Variant report

Variant	rs7699486
Chromosome Location	chr4:78399133-78399134
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11930677	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11936117	0.83[ASN][1000 genomes]
rs11939449	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11942781	0.83[ASN][1000 genomes]
rs11945282	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17002681	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17002682	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17002687	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17002700	0.89[EUR][1000 genomes]
rs1867107	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1992489	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2083702	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2119977	0.90[ASN][1000 genomes]
rs2866292	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2903241	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2903242	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4152	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4859499	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4859842	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4859843	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4859844	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4859845	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4859846	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55685718	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55729445	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55915318	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56092580	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56107646	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56164638	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62302436	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62302437	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62302438	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62302439	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62302442	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62302445	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6826277	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72650428	0.81[ASN][1000 genomes]
rs72650458	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7670432	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7676991	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7681293	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829974	chr4:78240718-78415642	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3434529	chr4:78388030-78470631	Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:78398600-78402400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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