Variant report

Variant	rs1886607
Chromosome Location	chr10:58618956-58618957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10740688	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10763432	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10763436	0.92[ASN][1000 genomes]
rs10825869	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10825913	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10825914	0.96[ASN][1000 genomes]
rs10825915	0.92[ASN][1000 genomes]
rs10825918	0.96[ASN][1000 genomes]
rs10825919	0.96[ASN][1000 genomes]
rs11005567	0.96[ASN][1000 genomes]
rs11005570	0.96[ASN][1000 genomes]
rs1536082	0.96[ASN][1000 genomes]
rs1914560	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1925286	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1925287	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1925292	0.96[ASN][1000 genomes]
rs1925293	0.96[ASN][1000 genomes]
rs1925294	0.96[ASN][1000 genomes]
rs1925297	0.96[ASN][1000 genomes]
rs1925298	0.96[ASN][1000 genomes]
rs1925299	0.96[ASN][1000 genomes]
rs1925310	0.96[ASN][1000 genomes]
rs2025564	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2031461	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2224958	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2255193	0.87[ASN][1000 genomes]
rs2578094	0.87[ASN][1000 genomes]
rs2578095	0.87[ASN][1000 genomes]
rs2578096	0.85[ASN][1000 genomes]
rs2818847	0.87[ASN][1000 genomes]
rs2818848	0.87[ASN][1000 genomes]
rs2818849	0.87[ASN][1000 genomes]
rs2818850	0.87[ASN][1000 genomes]
rs4370856	0.96[ASN][1000 genomes]
rs4443998	0.92[ASN][1000 genomes]
rs4935670	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4935674	0.96[ASN][1000 genomes]
rs7081437	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7085248	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7914070	0.96[ASN][1000 genomes]
rs7917259	0.96[ASN][1000 genomes]
rs991653	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs993717	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv551064	chr10:58457011-58702440	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2758223	chr10:58490630-58689953	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2759758	chr10:58490630-58689953	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2757390	chr10:58567723-58644512	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv551100	chr10:58602006-58636572	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv895510	chr10:58602006-58672533	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:58618600-58636000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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