Variant report

Variant	rs7039686
Chromosome Location	chr9:71086433-71086434
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10116868	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10123848	0.82[CEU][hapmap]
rs10511958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10735596	0.86[JPT][hapmap]
rs10780960	1.00[CEU][hapmap];0.81[YRI][hapmap];0.86[EUR][1000 genomes]
rs10780962	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10780963	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10780967	0.90[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs10868795	0.86[JPT][hapmap]
rs10868803	0.82[JPT][hapmap]
rs10868851	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10868852	0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10868876	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10868877	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10868879	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11142075	0.86[JPT][hapmap]
rs11142199	0.86[JPT][hapmap]
rs11142468	0.86[ASN][1000 genomes]
rs11142541	0.88[EUR][1000 genomes]
rs11142543	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11142549	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11142650	0.85[JPT][hapmap]
rs11789244	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs11792137	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12000789	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12238439	0.85[CEU][hapmap]
rs12353500	0.81[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs1353009	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1353010	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs1492824	0.86[JPT][hapmap]
rs17056009	0.87[JPT][hapmap];0.84[ASN][1000 genomes]
rs2026033	0.86[JPT][hapmap]
rs265083	0.85[CEU][hapmap]
rs265087	1.00[CEU][hapmap]
rs35011246	0.91[ASN][1000 genomes]
rs4237244	0.92[ASN][1000 genomes]
rs4237245	0.85[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4744594	0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs4745041	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4745083	0.80[EUR][1000 genomes]
rs6560144	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7020465	0.86[JPT][hapmap]
rs7022220	0.85[JPT][hapmap]
rs7022394	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7025140	0.86[JPT][hapmap]
rs7026163	1.00[ASN][1000 genomes]
rs7030076	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7031619	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7035038	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7039149	0.90[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs7042123	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7042601	0.91[ASN][1000 genomes]
rs7042721	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7855134	1.00[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7860270	0.85[ASN][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	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:20 , 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	chr9:71078200-71103400	Weak transcription	HSMMtube	muscle
10	chr9:71078400-71087000	Weak transcription	Fetal Stomach	stomach
11	chr9:71081000-71098800	Weak transcription	Fetal Kidney	kidney
12	chr9:71082200-71088200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:71082200-71088400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr9:71083200-71091600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:71085800-71091400	Weak transcription	Fetal Lung	lung
16	chr9:71086000-71087000	Weak transcription	Left Ventricle	heart
17	chr9:71086000-71087000	Weak transcription	Stomach Smooth Muscle	stomach
18	chr9:71086200-71087600	Enhancers	Colon Smooth Muscle	Colon
19	chr9:71086200-71092000	Weak transcription	Right Atrium	heart
20	chr9:71086400-71088000	Weak transcription	Fetal Heart	heart

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