Variant report

Variant	rs72866841
Chromosome Location	chr3:43674493-43674494
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12495394	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12497714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2135510	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4420837	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4569634	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4618196	1.00[AMR][1000 genomes]
rs4682688	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4682889	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58089657	1.00[AMR][1000 genomes]
rs6767741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6784075	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72866835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72866848	1.00[AMR][1000 genomes]
rs72866873	1.00[AMR][1000 genomes]
rs7618790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7620124	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7628620	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7647197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906156	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906157	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9311342	1.00[AMR][1000 genomes]
rs937827	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9757381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9847454	1.00[AFR][1000 genomes]
rs9863775	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9872346	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9876963	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834673	chr3:43622985-43799876	Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 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	chr3:43664200-43688400	Weak transcription	Aorta	Aorta
2	chr3:43671200-43680200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:43672200-43680000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:43672400-43675400	Enhancers	K562	blood
5	chr3:43673400-43675000	Enhancers	HUVEC	blood vessel
6	chr3:43673400-43675000	Enhancers	Osteobl	bone
7	chr3:43673600-43674800	Enhancers	HSMM	muscle
8	chr3:43673600-43675000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr3:43674000-43675000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:43674000-43676400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:43674200-43677600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr3:43674400-43674600	Weak transcription	A549	lung
13	chr3:43674400-43675600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr3:43674400-43680200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:43674400-43682800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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