Variant report

Variant	nsv547857
Chromosome Location	chr1:152235564-152240504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548287633	chr1:152235623-152235624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377378127	chr1:152235624-152235625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140597673	chr1:152235692-152235693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557202859	chr1:152235700-152235701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74783083	chr1:152235732-152235733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77480409	chr1:152235759-152235760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570688958	chr1:152235799-152235800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538185083	chr1:152235839-152235840	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367646753	chr1:152235847-152235848	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188826122	chr1:152235888-152235889	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553052508	chr1:152235895-152235896	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557075819	chr1:152235945-152235946	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190378433	chr1:152235962-152235963	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535501344	chr1:152235992-152235993	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150464535	chr1:152235999-152236000	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6661487	chr1:152236011-152236012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543683813	chr1:152236026-152236027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11204956	chr1:152236058-152236059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542510004	chr1:152236065-152236066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145062671	chr1:152236066-152236067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12048637	chr1:152236079-152236080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545786992	chr1:152236125-152236126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56244386	chr1:152236148-152236149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs560680503	chr1:152236166-152236167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528484294	chr1:152236175-152236176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182842707	chr1:152236198-152236199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187520411	chr1:152236204-152236205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530716360	chr1:152236238-152236239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550545310	chr1:152236246-152236247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527922690	chr1:152236252-152236253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570724180	chr1:152236260-152236261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558835924	chr1:152236276-152236277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374320104	chr1:152236277-152236278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539309861	chr1:152236336-152236337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546927760	chr1:152236362-152236363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191673864	chr1:152236377-152236378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535462570	chr1:152236399-152236400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152230400-152235800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:152231200-152236400	Weak transcription	Fetal Kidney	kidney
3	chr1:152235800-152236000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:152236000-152236200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links