Variant report

Variant	rs13099482
Chromosome Location	chr3:85916542-85916543
allele	A/T
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:35)

rs_ID	r²[population]
rs11127912	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11127913	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11127914	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11708377	0.92[CEU][hapmap];0.82[YRI][hapmap]
rs11719943	0.82[AMR][1000 genomes]
rs12486982	0.82[YRI][hapmap]
rs12488773	0.82[YRI][hapmap]
rs12489145	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12491363	0.82[CEU][hapmap];0.82[YRI][hapmap]
rs12492459	0.83[CEU][hapmap];0.82[YRI][hapmap]
rs12493341	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12633520	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13079014	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13082138	0.91[CEU][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13085427	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17879296	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2325006	0.82[CEU][hapmap];0.82[YRI][hapmap]
rs34420989	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34803122	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs36080783	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3911063	0.99[ASN][1000 genomes]
rs4368495	0.83[CEU][hapmap];0.82[YRI][hapmap]
rs4464472	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4600827	0.91[CEU][hapmap];0.82[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4688895	0.82[YRI][hapmap]
rs4856604	0.82[YRI][hapmap]
rs56760958	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62261744	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62261747	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62261750	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71316818	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7620825	1.00[CEU][hapmap]
rs7627287	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9860792	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9879903	0.83[CEU][hapmap];0.82[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877106	chr3:85814620-86006210	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv877107	chr3:85814620-86037162	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv877108	chr3:85870363-86037162	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv877109	chr3:85892098-86006210	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv877110	chr3:85892098-86037162	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv877111	chr3:85892098-86044224	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	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
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