGCAGA TTGCTTGAGC 1430
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