Variant report

Variant	rs9834708
Chromosome Location	chr3:85718170-85718171
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10049108	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11705717	1.00[ASN][1000 genomes]
rs12714636	0.91[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12714640	1.00[CHD][hapmap];0.95[MKK][hapmap]
rs13059866	1.00[CHD][hapmap];0.95[MKK][hapmap]
rs13061681	0.91[CEU][hapmap];1.00[YRI][hapmap]
rs13076821	1.00[CEU][hapmap]
rs13077660	1.00[CHD][hapmap];0.91[MKK][hapmap]
rs13078807	1.00[CHD][hapmap];0.95[MKK][hapmap]
rs13083873	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13087042	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13096280	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13097865	1.00[YRI][hapmap]
rs13098327	0.81[MKK][hapmap]
rs13101056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1375547	0.91[MKK][hapmap]
rs1448602	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1448608	1.00[CEU][hapmap]
rs1449395	0.91[CEU][hapmap]
rs1449396	0.91[CEU][hapmap]
rs35326689	0.85[EUR][1000 genomes]
rs4129299	1.00[CEU][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4306872	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4464471	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7355953	1.00[CHD][hapmap];0.90[MEX][hapmap];0.95[MKK][hapmap];0.94[TSI][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7611991	0.88[CEU][hapmap];0.94[TSI][hapmap];0.91[EUR][1000 genomes]
rs7612213	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7620339	1.00[CHD][hapmap]
rs7622475	1.00[CHD][hapmap];0.95[MKK][hapmap]
rs7628948	1.00[CHD][hapmap];0.91[MKK][hapmap]
rs7640660	1.00[CHD][hapmap]
rs7643091	0.91[CEU][hapmap]
rs9309985	0.91[CEU][hapmap]
rs9309986	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9812845	0.91[CEU][hapmap];0.97[TSI][hapmap]
rs9813436	0.95[CEU][hapmap];1.00[YRI][hapmap]
rs9818122	1.00[CHD][hapmap]
rs9819476	0.96[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs9825885	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9840636	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9841144	1.00[CHD][hapmap]
rs9844512	1.00[CHD][hapmap];0.91[MKK][hapmap]
rs9852859	0.95[MKK][hapmap]
rs9858244	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
2	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
3	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1010541	chr3:85505839-85870597	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv536625	chr3:85505839-85870597	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv877104	chr3:85646426-85737646	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85712800-85719600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:85714800-85719800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:85717800-85718400	Weak transcription	Brain Hippocampus Middle	brain

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