Variant report

Variant	rs12414726
Chromosome Location	chr10:92609598-92609599
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	chr10:92605355..92608309-chr10:92609468..92612446,2	MCF-7	breast:

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10509612	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11186309	0.97[ASN][1000 genomes]
rs11591238	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11594126	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11594548	0.97[ASN][1000 genomes]
rs11594649	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11813096	0.99[ASN][1000 genomes]
rs11813240	0.97[ASN][1000 genomes]
rs11814840	0.99[ASN][1000 genomes]
rs11817810	0.97[ASN][1000 genomes]
rs12411309	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12412496	0.96[ASN][1000 genomes]
rs12413941	0.94[ASN][1000 genomes]
rs12414389	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12415970	0.99[ASN][1000 genomes]
rs12761105	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12761148	0.89[ASN][1000 genomes]
rs12764332	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12764938	0.97[ASN][1000 genomes]
rs12766523	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12766851	0.97[ASN][1000 genomes]
rs12772924	0.99[ASN][1000 genomes]
rs12774947	0.96[ASN][1000 genomes]
rs12777881	0.87[ASN][1000 genomes]
rs12778269	0.96[ASN][1000 genomes]
rs12779377	0.96[ASN][1000 genomes]
rs12779610	0.96[ASN][1000 genomes]
rs12783703	0.97[ASN][1000 genomes]
rs12784621	0.85[ASN][1000 genomes]
rs12785051	0.97[ASN][1000 genomes]
rs1418214	0.97[ASN][1000 genomes]
rs1935346	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1935348	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1935349	0.94[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1935350	0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1935351	0.97[ASN][1000 genomes]
rs2153779	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2185706	0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2185707	0.89[ASN][1000 genomes]
rs2420368	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28842222	0.80[ASN][1000 genomes]
rs34871116	0.99[ASN][1000 genomes]
rs35449520	0.99[ASN][1000 genomes]
rs35598406	0.97[ASN][1000 genomes]
rs35731058	0.96[ASN][1000 genomes]
rs35863839	0.81[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs36101610	0.96[ASN][1000 genomes]
rs4144423	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4272713	0.97[ASN][1000 genomes]
rs4350278	0.87[ASN][1000 genomes]
rs4350279	0.86[ASN][1000 genomes]
rs4406742	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4459202	0.97[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4933195	0.97[ASN][1000 genomes]
rs4933199	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4933200	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4933607	0.96[ASN][1000 genomes]
rs4933608	0.97[ASN][1000 genomes]
rs4933613	0.99[ASN][1000 genomes]
rs4933620	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4933621	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57825126	0.94[ASN][1000 genomes]
rs58460916	0.99[ASN][1000 genomes]
rs58586220	0.99[ASN][1000 genomes]
rs58868307	0.96[ASN][1000 genomes]
rs59277098	0.95[ASN][1000 genomes]
rs60135579	0.95[ASN][1000 genomes]
rs60748043	0.96[ASN][1000 genomes]
rs61218433	0.95[ASN][1000 genomes]
rs7074715	0.89[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7075333	0.97[ASN][1000 genomes]
rs7078682	0.96[ASN][1000 genomes]
rs7079426	0.99[ASN][1000 genomes]
rs7084468	0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7086484	0.93[ASN][1000 genomes]
rs7089533	0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090415	0.97[ASN][1000 genomes]
rs7090941	0.97[ASN][1000 genomes]
rs7093602	0.93[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7096934	0.99[ASN][1000 genomes]
rs71479059	0.99[ASN][1000 genomes]
rs71479062	0.80[ASN][1000 genomes]
rs7893260	0.99[ASN][1000 genomes]
rs7893391	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7897751	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv948363	chr10:92084520-92614402	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv831945	chr10:92590576-92793582	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92597800-92616200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:92605600-92610000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:92606800-92609600	Weak transcription	Psoas Muscle	Psoas
4	chr10:92607400-92609600	Weak transcription	HSMMtube	muscle
5	chr10:92607400-92610200	Enhancers	HMEC	breast
6	chr10:92607600-92609600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:92607600-92609600	Weak transcription	NH-A	brain
8	chr10:92607600-92609600	Weak transcription	Osteobl	bone
9	chr10:92607800-92609600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:92607800-92609600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr10:92609200-92609800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:92609200-92610200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr10:92609200-92610200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr10:92609200-92610200	Enhancers	HSMM	muscle
15	chr10:92609200-92610200	Flanking Active TSS	NHEK	skin
16	chr10:92609400-92610200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr10:92609400-92610400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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