| Tag | Content |
|---|
EnhancerAtlas ID | HS091-19124 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:18042930-18043830 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:18043420-18043439 | CGGCCAGCAGATGGCCCTA | + | 6.48 | | INSM1 | MA0155.1 | chr17:18042954-18042966 | TGCCCCCAGGCA | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 18043075 | 18043690 | | chr17 | 18043000 | 18043200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I018140 | chr17 | 18043361 | 18043530 |
|
Enhancer Sequence | CCTCGCCTCC CACCGCTCTG GCCCTGCCCC CAGGCATGTC CCCACCCCCA CACCCAGCCT 60
GCCTTCAGGC CTGGGACCGT GTTGCCACGT CCTGGCTCCG CTTAGCTTTG GCCAGACAAA 120
GACAAGGGTG GCCTGGACAC CCTGTTCCTG GCCTGTTCCC ACCTAGCTTG GCTCCGCCCT 180
AAACCTAGCG CCTCATCCTG ATCCTGTCCT CTGGCTCCCC ACAGCCCCAG TGGCTAGACT 240
CTGGCCCCGC TCCCAGTTCT AACCCTGTAC CCCACCAGCT GTGGCCTTGC CCTGTACTTA 300
CCCCACTCTG GGCCCCACCC CATTCCCTGG CCCATTCTTT CCTGGCTTCT TGCCAGACCT 360
GTTCCCCCAG TCCCACCTCC TGGTGTTCTC AGTTTCTCCC ACCCCACCCA TAAGGCCCCG 420
GGGAAGAGCT TGGGGGACCA ACTTTGGGTT CCTTGAAGGC TTGGGGAGGC CCTGCATCCC 480
AGCTACACTA CGGCCAGCAG ATGGCCCTAT GACAGAGCAC AGGCCTGGTA ACATCACCTC 540
CCCTATCTGG CCCTCCGCTT CCTCCTGTCA ACTGGGCAAC CTCCTCATGA GGTCATAGCC 600
AGAGTTCACA ACCATGTATC TAACAGGCCA CCCTGGGGCC AGGCACACAG TCAGTAACTG 660
TGTGTTCCTT AGACTGAAGG GGAAAAAGCC AGTTATGGGA TGGATCCCTT GGAAGATGCT 720
GAGCCCCACC TGTTTTGAGA AGCATGCAAG CCAGGATGAC AGAGGCCTTG CAGAGAGAAC 780
AGGGGTCCAG TTAGTCTTCA GATCCCCCTG GTCCGGAGAT TTACTCCTGC TCTCTCTTCC 840
TCCTCATTTC GGTCTCCCGG ACCCTGCCTG TCTGTTTTCC CTGCCCCGAC CCCTGCCCAG 900
|
