Variant report

Variant	esv3408855
Chromosome Location	chr8:1551220-1551783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185518713	chr8:1551249-1551250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs550122661	chr8:1551257-1551258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112432538	chr8:1551274-1551275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113936724	chr8:1551279-1551280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374367107	chr8:1551291-1551292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56677028	chr8:1551297-1551298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558854074	chr8:1551302-1551303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57812872	chr8:1551332-1551333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572393178	chr8:1551335-1551336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10098115	chr8:1551363-1551364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs60320941	chr8:1551370-1551371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2469739	chr8:1551373-1551374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201443783	chr8:1551374-1551375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183173962	chr8:1551399-1551400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58081209	chr8:1551407-1551408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60230362	chr8:1551408-1551409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574465620	chr8:1551416-1551417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188576227	chr8:1551429-1551430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57107071	chr8:1551430-1551431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57798201	chr8:1551445-1551446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58871247	chr8:1551446-1551447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4876109	chr8:1551468-1551469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61086208	chr8:1551482-1551483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56093927	chr8:1551484-1551485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs60768483	chr8:1551499-1551500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62485533	chr8:1551506-1551507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60849014	chr8:1551520-1551521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs58252085	chr8:1551521-1551522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577143435	chr8:1551527-1551528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58964295	chr8:1551537-1551538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11994543	chr8:1551543-1551544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs55873486	chr8:1551559-1551560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56045942	chr8:1551560-1551561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559732556	chr8:1551566-1551567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528347719	chr8:1551575-1551576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113680807	chr8:1551582-1551583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367645286	chr8:1551590-1551591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59209629	chr8:1551597-1551598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs57823554	chr8:1551598-1551599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58330935	chr8:1551620-1551621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113417458	chr8:1551622-1551623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59426452	chr8:1551634-1551635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58106326	chr8:1551635-1551636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112545525	chr8:1551636-1551637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547482366	chr8:1551638-1551639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563004509	chr8:1551650-1551651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs55952683	chr8:1551657-1551658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs60456968	chr8:1551658-1551659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61660667	chr8:1551666-1551667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114634914	chr8:1551669-1551670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1550800-1553400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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