Variant report

Variant	rs10817465
Chromosome Location	chr9:116005783-116005784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10081797	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10121845	0.90[YRI][hapmap]
rs10739391	0.81[AFR][1000 genomes]
rs10759631	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10759632	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs10759635	0.95[AFR][1000 genomes]
rs10817470	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs10981693	0.88[ASW][hapmap];0.89[GIH][hapmap];0.90[YRI][hapmap]
rs10981698	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs12338001	0.95[AFR][1000 genomes]
rs3810914	0.90[YRI][hapmap]
rs4978536	0.88[ASW][hapmap];0.87[GIH][hapmap];0.90[YRI][hapmap]
rs4979224	0.88[ASW][hapmap];0.87[GIH][hapmap];0.90[YRI][hapmap]
rs4979225	0.90[YRI][hapmap]
rs6477997	0.88[ASW][hapmap];0.87[GIH][hapmap];0.89[YRI][hapmap]

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	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv893745	chr9:115955271-116005783	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1041112	chr9:115960704-116005783	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv893746	chr9:115983540-116022826	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10817465	SVEP1	cis	parietal	SCAN
rs10817465	CDC26	cis	cerebellum	SCAN
rs10817465	WDR31	cis	parietal	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115985000-116020800	Weak transcription	Aorta	Aorta
2	chr9:115985600-116020800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:115985800-116018400	Weak transcription	NHEK	skin
4	chr9:115985800-116019000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:115985800-116021000	Weak transcription	Fetal Stomach	stomach
6	chr9:115986400-116013000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr9:115987600-116017800	Weak transcription	Fetal Muscle Trunk	muscle
8	chr9:115987600-116018200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr9:115987800-116011000	Weak transcription	A549	lung
10	chr9:115987800-116021000	Weak transcription	Hela-S3	cervix
11	chr9:115989000-116019200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:115991000-116011600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:115995200-116017800	Weak transcription	Left Ventricle	heart
14	chr9:115995400-116009200	Weak transcription	K562	blood
15	chr9:115995400-116018000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:115996000-116022200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr9:115996000-116031600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr9:115996200-116018600	Weak transcription	Primary T cells from cord blood	blood
19	chr9:115996200-116022400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr9:115996600-116019200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr9:115998400-116018200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:115998600-116013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:116000000-116017400	Weak transcription	HepG2	liver
24	chr9:116002000-116018400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:116002200-116018400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:116004400-116020400	Weak transcription	Fetal Thymus	thymus
27	chr9:116004600-116006000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:116004800-116013000	Weak transcription	Liver	Liver
29	chr9:116005200-116006000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:116005200-116017600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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