Variant report

Variant	rs11157067
Chromosome Location	chr14:39952181-39952182
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs11847057	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12587625	0.86[AFR][1000 genomes]
rs12588110	0.86[AFR][1000 genomes]
rs12588175	0.84[AFR][1000 genomes]
rs12588483	0.87[AFR][1000 genomes]
rs12589427	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12590172	0.86[AFR][1000 genomes]
rs12880644	0.86[AFR][1000 genomes]
rs12884747	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12886769	0.80[AFR][1000 genomes]
rs12896502	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17109300	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17109328	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1950329	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1950334	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1950336	0.89[AFR][1000 genomes]
rs1950338	0.88[AFR][1000 genomes]
rs1955718	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2057137	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2057138	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2207291	0.88[AFR][1000 genomes]
rs2274395	0.86[AFR][1000 genomes]
rs2415549	0.86[AFR][1000 genomes]
rs2415550	0.89[AFR][1000 genomes]
rs2899889	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34649642	0.87[AFR][1000 genomes]
rs34687394	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35459433	0.86[AFR][1000 genomes]
rs35553183	0.86[AFR][1000 genomes]
rs35643160	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35693868	0.84[AFR][1000 genomes]
rs35923045	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs36010374	0.89[AFR][1000 genomes]
rs3814860	0.86[AFR][1000 genomes]
rs4899277	0.86[AFR][1000 genomes]
rs4899278	0.90[AFR][1000 genomes]
rs4899287	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4899291	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4902622	0.87[AFR][1000 genomes]
rs4902636	0.87[AFR][1000 genomes]
rs4902637	0.87[AFR][1000 genomes]
rs4902648	0.87[AFR][1000 genomes]
rs4902665	0.86[AFR][1000 genomes]
rs4902676	0.88[AFR][1000 genomes]
rs4902692	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56046902	0.86[AFR][1000 genomes]
rs71407789	0.88[AFR][1000 genomes]
rs7140983	0.80[AFR][1000 genomes]
rs7152341	0.86[AFR][1000 genomes]
rs7152935	0.88[AFR][1000 genomes]
rs7158709	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72675487	0.86[AFR][1000 genomes]
rs8003397	0.87[AFR][1000 genomes]
rs8003621	0.83[AFR][1000 genomes]
rs8006123	0.86[AFR][1000 genomes]
rs8006321	0.86[AFR][1000 genomes]
rs8020250	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs910370	0.85[AFR][1000 genomes]
rs910371	0.88[AFR][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	esv3523177	chr14:39875036-40128325	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	esv3523178	chr14:39875036-40128325	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv832774	chr14:39897746-40060823	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv915558	chr14:39944831-40165370	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr14:39939000-39954600	Weak transcription	Brain Hippocampus Middle	brain

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