Tag | Content |
---|
EnhancerAtlas ID | HS072-01342 | Organism | Homo sapiens | Tissue/cell | GM19193 | Coordinate | chr20:61076470-61078280 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr20:61077778-61077799 | TCTCCACGTCCCTGCTCCTCC | - | 6.18 |
| | 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 |
GH20I062500 | chr20 | 61075301 | 61078056 |
| Enhancer Sequence | GTGTTCATGT GTGCGGGTGA GCGTGTGTCT GCGTGTACTG TCGTGAGTTG GGAGCCGTGG 60 ATGCCACGCA AGCCCCGAAG CCCCAGCTTT CTGAGCAGCT GGCCTGTGAC GGCGGCATCT 120 CAGGCGGCTT GGCTGTGTAG TGGGGATCCC CCAGCAGGCT CCAGGACCAG GGTCTTCTCT 180 TTGGCTCCAG GTGACCCCAG CAGACTGGCC CTGCACCTGG CCCTGTGTTG ACATCTCCAG 240 AGGGTTTGTG AGCAGAGATG AGGGCACCTG TGAGGTCAAG GATAGTCTCT GTGTGGCAGC 300 GGGACCTTGG GCCCAGGGGC AGCCTGTGGC TCTGAGGATG GCTGTGAGTA CTTGGCAATG 360 ACCCTGTTAG TTGAGCTTGT GCCCGGCAGG GCTGAGATCT CCCAGCATGT GGCATGGGCC 420 CCTCACCACC CCGAGTATGG ACCCTGATAT GGTCTGGCTC TGTGTCCTCA CCCAGATCTC 480 ATCTTGAGTT GTAACTGAAT TGTAATCCTC ATGTGTTGGT TGGCAGAGGG ACCTCGTGGA 540 GGTGATGAGA TCATGGGGGC GGTTCCCCCA TGCTGTTCTC AAGACAGTGA ATGAGTCTCA 600 TGTGATCTGA TGGTCTCATA AGGGCTTTTC CCCCTTTTGC TCTGTGCTCA TTCTTTCTCC 660 TGTCACCCTG TGAGGAGGTG CCTTCCGCCA TGATTGTAAG TTTCCTGGGG CTTTCCCAAC 720 CAGGCGGAAC GGTGAGTCAA CCAAACCTCT TTTCTTTATA CATTACCCAG TTGAGTATTT 780 CTTCATAGCA GTGTGAGAGA GGCCTCATAA AGACCCACTT CGTAGATGCA CCGAGACTCA 840 GACCCTGAGG TGGGGCTGGG TGGCCGCAGG CTGCTCAGGG GTCTCAAGTG AGTGTGGTGG 900 GCTAGGCCAC CCGCGGTTAT GCTGCCCATT TCATCCCCCT GCCTGGGTGT GGGTCTTGGT 960 GTGTGGGGTG GGATTACAGG AAGGAGCAGT GCCCTGGGCT GGCCTGCTAG GGGTGGCCCA 1020 GCCAGGAGGC TCCCAGCAGG GTCGGCTCTC GGGAGCTGGG TCATGGAGGG TGGGGACATG 1080 AGGGTCAGGG AGAGGGCCCA GCTCCCTGAC AGCTCCTGGG GCTCTGTGGC AGGGAGAGCA 1140 GGTCTGCTGG GGCCAGCTCA TGCTTCTGGG GCGCAGCCTT GCCCTGACCC ATGGGCTCAA 1200 CGGAGGGCCG GGTGGGGCTC CCACAGAGCA GTGGGCCTTG GGCCTCAGCT CTTCCCAGAT 1260 GGAAGCTCTC GAGCAGATGA GAGGGGCTGT GAGCTCCTAT GCGCTGGCTC TCCACGTCCC 1320 TGCTCCTCCT CTTCCTGGTC ACCCCTGCCA GCCCCTTCCT CTGGTGCTTG ACCTCGCCCT 1380 ACTCCCCACC TCCCGGCCTG TGAGCAGCCT TGGCCCGGAG CTGCCCTTCC TGATCATGGT 1440 CGGGACCCCA GGCATCTGCC CCTACGTTGG CCTTTGCCAA CAGCTGCTCA ACCTGCGAGG 1500 AGGTGCAGGG AGCCGCCGGC CCCGCTCCTT GGACCTGATC ATGGGCAGGT GGAAGCAAAC 1560 CGCCTCTGAG AAGGGCTGCT CCACAGACAC TGCAGGAGTG CCTGGGTCCC AGGACAGACC 1620 CTCTGTTGGG TGCAAGGGAT GAGGATGGCT GTCCCCACAT GTCTCCTAGA GAACCTTCAG 1680 GTGGGAATCC TTTTAAGTGA AAATATTCAA AACAACCAAG CTCTCCAAGC TGTGGAGGGC 1740 GATTCTCAGA CTTCTCGCCC GGCGCTGCCA AAATCCTGTA GCCGGGGTGG ATGGGGTGCC 1800 CTGGCTGCCT 1810
|
| |
|
|
|