Variant report

Variant	rs6533426
Chromosome Location	chr4:110293437-110293438
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10000545	0.85[JPT][hapmap]
rs10002595	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs10005198	0.94[EUR][1000 genomes]
rs10007410	0.87[EUR][1000 genomes]
rs10016533	1.00[MEX][hapmap]
rs10028250	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10155127	0.85[JPT][hapmap]
rs10155246	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs11098033	0.90[CHD][hapmap];0.85[JPT][hapmap]
rs11098035	0.86[CHD][hapmap];0.85[JPT][hapmap]
rs11929713	0.82[JPT][hapmap]
rs11930655	0.82[JPT][hapmap]
rs11933172	1.00[CEU][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.90[TSI][hapmap];0.94[EUR][1000 genomes]
rs11939924	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11942140	0.87[AMR][1000 genomes]
rs11942291	0.85[JPT][hapmap]
rs11942858	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs11943384	0.82[JPT][hapmap]
rs11943430	0.85[JPT][hapmap]
rs12640049	0.87[AMR][1000 genomes]
rs12641197	0.89[EUR][1000 genomes]
rs12641272	0.88[EUR][1000 genomes]
rs12643055	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs12648138	0.85[JPT][hapmap]
rs12648965	0.81[CHD][hapmap]
rs12650654	0.90[CHD][hapmap];0.85[JPT][hapmap]
rs13103034	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs13104799	0.91[EUR][1000 genomes]
rs13113384	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13119700	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13123618	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs13126829	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13128445	0.85[MEX][hapmap]
rs13138833	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13142698	0.85[CHD][hapmap];1.00[MEX][hapmap]
rs13143825	0.85[JPT][hapmap]
rs13145066	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs1509314	0.85[JPT][hapmap]
rs1509315	0.85[JPT][hapmap]
rs1557804	0.89[EUR][1000 genomes]
rs17040436	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs17040439	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs17040461	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs17585970	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs17619262	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs17842269	0.89[EUR][1000 genomes]
rs1859144	0.90[EUR][1000 genomes]
rs1859146	0.89[EUR][1000 genomes]
rs1859147	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1981540	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1981541	0.89[EUR][1000 genomes]
rs2079108	0.94[EUR][1000 genomes]
rs2214377	0.89[EUR][1000 genomes]
rs2346014	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28374470	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28463999	0.89[EUR][1000 genomes]
rs28542804	0.91[EUR][1000 genomes]
rs28585579	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28628718	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28681408	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs28749845	0.94[EUR][1000 genomes]
rs4524460	0.94[EUR][1000 genomes]
rs6533434	1.00[MEX][hapmap]
rs6815455	0.85[JPT][hapmap]
rs6818911	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs6825928	1.00[CEU][hapmap];0.88[MEX][hapmap];0.83[TSI][hapmap]
rs6827985	0.94[EUR][1000 genomes]
rs6835683	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs6841133	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6841198	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs6841222	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6848452	0.82[AMR][1000 genomes]
rs6856291	0.85[JPT][hapmap]
rs7436583	0.90[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.82[AMR][1000 genomes]
rs7436745	0.90[CHD][hapmap];0.85[JPT][hapmap]
rs7440570	0.85[JPT][hapmap]
rs7665024	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7673595	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7673867	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7675344	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7675602	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs7680752	0.89[EUR][1000 genomes]
rs7680920	0.89[EUR][1000 genomes]
rs7684744	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7685787	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7687245	0.85[JPT][hapmap]
rs7694523	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7695754	1.00[CEU][hapmap]
rs7699247	0.84[EUR][1000 genomes]
rs876464	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9307329	0.89[EUR][1000 genomes]
rs9985632	0.81[CHD][hapmap];0.85[JPT][hapmap];0.88[MEX][hapmap]
rs9985964	0.85[JPT][hapmap]
rs9993228	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9994676	0.81[CHD][hapmap];0.85[JPT][hapmap]
rs9996165	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs9996432	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9996537	0.89[EUR][1000 genomes]
rs9996920	0.89[EUR][1000 genomes]
rs9999270	0.89[EUR][1000 genomes]
rs9999278	0.89[EUR][1000 genomes]
rs9999570	0.81[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap]
rs9999751	0.89[EUR][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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110291000-110294600	Weak transcription	HSMMtube	muscle
2	chr4:110292800-110297000	Weak transcription	Placenta	Placenta

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