Variant report

Variant	esv3433614
Chromosome Location	chr1:210399593-210400031
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	chr1:210398376..210400495-chr1:210402941..210405832,2	K562	blood:
2	chr1:210398543..210400945-chr1:210545064..210546589,2	MCF-7	breast:

Extended variants
information (count: 21 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573147889	chr1:210399633-210399634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs677520	chr1:210399652-210399653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563933664	chr1:210399669-210399670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2494186	chr1:210399713-210399714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs189841451	chr1:210399730-210399731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567790361	chr1:210399752-210399753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9430037	chr1:210399786-210399787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182006177	chr1:210399801-210399802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115704564	chr1:210399815-210399816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539578250	chr1:210399817-210399818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376530396	chr1:210399840-210399841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186988424	chr1:210399844-210399845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553903565	chr1:210399847-210399848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386638991	chr1:210399854-210399855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78123484	chr1:210399855-210399856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192507139	chr1:210399866-210399867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141330431	chr1:210399870-210399871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145174191	chr1:210399873-210399874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559355384	chr1:210399908-210399909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79532118	chr1:210399917-210399918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545548828	chr1:210399930-210399931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	20967226	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210397200-210400600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr1:210397200-210400800	Weak transcription	Colon Smooth Muscle	Colon
3	chr1:210397200-210405000	Weak transcription	Stomach Smooth Muscle	stomach

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