Variant report

Variant	rs1491925
Chromosome Location	chr12:40564945-40564946
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10878123	0.90[JPT][hapmap]
rs10878208	0.95[CHB][hapmap];0.96[ASN][1000 genomes]
rs11175256	0.90[JPT][hapmap]
rs11175332	0.90[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11175371	0.95[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11175401	0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs11175405	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11175422	0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs11175458	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11175540	0.85[ASN][1000 genomes]
rs11175558	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap]
rs11564115	0.90[JPT][hapmap]
rs12581617	0.94[ASN][1000 genomes]
rs1472117	0.90[JPT][hapmap]
rs1491922	0.96[ASN][1000 genomes]
rs1491923	0.96[ASN][1000 genomes]
rs1491924	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1491942	0.95[JPT][hapmap]
rs17443199	0.95[CEU][hapmap];0.87[CHB][hapmap];0.89[JPT][hapmap];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17461429	0.85[ASN][1000 genomes]
rs2046931	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2131088	0.90[JPT][hapmap]
rs2201144	0.90[JPT][hapmap]
rs2253736	0.87[ASN][1000 genomes]
rs2638224	0.91[ASN][1000 genomes]
rs2638244	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2638247	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638250	0.96[ASN][1000 genomes]
rs2638268	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2638269	0.95[ASN][1000 genomes]
rs2638270	0.85[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2638271	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2708437	0.90[JPT][hapmap]
rs2708438	0.90[JPT][hapmap]
rs2708463	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2708465	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2708478	0.96[ASN][1000 genomes]
rs2723269	0.90[JPT][hapmap]
rs72644819	0.85[ASN][1000 genomes]
rs7310104	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs949640	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv558596	chr12:40413698-40591117	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv899030	chr12:40509341-40580440	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv899031	chr12:40520684-40580440	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1045516	chr12:40543200-40589557	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a
5	esv3398206	chr12:40556364-40581392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1491925	LRRK2	cis	Muscle Skeletal	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40562800-40565600	Enhancers	GM12878-XiMat	blood
2	chr12:40564400-40565200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr12:40564400-40566600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr12:40564600-40566200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr12:40564800-40565200	Weak transcription	Primary B cells from cord blood	blood

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