| Tag | Content |
|---|
EnhancerAtlas ID | HS091-18557 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:89794740-89795640 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr16:89795261-89795272 | AGTGACTCATG | + | 6.14 | | JUN(var.2) | MA0489.1 | chr16:89795257-89795271 | TAGAAGTGACTCAT | + | 6 | | Nr2f6(var.2) | MA0728.1 | chr16:89795163-89795178 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCCCGCCTCA GCCTCCCGAG TAGCTGGGAT TACAGGCGCC CGCCACCACA CCCAGCTAAG 60
TTTTGTATTT ATTTATTTTT TTTTTATTTG AGACGGAGTC TCGCTGTGTT GCCCAGGCTG 120
GAGTGCAGTG GCACAATCTC GGCTCACTGC AAGCTCTGCC TCCCGGGTTC ACGCCATTCT 180
CCGGCCTCAG CCTCTGAGTC GCTGGGACTA CAGGCACCCG CCACCACGCC CGGCTAATTT 240
TTTGTATTTT TAGCAGAGAC GGGGTTTCAC TTTGTTAGCC GGGATGGTCT TGATCTCCTG 300
ACCTCGTGAT CCGCCCGCCT CTGCCTCCCA AAGTGCTGGG ATTACAGGTG TTAGCCACCG 360
CACCCGGCCA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT CACGGTATTG GCCAGGCTGG 420
TCTTGAACTC CTGACCTCAT GCGATCCACC TACGTCACCC TCCCAAAGTG CTGGGATTAC 480
AGGAGTTAGC CTCTGCACCC AGCCACTTTT GTGAACTTAG AAGTGACTCA TGGCAAACCC 540
ATCAGTTGCA TAGGGTTCGC AGTTATGGGG TGAGGTGGTC GATTTCTCAA AGTCTGCTTA 600
GCAGGAAGCT ACCTTTGAGC GCCTCCACCC CTTCTGGGCC GCTGTGGAAA GGGCTGTTTC 660
CAAGTCCAGT GTCCTGGTGC CCAGAGCACA TGGCTTGTGG GGATTGCTGG CTTGTGAGCC 720
TGGCTGGCCC TTTGTGTTCG GAAACGGGAT TGGAAATTTG GGGATTTTAG ATTTAAGACA 780
TTTTCAGAAG AACTCAAATG TGGGACATGG GGGTCCATTT GGTATCTTTA GGCAGGAGGT 840
CGTGTTGGGT CTGTCACTGC CCAGGCCCAG GGCTTTGCTG AAGATTCTCT CTTAATTCCT 900
|
