| Tag | Content |
|---|
EnhancerAtlas ID | HS105-12469 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr11:641870-643080 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr11:642867-642878 | GGGCAGGTGGG | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGAGAGAGG ACCAAGCCCA ATTACTACTT TAGTGCGGCT GCCCCGTCCC GTCTGGTGAC 60
CACGCACTTC TGTGATGGCC TCAGCGGCTG CCTCCTCCAG GACACCTTCT CCGACTACCT 120
GCTTCCCAGG ACCAGCCTGT CCCAGTCACC CCCGGAACAG ACTGAGTCAC AGTGGATTCC 180
TCTCAGACAC CCGTGAGAGT GAAGGAGGGG CTCCCGCCAG CTTTGTCCCA GGACCCACAG 240
CCCCACACGT GCCTGACAGC GCTGGAGGCC ATGGGAGGTG CACATGCATC TGGGGGTCCT 300
GGGGGTGCTG ACAGCCCTGG GGCAGGGCGA CCTCTGACCA TCAGCCTCCC AGGCTTGGAA 360
AGGAGGAGCT GTGGAAACCT GGGATCCCAA CAGACGCGTG GTGCTTGGCT TCTGTTTTAC 420
GGAAAGTTGG GGAAGAGTAA GTGGCCCCCA CAATTCCAGG GAATACCCCC ACTCCATTCC 480
TGCAGGGCCT GGCGCAGGAA GCCAGGTGGC ATCACTGCTG GCGGGGGTCA CTGTGCCAGA 540
GGGCTCCCAC GGTGCCTCCC CCACCAGGCA GGGGTTCAGC TACTTCCTGC AGCTGTGCTC 600
TCTGCAGAGA TGCTGGTGTT CTCAGCTTTG GGGGATTATT CTTAAGAGGT GCAGGTCCTC 660
AATTGCCTGC CACCTTTATG TTGGTTAAAA CCCAAAGGAG CAGGCCCAGC CCTGCTGTCT 720
CATGGAGGTC AACCCACGGC CCGCCTGCCT GGACAGGGCA AGGCCAAGCA GGGCCTCTGA 780
GATGCCTCCA CCTTGCGGCA ATGGCAGACC CTGCTGGGTT GGATGAAAAG CCATTGTAGA 840
GTCTCAGAGG AAGGGCCAGG CGGGCTGAGG GTCAGAGGAA GGGCCAGGCG GGCTGAGGGT 900
CACAGGAAGG GCCAGGCGGG GTGAGGGTCA CAGGAAGGGC CAGGCGGGCT GAGGGTCACA 960
GGAAGGGCCA GGCGGGGTGA GGGACAGGCG GGGTGAGGGG CAGGTGGGGT GAGGTGCAGC 1020
ATCTGGAGCG CGTCCTGCAG CAGCCCAGAC ACCTTTTCCA GCCTCCACTG CTCACTGGCA 1080
GCACCAACGG TGCAGCACCG GGCACGCCTG AGCAGGATGA TGAAACATCA GTGAGGGCTT 1140
GGCCTGGCTG GGCAGAGACT TTACTAAGTA AATAGGCCAG GGCGGTGGCT CACACCTGTA 1200
ATCCCAGCAC 1210
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