Variant report

Variant	rs1447127
Chromosome Location	chr6:55771967-55771968
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:55765849..55767461-chr6:55770096..55772220,2	MCF-7	breast:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10498808	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12198217	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12199367	0.95[ASN][1000 genomes]
rs12209768	0.92[ASN][1000 genomes]
rs1447128	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1562407	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1562408	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs16887395	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1838946	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1868031	0.91[ASN][1000 genomes]
rs2028956	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2044542	0.92[ASN][1000 genomes]
rs2044543	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2056424	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4560651	0.88[ASN][1000 genomes]
rs4574618	0.92[ASN][1000 genomes]
rs4599631	0.92[ASN][1000 genomes]
rs4715570	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4715571	0.92[ASN][1000 genomes]
rs6459111	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6459112	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6459113	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6459115	0.91[ASN][1000 genomes]
rs6459116	0.92[ASN][1000 genomes]
rs6459118	0.91[ASN][1000 genomes]
rs6925961	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6932412	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7752119	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7755388	0.90[ASN][1000 genomes]
rs7755393	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs895641	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs895642	0.94[ASN][1000 genomes]
rs895643	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9296809	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9296810	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9464303	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9475467	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9475469	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9475471	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9475472	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9475473	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9475477	0.94[ASN][1000 genomes]
rs9475480	0.92[ASN][1000 genomes]
rs9885708	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2752670	chr6:55614978-55781605	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1024174	chr6:55713889-55829936	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1029301	chr6:55713889-55834480	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv830665	chr6:55755560-55920219	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55768000-55772200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:55768200-55772400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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