Variant report

Variant	rs73400825
Chromosome Location	chr15:50369012-50369013
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50367668..50369277-chr15:50371456..50373919,2	MCF-7	breast:
2	chr15:50368228..50370231-chr15:50409424..50412316,2	MCF-7	breast:
3	chr15:50366775..50369568-chr15:50372000..50374396,2	K562	blood:

Variant related genes	Relation type
ENSG00000104043	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10162988	1.00[AMR][1000 genomes]
rs28378462	1.00[AMR][1000 genomes]
rs28430678	1.00[AMR][1000 genomes]
rs28435529	1.00[AMR][1000 genomes]
rs28452447	1.00[AMR][1000 genomes]
rs28483908	1.00[AMR][1000 genomes]
rs28488704	1.00[AMR][1000 genomes]
rs28503500	1.00[AMR][1000 genomes]
rs28547013	1.00[AMR][1000 genomes]
rs28624511	1.00[AMR][1000 genomes]
rs28665904	1.00[AMR][1000 genomes]
rs28694140	1.00[AMR][1000 genomes]
rs28694493	1.00[AMR][1000 genomes]
rs28695746	1.00[AMR][1000 genomes]
rs28720873	1.00[AMR][1000 genomes]
rs56654392	1.00[AMR][1000 genomes]
rs57191911	1.00[AMR][1000 genomes]
rs57210505	1.00[AMR][1000 genomes]
rs59021616	1.00[AMR][1000 genomes]
rs60436593	1.00[AMR][1000 genomes]
rs60959211	1.00[AMR][1000 genomes]
rs61626064	1.00[AMR][1000 genomes]
rs7163385	1.00[AMR][1000 genomes]
rs73400834	1.00[AMR][1000 genomes]
rs73400842	1.00[AMR][1000 genomes]
rs73400860	1.00[AMR][1000 genomes]
rs73400867	1.00[AMR][1000 genomes]
rs73400871	1.00[AMR][1000 genomes]
rs73400878	1.00[AMR][1000 genomes]
rs73400879	1.00[AMR][1000 genomes]
rs73400880	1.00[AMR][1000 genomes]
rs9920507	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	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1035983	chr15:50223334-50595170	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv542382	chr15:50223334-50595170	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv569395	chr15:50345393-50437494	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50367200-50369800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr15:50367200-50380600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr15:50367400-50381600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr15:50368000-50369200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr15:50368000-50370000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:50368000-50380800	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr15:50368800-50370400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:50368800-50370600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:50368800-50371000	Enhancers	Colon Smooth Muscle	Colon
10	chr15:50369000-50370200	Enhancers	Fetal Intestine Large	intestine
11	chr15:50369000-50370200	Enhancers	Rectal Smooth Muscle	rectum
12	chr15:50369000-50370600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr15:50369000-50371000	Enhancers	Primary hematopoietic stem cells	blood

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