Variant report

Variant	rs806850
Chromosome Location	chr6:81030941-81030942
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:81029449..81030983-chr6:81039020..81041203,2	MCF-7	breast:

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1040593	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1179571	0.83[ASN][1000 genomes]
rs12174405	1.00[CHB][hapmap]
rs12525046	0.83[ASN][1000 genomes]
rs12526876	0.83[ASN][1000 genomes]
rs12527244	0.83[ASN][1000 genomes]
rs12527712	0.83[ASN][1000 genomes]
rs12530290	0.83[ASN][1000 genomes]
rs16891532	0.83[ASN][1000 genomes]
rs16891545	0.83[ASN][1000 genomes]
rs4706116	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4706829	1.00[LWK][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs4706830	0.83[ASN][1000 genomes]
rs55755254	0.83[ASN][1000 genomes]
rs57913486	0.83[ASN][1000 genomes]
rs584372	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs585506	0.83[ASN][1000 genomes]
rs587999	0.83[ASN][1000 genomes]
rs588009	0.83[ASN][1000 genomes]
rs590686	0.83[ASN][1000 genomes]
rs598234	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs59973779	0.83[ASN][1000 genomes]
rs610946	0.83[ASN][1000 genomes]
rs612208	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs613577	0.83[ASN][1000 genomes]
rs623085	0.83[ASN][1000 genomes]
rs631367	0.83[ASN][1000 genomes]
rs634499	0.83[ASN][1000 genomes]
rs636499	0.83[ASN][1000 genomes]
rs638921	0.83[ASN][1000 genomes]
rs640568	0.83[ASN][1000 genomes]
rs641229	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs642943	0.83[ASN][1000 genomes]
rs644666	0.83[ASN][1000 genomes]
rs6454149	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs646369	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs649148	0.83[ASN][1000 genomes]
rs651065	0.83[ASN][1000 genomes]
rs66518170	0.83[ASN][1000 genomes]
rs66560352	0.83[ASN][1000 genomes]
rs669420	0.83[ASN][1000 genomes]
rs670119	0.83[ASN][1000 genomes]
rs670390	0.83[ASN][1000 genomes]
rs67379633	0.83[ASN][1000 genomes]
rs67456645	0.83[ASN][1000 genomes]
rs67597629	0.83[ASN][1000 genomes]
rs67632695	0.83[ASN][1000 genomes]
rs677134	0.83[ASN][1000 genomes]
rs67851250	0.83[ASN][1000 genomes]
rs67988458	0.83[ASN][1000 genomes]
rs688442	0.83[ASN][1000 genomes]
rs6906403	0.83[ASN][1000 genomes]
rs6908084	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs6920430	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6924011	0.83[ASN][1000 genomes]
rs723308	0.83[ASN][1000 genomes]
rs72892417	0.83[ASN][1000 genomes]
rs72892426	0.83[ASN][1000 genomes]
rs72892441	0.83[ASN][1000 genomes]
rs72892456	0.83[ASN][1000 genomes]
rs72892458	0.83[ASN][1000 genomes]
rs72908809	0.83[ASN][1000 genomes]
rs72908854	0.83[ASN][1000 genomes]
rs73479994	0.83[ASN][1000 genomes]
rs764442	0.83[ASN][1000 genomes]
rs7757610	0.83[ASN][1000 genomes]
rs7771726	0.83[ASN][1000 genomes]
rs7772483	0.83[ASN][1000 genomes]
rs806781	0.83[ASN][1000 genomes]
rs806839	0.83[ASN][1000 genomes]
rs806841	1.00[YRI][hapmap]
rs806844	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs806846	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs811567	1.00[LWK][hapmap];1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs932463	0.83[ASN][1000 genomes]
rs9443739	1.00[YRI][hapmap];0.83[ASN][1000 genomes]
rs9688524	0.83[ASN][1000 genomes]
rs9688535	0.83[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	nsv1034096	chr6:80856135-81150170	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv932996	chr6:80880896-81134991	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv497995	chr6:80883701-81134991	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81005200-81056200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:81015600-81036400	Weak transcription	Ovary	ovary
3	chr6:81015600-81037400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:81026800-81037400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:81027000-81044600	Weak transcription	Aorta	Aorta
6	chr6:81029400-81038200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:81029400-81038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:81029400-81079600	Weak transcription	HSMM	muscle

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