Variant report

Variant	rs603956
Chromosome Location	chr2:141099143-141099144
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10202846	0.82[ASN][1000 genomes]
rs10204667	0.86[ASN][1000 genomes]
rs12692042	0.86[ASN][1000 genomes]
rs12692048	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12692049	0.86[ASN][1000 genomes]
rs12992137	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13002228	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13009775	0.86[ASN][1000 genomes]
rs13017246	0.82[ASN][1000 genomes]
rs13022878	0.86[ASN][1000 genomes]
rs13028524	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13028948	0.86[ASN][1000 genomes]
rs13031109	0.86[ASN][1000 genomes]
rs13382933	0.85[ASN][1000 genomes]
rs13407545	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13414281	0.81[ASN][1000 genomes]
rs1386355	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1401121	0.85[ASN][1000 genomes]
rs1401122	0.89[ASN][1000 genomes]
rs1401123	0.89[ASN][1000 genomes]
rs1518450	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1968911	0.89[ASN][1000 genomes]
rs2046563	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2945572	0.90[AMR][1000 genomes]
rs35000420	0.83[ASN][1000 genomes]
rs35699793	0.89[ASN][1000 genomes]
rs35871598	0.89[ASN][1000 genomes]
rs35958180	0.86[ASN][1000 genomes]
rs591185	0.81[ASN][1000 genomes]
rs597222	0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs600802	1.00[YRI][hapmap]
rs623670	1.00[YRI][hapmap]
rs639195	0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs650706	0.84[YRI][hapmap];0.90[AMR][1000 genomes]
rs655308	0.84[YRI][hapmap]
rs667446	0.88[YRI][hapmap]
rs682371	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7563544	0.93[ASN][1000 genomes]
rs825429	0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv875185	chr2:141055080-141179257	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv1002168	chr2:141056296-141157971	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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