Variant report

Variant	rs31352
Chromosome Location	chr14:79389766-79389767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11159385	0.86[ASN][1000 genomes]
rs11159386	0.86[ASN][1000 genomes]
rs11159387	0.86[ASN][1000 genomes]
rs11159388	0.84[ASN][1000 genomes]
rs11159389	0.84[ASN][1000 genomes]
rs11159390	0.83[ASN][1000 genomes]
rs11845894	0.88[ASN][1000 genomes]
rs11847534	0.84[ASN][1000 genomes]
rs11847702	0.84[ASN][1000 genomes]
rs12050287	0.86[ASN][1000 genomes]
rs149088	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs154329	0.96[ASN][1000 genomes]
rs154330	0.96[ASN][1000 genomes]
rs154333	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs154334	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs154336	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs154343	0.90[ASN][1000 genomes]
rs17108401	0.93[ASN][1000 genomes]
rs17108405	0.93[ASN][1000 genomes]
rs17108413	0.90[ASN][1000 genomes]
rs220103	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs220104	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2272292	0.84[ASN][1000 genomes]
rs2272293	0.84[ASN][1000 genomes]
rs31349	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs31351	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs31426	0.80[ASN][1000 genomes]
rs31436	0.92[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs31437	0.93[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs31439	0.92[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs31450	0.96[ASN][1000 genomes]
rs3817535	0.92[ASN][1000 genomes]
rs60746359	0.83[ASN][1000 genomes]
rs61330422	0.96[ASN][1000 genomes]
rs7157841	0.84[ASN][1000 genomes]
rs8003966	0.84[ASN][1000 genomes]
rs8007109	0.83[ASN][1000 genomes]
rs8007461	0.93[ASN][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	nsv832838	chr14:79306627-79445382	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1048274	chr14:79323592-79417906	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv917249	chr14:79388181-79574717	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:79387000-79390400	Enhancers	HUVEC	blood vessel
2	chr14:79389200-79390000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:79389400-79390000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr14:79389600-79390000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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