| Tag | Content |
|---|
EnhancerAtlas ID | HS040-14390 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr16:89671720-89672740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:89672459-89672480 | CCTTCCCCTTCCCCTGCCTCC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I089605 | chr16 | 89672117 | 89672737 |
| Enhancer Sequence | CAATGTCACC AGGTGGACGT CGGTGTCCTG GGACTGGAAG TTACGTGCGT CCTGCCAGGG 60
CTCCTGGGCG CGCATGTTCC CTGGCAAGCA GGTGCAGGTG ATGGCCTGGA CCACGTCCCT 120
GTCTACTGCG TCCTCTGCTG TGGGTCAGTG CCTGCCGGGT GGCGCAGGCA GGGAGTGCAG 180
CCGGAGGGCT CCGTGGGGGG GTCTGTTATC CACACGTGCC CTACCAGAGG CCCAGGCAGG 240
TTCTAGCAGG TGGACACCAG CTCCGCCATC CCCACCGTTA AATACTAGCA GAGGCCCACA 300
TTCAGGTGCC CTCCCAGGAC CAGCCTCAGC CCTCGTCAGC CTTGCCTGCC GCCTTGGCCA 360
GGGAAGGCCT TTCCTCAGCA GGAGAGAGAC GGTGCTCTGG GCAAGTACCC GCTGGCCCCG 420
GGGCTGTGGG ATTCCGCTGC CAGCACCACC CACGGTCCCT GTAGTCTGCT CTTCAGTGGC 480
AAACGGGCGT GGCTGGGATG CGTGGGCCTC CGGTGGGAAG GGCCCTTGGG GAGTACCTGT 540
CTCCCTCCCA GAAGCCTCAG AGCCACGGTG GGGCGGCCGT GGTAGATTCT GCCACAGTCC 600
TCACCTCCCA GGCAAAAACC TCCATTCAAT CTTCACGTAG CAGCTGCCCG GCCTGGGCTG 660
GTGTGAGGGG GGGCTCCCGC AGGCAGGGGT GGGTCTGGAT TCCCAGGCAG CCCCTGCCAT 720
CAGTCCTCAT GCTGTCTTGC CTTCCCCTTC CCCTGCCTCC AGGGAGGACG GCAGAACAGC 780
CCAGGTGCCT GAGGTCGAGT CCCCGCACTC ACCACCACGT CACCTCCACC GGCCGTGCCA 840
AGAAAGCTCC TCTCTGGAAA CATCTGTGCC ACGAAGCCCA GGAGCAGGTG GTGGCCAAGG 900
CAGGGGCAGG CCAGAGTGGG GAGGGATGGG ATTGGACTAA CCTGGGTCAG AAGGCTCCGG 960
GGGGCGGGGA GAGGATCTGG GATGCCTCCA GGGCTGTTCC CCCAGCCCTG GGTGTCAGCT 1020
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