Tag | Content |
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EnhancerAtlas ID | HS017-06446 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr11:94885760-94887230 |
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) |
Foxd3 | MA0041.1 | chr11:94885951-94885963 | GATTGTTTTTTT | + | 6.44 | IRF1 | MA0050.2 | chr11:94886462-94886483 | GTAATGAAAGTGAAACTGCGT | - | 7 | IRF8 | MA0652.1 | chr11:94886465-94886479 | ATGAAAGTGAAACT | + | 6.06 | IRF9 | MA0653.1 | chr11:94886464-94886479 | AATGAAAGTGAAACT | + | 6.38 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_36837 | chr11:94885982-94887101 | HMEC |
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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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Enhancer Sequence | TCAATCAATC AATCAATAAA AATACAAAAC ATTAGCTGGG TGTGATGGTG TGCACCCTTA 60 ATCCCACCTA CTCGGGAGGC TGAGGCAAGA GAATAGCGTG AACCCAGGAG GCAGAGGTTT 120 CAGTGAGCCG AGATTGCGCC ATTGCACTCC AACCGGGGCG AAGATTTACA TATATATAAG 180 ATTTTCTGTC TGATTGTTTT TTTGGGTATG AGAAAAAGAC AGGAATCAGG GATGACTCCA 240 AGCAGCTGGA AAAACGGAGA TGCTGCTGGC TGAGATTGGA AGATGCTGGG GTAGAGGGAT 300 AAGACAGCTT AATGTTATAT ATTTTAGGTT TGAGGTGTTC ATTAGAAAAA CAAGTGGAGA 360 GATTGATTGG GCAGACACAC AGGTCTGGAG AGGGCTGGGC TGGAGATAGA AATATGGGTT 420 GCCATGATAC AGGCATGGGA CTGAAAGCCC CATCAGTCCC TTGGAGAGAT CATCAGAGAG 480 TGAGTAGAGA CATAGCAGGG CGAAGCCCTG AGCCCCGGTT CCCCCAGCAT GTACCTGCAG 540 TCTGTTTCCT CTTCTCAACT ACAATTCCCA TGGTCTTGTC TTGTTCACAG AACCTGCTCA 600 AGGAGCATCT ATTAAATGAA GGAACCCAAC TTTCATCACA TGTAAAATAA ACATCATTAT 660 AATCCTACCT CATAAGGTTG TTGTCAGAAA AAGTTAAACG TCGTAATGAA AGTGAAACTG 720 CGTTATGATT GGTAGATGCC TGCTATATTT TAAAATGTAG GCTTCATTAT CTCATTCTGT 780 ACAGCTTGTA TTACTTGATT GTATCTTCAC AGTTTCTGAT GCATGCAAGG CAGACACTCT 840 CGTTCTCACT TTATTGACGA GGAAAGTAGG ATTGGTGAGA CAAAATAAGT CCCTGAAGCT 900 GCATATCTAA TGGTAACACC AGTGGCTGAC CTGTTTGAGC ACATCTGCGG CAGGCACTGT 960 GTTAATGATT TTGCATGTGT TATCTGGCAA CAACACAGCG AGGTGGGGGT TATTATCTTC 1020 ACTTGCACAT GAGGAAACTG AAGCATAGAG AGGGTGGTTA ACTTAGCCAA GGTCCCATAG 1080 TGAGTGGTTG GAAGAGTCTG GGCCATGAAG CAGACCTGCC CATCCTGATT CAATGTTCTT 1140 TTTGCAGCCT GATAGCTCCT CTTCTTCATC CCCCTACTAG ACTCCTGCCA GGGCCAAGCC 1200 TCACCACTCC TTCCCTTGAC ATTGGCAACA TTCCTCTCTC CTTAACGTTT CTCTCCTACC 1260 AAGCCTGCTT GCTGCAGGAT ACAAGAGTTC AGTCACTCCT TGGGAACAAC CTGCAGGTCA 1320 AAACATTTTG GCTTATTGCT TCCCCTTTCT GGAAAGTCCT TTCCCTTCCT CTCTGCCTTA 1380 TGAACTCCTA TGTGTTCTTC CAAACCCTGG TGAACTCCTA TGTGGTTTTC CAAGTCCAAT 1440 TAATATGTCA CCTCTGTTGT GAAGCTTTCC 1470
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