| Tag | Content |
|---|
EnhancerAtlas ID | HS091-06833 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:788660-790020 |
Target genes | | Number: 46 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr11:789685-789702 | AGGTCACCCGAAGGTCA | + | 8.29 | | ZNF263 | MA0528.1 | chr11:789149-789170 | GGAGGAGGGCGGGGAGGGGCA | + | 7.64 | | ZNF263 | MA0528.1 | chr11:789146-789167 | GGGGGAGGAGGGCGGGGAGGG | + | 7.79 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGAGGGAGAC ACAAGGGAGG CTGCGCGCGG GTCCAGTCCC CCCTGTGCTG CCCCGACCAC 60
CTGGTCCCCA GGCAGCCCCT GCCCAGTTCT CTGGACTCTC TGGAGCCCCA GCTCAGGGGC 120
CTCCCGTGGG CCTCTGACAC TTCTCTTTCA CGGCCTGGAC TCCATCTGTC CATGACCACT 180
CCTCAAGGGG CCCCTCCAGC CGCAGAGGCA AGGGCCACGC ACAGGTGGGA GGAGGTAGGG 240
GACCCCACTG TGCTCCATAA AATGGCCCAT GCAAATGCCA CATCCTCCCA CCAGCCGGGG 300
GCAGGAGGCT CTTGGTGGGG AAGTAAGGAT CAGGCCCAGA GAACTCGAAG GAAGAGCATT 360
CTCCCCTCCA AGGAGGTGAT CGGAGCCCCA GTGGGAGAGC TGACTGCATC CCCTCCTCAG 420
GAGAGCATTC CTGCTTTGCA GAGATGGACA CTAAAGCACG GAGGCTGTGA CCTGGCCAGG 480
GTCCCAGGGG GAGGAGGGCG GGGAGGGGCA GGAGCTGGGA TCTCAGGCAG CCATCAGGGT 540
GGGTGGGCCC ACAAGAACCC AGACTTGAGA AAACTGGGGT GTCTCTCCAG GAAGTCAGCG 600
TGGGGCTGTG CTTCCAAGGG CCGTCTGCCC CTCCCCAGCC TCTGGGGCCC CCTCCTCAGC 660
ATGGGCCGTG CCTGCCTCCA GCCCTGGAGC AGGGAGTCCT CGCCCAGCCC AAGGCTGTGC 720
TGTCTCTGTG GGCAGAGGGT TCCTGGCGTT AAACAGGGTG GGCACATGCT GCACTTGGCC 780
CGCGGGTCAG GGCGGAGGAC AGGGTTCTGG GCTGTGGGAA AGGCGGTGCC CAGATTCTCA 840
ATGACCGAGG CAGAGGTGGG AAGGGCCCTG GGGGCCCAGC CGCCCTGAAC CTGAGTGGGT 900
CTTGCCCCAA AGCCCCAGAG GCCGCCTGTC TGCCTCTCCC AGGGAAGGAT GAGAAATGCC 960
CTCCAGACCT GCAGAGAAAG GGAGGCACGT TCCCCACCCC CCGCCAGGTG CATTGACCAC 1020
ACTGAAGGTC ACCCGAAGGT CACAGCATGA TGAGGGCGTC TCCAGAAGAG GCCCAGCTGC 1080
TGCCACCTCC CAGGGAAGCC CAGCCGTCCC TTCACCCCTG CAGTTCTCGG GGGGCTCAGC 1140
TGCTGGGCAT CAAGTTTGCA AAGAGCAGGT GGTCTGCCCC CCCAACCTCG CTATTTGTGG 1200
CACTTACATC CCGGCCGCCG CCTCCCTCTC CCGGGATCAA CTGAGCCCTG GAGAACTGGG 1260
GGGCCCGCGC GCAAACCCAG TGACCTTCAA GGCCCGGAGC CGCCTCCTCG CCCCGCAGGA 1320
CGCCGCGCCC GCCCCGCCCG CCCCGCCCGC CGGGAGCCCC 1360
|
