Variant report

Variant	rs10221326
Chromosome Location	chr18:13036034-13036035
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:13031424..13033227-chr18:13033629..13036334,2	K562	blood:
2	chr18:13016492..13018767-chr18:13034776..13036478,2	K562	blood:
3	chr18:13032939..13034812-chr18:13035452..13038047,2	MCF-7	breast:
4	chr18:13034897..13036714-chr18:13150744..13153648,2	K562	blood:

Variant related genes	Relation type
ENSG00000267032	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10221384	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11080620	0.92[CHB][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11663049	0.92[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12605638	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12954256	0.92[CHB][hapmap];0.85[EUR][1000 genomes]
rs12955780	0.85[CHB][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1474043	0.85[CHB][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1786263	0.92[CHB][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1786270	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1786279	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1787000	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1787003	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1787004	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1787008	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1973779	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28619103	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28641764	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2902856	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35790309	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3809912	0.92[CHB][hapmap]
rs472702	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs472992	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs473580	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs474337	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs475139	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs478006	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs478399	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs482360	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs482577	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs490853	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs491349	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs492723	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs498685	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4995995	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs518145	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs527839	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs529620	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs547084	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs554719	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs554854	0.92[CHB][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs556371	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs556536	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs557846	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs562151	0.92[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs565832	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs567031	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs569453	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs570505	0.92[CHB][hapmap]
rs576963	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs578208	0.92[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6505775	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6505776	0.92[CHB][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6505777	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6505780	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs692833	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs692964	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs71353243	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7226616	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7229870	0.92[CHB][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7233600	0.92[CHB][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7233814	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7234094	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7234960	0.92[CHB][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7236162	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7236764	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7237236	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7241536	0.92[CHB][hapmap]
rs7243660	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8088313	0.92[CHB][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8089123	0.92[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8097038	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8097125	0.92[CHB][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9783859	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9783903	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9948139	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9949589	0.92[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9949682	0.92[CHB][hapmap]
rs9952698	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9958369	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9961669	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9964466	0.92[CHB][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1057083	chr18:12916779-13207538	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
4	nsv576524	chr18:12918318-13183609	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1056593	chr18:12926314-13183383	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv1064364	chr18:12926314-13207686	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv1062413	chr18:12988947-13039941	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv543657	chr18:12988947-13039941	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs10221326	CEP192	cis	Nerve Tibial	GTEx
rs10221326	CEP192	cis	Skin Sun Exposed Lower leg	GTEx
rs10221326	CEP192	cis	multi-tissue	Pritchard
rs10221326	CEP192	cis	lung	GTEx
rs10221326	CEP192	Cis_1M	lymphoblastoid	RTeQTL
rs10221326	CEP192	cis	Artery Tibial	GTEx
rs10221326	CEP192	cis	Esophagus Mucosa	GTEx
rs10221326	CEP192	cis	Adipose Subcutaneous	GTEx
rs10221326	CEP192	cis	Stomach	GTEx
rs10221326	CEP192	cis	Whole Blood	GTEx
rs10221326	CEP192	cis	Thyroid	GTEx
rs10221326	CEP192	cis	Esophagus Muscularis	GTEx
rs10221326	CEP192	cis	Artery Aorta	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12995200-13042000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:12998400-13041600	Strong transcription	Dnd41	blood
3	chr18:12999200-13039000	Strong transcription	Fetal Thymus	thymus
4	chr18:13005000-13039200	Strong transcription	Primary B cells from peripheral blood	blood
5	chr18:13007200-13044000	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr18:13008000-13046000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr18:13008400-13047200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr18:13011400-13038800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr18:13013800-13052000	Weak transcription	Right Ventricle	heart
10	chr18:13013800-13053200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr18:13014200-13047200	Weak transcription	Psoas Muscle	Psoas
12	chr18:13015400-13036400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr18:13015600-13048800	Weak transcription	Small Intestine	intestine
14	chr18:13016400-13036200	Weak transcription	Gastric	stomach
15	chr18:13016800-13053200	Weak transcription	Esophagus	oesophagus
16	chr18:13017200-13056000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr18:13017600-13042200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr18:13018400-13038400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr18:13018600-13117400	Weak transcription	Stomach Mucosa	stomach
20	chr18:13023800-13037200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr18:13024000-13038600	Strong transcription	Fetal Intestine Large	intestine
22	chr18:13024000-13039400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr18:13024000-13042400	Weak transcription	Fetal Brain Female	brain
24	chr18:13024200-13041800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr18:13024200-13042200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr18:13024800-13039800	Strong transcription	Fetal Muscle Leg	muscle
27	chr18:13026200-13039200	Strong transcription	Primary T cells from cord blood	blood
28	chr18:13027200-13036400	Weak transcription	NHLF	lung
29	chr18:13028200-13036200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr18:13028400-13052000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr18:13030000-13048600	Weak transcription	Brain Substantia Nigra	brain
32	chr18:13031000-13036600	Weak transcription	Fetal Heart	heart
33	chr18:13031000-13040600	Strong transcription	Fetal Stomach	stomach
34	chr18:13031000-13048400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr18:13031000-13048600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr18:13032000-13047000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr18:13032000-13048000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr18:13032000-13048200	Weak transcription	Colon Smooth Muscle	Colon
39	chr18:13032000-13056000	Weak transcription	HSMMtube	muscle
40	chr18:13032200-13042000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr18:13032200-13043000	Weak transcription	Pancreas	Pancrea
42	chr18:13032400-13038800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr18:13032400-13041000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr18:13032400-13048600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr18:13032600-13041600	Weak transcription	A549	lung
46	chr18:13032600-13042000	Weak transcription	Brain Hippocampus Middle	brain
47	chr18:13032600-13048600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr18:13032800-13042000	Weak transcription	NH-A	brain
49	chr18:13033000-13036200	Weak transcription	Brain Anterior Caudate	brain
50	chr18:13033000-13036200	Weak transcription	Left Ventricle	heart

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