Variant report

Variant	rs34211399
Chromosome Location	chr13:53663494-53663495
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10507575	0.83[EUR][1000 genomes]
rs12860364	0.81[EUR][1000 genomes]
rs12864008	0.88[ASN][1000 genomes]
rs12865218	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12866736	0.88[ASN][1000 genomes]
rs12867491	0.97[EUR][1000 genomes]
rs12868253	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12869523	0.97[EUR][1000 genomes]
rs12870777	0.97[EUR][1000 genomes]
rs12871248	0.97[EUR][1000 genomes]
rs12874939	0.97[EUR][1000 genomes]
rs12876105	0.97[EUR][1000 genomes]
rs12876387	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12876786	0.94[EUR][1000 genomes]
rs12877178	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12877599	0.97[EUR][1000 genomes]
rs12877758	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12877912	0.94[EUR][1000 genomes]
rs1343608	0.97[EUR][1000 genomes]
rs17053814	0.81[ASN][1000 genomes]
rs17053823	0.85[ASN][1000 genomes]
rs17053844	0.89[ASN][1000 genomes]
rs17053849	0.89[ASN][1000 genomes]
rs17053872	0.89[ASN][1000 genomes]
rs17054812	0.97[EUR][1000 genomes]
rs17054937	0.94[EUR][1000 genomes]
rs1891947	0.88[ASN][1000 genomes]
rs1909651	0.83[EUR][1000 genomes]
rs2275840	0.81[ASN][1000 genomes]
rs2799344	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2799345	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2806957	0.83[EUR][1000 genomes]
rs34030659	0.97[EUR][1000 genomes]
rs34031649	0.97[EUR][1000 genomes]
rs34059997	0.97[EUR][1000 genomes]
rs34110102	0.88[ASN][1000 genomes]
rs34162017	0.82[ASN][1000 genomes]
rs34163916	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34201111	0.97[EUR][1000 genomes]
rs34298498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34330988	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34374288	0.88[ASN][1000 genomes]
rs34531708	0.97[EUR][1000 genomes]
rs34557321	0.94[EUR][1000 genomes]
rs34610752	0.80[EUR][1000 genomes]
rs34642277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34687272	0.97[EUR][1000 genomes]
rs34708622	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34756826	0.94[EUR][1000 genomes]
rs34820311	0.83[EUR][1000 genomes]
rs34902019	0.97[EUR][1000 genomes]
rs35003538	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35007240	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35114755	0.97[EUR][1000 genomes]
rs35121580	0.88[ASN][1000 genomes]
rs35137422	0.82[ASN][1000 genomes]
rs35226075	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35340650	0.94[EUR][1000 genomes]
rs35397855	0.89[ASN][1000 genomes]
rs35472513	0.89[ASN][1000 genomes]
rs35575822	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35625606	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35628629	0.92[EUR][1000 genomes]
rs35666947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35727089	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35756659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35765587	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35800707	0.94[EUR][1000 genomes]
rs36081995	0.88[ASN][1000 genomes]
rs55972529	0.97[EUR][1000 genomes]
rs57273256	0.97[EUR][1000 genomes]
rs57454139	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59155861	0.86[EUR][1000 genomes]
rs59297590	0.97[EUR][1000 genomes]
rs59345770	0.88[ASN][1000 genomes]
rs59513810	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59960345	0.97[EUR][1000 genomes]
rs60408242	0.97[EUR][1000 genomes]
rs61950074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61950078	0.83[EUR][1000 genomes]
rs61950079	0.97[EUR][1000 genomes]
rs61950086	0.97[EUR][1000 genomes]
rs61950491	0.88[ASN][1000 genomes]
rs61950492	0.89[ASN][1000 genomes]
rs61950504	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61950522	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6561705	0.92[EUR][1000 genomes]
rs6561706	0.97[EUR][1000 genomes]
rs6561707	0.97[EUR][1000 genomes]
rs7320513	0.97[EUR][1000 genomes]
rs7325509	0.89[EUR][1000 genomes]
rs74086489	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7998204	0.97[EUR][1000 genomes]
rs7998385	0.89[EUR][1000 genomes]
rs912053	0.89[EUR][1000 genomes]
rs9563134	0.88[EUR][1000 genomes]
rs9563136	0.94[EUR][1000 genomes]
rs9563137	0.94[EUR][1000 genomes]
rs9563138	0.94[EUR][1000 genomes]
rs9568814	0.94[EUR][1000 genomes]
rs9568815	0.94[EUR][1000 genomes]
rs9568816	0.94[EUR][1000 genomes]
rs9568817	0.94[EUR][1000 genomes]
rs9568820	0.94[EUR][1000 genomes]
rs9568821	0.94[EUR][1000 genomes]
rs9568822	0.94[EUR][1000 genomes]
rs9568823	0.94[EUR][1000 genomes]
rs9568824	0.94[EUR][1000 genomes]
rs9568825	0.94[EUR][1000 genomes]
rs9568827	0.89[EUR][1000 genomes]
rs995821	0.83[EUR][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	nsv530719	chr13:53173014-53675953	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv3440613	chr13:53307609-53671072	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv832613	chr13:53524319-53687188	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53658600-53666000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr13:53662400-53663600	Enhancers	Brain Cingulate Gyrus	brain
3	chr13:53663000-53664200	Weak transcription	Brain Substantia Nigra	brain
4	chr13:53663200-53664200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:53663200-53664200	Weak transcription	Brain Germinal Matrix	brain
6	chr13:53663200-53664200	Weak transcription	Brain Hippocampus Middle	brain
7	chr13:53663400-53664600	Weak transcription	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links