Variant report

Variant	rs73939353
Chromosome Location	chr18:7728275-7728276
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs1446075	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57210096	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73939346	1.00[AMR][1000 genomes]
rs73939351	0.89[AFR][1000 genomes];0.83[AMR][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	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	nsv458017	chr18:7689201-7747873	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv576420	chr18:7689201-7747873	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv470406	chr18:7700462-7747873	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7723000-7733800	Weak transcription	A549	lung
2	chr18:7723800-7728400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr18:7723800-7728400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr18:7723800-7728400	Weak transcription	Pancreas	Pancrea
5	chr18:7724000-7728400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr18:7724000-7728400	Weak transcription	Right Atrium	heart
7	chr18:7724000-7734200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr18:7724600-7730400	Weak transcription	Fetal Kidney	kidney
9	chr18:7726000-7728600	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr18:7726000-7734200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr18:7726200-7728400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr18:7726200-7728400	Weak transcription	Left Ventricle	heart
13	chr18:7726200-7728600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr18:7726200-7733600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr18:7726200-7733800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr18:7726200-7733800	Weak transcription	Psoas Muscle	Psoas
17	chr18:7726400-7728400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr18:7726600-7728400	Weak transcription	Gastric	stomach
19	chr18:7726600-7729600	Enhancers	Fetal Lung	lung
20	chr18:7727000-7728600	Enhancers	Adipose Nuclei	Adipose
21	chr18:7727000-7728600	Enhancers	Fetal Stomach	stomach
22	chr18:7727000-7728800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr18:7727200-7728400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr18:7727200-7728600	Enhancers	Colon Smooth Muscle	Colon
25	chr18:7727200-7728600	Enhancers	Fetal Muscle Leg	muscle
26	chr18:7727200-7728800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr18:7727400-7728600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr18:7727400-7732800	Weak transcription	Right Ventricle	heart
29	chr18:7727400-7734000	Weak transcription	Aorta	Aorta
30	chr18:7727800-7728400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr18:7727800-7728600	Enhancers	Ovary	ovary
32	chr18:7728000-7738800	Weak transcription	Thymus	Thymus
33	chr18:7728200-7728400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr18:7728200-7728400	Flanking Active TSS	Fetal Heart	heart
35	chr18:7728200-7728600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr18:7728200-7728800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:7728200-7728800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr18:7728200-7728800	Enhancers	HMEC	breast
39	chr18:7728200-7731800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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