Variant report

Variant	rs17046703
Chromosome Location	chr4:166469186-166469187
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10017297	0.84[EUR][1000 genomes]
rs17046745	0.84[EUR][1000 genomes]
rs17046756	0.84[EUR][1000 genomes]
rs1914834	0.84[EUR][1000 genomes]
rs1914835	0.84[EUR][1000 genomes]
rs1914836	0.84[EUR][1000 genomes]
rs28391070	0.84[EUR][1000 genomes]
rs28487969	0.84[EUR][1000 genomes]
rs28583482	0.84[EUR][1000 genomes]
rs6819473	0.84[EUR][1000 genomes]
rs6831798	0.84[EUR][1000 genomes]
rs6855033	0.84[EUR][1000 genomes]
rs7658683	0.84[EUR][1000 genomes]
rs7694281	0.84[EUR][1000 genomes]
rs7694612	0.84[EUR][1000 genomes]
rs9992314	0.84[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	nsv508327	chr4:166424440-166475679	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv596052	chr4:166454826-166488615	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	1 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	chr4:166468600-166469200	Enhancers	Primary T killer memory cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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