Variant report

Variant	rs7023928
Chromosome Location	chr9:94360716-94360717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10992008	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10992015	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1319000	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4451437	0.81[ASN][1000 genomes]
rs4744080	0.81[ASN][1000 genomes]
rs55798203	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7020635	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7022528	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7023804	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7033293	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7849723	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9409623	0.90[AMR][1000 genomes];0.96[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	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr9:94352000-94365800	Weak transcription	Pancreas	Pancrea

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

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