Variant report

Variant	rs72680497
Chromosome Location	chr4:121845067-121845068
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10518380	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11943025	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12499872	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12501914	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12503895	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12510578	0.95[ASN][1000 genomes]
rs12511422	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12639719	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12639772	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12640648	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12644883	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12648660	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1470695	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1597491	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17051271	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17051275	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2167208	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3806807	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4833688	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4833689	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57023921	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72680432	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72680433	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72680438	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72680440	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72680445	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72680451	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72680462	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72680468	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72680474	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72680476	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72680477	0.95[ASN][1000 genomes]
rs72680480	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680484	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680490	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72680498	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs994831	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[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	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1009395	chr4:121841442-122557363	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv537235	chr4:121841442-122557363	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121844800-121845200	Enhancers	Fetal Intestine Small	intestine
2	chr4:121844800-121845400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:121844800-121845600	Weak transcription	Pancreas	Pancrea
4	chr4:121844800-121846400	Enhancers	HUVEC	blood vessel
5	chr4:121844800-121848800	Weak transcription	NHDF-Ad	bronchial
6	chr4:121845000-121845200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:121845000-121845400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:121845000-121845400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:121845000-121845400	Weak transcription	Ovary	ovary
10	chr4:121845000-121845400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr4:121845000-121845600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:121845000-121845600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:121845000-121845600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr4:121845000-121845600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:121845000-121849000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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