Tag | Content |
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EnhancerAtlas ID | HS020-33136 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr4:2688780-2691230 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr4:2691180-2691192 | AGGTAAACAGAA | + | 6.14 | HNF4G | MA0484.1 | chr4:2689219-2689234 | AGAGCCCAAAGGCCA | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I002689 | chr4 | 2691055 | 2694415 |
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Enhancer Sequence | TGAGTCCTGA GTGTCTGCTC TACCCTCCTC TCCCCCTTTG CCTTCCTGGG CCTGTTCCAG 60 GTCAGTGGAC TCGCTGAGCT GTCCAGCAGC CCAGAGGGGA GTGCTTCCTC TCTGCTCCGA 120 AGCACTGTGG AAGAAGGGCA AGGTGGAAAG GTTTGGTCGG TTGGTCAGGT GTTTTGTGTC 180 CAGGGACTCT ATGTCTATAT AAGTAGTCTC TATATAGTAG TCTCTAAGAC TATTGTCCTA 240 GAAAATCAAA GCAGTGCACC ATCACACTCA CTGAATACTT ACTATGGGCC AGGCAGTGTG 300 CTCAACTCTT ACCATACCCC TGGAGGTAGG TATTTCCAGA TTACAGATGA GAAAACTAAA 360 GCACAAAAAG ATTGAGTGAT TTGCCTGAGG TCACACAGCT AGCAAAAGGG AGAGCTGGCA 420 TCCGAGCTCG CCAGACTCCA GAGCCCAAAG GCCAAGACGT GGGACTAGAG TTCAGATCTA 480 GCTGTCACCT GACCGTGCCT CCTCATAGTG GAGCCAGCAG TGGTAGCTCC TGGACTAGAT 540 GTGCAGTCCC AGCTTTCATC TTGATAGCTC CAGAATTCCT CCTTTCCTTG CCACCTTCAC 600 TGCCATTGCT TCATCCTTTC TCATCCCCTG ACTAACCTAC TCGTCCTCCT TCCGCCTTCT 660 GGTTCATCCA CAGCATTGCC ACAAATTGAT CTTTCCACAA AGCTGACCAA ATCATCTCAC 720 TCTGCTGTTT AAATCCCTCT GTGACTCCCC AGCCCCTTCA GAACAAAGTG GTACAAAGTT 780 GTCTTTGGCC TGGCTGCTGC CCACACTCAA CCTGGAGCCT GTCAGGGTGT AGCACTGTCA 840 TCCCTGTACG TGCGCCATCC CTTTGCTCCT AACCTCTTCC TGTCCTCCCT CTGCCCCAGC 900 CAGGCCAGCA GGATTCTGCC GAACCATCGC CCATTCTTAA GAACCCTCCA GGGAACCCTC 960 CCACTTGAGT TTAAAGAATT CACTACTCAT TTCTGCATCC CAGAGGATGT GATGACCAGG 1020 TTGCCCATAA CTGGGCACTT CTCCTCTCCA GCAGACAGAA GTCCTGCTGA GGGAGAACCG 1080 TATGTCTGCC CAGCATTAGC AAGGACTGGG GGAGAAGGGC CAGGACCCAG ATGTCCCACC 1140 TCATCCTAGA GCGCATATAA TTTGGGGAAA GGCAGACATC AAACCAACAG GCTACAAGTA 1200 GGTCTCGAAT TATAACTGTG GTAAGTGCTA AGAGGGAAAA TGACGGATTT TAGTGTGTTC 1260 AGTGGGAAGG CTCGCCTTGG TCTTGGGTGT TGGTTCCTGG GAGGTGACAG CAAAGGCAAC 1320 GCCGGCTTCT CTGAGGAAGC GATCTTTAGG CCGAGGCCTG CAGGATGAGT GCGAGTGTGG 1380 TAGCGAGCTG AGGCTTGCAC ATTCTAGAGC ATGGACACAG CACAAGCAGA ACTTAGGGCC 1440 AAGAAGGTGA ATAGGCGTGT GCCGGCCAAG GGGAGGCCTG TGTGTCCAGG GCTTTGGTGA 1500 GCAGGAAGGG TGGAGGTGGT GGGCCCAGCT CCCTTGGAAC TTTGCAGGCC AGAGCCTTGG 1560 GAAGCCATTG CTGCATCCTG AGCAGGGGAG TGACATGCTC GAATTTACAT TCAACAAAGA 1620 TCACTCTGGC TGTAGTGGGG AGAAGGACTG GGAAGAGTTC GTGGTGCAAA TGTGCAGGCT 1680 GTTGCACTGC GCCACTGTGA GAACATGGTG CTCAGGATCT CCTAAGGAGG TCAGCAGCCA 1740 GGGCCTGTTG CCTGGATAGT GGCTGAGGCA GAGGGAGGAC CCAAGGGGGC CCCAGCCTGT 1800 GCAGGAGCAG CCAGATGGCT AGTGGCTCAA TAAATGCATG GATGTTGGCT AGCCAGCTGG 1860 CCAGACCCTG CTCACCTTCC CTTGGTGCCT TCAACAATGG TCTGCCCCAC AGGGCCCAGG 1920 GCGGGGCTTG CCAATGAGGC AGCTCCTTTG AGAACGCCCT GGTCTTTAGA GCACAGTATA 1980 CAAATTTCTC TAGGTCATTA GATTTGTGCT GTACCTTGCC TGGGTATAAG AGGTCAGTGT 2040 AAGGGTTTTA TCCATTTTCA TCAGTGATTC CAAAGTTGAC TTATTAGTGA TGATCATTAA 2100 AATGCTTGCT GAGATTAAGC CGTAGAAACA GATCTTACGA CGCACATGGC ACACTCACAT 2160 GTGACCCAGT AGGAATGTGA GAAGTTACTG AGTTGTCTAA AGTTTGTTCA GATATACTCC 2220 TCAAGGCATC GGTTGCTTTT CATATCTACA TCTGGTTGAA ATTTGACCTG TCGTGTACAG 2280 TCTCATAAAT CAAGTCCATG TTTTGTGAGA TGTGCTCCCC CTGGGCTGAG CTCAGCTCAT 2340 GGCGAGCACA TCCCATGAGG CTCATAATGA ATTGTCTGTC TGTAGTTTAA CTACTTACCT 2400 AGGTAAACAG AATATTAATT TTGATATGTG ATTAGAAAAT TTTTTTTTGT 2450
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