Variant report

Variant	rs11792137
Chromosome Location	chr9:71082877-71082878
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10123848	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs10511957	1.00[CHB][hapmap];1.00[MEX][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10511958	1.00[CEU][hapmap];0.89[TSI][hapmap];0.97[EUR][1000 genomes]
rs10780960	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs10868876	0.84[EUR][1000 genomes]
rs10868879	0.85[CEU][hapmap];0.97[EUR][1000 genomes]
rs11142541	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11142543	0.97[EUR][1000 genomes]
rs11789244	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes]
rs11791213	1.00[ASN][1000 genomes]
rs11794424	1.00[CHB][hapmap];1.00[MEX][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11795356	1.00[ASN][1000 genomes]
rs12000789	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs12238439	0.85[CEU][hapmap]
rs12343961	1.00[ASN][1000 genomes]
rs12343980	1.00[ASN][1000 genomes]
rs12350942	1.00[ASN][1000 genomes]
rs1353009	1.00[CEU][hapmap];0.89[TSI][hapmap];0.97[EUR][1000 genomes]
rs1353010	0.85[CEU][hapmap];1.00[EUR][1000 genomes]
rs17053702	1.00[CHB][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17054803	1.00[CHB][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17059173	1.00[CHB][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs265083	0.85[CEU][hapmap]
rs265087	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs4745041	1.00[CEU][hapmap];0.89[TSI][hapmap];0.97[EUR][1000 genomes]
rs4745083	0.85[EUR][1000 genomes]
rs6560144	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs7022394	0.84[EUR][1000 genomes]
rs7030076	0.97[EUR][1000 genomes]
rs7031619	0.97[EUR][1000 genomes]
rs7035038	0.97[EUR][1000 genomes]
rs7039686	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7042123	0.85[CEU][hapmap];0.97[EUR][1000 genomes]
rs7042721	0.97[EUR][1000 genomes]
rs7855134	1.00[CEU][hapmap];0.89[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7866604	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs984109	1.00[GIH][hapmap]

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	nsv427847	chr9:70318730-71153527	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71051200-71091800	Weak transcription	Psoas Muscle	Psoas
2	chr9:71070200-71087000	Weak transcription	Aorta	Aorta
3	chr9:71070800-71100800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:71075200-71098800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:71076400-71098800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:71077400-71087000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr9:71077600-71098800	Weak transcription	Fetal Muscle Leg	muscle
8	chr9:71077800-71103400	Weak transcription	Right Ventricle	heart
9	chr9:71078200-71084400	Weak transcription	Fetal Heart	heart
10	chr9:71078200-71103400	Weak transcription	HSMMtube	muscle
11	chr9:71078400-71084400	Weak transcription	Ovary	ovary
12	chr9:71078400-71087000	Weak transcription	Fetal Stomach	stomach
13	chr9:71080200-71085600	Weak transcription	Right Atrium	heart
14	chr9:71081000-71098800	Weak transcription	Fetal Kidney	kidney
15	chr9:71081200-71085600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr9:71082000-71085200	Weak transcription	Fetal Lung	lung
17	chr9:71082200-71083200	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr9:71082200-71083800	Enhancers	Colon Smooth Muscle	Colon
19	chr9:71082200-71088200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:71082200-71088400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:71082400-71085600	Weak transcription	Left Ventricle	heart

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