Variant report

Variant	rs13279687
Chromosome Location	chr8:118145265-118145266
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10107643	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10505310	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10505312	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10505313	0.88[AFR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10505314	0.85[AFR][1000 genomes]
rs10955804	0.87[ASN][1000 genomes]
rs12679333	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13254783	0.80[AFR][1000 genomes]
rs13269408	0.97[AFR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13270550	0.90[EUR][1000 genomes]
rs13281296	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17745149	0.88[ASN][1000 genomes]
rs17813200	0.91[ASN][1000 genomes]
rs1876080	0.94[ASN][1000 genomes]
rs35228127	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35934480	0.90[ASN][1000 genomes]
rs4876370	0.83[EUR][1000 genomes]
rs4876371	0.83[EUR][1000 genomes]
rs4876702	0.83[AFR][1000 genomes]
rs4876703	0.92[ASN][1000 genomes]
rs58516434	0.83[AFR][1000 genomes]
rs62510556	0.89[EUR][1000 genomes]
rs6469675	0.90[ASN][1000 genomes]
rs6469676	0.91[ASN][1000 genomes]
rs6469677	0.90[ASN][1000 genomes]
rs67425784	0.91[EUR][1000 genomes]
rs6982630	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6983495	0.90[ASN][1000 genomes]
rs6984249	0.88[ASN][1000 genomes]
rs6990569	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6998536	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7000505	0.88[ASN][1000 genomes]
rs7007057	0.91[ASN][1000 genomes]
rs7014190	0.94[ASN][1000 genomes]
rs7015338	0.89[EUR][1000 genomes]
rs7015397	0.90[ASN][1000 genomes]
rs7826750	0.92[ASN][1000 genomes]
rs868651	0.88[ASN][1000 genomes]
rs924922	0.91[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	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1031711	chr8:118134669-118322562	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1027039	chr8:118143762-118460954	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:118145200-118145400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet

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