Variant report

Variant	rs60554782
Chromosome Location	chr4:21901393-21901394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10000092	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10023378	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10028678	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10029164	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10155094	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11723357	0.92[ASN][1000 genomes]
rs12640849	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1513566	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1606537	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16872048	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16872074	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17569897	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2323161	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28476598	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28485804	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28593399	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28633789	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4697246	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4697247	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56102367	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56695493	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57592786	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58741960	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58985230	0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs907790	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	esv2757924	chr4:21873204-21980559	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2759231	chr4:21873204-21980559	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv428440	chr4:21873204-21980559	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv987707	chr4:21900601-21908051	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21899400-21901400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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