Variant report

Variant	rs9356308
Chromosome Location	chr6:165355357-165355358
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs4515355	0.82[EUR][1000 genomes]
rs6919089	1.00[EUR][1000 genomes]
rs6919144	0.95[EUR][1000 genomes]
rs6939583	0.95[EUR][1000 genomes]
rs6942200	0.95[EUR][1000 genomes]
rs73247835	0.95[EUR][1000 genomes]
rs9347051	0.85[EUR][1000 genomes]
rs9347950	0.95[EUR][1000 genomes]
rs9347953	0.95[EUR][1000 genomes]
rs9365815	0.95[EUR][1000 genomes]
rs9365826	0.95[EUR][1000 genomes]
rs9365837	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9365838	0.85[EUR][1000 genomes]
rs9457018	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv605232	chr6:164994771-165401154	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv886925	chr6:165319631-165705488	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr6:165350800-165356200	Weak transcription	Placenta	Placenta
2	chr6:165355200-165355400	ZNF genes & repeats	Aorta	Aorta

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

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