Variant report

Variant	rs10272186
Chromosome Location	chr7:40846595-40846596
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:40839610..40841601-chr7:40845220..40847169,2	MCF-7	breast:

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10225209	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10225445	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10226900	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs10231324	0.88[ASN][1000 genomes]
rs10231545	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10235458	1.00[CEU][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes]
rs10243080	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10247275	0.85[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs10252053	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs10268219	0.86[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs10276001	0.89[ASN][1000 genomes]
rs10276629	0.90[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1029621	0.95[CEU][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes]
rs1115714	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs1115715	0.91[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs12666544	0.90[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12701835	0.90[ASN][1000 genomes]
rs12701836	0.86[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs12701837	0.86[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs13237870	0.90[ASN][1000 genomes]
rs13240894	0.88[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs17530165	0.91[CHB][hapmap];0.86[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs17530213	0.94[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs17621030	0.91[CHB][hapmap];0.90[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs17688285	0.90[ASN][1000 genomes]
rs17688414	0.90[ASN][1000 genomes]
rs17770843	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17770991	0.86[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs1921743	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1921745	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1921746	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1921747	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1921748	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1974547	0.86[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs2302025	0.86[CHB][hapmap];0.80[CHD][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs2302026	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35146091	0.90[ASN][1000 genomes]
rs35570092	0.90[ASN][1000 genomes]
rs35628600	0.84[ASN][1000 genomes]
rs35712272	0.90[ASN][1000 genomes]
rs36200804	0.82[ASN][1000 genomes]
rs3815265	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs4050963	0.88[ASN][1000 genomes]
rs4460274	0.95[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs59027414	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62449401	0.90[ASN][1000 genomes]
rs62449405	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62449407	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68023334	0.90[ASN][1000 genomes]
rs73125791	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs763714	0.86[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs7784052	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7801192	0.90[ASN][1000 genomes]
rs7804009	0.90[ASN][1000 genomes]
rs7807596	0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs7808211	0.91[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs886831	0.91[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.90[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	nsv1030648	chr7:40218618-41032599	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830972	chr7:40814709-40945917	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv830973	chr7:40816419-40851594	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10272186	STK33	trans	parietal	SCAN

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40835400-40847800	Weak transcription	Aorta	Aorta
2	chr7:40842400-40847200	Weak transcription	Ovary	ovary
3	chr7:40842400-40847600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:40842400-40847800	Weak transcription	HMEC	breast
5	chr7:40843600-40850000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:40844200-40848600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:40844400-40850600	Enhancers	HSMM	muscle
8	chr7:40844600-40850400	Enhancers	HSMMtube	muscle
9	chr7:40844800-40848200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:40845000-40847600	Weak transcription	NH-A	brain
11	chr7:40845000-40849600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:40845200-40847800	Weak transcription	Colonic Mucosa	Colon
13	chr7:40845400-40847000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:40845400-40847200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:40845400-40847800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr7:40845400-40847800	Weak transcription	Hela-S3	cervix
17	chr7:40845400-40850000	Enhancers	NHDF-Ad	bronchial
18	chr7:40845600-40846600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:40845600-40847000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:40845600-40847000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:40845600-40847400	Weak transcription	NHLF	lung
22	chr7:40846000-40847000	Weak transcription	Osteobl	bone
23	chr7:40846400-40849200	Enhancers	Primary B cells from cord blood	blood
24	chr7:40846400-40850000	Enhancers	Primary B cells from peripheral blood	blood

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