Variant report

Variant	rs7855134
Chromosome Location	chr9:71074851-71074852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10123848	0.82[CEU][hapmap]
rs10511957	0.90[EUR][1000 genomes]
rs10511958	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs10780955	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10780960	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10780967	0.91[GIH][hapmap]
rs10781002	0.82[GIH][hapmap]
rs10868817	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs10868851	0.91[GIH][hapmap]
rs10868852	0.91[GIH][hapmap]
rs10868876	0.98[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10868877	0.91[GIH][hapmap]
rs10868879	0.85[CEU][hapmap];0.97[EUR][1000 genomes]
rs11142391	1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap]
rs11142449	1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap]
rs11142461	1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap]
rs11142499	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11142500	1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11142541	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11142543	0.94[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs11142616	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11789244	0.85[CEU][hapmap];0.91[EUR][1000 genomes]
rs11792137	1.00[CEU][hapmap];0.89[TSI][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11794424	0.90[EUR][1000 genomes]
rs12000789	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs12238439	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[TSI][hapmap];0.93[ASN][1000 genomes]
rs12353500	1.00[GIH][hapmap];0.90[TSI][hapmap]
rs13439981	1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[ASN][1000 genomes]
rs1353009	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];1.00[TSI][hapmap];0.80[YRI][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs1353010	0.85[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17053702	0.90[EUR][1000 genomes]
rs17054803	0.90[EUR][1000 genomes]
rs17059173	0.90[EUR][1000 genomes]
rs265083	0.85[CEU][hapmap];0.91[GIH][hapmap]
rs265087	1.00[CEU][hapmap];0.86[GIH][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs28510448	0.83[ASN][1000 genomes]
rs4745041	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs4745083	0.85[EUR][1000 genomes]
rs59478866	0.80[ASN][1000 genomes]
rs6560144	1.00[CEU][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs7019238	0.80[ASW][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.90[TSI][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs7021955	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7022394	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7030076	0.97[EUR][1000 genomes]
rs7031619	0.99[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs7035038	0.97[EUR][1000 genomes]
rs7039686	1.00[CEU][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7042123	0.85[CEU][hapmap];0.97[EUR][1000 genomes]
rs7042721	0.97[EUR][1000 genomes]
rs7875408	1.00[JPT][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:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71051200-71091800	Weak transcription	Psoas Muscle	Psoas
2	chr9:71062200-71075800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr9:71065800-71080000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:71067800-71077000	Weak transcription	Lung	lung
5	chr9:71069800-71075600	Weak transcription	Right Ventricle	heart
6	chr9:71070200-71087000	Weak transcription	Aorta	Aorta
7	chr9:71070600-71076000	Weak transcription	Right Atrium	heart
8	chr9:71070800-71100800	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr9:71071600-71076800	Enhancers	Rectal Smooth Muscle	rectum
10	chr9:71071800-71078200	Enhancers	Colon Smooth Muscle	Colon
11	chr9:71072200-71075400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr9:71073000-71075600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:71073000-71075800	Weak transcription	Fetal Stomach	stomach
14	chr9:71073000-71076000	Weak transcription	Ovary	ovary
15	chr9:71073000-71077200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:71073200-71076800	Weak transcription	Fetal Heart	heart
17	chr9:71073400-71075800	Weak transcription	Fetal Lung	lung
18	chr9:71073400-71077000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr9:71074000-71075200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr9:71074800-71075000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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