Tag | Content |
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EnhancerAtlas ID | HS167-02771 | Organism | Homo sapiens | Tissue/cell | Retina | Coordinate | chr2:45199400-45200880 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr2:45199633-45199654 | TTCAGCCCCAAGGATAGAGGC | + | 6.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 45199818 | 45200000 | chr2 | 45200000 | 45200797 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I044973 | chr2 | 45200340 | 45200539 |
| Enhancer Sequence | GTGAAACCCC GTCTCTACTA AAAATACAAA AATTATCTGG GTGTGGTGGT ACACACCTGT 60 AGTCCCAGCT ACTTGGGAGC CTGAGGCAGG AGAATCACTT GAACCTGGAA GGCAGAGGTT 120 GCAGTGAGCC AAGATGGTGC CACTGCACTG CACTCCAGCC TGGTCTGGGG ACCGAGCTAG 180 ACTCCGTCTC AAAAAAAAAA AAAAAAATGC AGCTCTCTCA TGAGAGTCCA TTCTTCAGCC 240 CCAAGGATAG AGGCTGCAAA AACTGCCCAC GTCATCTGGC CCAGGACACA TCCTGCCTGT 300 GGGGTGGGCT GACCTCATAC CTGCCACATA CTGGGAGCCC AGAGTCCTCC CACTCCAGCC 360 CAGCCCAGTC CAGGGCCACC AGCTCTTAGG TTCTGAAGTA GCCCTTTGAG AGGGTGAGGG 420 TGACATGCCA TGTCTCTCTG TTCCCATCCT CCTGCCAGTC TTCTCTCCAC CCTAGCATTT 480 CAGGCAAAGG AACAGAAAGC CAGTCTGTGC CCCCACCTGA CACTCTCTCC AGGAAGTGTC 540 AGGGAGTGGG CTCTGCTGCC TGGCCCCTCA CGCCAGGCTT CAGGATGAAA GGAAACTCCA 600 GAATGACAAT TTGGGATTAT CTAGTGCCCT GGGCCAGATA GTCTCCTGTG AGGATTAGTG 660 GCATCTTTGA AAAGCAGCGG CCACTCCTTT ACACAATACC TCCTCTTCAG GGGATCTCCT 720 CCCACTCTCC CATACAGGGA GCTCTGAATC TGCAGAGGAC AGCTTATCTT GGAACACCTT 780 TGGGATGGGA AACTGATCAC CTTTCAAGGA AGCCCAGTCC ATCTGCATCT GTGCTAGAAA 840 GTTCTTCCTT CTACCGACTC AGAAGCAGTC TCCCTGCTGT TTCCTCCTTG CATCACGGAG 900 CAAAGCCTGC TGCTTTTTCC AGGAGCAGTG GGGGCACGAA ATGTCCTATT GTTTACGTAC 960 CCAAAGAGTG CTTGCTCTAA GCTCCTTCTC CACGAGAACT CTGCAGCTGC CGCTGACCAC 1020 AGGATGCTCG TTTGGACAAT GAAGCCCCTT TCTAATGGGA GGATACTTTC AGGATTGTTG 1080 CCCCTAGTGA GCTTCCTACT CCTCCCCTTC CGGTTGCCCC CGGTGTGCCC TCAGGCTCCT 1140 GGCAACTCCA CTGCTTCACT CAGCCATCAC TCCAACTAGC TTTCTATATC TCCATGCCCC 1200 TGTGTTCAGT CCTAAGTGGA GCTACTGGAT ATTTGAGCCT CTCACTCAGC AAGCCTTGGA 1260 GCTCCTTCCC TTAAGCCCTA CTAGCACCCT TCCCCCATGC ATGTAGGTCC CGGGGCCCAG 1320 CCACCACTGC AGGCATGGAG GAAGGGGGTG GGCAGTGCAC AGGTATCCAT GGCAAAGGGC 1380 CAGCGGGCTG TATCTGTGGA AACAGAATCT GTAGCCTCCC TCACTGATCC TCTCTGAATC 1440 CCCAGCGCTG GAGGGTGTAA TTTTTTATTG TGAAATATAT 1480
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