Variant report

Variant	rs10484547
Chromosome Location	chr6:29452774-29452775
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs16894919	0.94[ASN][1000 genomes]
rs16894964	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16894967	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16894969	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17184114	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2066951	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2073148	0.82[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2107189	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3025657	0.84[ASN][1000 genomes]
rs3025669	0.84[ASN][1000 genomes]
rs57396831	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58008302	0.84[ASN][1000 genomes]
rs58211986	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs60219685	0.84[ASN][1000 genomes]
rs6907104	0.80[ASN][1000 genomes]
rs6908631	0.84[ASN][1000 genomes]
rs6913746	0.81[ASN][1000 genomes]
rs6920668	0.84[ASN][1000 genomes]
rs6925408	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925744	0.90[ASN][1000 genomes]
rs6925869	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6931702	0.84[ASN][1000 genomes]
rs6933331	0.84[ASN][1000 genomes]
rs72500877	0.90[ASN][1000 genomes]
rs73402748	0.84[ASN][1000 genomes]
rs73402770	0.84[ASN][1000 genomes]
rs73402788	0.81[ASN][1000 genomes]
rs7739905	0.84[ASN][1000 genomes]
rs7739937	0.92[ASN][1000 genomes]
rs9468551	0.83[ASN][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	esv3424039	chr6:29439297-29504564	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv883528	chr6:29447724-29494897	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	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	chr6:29452200-29457000	Weak transcription	Liver	Liver

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