Variant report

Variant	rs7019399
Chromosome Location	chr9:18485876-18485877
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1006022	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs10453192	0.87[EUR][1000 genomes]
rs10733354	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10738510	0.80[ASN][1000 genomes]
rs10738511	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10810973	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10963613	0.82[CEU][hapmap]
rs11793923	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1281350	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1281352	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1340039	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1417035	0.84[EUR][1000 genomes]
rs1417037	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1538999	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs16936745	0.86[CEU][hapmap]
rs1832747	0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1888068	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1888069	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2149875	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2153415	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2153416	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2277160	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3898100	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4246142	0.86[EUR][1000 genomes]
rs4246143	0.88[EUR][1000 genomes]
rs4590536	0.88[EUR][1000 genomes]
rs4961650	0.92[ASN][1000 genomes]
rs4961651	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4961652	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6475219	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6475220	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6475221	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7032393	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7036515	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7046502	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7856703	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7864856	0.99[ASN][1000 genomes]
rs7867766	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][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:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18477400-18489200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr9:18479200-18490000	Weak transcription	Aorta	Aorta
3	chr9:18482600-18492200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr9:18484000-18486000	Genic enhancers	NHDF-Ad	bronchial
5	chr9:18484000-18486800	Genic enhancers	HSMM	muscle
6	chr9:18484400-18486200	Genic enhancers	Muscle Satellite Cultured Cells	--
7	chr9:18484400-18486200	Enhancers	Colon Smooth Muscle	Colon
8	chr9:18484600-18486000	Enhancers	Fetal Muscle Leg	muscle
9	chr9:18484600-18486000	Enhancers	Stomach Smooth Muscle	stomach
10	chr9:18485200-18486000	Genic enhancers	NH-A	brain
11	chr9:18485200-18486200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:18485200-18486400	Enhancers	Fetal Heart	heart
13	chr9:18485400-18486000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr9:18485400-18486000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr9:18485400-18486000	Genic enhancers	Osteobl	bone
16	chr9:18485400-18486400	Enhancers	HSMMtube	muscle
17	chr9:18485400-18488600	Weak transcription	HUVEC	blood vessel
18	chr9:18485600-18486000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr9:18485600-18486000	Enhancers	NHLF	lung
20	chr9:18485600-18486200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:18485600-18486200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:18485600-18486200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr9:18485600-18486200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr9:18485600-18486200	Enhancers	Fetal Stomach	stomach
25	chr9:18485800-18487200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:18485800-18490800	Weak transcription	Fetal Brain Female	brain

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