Variant report

Variant	rs11721105
Chromosome Location	chr3:110385315-110385316
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10934065	0.87[ASN][1000 genomes]
rs1154944	0.82[EUR][1000 genomes]
rs1156743	0.88[ASN][1000 genomes]
rs1156744	0.88[ASN][1000 genomes]
rs11708284	0.81[EUR][1000 genomes]
rs11712535	0.90[EUR][1000 genomes]
rs11713871	0.89[EUR][1000 genomes]
rs11714695	0.82[EUR][1000 genomes]
rs11718338	0.82[EUR][1000 genomes]
rs11721109	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11920731	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11920740	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11923966	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12639004	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1303902	0.88[ASN][1000 genomes]
rs13060004	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13061277	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13062747	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13065410	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13067662	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13071834	0.90[EUR][1000 genomes]
rs13073901	0.81[EUR][1000 genomes]
rs13074289	0.81[EUR][1000 genomes]
rs13075730	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13077386	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13077450	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13077986	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13082127	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13082391	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13082702	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13085701	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13087274	0.90[EUR][1000 genomes]
rs13088357	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13089778	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13092632	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13094610	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13097489	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1398356	0.82[EUR][1000 genomes]
rs1462296	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1462311	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1462314	0.88[ASN][1000 genomes]
rs1512532	0.81[EUR][1000 genomes]
rs1512537	0.82[EUR][1000 genomes]
rs1599570	0.84[ASN][1000 genomes]
rs1599572	0.88[ASN][1000 genomes]
rs17202466	0.88[ASN][1000 genomes]
rs2175607	0.82[EUR][1000 genomes]
rs35947928	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4234398	0.85[ASN][1000 genomes]
rs4267670	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4510407	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4682187	0.82[EUR][1000 genomes]
rs56203101	0.88[ASN][1000 genomes]
rs61188814	0.83[EUR][1000 genomes]
rs62270154	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7629191	0.87[ASN][1000 genomes]
rs7633936	0.87[ASN][1000 genomes]
rs7647181	0.87[ASN][1000 genomes]
rs7647421	0.87[ASN][1000 genomes]
rs9830854	0.88[ASN][1000 genomes]
rs9836371	0.87[ASN][1000 genomes]
rs9837589	0.88[ASN][1000 genomes]
rs9857228	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520365	chr3:110155172-110441165	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1001144	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv536687	chr3:110158316-110431113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1001810	chr3:110158316-110522247	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1010230	chr3:110204439-110588814	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv536688	chr3:110204439-110588814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1011034	chr3:110209344-110559021	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv536689	chr3:110209344-110559021	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv1014199	chr3:110293896-110754155	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv829673	chr3:110378069-110530815	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110381800-110389200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:110383200-110385800	Enhancers	Stomach Mucosa	stomach
3	chr3:110384200-110389400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr3:110384400-110385400	Weak transcription	Gastric	stomach
5	chr3:110384400-110389400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:110385000-110385400	Enhancers	Fetal Lung	lung
7	chr3:110385000-110386200	Enhancers	Fetal Intestine Large	intestine
8	chr3:110385200-110385400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:110385200-110386200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:110385200-110386200	Enhancers	Pancreas	Pancrea
11	chr3:110385200-110386400	Enhancers	Fetal Intestine Small	intestine
12	chr3:110385200-110386400	Enhancers	Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links