Variant report

Variant	rs34913116
Chromosome Location	chr11:49202163-49202164
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12099184	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12574187	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12574928	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12788284	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12790852	0.85[ASN][1000 genomes]
rs12806991	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs16906205	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17743650	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs202694	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs202706	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs202715	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs202718	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs202721	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2299649	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34279527	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34397699	0.85[ASN][1000 genomes]
rs34460216	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs34966829	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34983822	0.83[AMR][1000 genomes]
rs35777887	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35839246	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs36067143	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs383028	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs3903422	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57165791	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs583850	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs617528	0.92[ASN][1000 genomes]
rs646131	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67736905	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71477493	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71477497	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs71477498	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72908309	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][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	nsv469956	chr11:48922645-49862647	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv554347	chr11:49111467-49862647	Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1044070	chr11:49147743-49448774	Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv525454	chr11:49156039-49570587	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv518571	chr11:49162948-49627833	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv972015	chr11:49187522-49240719	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	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	chr11:49184800-49208400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr11:49186800-49204200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr11:49194600-49205200	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:49197000-49206400	Weak transcription	Fetal Intestine Small	intestine
5	chr11:49197800-49208400	Weak transcription	Brain Substantia Nigra	brain
6	chr11:49199800-49204000	Weak transcription	Fetal Intestine Large	intestine
7	chr11:49201200-49202400	Enhancers	Liver	Liver
8	chr11:49202000-49202400	Weak transcription	Fetal Lung	lung

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