Variant report

Variant	rs13042875
Chromosome Location	chr20:14503625-14503626
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAZ	chr20:14503585-14503701	HepG2	liver:	n/a	n/a

Variant related genes	Relation type
MACROD2	TF binding region

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs13036305	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13036870	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13037403	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13039094	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13039304	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13040047	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13043292	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17227062	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17812701	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17812707	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17812713	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17812749	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1998103	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1998104	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2327859	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2423789	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423795	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423796	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423797	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423798	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423799	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2423801	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34202312	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34366310	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35658161	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36023726	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs365225	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs373874	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs376577	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs376972	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs384498	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs391092	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs398372	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs405620	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs405993	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs406307	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs406441	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs407908	0.94[EUR][1000 genomes]
rs408176	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs412345	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs416436	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs420299	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs429495	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs429643	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs430452	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs436322	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs441540	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs441647	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs475471	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4814307	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6079476	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6110316	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62202873	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055499	chr20:14224873-14848061	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1064721	chr20:14384931-14648223	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv833926	chr20:14410153-14572336	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1059770	chr20:14432394-14549781	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv544187	chr20:14432394-14549781	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv529577	chr20:14434373-14799157	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1064008	chr20:14477895-14540691	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1060786	chr20:14486713-14648467	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv544188	chr20:14486713-14648467	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv912690	chr20:14488761-14553745	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1060985	chr20:14488785-14759939	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv912691	chr20:14495489-14536808	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1060291	chr20:14498526-14578899	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14501200-14504600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:14501400-14504800	Enhancers	HMEC	breast
3	chr20:14501600-14504800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr20:14502600-14503800	Flanking Active TSS	NHEK	skin
5	chr20:14502600-14504000	Enhancers	Esophagus	oesophagus
6	chr20:14503600-14503800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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