Variant report

Variant	rs9404069
Chromosome Location	chr6:101458728-101458729
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	chr6:101452622..101455428-chr6:101458387..101460104,2	MCF-7	breast:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs13205402	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13212730	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs13220881	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1337385	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1406894	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17801075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1923013	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2004276	0.87[ASN][1000 genomes]
rs2024842	0.84[ASN][1000 genomes]
rs2024843	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2398247	0.86[ASN][1000 genomes]
rs34555727	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4240589	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4464803	0.93[ASN][1000 genomes]
rs4840160	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4840164	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4840169	0.84[ASN][1000 genomes]
rs4840170	0.84[ASN][1000 genomes]
rs55967215	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56359216	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588204	0.91[ASN][1000 genomes]
rs599934	0.93[ASN][1000 genomes]
rs62419249	0.84[ASN][1000 genomes]
rs62420689	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs62420692	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs652335	0.95[ASN][1000 genomes]
rs669543	0.90[ASN][1000 genomes]
rs679444	0.86[ASN][1000 genomes]
rs684140	0.95[ASN][1000 genomes]
rs694418	0.90[ASN][1000 genomes]
rs7453078	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7740902	0.88[EUR][1000 genomes]
rs7758630	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7760958	1.00[EUR][1000 genomes]
rs7769142	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7772462	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9322270	0.86[ASN][1000 genomes]
rs9322271	0.87[ASN][1000 genomes]
rs9322276	0.86[ASN][1000 genomes]
rs9377251	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9404060	0.87[ASN][1000 genomes]
rs9404070	1.00[EUR][1000 genomes]
rs9791225	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
6	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101458000-101459000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:101458400-101459000	Weak transcription	Fetal Brain Male	brain
3	chr6:101458400-101459800	Enhancers	Fetal Thymus	thymus
4	chr6:101458400-101460000	Enhancers	Primary B cells from peripheral blood	blood
5	chr6:101458600-101458800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr6:101458600-101459000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:101458600-101459000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:101458600-101459200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr6:101458600-101459200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:101458600-101459600	Enhancers	Primary B cells from cord blood	blood
11	chr6:101458600-101459800	Flanking Active TSS	Dnd41	blood
12	chr6:101458600-101460000	Enhancers	Thymus	Thymus

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