Variant report

Variant	rs55735972
Chromosome Location	chr4:28575886-28575887
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1024126	0.83[ASN][1000 genomes]
rs10805276	0.81[ASN][1000 genomes]
rs10805277	0.81[ASN][1000 genomes]
rs10939218	0.86[ASN][1000 genomes]
rs10939219	0.83[ASN][1000 genomes]
rs10939220	0.81[ASN][1000 genomes]
rs10939222	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11723657	0.81[ASN][1000 genomes]
rs11729559	0.81[ASN][1000 genomes]
rs11937307	0.90[ASN][1000 genomes]
rs11943453	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11944357	0.91[ASN][1000 genomes]
rs12331108	0.93[ASN][1000 genomes]
rs12509357	0.81[ASN][1000 genomes]
rs12648749	0.84[EUR][1000 genomes]
rs13107472	0.81[ASN][1000 genomes]
rs13144499	0.81[ASN][1000 genomes]
rs13151535	0.81[ASN][1000 genomes]
rs17643041	0.86[ASN][1000 genomes]
rs17643347	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17699520	0.86[ASN][1000 genomes]
rs17699721	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17699827	0.86[ASN][1000 genomes]
rs17701516	0.81[ASN][1000 genomes]
rs17702089	0.83[ASN][1000 genomes]
rs2309830	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2471693	0.83[ASN][1000 genomes]
rs2471694	0.83[ASN][1000 genomes]
rs2471722	0.83[ASN][1000 genomes]
rs34933409	0.81[ASN][1000 genomes]
rs35093995	0.81[ASN][1000 genomes]
rs35639254	0.81[ASN][1000 genomes]
rs4075471	0.81[ASN][1000 genomes]
rs4368591	0.81[ASN][1000 genomes]
rs4368592	0.81[ASN][1000 genomes]
rs4373152	0.81[ASN][1000 genomes]
rs4374613	0.81[ASN][1000 genomes]
rs4398515	0.81[ASN][1000 genomes]
rs4438752	0.81[ASN][1000 genomes]
rs4533764	0.81[ASN][1000 genomes]
rs4544697	0.81[ASN][1000 genomes]
rs4568230	0.81[ASN][1000 genomes]
rs4593119	0.81[ASN][1000 genomes]
rs4604048	0.81[ASN][1000 genomes]
rs4637390	0.81[ASN][1000 genomes]
rs4692331	0.83[ASN][1000 genomes]
rs4692333	0.93[ASN][1000 genomes]
rs57767930	0.88[ASN][1000 genomes]
rs58438669	0.82[ASN][1000 genomes]
rs67683753	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6811230	0.81[EUR][1000 genomes]
rs6824212	0.81[ASN][1000 genomes]
rs6830893	0.82[EUR][1000 genomes]
rs6844131	0.86[ASN][1000 genomes]
rs73215429	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73215462	0.86[EUR][1000 genomes]
rs7656263	0.81[ASN][1000 genomes]
rs7657422	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7659143	0.81[ASN][1000 genomes]
rs7662061	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7680975	0.81[ASN][1000 genomes]
rs7682822	0.81[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	nsv1010133	chr4:28273244-28642942	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1014938	chr4:28277683-28642942	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2757926	chr4:28543958-28839437	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759239	chr4:28543958-28839437	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv878781	chr4:28568780-28680520	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	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	chr4:28570600-28587400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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