Variant report

Variant	rs870019
Chromosome Location	chr9:18489961-18489962
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10511658	1.00[AMR][1000 genomes]
rs11999281	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12000949	0.93[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12000950	0.93[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12001004	0.91[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12001790	0.93[YRI][hapmap]
rs12002126	1.00[AMR][1000 genomes]
rs12003118	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs12003267	0.81[LWK][hapmap];0.96[MKK][hapmap];0.85[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12003900	1.00[AMR][1000 genomes]
rs12005242	1.00[AMR][1000 genomes]
rs16936711	1.00[AMR][1000 genomes]
rs16936775	0.85[YRI][hapmap];1.00[AMR][1000 genomes]
rs16936780	0.92[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16936815	0.81[LWK][hapmap];0.93[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1856705	1.00[AMR][1000 genomes]
rs1888064	1.00[AMR][1000 genomes]
rs57153018	1.00[AMR][1000 genomes]
rs58068158	1.00[AMR][1000 genomes]
rs58526635	1.00[AMR][1000 genomes]
rs60199560	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60288112	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60561389	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6475217	1.00[AMR][1000 genomes]
rs7019792	0.91[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7040544	1.00[AMR][1000 genomes]
rs73417101	1.00[AMR][1000 genomes]
rs73418922	1.00[AMR][1000 genomes]
rs73418924	1.00[AMR][1000 genomes]
rs73418940	1.00[AMR][1000 genomes]
rs73421011	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73421013	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73421023	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73421030	1.00[AMR][1000 genomes]
rs73421031	1.00[AMR][1000 genomes]
rs73421035	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv892688	chr9:18385143-18551247	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1029449	chr9:18414752-18829127	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv540077	chr9:18414752-18829127	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv1030931	chr9:18414752-18903530	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
8	nsv892689	chr9:18485434-18537444	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv892690	chr9:18485434-18592374	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18479200-18490000	Weak transcription	Aorta	Aorta
2	chr9:18482600-18492200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr9:18485800-18490800	Weak transcription	Fetal Brain Female	brain
4	chr9:18486000-18490000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:18486000-18490000	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:18486000-18490200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr9:18486000-18490400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:18486200-18490000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:18486200-18490000	Weak transcription	Fetal Stomach	stomach
10	chr9:18486200-18490800	Weak transcription	Fetal Lung	lung
11	chr9:18487200-18490200	Enhancers	Osteobl	bone
12	chr9:18487400-18495600	Enhancers	Fetal Heart	heart
13	chr9:18487800-18490000	Weak transcription	Ovary	ovary
14	chr9:18488000-18490000	Weak transcription	Adipose Nuclei	Adipose
15	chr9:18488000-18490200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:18488000-18490200	Enhancers	NHDF-Ad	bronchial
17	chr9:18488200-18490000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr9:18488200-18490200	Weak transcription	Colon Smooth Muscle	Colon
19	chr9:18488400-18490000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr9:18488400-18490000	Enhancers	NH-A	brain
21	chr9:18488600-18490200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:18488600-18490400	Enhancers	HUVEC	blood vessel
23	chr9:18488800-18490200	Enhancers	HSMMtube	muscle
24	chr9:18488800-18490200	Enhancers	NHLF	lung
25	chr9:18489000-18490000	Enhancers	HSMM	muscle
26	chr9:18489000-18490600	Weak transcription	Brain Germinal Matrix	brain
27	chr9:18489200-18490000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr9:18489200-18491000	Enhancers	HMEC	breast
29	chr9:18489200-18491800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr9:18489400-18490800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:18489600-18490200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:18489600-18490200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr9:18489800-18490800	Enhancers	NHEK	skin

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