| Tag | Content |
|---|
EnhancerAtlas ID | HS042-29047 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr20:62055550-62056630 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr20:62056546-62056559 | ATGACCTCATCTC | - | 6.11 | | JUND(var.2) | MA0492.1 | chr20:62056545-62056560 | GATGACCTCATCTCA | - | 6.6 | | MYB | MA0100.3 | chr20:62056075-62056085 | ACCAACTGTC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGTCCTTCC TTCAAACAGA AGCAACAGAG AGTTAGTGGC CGCCCACTCA GCACCCATGA 60
GGGTCCCCCA ACCAGTCCAG CCCCCCACAG TCCCATGGGT CAGGGGCTGC AGGGGAGGGG 120
GGTCTCAGAA AAGGCTGGGC AGGGGTGGAG CTGGCCCACC CACCCCAGAG AGCCCACGGC 180
CCCAGGAACG GGCACCCCAG GGCCCACGGA GGCAGCTCCG AGAGGGAAGA GGGACTCCAT 240
GGGGCGGGGG CCTCTGCTCT TCTGACCTGG GGGTCTCTAC CCCTCCACAT TTACAGACAC 300
TCATTTTAAT CAGAACCACA CCAATATTAA TAAAGTTCCA AAAAGCACGT GTTTGCTGAA 360
GGAAGCTCTG GAAGGGAGTT TAATTTACAA TCAATTTTCG AGACAGAGTG AGCTGCTCCG 420
ACTCTTTTTT CCACGCTCAT CCTAATGGAA TGATTCTCTT CCGCGTGACT TTCCAGGGGT 480
GGCTCCACTG CGCCACAGTC AGTGAGCCCA GGGTTTGCAC CGCTGACCAA CTGTCCCGGC 540
CTCGTCCTGC AGGCAAAGCT GTCTGGGCCT TCCGGCGTCT CATCTGGGGC TGTTTCCGCG 600
GGTAAAGGCG TTATGGATTG AGTGAGAGAT CGGCGGATCG TGATTTGGCT CATCCATGGG 660
GAGGCCCCAG CGATCTCATT CGAACACCTG GGCTGGTGCC CCGGCTGGTA CGCCGTGTTA 720
CAAGCAGGCT CTTTGGTGCA CTTCCAAATA CTTCATGTGA CAGGGACCGT GTTGCCGTGG 780
AACATGGTCC ACGCTCTCGG GGAGGGTCCC TCATCACCTC CTGCAGCTCC CGGTGGCCCA 840
GGTGTCCTTG GCTTGTGGCT GCACCGCCCC GTCTCTGCCT CCGTCTCTAC ACGACATTCT 900
CTGTGTCTCT GTGTCTTCTC CTCCTCTACC TCTGTAAGGA CAGCTGTCAC CGGGCTAGGG 960
CTCAAGCTGT CACCAGGCTC ATCAGGATGT TCCAGGATGA CCTCATCTCA AGATCCCAAG 1020
CTCAGTTACA GCTGCAAGGA CCCTTTCTCC AAATCAGGTC ACATTTGCAA ATTCTGGGAC 1080
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