Variant report

Variant	rs9357918
Chromosome Location	chr6:56296009-56296010
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1547625	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17825773	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58705220	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs594435	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs606894	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs607271	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs656550	0.89[ASN][1000 genomes]
rs656988	0.89[ASN][1000 genomes]
rs657057	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6911307	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6911502	0.87[ASN][1000 genomes]
rs6914325	0.83[ASN][1000 genomes]
rs6916287	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9349822	0.83[ASN][1000 genomes]
rs9396210	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9396211	0.84[ASN][1000 genomes]
rs9464388	0.81[EUR][1000 genomes];0.94[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	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv830666	chr6:56243743-56419599	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv965727	chr6:56294729-56298343	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 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	chr6:56295800-56297200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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