Variant report

Variant	rs60927673
Chromosome Location	chr10:116936636-116936637
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10399963	1.00[EUR][1000 genomes]
rs10400160	1.00[EUR][1000 genomes]
rs10466204	1.00[EUR][1000 genomes]
rs10885652	1.00[EUR][1000 genomes]
rs10885665	1.00[EUR][1000 genomes]
rs11197025	1.00[EUR][1000 genomes]
rs11197057	1.00[EUR][1000 genomes]
rs11197058	1.00[EUR][1000 genomes]
rs11197060	1.00[EUR][1000 genomes]
rs11197061	1.00[EUR][1000 genomes]
rs11197067	1.00[EUR][1000 genomes]
rs11197070	1.00[EUR][1000 genomes]
rs11197082	1.00[EUR][1000 genomes]
rs11197089	1.00[EUR][1000 genomes]
rs11197090	1.00[EUR][1000 genomes]
rs11197092	1.00[EUR][1000 genomes]
rs11197096	1.00[EUR][1000 genomes]
rs11197097	1.00[EUR][1000 genomes]
rs11197104	1.00[EUR][1000 genomes]
rs11197119	1.00[EUR][1000 genomes]
rs11197121	1.00[EUR][1000 genomes]
rs11819446	1.00[EUR][1000 genomes]
rs12241864	1.00[EUR][1000 genomes]
rs12245856	1.00[EUR][1000 genomes]
rs12248612	1.00[EUR][1000 genomes]
rs12248846	1.00[EUR][1000 genomes]
rs12252344	1.00[EUR][1000 genomes]
rs12255157	1.00[EUR][1000 genomes]
rs12264153	1.00[EUR][1000 genomes]
rs12267097	1.00[EUR][1000 genomes]
rs13376959	1.00[EUR][1000 genomes]
rs2197305	1.00[EUR][1000 genomes]
rs2252627	1.00[EUR][1000 genomes]
rs28564357	1.00[EUR][1000 genomes]
rs28842563	1.00[EUR][1000 genomes]
rs56866557	1.00[EUR][1000 genomes]
rs57423028	1.00[EUR][1000 genomes]
rs58042685	1.00[EUR][1000 genomes]
rs7070487	1.00[EUR][1000 genomes]
rs7074608	1.00[EUR][1000 genomes]
rs7077627	1.00[EUR][1000 genomes]
rs7077957	1.00[EUR][1000 genomes]
rs7078359	1.00[EUR][1000 genomes]
rs7082007	1.00[EUR][1000 genomes]
rs7082592	1.00[EUR][1000 genomes]
rs7085221	1.00[EUR][1000 genomes]
rs7097441	1.00[EUR][1000 genomes]
rs7098585	1.00[EUR][1000 genomes]
rs73363470	1.00[EUR][1000 genomes]
rs74159822	1.00[EUR][1000 genomes]
rs74159823	1.00[EUR][1000 genomes]
rs74159827	1.00[EUR][1000 genomes]
rs7893964	1.00[EUR][1000 genomes]
rs7894112	1.00[EUR][1000 genomes]
rs7896027	1.00[EUR][1000 genomes]
rs7897375	1.00[EUR][1000 genomes]
rs7899382	1.00[EUR][1000 genomes]
rs7899771	1.00[EUR][1000 genomes]
rs7900110	1.00[EUR][1000 genomes]
rs7902966	1.00[EUR][1000 genomes]
rs7906551	1.00[EUR][1000 genomes]
rs7907668	1.00[EUR][1000 genomes]
rs7908005	1.00[EUR][1000 genomes]
rs7910204	1.00[EUR][1000 genomes]
rs7913288	1.00[EUR][1000 genomes]
rs7917672	1.00[EUR][1000 genomes]
rs7918291	1.00[EUR][1000 genomes]
rs7920152	1.00[EUR][1000 genomes]
rs7920260	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3435429	chr10:116394152-117006347	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv831998	chr10:116847998-116969618	Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv869279	chr10:116884639-117032437	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv868940	chr10:116933802-117032437	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116926600-116951400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:116932400-116940400	Weak transcription	Aorta	Aorta

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