Variant report

Variant	rs73222477
Chromosome Location	chr3:111492748-111492749
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	chr3:111485439..111489234-chr3:111490972..111493959,3	MCF-7	breast:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13321524	0.96[ASN][1000 genomes]
rs13322494	0.96[ASN][1000 genomes]
rs28479130	0.87[ASN][1000 genomes]
rs28534728	0.96[ASN][1000 genomes]
rs28648833	0.96[ASN][1000 genomes]
rs28675079	0.83[ASN][1000 genomes]
rs3922706	0.83[ASN][1000 genomes]
rs3922780	0.83[ASN][1000 genomes]
rs4075549	0.83[ASN][1000 genomes]
rs4390898	0.96[ASN][1000 genomes]
rs4516581	0.83[ASN][1000 genomes]
rs4542994	0.83[ASN][1000 genomes]
rs4634085	0.96[ASN][1000 genomes]
rs4682313	0.83[ASN][1000 genomes]
rs56005252	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56052712	0.87[ASN][1000 genomes]
rs57902958	0.91[ASN][1000 genomes]
rs58124137	0.96[ASN][1000 genomes]
rs58663746	0.96[ASN][1000 genomes]
rs60867472	0.96[ASN][1000 genomes]
rs6438012	0.83[ASN][1000 genomes]
rs66651424	0.83[ASN][1000 genomes]
rs66786213	0.96[ASN][1000 genomes]
rs66856712	0.96[ASN][1000 genomes]
rs66975684	0.87[ASN][1000 genomes]
rs6762246	0.96[ASN][1000 genomes]
rs6762572	0.83[ASN][1000 genomes]
rs6778818	0.83[ASN][1000 genomes]
rs6782513	0.83[ASN][1000 genomes]
rs6787278	0.96[ASN][1000 genomes]
rs6789977	0.96[ASN][1000 genomes]
rs6790355	0.96[ASN][1000 genomes]
rs6790521	0.96[ASN][1000 genomes]
rs6790612	0.96[ASN][1000 genomes]
rs6790825	0.96[ASN][1000 genomes]
rs6790977	0.96[ASN][1000 genomes]
rs6795947	0.83[ASN][1000 genomes]
rs67970120	0.83[ASN][1000 genomes]
rs6800047	0.96[ASN][1000 genomes]
rs6800065	0.96[ASN][1000 genomes]
rs6800922	0.96[ASN][1000 genomes]
rs6802960	0.96[ASN][1000 genomes]
rs73220212	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73222475	0.96[ASN][1000 genomes]
rs73222500	0.96[ASN][1000 genomes]
rs7614433	0.83[ASN][1000 genomes]
rs7627909	0.83[ASN][1000 genomes]
rs9843288	0.83[ASN][1000 genomes]
rs9858064	0.91[ASN][1000 genomes]
rs9858228	0.96[ASN][1000 genomes]
rs9862472	0.96[ASN][1000 genomes]
rs9868898	0.83[ASN][1000 genomes]
rs9871034	0.96[ASN][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	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv829676	chr3:111464087-111619200	Genic enhancers Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111487800-111493000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:111487800-111521000	Weak transcription	Gastric	stomach
3	chr3:111488000-111493000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:111488000-111493400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:111488000-111501400	Weak transcription	Psoas Muscle	Psoas
6	chr3:111488400-111496800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:111489000-111495200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:111489400-111500600	Weak transcription	Fetal Lung	lung
9	chr3:111492000-111493000	Weak transcription	Liver	Liver
10	chr3:111492400-111492800	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:111492400-111493000	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr3:111492400-111493200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:111492400-111494200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:111492600-111493400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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