Variant report

Variant	rs12279585
Chromosome Location	chr11:66765472-66765473
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:66764153..66769079-chr11:66769260..66775339,9	MCF-7	breast:
2	chr11:66764015..66766435-chr11:66822154..66824249,3	MCF-7	breast:
3	chr11:66764180..66766583-chr11:66780585..66782268,2	MCF-7	breast:
4	chr11:66765257..66769768-chr11:66775296..66778044,4	MCF-7	breast:
5	chr11:66762811..66772502-chr11:66787021..66797000,34	MCF-7	breast:
6	chr11:66761490..66778711-chr11:66821814..66832221,36	MCF-7	breast:
7	chr11:66622879..66624462-chr11:66764748..66766385,2	MCF-7	breast:
8	chr11:66762967..66768319-chr11:66788576..66792799,9	MCF-7	breast:
9	chr11:66764346..66765886-chr11:66766577..66769051,2	MCF-7	breast:
10	chr11:66610071..66611807-chr11:66762959..66765909,2	MCF-7	breast:
11	chr11:66764654..66766748-chr11:66793832..66796764,2	MCF-7	breast:
12	chr11:66761666..66763201-chr11:66763495..66765562,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000173227	Chromatin interaction
ENSG00000173653	Chromatin interaction
ENSG00000252709	Chromatin interaction
ENSG00000173156	Chromatin interaction
ENSG00000173621	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10160663	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10896146	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10896147	1.00[EUR][1000 genomes]
rs10896148	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227654	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227659	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227662	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227664	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12222286	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12270068	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12270183	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12273240	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12274897	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12275124	0.96[AFR][1000 genomes]
rs12275370	0.93[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12276046	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12277065	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12277720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12281292	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12281335	1.00[EUR][1000 genomes]
rs12281512	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12282433	0.81[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12282440	0.82[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12284422	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12284764	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12284808	0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12284860	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12285661	1.00[EUR][1000 genomes]
rs12287658	0.93[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12288309	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12288354	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12290308	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12290429	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12290836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12290886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12290950	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12292728	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12293275	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12788732	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56173916	1.00[EUR][1000 genomes]
rs56973649	1.00[EUR][1000 genomes]
rs57604888	1.00[EUR][1000 genomes]
rs57946225	1.00[EUR][1000 genomes]
rs60751057	1.00[EUR][1000 genomes]
rs7109580	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7123934	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7128943	0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73493529	1.00[EUR][1000 genomes]
rs73493531	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs7924894	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7925264	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7941982	1.00[EUR][1000 genomes]
rs7942885	1.00[EUR][1000 genomes]
rs7948985	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv428574	chr11:66619002-66804133	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv832194	chr11:66634462-66805980	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
4	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
5	esv1817552	chr11:66751014-66839985	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66763400-66765800	Enhancers	HSMMtube	muscle
2	chr11:66763800-66765800	Enhancers	HepG2	liver
3	chr11:66764800-66766400	Weak transcription	K562	blood
4	chr11:66764800-66769400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:66764800-66769800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:66765000-66769400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:66765000-66769600	Weak transcription	Liver	Liver
8	chr11:66765200-66770000	Weak transcription	Hela-S3	cervix
9	chr11:66765200-66770200	Weak transcription	A549	lung

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