Variant report

Variant	rs9710023
Chromosome Location	chr18:12601176-12601177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:12600695..12603563-chr18:12609773..12612258,2	K562	blood:
2	chr18:12601083..12604521-chr18:12605372..12609062,5	MCF-7	breast:
3	chr18:12594070..12599084-chr18:12599553..12605396,7	K562	blood:
4	chr18:12407681..12409442-chr18:12599712..12601429,2	K562	blood:

Variant related genes	Relation type
ENSG00000141391	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10401097	0.80[ASN][1000 genomes]
rs11080585	0.80[ASN][1000 genomes]
rs11080586	0.81[ASN][1000 genomes]
rs11659854	0.82[ASN][1000 genomes]
rs11664765	0.80[ASN][1000 genomes]
rs11664927	0.85[ASN][1000 genomes]
rs11664936	0.80[ASN][1000 genomes]
rs11665543	0.82[ASN][1000 genomes]
rs12326271	0.81[ASN][1000 genomes]
rs12454931	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12455909	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12604184	0.80[ASN][1000 genomes]
rs12604385	0.83[ASN][1000 genomes]
rs12604400	0.84[EUR][1000 genomes]
rs12604541	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12605240	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12606465	0.83[ASN][1000 genomes]
rs12606482	0.80[ASN][1000 genomes]
rs12606506	0.87[EUR][1000 genomes]
rs12953578	0.80[ASN][1000 genomes]
rs12954614	0.84[EUR][1000 genomes]
rs12956133	0.80[ASN][1000 genomes]
rs12957688	0.84[ASN][1000 genomes]
rs12958200	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12959015	0.87[EUR][1000 genomes]
rs12960150	0.80[ASN][1000 genomes]
rs12962476	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12963179	0.84[ASN][1000 genomes]
rs12965094	0.86[EUR][1000 genomes]
rs12970025	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12970174	0.81[EUR][1000 genomes]
rs1893193	0.81[ASN][1000 genomes]
rs1940974	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1940975	0.82[ASN][1000 genomes]
rs2155698	0.82[ASN][1000 genomes]
rs2186907	0.81[ASN][1000 genomes]
rs28414067	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28457089	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28496036	0.83[ASN][1000 genomes]
rs28582228	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28647784	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28886423	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34072260	0.86[EUR][1000 genomes]
rs34438212	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34814556	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34899007	0.87[EUR][1000 genomes]
rs35449211	0.86[EUR][1000 genomes]
rs35630805	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4389196	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4493131	0.81[EUR][1000 genomes]
rs4627434	0.82[ASN][1000 genomes]
rs4629035	0.80[ASN][1000 genomes]
rs62097102	0.80[EUR][1000 genomes]
rs62097126	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62097148	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62097149	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62097153	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67045810	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7234697	0.84[ASN][1000 genomes]
rs7238546	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7242395	0.86[EUR][1000 genomes]
rs8088786	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8089081	0.85[EUR][1000 genomes]
rs8093571	0.88[EUR][1000 genomes]
rs8095160	0.82[ASN][1000 genomes]
rs8096455	0.80[ASN][1000 genomes]
rs9303772	0.80[ASN][1000 genomes]
rs9303773	0.80[ASN][1000 genomes]
rs9945339	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9945374	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9948505	0.80[ASN][1000 genomes]
rs9948618	0.82[ASN][1000 genomes]
rs9951147	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9954054	0.80[ASN][1000 genomes]
rs9954419	0.81[ASN][1000 genomes]
rs9958409	0.80[ASN][1000 genomes]
rs9959759	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9961705	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9961851	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9964759	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9965123	0.80[ASN][1000 genomes]
rs9967123	0.81[ASN][1000 genomes]
rs9989506	0.80[ASN][1000 genomes]
rs9989568	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	nsv491873	chr18:12159445-12739784	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
3	esv3528039	chr18:12396582-12851293	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	esv3528041	chr18:12396641-12851245	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv523743	chr18:12474505-12742809	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9710023	RP11-861E21.2	cis	Muscle Skeletal	GTEx
rs9710023	SPIRE1	cis	Muscle Skeletal	GTEx

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12597000-12605800	Weak transcription	Gastric	stomach
2	chr18:12597000-12605800	Weak transcription	K562	blood
3	chr18:12597000-12606800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr18:12597800-12610800	Weak transcription	Right Ventricle	heart
5	chr18:12597800-12634600	Weak transcription	Aorta	Aorta
6	chr18:12598000-12601800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr18:12598000-12601800	Weak transcription	Brain Hippocampus Middle	brain
8	chr18:12598000-12601800	Weak transcription	Fetal Thymus	thymus
9	chr18:12598000-12606600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr18:12598000-12607000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr18:12598000-12607200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr18:12598000-12610000	Weak transcription	Lung	lung
13	chr18:12598200-12606800	Weak transcription	Brain Anterior Caudate	brain
14	chr18:12598600-12608600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr18:12598800-12606000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr18:12598800-12606000	Weak transcription	Left Ventricle	heart
17	chr18:12598800-12606800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr18:12598800-12607000	Weak transcription	Brain Angular Gyrus	brain
19	chr18:12598800-12609000	Weak transcription	Right Atrium	heart
20	chr18:12599000-12601800	Weak transcription	Fetal Brain Male	brain
21	chr18:12599000-12606800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr18:12599000-12606800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr18:12599400-12601800	Weak transcription	Fetal Heart	heart
24	chr18:12599800-12601800	Weak transcription	Fetal Brain Female	brain
25	chr18:12599800-12606200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr18:12599800-12607000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr18:12600000-12604600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr18:12600000-12606200	Weak transcription	A549	lung
29	chr18:12600000-12607400	Weak transcription	Pancreas	Pancrea
30	chr18:12600200-12607000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:12600400-12601600	Weak transcription	Primary T cells from cord blood	blood
32	chr18:12600400-12601600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr18:12600400-12601600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr18:12600400-12601600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr18:12600400-12601800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr18:12600400-12601800	Weak transcription	HUVEC	blood vessel
37	chr18:12600400-12604600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr18:12600400-12605800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr18:12600400-12605800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr18:12600400-12605800	Weak transcription	Hela-S3	cervix
41	chr18:12600400-12606600	Weak transcription	HepG2	liver
42	chr18:12600400-12606800	Weak transcription	HSMM	muscle
43	chr18:12600400-12607000	Weak transcription	NHLF	lung
44	chr18:12600400-12608600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr18:12600600-12601600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr18:12600600-12602000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr18:12600600-12605000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr18:12600600-12606000	Weak transcription	NHEK	skin
49	chr18:12600600-12606400	Weak transcription	HSMMtube	muscle
50	chr18:12600600-12606800	Weak transcription	NHDF-Ad	bronchial

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