Variant report

Variant	rs1939432
Chromosome Location	chr11:101613940-101613941
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:101611797..101613703-chr11:101613756..101615793,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10501990	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10736621	0.86[EUR][1000 genomes]
rs10750622	0.87[EUR][1000 genomes]
rs10791523	0.95[EUR][1000 genomes]
rs10791524	0.95[EUR][1000 genomes]
rs10791534	0.81[EUR][1000 genomes]
rs10791539	0.85[EUR][1000 genomes]
rs10791540	0.86[EUR][1000 genomes]
rs10895192	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10895202	0.92[EUR][1000 genomes]
rs1372415	0.82[EUR][1000 genomes]
rs1441932	0.84[EUR][1000 genomes]
rs17745489	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1815903	0.90[EUR][1000 genomes]
rs1815904	0.90[EUR][1000 genomes]
rs1815905	0.88[EUR][1000 genomes]
rs1939028	0.81[EUR][1000 genomes]
rs1939031	0.94[EUR][1000 genomes]
rs1939033	0.84[EUR][1000 genomes]
rs1939036	0.91[EUR][1000 genomes]
rs1939041	0.96[EUR][1000 genomes]
rs1939044	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1939045	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1939056	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1939063	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1939069	0.92[EUR][1000 genomes]
rs1939070	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1939461	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2000535	0.92[EUR][1000 genomes]
rs2155064	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2155065	0.82[AMR][1000 genomes]
rs2155066	0.95[EUR][1000 genomes]
rs4084123	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4237604	0.92[EUR][1000 genomes]
rs4445600	0.89[EUR][1000 genomes]
rs4576789	0.87[EUR][1000 genomes]
rs4754020	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4754021	0.94[EUR][1000 genomes]
rs4754023	0.83[EUR][1000 genomes]
rs4754027	0.88[EUR][1000 genomes]
rs4754031	0.88[EUR][1000 genomes]
rs4754799	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4754802	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4754805	0.92[EUR][1000 genomes]
rs4754810	0.92[EUR][1000 genomes]
rs4754812	0.88[EUR][1000 genomes]
rs4754814	0.86[EUR][1000 genomes]
rs6590920	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6590923	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7101850	0.94[EUR][1000 genomes]
rs7117680	0.94[EUR][1000 genomes]
rs7128050	0.88[EUR][1000 genomes]
rs7944440	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7950837	0.86[EUR][1000 genomes]
rs894255	0.83[EUR][1000 genomes]
rs894256	0.82[EUR][1000 genomes]
rs894257	0.83[EUR][1000 genomes]
rs947993	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs947994	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898330	chr11:101243644-101722031	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1052159	chr11:101439655-101853293	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1051457	chr11:101446705-101837650	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv530645	chr11:101451416-101778666	Bivalent/Poised TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv468853	chr11:101539408-101616696	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv556139	chr11:101539408-101616696	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv898332	chr11:101562004-101732566	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv832249	chr11:101571819-101749073	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1044223	chr11:101586478-101626839	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101598600-101614400	Weak transcription	Fetal Lung	lung
2	chr11:101613200-101619400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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