Variant report

Variant	rs1569346
Chromosome Location	chr3:60750062-60750063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11130781	0.94[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs11130782	0.90[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs11710207	0.90[CHD][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs12185984	1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs13059280	0.87[ASN][1000 genomes]
rs13065371	0.90[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs13067083	0.86[ASN][1000 genomes]
rs13073028	0.87[CHD][hapmap]
rs13098348	0.87[ASN][1000 genomes]
rs13098466	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs13098545	0.87[ASN][1000 genomes]
rs13099811	0.90[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2064012	1.00[CHB][hapmap];0.93[CHD][hapmap];0.89[ASN][1000 genomes]
rs2142294	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2142296	0.87[CHD][hapmap]
rs2205342	0.86[ASN][1000 genomes]
rs2205343	0.87[ASN][1000 genomes]
rs2205344	0.87[ASN][1000 genomes]
rs2364293	0.90[ASN][1000 genomes]
rs2736736	0.87[CHD][hapmap]
rs2736737	0.81[CHD][hapmap]
rs4974227	0.90[CHD][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs4974230	0.83[CHB][hapmap]
rs57203484	0.87[ASN][1000 genomes]
rs57595293	0.87[ASN][1000 genomes]
rs60858106	0.84[ASN][1000 genomes]
rs6771383	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6786213	0.81[CHB][hapmap]
rs6787897	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7429680	0.85[ASN][1000 genomes]
rs926139	0.90[ASN][1000 genomes]
rs9823013	0.88[CHB][hapmap]
rs9840977	0.85[ASN][1000 genomes]
rs9842407	1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs9847131	0.98[ASN][1000 genomes]
rs9878766	0.83[CHB][hapmap]
rs9881274	0.86[ASN][1000 genomes]
rs9882068	0.87[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]

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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60743800-60751600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:60746200-60756200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:60747200-60756000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:60747200-60756400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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