Variant report

Variant	rs13015726
Chromosome Location	chr2:212044685-212044686
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10168717	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176880	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10177360	0.97[ASN][1000 genomes]
rs10932369	0.97[ASN][1000 genomes]
rs11681093	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12105101	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12105447	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12105448	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12620896	0.81[EUR][1000 genomes]
rs13009135	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1344906	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1370611	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1370612	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1370613	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1437912	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1837054	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1837055	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1866196	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2164839	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2371169	0.97[ASN][1000 genomes]
rs2887949	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34684280	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35259140	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35647425	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36018701	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4271704	0.95[ASN][1000 genomes]
rs4422100	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4591289	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4672606	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4673587	0.97[ASN][1000 genomes]
rs4673588	0.97[ASN][1000 genomes]
rs4673589	0.97[ASN][1000 genomes]
rs57547487	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62178182	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62178183	0.97[ASN][1000 genomes]
rs62179779	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6435608	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6435609	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6714948	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6716813	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6720898	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6720925	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6726901	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6744625	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7572040	0.95[ASN][1000 genomes]
rs7575042	0.97[ASN][1000 genomes]
rs7575077	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv834521	chr2:211918881-212057872	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv875774	chr2:212016056-212047120	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv875775	chr2:212021755-212047120	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212039000-212045800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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