Variant report

Variant	esv2335143
Chromosome Location	chr10:27731899-27732419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200756155	chr10:27731901-27731902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530360899	chr10:27731918-27731919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372823774	chr10:27731920-27731921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs67475231	chr10:27731922-27731923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375782559	chr10:27731924-27731925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62636305	chr10:27731941-27731942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56175138	chr10:27731942-27731943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182772077	chr10:27731955-27731956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12776112	chr10:27731964-27731965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12782086	chr10:27731966-27731967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151312626	chr10:27731975-27731976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111218174	chr10:27731979-27731980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139670812	chr10:27731991-27731992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187136984	chr10:27731993-27731994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368988909	chr10:27732002-27732003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372028175	chr10:27732005-27732006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12782267	chr10:27732018-27732019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12774780	chr10:27732020-27732021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146700597	chr10:27732036-27732037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12776313	chr10:27732045-27732046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12782287	chr10:27732047-27732048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12782290	chr10:27732054-27732055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567440559	chr10:27732056-27732057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62650800	chr10:27732063-27732064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548634196	chr10:27732072-27732073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568431024	chr10:27732074-27732075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200210249	chr10:27732081-27732082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368518321	chr10:27732082-27732083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369464317	chr10:27732089-27732090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62650801	chr10:27732119-27732120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12782488	chr10:27732120-27732121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12782496	chr10:27732130-27732131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536196638	chr10:27732133-27732134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199878996	chr10:27732147-27732148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533887245	chr10:27732150-27732151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12782514	chr10:27732153-27732154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12776549	chr10:27732157-27732158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554035466	chr10:27732165-27732166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184131984	chr10:27732198-27732199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370219034	chr10:27732200-27732201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201054160	chr10:27732202-27732203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199842865	chr10:27732203-27732204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200796089	chr10:27732204-27732205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372260474	chr10:27732205-27732206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200088811	chr10:27732206-27732207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201066203	chr10:27732207-27732208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539267229	chr10:27732208-27732209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555915642	chr10:27732231-27732232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189067929	chr10:27732246-27732247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575763398	chr10:27732253-27732254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

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
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
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27730000-27734800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:27730200-27735200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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