Variant report

Variant	rs17168064
Chromosome Location	chr7:14342940-14342941
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10950517	0.85[ASW][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes]
rs11982440	0.90[AMR][1000 genomes]
rs16878125	0.83[ASW][hapmap];1.00[TSI][hapmap]
rs17168050	0.96[YRI][hapmap]
rs4483055	1.00[TSI][hapmap]
rs62443937	0.83[AMR][1000 genomes]
rs6953240	1.00[EUR][1000 genomes]
rs6960014	0.85[ASW][hapmap];0.96[YRI][hapmap]
rs6975629	1.00[TSI][hapmap]
rs73281232	1.00[EUR][1000 genomes]
rs969689	0.96[YRI][hapmap]

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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv606280	chr7:14327966-14352001	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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