Tag | Content |
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EnhancerAtlas ID | HS196-02946 | Organism | Homo sapiens | Tissue/cell | ZR75-1 | Coordinate | chr1:183339300-183340690 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:183339763-183339784 | GAATGAGGAAGAGGAAGAGGC | + | 6.58 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATTTCTACT GCTCTGTTTA TCCACTCCTA GTACTTCCTA CCACTACTAT CAACACATAC 60 ACACACACAC ACACACACAC ACACACACAC ACACACACAC ACACACACAC AGGCTGCAGT 120 GGCAAGAATT TGAGTTCTGG TACCAGACAG ACCTAGTTCC AGGTACAGTT CTGTGATGTG 180 CTAAATGTCT GCCCTTTACT GAGTTTCCAT TTCTGCTTCA TTCATGTGGG GATGGTGTTA 240 TCTATCTTAC TGGTATGCTG AGAATAAGGG TTAAATGAAA TGAAGTTGTG AAATCATCAG 300 GCAGAGTGTC TGACAGACAG CAGAAACTCA ATAATTGTGA ACTCCTGTCC CACTTCTCCA 360 CTTCTCCACT TCACCATAGA AGGAAACTGA AAAACCTCTG TGAATGCCCT GGAGCCCAGC 420 CAGCCTAGGA GTGCTCTCCA TATCAGGTGT GCTCGGGCAC AAGGAATGAG GAAGAGGAAG 480 AGGCAGCGTT GAGGAGAGTA CTGGTGGGGA TCCATTGATT CTGGGGGAAT GAAATAAAAT 540 CCCCAGAAAA ATATGCATGC CTCTTGTATC TCAAGTATTG GCAGGACAAT TAGAACAAGG 600 GGATGCTGGT GGGCTCCCAG TAACACTGAC GCTGTAAAAA GCCAAGCTTC TGCCTGAACT 660 TCTGTCCCTT GACTGGCGGG CAGATTGGAC AGCTCCTGCC CTGTCCGGTG TGCTTTCCCA 720 CTATAGCCCC AGAGCCTCAG GGAGGGTTGA GGATGCTGGG GAGGTTGTGG TATATACATG 780 TTGAACCAAT GAGTGAGTGA GTAAATGCAT GGTGCCTGAC CACGGTGCGC CGCATGTTTT 840 TACTTAGGAA AAGCAAACAA ATGACCTGGA CAAATATTTC AGAATGGATT CCCCCACACC 900 TCCACAGGAG AAAAAAAAGG CCAGGGGCAG GAGTGGTATA TGCGGACAGA CTGATTTTGA 960 TTGATACTTC CAGCCACCTG GGGCATTAGA CGCACCTGAT AAAACTCTTC ATCCCAGAAG 1020 AAGTTGATTA CTAAGTGAAA GAAGCTGATG TGAAAAAGGC TATATACAGC ATGATTCCAA 1080 TGATAGGACA TTTTGAAAAA GGCAAAACTG TGGACACTGT AAAAAGATCA GTGGTTGCCA 1140 GAAGTTGAGG GGAGGGAAGG ATGGGCAGGC AGAGCACAGA GGATGGTTAG GGCAACGCAA 1200 CTACTCTATG TGATACTGTG GAGGTGGTTA CATGTCAATA AACATTGTCC AAAACCATAG 1260 GATGCACAAC ACCCCGAATG AGCTCTGGTG TAAACCATGG CCTCTGAGTG GTGTGTGGAT 1320 GCCGCTCCAT CAGCTGTAAT TAATGTACCC CTCTGGTGGG GGATGTTGAT AATGGGCAAG 1380 GCTGTGCATG 1390
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