Variant report

Variant	rs73647260
Chromosome Location	chr9:72216594-72216595
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11139414	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11999656	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12000827	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12000908	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12006272	0.83[EUR][1000 genomes]
rs12552474	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12553894	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12553941	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12554978	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12555100	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1411439	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1411441	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1411442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3927537	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4636268	0.83[EUR][1000 genomes]
rs56654380	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57512468	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58638129	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58667541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58898534	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59791186	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60759202	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7036538	0.83[EUR][1000 genomes]
rs72717199	0.83[EUR][1000 genomes]
rs72719005	0.83[EUR][1000 genomes]
rs72719017	0.83[EUR][1000 genomes]
rs72719024	0.95[EUR][1000 genomes]
rs73647250	0.83[EUR][1000 genomes]
rs73647252	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73647254	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73647255	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73647256	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73647257	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73647259	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73647261	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73647262	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73647263	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73647264	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73647265	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73647266	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7849601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7861451	0.83[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893437	chr9:72118962-72223176	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72207000-72216600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr9:72207800-72220200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:72208600-72217400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr9:72209200-72219600	Weak transcription	Gastric	stomach
5	chr9:72209800-72217600	Weak transcription	Fetal Lung	lung
6	chr9:72212000-72219200	Weak transcription	Liver	Liver
7	chr9:72214400-72217600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:72215000-72219600	Weak transcription	Right Ventricle	heart
9	chr9:72215000-72220200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:72215200-72219600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:72215200-72221000	Weak transcription	Right Atrium	heart
12	chr9:72215400-72217200	Weak transcription	Ovary	ovary
13	chr9:72215400-72217600	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:72215400-72217800	Weak transcription	Fetal Heart	heart
15	chr9:72215400-72219200	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:72215600-72235200	Weak transcription	Aorta	Aorta
17	chr9:72215800-72218400	Enhancers	HUVEC	blood vessel
18	chr9:72216400-72216800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr9:72216400-72217000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:72216400-72217000	Enhancers	Dnd41	blood

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