Tag | Content |
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EnhancerAtlas ID | HS136-13254 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr3:23765210-23766190 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:23765298-23765319 | AAAAAGAAAAAGAAAGTAAGT | - | 7.51 | ONECUT3 | MA0757.1 | chr3:23765884-23765898 | CCAAAATCAATAAA | + | 6.02 | SPI1 | MA0080.4 | chr3:23765628-23765642 | GTAAAGAGGAAGTA | + | 6.05 | SPIC | MA0687.1 | chr3:23765628-23765642 | GTAAAGAGGAAGTA | + | 6.53 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTGAACCCG GGAGGTGGAG GTTGTGGTAA GCCAAGATCG CACCACTGCA CTCCAGCCTA 60 GGCAACAAGA GCGAGACTCT GTCTCAAAAA AAAGAAAAAG AAAGTAAGTT TGGAGGCAGG 120 CATCCAGGGT TGGTGGGACC TAGGTTTCAT CAGTCTTTCT GCTGCTGCAT TCTAGCATAT 180 GGCTTCCATC CTTCAGATTG CTTCATGGTC CAAAATGGGC TTCTGGAGTT ATAAGCCAGA 240 AAAAGAAGGA AAGTAAAGAA AAAGAGAGGC CTTCCATGCT AAGTTAGCTC TCTTTAGACT 300 GCCTTCCTGA AAGGCCCACT GAATTCAGCT TTCTGGGCCA CAAGTCACAT GGTCATATCT 360 AGCAGCAAGG GAGGCTGGGA GATTAATATT TTATTTTTGG TCACAATGTG GCTAGCAAGT 420 AAAGAGGAAG TAAGGAGAAG TAGAGAAGTG ATACTGGAAG TAGCCACTAA CCATCTCTGC 480 ATCTGGCAAG ACATGAAGGC AGGACTAGCC TTGGAACAAT GTCTGGGGCT CAAGTTTTTC 540 TAGGCCCTTA AGAGAATGCT TGCTCCAACT AGGCTTTTCT GCTCTGTTTA GGCTTTTTCT 600 GGGTAGAGGG CAATCCTAAG GACTGGAATA GCCTAGTTCT CACAACTGTG TTTATTTGTC 660 CAGAAGCCTC AGGCCCAAAA TCAATAAAAA TGCACAAGGA TCCACTGAGC ACACTTCATA 720 TGGGCTGCAC TGATGTAGAC ATAACAGTGG AGCCAGGGTG ATGGGAAGCT CTTTCCTGAG 780 TGGCTTTCAA GCTAAGAGGG TAGCTTAGAA CCATGTTTCT CAAACTACTT TCTTCCAGTT 840 TATAGCAGAC CACTATGTGT TCCTACTGTG ATAACCATAG GAGTTCAGCA ATACCCAGCC 900 TCGTCTATTT CTTGTTCAAA AAGATGAGTC CTCTAATCAT ACACTTGGGT GTCACAATGT 960 CAACTTGCTA TATATATTTT 980
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