Variant report

Variant	rs659059
Chromosome Location	chr1:193983693-193983694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10737634	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10737635	0.83[ASN][1000 genomes]
rs10801279	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10921478	0.80[ASN][1000 genomes]
rs12239212	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16836057	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs608100	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs616204	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs617952	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs618961	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs619489	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs629872	0.93[EUR][1000 genomes]
rs643380	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs646090	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs650350	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs652268	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67104929	0.81[ASN][1000 genomes]
rs681469	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs958096	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3372415	chr1:193612172-193988265	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv872834	chr1:193889533-194482304	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv548664	chr1:193938944-194000953	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs659059	RGS18	cis	cerebellum	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193982600-193984000	Enhancers	NHEK	skin
2	chr1:193983000-193984000	Enhancers	Hela-S3	cervix
3	chr1:193983600-193984000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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