Variant report

Variant	rs10770891
Chromosome Location	chr12:22283236-22283237
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10492281	0.83[ASN][1000 genomes]
rs10770890	0.88[CHB][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs11046301	0.89[ASN][1000 genomes]
rs12303121	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12306254	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12829732	0.83[ASN][1000 genomes]
rs12831501	0.83[ASN][1000 genomes]
rs1861710	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2080551	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2080554	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2111353	0.82[ASN][1000 genomes]
rs2193382	0.84[ASN][1000 genomes]
rs2193384	0.86[ASN][1000 genomes]
rs2193385	0.83[ASN][1000 genomes]
rs2193386	0.83[ASN][1000 genomes]
rs2193387	0.81[ASN][1000 genomes]
rs2900495	0.89[ASN][1000 genomes]
rs2909067	0.89[ASN][1000 genomes]
rs2970797	0.86[ASN][1000 genomes]
rs34299716	0.83[ASN][1000 genomes]
rs34533494	0.81[ASN][1000 genomes]
rs35253752	0.86[ASN][1000 genomes]
rs35683388	0.86[ASN][1000 genomes]
rs3937473	0.81[ASN][1000 genomes]
rs6487285	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7138641	0.88[ASN][1000 genomes]
rs71448629	0.85[ASN][1000 genomes]
rs7296982	0.88[CHB][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs7300750	0.83[ASN][1000 genomes]
rs7304110	0.89[ASN][1000 genomes]
rs7304537	0.86[ASN][1000 genomes]
rs7968893	0.85[ASN][1000 genomes]
rs7969364	0.89[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	esv2758298	chr12:22140834-22339299	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2759883	chr12:22140834-22736907	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:22282800-22285000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:22283000-22285000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:22283200-22285000	Enhancers	HMEC	breast
4	chr12:22283200-22285200	Enhancers	NHEK	skin

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