Variant report

Variant	rs12523622
Chromosome Location	chr5:92401045-92401046
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1027429	0.91[ASN][1000 genomes]
rs1027430	0.93[ASN][1000 genomes]
rs10514368	0.89[ASN][1000 genomes]
rs10514369	0.90[ASN][1000 genomes]
rs1075873	0.93[ASN][1000 genomes]
rs11951873	0.91[ASN][1000 genomes]
rs11958890	0.90[ASN][1000 genomes]
rs12514052	0.88[ASN][1000 genomes]
rs12514544	0.90[ASN][1000 genomes]
rs12515643	0.91[ASN][1000 genomes]
rs1390614	0.91[ASN][1000 genomes]
rs1496336	0.98[ASN][1000 genomes]
rs1496338	0.95[ASN][1000 genomes]
rs1496339	0.91[ASN][1000 genomes]
rs1496341	0.94[ASN][1000 genomes]
rs1603407	0.90[ASN][1000 genomes]
rs17082878	0.90[ASN][1000 genomes]
rs17082886	0.99[ASN][1000 genomes]
rs1845837	0.91[ASN][1000 genomes]
rs1845838	0.91[ASN][1000 genomes]
rs1845839	0.91[ASN][1000 genomes]
rs1961168	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2017806	0.95[ASN][1000 genomes]
rs2132535	0.95[ASN][1000 genomes]
rs2173008	0.91[ASN][1000 genomes]
rs2342063	0.90[ASN][1000 genomes]
rs2438470	0.95[ASN][1000 genomes]
rs2578487	0.91[ASN][1000 genomes]
rs2578488	0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2578489	0.91[ASN][1000 genomes]
rs2578491	0.95[ASN][1000 genomes]
rs2578492	0.96[ASN][1000 genomes]
rs2578493	0.95[ASN][1000 genomes]
rs2644787	0.95[ASN][1000 genomes]
rs34524	0.91[ASN][1000 genomes]
rs3925782	0.91[ASN][1000 genomes]
rs4301219	0.86[ASN][1000 genomes]
rs56993733	0.91[ASN][1000 genomes]
rs57308733	0.90[ASN][1000 genomes]
rs58430736	0.87[ASN][1000 genomes]
rs59564433	0.99[ASN][1000 genomes]
rs59998698	0.95[ASN][1000 genomes]
rs60548086	0.87[ASN][1000 genomes]
rs6557059	0.96[ASN][1000 genomes]
rs67020389	0.93[ASN][1000 genomes]
rs67939833	0.98[ASN][1000 genomes]
rs68112398	0.94[ASN][1000 genomes]
rs6861529	0.91[ASN][1000 genomes]
rs6866281	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6870541	0.95[ASN][1000 genomes]
rs7732596	0.98[ASN][1000 genomes]
rs7735078	0.91[ASN][1000 genomes]
rs9314229	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9314230	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs990959	0.91[ASN][1000 genomes]
rs991235	0.95[ASN][1000 genomes]
rs995626	0.98[ASN][1000 genomes]
rs998492	0.90[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	nsv1015770	chr5:91911877-92498264	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1022712	chr5:92191693-92415111	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1028930	chr5:92194772-92415111	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv830399	chr5:92290915-92462490	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92395200-92408000	Weak transcription	Muscle Satellite Cultured Cells	--

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