Variant report

Variant	rs8027586
Chromosome Location	chr15:39846299-39846300
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:39845301..39848272-chr15:39850823..39852507,2	MCF-7	breast:
2	chr15:39826333..39829143-chr15:39844610..39847564,2	MCF-7	breast:
3	chr15:39841161..39843886-chr15:39846091..39848223,2	MCF-7	breast:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10520134	1.00[AMR][1000 genomes]
rs1551946	1.00[CHB][hapmap]
rs1551947	0.86[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16969237	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16969254	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1876850	0.83[AMR][1000 genomes]
rs1876851	0.83[AMR][1000 genomes]
rs1961097	0.83[AMR][1000 genomes]
rs28390974	0.83[AMR][1000 genomes]
rs28605448	0.83[AMR][1000 genomes]
rs58789628	0.83[AMR][1000 genomes]
rs59284692	0.83[AMR][1000 genomes]
rs6492901	0.83[AMR][1000 genomes]
rs6492902	1.00[AMR][1000 genomes]
rs6492903	0.83[AMR][1000 genomes]
rs6492904	0.83[AMR][1000 genomes]
rs7162828	1.00[EUR][1000 genomes]
rs7163169	1.00[EUR][1000 genomes]
rs7167136	1.00[AMR][1000 genomes]
rs7167206	0.83[AMR][1000 genomes]
rs7168679	0.83[AMR][1000 genomes]
rs7168836	0.83[AMR][1000 genomes]
rs7174585	1.00[AMR][1000 genomes]
rs7175706	1.00[EUR][1000 genomes]
rs7183198	0.83[AMR][1000 genomes]
rs73385184	0.83[AMR][1000 genomes]
rs73385188	0.83[AMR][1000 genomes]
rs73387008	0.83[AMR][1000 genomes]
rs73387042	0.83[AMR][1000 genomes]
rs73387053	0.83[AMR][1000 genomes]
rs73387054	0.83[AMR][1000 genomes]
rs73389094	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73401235	1.00[AMR][1000 genomes]
rs73401240	1.00[AMR][1000 genomes]
rs8024038	1.00[CHB][hapmap]
rs8024886	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8030858	1.00[AMR][1000 genomes]
rs8038776	1.00[EUR][1000 genomes]
rs8039379	0.83[AMR][1000 genomes]
rs937955	0.83[AMR][1000 genomes]
rs9673056	1.00[CHB][hapmap]

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	nsv1049682	chr15:39657279-40027403	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv542361	chr15:39657279-40027403	Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv3373125	chr15:39691567-40061262	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv904094	chr15:39738006-39976057	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv832977	chr15:39817512-39981520	Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:39839000-39848200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:39844400-39851200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr15:39844600-39849600	Enhancers	Colon Smooth Muscle	Colon
4	chr15:39844800-39846400	Enhancers	GM12878-XiMat	blood
5	chr15:39844800-39848600	Enhancers	Ovary	ovary
6	chr15:39844800-39849000	Enhancers	Fetal Lung	lung
7	chr15:39845200-39847000	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr15:39845200-39848200	Enhancers	Rectal Smooth Muscle	rectum
9	chr15:39845400-39846600	Enhancers	Fetal Kidney	kidney
10	chr15:39845600-39847600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr15:39845800-39849800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr15:39846000-39846800	Enhancers	Fetal Heart	heart
13	chr15:39846000-39846800	Weak transcription	Left Ventricle	heart
14	chr15:39846200-39846600	Weak transcription	Pancreas	Pancrea
15	chr15:39846200-39846800	Enhancers	Hela-S3	cervix
16	chr15:39846200-39847000	Enhancers	HSMMtube	muscle
17	chr15:39846200-39848400	Enhancers	Fetal Stomach	stomach

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