Variant report

Variant	rs55983357
Chromosome Location	chr18:7632723-7632724
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11876323	0.96[ASN][1000 genomes]
rs11876394	0.96[ASN][1000 genomes]
rs13313691	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs13381320	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs16952317	0.91[ASN][1000 genomes]
rs28375830	0.89[ASN][1000 genomes]
rs28507304	0.89[ASN][1000 genomes]
rs55669819	0.89[ASN][1000 genomes]
rs55793264	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56079905	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56165536	0.89[ASN][1000 genomes]
rs57109716	0.96[ASN][1000 genomes]
rs58291169	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58361187	0.97[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs73387558	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73387584	0.86[AFR][1000 genomes]
rs73387591	0.96[ASN][1000 genomes]
rs9946337	1.00[ASN][1000 genomes]
rs9954075	0.89[ASN][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:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7620400-7633400	Weak transcription	Aorta	Aorta
2	chr18:7627200-7636000	Weak transcription	Gastric	stomach
3	chr18:7627200-7637800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr18:7627400-7633000	Weak transcription	HSMM	muscle
5	chr18:7627600-7636600	Weak transcription	Fetal Muscle Leg	muscle
6	chr18:7627800-7633000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr18:7627800-7637200	Weak transcription	NHLF	lung
8	chr18:7627800-7637400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr18:7628000-7632800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:7628200-7632800	Weak transcription	HMEC	breast
11	chr18:7628200-7633000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr18:7628200-7633000	Weak transcription	A549	lung
13	chr18:7628200-7636000	Weak transcription	Lung	lung
14	chr18:7628400-7635800	Weak transcription	HepG2	liver
15	chr18:7628800-7633000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr18:7629000-7646200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr18:7629600-7634200	Enhancers	Left Ventricle	heart
18	chr18:7629600-7634600	Enhancers	Right Ventricle	heart
19	chr18:7630600-7641800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr18:7631000-7636600	Weak transcription	Fetal Lung	lung
21	chr18:7631000-7637400	Weak transcription	Ovary	ovary
22	chr18:7631000-7662800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr18:7631200-7632800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr18:7632000-7633200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr18:7632000-7634400	Enhancers	Psoas Muscle	Psoas
26	chr18:7632200-7633000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr18:7632200-7633400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr18:7632200-7636800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr18:7632400-7632800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr18:7632400-7633000	Enhancers	Fetal Brain Female	brain
31	chr18:7632400-7633200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr18:7632600-7633000	Enhancers	Stomach Smooth Muscle	stomach
33	chr18:7632600-7633200	Weak transcription	Right Atrium	heart
34	chr18:7632600-7633600	Enhancers	NHDF-Ad	bronchial

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