Variant report

Variant	rs4767965
Chromosome Location	chr12:40592340-40592341
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10506143	1.00[JPT][hapmap]
rs10506144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs10506146	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs10506147	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10506154	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs10878244	1.00[JPT][hapmap]
rs11174697	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs11175186	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs11175593	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11564107	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11564108	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11564123	1.00[JPT][hapmap]
rs11564131	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes]
rs11564152	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs11564153	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11564185	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs11564187	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11564190	0.94[AMR][1000 genomes]
rs11564196	1.00[JPT][hapmap]
rs11564199	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11564209	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs11564210	1.00[CEU][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11564212	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11564216	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs11564218	1.00[JPT][hapmap]
rs11564266	1.00[CEU][hapmap]
rs11564271	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs12422544	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12422796	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs12423419	1.00[JPT][hapmap]
rs12423551	1.00[JPT][hapmap]
rs12424040	0.93[EUR][1000 genomes]
rs12424294	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12425561	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs12426378	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs12426639	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs12426643	0.80[AMR][1000 genomes]
rs12427022	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12427245	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs1365768	1.00[CEU][hapmap]
rs1365769	1.00[CEU][hapmap]
rs1388585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs1388597	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1463717	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs1491945	0.90[AMR][1000 genomes]
rs17442924	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs17443078	0.86[EUR][1000 genomes]
rs17443178	0.80[EUR][1000 genomes]
rs17443185	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs17443206	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs17443600	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs17443656	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs17443909	0.87[EUR][1000 genomes]
rs17444028	0.94[EUR][1000 genomes]
rs17444054	1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs17444103	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs17458549	0.93[EUR][1000 genomes]
rs17458808	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17461387	0.80[AMR][1000 genomes]
rs17461575	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17461664	0.94[EUR][1000 genomes]
rs17465610	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17465946	0.87[EUR][1000 genomes]
rs17466016	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs17466626	1.00[CEU][hapmap]
rs17466907	1.00[CEU][hapmap]
rs17466969	1.00[CEU][hapmap]
rs17483919	1.00[CHB][hapmap];0.80[AMR][1000 genomes]
rs17484003	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17484141	1.00[JPT][hapmap];0.80[AMR][1000 genomes]
rs17484342	0.94[EUR][1000 genomes]
rs17484493	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs2131081	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs2638223	0.86[EUR][1000 genomes]
rs2708460	0.86[EUR][1000 genomes]
rs28365169	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs28365173	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs28365206	1.00[CHB][hapmap];0.90[AMR][1000 genomes]
rs28365229	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs28365689	0.93[EUR][1000 genomes]
rs28370649	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs28370650	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs28370664	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs28370682	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs28370830	0.87[EUR][1000 genomes]
rs36212067	0.94[EUR][1000 genomes]
rs36220738	0.94[EUR][1000 genomes]
rs3789329	1.00[CEU][hapmap]
rs4628750	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs4767962	0.88[AMR][1000 genomes]
rs4767964	0.94[AMR][1000 genomes]
rs4768213	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes]
rs4768226	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs4768228	1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs72547977	0.87[EUR][1000 genomes]
rs729215	0.93[EUR][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	nsv1044685	chr12:40574460-40771612	Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40590200-40595400	Weak transcription	Primary B cells from cord blood	blood
2	chr12:40590400-40595200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:40590400-40595600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr12:40590400-40596600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr12:40591000-40595600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr12:40591600-40594600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr12:40592200-40595200	Weak transcription	Monocytes-CD14+_RO01746	blood

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