Variant report

Variant	rs6533428
Chromosome Location	chr4:110321074-110321075
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:110308992..110311628-chr4:110320661..110323611,2	K562	blood:

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10000545	0.84[ASN][1000 genomes]
rs10002595	0.84[ASN][1000 genomes]
rs10005355	0.80[ASN][1000 genomes]
rs10155127	0.80[ASN][1000 genomes]
rs10516558	0.80[ASN][1000 genomes]
rs11098033	0.95[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11098035	0.86[ASN][1000 genomes]
rs11929713	0.80[ASN][1000 genomes]
rs11933971	0.84[ASN][1000 genomes]
rs11934486	0.94[ASN][1000 genomes]
rs11935440	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11935629	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11938593	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11941344	0.84[ASN][1000 genomes]
rs11942140	0.94[ASN][1000 genomes]
rs11942858	0.84[ASN][1000 genomes]
rs11942928	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11943384	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11943430	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11944375	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11944427	0.90[ASN][1000 genomes]
rs11944659	0.94[ASN][1000 genomes]
rs12639832	0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12640049	0.94[ASN][1000 genomes]
rs12640161	0.86[ASN][1000 genomes]
rs12642304	0.80[ASN][1000 genomes]
rs12643055	0.80[ASN][1000 genomes]
rs12643844	0.80[ASN][1000 genomes]
rs12644055	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12647695	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12648138	0.88[ASN][1000 genomes]
rs12648965	0.80[ASN][1000 genomes]
rs12650654	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12650873	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13103034	0.84[ASN][1000 genomes]
rs13123618	0.84[ASN][1000 genomes]
rs13128124	0.80[ASN][1000 genomes]
rs13134239	0.80[ASN][1000 genomes]
rs13141701	0.80[ASN][1000 genomes]
rs13142698	0.86[ASN][1000 genomes]
rs13143825	0.80[ASN][1000 genomes]
rs13145066	0.80[ASN][1000 genomes]
rs1509314	0.82[ASN][1000 genomes]
rs1509315	0.84[ASN][1000 genomes]
rs17040410	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17040436	0.84[ASN][1000 genomes]
rs17040439	0.84[ASN][1000 genomes]
rs17040461	0.84[ASN][1000 genomes]
rs17040488	0.80[ASN][1000 genomes]
rs17040510	0.80[ASN][1000 genomes]
rs28681408	0.80[ASN][1000 genomes]
rs34153531	0.80[ASN][1000 genomes]
rs34224638	0.80[ASN][1000 genomes]
rs34274964	0.80[ASN][1000 genomes]
rs34441811	0.84[ASN][1000 genomes]
rs34482781	0.84[ASN][1000 genomes]
rs34836476	0.84[ASN][1000 genomes]
rs35110951	0.80[ASN][1000 genomes]
rs35359830	0.84[ASN][1000 genomes]
rs35594044	0.80[ASN][1000 genomes]
rs35762958	0.80[ASN][1000 genomes]
rs35791246	0.84[ASN][1000 genomes]
rs35940980	0.80[ASN][1000 genomes]
rs36115572	0.80[ASN][1000 genomes]
rs3775962	0.80[ASN][1000 genomes]
rs60957336	0.84[ASN][1000 genomes]
rs61004219	0.84[ASN][1000 genomes]
rs61439452	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61553525	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6533429	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66642182	0.84[ASN][1000 genomes]
rs66667140	0.80[ASN][1000 genomes]
rs68041341	0.80[ASN][1000 genomes]
rs6812469	0.80[ASN][1000 genomes]
rs6815455	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6817954	0.81[ASN][1000 genomes]
rs6818911	0.80[ASN][1000 genomes]
rs6823032	0.80[ASN][1000 genomes]
rs6827006	0.80[ASN][1000 genomes]
rs6835683	0.80[ASN][1000 genomes]
rs6837199	0.88[ASN][1000 genomes]
rs6841198	0.80[ASN][1000 genomes]
rs6845371	0.80[ASN][1000 genomes]
rs6848452	0.88[ASN][1000 genomes]
rs6851517	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6852037	0.80[ASN][1000 genomes]
rs6856291	0.80[ASN][1000 genomes]
rs6856446	0.80[ASN][1000 genomes]
rs72896619	0.86[ASN][1000 genomes]
rs72896622	0.86[ASN][1000 genomes]
rs72896625	0.86[ASN][1000 genomes]
rs72896629	0.86[ASN][1000 genomes]
rs73838809	0.80[ASN][1000 genomes]
rs7436583	0.90[ASN][1000 genomes]
rs7436745	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7440371	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7440570	0.84[ASN][1000 genomes]
rs7675602	0.80[ASN][1000 genomes]
rs7679836	0.80[ASN][1000 genomes]
rs9985632	0.80[ASN][1000 genomes]
rs9994676	0.80[ASN][1000 genomes]
rs9994985	0.80[ASN][1000 genomes]
rs9999570	0.80[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	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv1799708	chr4:110309234-110333106	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110311200-110327800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:110311600-110331400	Weak transcription	HSMMtube	muscle
3	chr4:110317200-110321800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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