Variant report

Variant	rs12051093
Chromosome Location	chr16:71276067-71276068
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:71274750..71277608-chr16:71280873..71283988,3	MCF-7	breast:
2	chr16:71273768..71276073-chr16:71277133..71279067,2	K562	blood:
3	chr16:71274627..71276994-chr20:52214736..52216358,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1155052	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1155054	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12448046	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12449210	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12933427	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13332757	0.80[ASN][1000 genomes]
rs1424134	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1424136	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1424137	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1557761	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1559420	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1895528	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2042423	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2081253	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2098746	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2158102	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28663037	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2883938	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35645515	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3743954	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3785346	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3902443	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4636918	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4788534	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4788536	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6499489	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7193051	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7498840	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs757106	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs764600	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8052442	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8063809	0.81[ASN][1000 genomes]
rs987958	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9924525	0.80[ASN][1000 genomes]
rs9928164	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9930115	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9932494	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9934510	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9936084	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9939194	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9939836	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9940569	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758429	chr16:70807122-71316983	Active TSS ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv2758653	chr16:70807122-71316983	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1060754	chr16:71008303-71276778	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv482374	chr16:71228600-71401617	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1860	chr16:71269156-71313852	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71275800-71277800	Enhancers	Fetal Intestine Large	intestine
2	chr16:71275800-71277800	Enhancers	Fetal Intestine Small	intestine

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