Variant report

Variant	rs4425262
Chromosome Location	chr3:69190615-69190616
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:69183723..69185886-chr3:69189955..69191851,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1051901	0.81[GIH][hapmap]
rs10865644	0.98[ASN][1000 genomes]
rs10865645	0.98[ASN][1000 genomes]
rs11128114	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11128118	0.89[MEX][hapmap]
rs1131960	0.81[GIH][hapmap]
rs11719988	0.97[ASN][1000 genomes]
rs17005366	0.81[GIH][hapmap]
rs17005393	0.98[ASN][1000 genomes]
rs28591428	0.94[ASN][1000 genomes]
rs34890270	0.94[ASN][1000 genomes]
rs3772980	0.81[GIH][hapmap]
rs3796213	0.81[GIH][hapmap]
rs3796214	0.81[GIH][hapmap]
rs4241384	0.93[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4241395	0.94[ASN][1000 genomes]
rs4389485	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4407408	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4446215	0.83[EUR][1000 genomes]
rs4461426	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4493438	0.83[EUR][1000 genomes]
rs4504171	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4508787	0.83[EUR][1000 genomes]
rs4522769	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4525874	1.00[GIH][hapmap]
rs4541413	0.89[MEX][hapmap]
rs4560302	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4563416	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4563417	0.95[ASN][1000 genomes]
rs4589943	0.89[ASN][1000 genomes]
rs4621333	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57774890	0.83[EUR][1000 genomes]
rs58181265	0.83[EUR][1000 genomes]
rs58860053	0.83[EUR][1000 genomes]
rs61006449	0.83[EUR][1000 genomes]
rs6763046	0.81[GIH][hapmap]
rs6779055	0.83[EUR][1000 genomes]
rs6792358	1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6797538	0.83[EUR][1000 genomes]
rs6799247	0.83[EUR][1000 genomes]
rs6804718	0.83[EUR][1000 genomes]
rs72924889	0.91[ASN][1000 genomes]
rs72924892	0.94[ASN][1000 genomes]
rs72924899	0.83[EUR][1000 genomes]
rs72924901	0.83[EUR][1000 genomes]
rs72926297	1.00[EUR][1000 genomes]
rs72926723	0.83[EUR][1000 genomes]
rs72926734	0.83[EUR][1000 genomes]
rs7635939	0.83[EUR][1000 genomes]
rs7638543	0.83[EUR][1000 genomes]
rs937863	0.96[GIH][hapmap]
rs9853587	0.89[MEX][hapmap];0.83[EUR][1000 genomes]
rs9883017	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[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	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 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	chr3:69178000-69193600	Weak transcription	Psoas Muscle	Psoas
2	chr3:69190400-69194200	Enhancers	Hela-S3	cervix
3	chr3:69190600-69191200	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr3:69190600-69192200	Enhancers	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links