Variant report

Variant	rs74081028
Chromosome Location	chr12:42640987-42640988
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:42631376..42634368-chr12:42640313..42643094,3	MCF-7	breast:
2	chr12:42630899..42632760-chr12:42639742..42641533,2	K562	blood:
3	chr12:42629596..42634057-chr12:42635851..42641617,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000015153	Chromatin interaction
ENSG00000134283	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1079985	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17090974	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17090988	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17091121	0.90[AFR][1000 genomes]
rs1982507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55699566	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56000886	0.87[AFR][1000 genomes]
rs56126783	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56183709	1.00[AMR][1000 genomes]
rs56315321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56400220	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56404347	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57096261	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58745493	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60164617	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60635137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74077499	1.00[AMR][1000 genomes]
rs74077816	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078011	1.00[AMR][1000 genomes]
rs74078049	0.90[AFR][1000 genomes]
rs74078160	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078165	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078171	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078173	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078174	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078176	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078178	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078179	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078180	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078194	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74078197	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74079127	0.87[AFR][1000 genomes]
rs74081009	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74081065	1.00[AFR][1000 genomes];1.00[AMR][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	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv826351	chr12:42584218-42676281	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv826352	chr12:42593124-42675255	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	esv3397788	chr12:42636734-42665519	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42640800-42641200	Enhancers	Primary monocytes fromperipheralblood	blood

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