Variant report

Variant	rs12466697
Chromosome Location	chr2:113709876-113709877
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:113703635..113706262-chr2:113709716..113711603,3	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10864907	0.85[CHB][hapmap]
rs11123151	0.89[AMR][1000 genomes]
rs11683383	0.82[ASN][1000 genomes]
rs11683399	0.80[ASN][1000 genomes]
rs11690185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11690539	0.81[AMR][1000 genomes]
rs11690879	0.81[AMR][1000 genomes]
rs11695077	0.82[ASN][1000 genomes]
rs11696039	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11893071	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12053091	0.83[AMR][1000 genomes]
rs12105482	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12464758	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12465526	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12466604	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12466653	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12467810	0.90[ASN][1000 genomes]
rs12467847	0.90[ASN][1000 genomes]
rs12470439	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12471839	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12472089	0.82[AMR][1000 genomes]
rs12477661	0.84[AMR][1000 genomes]
rs12479173	0.85[AMR][1000 genomes]
rs12614316	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12614988	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12616801	0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs12617864	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12618418	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12621220	0.82[AMR][1000 genomes]
rs12623837	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12993351	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12995439	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13008855	0.81[AMR][1000 genomes]
rs13021862	0.85[AMR][1000 genomes]
rs13026837	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13033104	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1317913	0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13418326	0.85[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs2305152	0.85[CHB][hapmap];0.90[JPT][hapmap]
rs34027384	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34899562	0.85[AMR][1000 genomes]
rs35520189	0.81[AMR][1000 genomes]
rs35880601	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4077216	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs58788639	0.84[AMR][1000 genomes]
rs66591921	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6705432	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6716380	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6720230	0.84[AMR][1000 genomes]
rs6722962	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6723197	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6723582	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6733001	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6733003	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67721272	0.83[AMR][1000 genomes]
rs67995749	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72825577	0.82[AMR][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	nsv532471	chr2:113682449-113862981	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv997348	chr2:113688093-113986508	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 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	chr2:113703000-113711400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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