Variant report

Variant	rs73603370
Chromosome Location	chr10:4726169-4726170
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:4724736..4726805-chr10:4727300..4730027,2	MCF-7	breast:
2	chr10:4720784..4722788-chr10:4723962..4726842,2	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs6601856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7080358	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7080362	0.81[AFR][1000 genomes]
rs73585603	1.00[AMR][1000 genomes]
rs73585605	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73585607	1.00[AMR][1000 genomes]
rs73585608	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603357	1.00[AMR][1000 genomes]
rs73603358	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603363	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603367	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603369	1.00[AMR][1000 genomes]
rs73603372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73603373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7904029	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7915099	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7915596	1.00[AMR][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	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv1798456	chr10:4689138-4731081	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv1817443	chr10:4689138-4731081	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1831014	chr10:4689138-4731081	Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv1838419	chr10:4689138-4731081	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4716400-4726600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr10:4717800-4727000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:4721000-4727800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr10:4721200-4728400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:4721200-4729000	Weak transcription	NHDF-Ad	bronchial
6	chr10:4721200-4733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:4721400-4727000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:4721600-4727200	Weak transcription	HUVEC	blood vessel
9	chr10:4721800-4726400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr10:4721800-4726600	Weak transcription	NH-A	brain
11	chr10:4721800-4727200	Weak transcription	Psoas Muscle	Psoas
12	chr10:4725600-4728800	Enhancers	A549	lung
13	chr10:4725800-4726400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:4725800-4728400	Enhancers	HMEC	breast
15	chr10:4725800-4729000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr10:4725800-4730000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr10:4725800-4730800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:4726000-4726600	Enhancers	Osteobl	bone
19	chr10:4726000-4727800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:4726000-4728200	Enhancers	NHEK	skin
21	chr10:4726000-4730800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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