Variant report

Variant	rs9463491
Chromosome Location	chr6:49475092-49475093
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10755760	0.92[AFR][1000 genomes]
rs12190131	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12214753	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1480611	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1480612	0.88[ASN][1000 genomes]
rs1480613	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1480614	0.91[AFR][1000 genomes]
rs1480615	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1947861	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2061972	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2061973	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2127754	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2127755	0.92[AFR][1000 genomes]
rs2396911	0.92[AFR][1000 genomes]
rs2498470	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2498471	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2498472	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2501969	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2501970	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2501971	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4367370	0.92[AFR][1000 genomes]
rs4715134	0.88[ASN][1000 genomes]
rs6942364	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7453050	0.89[AFR][1000 genomes]
rs7740682	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7757014	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9296618	0.88[ASN][1000 genomes]
rs9357618	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9367357	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9369904	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9381791	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9381792	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9395499	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395500	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9463489	0.91[AFR][1000 genomes]
rs9463492	0.93[AFR][1000 genomes]
rs9463493	0.91[AFR][1000 genomes]
rs9473567	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9473568	0.89[AFR][1000 genomes]
rs9473582	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024959	chr6:49290141-49652124	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1021136	chr6:49295037-49631278	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv885881	chr6:49439805-49575141	Weak transcription Bivalent Enhancer Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv3398270	chr6:49468042-49488082	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
5	esv3326724	chr6:49469324-49476170	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49473600-49475200	Enhancers	Stomach Mucosa	stomach
2	chr6:49474400-49475600	Enhancers	Liver	Liver
3	chr6:49474600-49475400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr6:49474800-49475400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr6:49475000-49478200	Enhancers	HepG2	liver

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