Variant report

Variant	rs71587999
Chromosome Location	chr5:128288376-128288377
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs13166325	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13190393	0.82[ASN][1000 genomes]
rs17616784	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1898543	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1898544	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1898549	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526196	0.82[ASN][1000 genomes]
rs2526201	0.82[ASN][1000 genomes]
rs2526202	0.82[ASN][1000 genomes]
rs2526209	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526210	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526211	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526212	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526213	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526214	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526225	0.82[AMR][1000 genomes]
rs2526239	0.82[AMR][1000 genomes]
rs2526240	0.82[ASN][1000 genomes]
rs2526241	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2526243	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577399	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577402	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577403	0.82[ASN][1000 genomes]
rs2577445	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577446	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577504	0.82[ASN][1000 genomes]
rs2577506	0.82[ASN][1000 genomes]
rs2577507	0.82[ASN][1000 genomes]
rs2577508	0.82[ASN][1000 genomes]
rs2577509	0.82[ASN][1000 genomes]
rs2577510	0.82[ASN][1000 genomes]
rs2577511	0.82[ASN][1000 genomes]
rs2577512	0.82[ASN][1000 genomes]
rs2577513	0.82[ASN][1000 genomes]
rs2577514	0.82[ASN][1000 genomes]
rs2577528	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577529	0.82[AMR][1000 genomes]
rs2577530	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577533	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577534	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577535	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577537	0.81[AMR][1000 genomes]
rs2577538	0.81[AMR][1000 genomes]
rs2577555	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577556	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577560	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577561	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2577562	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34075274	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34299037	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34683252	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34813132	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34831887	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35044703	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35388070	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35696888	0.80[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35767068	0.82[ASN][1000 genomes]
rs62391271	0.82[ASN][1000 genomes]
rs62391272	0.82[ASN][1000 genomes]
rs62391297	0.84[AMR][1000 genomes]
rs71587998	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71588000	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71592877	0.84[AMR][1000 genomes]
rs7349831	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462443	chr5:128172808-128298437	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv599700	chr5:128172808-128298437	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv882839	chr5:128205828-128390167	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv882840	chr5:128205828-128428962	Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:128287800-128288400	Enhancers	Placenta Amnion	Placenta Amnion

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