Variant report

Variant	rs12545245
Chromosome Location	chr8:63900084-63900085
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10464903	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10464904	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10464905	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10957265	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10957266	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10957268	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10957269	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10957270	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12056582	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12541047	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12541993	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12543020	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12543961	0.94[AMR][1000 genomes]
rs12545230	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12547772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12547848	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12548729	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12549172	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12675369	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12676348	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12678042	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12678214	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12681795	0.81[EUR][1000 genomes]
rs12682385	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16929963	0.96[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16929988	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1963949	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3758147	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4534128	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4737621	0.94[AMR][1000 genomes]
rs4737626	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4737627	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4739028	0.92[AMR][1000 genomes]
rs4739031	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4739032	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4739046	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4739047	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73684520	0.83[EUR][1000 genomes]
rs7818582	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs930840	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9643545	0.83[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	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv6227	chr8:63892087-63936952	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63896400-63901000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr8:63896600-63900600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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