Variant report

Variant	rs9832396
Chromosome Location	chr3:79354187-79354188
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11127642	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11918896	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs12629261	0.89[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs12629799	0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12635896	0.80[JPT][hapmap]
rs12638565	0.82[ASN][1000 genomes]
rs13067596	0.80[JPT][hapmap]
rs13073607	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs13084290	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs1387668	0.89[ASN][1000 genomes]
rs1489844	0.86[CHB][hapmap];0.93[JPT][hapmap]
rs1489849	0.87[JPT][hapmap]
rs1489850	0.89[CHB][hapmap];0.89[CHD][hapmap];0.90[JPT][hapmap]
rs1565345	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs17395749	0.89[ASN][1000 genomes]
rs2130377	0.89[CHB][hapmap];0.80[JPT][hapmap]
rs57012643	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6548616	0.87[JPT][hapmap]
rs6782763	0.89[CHB][hapmap];0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs6785230	0.90[ASN][1000 genomes]
rs6788829	0.89[CHB][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs6788970	0.81[ASN][1000 genomes]
rs6801558	0.89[CHB][hapmap];0.83[CHD][hapmap];0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs73110997	0.90[ASN][1000 genomes]
rs73112706	0.89[ASN][1000 genomes]
rs73122554	0.89[ASN][1000 genomes]
rs73122569	0.89[ASN][1000 genomes]
rs73122578	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73122579	0.86[ASN][1000 genomes]
rs73122586	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73122590	0.86[ASN][1000 genomes]
rs73122600	0.84[ASN][1000 genomes]
rs73125241	0.81[ASN][1000 genomes]
rs73125242	0.81[ASN][1000 genomes]
rs73125244	0.81[ASN][1000 genomes]
rs73125248	0.81[ASN][1000 genomes]
rs7610397	0.89[CHB][hapmap];0.89[CHD][hapmap];0.93[JPT][hapmap]
rs7618575	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs902164	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs964137	0.91[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9842630	0.80[JPT][hapmap]
rs9855638	0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763281	chr3:79246361-79489765	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv460727	chr3:79264611-79406519	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv590736	chr3:79264611-79406519	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv460730	chr3:79286801-79411014	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv590737	chr3:79286801-79411014	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	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	chr3:79348800-79356000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:79351600-79357400	Weak transcription	Fetal Heart	heart

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