Variant report

Variant	rs2891072
Chromosome Location	chr9:16553933-16553934
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10116857	1.00[CEU][hapmap]
rs10117448	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10121959	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10123480	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs10123558	0.82[CEU][hapmap]
rs10511622	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10733312	1.00[CEU][hapmap]
rs10738437	0.82[CEU][hapmap]
rs10738439	1.00[CEU][hapmap]
rs10756763	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10810576	0.82[CEU][hapmap]
rs10962488	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10962492	0.82[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10962493	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10962494	0.82[CEU][hapmap]
rs10962511	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12000426	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12002673	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12004947	0.86[ASN][1000 genomes]
rs12335443	1.00[JPT][hapmap]
rs12337676	1.00[CEU][hapmap]
rs12338548	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12343239	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12343306	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12350242	1.00[CEU][hapmap]
rs12350853	0.82[CEU][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12352543	1.00[CEU][hapmap];0.89[AMR][1000 genomes]
rs1337393	1.00[CEU][hapmap]
rs1337400	1.00[CEU][hapmap]
rs1415473	1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1415474	1.00[CEU][hapmap]
rs1415476	1.00[CEU][hapmap]
rs16934806	1.00[JPT][hapmap]
rs1807023	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1927616	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1927617	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1927618	0.82[CEU][hapmap]
rs1927626	1.00[CEU][hapmap]
rs1952345	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes]
rs1952346	1.00[CEU][hapmap]
rs2065937	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2382808	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2382809	1.00[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2382810	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28414647	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28483319	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28593297	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28602416	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28714603	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28733737	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56170891	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6475059	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6475060	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6475062	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6475063	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7018594	1.00[JPT][hapmap]
rs7021199	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7022328	0.87[ASN][1000 genomes]
rs7022813	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7029578	1.00[JPT][hapmap]
rs7029648	1.00[JPT][hapmap]
rs7030387	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7035791	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs725011	1.00[CEU][hapmap]
rs7350234	1.00[CEU][hapmap]
rs7470623	1.00[CEU][hapmap]
rs7847768	1.00[JPT][hapmap]
rs7850123	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs7856477	1.00[CEU][hapmap]
rs7858025	0.82[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7863885	0.82[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7870380	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes]
rs7872747	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7872838	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs943744	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs943745	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs943748	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16542600-16564000	Weak transcription	HUVEC	blood vessel
2	chr9:16542800-16554800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr9:16543800-16554600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr9:16543800-16567000	Weak transcription	HSMMtube	muscle
5	chr9:16544000-16559600	Weak transcription	Small Intestine	intestine
6	chr9:16545000-16554000	Weak transcription	Fetal Kidney	kidney
7	chr9:16546000-16554600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr9:16546000-16559600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:16546000-16559800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr9:16546000-16568400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr9:16550000-16556400	Weak transcription	Fetal Intestine Small	intestine
12	chr9:16550200-16554000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:16550800-16559800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr9:16551600-16554000	Weak transcription	Fetal Lung	lung
15	chr9:16551800-16567800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr9:16552000-16559600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr9:16552000-16567800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr9:16552200-16559000	Weak transcription	Colon Smooth Muscle	Colon
19	chr9:16552600-16554600	Weak transcription	NH-A	brain
20	chr9:16552600-16555400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr9:16552600-16556000	Weak transcription	HSMM	muscle
22	chr9:16552800-16554000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:16552800-16554600	Weak transcription	Adipose Nuclei	Adipose
24	chr9:16552800-16554600	Weak transcription	Fetal Muscle Leg	muscle
25	chr9:16552800-16556000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:16552800-16557600	Weak transcription	Fetal Intestine Large	intestine
27	chr9:16552800-16557800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:16552800-16558400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:16552800-16559800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr9:16552800-16566600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:16552800-16570200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:16552800-16571000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr9:16552800-16571400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr9:16553000-16557800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:16553000-16559600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr9:16553000-16570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:16553000-16575200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr9:16553200-16554000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr9:16553200-16554600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr9:16553400-16554000	Weak transcription	NHDF-Ad	bronchial
41	chr9:16553400-16554600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:16553600-16554000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr9:16553600-16554800	Enhancers	Fetal Stomach	stomach
44	chr9:16553800-16554400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:16553800-16554600	Enhancers	NHLF	lung
46	chr9:16553800-16554800	Enhancers	Osteobl	bone
47	chr9:16553800-16555000	Enhancers	Ovary	ovary

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