Tag | Content |
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EnhancerAtlas ID | HS136-13512 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:50487070-50489020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr3:50487155-50487166 | AATGACCTTGA | - | 6.32 | Esrra | MA0592.2 | chr3:50487156-50487167 | ATGACCTTGAG | - | 6.02 | Esrrg | MA0643.1 | chr3:50487156-50487166 | ATGACCTTGA | - | 6.02 | FOXP1 | MA0481.2 | chr3:50487797-50487809 | GTGTAAACAGAA | + | 6.22 | IRF9 | MA0653.1 | chr3:50488580-50488595 | AGTTTCACTTTTGTT | - | 6.15 | MEOX1 | MA0661.1 | chr3:50488959-50488969 | GCTAATTAAC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr3:50488775-50488790 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr3 | 50487601 | 50488521 | chr3 | 50487622 | 50487847 | chr3 | 50488140 | 50488331 | chr3 | 50487400 | 50488140 | chr3 | 50488144 | 50488400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I050449 | chr3 | 50486750 | 50489034 |
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Enhancer Sequence | ATGAAAATAG TGTCAGCCTG AAAGGACACC ATTAAGAAGG GTCTTAAAGC GTGGCCCTGT 60 GATGCCTCCG CCACACCACA CTCAGAATGA CCTTGAGGCC ATGAAGAGAG GGTGGCCTGG 120 GGCGGGGGGA GCCTGTACTC CCAGGACTGC CCACCACACT CCCCATCAGA GACACAGGCA 180 TTCAGCCCGG GCCCTAGGGA CTGAGTAGGT GGGAGAGAGA CCTAGGGCTG GGTTCTGGGG 240 CTTCACCCAT GAAGTGGAGC TGCTTCTCCC ACACAATGAC AGGACTGTCA CCACCCAAGC 300 TCACAAGGGC TGTGGAGGGG ACATAGTGGG AGGTGAGGCT CCATGTGAGG AGGGGTCCAT 360 GGAGCCTGAC TCAAAGCAAA CTGCAGCCTC CAGAGTTTGT GAGCCCCAAG CCACAGAAGG 420 GGGCAAGCTA AAGGTGGCCC CCAGGTCTCA ACCAGTCCTC TCAGTGGAGA CTTAGGCCAA 480 CCTGAAAGCC CAATATTCTT GATTTGCCCC CAAAATCACT ATACAGCCCC ACCTTCCATG 540 CACACAGGAC ATCTAAAATG GGGCAGGATT CACACATTCT TTTGACAGCG GATCGGCCTG 600 GCTCCCTTTG AGGGCCCTCG GGTCAGGTGA GGCAGTCCCT GACCCAGTTC CTGTGTGGGC 660 TTCCTGTGCA AATGGGCCCC AAGCCCCACC TACCCCCGCA CCGCCTCCCC TACCCTGCCC 720 CCGCCCCGTG TAAACAGAAC CCGCCACTCT CTCCCAGGAG CTGCTAATTC CTCGCCAGAA 780 CTGCTCGGAC GTGAAATTGG AGTGAGACAA TGTGTGTTTA AGGAAATGAA TCTCGAATCT 840 TAAGAGGCTC TGGAGCCCGC CCTGCACCCC CATCACCCTG CTCTCGCCCA CCAGAGCCAG 900 GAAAGGAGCA CTTGGCATCA GAGAAGAGAA AGGCGGAGGT GACATTCAGC GCCAAATTAG 960 CAGCCGCCAC AGCCAAATAT TGTACTTGCC TCCAATCTTC TTTTATTTTT CCAAAGAAAA 1020 GGCTTTTACA GAGTGAAAGA GGCTGTTGGA ACACTGAGGC TGATGATCGT TTGTAAAAGG 1080 CAGGCCTGCT GCGCGCATGC CTGACTCAGA GCCTTCCCTT CCCATCGGCA GGCCTCCCCT 1140 CCCTGCCCAC AGTCACATCC GCAAGACGCC CGCCGACGTC ACACCCCACC GCACCAGCCA 1200 CACTGGCCGA TGTCACGGGT GTCCTTAGCC AACAAGACCC AGGGGCTCTG ACCCTGTGCC 1260 AGTCCTGGAC ATGGGACCTG CCTCTGAGCT GTCTCCCCGC CTACATGGGG CCCTTGGAAA 1320 TGAGGACTCA TTTGTGGTGT GTACAAAACC ACTGTGCCTA CAGAGGCCTC AAAAGTGACC 1380 AGTCCATGAC CTCTGTAGGG GCTCCTCATC CACCCCAATG GCCCTTAGTG CCCCCTCCAT 1440 GGACAGCCAC CCTGCCTCTG CCATCATCAC TTTTATCCCT CCCACCAGGG GCTGTTTTTT 1500 TTTGAGACGG AGTTTCACTT TTGTTGCCCA GGCTGGAGTG CAATGGCGCG ATCTCGGCTC 1560 ATTGCAACCT CTGCCCCCTG GGTTCAAGCG ATTCCCCTGC CTCAGCCTCC CGAGTACCTG 1620 GGATTACAGG TGTGCGCCAC CATGCCCAGC TAATTTTTTG TATTTTTAGT AAAGATGGGT 1680 TTCACCATAT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCTG CCCACCTCGG 1740 CCTCCCAAAG TGCTGGGATT ACAGGCATGA GTCAACACGC ACGGCCCAGG GGCTGTTTTA 1800 AGGCCCCTCC CCAGGCTGCC TGACACTTTG TTGAACACTA CCAGTCATCC TGAAGTTCAG 1860 GCCCCTGAAC CCAGCCTACC TCCATCCACG CTAATTAACC CACTGAGCAG GCTGAGCAGA 1920 TACCCTCTGC ATGCCCCTCC ACTATTTTCA 1950
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