Variant report

Variant	rs34737391
Chromosome Location	chr1:192750839-192750840
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10737613	0.83[ASN][1000 genomes]
rs10737615	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10737616	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10754026	0.83[ASN][1000 genomes]
rs10754027	0.83[ASN][1000 genomes]
rs10754028	0.81[EUR][1000 genomes]
rs10754029	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10801143	0.83[ASN][1000 genomes]
rs10801144	0.83[ASN][1000 genomes]
rs10801145	0.83[ASN][1000 genomes]
rs10801146	0.83[ASN][1000 genomes]
rs10801147	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10921252	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10921253	0.83[ASN][1000 genomes]
rs10921254	0.83[ASN][1000 genomes]
rs10921256	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10921257	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10921262	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10921263	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12022694	0.83[ASN][1000 genomes]
rs12027961	0.83[ASN][1000 genomes]
rs12030009	0.83[ASN][1000 genomes]
rs12030545	0.82[ASN][1000 genomes]
rs12058129	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12143838	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12145127	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12568780	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1418720	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1418721	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1592232	0.83[ASN][1000 genomes]
rs1592233	0.83[ASN][1000 genomes]
rs1933696	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1933701	0.83[ASN][1000 genomes]
rs1933702	0.82[ASN][1000 genomes]
rs1935825	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2066410	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2146603	0.83[ASN][1000 genomes]
rs2146604	0.83[ASN][1000 genomes]
rs2146606	0.83[ASN][1000 genomes]
rs2369895	0.83[ASN][1000 genomes]
rs2369896	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6428134	0.80[EUR][1000 genomes]
rs6657274	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs720829	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7525732	0.83[ASN][1000 genomes]
rs7534794	0.83[ASN][1000 genomes]
rs7537443	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	nsv532618	chr1:192537006-193149179	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv548660	chr1:192609268-192945348	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs34737391	RGS2	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192747000-192752600	Weak transcription	NHEK	skin

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