Variant report

Variant	rs73145345
Chromosome Location	chr3:89598696-89598697
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1080592	0.93[EUR][1000 genomes]
rs12629165	0.86[EUR][1000 genomes]
rs12629758	0.92[EUR][1000 genomes]
rs12631313	0.86[EUR][1000 genomes]
rs12633325	0.93[EUR][1000 genomes]
rs12634269	0.85[EUR][1000 genomes]
rs12634341	0.86[EUR][1000 genomes]
rs12636710	0.86[EUR][1000 genomes]
rs17026990	0.92[EUR][1000 genomes]
rs17801380	0.80[EUR][1000 genomes]
rs2048518	0.90[EUR][1000 genomes]
rs2048519	0.91[EUR][1000 genomes]
rs2048520	0.91[EUR][1000 genomes]
rs2048521	0.91[EUR][1000 genomes]
rs2069183	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2117138	0.86[EUR][1000 genomes]
rs2346840	0.86[EUR][1000 genomes]
rs3762717	0.86[EUR][1000 genomes]
rs73139121	0.80[EUR][1000 genomes]
rs73139127	0.80[EUR][1000 genomes]
rs73139129	0.80[EUR][1000 genomes]
rs73139133	0.82[EUR][1000 genomes]
rs73139134	0.81[EUR][1000 genomes]
rs73139135	0.86[EUR][1000 genomes]
rs73139139	0.86[EUR][1000 genomes]
rs73139144	0.86[EUR][1000 genomes]
rs73139147	0.86[EUR][1000 genomes]
rs73139148	0.85[EUR][1000 genomes]
rs73144998	0.91[EUR][1000 genomes]
rs73145303	0.85[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs73145304	0.94[EUR][1000 genomes]
rs73145305	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145307	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145309	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145310	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145312	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145316	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73145353	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73145357	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73146907	0.91[EUR][1000 genomes]
rs73146968	0.91[EUR][1000 genomes]
rs73146970	0.92[EUR][1000 genomes]
rs73146972	0.92[EUR][1000 genomes]
rs73149109	0.93[EUR][1000 genomes]
rs73149113	0.93[EUR][1000 genomes]
rs73149115	0.82[EUR][1000 genomes]
rs73153218	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7650466	0.86[EUR][1000 genomes]
rs819293	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907548	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs972030	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008018	chr3:89382031-90254063	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv536639	chr3:89382031-90254063	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1010932	chr3:89424428-90192503	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv590952	chr3:89493167-89727198	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1010021	chr3:89521983-90141988	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv530024	chr3:89548440-90304841	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv428743	chr3:89584946-89689096	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	3 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	chr3:89598200-89599000	Enhancers	Fetal Heart	heart

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