Variant report

Variant	rs72626932
Chromosome Location	chr3:68057966-68057967
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1351957	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140939	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140941	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140947	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17140948	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55780642	0.93[AMR][1000 genomes]
rs57457619	1.00[AMR][1000 genomes]
rs58063220	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59728287	0.81[AMR][1000 genomes]
rs60547129	0.93[AMR][1000 genomes]
rs61737909	1.00[AMR][1000 genomes]
rs61739210	1.00[AMR][1000 genomes]
rs73834808	0.86[AMR][1000 genomes]
rs73834809	0.93[AMR][1000 genomes]
rs73834814	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73834815	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs73834816	0.93[AMR][1000 genomes]
rs73834820	1.00[AMR][1000 genomes]
rs73834821	0.93[AMR][1000 genomes]
rs73834822	1.00[AMR][1000 genomes]
rs73834823	1.00[AMR][1000 genomes]
rs73834824	0.81[AMR][1000 genomes]
rs73834825	0.93[AMR][1000 genomes]
rs73834826	1.00[AMR][1000 genomes]
rs73834828	1.00[AMR][1000 genomes]
rs73834833	1.00[AMR][1000 genomes]
rs73834835	1.00[AMR][1000 genomes]
rs73834837	1.00[AMR][1000 genomes]
rs73834838	1.00[AMR][1000 genomes]
rs73834839	1.00[AMR][1000 genomes]
rs73834844	1.00[AMR][1000 genomes]
rs73834845	1.00[AMR][1000 genomes]
rs73834846	1.00[AMR][1000 genomes]
rs73834847	1.00[AMR][1000 genomes]
rs73834852	1.00[AMR][1000 genomes]
rs73837231	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73837233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73837236	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73837237	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73837249	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73837250	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73837251	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73837263	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837269	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73837270	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7426725	0.85[AMR][1000 genomes]
rs7433199	0.93[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1009871	chr3:67862617-68312064	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv536583	chr3:67862617-68312064	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1010231	chr3:67894825-68117879	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1013531	chr3:67917771-68070027	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3442201	chr3:67925312-68064610	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv3338669	chr3:67925912-68064160	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv3395568	chr3:67955462-68064660	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv876924	chr3:67978367-68063259	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68053600-68058000	Active TSS	Brain Inferior Temporal Lobe	brain
2	chr3:68057400-68058000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:68057400-68058400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:68057400-68060400	Weak transcription	Spleen	Spleen
5	chr3:68057600-68058000	Flanking Active TSS	Fetal Brain Female	brain
6	chr3:68057600-68059200	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:68057600-68059200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr3:68057800-68058000	Bivalent Enhancer	Fetal Brain Male	brain

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