Variant report

Variant	rs12526640
Chromosome Location	chr6:121400981-121400982
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:121399181..121401952-chr6:121402264..121404345,2	K562	blood:
2	chr6:121394181..121397153-chr6:121399643..121401552,2	K562	blood:
3	chr6:121400057..121403003-chr6:121403745..121405643,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12523922	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12524258	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12524754	0.87[AMR][1000 genomes]
rs12525337	0.85[CEU][hapmap];1.00[AFR][1000 genomes]
rs12525794	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12527407	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12529567	1.00[AFR][1000 genomes]
rs1273721	0.84[MEX][hapmap]
rs1273722	0.84[MEX][hapmap]
rs1273725	0.84[MEX][hapmap]
rs1273726	0.84[MEX][hapmap]
rs1273745	0.84[MEX][hapmap]
rs1273757	0.85[CEU][hapmap]
rs1273759	0.85[CEU][hapmap]
rs1273760	0.85[CEU][hapmap]
rs1273775	0.85[CEU][hapmap]
rs1697446	0.85[CEU][hapmap]
rs17083122	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2133993	0.85[CEU][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2173837	0.85[CEU][hapmap]
rs2173838	0.82[CEU][hapmap]
rs2455056	0.89[MEX][hapmap]
rs2884396	0.85[CEU][hapmap]
rs2995680	0.84[MEX][hapmap]
rs4257888	0.85[CEU][hapmap]
rs4527742	0.85[CEU][hapmap];0.84[MEX][hapmap]
rs4585603	0.85[CEU][hapmap];0.84[MEX][hapmap]
rs4945676	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4945681	0.82[CEU][hapmap];1.00[AFR][1000 genomes]
rs4946540	0.85[CEU][hapmap];0.94[MEX][hapmap];1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4946546	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs4946548	0.85[CEU][hapmap]
rs4946551	0.82[CEU][hapmap]
rs6569179	0.85[CEU][hapmap];0.84[MEX][hapmap]
rs6569182	0.85[CEU][hapmap]
rs6912500	0.82[CEU][hapmap]
rs6916425	0.85[CEU][hapmap]
rs6933263	0.85[CEU][hapmap]
rs6935039	0.85[CEU][hapmap]
rs7762181	0.85[CEU][hapmap]
rs7762977	0.85[CEU][hapmap]
rs7766150	0.85[CEU][hapmap]
rs810826	0.85[CEU][hapmap]
rs811484	0.82[CEU][hapmap];0.84[MEX][hapmap]
rs813068	0.85[CEU][hapmap];0.84[MEX][hapmap]
rs9385188	0.85[CEU][hapmap]
rs975679	0.84[MEX][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	nsv1023384	chr6:121235867-121683448	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv886592	chr6:121260089-121425387	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv464037	chr6:121261915-121400981	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv604571	chr6:121261915-121400981	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv530527	chr6:121298528-121789855	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv886593	chr6:121362591-121414770	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1830193	chr6:121392847-121425387	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121390800-121444000	Weak transcription	Ovary	ovary

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