Variant report

Variant	rs11206663
Chromosome Location	chr1:56239599-56239600
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1165490	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1165491	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1165493	0.86[AFR][1000 genomes]
rs1165494	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1165495	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1165496	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1165498	0.87[AFR][1000 genomes]
rs1165502	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1165508	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1165509	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1183209	0.87[AFR][1000 genomes]
rs12095642	0.82[EUR][1000 genomes]
rs1926909	0.80[EUR][1000 genomes]
rs2767499	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2767500	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2819484	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs749330	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv829926	chr1:56188492-56360745	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a
2	nsv546304	chr1:56195659-56240015	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56237800-56239600	Enhancers	Fetal Lung	lung
2	chr1:56239200-56239600	Enhancers	NHLF	lung

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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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