Variant report

Variant	nsv467207
Chromosome Location	chr10:55378668-55391418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 422 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9416282	chr10:55378668-55378669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187481089	chr10:55378719-55378720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574773280	chr10:55378776-55378777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201629948	chr10:55378801-55378802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559131703	chr10:55378824-55378825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371756296	chr10:55378845-55378846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560429821	chr10:55378863-55378864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12572437	chr10:55378868-55378869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545258215	chr10:55378913-55378914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545949803	chr10:55378922-55378923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565009049	chr10:55379006-55379007	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190799405	chr10:55379025-55379026	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147288682	chr10:55379046-55379047	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541816695	chr10:55379221-55379222	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183720230	chr10:55379256-55379257	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34950396	chr10:55379260-55379261	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547371274	chr10:55379275-55379276	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141026644	chr10:55379298-55379299	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567981351	chr10:55379299-55379300	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556365524	chr10:55379310-55379311	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536922129	chr10:55379383-55379384	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569893348	chr10:55379521-55379522	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535729441	chr10:55379527-55379528	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144900527	chr10:55379534-55379535	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574773837	chr10:55379540-55379541	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550430085	chr10:55379630-55379631	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540217316	chr10:55379643-55379644	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369927505	chr10:55379644-55379645	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570219770	chr10:55379698-55379699	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576892925	chr10:55379713-55379714	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538800847	chr10:55379715-55379716	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559009462	chr10:55379743-55379744	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562723479	chr10:55379841-55379842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs60993664	chr10:55379852-55379853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542502553	chr10:55379855-55379856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562195908	chr10:55379875-55379876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189100435	chr10:55379906-55379907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571655537	chr10:55379969-55379970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199607088	chr10:55379977-55379978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs202240551	chr10:55379978-55379979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540904679	chr10:55379979-55379980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs398054354	chr10:55379985-55379986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs398013483	chr10:55379986-55379987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35219027	chr10:55380007-55380008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147881716	chr10:55380024-55380025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533037644	chr10:55380092-55380093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371094579	chr10:55380107-55380108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549936935	chr10:55380133-55380134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200689624	chr10:55380155-55380156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9416283	chr10:55380159-55380160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55368000-55379000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:55371600-55381800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:55379000-55379400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
4	chr10:55379200-55379800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:55379200-55380200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr10:55379400-55379800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr10:55379400-55379800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:55379400-55379800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:55379400-55379800	Enhancers	NHEK	skin
10	chr10:55379400-55380400	Enhancers	HMEC	breast
11	chr10:55379800-55381600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr10:55379800-55387600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr10:55390400-55390600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr10:55390600-55394000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links