Variant report

Variant	rs17014588
Chromosome Location	chr12:87705715-87705716
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10219442	0.85[ASN][1000 genomes]
rs10219627	0.85[ASN][1000 genomes]
rs10219675	0.85[ASN][1000 genomes]
rs10219690	0.85[ASN][1000 genomes]
rs10219753	0.85[ASN][1000 genomes]
rs11104398	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11104430	0.87[ASN][1000 genomes]
rs11104431	0.87[ASN][1000 genomes]
rs12302125	0.87[ASN][1000 genomes]
rs12309007	0.87[ASN][1000 genomes]
rs12315201	0.85[ASN][1000 genomes]
rs12317796	0.87[ASN][1000 genomes]
rs17014535	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17014615	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17577858	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17577874	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17577881	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17577888	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17577895	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17577944	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17605650	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17605679	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17605785	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4485182	0.87[ASN][1000 genomes]
rs4522255	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4564411	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57967943	0.92[EUR][1000 genomes]
rs57972376	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58322011	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59038161	0.95[EUR][1000 genomes]
rs59786711	0.95[EUR][1000 genomes]
rs6538070	0.87[ASN][1000 genomes]
rs6538071	0.87[ASN][1000 genomes]
rs67318846	0.85[ASN][1000 genomes]
rs68056248	0.85[ASN][1000 genomes]
rs7297021	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7300553	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7306472	0.95[EUR][1000 genomes]
rs7308449	0.85[ASN][1000 genomes]
rs7314876	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7952911	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7955357	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7958392	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7958524	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7966191	0.87[ASN][1000 genomes]
rs7968168	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7968238	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7968297	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7968474	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7968621	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7971539	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7972428	0.90[EUR][1000 genomes]
rs7972666	1.00[CEU][hapmap];0.80[CHB][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7972720	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7975468	0.95[EUR][1000 genomes]
rs7977794	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7977925	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7978511	0.95[EUR][1000 genomes]
rs7980888	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916862	chr12:86837694-87718558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv427918	chr12:87647585-87786660	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:87703200-87705800	Enhancers	Primary B cells from cord blood	blood
2	chr12:87703200-87706200	Enhancers	Primary B cells from peripheral blood	blood
3	chr12:87703600-87706000	Enhancers	Primary hematopoietic stem cells	blood
4	chr12:87703800-87706000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:87704200-87706000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr12:87704200-87706000	Enhancers	Fetal Kidney	kidney
7	chr12:87704600-87706000	Enhancers	GM12878-XiMat	blood
8	chr12:87705000-87705800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:87705200-87705800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr12:87705200-87706000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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