Tag | Content |
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EnhancerAtlas ID | HS127-15662 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr19:45786370-45788070 |
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 | AGCAATCAAC TTCCAGGCAG GGCATGGTGG CTCATGCCCG TAATCCTAGC ACTTTGGGAG 60 ACTGAGGCAG GCAGATCACC TGAGCGCAGG AGTTCGAGAC CACTGGGCAA CATGGCGAAA 120 CCCCATCTCC ACTATAAAAT ACAAAAATTA GCCGGGCGTA GTGGCAGGCG TCTGTAATCC 180 CAGCTACTCA GGAGTCTGAG GCAGGAGAAT TGCTTGAACC TGGGAGGCGG AGGTTGCAGT 240 AAGCTGAGAT CGCGCCACTA CACTCTAGCC TGGGCGATAA GAGTGAGACT TCCTCTCAAA 300 AAAAAAAAAA AAAAAAAAAA AAAATCAACT TCCAATCCCC CTTCCACCCT CAGCTACTAA 360 TCTACTTTCT ATGTCGATGA ATTTGGCTAT TCTAGACATT TCAGGTAAAT GGAATTACAC 420 GATGTGTGGC CTTCAGTGAC TGGCTTCTTT CATTTAGCAG AAAGTTTTCA AGGTTCATCC 480 ATGATATGGG TATCAGCACT TCATTCCTTT TCATTGGCAA GTAATATTCC ATTGCATAGA 540 TAGACCACAT TTTGTTTATC CATTCATGAA CACGTGGATT GCCTCCACTT TTTGGCTGTT 600 GTGAATGATG CTGCTGTGAA CATTTGTATC CGTGTTTTTG TGTGGCTGTG TTTTGCCGTC 660 ATTTCTCTTG GGTACGTATC TGGGAGTGGA ATTGCTGAGT CATCTGGTAA CTGTGTGTTT 720 AATAATAGTT TGAGGAACTT TCAGGGTGTT TTCCAACTCT GTTCGTTTTA CAGCCCTGCT 780 TGTCTGCAGG GGTGAAGTTC TTACTCTGGG ACAGGTACTA GGCTGTCTGC TTGTCTAATC 840 TTTTTTTTCT CTGTCTTACA TATCTCACCT TATCTTTTTC TAGATCTCTC AGCTCCTAGA 900 TTTCTTCTTT TTTTTCTTTT TTTGAGACAG AGTCTCACTC TGTCGCCCAG GCTGGAGTAC 960 AGTGGTGCGA TGGTGGCTCA CTGAAACCTC AGTCTCCCAG GTTCAACTGA TTCTCCTGCC 1020 TCAGGCCCCC GAGCTGGAAT TACAAGCCAC CTTGCCCAGC TAATTTTGTA TTTTTAGTAG 1080 AGACAGGGTT TCACCGTGTT GGCCTGGCTG GTCTTGAATT CCTGACCTGA GGTGATCCAC 1140 CCGCCTCGGC CTCCCAAAGT GCTGGGATTG CAGGCGTGAG CCACTGTGCC CAGCCACTCC 1200 TAGATTTCTT TTCTTTTTTT TTTTTTTGGA GGCAAAGTCT CGCTCCGTTG CCCAAGCTGG 1260 AGTGCAGTGG CGCAATCTTG GCTCACTGCA AGCTCCACCT CCCGGGTTCA TGCCATTCTC 1320 CTGCCTCAGC CTCCCGAGTA GCTGGGACTA TAGGTGTCCA CCACCACGCC CAGCTAATTT 1380 TTTGTATTTT TAGTAGAGAT GGGGTTTCAC TGTGTTAGCC AGGATGGTCT TGATCGCCTG 1440 ACCTCATGAT CCACCTGCTT TGGCTTTGGC TTCCCAAAGT GCTGGGATTA CAGGCATGAG 1500 CCACCGCGCC TGGCCCGCTC CTAGATTTCT TACATCTCAG TTTTAGAATC CAGCCCAGGG 1560 CTGAGTGCAG TGGCTTACGC CTGTAATCCC AGCACTTTGG GAGGCTGAAT TGGGTGGATC 1620 ACTTGAGCTC TCAAGTTCGA CACCAGCCTG GGCAACATGA TGAAACCTCA TCTCTACAGA 1680 AAAATACAAA AATTAGGCTG 1700
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