Variant report

Variant	rs7769064
Chromosome Location	chr6:74495849-74495850
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	chr6:74482741..74484396-chr6:74495727..74498178,3	MCF-7	breast:
2	chr6:74495117..74497243-chr6:75916088..75918968,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10455097	0.95[EUR][1000 genomes]
rs10805980	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10943130	0.91[EUR][1000 genomes]
rs10943131	0.91[EUR][1000 genomes]
rs11757360	0.91[EUR][1000 genomes]
rs12189952	0.91[EUR][1000 genomes]
rs12209909	0.90[EUR][1000 genomes]
rs12211905	0.86[EUR][1000 genomes]
rs12660627	0.91[EUR][1000 genomes]
rs12663597	0.91[EUR][1000 genomes]
rs12663978	0.91[EUR][1000 genomes]
rs1973482	0.86[EUR][1000 genomes]
rs1973483	0.87[EUR][1000 genomes]
rs4708084	0.91[EUR][1000 genomes]
rs4708085	0.90[EUR][1000 genomes]
rs4708086	0.91[EUR][1000 genomes]
rs4708087	0.91[EUR][1000 genomes]
rs6453696	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6903575	0.90[EUR][1000 genomes]
rs6907989	0.91[EUR][1000 genomes]
rs6908109	0.91[EUR][1000 genomes]
rs6909201	0.91[EUR][1000 genomes]
rs6918540	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6925924	0.90[EUR][1000 genomes]
rs71309314	0.91[EUR][1000 genomes]
rs7745364	0.91[EUR][1000 genomes]
rs7749499	0.91[EUR][1000 genomes]
rs7751343	0.90[EUR][1000 genomes]
rs7751523	0.91[EUR][1000 genomes]
rs7751558	0.91[EUR][1000 genomes]
rs7751669	0.91[EUR][1000 genomes]
rs7751758	0.91[EUR][1000 genomes]
rs7762920	0.91[EUR][1000 genomes]
rs7763030	0.91[EUR][1000 genomes]
rs7763254	0.91[EUR][1000 genomes]
rs7772434	0.90[EUR][1000 genomes]
rs7773872	0.90[EUR][1000 genomes]
rs9293942	0.89[EUR][1000 genomes]
rs9293944	0.91[EUR][1000 genomes]
rs9343072	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9343075	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9343078	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9350507	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9442968	0.91[EUR][1000 genomes]
rs9447004	0.89[EUR][1000 genomes]
rs9447013	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9447030	0.91[EUR][1000 genomes]
rs997767	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027968	chr6:74155378-74521923	Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
2	nsv538305	chr6:74155378-74521923	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
3	nsv1023250	chr6:74189642-74605976	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
4	nsv538306	chr6:74189642-74605976	Strong transcription Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	172 gene(s)	inside rSNPs	diseases
5	nsv463154	chr6:74412048-74775904	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv603695	chr6:74412048-74775904	Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74438400-74527200	Weak transcription	Esophagus	oesophagus
2	chr6:74441400-74544400	Weak transcription	Aorta	Aorta
3	chr6:74444000-74498600	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:74469800-74502800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr6:74474800-74498200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:74475200-74513600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr6:74476000-74510800	Weak transcription	Fetal Heart	heart
8	chr6:74477400-74543400	Weak transcription	Lung	lung
9	chr6:74484400-74505800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:74484600-74498000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:74484600-74500200	Weak transcription	Left Ventricle	heart
12	chr6:74484600-74507800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr6:74484600-74508200	Weak transcription	Colon Smooth Muscle	Colon
14	chr6:74484600-74542000	Weak transcription	Right Ventricle	heart
15	chr6:74484800-74497800	Weak transcription	Adipose Nuclei	Adipose
16	chr6:74484800-74498600	Weak transcription	NH-A	brain
17	chr6:74484800-74508200	Weak transcription	Hela-S3	cervix
18	chr6:74484800-74512600	Weak transcription	HSMM	muscle
19	chr6:74485400-74498400	Weak transcription	Osteobl	bone
20	chr6:74487000-74509600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:74489400-74498200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:74489800-74497600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:74489800-74510000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:74490000-74498000	Strong transcription	HMEC	breast
25	chr6:74490200-74508200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr6:74490400-74527800	Weak transcription	Thymus	Thymus
27	chr6:74490600-74498000	Strong transcription	NHDF-Ad	bronchial
28	chr6:74490600-74503600	Strong transcription	Primary hematopoietic stem cells	blood
29	chr6:74490600-74507400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:74490800-74500200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:74490800-74507200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:74491000-74499800	Weak transcription	Primary T cells from cord blood	blood
33	chr6:74491200-74497800	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr6:74491400-74498200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:74491600-74508000	Weak transcription	Brain Anterior Caudate	brain
36	chr6:74492400-74510800	Weak transcription	A549	lung
37	chr6:74492600-74504600	Weak transcription	Stomach Mucosa	stomach
38	chr6:74492800-74497400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:74493400-74497200	Strong transcription	Fetal Muscle Trunk	muscle
40	chr6:74494000-74496800	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr6:74494000-74505400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr6:74494200-74496000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr6:74494400-74502800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:74494400-74510800	Weak transcription	Fetal Lung	lung
45	chr6:74494400-74530800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr6:74495000-74497800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:74495200-74496800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:74495400-74496600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:74495400-74497000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr6:74495400-74498200	Strong transcription	NHEK	skin

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