Variant report

Variant	rs62382864
Chromosome Location	chr5:113484323-113484324
allele	C/T
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:33)

rs_ID	r²[population]
rs10045738	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10066191	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10078772	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747036	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17350454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17429055	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2974468	0.96[ASN][1000 genomes]
rs4260657	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4272124	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4365834	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4368718	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4416597	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4519916	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4537051	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4583880	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4612056	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705487	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705488	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705625	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705626	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4705628	0.89[EUR][1000 genomes]
rs62382892	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6594791	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6594793	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6871846	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6873105	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6873190	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6875528	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6879669	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7720919	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7721332	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7721339	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9326911	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[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	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1020064	chr5:113418512-113492951	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2763899	chr5:113474771-113533857	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113483400-113484800	Enhancers	Stomach Mucosa	stomach
2	chr5:113484200-113485200	Enhancers	Pancreas	Pancrea

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