Tag | Content |
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EnhancerAtlas ID | HS021-00128 |
Organism | Homo sapiens |
Tissue/cell | CD36+ |
Coordinate | chr12:122308950-122309940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:122309920-122309935 | AAGGTCAGGAGTTCA | + | 6.04 | Zfx | MA0146.2 | chr12:122309898-122309912 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122309381 | 122309707 | chr12 | 122309456 | 122309717 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121871 | chr12 | 122309456 | 122312164 |
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Enhancer Sequence | TAGGTTTGGG GAAGATAAGT AAACCAAGAA GCTTTACATT TAAAAATTGG ATCTAGGCTG 60 TAATCCCCTC ACTTTGGGAG GCCGAGGCAG ACAGATCGCT TGAGCCTAGG AATTCAACAT 120 GACCCTGGGT AACATGGCAA AACCCCATTT CTACAAAAAA AAACCCCAAA ATCAGCCAGG 180 TGTGGTGGGG CACACCTGTA GTCCTAGCTG CTCAGGAGGC TGAGACGGGT GAATCGATTG 240 AGCCCAGGAG GTTGAGGCTA CAGTGAGCTG TGATTATGCC ACTGCACTCC AGCCTGGGTG 300 ACAGAGTGAG ACCCTGTCTC AATTAAAAAA AAAAAATGCA TCTAAAAGCA GTCAAATAGC 360 CCTGTGCTCT GCTTCCTGCA ATCTACAACT GGAGACTCCC AAACAGGCAG AACTAGTGAG 420 GATTCAGAGG CAGAAGTCCA TGGACAGAAC CTCACCCCTC CCCTGCCAGG CCCCACAGCT 480 CTCCCAAGCA AGGGCAGCTG GGACCAGAGC AGGTGAAGGC TGGCCCGGGT GCCCAGCTAG 540 TCTTGTTATC AGGGCTGGTG ATCCTGGGCA GGGCCACTTA GGTGGGGCTG GTCTTTATCT 600 CTTGAGGTAC AGAGCCCATG TGTCTGAGCT TTGTGGTGAC AGGAAGCTGT ATCACCAGGC 660 ACCAGTGATG GCTGGGAGGG ACCAGAGAGT TGGTGGCACG GGACATAGGA CCCCTGGGCT 720 CTGAAGACTG TGTAATCTTG GGCCACTCCT GGCATCCTCT GAGTCTTAGT GTCCTAACTG 780 TGCAAGCCAG GGAGCACTGG AGCTGGTGTG GACCGTAGGA TGTCCTCTGT TCCTGGCACC 840 GGGGCATTGA GGAGTGTCCT GGAGATTTCT TTTCTCTCTT TTTTTTCTTT TTGAGATGGA 900 GTCTCGGGCT GGGCGCGGTG GCTCACGACT GTAATCCCAG CACTTTGGGA GGCCGAGGCG 960 GGTGGATCAC AAGGTCAGGA GTTCAAGACC 990
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