Tag | Content |
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EnhancerAtlas ID | HS147-04898 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:231414450-231415470 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:231414993-231415004 | AATGAGTCAGA | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGCACATTG GGTTAAAGGT TTCAACATAT GAATTTGATT CATGTTGGGA TTACAGGCAT 60 AAGCCACTGC GCCCGGCCTC AAAAGTCTCT TAAGGCGGGA TTCTGGGATT ACCTGCATTC 120 AGGGGTCCTG CAATGTGTGT GTGTGTTCCC CAGGACCAGG CTGTTTCTGC TGCACATTGA 180 GATCGGAGAG CCATCTTCTC CATGCATTGG TGACCAGGAG GCCCTCTCTG TGGCTCTGCT 240 TGGGGCTGGT TCTCGATTTC TTTGGGAAGC CAGGGAGGAG TCTGTTGAGA TTGACCAAGA 300 GCGAGTTGAA GAGTCAGTTG AACAGTGTTC CTGGCTGAGG ACTCTCCTGT ATGCCTGTTG 360 AATAGGGGAC CTGAGCTGCT GTTCTCCAGG GAGAGAAAAG CTGTGAGTCC AGGGCAATTG 420 GGAGAACAGG ACCCTGGCCA ATTCTTGCAA TGTAGACATG CCTTAGAAAG AATCCCCATA 480 CACCCAATTC GTTACTTGTT TTTCTTTACC CTGACACTCA TGCTGTGCAT GTACATGTTG 540 AAGAATGAGT CAGATGACCT TTATTTCCTT GTAGGTCTGT TTGTAACACA TGCCAAGTTT 600 AGACAAAGAC TTTGGAGTTT TGGGTGCAAG TGGCTAGACT TGTCTCCTGG CCAGCTCTGT 660 CATTAGTCAA GCAAGCAGAC AATGTGGAGG TGAAAGGAAA ATGGGGTGCA GTGAAAACCA 720 AATGAGGCTC TGCAGCAGAA GCAGCTCTAG GTGGCTGGGC ATGGTGGCTC ACACCTGTGA 780 TCCCAGCACT TTGGGAGGCT GAGGCCAGCG GATCATGAGG TCAAGATATC AAGACCAGCC 840 TGGCCAACAT GGTGAAACCC CATCTCTACT AAAAATACAA AAGATTAGCT GGGCGTGGTG 900 ACACGCGCCT GTAGTCCCAG CTACTTGTGA GGCTGAGGCA GGACAATTAC TTGAACCCGG 960 GAGACAGAGG TTACAGTGAG CCAAGATAGC GCCACTGCCT GGTGACAGAG CGAGACTCCG 1020
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