Variant report

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:53083713..53086465-chr20:53104546..53106950,2	MCF-7	breast:
2	chr20:53084969..53087855-chr20:53094880..53097639,2	MCF-7	breast:
3	chr20:52834058..52838026-chr20:53082960..53086578,4	MCF-7	breast:
4	chr19:39323028..39324723-chr20:53082309..53085056,2	MCF-7	breast:
5	chr20:53084412..53085133-chr20:53323833..53324690,2	MCF-7	breast:
6	chr20:52209472..52211253-chr20:53083989..53086428,2	MCF-7	breast:
7	chr20:53082885..53085495-chr20:53250896..53253910,3	MCF-7	breast:
8	chr20:53082818..53085398-chr20:53109115..53112066,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000171940	Chromatin interaction

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs16999643	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs55665963	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55957910	0.85[EUR][1000 genomes]
rs56302497	0.85[EUR][1000 genomes]
rs58143732	0.93[EUR][1000 genomes]
rs6014019	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6014020	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6023247	0.88[AMR][1000 genomes]
rs6023251	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6023253	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6023254	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6023258	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6023262	0.85[AMR][1000 genomes]
rs6023263	0.81[AMR][1000 genomes]
rs6023266	0.83[EUR][1000 genomes]
rs60780716	0.93[EUR][1000 genomes]
rs6091886	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6091887	0.87[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs6097986	0.88[AMR][1000 genomes]
rs6097987	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6097988	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6097998	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6097999	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6098002	0.80[AMR][1000 genomes]
rs68091706	0.83[EUR][1000 genomes]
rs7264053	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7264143	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7271481	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73141254	0.85[EUR][1000 genomes]
rs73141258	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv834011	chr20:52858341-53086042	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv834012	chr20:52921007-53097177	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:53084000-53085200	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr20:53084800-53091800	Weak transcription	Aorta	Aorta

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