Variant report

Variant	rs6569084
Chromosome Location	chr6:120001440-120001441
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	chr17:56707777..56710007-chr6:119999484..120001764,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000212195	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1040656	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11153841	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1159767	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1160757	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1341496	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1341500	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1341501	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1341503	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1884255	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1884256	0.88[CEU][hapmap]
rs2064568	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2064569	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2103845	0.82[CEU][hapmap];0.90[JPT][hapmap]
rs2144360	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2207611	0.86[JPT][hapmap]
rs6569088	0.80[EUR][1000 genomes]
rs6913597	0.80[EUR][1000 genomes]
rs6916609	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6930071	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6933847	0.80[EUR][1000 genomes]
rs6939299	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs706858	0.97[EUR][1000 genomes]
rs7747886	0.80[EUR][1000 genomes]
rs7757918	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7758447	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7771532	0.80[EUR][1000 genomes]
rs7772968	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7776137	0.80[EUR][1000 genomes]
rs807310	0.93[EUR][1000 genomes]
rs807311	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9320699	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9372545	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9372546	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9372547	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9374816	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9374818	0.81[EUR][1000 genomes]
rs9385082	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9385083	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9387664	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9387668	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9387669	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9387670	0.80[EUR][1000 genomes]
rs9387672	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9387675	0.85[JPT][hapmap]
rs9387678	0.81[EUR][1000 genomes]
rs9387679	0.81[EUR][1000 genomes]
rs9401162	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9481955	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9489765	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[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	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1027904	chr6:119709488-120001986	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv3442553	chr6:119742069-120076777	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1027370	chr6:119869409-120056608	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv538431	chr6:119869409-120056608	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119991800-120008000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr6:119992800-120009600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:119999400-120004200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr6:120000000-120002200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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