Variant report

Variant	rs9472171
Chromosome Location	chr6:43930962-43930963
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs4382251	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4481426	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4714719	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6916540	0.82[ASN][1000 genomes]
rs7745183	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7745184	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs943075	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9462949	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9472170	0.94[AMR][1000 genomes];0.92[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	nsv931987	chr6:43624625-44350167	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:43923400-43932000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:43929800-43936600	Enhancers	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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