Variant report

Variant	rs71434747
Chromosome Location	chr13:30297596-30297597
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs12853894	1.00[AFR][1000 genomes]
rs12864282	0.93[AFR][1000 genomes]
rs12865724	0.85[AFR][1000 genomes]
rs12866411	1.00[AFR][1000 genomes]
rs12868072	0.93[AFR][1000 genomes]
rs12872620	1.00[AFR][1000 genomes]
rs12872872	1.00[AFR][1000 genomes]
rs12873674	0.85[AFR][1000 genomes]
rs12877965	1.00[AFR][1000 genomes]
rs13378487	0.81[AFR][1000 genomes]
rs34117941	1.00[AFR][1000 genomes]
rs34279165	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34492142	1.00[AFR][1000 genomes]
rs34867854	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34879256	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35145379	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35227498	1.00[AFR][1000 genomes]
rs35566813	1.00[AFR][1000 genomes]
rs35569918	1.00[AFR][1000 genomes]
rs35587642	0.92[AFR][1000 genomes]
rs35809262	1.00[AFR][1000 genomes]
rs35820783	0.86[AFR][1000 genomes]
rs35901321	0.85[AFR][1000 genomes]
rs71427279	1.00[AFR][1000 genomes]
rs71427280	1.00[AFR][1000 genomes]
rs71434744	0.86[AFR][1000 genomes]
rs71434746	1.00[AFR][1000 genomes]
rs7320198	0.85[AFR][1000 genomes]
rs7986326	0.85[AFR][1000 genomes]
rs9314968	0.85[AFR][1000 genomes]
rs9578121	0.85[AFR][1000 genomes]
rs9578122	0.85[AFR][1000 genomes]
rs9578125	0.85[AFR][1000 genomes]
rs9578127	0.85[AFR][1000 genomes]
rs9578128	0.85[AFR][1000 genomes]
rs9578130	0.86[AFR][1000 genomes]
rs9578131	0.86[AFR][1000 genomes]
rs9578133	1.00[AFR][1000 genomes]
rs9578134	0.93[AFR][1000 genomes]
rs9579442	0.85[AFR][1000 genomes]
rs9579445	0.85[AFR][1000 genomes]
rs9579446	0.85[AFR][1000 genomes]
rs9579447	0.85[AFR][1000 genomes]
rs9579449	0.85[AFR][1000 genomes]
rs9579451	0.85[AFR][1000 genomes]
rs9579454	0.85[AFR][1000 genomes]
rs9579455	0.85[AFR][1000 genomes]
rs9579457	0.85[AFR][1000 genomes]
rs9579459	0.85[AFR][1000 genomes]
rs9579462	0.85[AFR][1000 genomes]
rs9579463	0.85[AFR][1000 genomes]
rs9579464	0.86[AFR][1000 genomes]
rs9579465	0.86[AFR][1000 genomes]
rs9579466	1.00[AFR][1000 genomes]
rs9579468	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899961	chr13:30226924-30407273	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr13:30297000-30297600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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