Variant report

Variant	rs13030747
Chromosome Location	chr2:178866494-178866495
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1020010	0.94[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10211367	0.85[ASN][1000 genomes]
rs10930820	0.91[ASN][1000 genomes]
rs11677176	0.86[EUR][1000 genomes]
rs11687117	0.84[EUR][1000 genomes]
rs11695452	0.86[EUR][1000 genomes]
rs12473461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12478277	0.86[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12618606	0.84[ASN][1000 genomes]
rs12621562	0.94[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1527286	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1527287	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1527293	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1534289	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1546813	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1554776	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17687590	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs17687668	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1821629	0.85[ASN][1000 genomes]
rs1836672	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1852496	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1852497	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1852499	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1852501	0.86[EUR][1000 genomes]
rs1852502	0.86[EUR][1000 genomes]
rs1982131	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1991994	0.91[ASN][1000 genomes]
rs2060490	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2060491	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2117738	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2117740	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2573079	0.92[EUR][1000 genomes]
rs2573087	0.84[EUR][1000 genomes]
rs2695107	0.81[EUR][1000 genomes]
rs2695728	0.84[EUR][1000 genomes]
rs2695739	0.81[EUR][1000 genomes]
rs4335982	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4567975	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4893994	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4893995	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62183411	0.84[EUR][1000 genomes]
rs62183412	0.84[EUR][1000 genomes]
rs62183413	0.92[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs62183443	0.85[EUR][1000 genomes]
rs62183445	0.86[EUR][1000 genomes]
rs6711886	0.83[EUR][1000 genomes]
rs6738831	0.86[EUR][1000 genomes]
rs6750869	0.88[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6758442	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6759109	0.84[EUR][1000 genomes]
rs744397	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs744398	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7570423	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7588973	0.86[EUR][1000 genomes]
rs764780	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs934568	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9679090	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533377	chr2:178718801-178963463	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1007579	chr2:178729330-178890946	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv875451	chr2:178748294-178953409	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv998304	chr2:178756380-178924378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv536056	chr2:178756380-178924378	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr2:178863600-178873400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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