Variant report

Variant	rs7454742
Chromosome Location	chr6:128900153-128900154
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:127)

rs_ID	r²[population]
rs10085245	1.00[ASN][1000 genomes]
rs10085247	1.00[ASN][1000 genomes]
rs10085248	1.00[ASN][1000 genomes]
rs10223535	1.00[ASN][1000 genomes]
rs10872331	1.00[ASN][1000 genomes]
rs11154439	1.00[ASN][1000 genomes]
rs11154440	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11751628	1.00[ASN][1000 genomes]
rs11752256	1.00[ASN][1000 genomes]
rs11753496	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11758545	1.00[ASN][1000 genomes]
rs11758690	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11963575	1.00[ASN][1000 genomes]
rs12524679	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12525214	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12526634	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12526667	1.00[ASN][1000 genomes]
rs12527086	0.86[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12527265	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529229	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529511	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529947	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529948	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341584	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341585	0.85[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341588	0.81[EUR][1000 genomes]
rs13437323	1.00[ASN][1000 genomes]
rs1417896	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1572964	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17055952	1.00[ASN][1000 genomes]
rs17056043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17364020	1.00[ASN][1000 genomes]
rs17364090	1.00[ASN][1000 genomes]
rs17364118	1.00[ASN][1000 genomes]
rs17364153	1.00[ASN][1000 genomes]
rs17461370	1.00[ASN][1000 genomes]
rs17461759	0.86[CEU][hapmap];1.00[ASN][1000 genomes]
rs1935131	1.00[ASN][1000 genomes]
rs2144376	1.00[CEU][hapmap]
rs2326702	1.00[ASN][1000 genomes]
rs55988836	1.00[ASN][1000 genomes]
rs57922933	1.00[ASN][1000 genomes]
rs62425737	1.00[ASN][1000 genomes]
rs62425738	1.00[ASN][1000 genomes]
rs62425739	1.00[ASN][1000 genomes]
rs62425740	1.00[ASN][1000 genomes]
rs62425742	1.00[ASN][1000 genomes]
rs62425743	1.00[ASN][1000 genomes]
rs62425744	1.00[ASN][1000 genomes]
rs62426790	1.00[ASN][1000 genomes]
rs62426791	1.00[ASN][1000 genomes]
rs62426792	1.00[ASN][1000 genomes]
rs62426793	1.00[ASN][1000 genomes]
rs62426794	1.00[ASN][1000 genomes]
rs62426795	1.00[ASN][1000 genomes]
rs62426796	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426797	1.00[ASN][1000 genomes]
rs62426798	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426799	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62426800	1.00[ASN][1000 genomes]
rs62426801	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426804	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426805	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426806	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426840	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426841	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426842	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426844	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426845	0.93[EUR][1000 genomes]
rs62426846	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426847	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426848	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426849	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426850	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62426851	1.00[ASN][1000 genomes]
rs62426853	1.00[ASN][1000 genomes]
rs62427780	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62427781	1.00[ASN][1000 genomes]
rs6569529	1.00[ASN][1000 genomes]
rs6569535	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6569536	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6916294	0.92[EUR][1000 genomes]
rs714782	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717617	0.87[CEU][hapmap]
rs7356818	1.00[ASN][1000 genomes]
rs7356823	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7356912	1.00[ASN][1000 genomes]
rs766306	1.00[ASN][1000 genomes]
rs7738739	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7739600	1.00[ASN][1000 genomes]
rs7748742	1.00[ASN][1000 genomes]
rs7751094	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7751265	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs7752487	1.00[ASN][1000 genomes]
rs7754729	0.96[EUR][1000 genomes]
rs7760287	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760572	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760682	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7765212	1.00[ASN][1000 genomes]
rs7768240	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771701	1.00[ASN][1000 genomes]
rs9321122	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9375578	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs9388647	0.96[EUR][1000 genomes]
rs9388648	0.92[EUR][1000 genomes]
rs9388649	0.96[EUR][1000 genomes]
rs9388650	0.96[EUR][1000 genomes]
rs9402055	0.96[EUR][1000 genomes]
rs9482892	1.00[ASN][1000 genomes]
rs9482893	1.00[ASN][1000 genomes]
rs9482897	1.00[ASN][1000 genomes]
rs9482902	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9482904	1.00[ASN][1000 genomes]
rs9491988	1.00[ASN][1000 genomes]
rs9492000	0.86[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492002	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492003	0.96[EUR][1000 genomes]
rs9492004	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492005	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492008	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492011	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492013	1.00[ASN][1000 genomes]
rs9492014	1.00[ASN][1000 genomes]
rs9492017	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492018	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9492020	1.00[ASN][1000 genomes]
rs9492021	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv969326	chr6:128899447-128900483	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128895800-128901200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:128898200-128901400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:128899800-128900200	Enhancers	Fetal Brain Male	brain

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