Variant report

Variant	rs73548453
Chromosome Location	chr9:116506574-116506575
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:116504620..116507009-chr9:116507606..116509434,2	K562	blood:
2	chr9:116505256..116507390-chr9:116545375..116548005,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12003007	0.96[ASN][1000 genomes]
rs12003025	0.96[ASN][1000 genomes]
rs12003036	0.96[ASN][1000 genomes]
rs12005142	0.96[ASN][1000 genomes]
rs12682750	0.96[ASN][1000 genomes]
rs12684806	0.96[ASN][1000 genomes]
rs12684822	0.96[ASN][1000 genomes]
rs16908738	0.96[ASN][1000 genomes]
rs16908750	0.96[ASN][1000 genomes]
rs16908763	0.96[ASN][1000 genomes]
rs16908769	0.96[ASN][1000 genomes]
rs16908826	0.96[ASN][1000 genomes]
rs16908828	0.96[ASN][1000 genomes]
rs16908855	0.81[ASN][1000 genomes]
rs16908863	0.81[ASN][1000 genomes]
rs56828590	0.96[ASN][1000 genomes]
rs56929719	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58640994	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59524940	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59945200	0.85[ASN][1000 genomes]
rs60505560	0.96[ASN][1000 genomes]
rs60726370	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61265469	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61421261	0.96[ASN][1000 genomes]
rs62557116	0.93[ASN][1000 genomes]
rs62557117	0.93[ASN][1000 genomes]
rs62557118	0.96[ASN][1000 genomes]
rs62557120	0.96[ASN][1000 genomes]
rs62557121	0.96[ASN][1000 genomes]
rs62557122	0.96[ASN][1000 genomes]
rs62557123	0.96[ASN][1000 genomes]
rs62557125	0.96[ASN][1000 genomes]
rs62557126	0.96[ASN][1000 genomes]
rs62557127	0.96[ASN][1000 genomes]
rs62557129	0.96[ASN][1000 genomes]
rs62557134	0.96[ASN][1000 genomes]
rs62557135	0.96[ASN][1000 genomes]
rs62558193	0.96[ASN][1000 genomes]
rs62558194	0.96[ASN][1000 genomes]
rs7031265	0.96[ASN][1000 genomes]
rs7045057	0.96[ASN][1000 genomes]
rs7045864	0.95[ASN][1000 genomes]
rs73548455	0.96[ASN][1000 genomes]
rs73548463	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73548475	0.96[ASN][1000 genomes]
rs73548490	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73550914	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv12963	chr9:116506433-116509946	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116505400-116508400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:116505800-116508400	Weak transcription	Pancreas	Pancrea

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