Variant report

Variant	rs7099184
Chromosome Location	chr10:44744492-44744493
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44744429..44746085-chr10:44747966..44749573,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11594522	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11597208	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11598523	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12570720	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12571719	0.87[ASN][1000 genomes]
rs12572886	0.85[ASN][1000 genomes]
rs12572910	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12573602	0.85[ASN][1000 genomes]
rs12573610	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17155437	0.81[AMR][1000 genomes]
rs17155635	0.91[ASN][1000 genomes]
rs17155733	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17389211	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17480411	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17480530	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17657853	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2224769	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3865770	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3952245	0.87[ASN][1000 genomes]
rs55769846	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs56043323	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56095445	0.81[AMR][1000 genomes]
rs56284808	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56366664	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs58189594	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6593403	0.84[AMR][1000 genomes]
rs7069262	0.82[AMR][1000 genomes]
rs7083765	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7086461	0.96[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72788727	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs72788733	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs72788737	0.87[ASN][1000 genomes]
rs72788749	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72788751	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72788758	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72788791	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs736136	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7894238	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7895640	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7896736	0.81[AMR][1000 genomes]
rs7897728	0.91[ASN][1000 genomes]
rs7899802	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7901938	0.91[ASN][1000 genomes]
rs7906240	0.85[ASN][1000 genomes]
rs7906368	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7913299	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs881828	0.85[ASN][1000 genomes]
rs9787462	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9787518	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv508579	chr10:44709770-44799256	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44738000-44745200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:44740400-44745000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr10:44741000-44745000	Weak transcription	Placenta	Placenta
4	chr10:44741400-44744800	Weak transcription	HepG2	liver

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