Variant report

Variant	rs7650575
Chromosome Location	chr3:179638781-179638782
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12696482	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1567622	0.83[ASN][1000 genomes]
rs1567624	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.90[TSI][hapmap]
rs1609981	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1973797	0.82[ASN][1000 genomes]
rs2037633	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2177591	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2287224	0.83[ASN][1000 genomes]
rs2339917	0.88[MEX][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes]
rs2879636	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs3774253	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3821798	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4146790	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4854954	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6443675	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6784136	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7616210	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7634271	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9290684	1.00[CHD][hapmap];0.89[TSI][hapmap]
rs9836550	0.87[ASN][1000 genomes]
rs9862706	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7650575	PARL	cis	parietal	SCAN
rs7650575	CHRD	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179624800-179639000	Weak transcription	Brain Substantia Nigra	brain
2	chr3:179630000-179638800	Weak transcription	Brain Angular Gyrus	brain
3	chr3:179633000-179638800	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:179637000-179639000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:179637400-179638800	Weak transcription	Dnd41	blood

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