Variant report

Variant	rs8089761
Chromosome Location	chr18:7596538-7596539
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11876394	0.97[EUR][1000 genomes]
rs13313691	0.97[EUR][1000 genomes]
rs28375830	0.97[EUR][1000 genomes]
rs28507304	0.97[EUR][1000 genomes]
rs4798572	0.83[EUR][1000 genomes]
rs55669819	0.97[EUR][1000 genomes]
rs56165536	0.97[EUR][1000 genomes]
rs58291169	0.97[EUR][1000 genomes]
rs58361187	0.97[EUR][1000 genomes]
rs7235826	0.93[EUR][1000 genomes]
rs73387558	0.97[EUR][1000 genomes]
rs73387591	0.97[EUR][1000 genomes]
rs9946337	0.97[EUR][1000 genomes]
rs9954075	0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2656232	chr18:7111033-7658679	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv532282	chr18:7115075-7608218	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1064597	chr18:7169490-7762738	Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv543636	chr18:7169490-7762738	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1063350	chr18:7215275-7659999	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv534374	chr18:7438812-8412546	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv458016	chr18:7488133-7934001	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv576399	chr18:7488133-7934001	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	esv2762810	chr18:7492090-7924728	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1062911	chr18:7561991-8088274	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv543637	chr18:7561991-8088274	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv1064345	chr18:7562051-8088274	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv543638	chr18:7562051-8088274	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7580600-7600800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr18:7585000-7600600	Weak transcription	Spleen	Spleen
3	chr18:7585400-7600000	Weak transcription	A549	lung
4	chr18:7586400-7607600	Weak transcription	Aorta	Aorta
5	chr18:7591200-7597400	Enhancers	Left Ventricle	heart
6	chr18:7591400-7598200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr18:7591400-7599800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr18:7591400-7600400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr18:7591600-7598400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:7591600-7599800	Weak transcription	Brain Anterior Caudate	brain
11	chr18:7591600-7603800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr18:7592800-7600000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr18:7592800-7603400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr18:7593000-7599600	Weak transcription	Lung	lung
15	chr18:7593600-7597000	Weak transcription	Fetal Lung	lung
16	chr18:7593800-7598400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr18:7593800-7599600	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr18:7594800-7596600	Enhancers	Psoas Muscle	Psoas
19	chr18:7595000-7597400	Enhancers	Right Atrium	heart
20	chr18:7595000-7597600	Enhancers	Right Ventricle	heart
21	chr18:7595000-7597600	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr18:7595000-7598600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr18:7595400-7600600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:7595800-7596800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr18:7595800-7597200	Enhancers	HepG2	liver
26	chr18:7596000-7596600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr18:7596000-7596600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr18:7596000-7596600	Enhancers	Adipose Nuclei	Adipose
29	chr18:7596000-7596800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr18:7596000-7597000	Weak transcription	Fetal Heart	heart
31	chr18:7596000-7597200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr18:7596000-7597600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr18:7596200-7600200	Weak transcription	Small Intestine	intestine
34	chr18:7596400-7599000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr18:7596400-7599600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr18:7596400-7599800	Weak transcription	Gastric	stomach
37	chr18:7596400-7600200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr18:7596400-7600600	Weak transcription	NH-A	brain
39	chr18:7596400-7600800	Weak transcription	NHDF-Ad	bronchial
40	chr18:7596400-7603400	Weak transcription	Colon Smooth Muscle	Colon
41	chr18:7596400-7603400	Weak transcription	Pancreas	Pancrea
42	chr18:7596400-7603600	Weak transcription	Rectal Smooth Muscle	rectum

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