Variant report

Variant	rs11127967
Chromosome Location	chr3:86980246-86980247
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11708953	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11720259	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12496631	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12633088	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13073131	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13074417	0.88[EUR][1000 genomes]
rs13092422	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1347611	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1370032	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1370033	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1370034	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1370035	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1370036	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1370037	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1370038	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1473272	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1473273	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2028090	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34506181	0.90[EUR][1000 genomes]
rs4295171	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4859048	0.83[EUR][1000 genomes]
rs4859060	0.84[EUR][1000 genomes]
rs4859084	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6419886	0.84[EUR][1000 genomes]
rs6419887	0.84[EUR][1000 genomes]
rs6419888	0.84[EUR][1000 genomes]
rs6551477	0.84[EUR][1000 genomes]
rs6551498	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6551499	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6774777	0.84[EUR][1000 genomes]
rs6776393	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6781697	0.91[EUR][1000 genomes]
rs6791881	0.84[EUR][1000 genomes]
rs6794181	0.84[EUR][1000 genomes]
rs6797991	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6803815	0.91[EUR][1000 genomes]
rs7614681	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7623702	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7635070	0.84[EUR][1000 genomes]
rs7643907	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7649306	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7649317	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9837981	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9869786	0.82[EUR][1000 genomes]
rs9871001	0.90[EUR][1000 genomes]
rs9881446	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519148	chr3:86831077-86995124	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv534036	chr3:86967129-87283600	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86972600-86986400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:86973400-86986200	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:86973600-86982400	Weak transcription	NHLF	lung
4	chr3:86973600-86986000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr3:86978000-86980400	Enhancers	HSMM	muscle
6	chr3:86978000-86980400	Enhancers	Osteobl	bone
7	chr3:86978000-86981000	Enhancers	NHDF-Ad	bronchial
8	chr3:86978800-86980400	Enhancers	HSMMtube	muscle
9	chr3:86978800-86980800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:86979000-86986200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr3:86979200-86980400	Weak transcription	Placenta	Placenta
12	chr3:86979200-86980800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:86979800-86980600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:86980200-86980400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:86980200-86980600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:86980200-86980600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr3:86980200-86985800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links