Variant report

Variant	rs11691866
Chromosome Location	chr2:116037531-116037532
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10192079	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10199934	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11690705	0.84[AMR][1000 genomes]
rs11695752	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12474916	0.81[EUR][1000 genomes]
rs1356384	0.89[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs1516312	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1521078	0.88[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2176250	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4353659	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4353660	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4429481	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4493269	0.90[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs4610066	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4614945	0.82[AMR][1000 genomes]
rs4624386	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4848383	0.89[ASN][1000 genomes]
rs4849388	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7563562	0.84[AMR][1000 genomes]
rs7565854	0.92[ASN][1000 genomes]
rs7568698	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7587771	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7591002	0.98[ASN][1000 genomes]
rs7598070	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7605036	0.90[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7606313	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs975453	0.92[AFR][1000 genomes];0.86[EUR][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	nsv1001542	chr2:115920847-116082585	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv834339	chr2:115953298-116132979	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:116030600-116037800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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