Variant report

Variant	esv10658
Chromosome Location	chr10:1634481-1635471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:119 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531669757	chr10:1634496-1634497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542018790	chr10:1634502-1634503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10903504	chr10:1634511-1634512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199651146	chr10:1634512-1634513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71500146	chr10:1634515-1634516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561945539	chr10:1634516-1634517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112742867	chr10:1634518-1634519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10903505	chr10:1634519-1634520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10219018	chr10:1634522-1634523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10903506	chr10:1634530-1634531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113098659	chr10:1634535-1634536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528021699	chr10:1634538-1634539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12258188	chr10:1634559-1634560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570382819	chr10:1634567-1634568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7897168	chr10:1634576-1634577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7916743	chr10:1634579-1634580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs137988049	chr10:1634581-1634582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10218870	chr10:1634582-1634583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549477876	chr10:1634583-1634584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75281748	chr10:1634590-1634591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78402715	chr10:1634593-1634594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10219019	chr10:1634594-1634595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113628006	chr10:1634607-1634608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113184941	chr10:1634619-1634620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10219101	chr10:1634639-1634640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11250647	chr10:1634644-1634645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10218872	chr10:1634645-1634646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377531762	chr10:1634656-1634657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111944201	chr10:1634680-1634681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111493405	chr10:1634682-1634683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371157579	chr10:1634707-1634708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71500147	chr10:1634708-1634709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535497083	chr10:1634732-1634733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377444812	chr10:1634733-1634734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36210709	chr10:1634769-1634770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75176664	chr10:1634770-1634771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71500155	chr10:1634771-1634772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34546595	chr10:1634774-1634775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11250649	chr10:1634779-1634780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112999785	chr10:1634782-1634783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549239965	chr10:1634790-1634791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112451929	chr10:1634796-1634797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112644075	chr10:1634808-1634809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71500148	chr10:1634828-1634829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112582681	chr10:1634833-1634834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35281874	chr10:1634834-1634835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77108582	chr10:1634837-1634838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112704021	chr10:1634845-1634846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113118153	chr10:1634859-1634860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71500150	chr10:1634860-1634861	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:1634000-1637000	Weak transcription	Fetal Brain Male	brain
2	chr10:1634600-1648200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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