Variant report

Variant	nsv947847
Chromosome Location	chr10:37438104-37458506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 762 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574146977	chr10:37438104-37438105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543211278	chr10:37438117-37438118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190030891	chr10:37438128-37438129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545723915	chr10:37438145-37438146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576826529	chr10:37438180-37438181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544994936	chr10:37438195-37438196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117525070	chr10:37438205-37438206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527318864	chr10:37438229-37438230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370222883	chr10:37438276-37438277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541118856	chr10:37438280-37438281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561085248	chr10:37438281-37438282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138606756	chr10:37438288-37438289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549963234	chr10:37438326-37438327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369635206	chr10:37438330-37438331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182101286	chr10:37438337-37438338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373610331	chr10:37438347-37438348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187956280	chr10:37438377-37438378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552085686	chr10:37438393-37438394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149293826	chr10:37438414-37438415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533976863	chr10:37438423-37438424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530188143	chr10:37438470-37438471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116605061	chr10:37438471-37438472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139147209	chr10:37438482-37438483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556742059	chr10:37438508-37438509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576739383	chr10:37438515-37438516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142362140	chr10:37438528-37438529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557917811	chr10:37438531-37438532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200039777	chr10:37438538-37438539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572069400	chr10:37438539-37438540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376577847	chr10:37438547-37438548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201538199	chr10:37438587-37438588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369532435	chr10:37438591-37438592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560786304	chr10:37438619-37438620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202049333	chr10:37438622-37438623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72787532	chr10:37438647-37438648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201445322	chr10:37438653-37438654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543180343	chr10:37438702-37438703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192432374	chr10:37438712-37438713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs267602480	chr10:37438714-37438715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200260827	chr10:37438725-37438726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs267602481	chr10:37438727-37438728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552047613	chr10:37438730-37438731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201360743	chr10:37438746-37438747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199571878	chr10:37438753-37438754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527641248	chr10:37438767-37438768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376821949	chr10:37438772-37438773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368836727	chr10:37438802-37438803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373024622	chr10:37438807-37438808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377016392	chr10:37438808-37438809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142471234	chr10:37438810-37438811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	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
Oral squamous cell carcinoma	17134496	CNVD
Bethlem myopathy	20302629	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hepatocellular carcinoma	16785998	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:37436000-37439000	Weak transcription	A549	lung
2	chr10:37439000-37439400	Active TSS	A549	lung
3	chr10:37439400-37441200	Weak transcription	A549	lung
4	chr10:37441200-37441400	Enhancers	A549	lung
5	chr10:37446400-37447200	Weak transcription	A549	lung
6	chr10:37447800-37448400	ZNF genes & repeats	A549	lung
7	chr10:37448400-37454800	Weak transcription	A549	lung
8	chr10:37454800-37455200	Enhancers	A549	lung

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