Variant report

Variant	rs344229
Chromosome Location	chr8:62928715-62928716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10108997	0.82[EUR][1000 genomes]
rs1400512	0.87[ASN][1000 genomes]
rs1516994	0.90[ASN][1000 genomes]
rs1516995	0.87[ASN][1000 genomes]
rs1546639	0.87[ASN][1000 genomes]
rs1546640	0.87[ASN][1000 genomes]
rs1607125	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2176342	0.83[ASN][1000 genomes]
rs2351083	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28634373	0.87[ASN][1000 genomes]
rs28804830	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs344205	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs344208	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs344211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs344237	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs344239	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs344243	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs344244	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs344249	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs344253	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs344263	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs344264	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs344265	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs344266	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs344267	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs344271	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35035266	0.87[ASN][1000 genomes]
rs35999143	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs55819473	0.87[ASN][1000 genomes]
rs56098200	0.86[ASN][1000 genomes]
rs57027979	0.87[ASN][1000 genomes]
rs57232729	0.87[ASN][1000 genomes]
rs59040850	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs59691363	0.87[ASN][1000 genomes]
rs61402923	0.86[ASN][1000 genomes]
rs61475697	0.86[ASN][1000 genomes]
rs62508546	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7814557	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7818829	0.87[ASN][1000 genomes]
rs7832965	0.87[ASN][1000 genomes]
rs9694964	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs992841	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890951	chr8:62889169-62989464	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv890952	chr8:62898648-62989464	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv890953	chr8:62899559-62989464	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv890954	chr8:62919691-63023132	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv520442	chr8:62928715-62962071	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62928000-62928800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr8:62928000-62928800	Enhancers	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links