| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21571 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:79914950-79915680 |
Target genes | | Number: 54 | 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) |
| EWSR1-FLI1 | MA0149.1 | chr17:79915180-79915198 | CCTTCCTCCTCCCCTTCC | - | 6.2 | | ZNF263 | MA0528.1 | chr17:79915183-79915204 | TCCTCCTCCCCTTCCTCTCTC | - | 7.06 | | ZNF263 | MA0528.1 | chr17:79915174-79915195 | CTCTCCCCTTCCTCCTCCCCT | - | 7.45 | | ZNF263 | MA0528.1 | chr17:79915180-79915201 | CCTTCCTCCTCCCCTTCCTCT | - | 7.83 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 79914995 | 79915110 | | chr17 | 79915425 | 79915548 |
|
Enhancer Sequence | CTGCAAGGAG GGCCAGACGT GAGGCCAGGT GGCTGGGAAG AGGCACTCAC CTCCCCCGAG 60
TCTGCTCAGC GTCAGCCCGT GCCCCGAGGG GGGCAGGAGT CCTGATGCGT TCTGAACTGC 120
GGATGCATTC TGCATTCTCT GTTCACGTGC AAGACCCATG GCCGTCCCCT CCAGAGCAGG 180
CCAGGGCTCA GGCTGGCAGG CCACATTTCC CTGACACAGC CAGGCTCTCC CCTTCCTCCT 240
CCCCTTCCTC TCTCTGTCTC TTTACCTCAG GTTCCTTATC TGAAAATGAA GATAAACTAT 300
GTGGCCTCAG GCCCCATCAT CTATTCCCCA TTTGTCTCCT GGTCTCCTGT ATGCCTGCTG 360
GGATACAGGA ACCCACAGGG GTGATCCTCA TCTACCGGGC CCTGGAGAAG GAGCATTAGT 420
CCATGGCCAA CCCCTAACCA ACGACTTAGG TCCCTGCAGC CCAAACCTTC CCCTATATCC 480
AACAACCATG GCGTCCAGAA GCATCCTCTG GACAGTGTCT GGTTACCCAG CACTCTGAAG 540
CCAGGCCTCA GAGACGTCTC CAATGATGCG GGTTCTCCCA GCTCCAGCCT CTCACCCTCC 600
TAGCCACCTG CCAAGATCTG CACAGGCTCC ACTCCATCCT CGCCTCTCAT ACAACCCCAC 660
CCCACACCCC TTCCATGCAC CCTGCACACC GTCCTCACCC CTCACCTCCA GCCCTGCCCC 720
GCCCTGCCCA 730
|
