| Tag | Content |
|---|
EnhancerAtlas ID | HS118-18014 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr8:11631800-11632950 | 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 | chr8:11631837-11631848 | CGCACCTGCGC | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGAACCCAG GAGACAGAGG TTGCAGTGAG CTGAGATCGC ACCTGCGCTC CAGCCTCAGC 60
AACAGAGTGA GACTCCATCT GAAAAACAAC AACAACAAAA AACCCATCAG ATCTCTTGAG 120
ACTTATTTAC TATCACGAGA ACAGCCCCCA TGATTCAATT ACCTCCCACT GGGTACCTCC 180
CACCAGGTCC GTCCCATAAC ACATGGGAAT CATGGGAGTT ATATTATTCC ACCCCCAGGC 240
CCTTCCAAAG CACAAGTCCT CACATTTCAA AACCAATCAT GCCTTCCCAA CAGTCCCCAA 300
AAGTCTTAAT TCATTTCAGC ATTAATTTAA TAGGCCACAG TCCAAAGTCT CATCTGAGAC 360
AAGGCAGGTT GCTTCCACCT ATGAGCCTGT AAAATCAAAA GCAAGTTAGT TACTTCCTAG 420
ATACAATGGG GGTACAGGCA TTGGGTAAAT ACACCTGTTT CAAATGGGAG AAATTGGCCA 480
AAACGAAGGG GCTACAGGCC CCATGCAAGT CTGAAATCCA GTGAGGCAGT CAAATCTTAA 540
AGCTCCAAAA TGATCTTTGA CTCCATGTCT CTCATCCAGG GCACGCTGAT GCAAGAGGTA 600
GACTCCCACG GCCTTGGGCA GCTCTGCCTC TGTGGCTTTG GTAGGGTACA GTCCGTCATC 660
CTGGCTGCTT TCACAGGCTG GCATTGAGTG TCTGTGTGTT TTCCAGGGCA GGGTGCAAGC 720
TGTCAGTAGA TCTACCATTC TGGGGTCTGG AGGACAGTGG CCCTCTTCTC ACAGCTCTAC 780
TAGGCAGTGC CCCAGTGGGA ACTCTGCCTT GGGGCTCTAA CCCCGTCTTT TCCTTCTGCA 840
CTGCCCTAGC AGAGGTTCTC AATGAGGGCT CTGCCCCTGC AGCACACCTC TGCCTGGACA 900
TCCCGTTGTT TCTATACATC CTCAGAAATC TAGGTGGAGG TTTCCAAACC TCCATTCTTA 960
ACTTCTGTGC ACCTGCAGGC TCAACACCAC ATGTGAACCG CCAAGGCTTG GGGCTTGTAC 1020
CCTCTGAAGC AGCAGCCTGG GTTGTACATT GGCGCTTTTT AGCCATGGCT GGAGGGGCTA 1080
GGACACAGGG CACCAAGTCC CTAGGCTGCA CACAGCAGAG GGGGCCCTGG ATCTGGCCCA 1140
GGAAACCATT 1150
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