Variant report

Variant	rs16934875
Chromosome Location	chr9:16643147-16643148
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10118895	1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10120281	0.81[ASN][1000 genomes]
rs10122372	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[ASN][1000 genomes]
rs10125014	1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1029016	0.84[YRI][hapmap]
rs10733311	0.81[ASN][1000 genomes]
rs10738437	1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10738440	1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap];0.90[ASN][1000 genomes]
rs10738441	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10738442	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10738443	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10756764	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10756765	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[TSI][hapmap];0.90[ASN][1000 genomes]
rs10756766	0.90[ASN][1000 genomes]
rs10756767	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10756768	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10756770	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10962484	0.94[GIH][hapmap];0.91[TSI][hapmap]
rs10962510	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12004304	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12339625	1.00[GIH][hapmap];0.91[TSI][hapmap]
rs12350242	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs1415472	0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs1415474	1.00[JPT][hapmap]
rs1538102	1.00[JPT][hapmap];0.84[YRI][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16934816	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16934855	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16934886	1.00[JPT][hapmap];0.81[YRI][hapmap];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16934893	0.88[YRI][hapmap]
rs2095657	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs28490464	0.81[ASN][1000 genomes]
rs28501274	0.81[ASN][1000 genomes]
rs28651010	0.81[ASN][1000 genomes]
rs34950291	0.81[ASN][1000 genomes]
rs4466493	0.81[ASN][1000 genomes]
rs4961725	0.82[MEX][hapmap]
rs4961726	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59379949	0.84[AMR][1000 genomes]
rs7018877	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7019016	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7019105	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7034606	0.91[EUR][1000 genomes]
rs7035303	0.91[EUR][1000 genomes]
rs7049170	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73421425	0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7470623	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7854979	0.90[ASN][1000 genomes]
rs7859395	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs7870508	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7870730	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7873338	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv430000	chr9:16603483-16671045	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	esv2758627	chr9:16641966-16809203	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	esv2759673	chr9:16641966-16809203	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16629600-16653600	Weak transcription	HUVEC	blood vessel
2	chr9:16636400-16645800	Weak transcription	Ovary	ovary
3	chr9:16637800-16644600	Weak transcription	Fetal Lung	lung
4	chr9:16637800-16652600	Weak transcription	Fetal Stomach	stomach
5	chr9:16638000-16651200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr9:16638200-16644600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr9:16638400-16644800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:16640000-16670800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:16640600-16643400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:16641000-16644800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr9:16641000-16645000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:16641000-16645800	Weak transcription	HSMMtube	muscle
13	chr9:16641200-16644600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr9:16641200-16645000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr9:16641200-16646000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr9:16641200-16649400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr9:16641400-16651400	Weak transcription	A549	lung
18	chr9:16642400-16643200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:16642400-16643200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr9:16642400-16643200	Enhancers	NHDF-Ad	bronchial
21	chr9:16642600-16643200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:16642600-16643200	Enhancers	NHLF	lung
23	chr9:16642600-16643400	Enhancers	Osteobl	bone
24	chr9:16642800-16644200	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:16643000-16643200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:16643000-16644800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr9:16643000-16645000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:16643000-16645800	Weak transcription	HSMM	muscle
29	chr9:16643000-16651800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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