Variant report

Variant	rs62167332
Chromosome Location	chr2:56530192-56530193
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10183245	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10460555	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10460559	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11125623	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11125624	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11677428	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11679038	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11690074	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11902889	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12053439	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13382999	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13386846	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13390229	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13400915	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13403867	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13404434	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13410910	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13416084	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13416192	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13417930	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13427576	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1549029	0.83[EUR][1000 genomes]
rs17047813	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17047815	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1990758	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2032698	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2111473	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2216330	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2216331	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56832643	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58363543	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58390707	0.87[AFR][1000 genomes]
rs59132151	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62164360	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62164361	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62164363	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62164364	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62167333	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62167337	0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62167338	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6545565	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6751240	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6754471	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72916125	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72916129	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73940663	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73940664	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73940665	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7561764	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7591011	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7602941	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7606693	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9309275	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9309276	0.82[EUR][1000 genomes]
rs9309277	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9808063	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9808416	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530516	chr2:56447922-56633505	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv522006	chr2:56496589-56545845	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv874170	chr2:56496589-56590865	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56527400-56531200	Weak transcription	Adipose Nuclei	Adipose
2	chr2:56527400-56540600	Weak transcription	Left Ventricle	heart
3	chr2:56527400-56547400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:56527600-56561000	Weak transcription	HSMM	muscle
5	chr2:56530000-56530800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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