Variant report

Variant	rs1812952
Chromosome Location	chr2:116113983-116113984
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10180987	0.91[ASN][1000 genomes]
rs10181472	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1155664	0.88[ASN][1000 genomes]
rs1159302	0.89[ASN][1000 genomes]
rs11678564	0.82[AMR][1000 genomes]
rs11896853	0.89[ASN][1000 genomes]
rs11902350	0.88[ASN][1000 genomes]
rs12474916	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12478263	0.90[ASN][1000 genomes]
rs12478502	0.90[ASN][1000 genomes]
rs12611770	0.82[AMR][1000 genomes]
rs1356384	0.91[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1400667	0.91[ASN][1000 genomes]
rs1402445	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1517371	0.90[ASN][1000 genomes]
rs1521071	0.88[ASN][1000 genomes]
rs1521075	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1521078	0.87[AMR][1000 genomes]
rs1607914	0.81[AMR][1000 genomes]
rs1949402	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2176955	0.88[ASN][1000 genomes]
rs2420815	0.81[ASN][1000 genomes]
rs4493269	0.86[AMR][1000 genomes]
rs4849396	0.88[ASN][1000 genomes]
rs62167293	0.82[AMR][1000 genomes]
rs6714356	0.92[ASN][1000 genomes]
rs6716722	0.89[ASN][1000 genomes]
rs6749876	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6760151	0.92[ASN][1000 genomes]
rs7422121	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7564387	0.89[ASN][1000 genomes]
rs7568698	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7571103	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7578669	0.88[ASN][1000 genomes]
rs7605036	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs908599	0.80[ASN][1000 genomes]
rs949889	0.88[ASN][1000 genomes]
rs975453	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs992217	0.89[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	nsv834339	chr2:115953298-116132979	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv874918	chr2:116098665-116183946	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
3	nsv963924	chr2:116110836-116134022	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:116105200-116114800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:116108800-116114400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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