Variant report

Variant	rs10183674
Chromosome Location	chr2:125500086-125500087
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10164548	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178842	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs10179213	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10184800	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10185492	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10208814	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap]
rs11123062	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11680115	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11694621	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12468133	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12612581	0.82[CHB][hapmap]
rs12619688	1.00[JPT][hapmap]
rs12623831	0.84[CEU][hapmap];1.00[CHB][hapmap]
rs12992994	1.00[JPT][hapmap]
rs13021629	1.00[JPT][hapmap]
rs13386677	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13396871	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13400133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13406974	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13409512	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13427244	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6713505	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6736347	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6760383	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs717601	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs730468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7582461	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834359	chr2:125367872-125536022	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
2	nsv428727	chr2:125372897-125512949	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv834360	chr2:125492685-125683200	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125500000-125500800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:125500000-125501200	Enhancers	Fetal Stomach	stomach

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