Variant report

Variant	nsv818712
Chromosome Location	chr9:94148084-94154282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:94149933..94151504-chr9:94151649..94153455,2	MCF-7	breast:
2	chr9:94145262..94147906-chr9:94148347..94150501,2	MCF-7	breast:
3	chr9:94149933..94151504-chr9:94151649..94153455,2	MCF-7	breast:
4	chr9:94151920..94154917-chr9:94185254..94187129,2	K562	blood:

Variant related genes	Relation type
ENSG00000165030	chromatin interactions

Extended variants
information (count: 281 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2990343	chr9:94148084-94148085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530255223	chr9:94148097-94148098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565541109	chr9:94148105-94148106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186080505	chr9:94148114-94148115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527905136	chr9:94148154-94148155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537331047	chr9:94148158-94148159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541183721	chr9:94148170-94148171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558793295	chr9:94148180-94148181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189228681	chr9:94148185-94148186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376598846	chr9:94148254-94148255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146308026	chr9:94148331-94148332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370671956	chr9:94148343-94148344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181200915	chr9:94148351-94148352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112613491	chr9:94148372-94148373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553364399	chr9:94148382-94148383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139063472	chr9:94148412-94148413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370216604	chr9:94148415-94148416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542752338	chr9:94148445-94148446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79831899	chr9:94148460-94148461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149358512	chr9:94148465-94148466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576219266	chr9:94148466-94148467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543656078	chr9:94148467-94148468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534046439	chr9:94148468-94148469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565148856	chr9:94148470-94148471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10991915	chr9:94148471-94148472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76151707	chr9:94148474-94148475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143702426	chr9:94148477-94148478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186666465	chr9:94148478-94148479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2482364	chr9:94148481-94148482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148124666	chr9:94148482-94148483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74444129	chr9:94148486-94148487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559746052	chr9:94148490-94148491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530117252	chr9:94148494-94148495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548698517	chr9:94148531-94148532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570069023	chr9:94148538-94148539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531103348	chr9:94148542-94148543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552353699	chr9:94148582-94148583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2482365	chr9:94148584-94148585	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191264492	chr9:94148616-94148617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553352016	chr9:94148653-94148654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115593519	chr9:94148750-94148751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535951603	chr9:94148795-94148796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554615986	chr9:94148802-94148803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs386736243	chr9:94148846-94148847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs59655789	chr9:94148847-94148848	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs558794537	chr9:94148924-94148925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577205858	chr9:94148947-94148948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541365011	chr9:94148991-94148992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560540583	chr9:94149000-94149001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57541453	chr9:94149004-94149005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94142000-94153600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:94148600-94149200	Enhancers	HepG2	liver
3	chr9:94149000-94149200	Enhancers	Stomach Mucosa	stomach
4	chr9:94149200-94150000	Weak transcription	Stomach Mucosa	stomach
5	chr9:94149200-94156600	Weak transcription	HepG2	liver
6	chr9:94150000-94150200	Enhancers	Stomach Mucosa	stomach
7	chr9:94150200-94154400	Weak transcription	Stomach Mucosa	stomach
8	chr9:94152800-94153600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr9:94153400-94153800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:94153400-94154400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:94153400-94154400	Enhancers	NHDF-Ad	bronchial
12	chr9:94153400-94154400	Enhancers	Osteobl	bone
13	chr9:94153400-94154800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:94153600-94154000	Enhancers	NHLF	lung
15	chr9:94153600-94154200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:94153600-94154200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr9:94153600-94154200	Enhancers	Adipose Nuclei	Adipose
18	chr9:94153600-94154400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:94153600-94156600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr9:94153800-94154400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:94154000-94156000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:94154000-94157400	Weak transcription	NHLF	lung
23	chr9:94154200-94156000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:94154200-94157200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:94154200-94157400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:94154200-94157400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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