Variant report

Variant	rs710263
Chromosome Location	chr14:97421498-97421499
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1016637	1.00[ASN][1000 genomes]
rs10484167	1.00[ASN][1000 genomes]
rs11622799	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11627513	1.00[ASN][1000 genomes]
rs1385551	1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1683119	1.00[ASN][1000 genomes]
rs1683147	1.00[ASN][1000 genomes]
rs17191520	1.00[ASN][1000 genomes]
rs17686657	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17689806	1.00[ASN][1000 genomes]
rs17761028	1.00[ASN][1000 genomes]
rs1884065	1.00[ASN][1000 genomes]
rs1950268	1.00[ASN][1000 genomes]
rs1950269	1.00[ASN][1000 genomes]
rs1955579	1.00[ASN][1000 genomes]
rs1955581	1.00[ASN][1000 genomes]
rs2017852	1.00[ASN][1000 genomes]
rs2887582	1.00[ASN][1000 genomes]
rs5008068	1.00[ASN][1000 genomes]
rs61981058	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7147186	1.00[ASN][1000 genomes]
rs7154859	1.00[ASN][1000 genomes]
rs8011580	1.00[CHB][hapmap]
rs8013300	1.00[CHB][hapmap]
rs8018103	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs856245	1.00[ASN][1000 genomes]
rs856248	1.00[ASN][1000 genomes]
rs856268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957995	1.00[ASN][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	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948620	chr14:97334444-98133191	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv832867	chr14:97365919-97541763	Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv902212	chr14:97413032-97474908	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1048462	chr14:97421360-97804598	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs710263	VRK1	cis	cerebellum	SCAN

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97408600-97428600	Weak transcription	Thymus	Thymus
2	chr14:97416400-97425600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr14:97416600-97425000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr14:97417800-97426400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr14:97420200-97430800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:97420600-97426600	Weak transcription	Dnd41	blood

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