Variant report

Variant	rs6586829
Chromosome Location	chr8:19282019-19282020
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:19275354..19278233-chr8:19280534..19283813,3	MCF-7	breast:
2	chr8:19280974..19282712-chr8:19296114..19297888,2	MCF-7	breast:
3	chr8:19275542..19277855-chr8:19280462..19282722,2	K562	blood:
4	chr8:19277716..19280530-chr8:19280967..19283858,2	MCF-7	breast:

Extended variants
information (count: 20 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17407449	1.00[CHD][hapmap];0.89[ASN][1000 genomes]
rs4921639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4921640	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4922024	0.89[ASN][1000 genomes]
rs5009989	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6980861	1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[GIH][hapmap];0.97[TSI][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv949745	chr8:18826830-19363963	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv1016482	chr8:18834807-19339487	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1016993	chr8:18855623-19311731	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
10	nsv610751	chr8:19226335-19284889	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
11	esv3693374	chr8:19241970-19359184	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
12	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
13	nsv610752	chr8:19254816-19311496	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
14	nsv1022344	chr8:19270143-19324083	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs6586829	VPS37A	cis	parietal	SCAN
rs6586829	CSGALNACT1	cis	parietal	SCAN
rs6586829	TNFRSF10A	cis	cerebellum	SCAN
rs6586829	PSD3	cis	cerebellum	SCAN
rs6586829	FAM160B2	cis	parietal	SCAN
rs6586829	PIWIL2	cis	cerebellum	SCAN

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19266600-19283800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr8:19267200-19297000	Weak transcription	Brain Substantia Nigra	brain
3	chr8:19267400-19283600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr8:19267800-19295600	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:19268000-19283800	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:19270200-19288800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:19270400-19283000	Weak transcription	Brain Angular Gyrus	brain
8	chr8:19271000-19284200	Weak transcription	Thymus	Thymus
9	chr8:19271800-19283400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr8:19271800-19305200	Weak transcription	Pancreas	Pancrea
11	chr8:19275800-19287200	Weak transcription	Gastric	stomach
12	chr8:19275800-19288600	Weak transcription	Aorta	Aorta
13	chr8:19275800-19295600	Weak transcription	Brain Cingulate Gyrus	brain
14	chr8:19276200-19283400	Weak transcription	Ovary	ovary
15	chr8:19277400-19283200	Strong transcription	A549	lung
16	chr8:19277600-19295600	Weak transcription	Hela-S3	cervix
17	chr8:19277600-19307800	Weak transcription	Fetal Stomach	stomach
18	chr8:19277800-19283600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr8:19277800-19300200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr8:19278000-19283200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr8:19278000-19304800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr8:19278600-19283600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr8:19278600-19283800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:19279000-19282200	Weak transcription	Esophagus	oesophagus
25	chr8:19279600-19282400	Enhancers	Placenta Amnion	Placenta Amnion
26	chr8:19279600-19290600	Weak transcription	Primary B cells from cord blood	blood
27	chr8:19280400-19283200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr8:19280600-19282400	Genic enhancers	Primary T cells from cord blood	blood
29	chr8:19280800-19282400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr8:19280800-19284800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr8:19280800-19285000	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr8:19281000-19282400	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr8:19281000-19282400	Enhancers	Fetal Brain Male	brain
34	chr8:19281000-19282800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr8:19281000-19285000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr8:19281000-19285000	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr8:19281200-19282400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr8:19281400-19282200	Enhancers	Left Ventricle	heart
39	chr8:19281400-19282400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:19281400-19282400	Enhancers	Right Atrium	heart
41	chr8:19281400-19283800	Enhancers	Primary T cells fromperipheralblood	blood
42	chr8:19281600-19282200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr8:19281600-19283000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:19281800-19283400	Weak transcription	Spleen	Spleen
45	chr8:19281800-19283600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr8:19281800-19283800	Strong transcription	Placenta	Placenta
47	chr8:19281800-19296800	Weak transcription	Lung	lung

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