Tag | Content |
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EnhancerAtlas ID | HS017-21649 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr22:20817010-20819140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr22:20818711-20818732 | GAAGGGAAACTGAAACAACAT | - | 6.86 | KLF4 | MA0039.3 | chr22:20819091-20819102 | CCACACCCTCT | + | 6.02 | Klf1 | MA0493.1 | chr22:20817945-20817956 | GGCCACACCCA | + | 6.62 | PRDM1 | MA0508.2 | chr22:20817649-20817659 | GTGAAAGTGA | - | 6.02 | ZNF263 | MA0528.1 | chr22:20818836-20818857 | CTCTCCCCTCCCGTCTCCTCC | - | 6.79 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 20817133 | 20817240 | chr22 | 20817400 | 20818664 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I020462 | chr22 | 20816925 | 20819707 |
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Enhancer Sequence | TGTAGTTGGT GTTCAGTAAT CCACAGGGCT ATGGCTATGG GAAAGGTACA AGGAATGATG 60 CAGATAATAT AGATGCAAAG AAAGAAGGAA TGAAAGAGAA AAAGTAGTAT ATTGGAGACA 120 AACACCATTT GCTCCAAGAG AGGAAAGGTT TTTAAATATG CGGTTTCTGC ACCAATGCTT 180 TAAGATATAA CCTGGTAAGT AATAACTCCT CAAAATGCAA AGCCTAATTT ACTGCAAAAT 240 CTTGTTTCCT TATATTCTAA AAGCCTATAG CTTTTAGAAT TCACCAGTTC TAAGGCTGAT 300 GAAATGAGAA AGCAGAGAAA GAACCAAATC TTAGAATATT CAAATTAAGG ATTCATCTGG 360 AAGTTTTGAG TCCACTGGAA GGTTAATGAT GCCTTCATTC TGGAGAGATG ATACATCCCT 420 GGGTTAACCA GTAGGGCTGT GGTCCTTCCT GCCACCTCCA CTCTGTGGAT ACCTACTCTC 480 TCAAGGCAGG TCTTGCCGAC CCCACTTGCC ATTGTGATCC TACTCTCAGA CAGGAGTTTG 540 GGACTGGTTA TTGGTTACAG GGTCTAATAT TAGCATTACC CAGAGTTCAG CTTTGGTCTC 600 ACACCCCTTC ACAAGGGGAA ATTCAGACTC CTACTTTAAG TGAAAGTGAG ATCAATGGCC 660 CATAGCAGGT GGACAGAGGA CAGGGGCAGG CAGAATCCCA AGCTGTCACC CCCCTAGGGA 720 CAGCTCTGTG GAAACATCCA GCATTACTGC CAAGCACACA GCTGTCTCTA CCTTCTGCTA 780 AGGGCCAGAA GCCAAAACAC TCTGGAGAGA TTGGCTTTGC AGGTCTGTAG GTTACTCTCA 840 GCAGGGTGGT CTGGCCTTGG CCCCCCAACT GGGAAACCGA GCCCCCTAAA AAAGAAGGTT 900 TAAGGTTTGG CCAAAGGGAA GTCTAAACCT AGTGTGGCCA CACCCACTGG GGGCACAACT 960 TTGTTTAGAG AGGAAATGAA GGTAGCTGTT TCCTTTTTTC TGAAACCTGC CCTTCCTCAT 1020 ATTTAACCAC AATGTGTTAT TGCCAACCTC TGAGTCTCAT CAGCTTAACA AAGGAGATCA 1080 CTTCCTGGGG CCAGCAGTAG AGAGGTCGCT GAGAAATGGC CTTCTCCTCC TTGGCCAGGA 1140 TCACTATGCT TGATTCCAAG TGGCATGGCC AGGCCAGGCC CTACCCCACC CTGACCCCAG 1200 AAAATAGAAA CATGAACATG AACTCAGTCA GCATCTAGCT CATGGCTGCT GGAAATAGTT 1260 GGCAATCTCT CTCTCTCCAA CACAGCTCCA TCTTTCAGCA TGAAGGGTAG GGAGATTTCT 1320 CACATGCACC AAGGTAAGGT GGAGGGGTCC CTGGAAATCT AATGGTAGCT GAGTCTTGTG 1380 GGCCTGAACC ACTGTCCCTT GCTCTGCCCA GAAATGGATT TGTGAGATCA CAGCCTAAGT 1440 GACTGATGGA GCCAGGCGCA TCCTACGGAC CACAGCAGTC CACAAAACTC TCTCTTGGGA 1500 AAACTGCCTC TTCCCAGGGG AAATTGTGCC AAGTGCGTGG CAGACTGCAG GGCAGAGCGG 1560 AAATGTAGCA TGAGGCTCGG TGATGCTTGT TGGCCTTTAC CACGCCCCTG GGCTGAAGAC 1620 CGCATGCTGC TCAGGCACAG CAGCAGGAAG CCTGTTCCAC CATTAGCAAG CAGGTAAGAG 1680 AGAAGAGCAA AGCTGACTGG TGAAGGGAAA CTGAAACAAC ATGCATCAAA GCTCAGAGAG 1740 AGCATGATGG AGGGCGAGGC TGCTCAGCTG GCACTGCTCC TAGGTCCTCT CCATCCCAGT 1800 CCGACTGCCT TTCCTGCTGT GGGCTCCTCT CCCCTCCCGT CTCCTCCTGC ACAATGCACT 1860 CGCAACCTAG CCTACCCCAA AGAGGCTGAG CAAGGGTCCA GGGTAAGTGG GTTTCTGAGG 1920 AGTAGGGGAC ATGCAGGAAA GAAGGCGATC CACATGTCCC CTTCTCTTAT CTCACTGCTG 1980 TCCACCTTCT CTGAATTCAC CTAGACTTCA TTCCACAATG GCAAGTGATG CTCATGTGAA 2040 AGGCTGGGGG GAACCTGACC AGCTCTCTCA GCCCATGACT TCCACACCCT CTCATCACCT 2100 GAAGACAAAG GGACCAGCTA GCACCCTGTC 2130
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