Variant report

Variant	rs9957169
Chromosome Location	chr18:7626276-7626277
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs28465512	1.00[AMR][1000 genomes]
rs28524496	1.00[AMR][1000 genomes]
rs28570370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28674664	1.00[AMR][1000 genomes]
rs28870165	0.87[AFR][1000 genomes]
rs9953627	1.00[AMR][1000 genomes]
rs9955080	1.00[AMR][1000 genomes]
rs9958605	1.00[AMR][1000 genomes]
rs9958957	1.00[AMR][1000 genomes]
rs9959088	1.00[AMR][1000 genomes]
rs9959214	1.00[AMR][1000 genomes]
rs9962615	1.00[AMR][1000 genomes]
rs9963088	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7618200-7626400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr18:7619800-7626400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr18:7620000-7627200	Weak transcription	HSMMtube	muscle
4	chr18:7620000-7632000	Weak transcription	Fetal Kidney	kidney
5	chr18:7620200-7626800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr18:7620400-7626400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:7620400-7626400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr18:7620400-7626600	Weak transcription	Fetal Lung	lung
9	chr18:7620400-7633400	Weak transcription	Aorta	Aorta
10	chr18:7620600-7626400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr18:7620600-7632400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr18:7620800-7626400	Weak transcription	NHDF-Ad	bronchial
13	chr18:7621600-7626400	Enhancers	A549	lung
14	chr18:7622800-7626400	Weak transcription	Colon Smooth Muscle	Colon
15	chr18:7622800-7626600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr18:7623000-7626400	Weak transcription	NHEK	skin
17	chr18:7623000-7626600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr18:7623000-7626600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr18:7623000-7626800	Weak transcription	HMEC	breast
20	chr18:7623000-7627000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr18:7623800-7627800	Enhancers	Right Ventricle	heart
22	chr18:7624200-7629000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr18:7624400-7626400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr18:7624400-7626400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr18:7624800-7627800	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr18:7625000-7626400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:7625000-7626400	Weak transcription	Fetal Muscle Leg	muscle
28	chr18:7625000-7626400	Weak transcription	Lung	lung
29	chr18:7625000-7626600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr18:7625000-7627200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr18:7625600-7627600	Flanking Active TSS	HepG2	liver
32	chr18:7625800-7627200	Enhancers	Gastric	stomach
33	chr18:7625800-7627600	Enhancers	Pancreas	Pancrea
34	chr18:7625800-7628000	Enhancers	Left Ventricle	heart
35	chr18:7625800-7628200	Enhancers	Right Atrium	heart
36	chr18:7625800-7628400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr18:7625800-7631000	Enhancers	Psoas Muscle	Psoas
38	chr18:7626000-7627600	Enhancers	Liver	Liver
39	chr18:7626000-7628000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr18:7626000-7628000	Enhancers	Adipose Nuclei	Adipose
41	chr18:7626000-7628000	Enhancers	Fetal Heart	heart
42	chr18:7626000-7628200	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr18:7626200-7627400	Weak transcription	Small Intestine	intestine
44	chr18:7626200-7627600	Enhancers	Ovary	ovary
45	chr18:7626200-7627800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr18:7626200-7627800	Enhancers	Spleen	Spleen

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