Variant report

Variant	rs9493386
Chromosome Location	chr6:132910567-132910568
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs2788953	1.00[EUR][1000 genomes]
rs58707062	1.00[EUR][1000 genomes]
rs6901217	1.00[EUR][1000 genomes]
rs6919457	1.00[EUR][1000 genomes]
rs6921065	1.00[EUR][1000 genomes]
rs6929361	1.00[EUR][1000 genomes]
rs6929722	1.00[EUR][1000 genomes]
rs6929875	1.00[EUR][1000 genomes]
rs6934675	1.00[EUR][1000 genomes]
rs6935405	1.00[EUR][1000 genomes]
rs6936245	1.00[EUR][1000 genomes]
rs6936426	1.00[EUR][1000 genomes]
rs6942075	1.00[EUR][1000 genomes]
rs7745091	1.00[EUR][1000 genomes]
rs7745417	1.00[EUR][1000 genomes]
rs7751015	1.00[EUR][1000 genomes]
rs7751258	1.00[EUR][1000 genomes]
rs7754662	1.00[EUR][1000 genomes]
rs7765354	1.00[EUR][1000 genomes]
rs7766824	1.00[EUR][1000 genomes]
rs7770893	1.00[EUR][1000 genomes]
rs7772457	1.00[EUR][1000 genomes]
rs7772611	1.00[EUR][1000 genomes]
rs7772758	1.00[EUR][1000 genomes]
rs9483483	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132907000-132914800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr6:132908000-132910800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr6:132908000-132911200	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr6:132910200-132910600	Weak transcription	Pancreas	Pancrea
5	chr6:132910400-132911200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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