Variant report

Variant	rs9447399
Chromosome Location	chr6:75705617-75705618
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:120)

rs_ID	r²[population]
rs10080721	1.00[ASN][1000 genomes]
rs12661592	0.98[ASN][1000 genomes]
rs12663829	0.87[ASN][1000 genomes]
rs12663977	1.00[ASN][1000 genomes]
rs12664010	0.88[AMR][1000 genomes];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];0.94[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];0.87[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	0.98[ASN][1000 genomes]
rs16885971	1.00[ASN][1000 genomes]
rs16886197	1.00[CEU][hapmap]
rs2300791	1.00[CEU][hapmap]
rs2300794	1.00[CEU][hapmap]
rs2353249	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2353251	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2883118	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28832995	1.00[EUR][1000 genomes];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	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4085730	0.95[ASN][1000 genomes]
rs4085731	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4112825	0.95[ASN][1000 genomes]
rs4112826	0.95[ASN][1000 genomes]
rs4286732	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4388259	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4495246	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4612126	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];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[ASN][1000 genomes]
rs59695593	1.00[ASN][1000 genomes]
rs59848727	0.96[ASN][1000 genomes]
rs60108944	0.96[ASN][1000 genomes]
rs60321049	1.00[ASN][1000 genomes]
rs60356008	0.96[ASN][1000 genomes]
rs60555684	1.00[ASN][1000 genomes]
rs60909334	1.00[ASN][1000 genomes]
rs61308045	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	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453798	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs658592	1.00[CEU][hapmap]
rs6910855	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6916626	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6917149	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6922193	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6923380	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929192	0.95[ASN][1000 genomes]
rs6932000	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6932942	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6935326	0.95[ASN][1000 genomes]
rs73458044	0.83[ASN][1000 genomes]
rs73458047	0.83[ASN][1000 genomes]
rs7451287	1.00[ASN][1000 genomes]
rs7738809	1.00[CEU][hapmap]
rs7739660	1.00[ASN][1000 genomes]
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	0.98[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	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7769487	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7772503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772564	1.00[ASN][1000 genomes]
rs7775765	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7776027	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9293988	1.00[CEU][hapmap]
rs9293991	1.00[AFR][1000 genomes]
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	1.00[ASN][1000 genomes]
rs9443126	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443129	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];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];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9447371	0.96[ASN][1000 genomes]
rs9447374	0.96[ASN][1000 genomes]
rs9447376	0.96[ASN][1000 genomes]
rs9447377	0.96[ASN][1000 genomes]
rs9447378	0.98[ASN][1000 genomes]
rs9447379	0.98[ASN][1000 genomes]
rs9447380	0.98[ASN][1000 genomes]
rs9447386	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9447388	1.00[ASN][1000 genomes]
rs9447391	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9447394	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75703000-75716200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:75704000-75707200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:75704200-75707200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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