Variant report

Variant	rs73644683
Chromosome Location	chr9:15606695-15606696
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
2	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164975	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs11998843	1.00[AMR][1000 genomes]
rs11999047	0.88[AFR][1000 genomes]
rs11999354	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11999403	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12002030	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12002408	0.81[AFR][1000 genomes]
rs12002928	0.81[AFR][1000 genomes]
rs12003098	1.00[AMR][1000 genomes]
rs12003371	1.00[AMR][1000 genomes]
rs16933373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16933376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16933587	1.00[AMR][1000 genomes]
rs3082784	0.83[AFR][1000 genomes]
rs35546678	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55678381	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56304941	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56323052	0.83[AFR][1000 genomes]
rs56333848	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56754898	1.00[AMR][1000 genomes]
rs56818091	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56974853	1.00[AMR][1000 genomes]
rs57098037	1.00[AMR][1000 genomes]
rs57108331	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57201285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57471536	0.89[AFR][1000 genomes]
rs57688272	1.00[AMR][1000 genomes]
rs58027597	0.89[AFR][1000 genomes]
rs58596549	1.00[AMR][1000 genomes]
rs58892201	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59228819	1.00[AMR][1000 genomes]
rs59254174	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59736306	1.00[AMR][1000 genomes]
rs60294159	1.00[AMR][1000 genomes]
rs60651191	0.83[AFR][1000 genomes]
rs60911267	1.00[AMR][1000 genomes]
rs60918672	1.00[AMR][1000 genomes]
rs60940884	0.83[AFR][1000 genomes]
rs60997329	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61608504	1.00[AMR][1000 genomes]
rs7033545	0.90[AFR][1000 genomes]
rs73644661	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73644680	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73644681	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73644686	1.00[AMR][1000 genomes]
rs73644689	1.00[AMR][1000 genomes]
rs73644690	1.00[AMR][1000 genomes]
rs73644691	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73644692	1.00[AMR][1000 genomes]
rs73644693	1.00[AMR][1000 genomes]
rs73644695	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73644696	0.83[AFR][1000 genomes]
rs73644697	0.83[AFR][1000 genomes]
rs73644942	1.00[AMR][1000 genomes]
rs73644943	1.00[AMR][1000 genomes]
rs73644945	1.00[AMR][1000 genomes]
rs73644946	1.00[AMR][1000 genomes]
rs7468160	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892625	chr9:15326251-16064850	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv892626	chr9:15389610-15694690	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv892627	chr9:15397969-15909450	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats 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	28 gene(s)	inside rSNPs	diseases
4	nsv892629	chr9:15516375-15634326	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv3407839	chr9:15530438-15665653	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv892630	chr9:15554960-15694690	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1028357	chr9:15565670-15622556	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv2752286	chr9:15578017-15794897	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv613652	chr9:15579744-15661859	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv613653	chr9:15590116-15668606	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv892631	chr9:15590116-15694690	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv892632	chr9:15590116-15869845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv613654	chr9:15601971-15638364	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv613655	chr9:15602101-15670445	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	nsv892633	chr9:15604746-15889411	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15587000-15620400	Weak transcription	Pancreas	Pancrea
2	chr9:15589200-15609800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:15589400-15610600	Weak transcription	Thymus	Thymus
4	chr9:15592800-15614000	Weak transcription	Left Ventricle	heart
5	chr9:15599000-15617800	Weak transcription	Aorta	Aorta
6	chr9:15600200-15614400	Weak transcription	Gastric	stomach
7	chr9:15600600-15617600	Weak transcription	Fetal Stomach	stomach
8	chr9:15601000-15620000	Weak transcription	Ovary	ovary
9	chr9:15601200-15608000	Weak transcription	Fetal Thymus	thymus
10	chr9:15601200-15614000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr9:15605800-15606800	Enhancers	Dnd41	blood
12	chr9:15605800-15607200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:15606000-15607800	Enhancers	Primary hematopoietic stem cells	blood
14	chr9:15606000-15607800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr9:15606200-15607200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr9:15606200-15608000	Enhancers	HUVEC	blood vessel
17	chr9:15606400-15606800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:15606400-15606800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr9:15606400-15606800	Enhancers	Osteobl	bone
20	chr9:15606600-15606800	Enhancers	Fetal Kidney	kidney
21	chr9:15606600-15606800	Active TSS	Fetal Lung	lung
22	chr9:15606600-15608000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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