Variant report

Variant	rs1073381
Chromosome Location	chr12:47146303-47146304
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1008637	0.86[CEU][hapmap]
rs10785636	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10785637	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10785638	0.80[AMR][1000 genomes]
rs10880988	0.86[ASN][1000 genomes]
rs10880990	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10880991	0.80[ASN][1000 genomes]
rs10880993	0.86[ASN][1000 genomes]
rs10880995	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11183565	0.86[ASN][1000 genomes]
rs11183566	0.86[ASN][1000 genomes]
rs11183568	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11183570	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11183574	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11183580	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11183584	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11183597	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11520328	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12372653	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs180433	0.86[JPT][hapmap]
rs180434	0.86[JPT][hapmap]
rs2080688	0.90[EUR][1000 genomes]
rs2098510	0.81[EUR][1000 genomes]
rs2098513	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2408619	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2408620	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2429474	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2430914	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2430918	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2430922	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465583	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465613	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465644	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2715779	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2897980	0.82[EUR][1000 genomes]
rs4603389	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs4768748	0.81[EUR][1000 genomes]
rs4768752	0.83[EUR][1000 genomes]
rs4768753	0.83[EUR][1000 genomes]
rs6582672	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6582674	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7136299	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7305578	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7311780	0.86[ASN][1000 genomes]
rs7959739	0.85[EUR][1000 genomes]
rs7975961	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049525	chr12:46721742-47264172	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv541486	chr12:46721742-47264172	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
3	esv3416674	chr12:46988689-47178369	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1845143	chr12:47051076-47431496	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47145200-47146400	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr12:47145200-47146800	Enhancers	HepG2	liver
3	chr12:47145800-47146600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:47146000-47146600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:47146000-47146800	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr12:47146000-47146800	Enhancers	HMEC	breast
7	chr12:47146200-47146800	Enhancers	Primary T cells from cord blood	blood
8	chr12:47146200-47147000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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