Variant report

Variant	rs66794762
Chromosome Location	chr5:107848477-107848478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10515390	0.88[EUR][1000 genomes]
rs11743896	0.90[EUR][1000 genomes]
rs11957210	0.89[EUR][1000 genomes]
rs35639200	0.90[EUR][1000 genomes]
rs4072596	0.90[EUR][1000 genomes]
rs4075651	0.90[EUR][1000 genomes]
rs4128455	0.90[EUR][1000 genomes]
rs55644441	0.90[EUR][1000 genomes]
rs55679052	0.91[EUR][1000 genomes]
rs55882634	0.90[EUR][1000 genomes]
rs56188359	0.90[EUR][1000 genomes]
rs58634108	0.90[EUR][1000 genomes]
rs59162280	0.89[EUR][1000 genomes]
rs61356246	0.89[EUR][1000 genomes]
rs62360000	0.92[EUR][1000 genomes]
rs62360002	0.93[EUR][1000 genomes]
rs62360003	0.92[EUR][1000 genomes]
rs62360007	0.91[EUR][1000 genomes]
rs62360009	0.91[EUR][1000 genomes]
rs62360010	0.89[EUR][1000 genomes]
rs62360012	0.89[EUR][1000 genomes]
rs62360043	0.89[EUR][1000 genomes]
rs67714081	0.90[EUR][1000 genomes]
rs6861718	0.92[EUR][1000 genomes]
rs72799320	0.91[EUR][1000 genomes]
rs72799326	0.89[EUR][1000 genomes]
rs7447596	0.82[ASN][1000 genomes]
rs7707077	0.90[EUR][1000 genomes]
rs7707136	0.90[EUR][1000 genomes]
rs7707794	0.90[EUR][1000 genomes]
rs7720364	0.90[EUR][1000 genomes]
rs7722651	0.90[EUR][1000 genomes]
rs7734836	0.90[EUR][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	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv882690	chr5:107834247-107954485	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 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	chr5:107848000-107853800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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