Variant report

Variant	rs12191414
Chromosome Location	chr6:27278634-27278635
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:27275752..27278982-chr6:27286043..27289546,5	K562	blood:
2	chr6:27114741..27116846-chr6:27278241..27280578,2	K562	blood:

Variant related genes	Relation type
ENSG00000265565	Chromatin interaction
ENSG00000184825	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10456051	0.85[CEU][hapmap]
rs10456355	0.87[EUR][1000 genomes]
rs10946906	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12153912	0.86[CEU][hapmap]
rs12189640	0.85[CEU][hapmap]
rs12189835	0.87[CEU][hapmap]
rs12191649	0.85[CEU][hapmap]
rs12192560	0.81[EUR][1000 genomes]
rs12193557	0.85[CEU][hapmap]
rs12194842	0.85[CEU][hapmap]
rs12194893	0.85[CEU][hapmap]
rs12195750	0.86[AMR][1000 genomes]
rs12195783	0.85[CEU][hapmap]
rs12196084	0.87[CEU][hapmap]
rs12196452	0.83[EUR][1000 genomes]
rs12196970	0.83[EUR][1000 genomes]
rs12198077	0.87[CEU][hapmap]
rs12199685	0.83[EUR][1000 genomes]
rs12205921	0.87[CEU][hapmap]
rs12209393	0.87[CEU][hapmap]
rs12209456	0.86[CEU][hapmap]
rs12212348	0.85[CEU][hapmap]
rs12212389	0.83[EUR][1000 genomes]
rs12213533	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs12214930	0.86[CEU][hapmap]
rs12215289	0.85[CEU][hapmap]
rs12215878	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs12374607	0.83[EUR][1000 genomes]
rs12374649	0.81[EUR][1000 genomes]
rs28410967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3531	0.86[CEU][hapmap]
rs4636015	0.86[CEU][hapmap]
rs6902012	0.86[CEU][hapmap];1.00[AMR][1000 genomes]
rs72839451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72839468	0.94[EUR][1000 genomes]
rs72839469	0.94[EUR][1000 genomes]
rs72839470	0.93[EUR][1000 genomes]
rs72839471	0.83[EUR][1000 genomes]
rs72839474	0.83[EUR][1000 genomes]
rs72839479	0.83[EUR][1000 genomes]
rs858995	0.87[CEU][hapmap]
rs9348757	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9348759	1.00[CEU][hapmap]
rs9348763	0.94[EUR][1000 genomes]
rs9357034	1.00[AMR][1000 genomes]
rs9366690	1.00[CEU][hapmap]
rs9368498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9368499	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9368500	1.00[CEU][hapmap]
rs9379970	0.87[CEU][hapmap];0.93[AMR][1000 genomes]
rs9379975	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs9393802	0.82[CEU][hapmap]
rs9393803	0.87[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	nsv1017328	chr6:27177147-27369588	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv883505	chr6:27210614-27300580	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv883506	chr6:27271343-27288687	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27278600-27278800	Bivalent/Poised TSS	Placenta Amnion	Placenta Amnion

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