Variant report

Variant	rs12668579
Chromosome Location	chr7:41294895-41294896
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10214988	0.86[ASN][1000 genomes]
rs10215332	0.86[ASN][1000 genomes]
rs10215556	0.87[ASN][1000 genomes]
rs10215561	0.87[ASN][1000 genomes]
rs10215670	0.86[ASN][1000 genomes]
rs10225564	0.86[ASN][1000 genomes]
rs10225707	0.86[ASN][1000 genomes]
rs10230756	0.86[ASN][1000 genomes]
rs10238779	0.87[ASN][1000 genomes]
rs10281338	0.86[ASN][1000 genomes]
rs11505532	0.87[ASN][1000 genomes]
rs11760865	0.86[ASN][1000 genomes]
rs11762557	0.95[AFR][1000 genomes];0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11765463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766101	0.88[ASN][1000 genomes]
rs11768019	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11768122	0.86[EUR][1000 genomes]
rs11768187	0.83[ASN][1000 genomes]
rs11972895	0.87[ASN][1000 genomes]
rs11976671	0.87[ASN][1000 genomes]
rs12154794	0.83[ASN][1000 genomes]
rs12155345	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12155372	0.86[ASN][1000 genomes]
rs12701868	0.87[EUR][1000 genomes]
rs12701870	0.95[EUR][1000 genomes]
rs12701873	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12701874	0.87[EUR][1000 genomes]
rs12701875	0.92[CHB][hapmap]
rs12701876	0.81[ASN][1000 genomes]
rs12701877	0.86[ASN][1000 genomes]
rs12701879	0.87[ASN][1000 genomes]
rs12701880	0.87[ASN][1000 genomes]
rs13225532	0.81[EUR][1000 genomes]
rs13230373	0.88[ASN][1000 genomes]
rs13238496	0.81[ASN][1000 genomes]
rs13244372	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13311231	0.86[EUR][1000 genomes]
rs1545195	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1557928	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1557929	0.87[ASN][1000 genomes]
rs1557930	0.88[EUR][1000 genomes]
rs1557931	0.87[ASN][1000 genomes]
rs2051869	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2051871	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2158558	0.87[ASN][1000 genomes]
rs2189841	0.86[ASN][1000 genomes]
rs255014	0.85[EUR][1000 genomes]
rs255017	0.80[EUR][1000 genomes]
rs34965184	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35796717	0.87[ASN][1000 genomes]
rs56215033	0.80[ASN][1000 genomes]
rs6944817	0.87[ASN][1000 genomes]
rs6948410	0.87[ASN][1000 genomes]
rs6951425	0.85[CHB][hapmap];0.81[EUR][1000 genomes]
rs6955027	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6955172	0.86[ASN][1000 genomes]
rs6966153	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs718224	0.83[ASN][1000 genomes]
rs7782143	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv887989	chr7:41125447-41337044	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1028983	chr7:41165668-41635954	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv534465	chr7:41224437-41443498	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 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	chr7:41265000-41296600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:41288000-41296200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:41291800-41295800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:41291800-41296200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:41292400-41295800	Weak transcription	HMEC	breast
6	chr7:41293000-41295800	Weak transcription	NHEK	skin
7	chr7:41294600-41296200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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