Variant report

Variant	esv10455
Chromosome Location	chr10:26596407-26597670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:70 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs876845	chr10:26596420-26596421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552917600	chr10:26596422-26596423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536614810	chr10:26596424-26596425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs876848	chr10:26596496-26596497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs191697664	chr10:26596507-26596508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111977087	chr10:26596604-26596605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568354839	chr10:26596652-26596653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534338590	chr10:26596669-26596670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6482552	chr10:26596675-26596676	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs146431680	chr10:26596713-26596714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527766755	chr10:26596726-26596727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140798479	chr10:26596749-26596750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556050096	chr10:26596753-26596754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576240891	chr10:26596775-26596776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6482553	chr10:26596798-26596799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6482554	chr10:26596812-26596813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571924105	chr10:26596875-26596876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11432954	chr10:26596897-26596898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs397948898	chr10:26596899-26596900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201773095	chr10:26596900-26596901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143526537	chr10:26596916-26596917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7076001	chr10:26596932-26596933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577520613	chr10:26596933-26596934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183529929	chr10:26596938-26596939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs913960	chr10:26596954-26596955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs74126413	chr10:26596977-26596978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs74126414	chr10:26596983-26596984	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs1197125	chr10:26597017-26597018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556930330	chr10:26597068-26597069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74126416	chr10:26597114-26597115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs539913801	chr10:26597139-26597140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188224373	chr10:26597144-26597145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549988292	chr10:26597149-26597150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74126417	chr10:26597150-26597151	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs74126418	chr10:26597159-26597160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555345348	chr10:26597167-26597168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74126419	chr10:26597177-26597178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534554591	chr10:26597198-26597199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74126420	chr10:26597228-26597229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs74126421	chr10:26597285-26597286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543536322	chr10:26597290-26597291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112453130	chr10:26597297-26597298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74126422	chr10:26597300-26597301	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs368228655	chr10:26597305-26597306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1888251	chr10:26597316-26597317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs562210476	chr10:26597344-26597345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373571119	chr10:26597345-26597346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527689084	chr10:26597347-26597348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201483471	chr10:26597349-26597350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564137419	chr10:26597379-26597380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26587400-26599000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26592400-26598200	Weak transcription	Brain Germinal Matrix	brain

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