Variant report

Variant	rs8049333
Chromosome Location	chr16:71345736-71345737
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:71033431..71034148-chr16:71345247..71345906,2	MCF-7	breast:
2	chr16:71033432..71034748-chr16:71345163..71346194,8	MCF-7	breast:
3	chr16:71322082..71324513-chr16:71342713..71345948,3	MCF-7	breast:
4	chr16:71034869..71035905-chr16:71345260..71345928,3	MCF-7	breast:
5	chr16:71250267..71251239-chr16:71344784..71345862,3	MCF-7	breast:
6	chr16:71248492..71249558-chr16:71344873..71345896,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000180917	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1018910	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs12149475	0.83[ASN][1000 genomes]
rs12708908	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs12708909	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12708910	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs12708911	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs12918378	0.84[ASN][1000 genomes]
rs12919927	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12929550	0.84[ASN][1000 genomes]
rs13330156	0.84[ASN][1000 genomes]
rs1424141	0.83[ASN][1000 genomes]
rs2009763	0.85[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs2288048	0.86[ASN][1000 genomes]
rs28673886	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs34832413	0.91[ASN][1000 genomes]
rs3803704	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.85[ASN][1000 genomes]
rs4324135	0.83[ASN][1000 genomes]
rs4419068	0.91[ASN][1000 genomes]
rs4788786	0.81[ASN][1000 genomes]
rs4788787	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.84[ASN][1000 genomes]
rs6499492	0.83[ASN][1000 genomes]
rs6499493	0.84[ASN][1000 genomes]
rs713532	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7187450	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.84[ASN][1000 genomes]
rs7195330	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8050933	0.84[ASN][1000 genomes]
rs8056169	0.81[ASN][1000 genomes]
rs8059792	0.83[ASN][1000 genomes]
rs8060653	0.82[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs8061378	0.83[ASN][1000 genomes]
rs8062240	0.84[ASN][1000 genomes]
rs9927032	0.82[ASN][1000 genomes]
rs9928675	0.91[CHB][hapmap];0.92[JPT][hapmap];0.94[YRI][hapmap];0.86[ASN][1000 genomes]
rs9936354	0.84[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9941262	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv1062426	chr16:71307180-71423400	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv528229	chr16:71331728-71358937	Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71345200-71345800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:71345200-71346000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chr16:71345400-71346000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr16:71345400-71346000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr16:71345400-71346000	Enhancers	Fetal Brain Female	brain
6	chr16:71345600-71346800	Enhancers	HMEC	breast

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