| Tag | Content |
|---|
EnhancerAtlas ID | HS175-03881 | Organism | Homo sapiens | Tissue/cell | SK-N-MC | Coordinate | chr11:641850-643290 | 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 | AAAAGAAAAC GAGTATTGGG TGGAGAGAGG ACCAAGCCCA ATTACTACTT TAGTGCGGCT 60
GCCCCGTCCC GTCTGGTGAC CACGCACTTC TGTGATGGCC TCAGCGGCTG CCTCCTCCAG 120
GACACCTTCT CCGACTACCT GCTTCCCAGG ACCAGCCTGT CCCAGTCACC CCCGGAACAG 180
ACTGAGTCAC AGTGGATTCC TCTCAGACAC CCGTGAGAGT GAAGGAGGGG CTCCCGCCAG 240
CTTTGTCCCA GGACCCACAG CCCCACACGT GCCTGACAGC GCTGGAGGCC ATGGGAGGTG 300
CACATGCATC TGGGGGTCCT GGGGGTGCTG ACAGCCCTGG GGCAGGGCGA CCTCTGACCA 360
TCAGCCTCCC AGGCTTGGAA AGGAGGAGCT GTGGAAACCT GGGATCCCAA CAGACGCGTG 420
GTGCTTGGCT TCTGTTTTAC GGAAAGTTGG GGAAGAGTAA GTGGCCCCCA CAATTCCAGG 480
GAATACCCCC ACTCCATTCC TGCAGGGCCT GGCGCAGGAA GCCAGGTGGC ATCACTGCTG 540
GCGGGGGTCA CTGTGCCAGA GGGCTCCCAC GGTGCCTCCC CCACCAGGCA GGGGTTCAGC 600
TACTTCCTGC AGCTGTGCTC TCTGCAGAGA TGCTGGTGTT CTCAGCTTTG GGGGATTATT 660
CTTAAGAGGT GCAGGTCCTC AATTGCCTGC CACCTTTATG TTGGTTAAAA CCCAAAGGAG 720
CAGGCCCAGC CCTGCTGTCT CATGGAGGTC AACCCACGGC CCGCCTGCCT GGACAGGGCA 780
AGGCCAAGCA GGGCCTCTGA GATGCCTCCA CCTTGCGGCA ATGGCAGACC CTGCTGGGTT 840
GGATGAAAAG CCATTGTAGA GTCTCAGAGG AAGGGCCAGG CGGGCTGAGG GTCAGAGGAA 900
GGGCCAGGCG GGCTGAGGGT CACAGGAAGG GCCAGGCGGG GTGAGGGTCA CAGGAAGGGC 960
CAGGCGGGCT GAGGGTCACA GGAAGGGCCA GGCGGGGTGA GGGACAGGCG GGGTGAGGGG 1020
CAGGTGGGGT GAGGTGCAGC ATCTGGAGCG CGTCCTGCAG CAGCCCAGAC ACCTTTTCCA 1080
GCCTCCACTG CTCACTGGCA GCACCAACGG TGCAGCACCG GGCACGCCTG AGCAGGATGA 1140
TGAAACATCA GTGAGGGCTT GGCCTGGCTG GGCAGAGACT TTACTAAGTA AATAGGCCAG 1200
GGCGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGT CGAGGTGGGT GGATCACCTG 1260
AGGACAGGAG TTCGAGACCA GCCTGGCCAA CACGGAGAAA CCCCGTCTCT ACTAAAAATC 1320
CCTAAACTAG CTGGGTGTGC TGGTGGCCAC CTATAATCCC AGCTACTCGG GAGGCTGAGG 1380
CAGAAGAATC GCTTGAACCT GGGAGGCGAA GTTGCAGTGA GCCAAGATTG TGCCACCGCA 1440
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