Variant report

Variant	rs7762887
Chromosome Location	chr6:55384885-55384886
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	chr6:55377485..55380117-chr6:55381946..55384931,2	MCF-7	breast:

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

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

rs_ID	r²[population]
rs10223668	0.84[ASN][1000 genomes]
rs10948936	0.84[ASN][1000 genomes]
rs10948939	0.87[ASN][1000 genomes]
rs12209478	0.87[ASN][1000 genomes]
rs13206666	0.84[ASN][1000 genomes]
rs3800027	0.82[ASN][1000 genomes]
rs4144577	0.84[ASN][1000 genomes]
rs4236132	0.86[ASN][1000 genomes]
rs4404773	0.82[ASN][1000 genomes]
rs4496787	0.87[ASN][1000 genomes]
rs4537142	0.84[ASN][1000 genomes]
rs4538708	0.82[ASN][1000 genomes]
rs4599641	0.82[ASN][1000 genomes]
rs6459082	0.87[ASN][1000 genomes]
rs6908139	0.86[ASN][1000 genomes]
rs6914087	0.87[ASN][1000 genomes]
rs6925488	0.87[ASN][1000 genomes]
rs6928264	0.86[ASN][1000 genomes]
rs6936172	0.87[ASN][1000 genomes]
rs7452170	0.87[ASN][1000 genomes]
rs7740208	0.87[ASN][1000 genomes]
rs7744273	0.87[ASN][1000 genomes]
rs7744986	0.87[ASN][1000 genomes]
rs7745290	0.86[ASN][1000 genomes]
rs7756201	0.82[ASN][1000 genomes]
rs7760065	0.87[ASN][1000 genomes]
rs7761740	0.87[ASN][1000 genomes]
rs9382497	0.82[ASN][1000 genomes]
rs9464253	0.87[ASN][1000 genomes]
rs9464254	0.87[ASN][1000 genomes]
rs9464258	0.87[ASN][1000 genomes]
rs9475333	0.86[ASN][1000 genomes]
rs9475335	0.87[ASN][1000 genomes]
rs9475336	0.86[ASN][1000 genomes]
rs9475337	0.87[ASN][1000 genomes]
rs9475339	0.87[ASN][1000 genomes]
rs9475341	0.84[ASN][1000 genomes]
rs9791201	0.87[ASN][1000 genomes]
rs9791304	0.83[ASN][1000 genomes]
rs9791308	0.87[ASN][1000 genomes]
rs9791360	0.87[ASN][1000 genomes]
rs9885775	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv1029436	chr6:55237283-55386038	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1024550	chr6:55237723-55387481	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv948358	chr6:55351282-55477277	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1031992	chr6:55365469-55391815	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1026411	chr6:55372845-55653498	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr6:55376400-55399200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:55376800-55396400	Weak transcription	Left Ventricle	heart
3	chr6:55384400-55410200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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