| Tag | Content |
|---|
EnhancerAtlas ID | HS091-15937 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:849110-850440 |
Target genes | | Number: 34 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr16:849514-849524 | GCCCCGCCCC | + | 6.02 | | LHX2 | MA0700.1 | chr16:849317-849327 | ACTAATTAAC | + | 6.02 | | PLAG1 | MA0163.1 | chr16:849355-849369 | CCCCCATAGGCCCC | - | 6.08 | | PLAG1 | MA0163.1 | chr16:849356-849370 | CCCCATAGGCCCCC | - | 6.18 | | RREB1 | MA0073.1 | chr16:849918-849938 | CTTGGGAGGGTGGGTGGGGG | - | 6.06 | | mix-a | MA0621.1 | chr16:849317-849328 | ACTAATTAACT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTGGAGGGC ACAGGAGGAA GCCACAGGGC CGAGGCCACC AGCCTGTAGT CCCCACCCCC 60
GCTGCTCCCC GCAGGCCTGA GCTGAACCCC GCAGGATGAA GCGGGGAGAG TCCACACCAC 120
TGCCTGGGCC AGTCCCCTAG GCGTTGCTAG GGTGCAGGGC ACAGAGCGAG TTCCCACAAG 180
GCCCCAGCTC CCGCCTCCTG CACTGGGACT AATTAACTGC AAGAAACTTT ACATCCTCAG 240
CTACTCCCCC ATAGGCCCCC ACACCTTACG AAGATCCCTT GCAGGCAGGA GAAAGGGTGC 300
TCAGCACGGC AGGCCCCCAG CTCCTACCCT CCCACTGAGG CCCACGCAGG CTGACCCAGA 360
CCACGGTGTG AGGTGTGGGG CGAGGTCCTC AGGAGGTGGC CCCTGCCCCG CCCCGCTGTG 420
TGCCCCTTTG CTTTGCATGG CAGAGCCCAG TCCAGAGCCA GGACTCCTGG ACAGGAATGT 480
TCTGCTGCAG TTTGCTTCTC TGGCAGGTGG GGTGTGTGCT CAGGATCTTG GGGGCTCAGG 540
CTATACTACC CGAGTCTGGG ATATGGGCTG TGGGTGGCCC CTGGGTCCCC AGTGTGTCTG 600
GGAACCACAC ACGTTACCTG CGTGCTTTCT GCTTGTGGCC AGCCTGGGAA AGCCACAGGT 660
TGACACCCCT CAGAACTGCC ACAAGTTCGA GGCAAGTGGG GGTGGGTTGC CCCCTGCCTC 720
TCCCCCTACC CACTCCAGGG GCCCAGGGAG TCCCTCACTC CGTCCCAACT CTGGCCCCCG 780
TCCCCAAGGT TGGGAGACAG GGCTGAACCT TGGGAGGGTG GGTGGGGGTT GGCGTCAAGT 840
TTCGGGGAGC CTGCCTCTGG CTGTGAAGGG GGCTCCTGGC CCAACAGTCT CCCCATCCTT 900
TGGTCGTGCA GCTGCACCGG CCACCTAGGG AGGGGCCCAG GGCCTGAGGC TGGTGGGGTC 960
CCGGTGGTGA ATTGGGCAGA CTCCCAGCAG CCAGCAGAGG GTCTGCCCGT AGTGGGGTGG 1020
GAGGCCGGGG AGCGAGCGGG GGCAGGTTTC TGGGGGAGTG ATCAGGGTCA TGCAGAGGAT 1080
TCCCTCCCGG AGACTCTGGA GTTCCAGCAC CCCTACCCGC CCCCATCCCC GGTGCAGGCC 1140
TTTTCTCGGA GACCCTACAC TCAGCCCCGT GGGCGCAGGA CTAGCTGCGT GCGGGTCCTC 1200
CCAGGCCCGG GGTGTTGGCG CCCCGCCCAC AGCCCAGTCC TTGCTGCCCA GCCCTACCTT 1260
CGCGCAGCTG CCGCCAAGCC TGGCCACCCA CCCCGTGCAC CCCGTGGACG CCCCCAGCCA 1320
CGGGACTCGG 1330
|
