| Tag | Content |
|---|
EnhancerAtlas ID | HS019-12185 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr4:2688680-2690800 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr4:2689219-2689234 | AGAGCCCAAAGGCCA | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCTGGCTC TTGTCCCATG GGGCTCCCTT ACCAAAACAA TGACTTCAGG CCCTTTACTG 60
TATCCTGGGT GGCCCGTCTG GACCTGTTTA TTCCTGCTGT TGAGTCCTGA GTGTCTGCTC 120
TACCCTCCTC TCCCCCTTTG CCTTCCTGGG CCTGTTCCAG GTCAGTGGAC TCGCTGAGCT 180
GTCCAGCAGC CCAGAGGGGA GTGCTTCCTC TCTGCTCCGA AGCACTGTGG AAGAAGGGCA 240
AGGTGGAAAG GTTTGGTCGG TTGGTCAGGT GTTTTGTGTC CAGGGACTCT ATGTCTATAT 300
AAGTAGTCTC TATATAGTAG TCTCTAAGAC TATTGTCCTA GAAAATCAAA GCAGTGCACC 360
ATCACACTCA CTGAATACTT ACTATGGGCC AGGCAGTGTG CTCAACTCTT ACCATACCCC 420
TGGAGGTAGG TATTTCCAGA TTACAGATGA GAAAACTAAA GCACAAAAAG ATTGAGTGAT 480
TTGCCTGAGG TCACACAGCT AGCAAAAGGG AGAGCTGGCA TCCGAGCTCG CCAGACTCCA 540
GAGCCCAAAG GCCAAGACGT GGGACTAGAG TTCAGATCTA GCTGTCACCT GACCGTGCCT 600
CCTCATAGTG GAGCCAGCAG TGGTAGCTCC TGGACTAGAT GTGCAGTCCC AGCTTTCATC 660
TTGATAGCTC CAGAATTCCT CCTTTCCTTG CCACCTTCAC TGCCATTGCT TCATCCTTTC 720
TCATCCCCTG ACTAACCTAC TCGTCCTCCT TCCGCCTTCT GGTTCATCCA CAGCATTGCC 780
ACAAATTGAT CTTTCCACAA AGCTGACCAA ATCATCTCAC TCTGCTGTTT AAATCCCTCT 840
GTGACTCCCC AGCCCCTTCA GAACAAAGTG GTACAAAGTT GTCTTTGGCC TGGCTGCTGC 900
CCACACTCAA CCTGGAGCCT GTCAGGGTGT AGCACTGTCA TCCCTGTACG TGCGCCATCC 960
CTTTGCTCCT AACCTCTTCC TGTCCTCCCT CTGCCCCAGC CAGGCCAGCA GGATTCTGCC 1020
GAACCATCGC CCATTCTTAA GAACCCTCCA GGGAACCCTC CCACTTGAGT TTAAAGAATT 1080
CACTACTCAT TTCTGCATCC CAGAGGATGT GATGACCAGG TTGCCCATAA CTGGGCACTT 1140
CTCCTCTCCA GCAGACAGAA GTCCTGCTGA GGGAGAACCG TATGTCTGCC CAGCATTAGC 1200
AAGGACTGGG GGAGAAGGGC CAGGACCCAG ATGTCCCACC TCATCCTAGA GCGCATATAA 1260
TTTGGGGAAA GGCAGACATC AAACCAACAG GCTACAAGTA GGTCTCGAAT TATAACTGTG 1320
GTAAGTGCTA AGAGGGAAAA TGACGGATTT TAGTGTGTTC AGTGGGAAGG CTCGCCTTGG 1380
TCTTGGGTGT TGGTTCCTGG GAGGTGACAG CAAAGGCAAC GCCGGCTTCT CTGAGGAAGC 1440
GATCTTTAGG CCGAGGCCTG CAGGATGAGT GCGAGTGTGG TAGCGAGCTG AGGCTTGCAC 1500
ATTCTAGAGC ATGGACACAG CACAAGCAGA ACTTAGGGCC AAGAAGGTGA ATAGGCGTGT 1560
GCCGGCCAAG GGGAGGCCTG TGTGTCCAGG GCTTTGGTGA GCAGGAAGGG TGGAGGTGGT 1620
GGGCCCAGCT CCCTTGGAAC TTTGCAGGCC AGAGCCTTGG GAAGCCATTG CTGCATCCTG 1680
AGCAGGGGAG TGACATGCTC GAATTTACAT TCAACAAAGA TCACTCTGGC TGTAGTGGGG 1740
AGAAGGACTG GGAAGAGTTC GTGGTGCAAA TGTGCAGGCT GTTGCACTGC GCCACTGTGA 1800
GAACATGGTG CTCAGGATCT CCTAAGGAGG TCAGCAGCCA GGGCCTGTTG CCTGGATAGT 1860
GGCTGAGGCA GAGGGAGGAC CCAAGGGGGC CCCAGCCTGT GCAGGAGCAG CCAGATGGCT 1920
AGTGGCTCAA TAAATGCATG GATGTTGGCT AGCCAGCTGG CCAGACCCTG CTCACCTTCC 1980
CTTGGTGCCT TCAACAATGG TCTGCCCCAC AGGGCCCAGG GCGGGGCTTG CCAATGAGGC 2040
AGCTCCTTTG AGAACGCCCT GGTCTTTAGA GCACAGTATA CAAATTTCTC TAGGTCATTA 2100
GATTTGTGCT GTACCTTGCC 2120
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