Variant report

Variant	rs1716726
Chromosome Location	chr3:60695507-60695508
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11130780	1.00[CEU][hapmap]
rs11921025	1.00[CEU][hapmap]
rs11923899	1.00[CEU][hapmap]
rs11926456	1.00[CEU][hapmap]
rs11928674	1.00[CEU][hapmap]
rs13321532	1.00[CEU][hapmap]
rs17063781	1.00[CEU][hapmap]
rs1716723	0.89[AFR][1000 genomes]
rs1735463	0.87[AFR][1000 genomes]
rs4393862	1.00[CEU][hapmap]
rs62251537	0.82[AFR][1000 genomes]
rs6446150	1.00[CEU][hapmap]
rs6772346	0.82[AFR][1000 genomes]
rs6797892	1.00[CEU][hapmap]
rs72875002	0.82[AFR][1000 genomes]
rs7618351	1.00[CEU][hapmap];0.82[AFR][1000 genomes]
rs7636178	1.00[CEU][hapmap]
rs7638754	1.00[CEU][hapmap]
rs7641604	1.00[CEU][hapmap]
rs9311772	1.00[CEU][hapmap];0.83[AFR][1000 genomes]
rs9311773	1.00[CEU][hapmap]
rs9811304	1.00[CEU][hapmap]
rs9816956	0.82[AFR][1000 genomes]
rs9818734	1.00[CEU][hapmap]
rs9824756	1.00[CEU][hapmap]
rs9826128	1.00[CEU][hapmap]
rs9827312	1.00[CEU][hapmap]
rs9827340	1.00[CEU][hapmap]
rs9828898	1.00[CEU][hapmap]
rs9838172	1.00[CEU][hapmap]
rs9838335	1.00[CEU][hapmap]
rs9838669	1.00[CEU][hapmap]
rs9839778	1.00[CEU][hapmap];0.81[AFR][1000 genomes]
rs9840473	1.00[CEU][hapmap]
rs9844497	1.00[CEU][hapmap]
rs9861551	1.00[CEU][hapmap];0.80[AFR][1000 genomes]
rs9861707	1.00[CEU][hapmap];0.82[AFR][1000 genomes]
rs9866844	1.00[CEU][hapmap]
rs9868891	1.00[CEU][hapmap]
rs9874852	0.82[AFR][1000 genomes]
rs9875027	0.82[AFR][1000 genomes]
rs9876876	1.00[CEU][hapmap]
rs9878248	1.00[CEU][hapmap]
rs9881065	1.00[CEU][hapmap];0.82[AFR][1000 genomes]
rs9882477	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:60694800-60695600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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