Variant report

Variant	rs59552964
Chromosome Location	chr6:80905509-80905510
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12525046	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12526876	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12527244	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12527712	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12528770	0.82[EUR][1000 genomes]
rs12529191	0.82[EUR][1000 genomes]
rs12530290	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16891532	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16891545	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55755254	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57913486	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs57985210	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59973779	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66518170	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66560352	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs66606872	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67379633	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67456645	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67597629	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67632695	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67851250	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67988458	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6924011	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892417	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892426	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892441	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892456	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72892458	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72906886	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72906894	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72908809	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72908830	0.81[EUR][1000 genomes]
rs72908854	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73479994	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs764442	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7755034	0.82[EUR][1000 genomes]
rs7757610	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7771047	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7771726	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7772483	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9688524	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9688535	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][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	nsv830708	chr6:80844283-80996876	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	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
3	nsv886309	chr6:80880138-80959885	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv886310	chr6:80880138-81025879	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	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
6	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
7	nsv1033452	chr6:80888667-81000213	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80842200-80914200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:80855200-80907000	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:80855200-80907200	Weak transcription	Ovary	ovary
4	chr6:80863200-80907200	Weak transcription	Psoas Muscle	Psoas
5	chr6:80878000-80921000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:80878600-80916000	Weak transcription	Adipose Nuclei	Adipose
7	chr6:80878800-80907200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr6:80878800-80914200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:80880600-80914200	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr6:80882400-80935400	Weak transcription	Dnd41	blood
11	chr6:80883800-80913200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr6:80885800-80919000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr6:80891400-80907200	Weak transcription	Left Ventricle	heart
14	chr6:80891600-80907400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:80891600-80931200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:80892200-80913400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr6:80893000-80907400	Weak transcription	HSMM	muscle
18	chr6:80896200-80921000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:80896400-80927400	Weak transcription	Aorta	Aorta
20	chr6:80896400-80943800	Weak transcription	Right Ventricle	heart
21	chr6:80897800-80918800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:80898400-80907200	Weak transcription	Pancreas	Pancrea
23	chr6:80904200-80921800	Weak transcription	Fetal Thymus	thymus
24	chr6:80904400-80913000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:80904400-80916200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr6:80904600-80906600	Weak transcription	Liver	Liver
27	chr6:80904600-80906800	Weak transcription	Brain Germinal Matrix	brain
28	chr6:80905000-80919000	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr6:80905200-80907200	Weak transcription	Gastric	stomach
30	chr6:80905400-80905600	Enhancers	Small Intestine	intestine
31	chr6:80905400-80907600	Enhancers	Fetal Heart	heart

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