Variant report

Variant	esv3302276
Chromosome Location	chr10:1741202-1744450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187341823	chr10:1743405-1743406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368145324	chr10:1743450-1743451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371614490	chr10:1743452-1743453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113800091	chr10:1743476-1743477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112329323	chr10:1743503-1743504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375175432	chr10:1743519-1743520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368249348	chr10:1743531-1743532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372836263	chr10:1743603-1743604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375768556	chr10:1743611-1743612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77619529	chr10:1743629-1743630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371773756	chr10:1743671-1743672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374352098	chr10:1743700-1743701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562770704	chr10:1743710-1743711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74775971	chr10:1743715-1743716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376551642	chr10:1743731-1743732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56326508	chr10:1743733-1743734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531418056	chr10:1743739-1743740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74660836	chr10:1743757-1743758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7072134	chr10:1743773-1743774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74838696	chr10:1743788-1743789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs75241548	chr10:1743790-1743791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547451706	chr10:1743799-1743800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12777019	chr10:1743811-1743812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12771670	chr10:1743815-1743816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12769491	chr10:1743823-1743824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28422872	chr10:1743827-1743828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12770957	chr10:1743836-1743837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542511733	chr10:1743840-1743841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12771687	chr10:1743841-1743842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369794316	chr10:1743844-1743845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372751826	chr10:1743857-1743858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377161550	chr10:1743865-1743866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9663695	chr10:1743869-1743870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370640240	chr10:1743874-1743875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9663365	chr10:1743883-1743884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12771715	chr10:1743886-1743887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12356537	chr10:1743899-1743900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9663271	chr10:1743911-1743912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527270220	chr10:1743914-1743915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373862246	chr10:1743915-1743916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375573908	chr10:1743920-1743921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9663702	chr10:1743925-1743926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61831991	chr10:1743953-1743954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61831992	chr10:1743956-1743957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61831993	chr10:1743958-1743959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547561726	chr10:1743966-1743967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372070149	chr10:1743991-1743992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111327972	chr10:1743995-1743996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533007577	chr10:1743998-1743999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554737887	chr10:1744008-1744009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1743400-1751000	Weak transcription	Fetal Brain Male	brain

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