Variant report

Variant	rs1827591
Chromosome Location	chr4:21732186-21732187
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10006785	0.84[EUR][1000 genomes]
rs10012747	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10016234	0.84[EUR][1000 genomes]
rs10028323	0.99[ASN][1000 genomes]
rs10031539	1.00[CHB][hapmap];0.96[CHD][hapmap];0.83[JPT][hapmap]
rs10034603	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1040036	0.88[CEU][hapmap]
rs10516402	0.88[CEU][hapmap];0.87[TSI][hapmap]
rs10938858	0.89[CEU][hapmap];0.88[CHB][hapmap]
rs12498561	0.85[CEU][hapmap];0.88[CHB][hapmap]
rs12503736	0.89[CEU][hapmap];0.88[CHB][hapmap];0.95[TSI][hapmap]
rs12504827	0.81[CEU][hapmap]
rs12512316	0.81[CEU][hapmap]
rs12642992	0.89[CEU][hapmap]
rs12646630	1.00[CHB][hapmap];0.96[CHD][hapmap];0.83[JPT][hapmap]
rs1349383	0.92[CEU][hapmap]
rs1349384	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs1380270	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1459274	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1562815	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs168625	0.89[CEU][hapmap];0.88[CHB][hapmap]
rs17498679	1.00[CHB][hapmap];0.96[CHD][hapmap];0.83[JPT][hapmap]
rs17498715	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs1809267	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs1813583	0.89[CEU][hapmap]
rs1827590	0.99[ASN][1000 genomes]
rs1841185	0.89[CEU][hapmap];0.83[CHB][hapmap]
rs1841186	0.89[CEU][hapmap];0.83[CHB][hapmap]
rs1968778	0.89[CEU][hapmap];0.88[CHB][hapmap];0.95[TSI][hapmap]
rs1985182	0.96[ASN][1000 genomes]
rs2007970	0.88[CEU][hapmap];0.82[CHB][hapmap]
rs2007971	0.88[CEU][hapmap];0.87[CHB][hapmap]
rs2018175	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2063656	0.85[CEU][hapmap]
rs2063657	0.84[CEU][hapmap]
rs2063658	0.81[CEU][hapmap]
rs28667579	0.93[ASN][1000 genomes]
rs34833395	0.89[CEU][hapmap];0.83[CHB][hapmap];0.95[TSI][hapmap]
rs35609084	1.00[CHB][hapmap];0.96[CHD][hapmap];0.83[JPT][hapmap]
rs4101631	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4282162	0.85[CEU][hapmap];0.88[CHB][hapmap];0.95[TSI][hapmap]
rs4377576	0.89[CEU][hapmap];0.88[CHB][hapmap];0.93[TSI][hapmap]
rs4563486	0.89[CEU][hapmap];0.88[CHB][hapmap];0.95[TSI][hapmap]
rs6448069	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6448070	0.99[ASN][1000 genomes]
rs6448072	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6448073	0.99[ASN][1000 genomes]
rs6448075	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6840539	0.80[CEU][hapmap];0.82[CHB][hapmap]
rs6856781	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs7375384	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7378252	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7664617	0.85[CEU][hapmap];0.83[CHB][hapmap];0.84[TSI][hapmap]
rs9291430	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs966045	0.89[CEU][hapmap];0.83[CHB][hapmap];0.93[TSI][hapmap]
rs9884923	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap]
rs9994945	0.92[CEU][hapmap];0.87[CHB][hapmap]

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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv878751	chr4:21712050-21793807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region 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	chr4:21730600-21735600	Weak transcription	Colon Smooth Muscle	Colon

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