Variant report

Variant	rs153073
Chromosome Location	chr5:115023185-115023186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:115018021..115019776-chr5:115023115..115025620,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1067726	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1067728	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs149472	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs152416	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153074	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1651414	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1698097	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs171662	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs173733	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2431441	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2431443	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2434727	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2455447	0.91[ASN][1000 genomes]
rs2455450	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs249720	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs249721	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs251878	0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs251879	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2545847	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2561860	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2652663	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3105151	0.96[ASN][1000 genomes]
rs397908	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs403039	0.91[ASN][1000 genomes]
rs422161	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs425666	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs432032	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs440138	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs440925	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs441398	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs447079	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs455226	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs459180	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs459386	0.86[AMR][1000 genomes]
rs460451	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs461084	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs461105	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs461952	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs462799	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465126	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465457	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs465496	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465997	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs712556	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7733817	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs791565	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[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	nsv916273	chr5:114656592-115089901	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv868915	chr5:114723371-115252527	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115022400-115023400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr5:115022600-115023200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:115022800-115023800	Weak transcription	Aorta	Aorta

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