Variant report

Variant	rs28503500
Chromosome Location	chr15:50389627-50389628
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50372189..50373837-chr15:50387101..50389661,2	K562	blood:
2	chr15:50387437..50389948-chr15:52496988..52498573,2	K562	blood:
3	chr15:50387663..50389890-chr15:50394989..50396741,2	MCF-7	breast:

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[AFR][1000 genomes];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]
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[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56654392	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57191911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57210505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59021616	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60436593	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60959211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61626064	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7163385	1.00[AMR][1000 genomes]
rs73400825	1.00[AMR][1000 genomes]
rs73400834	1.00[AMR][1000 genomes]
rs73400842	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400860	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400867	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400878	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400879	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73400880	0.93[AFR][1000 genomes];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	chr15:50387200-50391200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr15:50387400-50390200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr15:50388200-50393600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr15:50388600-50391200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:50388800-50389800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:50389000-50390000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr15:50389000-50392400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr15:50389200-50389800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr15:50389200-50392800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr15:50389400-50390400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr15:50389400-50390600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr15:50389600-50390200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr15:50389600-50390200	Enhancers	iPS-15b Cell Line	embryonic stem cell

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