Variant report

Variant	rs793660
Chromosome Location	chr6:24366277-24366278
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12527102	0.83[EUR][1000 genomes]
rs1629620	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2025033	0.88[EUR][1000 genomes]
rs2328820	0.80[EUR][1000 genomes]
rs4382236	0.87[EUR][1000 genomes]
rs6456608	0.84[EUR][1000 genomes]
rs714452	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7758878	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs793649	0.83[EUR][1000 genomes]
rs793650	0.81[EUR][1000 genomes]
rs793658	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs793659	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs793662	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs793663	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs793666	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs793694	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs793698	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs793699	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs793701	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs793703	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs811102	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs811103	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs811578	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9366569	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9467123	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9467124	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9467126	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9467134	0.86[EUR][1000 genomes]
rs9467135	0.81[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	nsv1026638	chr6:24347972-24475300	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 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	chr6:24363400-24376200	Weak transcription	HepG2	liver

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