Variant report

Variant	rs11676026
Chromosome Location	chr2:184367502-184367503
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10497627	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10754996	0.95[ASN][1000 genomes]
rs10931086	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10931087	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11695835	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11897765	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12996552	0.96[ASN][1000 genomes]
rs13026970	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1406334	0.94[ASN][1000 genomes]
rs16824632	0.93[ASN][1000 genomes]
rs16824647	0.93[ASN][1000 genomes]
rs16824699	0.94[ASN][1000 genomes]
rs16824710	0.91[ASN][1000 genomes]
rs1919276	0.95[ASN][1000 genomes]
rs1919278	0.96[ASN][1000 genomes]
rs2118477	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2141414	0.94[ASN][1000 genomes]
rs4572562	0.94[ASN][1000 genomes]
rs4574075	0.93[ASN][1000 genomes]
rs4666922	0.93[ASN][1000 genomes]
rs56302218	0.94[ASN][1000 genomes]
rs58390523	0.93[ASN][1000 genomes]
rs59553799	0.93[ASN][1000 genomes]
rs59974361	0.93[ASN][1000 genomes]
rs60090891	0.93[ASN][1000 genomes]
rs60345524	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66879817	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6706093	0.94[ASN][1000 genomes]
rs6722136	0.89[ASN][1000 genomes]
rs6750117	0.93[ASN][1000 genomes]
rs6750378	0.87[ASN][1000 genomes]
rs67951091	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73044524	0.93[ASN][1000 genomes]
rs73044536	0.95[ASN][1000 genomes]
rs73977910	0.93[ASN][1000 genomes]
rs7558499	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv508188	chr2:184353162-184383232	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1012672	chr2:184363204-184571778	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184367000-184367800	Enhancers	HMEC	breast
2	chr2:184367200-184368000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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