Tag | Content |
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EnhancerAtlas ID | HS002-05732 | Organism | Homo sapiens | Tissue/cell | A375 | Coordinate | chr2:220381350-220382770 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr2:220382101-220382122 | GGTTCTGGCCCTGGTGCAGGA | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCCCACTCCA GCCCAGCCTC CAGCAGCCAG CCCCAGTGAT AGGGACCCCC GCCAGGTTCT 60 CACTCACCCG CTGCCTCAGG ATCACCAGGA AACATGCTCC AGCCAACGAG GTTCCTGGCC 120 CCCACCATGC CTGCAGTGTC TGGGGCCTCC CGCCATTGGG CAGGGGAGTT AGGTAGAAAT 180 AGAGGGACAG GAGCAGGAGC ATTGTGCAGG GAGAAGAGTC GGGGGCATTG GCCTGTTGTC 240 CGGCTGTACA CCCCCTTTCC TAGGGAAAAG CACTGCTCCC CAAAGCAAGG GTTGGTAGAG 300 TCCCCGAGGA GGAGGTGGGA TATGGAGGGT GAGTGTGGCC TTTGGGATCC ATAGGGCTCT 360 GCTGTCCTCA ATCCTCACCA CTCCGTATTG GGAGCTGGGC AGAGCTCAGT CTTAGCAGGT 420 GCTGTTGGGA CAGAAATCAA TGGGATCTTT GTGTCCCCGA GCGGGAGTTG GGGGTGGGCA 480 GGAAAGGGGA AGGGTGATGA GACCTCAGTG AGAGGAAAGG AGAGGAAGAG CTGGAGGGGG 540 TGAGGAAGTA AGGGGAGGGA GGCAGAGGGT TCTGCTTGGT CTCCAGGCTA GGAGGCGGTG 600 CCTGGAGGAT ACAGGAACGG GGATCCTCTG ATCAAGGCTG GTGAGTCCCC GGAATCCTGG 660 GGATGGCCTG GAGGAGTGTG GGTGGATTTC CCACAGGCCC TCTGGTACCC TGGGGCTGGA 720 GAAAGGAGGA TGGTAGAAGT CCGTGGGCTG AGGTTCTGGC CCTGGTGCAG GACAGTGGGG 780 GTAGAGGGCA TAGCTAGCAT TGGGGGACAG GAATTCCCCT TTGGGATTTC CATTTCCCCT 840 GTCTCCAGCC CAGCCTCCTA CTCTTCTGCA CATACTGCAT CCCCCGTCTG CTGAGTGTAA 900 CTCTGTCTTG GGTCTGGCAT TCAAGGGCTG AGTCTGCTGC AGATTCACCA GGGTCTGGAA 960 TTACAGATTG GGCTGGGGGC CCATGATCCA TGGTAGTGGG GAAGATGGGG TGTATTACAG 1020 GGGAAAGACT GGAGAATGGG CATGGAGATG AAGATATGGG GTCTCCAAAA AGGACGTGAG 1080 GTCCATAATC AGCTCTGTGG TGAGGACCTG GAGTCAATGA TGGGGATTTG GGGTCTATGG 1140 TGGGGAGATG GGTATGTGAG CTGGTTGGTG GGGAGCCTGC CGGGGTATGG GTGGTGAGAT 1200 GGTCAGAGAC AGGGACAGGC TTCACCAAGG GGCTGTTATG TGTTTTCTGT TGCTTTCCCT 1260 GTTTCCTCCT TCCCACTCCC CACTCTGCTG TGACCTTTCC TCTGGAATCC AAGTTAATAA 1320 ATGTCACATT TTCCAGCCTA TTTTTACTCC GGGTAATGTG CCCTCCCCCA GTCCCCTCTG 1380 CTGCTGCTCT TGCTTCTGTT ACCACTGCAA TCGCTCTCCC 1420
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