Variant report

Variant	rs12476869
Chromosome Location	chr2:116173371-116173372
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1037205	0.81[ASN][1000 genomes]
rs11123307	0.81[ASN][1000 genomes]
rs11674650	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11675299	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11675990	0.90[ASN][1000 genomes]
rs11680996	0.90[ASN][1000 genomes]
rs11683441	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12614808	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12711825	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12990043	0.81[ASN][1000 genomes]
rs13010997	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13016837	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13021167	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1517369	0.94[ASN][1000 genomes]
rs1517370	0.91[ASN][1000 genomes]
rs1517372	0.90[ASN][1000 genomes]
rs1521076	0.89[ASN][1000 genomes]
rs1521079	0.93[ASN][1000 genomes]
rs1589084	0.90[ASN][1000 genomes]
rs1589085	0.90[ASN][1000 genomes]
rs1589086	0.90[ASN][1000 genomes]
rs1626545	0.94[ASN][1000 genomes]
rs1711995	0.90[ASN][1000 genomes]
rs1712012	0.90[ASN][1000 genomes]
rs1717037	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1717038	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1717045	0.94[ASN][1000 genomes]
rs1717047	0.91[ASN][1000 genomes]
rs1717055	0.89[ASN][1000 genomes]
rs1829229	0.90[ASN][1000 genomes]
rs2030440	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2030441	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2138776	0.89[ASN][1000 genomes]
rs2677290	0.90[ASN][1000 genomes]
rs2683794	0.92[ASN][1000 genomes]
rs34790955	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34825131	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35275337	0.88[ASN][1000 genomes]
rs56280083	0.88[ASN][1000 genomes]
rs60118669	0.93[ASN][1000 genomes]
rs62164391	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62166081	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6542260	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs708649	0.93[ASN][1000 genomes]
rs843381	0.93[ASN][1000 genomes]
rs843388	0.93[ASN][1000 genomes]
rs843391	0.91[ASN][1000 genomes]
rs843395	0.91[ASN][1000 genomes]
rs843398	0.93[ASN][1000 genomes]
rs843399	0.92[ASN][1000 genomes]
rs843405	0.93[ASN][1000 genomes]
rs843408	0.85[ASN][1000 genomes]
rs843412	0.91[ASN][1000 genomes]
rs952747	0.91[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	nsv874918	chr2:116098665-116183946	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
2	nsv874919	chr2:116130709-116219686	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	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	chr2:116172400-116184600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:116173000-116184200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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