Variant report

Variant	rs7000020
Chromosome Location	chr8:63825220-63825221
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10090886	0.88[EUR][1000 genomes]
rs10093212	0.91[EUR][1000 genomes]
rs10100456	0.80[EUR][1000 genomes]
rs10808728	0.85[EUR][1000 genomes]
rs10957253	0.90[EUR][1000 genomes]
rs11992351	0.91[EUR][1000 genomes]
rs12679222	0.80[EUR][1000 genomes]
rs13272238	0.91[EUR][1000 genomes]
rs1378522	0.91[EUR][1000 genomes]
rs1378523	0.83[EUR][1000 genomes]
rs1455574	0.88[EUR][1000 genomes]
rs17273584	0.83[EUR][1000 genomes]
rs1869729	0.91[EUR][1000 genomes]
rs1869730	0.91[EUR][1000 genomes]
rs1869731	0.91[EUR][1000 genomes]
rs1869732	0.91[EUR][1000 genomes]
rs2353388	0.86[EUR][1000 genomes]
rs35185274	0.83[EUR][1000 genomes]
rs35478421	0.83[EUR][1000 genomes]
rs35583011	0.83[EUR][1000 genomes]
rs4237056	0.91[EUR][1000 genomes]
rs4237058	0.91[EUR][1000 genomes]
rs4237059	0.91[EUR][1000 genomes]
rs4237060	0.91[EUR][1000 genomes]
rs4237061	0.91[EUR][1000 genomes]
rs4276687	0.83[EUR][1000 genomes]
rs4284039	0.91[EUR][1000 genomes]
rs4292679	0.83[EUR][1000 genomes]
rs4352845	0.86[EUR][1000 genomes]
rs4360287	0.91[EUR][1000 genomes]
rs4368971	0.90[EUR][1000 genomes]
rs4374987	0.90[EUR][1000 genomes]
rs4376492	0.91[EUR][1000 genomes]
rs4412364	0.90[EUR][1000 genomes]
rs4413770	0.86[EUR][1000 genomes]
rs4434615	0.90[EUR][1000 genomes]
rs4466391	0.90[EUR][1000 genomes]
rs4478566	0.90[EUR][1000 genomes]
rs4504631	0.90[EUR][1000 genomes]
rs4509316	0.91[EUR][1000 genomes]
rs4521749	0.83[EUR][1000 genomes]
rs4573266	0.90[EUR][1000 genomes]
rs4593533	0.90[EUR][1000 genomes]
rs4626587	0.90[EUR][1000 genomes]
rs4739021	0.91[EUR][1000 genomes]
rs6998501	0.90[EUR][1000 genomes]
rs6999604	0.85[EUR][1000 genomes]
rs7000012	0.85[EUR][1000 genomes]
rs7463670	0.91[EUR][1000 genomes]
rs7830289	0.91[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	nsv831341	chr8:63658694-63852213	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63824800-63825400	Enhancers	Placenta	Placenta

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