Variant report

Variant	rs2306866
Chromosome Location	chr3:53766212-53766213
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1020822	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11130380	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11708934	0.91[ASN][1000 genomes]
rs17053417	0.93[ASN][1000 genomes]
rs2029331	0.93[ASN][1000 genomes]
rs2070616	0.84[ASN][1000 genomes]
rs2248381	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2306865	0.82[ASN][1000 genomes]
rs2633723	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2633726	0.89[EUR][1000 genomes]
rs3774548	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3796346	0.88[ASN][1000 genomes]
rs62253777	0.84[ASN][1000 genomes]
rs62253778	0.88[ASN][1000 genomes]
rs6800641	0.91[ASN][1000 genomes]
rs723540	0.91[ASN][1000 genomes]
rs7628839	0.86[ASN][1000 genomes]
rs898423	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1013783	chr3:53694418-53934781	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv1007655	chr3:53742148-53767689	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv1002452	chr3:53742148-53802811	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv1000280	chr3:53742736-53770588	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv520027	chr3:53762713-53784625	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53742600-53778000	Weak transcription	Pancreas	Pancrea
2	chr3:53761600-53781800	Weak transcription	Spleen	Spleen
3	chr3:53764200-53779800	Weak transcription	Liver	Liver
4	chr3:53764400-53767600	Strong transcription	Fetal Intestine Small	intestine
5	chr3:53764600-53770800	Strong transcription	Fetal Intestine Large	intestine
6	chr3:53764800-53766800	Strong transcription	Fetal Lung	lung
7	chr3:53764800-53767200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr3:53764800-53768600	Weak transcription	Right Ventricle	heart
9	chr3:53764800-53769400	Weak transcription	Right Atrium	heart
10	chr3:53764800-53783400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:53765000-53773600	Weak transcription	Fetal Brain Male	brain
12	chr3:53765000-53779800	Weak transcription	Brain Anterior Caudate	brain
13	chr3:53765000-53779800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:53765000-53788600	Weak transcription	Fetal Kidney	kidney
15	chr3:53765200-53783400	Weak transcription	Brain Angular Gyrus	brain
16	chr3:53765400-53774000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr3:53765400-53781600	Weak transcription	Brain Hippocampus Middle	brain
18	chr3:53765800-53767400	Enhancers	GM12878-XiMat	blood
19	chr3:53766000-53766600	Strong transcription	Duodenum Mucosa	Duodenum
20	chr3:53766200-53766600	ZNF genes & repeats	Lung	lung
21	chr3:53766200-53767200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:53766200-53769200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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