Variant report

Variant	rs10433823
Chromosome Location	chr4:21821848-21821849
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10006961	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10017728	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10034770	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10805229	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11736403	0.89[EUR][1000 genomes]
rs12500976	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12501059	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12508810	0.84[EUR][1000 genomes]
rs13102807	0.80[EUR][1000 genomes]
rs13108475	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13109215	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13122692	0.87[EUR][1000 genomes]
rs13147399	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1398830	0.90[EUR][1000 genomes]
rs1513572	0.88[EUR][1000 genomes]
rs16871968	0.87[EUR][1000 genomes]
rs17507672	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1841189	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1913327	0.83[EUR][1000 genomes]
rs2175783	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2323127	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28635318	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28726212	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35259948	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4434239	0.89[EUR][1000 genomes]
rs4470613	0.89[EUR][1000 genomes]
rs4696984	0.89[EUR][1000 genomes]
rs4697241	0.85[EUR][1000 genomes]
rs56318309	0.83[ASN][1000 genomes]
rs56703551	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6448092	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6448093	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6848840	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7654180	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7671494	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7696243	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7696754	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs921380	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs925574	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs925575	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs966922	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9985790	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[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	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	nsv1005221	chr4:21786702-21822000	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21821200-21829000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:21821800-21822600	Enhancers	Fetal Lung	lung

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