Variant report

Variant	rs67413955
Chromosome Location	chr8:20966010-20966011
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1015379	1.00[AMR][1000 genomes]
rs12543521	1.00[ASN][1000 genomes]
rs13249884	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13252980	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13261360	0.83[AMR][1000 genomes]
rs13274991	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13276572	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13281706	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1460975	0.83[AMR][1000 genomes]
rs1460979	0.83[AMR][1000 genomes]
rs1554459	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17093549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17093555	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17093564	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17093578	1.00[ASN][1000 genomes]
rs17423926	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17495702	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17495757	1.00[ASN][1000 genomes]
rs17495792	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17495841	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17495898	0.83[AMR][1000 genomes]
rs1841509	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34074802	0.83[AMR][1000 genomes]
rs34210663	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34224528	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34226603	0.83[AMR][1000 genomes]
rs34265291	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34702848	0.83[AMR][1000 genomes]
rs34757817	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34969903	0.83[AMR][1000 genomes]
rs35057769	0.83[AMR][1000 genomes]
rs35057973	1.00[ASN][1000 genomes]
rs35102574	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35248934	1.00[ASN][1000 genomes]
rs35325460	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35356390	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35549782	1.00[ASN][1000 genomes]
rs35627243	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35698958	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35703133	0.83[AMR][1000 genomes]
rs35741465	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35816769	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35853955	0.83[AMR][1000 genomes]
rs35888205	1.00[ASN][1000 genomes]
rs35899724	0.83[AMR][1000 genomes]
rs36033917	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs36082431	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs36096496	1.00[ASN][1000 genomes]
rs4582551	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs66823428	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67922235	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71512802	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs71513804	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71513806	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71513807	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71513808	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71513809	0.83[AMR][1000 genomes]
rs71513810	0.83[AMR][1000 genomes]
rs73623456	1.00[ASN][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	nsv1032450	chr8:20514995-21033577	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv539524	chr8:20514995-21033577	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1034265	chr8:20742935-21152545	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv539528	chr8:20742935-21152545	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv831260	chr8:20907266-21097125	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv469878	chr8:20955260-21128307	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv482339	chr8:20955260-21128307	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 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	chr8:20965200-20966400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:20965600-20966200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links