Variant report

Variant	rs7576329
Chromosome Location	chr2:76422485-76422486
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10084237	1.00[AMR][1000 genomes]
rs10169075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10170747	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11126521	1.00[AMR][1000 genomes]
rs11673996	1.00[AMR][1000 genomes]
rs11896158	1.00[AMR][1000 genomes]
rs12328296	1.00[AMR][1000 genomes]
rs12476472	1.00[AMR][1000 genomes]
rs12477363	1.00[AMR][1000 genomes]
rs12987628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13005979	1.00[AMR][1000 genomes]
rs13014046	1.00[AMR][1000 genomes]
rs1358177	1.00[AMR][1000 genomes]
rs1358178	1.00[AMR][1000 genomes]
rs1358180	1.00[AMR][1000 genomes]
rs1358181	1.00[AMR][1000 genomes]
rs1401837	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1401843	1.00[AMR][1000 genomes]
rs1401844	1.00[AMR][1000 genomes]
rs1404085	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1404088	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1405339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1405340	1.00[AMR][1000 genomes]
rs1405341	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1519897	1.00[AMR][1000 genomes]
rs1526613	1.00[AMR][1000 genomes]
rs1526622	1.00[AMR][1000 genomes]
rs1526625	1.00[AMR][1000 genomes]
rs1526626	1.00[AMR][1000 genomes]
rs1526628	1.00[AMR][1000 genomes]
rs1526640	1.00[AMR][1000 genomes]
rs1526642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1526648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1526651	1.00[AMR][1000 genomes]
rs1526652	1.00[AMR][1000 genomes]
rs1526653	1.00[AMR][1000 genomes]
rs1533985	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1554617	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1554618	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1660568	1.00[AFR][1000 genomes]
rs1852364	1.00[AMR][1000 genomes]
rs1949923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1980323	1.00[AMR][1000 genomes]
rs2049550	1.00[AMR][1000 genomes]
rs2090688	1.00[AMR][1000 genomes]
rs2139466	1.00[AMR][1000 genomes]
rs2139468	1.00[AMR][1000 genomes]
rs2139469	1.00[AMR][1000 genomes]
rs2860734	1.00[AMR][1000 genomes]
rs2860736	1.00[AMR][1000 genomes]
rs2860741	1.00[AMR][1000 genomes]
rs2860742	1.00[AMR][1000 genomes]
rs2901743	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs391688	1.00[AFR][1000 genomes]
rs393801	1.00[AFR][1000 genomes]
rs3961977	1.00[AMR][1000 genomes]
rs414148	1.00[AFR][1000 genomes]
rs4444560	1.00[AMR][1000 genomes]
rs4852401	1.00[AMR][1000 genomes]
rs4852404	1.00[AMR][1000 genomes]
rs4853208	1.00[AMR][1000 genomes]
rs4853224	1.00[AMR][1000 genomes]
rs4853225	1.00[AMR][1000 genomes]
rs4853239	1.00[AMR][1000 genomes]
rs4853240	1.00[AMR][1000 genomes]
rs6547060	1.00[AMR][1000 genomes]
rs6547062	1.00[AMR][1000 genomes]
rs6547063	1.00[AMR][1000 genomes]
rs6547074	1.00[AMR][1000 genomes]
rs6547076	1.00[AMR][1000 genomes]
rs6547077	1.00[AMR][1000 genomes]
rs6714618	1.00[AMR][1000 genomes]
rs6718886	1.00[AMR][1000 genomes]
rs6725074	1.00[AMR][1000 genomes]
rs6731474	1.00[AMR][1000 genomes]
rs6738864	1.00[AMR][1000 genomes]
rs6742237	1.00[AMR][1000 genomes]
rs6747521	1.00[AMR][1000 genomes]
rs6758608	1.00[AMR][1000 genomes]
rs7424136	1.00[AMR][1000 genomes]
rs7566339	1.00[AMR][1000 genomes]
rs7566454	1.00[AMR][1000 genomes]
rs7587657	1.00[AMR][1000 genomes]
rs7589273	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7601253	1.00[AMR][1000 genomes]
rs7602197	1.00[AMR][1000 genomes]
rs908960	1.00[AMR][1000 genomes]
rs964439	1.00[AMR][1000 genomes]
rs964440	1.00[AMR][1000 genomes]
rs964441	1.00[AMR][1000 genomes]
rs964443	1.00[AMR][1000 genomes]
rs975901	1.00[AMR][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	nsv834265	chr2:76275611-76450728	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv999645	chr2:76317006-76451354	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv874311	chr2:76389455-76492999	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 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	chr2:76420800-76424800	Weak transcription	HepG2	liver

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