Variant report

Variant	rs13078759
Chromosome Location	chr3:68222435-68222436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11921557	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1595489	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4302389	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs4419383	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs4508789	1.00[CEU][hapmap]
rs4602395	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs56831191	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57701717	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60993082	0.84[ASN][1000 genomes]
rs6548943	1.00[CEU][hapmap]
rs6548957	0.87[AMR][1000 genomes]
rs6548958	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6548964	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes]
rs6548970	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs6548977	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6548978	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6548979	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6548992	0.82[CEU][hapmap]
rs6549006	1.00[CEU][hapmap]
rs6549018	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6771439	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6777162	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs6781199	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs6785163	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6792628	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6809593	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7626911	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7630992	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7634100	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs9309966	0.82[CEU][hapmap]
rs961915	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs9860971	0.80[ASN][1000 genomes]
rs9874375	0.87[AMR][1000 genomes]

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	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009871	chr3:67862617-68312064	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536583	chr3:67862617-68312064	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1007450	chr3:68094416-68346546	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv876925	chr3:68180422-68288626	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv876926	chr3:68204939-68282529	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

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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