Variant report

Variant	rs73054405
Chromosome Location	chr1:185804330-185804331
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:185802813..185804569-chr1:185808059..185809582,2	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10127552	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12239000	0.97[AFR][1000 genomes]
rs28507443	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28571005	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41317459	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57642813	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57646071	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57647869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61492840	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6675790	0.97[AFR][1000 genomes]
rs6686746	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6689317	0.97[AFR][1000 genomes]
rs6701269	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6701921	0.97[AFR][1000 genomes]
rs6703750	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73054410	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73054419	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73054444	0.86[AFR][1000 genomes]
rs73054452	0.97[AFR][1000 genomes]
rs73054473	0.97[AFR][1000 genomes]
rs73058244	0.97[AFR][1000 genomes]
rs73058248	0.97[AFR][1000 genomes]
rs73058365	0.83[AFR][1000 genomes]
rs73058381	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73058387	1.00[AMR][1000 genomes]
rs73058389	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73058395	1.00[AMR][1000 genomes]
rs73060472	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73060496	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73062507	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070566	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070580	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070588	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070592	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070595	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73072044	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73072053	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73072054	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73072072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73072073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7514923	1.00[AMR][1000 genomes]
rs9727715	0.94[AFR][1000 genomes];1.00[AMR][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	nsv548398	chr1:185136458-186003094	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	esv3424090	chr1:185679718-186270877	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:185803200-185850000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:185803400-185804400	Enhancers	H9 Cell Line	embryonic stem cell
3	chr1:185803400-185805600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:185803800-185804400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:185803800-185812000	Weak transcription	Aorta	Aorta
6	chr1:185804200-185804600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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