Variant report

Variant	rs10096604
Chromosome Location	chr8:130795857-130795858
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10094445	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10097810	0.88[ASN][1000 genomes]
rs10098559	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10956495	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1600931	0.85[ASN][1000 genomes]
rs1905168	0.85[ASN][1000 genomes]
rs1967018	0.86[ASN][1000 genomes]
rs1979475	0.88[ASN][1000 genomes]
rs1979476	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1988911	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2128386	0.86[ASN][1000 genomes]
rs2894495	0.88[ASN][1000 genomes]
rs3912318	0.88[ASN][1000 genomes]
rs3957254	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4103049	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4260864	0.88[ASN][1000 genomes]
rs4383938	0.80[ASN][1000 genomes]
rs4412339	0.87[ASN][1000 genomes]
rs4500051	0.88[ASN][1000 genomes]
rs4733741	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6470781	0.86[ASN][1000 genomes]
rs6470782	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6470783	0.87[ASN][1000 genomes]
rs6983184	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73406845	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7821985	0.85[ASN][1000 genomes]
rs7823788	0.87[ASN][1000 genomes]
rs7834217	0.88[ASN][1000 genomes]
rs7834660	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9656980	0.84[EUR][1000 genomes];0.97[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	nsv428524	chr8:130731660-130894467	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130780400-130797000	Weak transcription	Esophagus	oesophagus
2	chr8:130790200-130796800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:130790400-130796000	Weak transcription	NHEK	skin
4	chr8:130794600-130796000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:130794800-130796600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin

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