Variant report

Variant	rs11945440
Chromosome Location	chr4:21775810-21775811
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11936372	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11936379	0.98[AFR][1000 genomes]
rs11944423	0.94[AFR][1000 genomes]
rs1398836	0.87[EUR][1000 genomes]
rs16871879	0.96[AFR][1000 genomes]
rs16871882	0.96[AFR][1000 genomes]
rs16871885	0.96[AFR][1000 genomes]
rs16871890	0.96[AFR][1000 genomes]
rs16871892	0.96[AFR][1000 genomes]
rs2044808	0.91[AFR][1000 genomes]
rs2323104	0.96[AFR][1000 genomes]
rs2323105	0.98[AFR][1000 genomes]
rs28445349	0.97[AFR][1000 genomes]
rs28459770	0.96[AFR][1000 genomes]
rs28679434	0.97[AFR][1000 genomes]
rs28700070	0.97[AFR][1000 genomes]
rs2874959	0.95[AFR][1000 genomes]
rs2874960	0.98[AFR][1000 genomes]
rs28762443	0.97[AFR][1000 genomes]
rs28767794	0.97[AFR][1000 genomes]
rs28808427	0.98[AFR][1000 genomes]
rs28850718	0.98[AFR][1000 genomes]
rs28860508	0.92[AFR][1000 genomes]
rs28871730	0.95[AFR][1000 genomes]
rs4469067	0.98[AFR][1000 genomes]
rs55819721	0.97[AFR][1000 genomes]
rs56329622	0.88[AFR][1000 genomes]
rs56340547	0.97[AFR][1000 genomes]
rs57244827	0.98[AFR][1000 genomes]
rs57329498	0.98[AFR][1000 genomes]
rs57893621	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58359333	0.97[AFR][1000 genomes]
rs58370602	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59093225	0.95[AFR][1000 genomes]
rs59388227	0.98[AFR][1000 genomes]
rs59714893	0.97[AFR][1000 genomes]
rs60071903	0.97[AFR][1000 genomes]
rs61456402	0.98[AFR][1000 genomes]
rs61708925	0.97[AFR][1000 genomes]
rs73102032	0.96[AFR][1000 genomes]
rs73102038	0.96[AFR][1000 genomes]
rs73102043	0.96[AFR][1000 genomes]
rs73119544	0.96[AFR][1000 genomes]
rs73119545	0.96[AFR][1000 genomes]
rs73800722	0.96[AFR][1000 genomes]
rs73800726	0.96[AFR][1000 genomes]
rs73800727	0.93[AFR][1000 genomes]
rs7656898	0.96[AFR][1000 genomes]
rs7677885	0.87[EUR][1000 genomes]
rs7697378	0.91[AFR][1000 genomes]
rs7697406	0.97[AFR][1000 genomes]
rs7697653	0.98[AFR][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	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv878751	chr4:21712050-21793807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv4269	chr4:21761429-21806056	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21766600-21780200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:21769400-21780400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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