Variant report

Variant	nsv892032
Chromosome Location	chr9:1491213-1538884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:1017972..1018656-chr9:1527877..1528623,2	MCF-7	breast:
2	chr9:1492000..1494748-chr9:1498884..1501267,2	MCF-7	breast:
3	chr9:1459862..1460804-chr9:1527712..1529112,4	MCF-7	breast:
4	chr9:1492000..1494748-chr9:1498884..1501267,2	MCF-7	breast:

Extended variants
information (count: 2838 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2838 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12379509	chr9:1491213-1491214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185381335	chr9:1491215-1491216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535021196	chr9:1491228-1491229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60023133	chr9:1491236-1491237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190194118	chr9:1491251-1491252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537186518	chr9:1491255-1491256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556317143	chr9:1491257-1491258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549547077	chr9:1491276-1491277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147053557	chr9:1491277-1491278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538882814	chr9:1491292-1491293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181421695	chr9:1491305-1491306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187013711	chr9:1491325-1491326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77720678	chr9:1491326-1491327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs530615890	chr9:1491331-1491332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540639182	chr9:1491334-1491335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551095719	chr9:1491356-1491357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75637935	chr9:1491398-1491399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552107287	chr9:1491423-1491424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574452280	chr9:1491435-1491436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536681062	chr9:1491437-1491438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563898118	chr9:1491446-1491447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116231004	chr9:1491470-1491471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191793577	chr9:1491495-1491496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140251486	chr9:1491499-1491500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74500249	chr9:1491502-1491503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548590917	chr9:1491605-1491606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113311838	chr9:1491637-1491638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374835815	chr9:1491652-1491653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201922861	chr9:1491680-1491681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs57068410	chr9:1491684-1491685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568406673	chr9:1491696-1491697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372619132	chr9:1491697-1491698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117922585	chr9:1491705-1491706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184032933	chr9:1491708-1491709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150379131	chr9:1491713-1491714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112233887	chr9:1491735-1491736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538467575	chr9:1491762-1491763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76012418	chr9:1491779-1491780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10756617	chr9:1491796-1491797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs576386050	chr9:1491798-1491799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149470563	chr9:1491805-1491806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574390690	chr9:1491808-1491809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543465772	chr9:1491810-1491811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188936458	chr9:1491838-1491839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144594235	chr9:1491846-1491847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111973855	chr9:1491855-1491856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10810256	chr9:1491861-1491862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528775840	chr9:1491862-1491863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75270122	chr9:1491876-1491877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562071063	chr9:1491884-1491885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1490800-1492000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:1491000-1492200	Weak transcription	Fetal Muscle Leg	muscle
3	chr9:1491000-1504000	Weak transcription	Adipose Nuclei	Adipose
4	chr9:1491200-1491400	Enhancers	GM12878-XiMat	blood
5	chr9:1491200-1492200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:1491200-1492400	Weak transcription	Psoas Muscle	Psoas
7	chr9:1492000-1493000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:1492200-1492800	Enhancers	Fetal Muscle Leg	muscle
9	chr9:1492400-1492600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:1492400-1492600	Enhancers	Psoas Muscle	Psoas
11	chr9:1495800-1496000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:1496200-1496400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:1496800-1497000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr9:1497000-1497200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:1504000-1504800	Strong transcription	Adipose Nuclei	Adipose
16	chr9:1504800-1513800	Weak transcription	Adipose Nuclei	Adipose
17	chr9:1511000-1511200	Enhancers	NHEK	skin
18	chr9:1512600-1513000	Enhancers	Fetal Muscle Leg	muscle
19	chr9:1512800-1514200	Enhancers	NHEK	skin
20	chr9:1513000-1513400	Weak transcription	Fetal Muscle Leg	muscle
21	chr9:1513000-1513800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr9:1513200-1514000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:1513400-1514800	Enhancers	Fetal Muscle Leg	muscle
24	chr9:1513800-1514600	Enhancers	Adipose Nuclei	Adipose
25	chr9:1514000-1514800	Enhancers	Psoas Muscle	Psoas
26	chr9:1514400-1515000	Enhancers	Fetal Stomach	stomach
27	chr9:1514400-1515800	Enhancers	GM12878-XiMat	blood
28	chr9:1514600-1522600	Weak transcription	Adipose Nuclei	Adipose
29	chr9:1514800-1521600	Weak transcription	Fetal Muscle Leg	muscle
30	chr9:1515000-1515600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr9:1515600-1516000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr9:1515600-1516000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:1515600-1516000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr9:1515800-1516200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr9:1521600-1522200	Enhancers	Fetal Muscle Leg	muscle
36	chr9:1521600-1523600	Enhancers	GM12878-XiMat	blood
37	chr9:1521800-1523000	Enhancers	Fetal Lung	lung
38	chr9:1522200-1522600	Weak transcription	Fetal Muscle Leg	muscle
39	chr9:1522600-1523400	Enhancers	Fetal Muscle Leg	muscle
40	chr9:1522600-1523800	Enhancers	Adipose Nuclei	Adipose
41	chr9:1523400-1527800	Weak transcription	Fetal Muscle Leg	muscle
42	chr9:1527800-1530000	Enhancers	Fetal Muscle Leg	muscle
43	chr9:1529600-1530000	Enhancers	Pancreas	Pancrea
44	chr9:1530000-1531200	Weak transcription	Pancreas	Pancrea
45	chr9:1531200-1532600	Enhancers	Pancreas	Pancrea
46	chr9:1531200-1533400	Enhancers	Fetal Muscle Leg	muscle
47	chr9:1531400-1533200	Enhancers	Fetal Stomach	stomach
48	chr9:1532400-1532600	Enhancers	Fetal Muscle Trunk	muscle
49	chr9:1533200-1533400	Enhancers	Fetal Muscle Trunk	muscle
50	chr9:1535400-1537400	Enhancers	GM12878-XiMat	blood

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