Variant report

Variant	rs2201148
Chromosome Location	chr3:46207036-46207037
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	chr3:46148102..46150678-chr3:46206152..46208391,2	MCF-7	breast:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs13059906	0.90[AFR][1000 genomes]
rs13086063	0.84[AFR][1000 genomes]
rs13089907	0.87[AFR][1000 genomes]
rs13090848	0.87[AFR][1000 genomes]
rs17078681	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3136664	1.00[EUR][1000 genomes]
rs3136665	1.00[EUR][1000 genomes]
rs34013035	0.87[AFR][1000 genomes]
rs34059564	0.80[AFR][1000 genomes]
rs34198655	0.87[AFR][1000 genomes]
rs35960950	0.91[AFR][1000 genomes]
rs41326147	1.00[EUR][1000 genomes]
rs41364446	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41366344	1.00[EUR][1000 genomes]
rs41424051	1.00[EUR][1000 genomes]
rs41465848	1.00[EUR][1000 genomes]
rs41480548	1.00[EUR][1000 genomes]
rs4547740	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56102061	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56129454	1.00[EUR][1000 genomes]
rs56947484	1.00[EUR][1000 genomes]
rs57522944	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58772082	1.00[EUR][1000 genomes]
rs59047782	1.00[EUR][1000 genomes]
rs59654809	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61145486	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61752589	1.00[EUR][1000 genomes]
rs6772596	1.00[EUR][1000 genomes]
rs6780714	1.00[EUR][1000 genomes]
rs6793690	1.00[EUR][1000 genomes]
rs6796282	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73830670	1.00[EUR][1000 genomes]
rs73833043	1.00[EUR][1000 genomes]
rs73833044	1.00[EUR][1000 genomes]
rs73833047	1.00[EUR][1000 genomes]
rs73833051	1.00[EUR][1000 genomes]
rs73833052	1.00[EUR][1000 genomes]
rs73833053	1.00[EUR][1000 genomes]
rs753110	1.00[EUR][1000 genomes]
rs7631551	0.83[AFR][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	nsv876734	chr3:45725031-46468467	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv498008	chr3:45733423-46319401	Strong transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr3:46206000-46207200	Weak transcription	Psoas Muscle	Psoas
2	chr3:46206200-46208400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:46206200-46211600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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