Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10167028	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10198382	0.86[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10203887	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13001078	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs13008111	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13033987	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13384786	0.86[AFR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13386998	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs13392156	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13402655	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13414973	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13424099	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13430450	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17182870	0.84[AFR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17183100	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28452374	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34287580	0.89[EUR][1000 genomes]
rs35341336	0.82[ASN][1000 genomes]
rs3771214	0.84[AFR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71418480	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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	nsv909659	chr18:53918924-54134488	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv458082	chr18:53950927-54667823	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv577020	chr18:53950927-54667823	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv1065207	chr18:53951439-54241108	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv833662	chr18:53974695-54108188	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:54074600-54089000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:54082600-54088600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr18:54082600-54088600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:54083000-54088400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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