Variant report

Variant	rs4864821
Chromosome Location	chr4:54647447-54647448
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1013508	0.95[ASN][1000 genomes]
rs1013509	0.95[ASN][1000 genomes]
rs11133287	0.95[ASN][1000 genomes]
rs11721806	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11723162	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11731952	0.97[ASN][1000 genomes]
rs11734520	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12646885	0.95[ASN][1000 genomes]
rs1498815	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1498816	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1498829	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1874915	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2102011	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2412491	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2412492	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2412496	0.95[ASN][1000 genomes]
rs2412498	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2412500	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4495107	0.92[ASN][1000 genomes]
rs4501282	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4561980	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56061807	0.95[ASN][1000 genomes]
rs60681996	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62297730	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs62297732	0.97[ASN][1000 genomes]
rs67780867	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6819547	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6819611	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6827313	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6827952	0.88[ASN][1000 genomes]
rs6834410	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6837405	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6837817	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6842213	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6842407	0.94[ASN][1000 genomes]
rs6843127	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6845180	0.89[ASN][1000 genomes]
rs6845286	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6846594	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6850939	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6854881	0.90[ASN][1000 genomes]
rs6858638	0.91[ASN][1000 genomes]
rs7686706	0.95[ASN][1000 genomes]
rs7688892	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879015	chr4:54596466-54665559	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv879016	chr4:54638218-54710952	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3379351	chr4:54646995-54650493	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:54644000-54648000	Weak transcription	NH-A	brain
2	chr4:54644200-54648000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:54644800-54652800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:54645200-54648000	Weak transcription	Fetal Stomach	stomach
5	chr4:54646400-54650000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:54646600-54649200	Enhancers	Osteobl	bone
7	chr4:54646600-54650200	Enhancers	NHDF-Ad	bronchial
8	chr4:54646800-54649200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:54646800-54649600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr4:54647000-54648000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:54647000-54648000	Enhancers	NHLF	lung
12	chr4:54647000-54648400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr4:54647000-54648800	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr4:54647000-54649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:54647200-54647800	Flanking Active TSS	A549	lung
16	chr4:54647200-54649200	Enhancers	HepG2	liver
17	chr4:54647400-54648000	Enhancers	Liver	Liver
18	chr4:54647400-54649200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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