Tag | Content |
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EnhancerAtlas ID | HS017-11910 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr16:11276050-11277620 |
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) |
ZNF263 | MA0528.1 | chr16:11276166-11276187 | CCTCCCTCTCCCTCCTCCCCG | - | 6.63 | ZNF263 | MA0528.1 | chr16:11276163-11276184 | GCCCCTCCCTCTCCCTCCTCC | - | 7.86 |
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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 |
GH16I011180 | chr16 | 11274029 | 11277997 |
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Enhancer Sequence | GCGTGCTGCT CCTGGGGGCT GTGGCAGGAG GCCGTGGCCT GGCACAGGGG AAGGTTCCCA 60 GCCAATGACC CCTCATCCCG GCGCAGCTGC TTGGCAGGGG TGTGGTGGCT GGAGCCCCTC 120 CCTCTCCCTC CTCCCCGCAC CAGGTTCCCT CCCATCCCCA GGTTCCTAAG AGGTTGTCGG 180 GGCTCATACA ACCCGGGAAT AACTGCTAAG GGGCAGTTGG CACCATCAGG AAATGTCCCC 240 GCCCTACCCC TGCCGGGTAC AGGGAGCGTG GTCCACATTC TGCATCTTTT CCCTGTTGGG 300 CAGGTGGCTG CCCATCCAAG CCTCAGGCTC TGCATCTGTG GATTTGGACA GCCAAGCCCT 360 ACCTCGCAGG ACAAGCGTAG CGAGCAGCGT CATTGTTGCC AGGCTGGGCC GAGGGAAGCA 420 GGAAGGCTCC CCACCGAGGA CAGAGGTGAA GTGCGGGGGT GGACATGACT CGGAAACACC 480 AACGTCCACC AGCGTGAAAC CCTGAAATCC CTGGAAACAG GATCACAGGT TCTCAAAATC 540 TCACCATCCA GCTTAAACCC TACCCAGAAA TGGCAGGGAA CTTCTGGGTC TTGAGAGGAT 600 AACCAAGTTG AGTCGAGAAA GAATGAACAA GGGACCCCCT TCCCCCACCG CATGCCAAGG 660 GTTGGGGTTA TGCCAACAGA AGGAGGAAGC CACTGCCCAG GGCAGAGCTG CCCTCCCATG 720 CCCCCGCCTC ACCCGGGTCT CAGGCCTCGT GGGCATTTAC ATGTCTGAGA CCCGCTGGGT 780 GACAGCTCCT CCCTCCTTGC ATTCCCAGCC CAGGTTCAAA CCCAGGGGTC GCCTGGGGCT 840 GGTTGAGAGG CTGGGGCCAC TTCTCTGGTG CCCCCAGAGC ATGTCTGTAT ATCCCCTGCT 900 CTGCGGTTGG AAGTGGCCTG CGTATACCGG CTGCTGTCAG TGTTTTCCCC AGGGCCTCGG 960 GAGGGTTCCC CTCGGTAGCC ATGAAGCGAA GCCTCGCAGG GTCCAGTGAT TATGCCCAAC 1020 AGGCCCAGAG CGTCCTGACT CTAGCCGGAG GGCGGGGCCA GCAAGGGCAG GTGGTAGTGA 1080 CCTGCCTGCG GGTGACCTCT AGGGGAAGAC CGATTGCCGG CCAGCCAGCT GCTGGAAACC 1140 CCCTTCCCCC ACGTCCTACT GCTCTGTGGC ACTTCATGGC GTTGGGAAAA AACCCTTAAC 1200 GTCTAAAGAG CTTTTCTCCA AAGGAAAGTT GGTTCTGAAT CACCCATGGG GTGAAGGGGC 1260 TTCCTGGGGA TTCACTTAAG GCTGCCCGAT GGGCAGTGTG AAGCTTCCCT TCCCTCCACA 1320 GGCCCCGGGG CTGCTGGCCC TGCTCCAGCC CTGGGTCTAC CTGCCCCACT TAGAGACCAG 1380 CCACCTGGGC TCCCAGGCCG TGCGCCTGCC TTGGGGCCCA GCCTGCTCTG CAGGTCCCTG 1440 CAGTCCTGAC ACTGCCTGGC TCAGTCTGAC TTCCTCCCAG AGGGCAGCAC GTGCCCCCTG 1500 AACACATGCC TGCCGCCTGC CTGTCACCTC CACTGACGCT TCCTTGCCCT TTTTTTTTTT 1560 TTTTTTTTTT 1570
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