Variant report

Variant	rs17085898
Chromosome Location	chr9:85567639-85567640
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12340476	0.81[TSI][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17085904	0.91[ASN][1000 genomes]
rs17672683	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17745151	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17745396	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17745511	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55642336	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs59684356	0.88[ASN][1000 genomes]
rs60164204	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61058280	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73651017	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73651019	0.92[AMR][1000 genomes];0.88[EUR][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	nsv1050771	chr9:85416931-85643417	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv893511	chr9:85495968-85833127	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv6585	chr9:85566659-85611489	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	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	chr9:85567400-85568000	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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