Variant report

Variant	rs72899983
Chromosome Location	chr2:185552032-185552033
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10497657	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10497659	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10497660	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1366843	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17430628	0.82[ASN][1000 genomes]
rs17431153	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17431603	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17508485	0.80[AMR][1000 genomes]
rs17508623	0.82[ASN][1000 genomes]
rs17508706	0.82[ASN][1000 genomes]
rs17509517	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1820847	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs722385	0.82[ASN][1000 genomes]
rs72897732	0.82[ASN][1000 genomes]
rs72897733	0.82[ASN][1000 genomes]
rs72897737	0.82[ASN][1000 genomes]
rs72897742	0.82[ASN][1000 genomes]
rs72897758	0.82[ASN][1000 genomes]
rs72897775	0.82[ASN][1000 genomes]
rs72897782	0.82[ASN][1000 genomes]
rs72897793	0.82[ASN][1000 genomes]
rs72897795	0.82[ASN][1000 genomes]
rs72897799	0.82[ASN][1000 genomes]
rs72897802	0.82[ASN][1000 genomes]
rs72899904	0.82[ASN][1000 genomes]
rs72899906	0.82[ASN][1000 genomes]
rs72899915	0.82[ASN][1000 genomes]
rs72899918	0.82[ASN][1000 genomes]
rs72899932	0.82[ASN][1000 genomes]
rs72899952	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899961	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899964	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899966	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899969	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899975	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899976	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899981	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72899986	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901820	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901831	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901834	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901836	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72901840	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901862	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901873	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901885	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72901891	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901893	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72901901	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72903719	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72903720	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72903723	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs72903763	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72903776	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72903778	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72903783	0.82[EUR][1000 genomes]
rs72903792	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72903798	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72905716	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72905722	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72905730	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72905749	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72905751	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72905782	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72905784	0.82[EUR][1000 genomes]
rs72905785	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72907715	1.00[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72907717	1.00[AMR][1000 genomes];0.84[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	nsv532412	chr2:185347334-186108701	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv834484	chr2:185550006-185762728	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185545200-185557000	Weak transcription	Fetal Stomach	stomach
2	chr2:185545800-185552200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:185548600-185552200	Enhancers	NHEK	skin

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