Tag | Content |
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EnhancerAtlas ID | HS017-09461 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr14:21316070-21318300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr14:21318232-21318247 | TGAACTCCTGACCTC | - | 6.22 | RARA(var.2) | MA0730.1 | chr14:21317637-21317654 | TGAACTTTCACTGACCT | - | 6.12 |
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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 |
GH14I020848 | chr14 | 21316514 | 21317829 |
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Enhancer Sequence | GGGTTATTGT GTGAACTAAA TAAAATAACC CAGGTAAAGC ATCTAGAACA GTTCAGCCAG 60 CTCAGTGATC AGAGTTGCAG CCTTATTTGC CTGAATAATG AAATAATTAT TGATTTAAGT 120 TCCCAGCTAT GAAACCATAT GTCCCAGTTT GCCCAGGATC TGCTCTATGT ATGCTGCTGT 180 CCTGGCTTAA TTACTAGTAG TATTCCTTCT CACTCTCAAA AGTATCACAG TTCAGACAGT 240 AAATTAGATG GGCACCCTAT TCAGAGCACA TAGTAAGCTC TCCATAGATA TCATTATATT 300 GTTATTATTA CCAGTTTAAT ATAGCTTCTG AAAAGGTCAC AATTAACAGG TAAGTTTGGC 360 TGGCACGGCG GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA AGTGGATCAC 420 CTGAGGTCAG GAGTTCGAGA CCAGCCTAGC CAACATGGTG AAACCTTGTC TCTACTAAAA 480 ATATGACAAT TAACCGGGTA TAGTGGCATG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG 540 AGGCAGAAGA ATCGCTTGAA CCTGGGAGGC AGAGGCTGCG ATGAGCCGAG ATTGAGTCAC 600 TGCACTCCAG CCTGGGTGAC AGAGCAAAAC TGTCTCAAAA AAGAAACAGT TAAGTTTACA 660 TTCTGAATTA GTAGGAGTGA CAATGATTGA AGTTTTTGAC TGGGCAGGAA AGATAGACTG 720 ACAGTTCCCT CATTCTATCT TTATATAGAA CTGGAGAGCA GCACAGAAGG AGGGGGACAT 780 GTCAAGGAAT ACCAGGCGGG CAGAGCCTGC TTTAAGGCAT CTTCCAAAGG TTATGAGTCA 840 CTGCAGACAC ACTGAGAGTC ACACTGGGGG AAGGTGCAGC AGACAGGGAG AAGTTCAAAG 900 TGGTGTTTCT GAGAGACTTG GGGCACTGTG TACAATTAAT CATCTCTCCA CATGGGTGAC 960 TGTGGGAGCC ACAGCAGTGC CTGAGTCTTC CAGGGGAAAC ACTGAACATG GAAATTTGTG 1020 GAAAGGAAAC GAAGGAGGTG GATGAAAGCT GGAGGAACAA GTGTTTAAAC AATGCAGCTT 1080 TTCTTGCCCT GGAAGGTTCT TTGGGTACTA ACCTTCTGTG TGGTAGACAG AGGGCGGCCG 1140 GGGAGAGGAA GGAAACTACC AAGAGAGAGC AGCAGCAGTC TTGCCTGTGC TCCCCTGTGG 1200 TGCCCTTTCT TTTGAACTCT TTCTTGAACC CTTAATCCCT GTCAGGCTCC TGGAGGAGCC 1260 TCACTGGGCA GCCTCAAATC TCCCCAGTTT GCCCTGTCCT CAGAAAAGCA GACCATTGAA 1320 ATTGCTATTT CAGAGCTGGA AGCTGGTCAG CCAGCTCAGA TGACCGGAGT TGCAGCTCTT 1380 ATTTGCCTGA ATAATAAAAT CATTATTGAC TTAAGTTCTC AGCAAACAGT GGGGTATTTG 1440 TTTCACATTT CTGAGCTGCT GCTCAAGTTC CAAAAAATGT CCCCTTCCAA AGAAAAGTAT 1500 TTAAAATTGG ATTGAGAGCG AAGAGTAGGT GGAATAGGCT ATTGTGGGGG AGGTCCTGGA 1560 TTTGCAGTGA ACTTTCACTG ACCTTTCAGC TCCTTAGGGC ATGCTCCTTG TCATCTGTCC 1620 ATCATGCCCA ATGGCCAGCC TAAGGGGAGA AAATAGAGTG CTCTCTCCAT GATGGCCAAA 1680 ACTACCTGCC TGGCTGGCTG TCCGTCCGTT ATCATCTCAG TCTCTAACCC ACTTCTTGCT 1740 GCTCCTGATT CTATGCCCAC TTAACTTGTC AACTGTGACT TTGTGGAACA TAATATAACA 1800 AAAAAAGGCA TGGGCTTTAG GGAAATTGGC CCCAATTTAG GCAGGAATTT GAGCCCCAGT 1860 GCCACTGCAT AACCTAAAGC TAATAACATC ATTTTGGTTA TCTGTTATTG CATAACACAC 1920 TTACTAAACA GTACTTTTTA TTTTATTTTA TTTTATTTTT TTAGATGGAG TCTCCCTCTG 1980 TCACCCAGGC TACAGTGCAG TGGCATGATC TCAGCTCACT GCAACCTCTG CCTCCTGGGT 2040 TCAAGCTATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA CTACAGGTGC AAGCCATCAT 2100 GCCCAGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTT GCTATGTTAG CTAGGCTGGT 2160 CTTGAACTCC TGACCTCAAG TGATCCAACT GCCCCAGCTT CCCAAAGTGC TGAGACTATA 2220 GGCATGAGCC 2230
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