Variant report

Variant	rs8088153
Chromosome Location	chr18:43531640-43531641
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10432160	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10432197	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11082498	0.87[ASN][1000 genomes]
rs11082501	0.86[ASN][1000 genomes]
rs12232683	0.83[ASN][1000 genomes]
rs12454420	0.86[ASN][1000 genomes]
rs12604430	0.84[ASN][1000 genomes]
rs12604492	0.83[ASN][1000 genomes]
rs1573404	0.84[ASN][1000 genomes]
rs2004084	0.86[ASN][1000 genomes]
rs28430300	0.86[ASN][1000 genomes]
rs3745000	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4629066	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs475452	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs481755	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57011365	0.91[ASN][1000 genomes]
rs58306126	0.80[ASN][1000 genomes]
rs58312765	0.86[ASN][1000 genomes]
rs584397	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59884993	0.86[ASN][1000 genomes]
rs60288752	0.81[ASN][1000 genomes]
rs60866799	0.84[ASN][1000 genomes]
rs61363974	0.83[ASN][1000 genomes]
rs61449207	0.87[ASN][1000 genomes]
rs61680317	0.86[ASN][1000 genomes]
rs630625	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7226881	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7230104	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7235629	0.84[ASN][1000 genomes]
rs7238724	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7242733	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72918390	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8087546	0.84[ASN][1000 genomes]
rs8093119	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8097415	0.83[ASN][1000 genomes]
rs8098175	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9948634	0.82[AMR][1000 genomes]
rs9957288	0.81[ASN][1000 genomes]
rs9958844	0.84[ASN][1000 genomes]
rs9959763	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9964220	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9964347	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv909588	chr18:43474795-43554371	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:43472000-43536800	Strong transcription	Primary monocytes fromperipheralblood	blood
2	chr18:43475200-43535800	Strong transcription	Placenta	Placenta
3	chr18:43477800-43536800	Strong transcription	Primary T cells from cord blood	blood
4	chr18:43478000-43536600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr18:43491600-43536000	Strong transcription	Fetal Intestine Large	intestine
6	chr18:43492400-43546600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:43494000-43546600	Weak transcription	Stomach Mucosa	stomach
8	chr18:43499800-43535200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr18:43501200-43535800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr18:43501200-43536000	Strong transcription	Primary B cells from peripheral blood	blood
11	chr18:43512200-43536400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr18:43512400-43535200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr18:43512400-43535600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr18:43514400-43536200	Strong transcription	Fetal Thymus	thymus
15	chr18:43514400-43536400	Strong transcription	Dnd41	blood
16	chr18:43514400-43537000	Strong transcription	Primary B cells from cord blood	blood
17	chr18:43514600-43536400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr18:43517600-43533400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr18:43517600-43535200	Strong transcription	Duodenum Mucosa	Duodenum
20	chr18:43517600-43535400	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr18:43517600-43535600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr18:43517600-43536200	Strong transcription	Liver	Liver
23	chr18:43517800-43533600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr18:43517800-43533600	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr18:43517800-43536000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr18:43517800-43536000	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr18:43517800-43536200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr18:43518000-43535200	Strong transcription	Lung	lung
29	chr18:43518000-43535200	Strong transcription	Thymus	Thymus
30	chr18:43518000-43535400	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr18:43518000-43535400	Strong transcription	Adipose Nuclei	Adipose
32	chr18:43518400-43535200	Strong transcription	Colon Smooth Muscle	Colon
33	chr18:43518600-43533600	Strong transcription	Left Ventricle	heart
34	chr18:43518600-43535200	Strong transcription	Fetal Muscle Trunk	muscle
35	chr18:43518600-43535200	Strong transcription	Ovary	ovary
36	chr18:43518600-43535600	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr18:43518600-43535600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr18:43518600-43536000	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr18:43518600-43536200	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr18:43518600-43536400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr18:43518800-43535600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr18:43519000-43535600	Strong transcription	Fetal Lung	lung
43	chr18:43519200-43532600	Strong transcription	Primary T helper cells PMA-I stimulated	--
44	chr18:43519200-43536200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr18:43519200-43546600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr18:43519400-43536000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr18:43519800-43533800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr18:43519800-43536200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr18:43519800-43536400	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr18:43519800-43539400	Weak transcription	A549	lung

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