Variant report

Variant	rs62570074
Chromosome Location	chr9:110264723-110264724
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10978886	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2236599	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4631527	0.81[EUR][1000 genomes]
rs58843994	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7033991	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110261200-110265600	Weak transcription	HepG2	liver
2	chr9:110263400-110266400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr9:110263600-110266400	Weak transcription	NHDF-Ad	bronchial
4	chr9:110263800-110266200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr9:110264000-110266200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:110264400-110264800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr9:110264600-110265200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr9:110264600-110265400	ZNF genes & repeats	A549	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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