| Tag | Content |
|---|
EnhancerAtlas ID | HS018-14456 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr20:61076470-61077850 | 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
|
| |
|
|
|
