Tag | Content |
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EnhancerAtlas ID | HS127-31221 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr8:144300700-144302570 |
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) |
Nr2f6(var.2) | MA0728.1 | chr8:144301184-144301199 | GAGGTCAGAAGTTCA | + | 6.38 | Nr5a2 | MA0505.1 | chr8:144300732-144300747 | GAGCTCAAGGTCACA | + | 6.38 | RARA | MA0729.1 | chr8:144301184-144301202 | GAGGTCAGAAGTTCACGT | + | 7.2 | RFX2 | MA0600.2 | chr8:144302497-144302513 | CGTTGCCTTGGAAACG | - | 6.19 | RFX2 | MA0600.2 | chr8:144302497-144302513 | CGTTGCCTTGGAAACG | + | 6.3 | RFX5 | MA0510.2 | chr8:144302497-144302513 | CGTTGCCTTGGAAACG | - | 6.41 | RFX5 | MA0510.2 | chr8:144302497-144302513 | CGTTGCCTTGGAAACG | + | 6.65 | ZNF263 | MA0528.1 | chr8:144302420-144302441 | CCATCCCTTTCCTCCTCCTTA | - | 6.29 |
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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 |
GH08I143217 | chr8 | 144299859 | 144303931 |
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Enhancer Sequence | GTACGAAAGC CTGCAGCTGC GACATGAGGC TCGAGCTCAA GGTCACACAG CTGGGCGGTG 60 CAGATCCAGG ATCCAGTCCC CGGGCTTCCT GCCAACCGCA CCCAGCTTCC CAGAGGTGTC 120 CCAGGCTCCA GGACGCCTCA GCTGGGGAGG AGCTGGATGT CAGCCAAGAG CCAGCCAGAT 180 TCCCAGGCCA AGTCGAGTCT GAGCCAGGCA AGTCAGCGGT GCCAACGGGC GGATGGTCAC 240 AGCCAAGACA CCCTGGGCCC CGTCTCAGAG CCCAACGCAT GCTGTCAGTC TCAAGAGTGA 300 ACATAGAGGG ACCTCCCTTT CTCATCCAGC CCAGCAGCAG GGAGACTGGG GGCTGGGGGG 360 CTGGGCAGGG AGGGGGCAGG GCCCTGGCCC AAGAACCCAT GTCCCTCTGT ACCAGTTTCC 420 CAGGGCTGCC ATAACAAATC ACCACGAACC TAGTGACTTA ACACAAGTTC ATGCTGTGGC 480 TCTGGAGGTC AGAAGTTCAC GTCAGGGCTC TGGCTGGGCT GCGTTTTCTT GGGAGAGAAT 540 CCACCCCCGC CCTCTCAGCT TCAAGAGGCC ACCTGCTCTC CTTGGCTCAT GGCCCTTCCT 600 CCACCTTCGA AGCCGCTCCA ACCACTGCTC CCTCACCAGC TTCCCGAGTC AGCTCTCCCT 660 CGGCCTCCTT CTTACAGGGA TCCTGTGACC ACAGTTAGGA CTCGCCTGGA GAATCCGGAG 720 CCATCTCCCA TCTCAGATCC TCCGCTTCCT CATGGCTGCA AAGTCCCTTT TGCCATAGAA 780 GGCACATTCA CAGGCTTGAG GATTTGAACC TGGGTATGTC AAAGACCTTT CCTGAGCCCA 840 CATCAGCCCT TCCCTGGACA CCTGCTCCGA GACTAGCTGT GCTCTGGAAG CCACGGTCCT 900 GGGGAGGATA AAGCCCAGCT CCCTGGCTCA AGGGGGCCAC AGTCCCAGGA AGGAGGCCTT 960 GCCGGGCCCC TGGTGGCCAC AGTCCAGAAG TCAGTCCCAC AGTGGTCTCT TCCTGCCCCA 1020 GAAGAATTCA GGCCCCTTCG CCTGTGCTCA TCACGAGAAG CCGGGCAGAG GCTTGTTCTC 1080 ACTCTGTCTC TCCCGCACCC CTTGGGTCTG CCCACACCCA GGTCTCCCCG CCATCAAAAC 1140 TGACCAAGAC CAGGGTGCAG TGCCTGACTC ACTCATGGGA CAAACCCTAA CCACGCCTCC 1200 CTCCTGACTC AACTCATGGG ACAGACCCTA ACCACGCCTC CCTCCTGACT CAACTCATCG 1260 GACAAACCTT AACCACGCCT CCCTCCTGAC TCAACTCATG GGACAGACCC TAACCACACC 1320 TCCCTCCTGA CTCAACTCAT CGGACAAACC CTAACCACGC CTCCCTCCTG ACTCAACTCA 1380 TGGGACAAAC CCTAACCACG CCTCCCTCCT GACTCAACTC ATGGGACAGA CCCTAACCAC 1440 ACCTCCCTCC TGGCTCAACT CATCGGACAA ACCTTAACCA CGCCTCCCTC CACCATGAGC 1500 TCTGGCCACT CCCACATAAG GACACACGAG GACACAAGGG GCGTCTGACA CCCCCGGGAC 1560 TGGGCCCCCA ACCTCTGCCC GCCAGCCATT CGGGGACAGG TGGACTCAGA TACGTGGGTG 1620 GGGGAGACCT GGGTGTGGCA GAGCCGAGGG AGTGCAGGAG AGACCGTGAG AGCAGGACTC 1680 TGCCTAGCAC CCTGGAGATC CTCCCCAGAA CCCACCAGAT CCATCCCTTT CCTCCTCCTT 1740 AGGGACTGGG GCCGGCAGGC ACTGCTCCGG CACCCACTCT CTGGAGGATG GAGCCAACGT 1800 TGCCTTGGAA ACGGGCATCC AGGAGTGGAG TTCATTCCTA ACACGTTCGG CTTTTTGTCT 1860 CTTAATTCAT 1870
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