Variant report

Variant	rs60763002
Chromosome Location	chr2:212637896-212637897
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10432443	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10432444	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10432445	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10432527	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10932397	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12104496	0.83[ASN][1000 genomes]
rs13005722	0.83[ASN][1000 genomes]
rs35623699	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35720933	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35870876	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4672625	0.86[ASN][1000 genomes]
rs4673633	0.82[ASN][1000 genomes]
rs56017633	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57367594	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs59568831	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs59804958	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60490270	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61019468	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6722576	0.82[AMR][1000 genomes]
rs73069350	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73069352	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73069355	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73069363	0.86[ASN][1000 genomes]
rs7422996	0.82[AMR][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	esv34128	chr2:212581485-212857122	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3445020	chr2:212636757-212638730	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212633200-212638000	Weak transcription	Aorta	Aorta

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