Variant report

Variant	rs4286732
Chromosome Location	chr6:75681252-75681253
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:75312619..75316343-chr6:75677557..75681482,3	MCF-7	breast:
2	chr6:75678710..75681421-chr6:75685866..75687554,2	MCF-7	breast:
3	chr6:75665143..75670328-chr6:75679224..75682641,4	MCF-7	breast:
4	chr6:75678289..75682945-chr6:75910306..75916824,17	MCF-7	breast:
5	chr6:75677800..75681711-chr6:75913586..75916557,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111799	Chromatin interaction

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10080721	0.88[ASN][1000 genomes]
rs12661592	0.86[ASN][1000 genomes]
rs12663977	0.88[ASN][1000 genomes]
rs12664010	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12664513	0.86[ASN][1000 genomes]
rs12664807	0.85[ASN][1000 genomes]
rs12664984	0.85[ASN][1000 genomes]
rs12665297	0.83[ASN][1000 genomes]
rs12665801	0.85[ASN][1000 genomes]
rs16885865	0.84[ASN][1000 genomes]
rs16885904	0.85[ASN][1000 genomes]
rs16885908	0.85[ASN][1000 genomes]
rs16885914	0.86[ASN][1000 genomes]
rs16885916	0.86[ASN][1000 genomes]
rs16885971	0.88[ASN][1000 genomes]
rs2353249	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2353251	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2883118	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28832995	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35129971	0.85[ASN][1000 genomes]
rs35835665	0.85[ASN][1000 genomes]
rs35871031	0.85[ASN][1000 genomes]
rs4085727	0.85[ASN][1000 genomes]
rs4085729	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4085730	0.84[ASN][1000 genomes]
rs4085731	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4112825	0.84[ASN][1000 genomes]
rs4112826	0.84[ASN][1000 genomes]
rs4388259	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4495246	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4612126	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57183891	0.85[ASN][1000 genomes]
rs57290574	0.85[ASN][1000 genomes]
rs57560334	0.85[ASN][1000 genomes]
rs58699375	0.85[ASN][1000 genomes]
rs59041629	0.85[ASN][1000 genomes]
rs59051124	0.83[AMR][1000 genomes]
rs59154474	0.85[ASN][1000 genomes]
rs59617477	0.88[ASN][1000 genomes]
rs59695593	0.88[ASN][1000 genomes]
rs59848727	0.85[ASN][1000 genomes]
rs60108944	0.85[ASN][1000 genomes]
rs60321049	0.88[ASN][1000 genomes]
rs60356008	0.85[ASN][1000 genomes]
rs60555684	0.88[ASN][1000 genomes]
rs60909334	0.88[ASN][1000 genomes]
rs61308045	0.88[ASN][1000 genomes]
rs61380374	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs61612838	0.85[ASN][1000 genomes]
rs6453795	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6453797	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6453798	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6910855	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6916626	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6917149	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6922193	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6923380	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6929192	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6932000	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6932942	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6935326	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7451287	0.88[ASN][1000 genomes]
rs7739660	0.88[ASN][1000 genomes]
rs7747261	0.80[AMR][1000 genomes]
rs7749000	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7749133	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7753238	0.86[ASN][1000 genomes]
rs7769481	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7769487	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7772503	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7772564	0.88[ASN][1000 genomes]
rs7775765	0.88[ASN][1000 genomes]
rs7776027	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9443095	0.83[AMR][1000 genomes]
rs9443100	0.83[AMR][1000 genomes]
rs9443124	0.88[ASN][1000 genomes]
rs9443126	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9443129	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9447337	0.83[AMR][1000 genomes]
rs9447343	0.83[AMR][1000 genomes]
rs9447370	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9447371	0.85[ASN][1000 genomes]
rs9447374	0.85[ASN][1000 genomes]
rs9447376	0.85[ASN][1000 genomes]
rs9447377	0.85[ASN][1000 genomes]
rs9447378	0.86[ASN][1000 genomes]
rs9447379	0.86[ASN][1000 genomes]
rs9447380	0.86[ASN][1000 genomes]
rs9447386	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9447388	0.88[ASN][1000 genomes]
rs9447391	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9447394	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9447399	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][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	nsv520746	chr6:75211546-75691814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv830696	chr6:75538316-75734609	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75679800-75682600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:75679800-75685800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:75679800-75686400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:75680000-75681400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:75680200-75681400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:75680200-75682200	Weak transcription	NHEK	skin
7	chr6:75680400-75682600	Weak transcription	HUVEC	blood vessel
8	chr6:75681000-75684000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr6:75681200-75681800	Enhancers	Muscle Satellite Cultured Cells	--

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