Variant report

Variant	rs11679253
Chromosome Location	chr2:145503097-145503098
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10200647	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10203655	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10205995	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10432351	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10496966	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10928225	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10928226	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10928227	0.92[ASN][1000 genomes]
rs11674690	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11900456	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12104619	0.90[ASN][1000 genomes]
rs12471698	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12478142	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12611966	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12623452	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12991932	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12997597	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13003467	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13008442	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13015001	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13016064	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs13032840	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13413613	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1351734	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1365902	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1365905	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1384779	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1384783	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1427509	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1483491	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1483499	0.90[ASN][1000 genomes]
rs1529386	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1529387	0.88[ASN][1000 genomes]
rs1559961	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1559962	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1564697	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1896453	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1896454	0.90[ASN][1000 genomes]
rs1905347	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1994155	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2086748	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2195114	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2195115	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2254435	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2381651	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs35099259	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3856364	0.93[ASN][1000 genomes]
rs4271712	0.81[ASN][1000 genomes]
rs4458150	0.88[ASN][1000 genomes]
rs4471836	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4662231	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4662232	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4662393	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61440197	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6707047	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6728198	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6745079	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72991962	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7575857	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7579453	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7580571	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs900554	0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs958500	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs958501	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs980772	0.81[AMR][1000 genomes];0.92[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	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv834397	chr2:145439528-145608628	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145502800-145503200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:145502800-145503600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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