Variant report

Variant	rs13009581
Chromosome Location	chr2:116264610-116264611
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1037205	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10496494	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10496496	0.81[EUR][1000 genomes]
rs10496497	0.81[EUR][1000 genomes]
rs11123306	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11123307	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11690107	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12618777	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12990043	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12990349	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12997176	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13002613	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1375144	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1448456	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1530689	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1584400	0.80[EUR][1000 genomes]
rs1584401	0.80[EUR][1000 genomes]
rs1597189	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1597193	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1712000	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1712002	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1839133	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2121998	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2421104	0.81[EUR][1000 genomes]
rs35511048	0.81[EUR][1000 genomes]
rs4383330	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4849398	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4849399	0.80[EUR][1000 genomes]
rs4849400	0.80[EUR][1000 genomes]
rs6732466	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6741692	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67984587	0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014859	chr2:116196951-116938584	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:116264400-116264800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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