Variant report

Variant	rs9390164
Chromosome Location	chr6:100700069-100700070
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:15)

rs_ID	r²[population]
rs2224068	0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6929694	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8180552	0.97[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9321991	0.85[AMR][1000 genomes]
rs9373411	0.90[AMR][1000 genomes]
rs9376805	0.85[AMR][1000 genomes]
rs9376810	0.92[AMR][1000 genomes]
rs9376821	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9376845	0.90[AMR][1000 genomes]
rs9376866	0.85[AMR][1000 genomes]
rs9386059	0.90[AMR][1000 genomes]
rs9386067	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9390163	0.97[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9390190	0.90[AMR][1000 genomes]
rs9399484	0.90[AMR][1000 genomes];0.85[ASN][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	nsv604262	chr6:100661336-100701917	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	1 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	chr6:100695200-100705600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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

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