Variant report

Variant	rs9381792
Chromosome Location	chr6:49480162-49480163
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:49477846..49480791-chr6:49486673..49489629,2	MCF-7	breast:
2	chr6:49479989..49482907-chr6:49513831..49515796,2	K562	blood:
3	chr6:49477015..49478603-chr6:49479650..49481514,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10755760	0.89[AFR][1000 genomes]
rs12190131	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12214753	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1480611	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1480612	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1480613	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1480614	0.94[AFR][1000 genomes]
rs1480615	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1947861	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2061972	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2061973	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2127754	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2127755	0.89[AFR][1000 genomes]
rs2396911	0.89[AFR][1000 genomes]
rs2498470	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2498471	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2498472	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2501969	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2501970	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2501971	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4367370	0.89[AFR][1000 genomes]
rs4715134	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6942364	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7453050	0.89[AFR][1000 genomes]
rs7740682	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7757014	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9296618	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9357618	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9367357	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9369904	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9381791	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9395499	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9395500	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9463489	0.88[AFR][1000 genomes]
rs9463491	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9463492	0.90[AFR][1000 genomes]
rs9463493	0.94[AFR][1000 genomes]
rs9473567	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9473568	0.86[AFR][1000 genomes]
rs9473582	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49475200-49481000	Weak transcription	Stomach Mucosa	stomach
2	chr6:49478200-49480200	Weak transcription	HepG2	liver
3	chr6:49479200-49481000	Enhancers	Liver	Liver

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