Variant report

Variant	rs11706897
Chromosome Location	chr3:155759612-155759613
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:15)

rs_ID	r²[population]
rs10936023	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11719280	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1817698	0.83[EUR][1000 genomes]
rs2087271	0.87[EUR][1000 genomes]
rs34533513	0.84[ASN][1000 genomes]
rs4680230	0.91[ASN][1000 genomes]
rs6441029	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6441030	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6441031	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6806441	0.98[ASN][1000 genomes]
rs6810368	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7643130	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs901862	0.86[EUR][1000 genomes]
rs9810320	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9875491	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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	nsv592084	chr3:155751484-155830578	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv521239	chr3:155755327-155762725	Weak transcription Enhancers Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv965225	chr3:155758196-155767076	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	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	chr3:155758000-155764800	Weak transcription	Right Atrium	heart

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

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