Variant report

Variant	rs9278006
Chromosome Location	chr6:33321431-33321432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1106606	0.89[EUR][1000 genomes]
rs11751696	0.90[EUR][1000 genomes]
rs11753355	0.90[EUR][1000 genomes]
rs11756267	0.90[EUR][1000 genomes]
rs11756767	0.90[EUR][1000 genomes]
rs2235982	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs41267647	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs41271245	0.90[EUR][1000 genomes]
rs4231	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55699469	0.90[EUR][1000 genomes]
rs7752202	0.84[EUR][1000 genomes]
rs9277997	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9278001	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9278004	0.83[EUR][1000 genomes]
rs9278005	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9278007	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9278015	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9278016	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9278019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9278027	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9278028	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9278034	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9278036	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9278038	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9278039	0.83[EUR][1000 genomes]
rs9278040	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9278043	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9278044	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9278045	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9278046	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9278049	0.94[AMR][1000 genomes];0.93[EUR][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	nsv830634	chr6:33161217-33330745	Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv830635	chr6:33238005-33413787	Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
3	nsv969386	chr6:33297665-33325116	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33313800-33322000	Weak transcription	Primary T cells from cord blood	blood
2	chr6:33317800-33323000	Weak transcription	Stomach Mucosa	stomach
3	chr6:33321200-33324000	Weak transcription	H9 Cell Line	embryonic stem cell

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