Variant report

Variant	esv3444468
Chromosome Location	chr13:93264751-93267099
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 87 )

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	rs549207697	chr13:93264754-93264755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184841756	chr13:93264757-93264758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534876876	chr13:93264891-93264892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547485296	chr13:93264892-93264893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570410906	chr13:93264900-93264901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577847348	chr13:93264917-93264918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539441229	chr13:93265005-93265006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11841741	chr13:93265019-93265020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570004430	chr13:93265026-93265027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535733929	chr13:93265051-93265052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537034927	chr13:93265056-93265057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11843052	chr13:93265074-93265075	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs188139559	chr13:93265141-93265142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180671005	chr13:93265179-93265180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558241534	chr13:93265180-93265181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577669408	chr13:93265187-93265188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34284645	chr13:93265240-93265241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185981091	chr13:93265324-93265325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563334026	chr13:93265333-93265334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189706964	chr13:93265335-93265336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529569432	chr13:93265372-93265373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372331833	chr13:93265445-93265446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181349578	chr13:93265522-93265523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9523727	chr13:93265524-93265525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9523728	chr13:93265532-93265533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9523729	chr13:93265533-93265534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186875040	chr13:93265536-93265537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528693408	chr13:93265542-93265543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190766633	chr13:93265552-93265553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377122841	chr13:93265569-93265570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183341612	chr13:93265572-93265573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9523730	chr13:93265574-93265575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374626518	chr13:93265577-93265578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367701248	chr13:93265586-93265587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569443327	chr13:93265594-93265595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370166309	chr13:93265595-93265596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9516095	chr13:93265601-93265602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9516096	chr13:93265604-93265605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9516097	chr13:93265624-93265625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538457864	chr13:93265626-93265627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9516098	chr13:93265627-93265628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548579408	chr13:93265629-93265630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61228489	chr13:93265633-93265634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56721406	chr13:93265639-93265640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71123417	chr13:93265642-93265643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71200592	chr13:93265647-93265648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9516100	chr13:93265649-93265650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56159649	chr13:93265655-93265656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551633658	chr13:93265656-93265657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533933022	chr13:93265659-93265660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93237200-93277400	Weak transcription	Right Atrium	heart

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