Variant report

Variant	rs7739660
Chromosome Location	chr6:75689747-75689748
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:75679003..75680747-chr6:75687605..75691074,3	MCF-7	breast:

Extended variants
information (count: 121 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs10080721	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12661592	0.98[ASN][1000 genomes]
rs12663829	0.87[ASN][1000 genomes]
rs12663977	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12664010	1.00[ASN][1000 genomes]
rs12664513	0.98[ASN][1000 genomes]
rs12664807	0.96[ASN][1000 genomes]
rs12664984	0.96[ASN][1000 genomes]
rs12665297	0.91[CHB][hapmap];0.80[JPT][hapmap];0.94[ASN][1000 genomes]
rs12665702	0.91[CHB][hapmap];0.87[ASN][1000 genomes]
rs12665801	0.96[ASN][1000 genomes]
rs13437111	1.00[CEU][hapmap]
rs16885835	0.90[CHB][hapmap];0.87[ASN][1000 genomes]
rs16885844	0.91[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs16885865	0.95[ASN][1000 genomes]
rs16885904	0.96[ASN][1000 genomes]
rs16885908	0.96[ASN][1000 genomes]
rs16885914	0.98[ASN][1000 genomes]
rs16885916	0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16885971	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16886197	1.00[CEU][hapmap]
rs2300791	1.00[CEU][hapmap]
rs2300794	1.00[CEU][hapmap]
rs2353249	0.96[ASN][1000 genomes]
rs2353251	0.94[ASN][1000 genomes]
rs2883118	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs28832995	1.00[ASN][1000 genomes]
rs35129971	0.96[ASN][1000 genomes]
rs35835665	0.96[ASN][1000 genomes]
rs35871031	0.96[ASN][1000 genomes]
rs4085727	0.96[ASN][1000 genomes]
rs4085729	0.95[ASN][1000 genomes]
rs4085730	0.95[ASN][1000 genomes]
rs4085731	0.94[ASN][1000 genomes]
rs4112825	0.95[ASN][1000 genomes]
rs4112826	0.95[ASN][1000 genomes]
rs4286732	0.88[ASN][1000 genomes]
rs4388259	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs4495246	1.00[ASN][1000 genomes]
rs4612126	0.98[ASN][1000 genomes]
rs545588	1.00[CEU][hapmap]
rs560250	1.00[CEU][hapmap]
rs57183891	0.96[ASN][1000 genomes]
rs57290574	0.96[ASN][1000 genomes]
rs57560334	0.96[ASN][1000 genomes]
rs57904603	0.89[ASN][1000 genomes]
rs58699375	0.96[ASN][1000 genomes]
rs59041629	0.96[ASN][1000 genomes]
rs59051124	0.84[ASN][1000 genomes]
rs59154474	0.96[ASN][1000 genomes]
rs59617477	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs59695593	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59848727	0.96[ASN][1000 genomes]
rs60108944	0.96[ASN][1000 genomes]
rs60321049	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60356008	0.96[ASN][1000 genomes]
rs60555684	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60909334	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61308045	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61380374	1.00[ASN][1000 genomes]
rs61612838	0.96[ASN][1000 genomes]
rs6453790	0.83[ASN][1000 genomes]
rs6453795	0.95[ASN][1000 genomes]
rs6453797	1.00[ASN][1000 genomes]
rs6453798	1.00[ASN][1000 genomes]
rs658592	1.00[CEU][hapmap]
rs6910855	0.98[ASN][1000 genomes]
rs6916626	1.00[ASN][1000 genomes]
rs6917149	0.96[ASN][1000 genomes]
rs6922193	1.00[ASN][1000 genomes]
rs6923380	1.00[ASN][1000 genomes]
rs6929192	0.95[ASN][1000 genomes]
rs6932000	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6932942	0.96[ASN][1000 genomes]
rs6935326	0.95[ASN][1000 genomes]
rs73458044	0.83[ASN][1000 genomes]
rs73458047	0.83[ASN][1000 genomes]
rs7451287	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7738809	1.00[CEU][hapmap]
rs7743883	1.00[CEU][hapmap]
rs7746348	0.81[ASN][1000 genomes]
rs7747261	0.85[ASN][1000 genomes]
rs7749000	1.00[CEU][hapmap];0.91[CHB][hapmap];0.94[ASN][1000 genomes]
rs7749133	0.91[CHB][hapmap];0.94[ASN][1000 genomes]
rs7753238	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7754400	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7755906	1.00[CEU][hapmap];0.90[CHB][hapmap];0.83[ASN][1000 genomes]
rs7769481	0.95[ASN][1000 genomes]
rs7769487	0.92[ASN][1000 genomes]
rs7772503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7772564	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775765	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776027	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9293988	1.00[CEU][hapmap]
rs9443092	0.84[ASN][1000 genomes]
rs9443095	0.84[ASN][1000 genomes]
rs9443096	0.83[ASN][1000 genomes]
rs9443100	0.83[ASN][1000 genomes]
rs9443124	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443126	1.00[ASN][1000 genomes]
rs9443129	1.00[ASN][1000 genomes]
rs9447317	1.00[CEU][hapmap]
rs9447335	0.80[ASN][1000 genomes]
rs9447337	0.83[ASN][1000 genomes]
rs9447339	0.83[ASN][1000 genomes]
rs9447343	0.83[ASN][1000 genomes]
rs9447370	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs9447371	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9447374	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9447376	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9447377	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9447378	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447379	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447380	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9447386	0.99[ASN][1000 genomes]
rs9447388	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447391	1.00[ASN][1000 genomes]
rs9447394	1.00[ASN][1000 genomes]
rs9447399	1.00[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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75685600-75690200	Enhancers	HMEC	breast
2	chr6:75687200-75695400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:75687200-75695600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:75688400-75690000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:75689200-75690400	Enhancers	NHEK	skin
6	chr6:75689200-75695400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:75689400-75695600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links