| Tag | Content |
|---|
EnhancerAtlas ID | HS024-05492 | Organism | Homo sapiens | Tissue/cell | Cerebellum | Coordinate | chr16:610660-612000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr16:610935-610948 | GGGGGGGGGGCAG | - | 6.33 | | ZNF740 | MA0753.2 | chr16:611445-611458 | GTGGGGGGGGCGG | - | 7.82 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTAGGAGCG GCGGGAGCCG CGGGGGCGGC CAGTTGGGCG TCGCGGGGCC GGCTGGACGC 60
GGGGCGCGGG GGCAGCGGGT GGCCAGGCGT GTGGGGGGCG CGGGGGGCGG CCGGGTCCCC 120
CCCACCCTCT TCTCGAAGTC CAGGAGCAGC GCGGGGGGAG GGAGGGCCGC CCTCAGGGGC 180
CAGGCGGGGA GGGCAGGGGC CGGGTCTGGG GTCTGGGGCA GACGCCTGAC CTCGCGCTCG 240
CCGCACCCGC CTGTGTGGGG CGCCCTGCGT TCCCGGGGGG GGGGGCAGCA GGATCTGCGG 300
GTGGCCGATC AGGGTCCCCG GCTGCTGGGT GCCCCCTCCT GCCCTGTGGG GGTGCCTGTG 360
CCCCCCGTGC CACCGGTTCT CCCCCAGCTC TCCCCCAAAC AGGGACAGGT GAGTGGGGCC 420
GGGTGTCGGG GCCTGGCACA GGGCTGCTGG CTGCCCCGGG AGCGATTGCC GGGTCCGGCT 480
GGGACGCGCG TGTGAGTGCG TATGCGTTTG TGTGTGCGTG TGGCTGCTGT CCAGGGGTGT 540
CTTTTGCTCT GTGTACACAC ACCAGGTGGG TGCCAGCTAT CCTCCGGGTC CCCAAGGGGT 600
CAGCAGCTGC TGAGACAGCC CCTTGGACAA GCCCCTGACC CGGGAGCCCC CGGTCCCTGC 660
TGGGAGGCGG GATGGGTTGT GGCATCGGCT GGCACAGCTG TGTGGCTCCC AGGGCTGGGT 720
GATCGATGGC CCGGCACAGC CGCCTCTGTC GCCGGAGCGC CCACACCCAT TTGTCATCCA 780
CATGGGTGGG GGGGGCGGCG GGCAGGGAGA AGGGGCCGCC TCTGCACCCA CCACCCAGTC 840
CAGGCCGGGT CTGCAGCCCC TCGGGGAGCC CCAGGACCTC TCCTGGCCCA GCCCCTGCCT 900
CCCGACCGCC ACCCTGTCTC AGCCACAGAC CAGCTGGTCA GCCTCTGCCT GCCCCTGCAG 960
CCCGTGACTG CCCTGCAGGG CCCCAAGCCT TTGGACGAGT GGACTTCTCC AGCCCTGTTG 1020
GTCGTCCCCC CAACGGCACC AACACAGTGT TTTGGGGGCA GCAGACAGCA GTGCCCCAGC 1080
CCTACCCTGC TCAACCCACT GGCCATGCAT GACCACGGGT GCGACCCCCA GCCAGGTCTG 1140
CGTGTGTCCT GGGGAGTCGG TGTGTAGGGC CTGTGTGAGC ATGTGAGTGC CGTGTTGGAG 1200
TGGTTTGGAA AGCCCCCCCA CACCTGGATG GGTGGTGAGT GTGTTATCAC GGACAAGCAG 1260
CCGTGTTCAC CGTGATGGAG TGTGAGGTGT GTGCAGCCAG GGCCCCGCAC TTGGTGGCAG 1320
ACTCCGTTCT GAGCTTAGGT 1340
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