Variant report

Variant	rs160019
Chromosome Location	chr6:39659516-39659517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF6-1	chr6:39657754-39659638	NONHSAT112438

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11752840	0.86[ASN][1000 genomes]
rs11754307	0.86[ASN][1000 genomes]
rs11754807	0.82[CEU][hapmap];0.82[MEX][hapmap]
rs1380343	0.95[YRI][hapmap]
rs149242	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs149607	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1563770	0.95[YRI][hapmap];0.85[AFR][1000 genomes]
rs159956	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs159957	0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs159958	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs160020	0.91[ASW][hapmap];1.00[CHD][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs160021	0.99[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs160023	1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs160024	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs160028	0.86[ASN][1000 genomes]
rs160030	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs160032	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2199174	0.86[ASN][1000 genomes]
rs2446644	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2446646	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2465672	1.00[CHB][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2466410	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2499450	0.91[ASW][hapmap];1.00[CHD][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.87[YRI][hapmap]
rs2499452	0.95[YRI][hapmap]
rs302548	0.86[ASN][1000 genomes]
rs302559	0.84[AFR][1000 genomes]
rs302560	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302561	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302562	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs302563	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302564	0.98[AFR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs302565	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302567	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302568	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302570	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[YRI][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302572	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs302573	0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302574	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302575	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302579	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302586	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302587	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302588	0.91[ASW][hapmap];1.00[CHD][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs302589	0.89[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302591	0.86[ASN][1000 genomes]
rs302592	0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302593	0.91[ASW][hapmap];1.00[CHD][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs302594	0.84[AFR][1000 genomes]
rs302595	1.00[YRI][hapmap]
rs302596	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303653	0.91[ASW][hapmap];1.00[CHD][hapmap];0.93[LWK][hapmap];0.82[MEX][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303661	0.93[LWK][hapmap];0.98[MKK][hapmap];0.87[YRI][hapmap]
rs303675	0.85[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303677	0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303678	0.91[ASW][hapmap];1.00[CHD][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303693	1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303699	0.90[YRI][hapmap];0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303700	0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs303701	0.91[ASW][hapmap];1.00[CHD][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs55815613	0.86[ASN][1000 genomes]
rs55941685	0.86[ASN][1000 genomes]
rs56130116	0.86[ASN][1000 genomes]
rs62402464	0.86[ASN][1000 genomes]
rs62402465	0.86[ASN][1000 genomes]
rs62403334	0.86[ASN][1000 genomes]
rs62403359	0.86[ASN][1000 genomes]
rs62405160	0.86[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885822	chr6:39327708-39721216	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39653600-39660200	Weak transcription	Fetal Lung	lung
2	chr6:39657000-39660800	Weak transcription	NHDF-Ad	bronchial
3	chr6:39657200-39660800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:39657200-39675000	Weak transcription	Brain Hippocampus Middle	brain
5	chr6:39658200-39665400	Weak transcription	Brain Substantia Nigra	brain

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