Variant report

Variant	rs9393862
Chromosome Location	chr6:27844117-27844118
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:26020549..26023198-chr6:27843330..27845730,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198366	Chromatin interaction
ENSG00000196176	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs12174918	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16867962	1.00[EUR][1000 genomes]
rs169287	0.93[ASN][1000 genomes]
rs175597	0.93[ASN][1000 genomes]
rs200481	0.84[ASN][1000 genomes]
rs200482	0.84[ASN][1000 genomes]
rs200483	0.86[ASN][1000 genomes]
rs200484	0.81[ASN][1000 genomes]
rs200485	0.84[ASN][1000 genomes]
rs200488	0.93[ASN][1000 genomes]
rs200489	0.93[ASN][1000 genomes]
rs200490	0.86[ASN][1000 genomes]
rs200497	0.91[ASN][1000 genomes]
rs200498	0.88[ASN][1000 genomes]
rs200499	0.86[ASN][1000 genomes]
rs200501	0.89[ASN][1000 genomes]
rs200948	0.98[ASN][1000 genomes]
rs200949	0.95[ASN][1000 genomes]
rs200950	0.98[ASN][1000 genomes]
rs200952	0.98[ASN][1000 genomes]
rs200953	0.95[ASN][1000 genomes]
rs200954	0.98[ASN][1000 genomes]
rs200964	0.93[ASN][1000 genomes]
rs200965	0.95[ASN][1000 genomes]
rs200966	0.93[ASN][1000 genomes]
rs200968	0.95[ASN][1000 genomes]
rs200973	0.93[ASN][1000 genomes]
rs200974	0.95[ASN][1000 genomes]
rs200975	0.86[ASN][1000 genomes]
rs200976	0.93[ASN][1000 genomes]
rs200977	1.00[ASN][1000 genomes]
rs200979	0.95[ASN][1000 genomes]
rs200980	0.95[ASN][1000 genomes]
rs200981	0.95[ASN][1000 genomes]
rs200983	0.93[ASN][1000 genomes]
rs200989	0.93[ASN][1000 genomes]
rs200990	0.91[ASN][1000 genomes]
rs200992	0.91[ASN][1000 genomes]
rs200995	0.93[ASN][1000 genomes]
rs200996	0.93[ASN][1000 genomes]
rs201002	0.91[ASN][1000 genomes]
rs2277104	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2394001	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2747054	0.91[ASN][1000 genomes]
rs34295134	0.93[ASN][1000 genomes]
rs36108923	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs370155	0.86[ASN][1000 genomes]
rs390764	0.91[ASN][1000 genomes]
rs401754	0.91[ASN][1000 genomes]
rs401763	0.88[ASN][1000 genomes]
rs4711161	1.00[EUR][1000 genomes]
rs4713117	1.00[EUR][1000 genomes]
rs4713122	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4713124	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4713127	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs483143	0.91[ASN][1000 genomes]
rs493161	1.00[ASN][1000 genomes]
rs494887	0.95[ASN][1000 genomes]
rs557042	1.00[ASN][1000 genomes]
rs56870390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59015666	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9348779	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9357052	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9368531	0.91[ASN][1000 genomes]
rs9368534	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9368535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9368536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9380009	1.00[EUR][1000 genomes]
rs9380013	1.00[EUR][1000 genomes]
rs9380014	1.00[EUR][1000 genomes]
rs9380015	1.00[EUR][1000 genomes]
rs9380018	0.84[ASN][1000 genomes]
rs9380026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9393855	1.00[EUR][1000 genomes]
rs9393858	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9393866	0.84[AMR][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	nsv1022797	chr6:27396961-27864277	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	390 gene(s)	inside rSNPs	diseases
2	nsv432858	chr6:27719375-28011652	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	387 gene(s)	inside rSNPs	diseases
3	nsv1017440	chr6:27734824-27864277	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	370 gene(s)	inside rSNPs	diseases
4	nsv1022173	chr6:27734824-27959408	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	379 gene(s)	inside rSNPs	diseases
5	nsv883512	chr6:27748631-27969004	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	379 gene(s)	inside rSNPs	diseases
6	nsv601208	chr6:27810626-27969004	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	237 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27841800-27847000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:27842200-27857000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:27842400-27844200	Enhancers	Dnd41	blood
4	chr6:27842400-27844400	Enhancers	Fetal Thymus	thymus
5	chr6:27842400-27847400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:27842400-27850600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr6:27842600-27855600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:27842800-27855600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:27843200-27849200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:27844000-27844200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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