Tag | Content |
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EnhancerAtlas ID | HS136-09796 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr19:45786310-45788100 |
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) |
MAFK | MA0496.2 | chr19:45787059-45787078 | AATTGCTGAGTCATCTGGT | - | 6.01 | MAFK | MA0496.2 | chr19:45787059-45787078 | AATTGCTGAGTCATCTGGT | + | 6.51 | NFE2L1 | MA0089.2 | chr19:45787060-45787075 | ATTGCTGAGTCATCT | - | 8.12 | Nfe2l2 | MA0150.2 | chr19:45787062-45787077 | TGCTGAGTCATCTGG | - | 6.48 | Zfx | MA0146.2 | chr19:45787509-45787523 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH19I045283 | chr19 | 45786461 | 45787658 |
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Enhancer Sequence | TATCATGATG ACCGATTTCA GAACATTTTC ATTACCCCAA AAAGAAAATT CACAACTTTT 60 AGCAATCAAC TTCCAGGCAG GGCATGGTGG CTCATGCCCG TAATCCTAGC ACTTTGGGAG 120 ACTGAGGCAG GCAGATCACC TGAGCGCAGG AGTTCGAGAC CACTGGGCAA CATGGCGAAA 180 CCCCATCTCC ACTATAAAAT ACAAAAATTA GCCGGGCGTA GTGGCAGGCG TCTGTAATCC 240 CAGCTACTCA GGAGTCTGAG GCAGGAGAAT TGCTTGAACC TGGGAGGCGG AGGTTGCAGT 300 AAGCTGAGAT CGCGCCACTA CACTCTAGCC TGGGCGATAA GAGTGAGACT TCCTCTCAAA 360 AAAAAAAAAA AAAAAAAAAA AAAATCAACT TCCAATCCCC CTTCCACCCT CAGCTACTAA 420 TCTACTTTCT ATGTCGATGA ATTTGGCTAT TCTAGACATT TCAGGTAAAT GGAATTACAC 480 GATGTGTGGC CTTCAGTGAC TGGCTTCTTT CATTTAGCAG AAAGTTTTCA AGGTTCATCC 540 ATGATATGGG TATCAGCACT TCATTCCTTT TCATTGGCAA GTAATATTCC ATTGCATAGA 600 TAGACCACAT TTTGTTTATC CATTCATGAA CACGTGGATT GCCTCCACTT TTTGGCTGTT 660 GTGAATGATG CTGCTGTGAA CATTTGTATC CGTGTTTTTG TGTGGCTGTG TTTTGCCGTC 720 ATTTCTCTTG GGTACGTATC TGGGAGTGGA ATTGCTGAGT CATCTGGTAA CTGTGTGTTT 780 AATAATAGTT TGAGGAACTT TCAGGGTGTT TTCCAACTCT GTTCGTTTTA CAGCCCTGCT 840 TGTCTGCAGG GGTGAAGTTC TTACTCTGGG ACAGGTACTA GGCTGTCTGC TTGTCTAATC 900 TTTTTTTTCT CTGTCTTACA TATCTCACCT TATCTTTTTC TAGATCTCTC AGCTCCTAGA 960 TTTCTTCTTT TTTTTCTTTT TTTGAGACAG AGTCTCACTC TGTCGCCCAG GCTGGAGTAC 1020 AGTGGTGCGA TGGTGGCTCA CTGAAACCTC AGTCTCCCAG GTTCAACTGA TTCTCCTGCC 1080 TCAGGCCCCC GAGCTGGAAT TACAAGCCAC CTTGCCCAGC TAATTTTGTA TTTTTAGTAG 1140 AGACAGGGTT TCACCGTGTT GGCCTGGCTG GTCTTGAATT CCTGACCTGA GGTGATCCAC 1200 CCGCCTCGGC CTCCCAAAGT GCTGGGATTG CAGGCGTGAG CCACTGTGCC CAGCCACTCC 1260 TAGATTTCTT TTCTTTTTTT TTTTTTTGGA GGCAAAGTCT CGCTCCGTTG CCCAAGCTGG 1320 AGTGCAGTGG CGCAATCTTG GCTCACTGCA AGCTCCACCT CCCGGGTTCA TGCCATTCTC 1380 CTGCCTCAGC CTCCCGAGTA GCTGGGACTA TAGGTGTCCA CCACCACGCC CAGCTAATTT 1440 TTTGTATTTT TAGTAGAGAT GGGGTTTCAC TGTGTTAGCC AGGATGGTCT TGATCGCCTG 1500 ACCTCATGAT CCACCTGCTT TGGCTTTGGC TTCCCAAAGT GCTGGGATTA CAGGCATGAG 1560 CCACCGCGCC TGGCCCGCTC CTAGATTTCT TACATCTCAG TTTTAGAATC CAGCCCAGGG 1620 CTGAGTGCAG TGGCTTACGC CTGTAATCCC AGCACTTTGG GAGGCTGAAT TGGGTGGATC 1680 ACTTGAGCTC TCAAGTTCGA CACCAGCCTG GGCAACATGA TGAAACCTCA TCTCTACAGA 1740 AAAATACAAA AATTAGGCTG GGCGCAGTGG CTCTTGCCTT GTAATCCCAG 1790
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