Tag | Content |
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EnhancerAtlas ID | HS017-31999 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr8:80634870-80636420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:80635693-80635711 | ACTTCCTTCCCTCTTTCG | - | 6.05 | ZNF263 | MA0528.1 | chr8:80635716-80635737 | TTCCTTCCTCTCTCTTCCTCC | - | 6.11 | ZNF263 | MA0528.1 | chr8:80635719-80635740 | CTTCCTCTCTCTTCCTCCTCA | - | 6.75 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAGCAATCA CAGCAGTGGG CAGAGCCCAG CAATGGGAAA GCAGGGTCCA CTACAGCAGA 60 AGCCCTGGCA AGCAGGCCAG TAGCATCTGG GAAGGCAATC AGGGCTCAGG TTTAAGGACA 120 TCCACAAGGA CACCATGAGA CAAGTGCCAG TCAGAAGGGC ACTGGCAGTA GTGGCTGCAG 180 AATTTCAATG TAGGAAGAAC TTACAGGGAG CATTTTGGTT GGAAAAGAAC TAGAGAAGCT 240 GTATTTGCAT AATACTCTAC ACAAGACTGA GAAAATGTCG ATTATCCGTG TCAAAAAATA 300 GGGATACCAT GGATAGTTGA GAGGAGAGCT AAAGCCTGCA GGACCAAGAA GTTTCCTGGA 360 TTCAGAATTC TCTGAGGTCA TCCCCAAGCA GAATGGTGCA TTCAGAAACC AGAACACACT 420 GCACGGGGCA GGCTCTGGCT GGAGAATTCA GCTGCAGGTG CTCTGTCCCA GCAGACAGGA 480 GGCAGGGGGA CAAGGAGGGC TTGTTGCCAT CCCCAGTGCA ATGCAGCAGC TCAAGCATTA 540 GCAGAGGGAC TTGCATCCTT GGTTAGCAAG CAGATCCATG AGGATGTCTG GAAGTAAGGA 600 GGGACTTGAT AGGTCTGCTT AATTGCTTCC TGCCTCAAGC CCAGATTGGT CTGGGAAAGA 660 GGCTGGGCCC AGGCTGCAGG TGGGAGATTG CGTGGCCAGC TGTGATGAAC TGGAGAGGCT 720 GAGTAAGGGG AAATAGAAAG GGAGGTGGGG GTGGGGAGAA CATGCTGAAA TAGATCCCTG 780 AATGTCCTGG GGCCGGAGCC GGGTCACTCA ATGTGGGGGA GGAACTTCCT TCCCTCTTTC 840 GTTATTTTCC TTCCTCTCTC TTCCTCCTCA CAGGCAACCA GCTAGAGGCA GGATGAGCTG 900 TCTCAAGGAA GAAGAAATCA AAACAGCCTT TAAATTACTG GAGGTCATGT CCTGTTTGAA 960 ACAACAACAA GAAAAGAGAG CAGAGTGCTA CCTCTCCTGC AGAGACCTTG CTGCCATGAT 1020 CTCTAGCCAA AGAGGTTACA TTAGTTCCAT CTTCATAGCC CAGGGACTGA GGCTTGAACC 1080 CACAAGTCTC TCTTTCTCAC TCCTTTAAAG AAACTGCTAA CCACTTCCAG GTCAACTGCT 1140 GAAAGTCATG TGTTTCTTTT ACTGCAGACA TTTCTGCAAA GCCTTCCCCT GAGAGCCGAG 1200 CACGGATGCA ATAGTCCAAG AGGTGGTGGC TGGCGCTCTT TCATCCTTGA CCCATGATCT 1260 AGAACATTTG GCTTAGAGCA TAAAGAGGAG ATTCCCAGCA CAATAAAATA GCCAGGGAGG 1320 GAACATTATT ATAGGTCCCC TTTTCAACTC AAATAGGTTA GGATTGACTG ACAACCTAAG 1380 AAATACTCAC CACTTTTTCA TTTTCAGATC AAACATAACT GTCTTCAGAG TATAAATCCT 1440 CTGAAGCCTG CCCTTCTTCC ATCCAGTCCC TTGGGTGGCA GGTATTAAAT GACTACTCCA 1500 TGTTCTCCAT AGGGAGGCAG GATGCCTTGG CAGCAGAGCA CACTGTTGTC 1550
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