Variant report

Variant	rs73587471
Chromosome Location	chr19:51288522-51288523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:51287157..51292690-chr19:51292694..51297699,7	MCF-7	breast:
2	chr19:51287088..51289490-chr19:51410149..51412690,2	MCF-7	breast:
3	chr19:51288460..51291986-chr19:51292271..51294566,4	MCF-7	breast:
4	chr19:51287149..51288654-chr19:51298573..51300535,2	MCF-7	breast:
5	chr19:51162808..51166425-chr19:51284462..51289034,5	K562	blood:
6	chr19:51286798..51289238-chr19:51306756..51308966,2	MCF-7	breast:
7	chr19:50885912..50887624-chr19:51286921..51288538,2	K562	blood:

Variant related genes	Relation type
ENSG00000142513	Chromatin interaction
ENSG00000062822	Chromatin interaction
ENSG00000268375	Chromatin interaction
ENSG00000167747	Chromatin interaction
ENSG00000167749	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10412862	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10412900	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12978675	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12979334	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12979351	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17800375	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2162784	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2560932	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2659060	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2659063	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2659064	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs266124	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36046465	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3810283	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3810284	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57028658	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57906560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58596241	0.95[ASN][1000 genomes]
rs59925776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60175380	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60471273	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60817149	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67085056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67367861	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73584988	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73584997	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73585002	0.90[EUR][1000 genomes]
rs73587469	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv1060760	chr19:50883425-51463712	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1058177	chr19:50984774-51463712	Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
3	nsv912288	chr19:51283791-51334355	Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
4	nsv912289	chr19:51283791-51335943	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
5	nsv912290	chr19:51283791-51344483	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51285000-51288800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr19:51286800-51289400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:51286800-51296800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr19:51287000-51289000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr19:51287000-51298400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:51287000-51298400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr19:51287200-51301200	Weak transcription	Primary B cells from cord blood	blood
8	chr19:51287400-51300000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:51288400-51289800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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