Variant report

Variant	rs13229182
Chromosome Location	chr7:71374028-71374029
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs12530530	1.00[CEU][hapmap];0.85[ASN][1000 genomes]
rs12537319	1.00[CEU][hapmap]
rs12540791	1.00[CEU][hapmap]
rs12668764	0.84[ASN][1000 genomes]
rs12669224	0.84[ASN][1000 genomes]
rs12670326	1.00[CEU][hapmap];0.86[ASN][1000 genomes]
rs12671022	1.00[CEU][hapmap]
rs12699101	0.82[CEU][hapmap]
rs12699108	0.84[ASN][1000 genomes]
rs12699109	0.84[ASN][1000 genomes]
rs12699110	1.00[CEU][hapmap];0.86[ASN][1000 genomes]
rs12699111	0.86[ASN][1000 genomes]
rs12699112	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13224623	1.00[CEU][hapmap];0.85[ASN][1000 genomes]
rs13225975	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13227550	1.00[CEU][hapmap];0.86[ASN][1000 genomes]
rs13229166	0.84[ASN][1000 genomes]
rs13230689	0.85[ASN][1000 genomes]
rs13231789	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13232386	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13235673	1.00[CEU][hapmap];0.84[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13239349	0.84[ASN][1000 genomes]
rs13241833	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13243279	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17137575	1.00[CEU][hapmap];0.85[ASN][1000 genomes]
rs17137582	0.84[ASN][1000 genomes]
rs17137587	0.86[ASN][1000 genomes]
rs17144018	1.00[CEU][hapmap]
rs17144069	0.84[ASN][1000 genomes]
rs17144079	1.00[CEU][hapmap];0.80[YRI][hapmap];0.85[ASN][1000 genomes]
rs17144089	0.86[ASN][1000 genomes]
rs17144092	0.86[ASN][1000 genomes]
rs17144104	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17144122	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1859554	1.00[CEU][hapmap]
rs2903599	0.83[ASN][1000 genomes]
rs34141892	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34603271	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34963824	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35066942	0.84[ASN][1000 genomes]
rs35296889	0.84[ASN][1000 genomes]
rs35316447	0.86[ASN][1000 genomes]
rs35490556	0.80[ASN][1000 genomes]
rs35708009	0.84[ASN][1000 genomes]
rs36088728	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4717617	0.86[ASN][1000 genomes]
rs4717620	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4719181	1.00[CEU][hapmap];0.84[ASN][1000 genomes]
rs4719182	0.87[CEU][hapmap];0.84[ASN][1000 genomes]
rs4719183	1.00[CEU][hapmap];0.94[YRI][hapmap];0.86[ASN][1000 genomes]
rs4719184	0.86[ASN][1000 genomes]
rs4719185	1.00[CEU][hapmap];0.94[YRI][hapmap];0.86[ASN][1000 genomes]
rs4719186	1.00[CEU][hapmap];0.86[ASN][1000 genomes]
rs4719188	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55748356	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56021743	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56139620	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56251697	0.86[ASN][1000 genomes]
rs57266099	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59305596	0.83[ASN][1000 genomes]
rs59902136	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61202888	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61687549	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61688132	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61692774	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71551226	0.81[EUR][1000 genomes]
rs71551228	0.85[ASN][1000 genomes]
rs71551229	0.85[ASN][1000 genomes]
rs71551230	0.86[ASN][1000 genomes]
rs71551231	0.86[ASN][1000 genomes]
rs71551232	0.84[ASN][1000 genomes]
rs71551234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs71551235	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71551236	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs71551237	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71551238	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs721235	1.00[CEU][hapmap];0.94[YRI][hapmap];0.86[ASN][1000 genomes]
rs73362196	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7806602	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 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	chr7:71366200-71375000	Weak transcription	Thymus	Thymus
2	chr7:71371400-71374400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:71373600-71374600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:71374000-71374800	Weak transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links