Variant report

Variant	rs13412147
Chromosome Location	chr2:21448887-21448888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1079457	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11694766	0.91[ASN][1000 genomes]
rs11900894	0.99[ASN][1000 genomes]
rs13420469	0.99[ASN][1000 genomes]
rs3106202	0.97[ASN][1000 genomes]
rs364381	0.97[ASN][1000 genomes]
rs364390	0.97[ASN][1000 genomes]
rs368523	0.97[ASN][1000 genomes]
rs377157	0.95[ASN][1000 genomes]
rs384429	0.97[ASN][1000 genomes]
rs393495	0.97[ASN][1000 genomes]
rs398532	0.96[ASN][1000 genomes]
rs401211	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs403772	0.97[ASN][1000 genomes]
rs405983	0.96[ASN][1000 genomes]
rs411617	0.97[ASN][1000 genomes]
rs412255	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs414611	0.97[ASN][1000 genomes]
rs416490	0.97[ASN][1000 genomes]
rs425953	0.95[ASN][1000 genomes]
rs426353	0.97[ASN][1000 genomes]
rs427075	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs427095	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs427642	0.97[ASN][1000 genomes]
rs430872	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs431802	0.97[ASN][1000 genomes]
rs434540	0.97[ASN][1000 genomes]
rs435647	0.96[ASN][1000 genomes]
rs436941	0.97[ASN][1000 genomes]
rs437362	0.96[ASN][1000 genomes]
rs437624	0.97[ASN][1000 genomes]
rs437775	0.97[ASN][1000 genomes]
rs452502	0.97[ASN][1000 genomes]
rs454826	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs540698	0.85[ASN][1000 genomes]
rs549973	0.93[ASN][1000 genomes]
rs7605304	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs949790	0.99[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	nsv873728	chr2:21250914-21460786	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21446400-21451200	Weak transcription	Aorta	Aorta
2	chr2:21448800-21449000	ZNF genes & repeats	Gastric	stomach
3	chr2:21448800-21449000	ZNF genes & repeats	Pancreas	Pancrea
4	chr2:21448800-21449000	Enhancers	Spleen	Spleen

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