Variant report

Variant	rs10912641
Chromosome Location	chr1:173519966-173519967
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1024266	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10399838	0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10494490	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10737301	0.95[CHB][hapmap]
rs10737303	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10753078	0.95[CHB][hapmap]
rs10753083	0.80[YRI][hapmap]
rs10798283	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10798284	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10798285	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10798290	0.87[CEU][hapmap]
rs10912624	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10912625	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10912626	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10912634	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10912635	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10912636	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10912642	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10912643	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10912651	0.86[CEU][hapmap]
rs12026427	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12026637	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12026677	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12026993	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12027451	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12027495	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12033623	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12034341	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12035105	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12037210	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12041114	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12065426	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs12406352	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12406500	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12744504	0.95[CHB][hapmap];0.80[JPT][hapmap]
rs1461014	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1461023	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1547155	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1547156	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16846113	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16846206	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1886639	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2017323	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2422433	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3934575	0.95[CHB][hapmap]
rs3934576	0.95[CHB][hapmap]
rs4244195	0.95[CHB][hapmap]
rs4294450	0.95[CHB][hapmap]
rs4310474	0.95[CHB][hapmap]
rs4336887	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4539167	0.95[CHB][hapmap]
rs4916365	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4916368	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60043192	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61828887	0.81[ASN][1000 genomes]
rs61828888	0.81[ASN][1000 genomes]
rs6425248	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6425249	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6425251	0.86[CEU][hapmap]
rs6660804	0.95[CHB][hapmap]
rs6675929	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6687872	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6699094	0.95[CHB][hapmap]
rs6702320	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72709325	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs728908	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs745573	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs745574	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7520814	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7524592	0.95[CHB][hapmap];0.90[JPT][hapmap]
rs7525100	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs7530469	0.95[CHB][hapmap]
rs7541082	0.87[CEU][hapmap]
rs7549074	0.95[CHB][hapmap];0.81[JPT][hapmap]
rs912767	0.95[CHB][hapmap];0.90[JPT][hapmap]

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	nsv872549	chr1:173509586-173546835	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173516600-173523600	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr1:173517200-173523000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr1:173518000-173523800	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr1:173518200-173523600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:173518400-173522600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:173518400-173523400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr1:173518600-173522800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr1:173518600-173523000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr1:173519000-173521200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:173519000-173522800	Enhancers	Primary T cells from cord blood	blood
11	chr1:173519000-173523600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr1:173519200-173520200	Weak transcription	K562	blood
13	chr1:173519200-173521000	Enhancers	Dnd41	blood
14	chr1:173519600-173520000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr1:173519800-173520200	Weak transcription	HUVEC	blood vessel
16	chr1:173519800-173521800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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