Variant report

Variant	rs62313056
Chromosome Location	chr4:91710846-91710847
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11097265	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17017577	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17247845	0.83[ASN][1000 genomes]
rs2123954	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2271591	0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3733453	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3733455	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62309559	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs62311071	0.81[ASN][1000 genomes]
rs62311072	0.83[ASN][1000 genomes]
rs62311076	0.81[ASN][1000 genomes]
rs62311111	0.81[ASN][1000 genomes]
rs62311114	0.81[ASN][1000 genomes]
rs62311118	0.84[ASN][1000 genomes]
rs62311119	0.86[ASN][1000 genomes]
rs62311125	0.81[ASN][1000 genomes]
rs62312977	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62312980	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312983	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312984	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312985	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312986	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312987	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312992	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312994	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62312997	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62313022	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62313025	0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62313055	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62313057	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62313058	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62314424	0.84[ASN][1000 genomes]
rs62314427	0.88[ASN][1000 genomes]
rs62314446	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6841566	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs720327	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72663610	0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs72663613	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72663663	0.81[ASN][1000 genomes]
rs7681018	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv534470	chr4:91342219-91842807	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv428766	chr4:91618397-91768647	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv879552	chr4:91691313-91729462	Enhancers Active TSS Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
5	nsv879553	chr4:91691313-91868576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv879554	chr4:91692287-91731886	Enhancers Weak transcription Active TSS ZNF genes & repeats	lncRNA	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	chr4:91700400-91713000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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