Variant report

Variant	rs6996727
Chromosome Location	chr8:52241068-52241069
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10099560	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10099699	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10110031	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11774588	0.84[AFR][1000 genomes]
rs11775272	0.84[AFR][1000 genomes]
rs11777020	0.96[AFR][1000 genomes]
rs11777663	0.96[AFR][1000 genomes]
rs11780044	0.92[AFR][1000 genomes]
rs11780126	0.96[AFR][1000 genomes]
rs11786018	0.96[AFR][1000 genomes]
rs11786053	0.96[AFR][1000 genomes]
rs11787165	0.96[AFR][1000 genomes]
rs1550235	1.00[EUR][1000 genomes]
rs16915981	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916019	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916021	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916023	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916024	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916051	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16916053	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2392834	0.96[AFR][1000 genomes]
rs2392835	0.96[AFR][1000 genomes]
rs6982243	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6984835	1.00[EUR][1000 genomes]
rs6985145	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6985579	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6986409	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6986594	1.00[EUR][1000 genomes]
rs6988739	1.00[EUR][1000 genomes]
rs6991317	1.00[EUR][1000 genomes]
rs6992306	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6993031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7010098	0.92[AFR][1000 genomes]
rs7818297	1.00[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	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv948338	chr8:52060314-52368754	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv890895	chr8:52190571-52615191	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:52238400-52241200	Weak transcription	Left Ventricle	heart
2	chr8:52240800-52245000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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