Variant report

Variant	rs67035385
Chromosome Location	chr8:94983810-94983811
allele	A/G
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:40)

rs_ID	r²[population]
rs10454346	0.87[EUR][1000 genomes]
rs10454352	0.91[EUR][1000 genomes]
rs10464832	0.89[EUR][1000 genomes]
rs10808664	0.88[EUR][1000 genomes]
rs10808665	0.85[EUR][1000 genomes]
rs10956891	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956892	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10956893	0.89[EUR][1000 genomes]
rs11774322	0.88[EUR][1000 genomes]
rs11783696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11784805	0.91[EUR][1000 genomes]
rs11787272	0.90[EUR][1000 genomes]
rs12675328	0.81[EUR][1000 genomes]
rs12681770	0.85[EUR][1000 genomes]
rs12681774	0.85[EUR][1000 genomes]
rs16916334	0.85[EUR][1000 genomes]
rs16916340	0.85[EUR][1000 genomes]
rs16916344	0.85[EUR][1000 genomes]
rs3115942	0.91[EUR][1000 genomes]
rs3115943	0.90[EUR][1000 genomes]
rs3115947	0.91[EUR][1000 genomes]
rs3134014	0.89[EUR][1000 genomes]
rs3134015	0.91[EUR][1000 genomes]
rs3134018	0.91[EUR][1000 genomes]
rs3134019	0.85[EUR][1000 genomes]
rs4236822	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4236823	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4415280	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4483119	0.85[EUR][1000 genomes]
rs4489299	0.85[EUR][1000 genomes]
rs4496935	0.85[EUR][1000 genomes]
rs55813436	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59369332	0.91[EUR][1000 genomes]
rs62523012	0.83[EUR][1000 genomes]
rs62523013	0.90[EUR][1000 genomes]
rs6471417	0.91[EUR][1000 genomes]
rs7812529	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7817292	0.90[EUR][1000 genomes]
rs7831416	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7835189	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:94982000-94984400	Weak transcription	HepG2	liver
2	chr8:94982000-94985200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:94982200-94984000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr8:94982200-94984000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr8:94982400-94984000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr8:94983800-94984600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr8:94983800-94984600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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