Variant report

Variant	nsv820026
Chromosome Location	chr21:17015941-17016855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:17015627..17017680-chr21:17022587..17025053,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551014907	chr21:17015946-17015947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373506295	chr21:17016011-17016012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386816530	chr21:17016012-17016013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202146296	chr21:17016022-17016023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564317316	chr21:17016052-17016053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111433695	chr21:17016189-17016190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570916927	chr21:17016237-17016238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533580210	chr21:17016255-17016256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536805989	chr21:17016264-17016265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567577062	chr21:17016270-17016271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2823412	chr21:17016271-17016272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs142329895	chr21:17016312-17016313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368481058	chr21:17016334-17016335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73892698	chr21:17016390-17016391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538354816	chr21:17016491-17016492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2205583	chr21:17016513-17016514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs578143039	chr21:17016514-17016515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192190133	chr21:17016529-17016530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75774759	chr21:17016638-17016639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574290241	chr21:17016667-17016668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372482474	chr21:17016675-17016676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550155117	chr21:17016750-17016751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73360906	chr21:17016775-17016776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531771508	chr21:17016791-17016792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182983249	chr21:17016794-17016795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564682602	chr21:17016810-17016811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527361613	chr21:17016847-17016848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548319483	chr21:17016855-17016856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Epilepsy	20502679	CNVD
22q11.2 microdeletion syndrome	19750312	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17012200-17018200	Weak transcription	HSMMtube	muscle
2	chr21:17014400-17021600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr21:17015400-17016000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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