Variant report

Variant	rs3765496
Chromosome Location	chr6:75800931-75800932
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:75794195..75796252-chr6:75800094..75801865,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10943236	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12662022	0.92[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12662415	0.99[ASN][1000 genomes]
rs12663939	0.93[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2015242	0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2295253	0.98[ASN][1000 genomes]
rs2300795	1.00[CEU][hapmap];0.88[CHD][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2300796	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734191	0.93[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3818138	1.00[CEU][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56091378	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59737607	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59740803	0.98[ASN][1000 genomes]
rs61656115	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs619607	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs636444	1.00[JPT][hapmap];0.88[MEX][hapmap];0.86[ASN][1000 genomes]
rs7758152	0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9343271	0.88[MEX][hapmap]
rs9343272	1.00[JPT][hapmap]
rs9443154	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443156	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447442	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447445	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022377	chr6:75762463-75919592	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv538309	chr6:75762463-75919592	Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv830697	chr6:75763095-75915029	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
4	nsv1016804	chr6:75775846-76188585	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv538310	chr6:75775846-76188585	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	nsv463155	chr6:75789526-75980419	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv603762	chr6:75789526-75980419	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75789800-75801000	Strong transcription	HSMM	muscle
2	chr6:75790000-75801200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:75793000-75804800	Strong transcription	HMEC	breast
4	chr6:75793200-75802400	Strong transcription	NHLF	lung
5	chr6:75793200-75803400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:75793800-75801000	Strong transcription	NHDF-Ad	bronchial
7	chr6:75795200-75802600	Weak transcription	Esophagus	oesophagus
8	chr6:75795200-75803000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:75795200-75804800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:75795200-75804800	Weak transcription	Aorta	Aorta
11	chr6:75795200-75808000	Weak transcription	HUVEC	blood vessel
12	chr6:75795200-75811600	Weak transcription	Right Ventricle	heart
13	chr6:75795400-75804400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr6:75795600-75801400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr6:75795600-75806800	Weak transcription	Fetal Kidney	kidney
16	chr6:75796600-75808200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr6:75797800-75806000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:75798000-75807400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:75798400-75803600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:75798400-75804400	Weak transcription	Colon Smooth Muscle	Colon
21	chr6:75799400-75801600	Genic enhancers	Fetal Intestine Large	intestine
22	chr6:75799400-75801600	Enhancers	Fetal Intestine Small	intestine
23	chr6:75799600-75802600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:75799600-75803400	Strong transcription	Fetal Muscle Trunk	muscle
25	chr6:75799600-75804200	Weak transcription	Fetal Lung	lung
26	chr6:75799800-75802800	Strong transcription	NHEK	skin
27	chr6:75799800-75808400	Weak transcription	Hela-S3	cervix
28	chr6:75800000-75801000	Strong transcription	Fetal Muscle Leg	muscle
29	chr6:75800000-75801400	Weak transcription	HSMMtube	muscle
30	chr6:75800000-75804400	Weak transcription	Ovary	ovary
31	chr6:75800000-75804400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr6:75800000-75808000	Weak transcription	Fetal Stomach	stomach
33	chr6:75800200-75804200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr6:75800200-75808000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:75800400-75808800	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:75800400-75815600	Genic enhancers	Osteobl	bone
37	chr6:75800600-75801600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr6:75800600-75801800	Strong transcription	Adipose Nuclei	Adipose
39	chr6:75800600-75809200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:75800800-75801000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:75800800-75802000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:75800800-75802400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr6:75800800-75804200	Weak transcription	NH-A	brain

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