Variant report

Variant	rs72897795
Chromosome Location	chr2:185510280-185510281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10497657	1.00[ASN][1000 genomes]
rs10497659	1.00[ASN][1000 genomes]
rs10497660	1.00[ASN][1000 genomes]
rs17430628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17430635	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17431153	1.00[ASN][1000 genomes]
rs17508623	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17508706	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17509517	0.90[ASN][1000 genomes]
rs722385	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897732	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897733	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897737	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897742	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897758	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897775	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72897802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899915	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899918	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72899952	1.00[ASN][1000 genomes]
rs72899961	1.00[ASN][1000 genomes]
rs72899964	1.00[ASN][1000 genomes]
rs72899966	1.00[ASN][1000 genomes]
rs72899969	1.00[ASN][1000 genomes]
rs72899975	1.00[ASN][1000 genomes]
rs72899976	1.00[ASN][1000 genomes]
rs72899981	1.00[ASN][1000 genomes]
rs72899983	0.82[ASN][1000 genomes]
rs72899986	1.00[ASN][1000 genomes]
rs72901820	1.00[ASN][1000 genomes]
rs72901831	1.00[ASN][1000 genomes]
rs72901834	1.00[ASN][1000 genomes]
rs72901840	1.00[ASN][1000 genomes]
rs72901862	1.00[ASN][1000 genomes]
rs72901873	1.00[ASN][1000 genomes]
rs72901891	1.00[ASN][1000 genomes]
rs72901893	1.00[ASN][1000 genomes]
rs72901901	1.00[ASN][1000 genomes]
rs72903719	1.00[ASN][1000 genomes]
rs72903720	1.00[ASN][1000 genomes]
rs72903723	1.00[ASN][1000 genomes]
rs72903763	1.00[ASN][1000 genomes]
rs72903776	0.90[ASN][1000 genomes]
rs72903778	0.90[ASN][1000 genomes]
rs72903792	0.82[ASN][1000 genomes]
rs72903798	0.90[ASN][1000 genomes]
rs72905716	0.90[ASN][1000 genomes]
rs72905722	0.90[ASN][1000 genomes]
rs72905730	0.90[ASN][1000 genomes]
rs990844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185509800-185510800	Weak transcription	Fetal Intestine Small	intestine
2	chr2:185509800-185512400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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