Variant report

Variant	rs34419229
Chromosome Location	chr3:116092739-116092740
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10511356	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11925640	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11927240	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16824815	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17645771	0.88[EUR][1000 genomes]
rs17646114	0.90[EUR][1000 genomes]
rs17646126	0.90[EUR][1000 genomes]
rs17646294	0.95[EUR][1000 genomes]
rs17646747	0.93[EUR][1000 genomes]
rs17702489	0.88[EUR][1000 genomes]
rs17702536	0.88[EUR][1000 genomes]
rs2116307	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs28590146	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs41457247	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59313401	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59428849	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60148139	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6771542	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6782605	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72950173	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72950188	1.00[EUR][1000 genomes]
rs72950190	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72950194	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72950202	0.90[EUR][1000 genomes]
rs72951910	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72951915	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72951916	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72951935	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72951938	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7433207	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7619749	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7630573	0.80[AMR][1000 genomes];0.93[EUR][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	nsv877361	chr3:116017931-116138039	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv437338	chr3:116076289-116110635	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757005	chr3:116085678-116121948	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv2759170	chr3:116085678-116121948	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:116088800-116093400	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:116089600-116093400	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:116089600-116093600	Weak transcription	Brain Anterior Caudate	brain

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