Variant report

Variant	nsv961741
Chromosome Location	chr2:184079546-184082834
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:184080634..184082480-chr2:184083427..184085243,2	K562	blood:
2	chr2:184081982..184083602-chr2:184085454..184088398,2	K562	blood:
3	chr2:184080700..184082212-chr2:184094955..184097317,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP35-2	chr2:184079047-184080128	ENSG00000272800.1
2	lnc-NUP35-2	chr2:184079117-184080015	NONHSAT075940

Extended variants
information (count: 115 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188098439	chr2:184079600-184079601	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs192709506	chr2:184079614-184079615	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs551793084	chr2:184079629-184079630	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs12474605	chr2:184079707-184079708	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs537579822	chr2:184079736-184079737	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs185164699	chr2:184079830-184079831	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs141290862	chr2:184079832-184079833	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs146229409	chr2:184079864-184079865	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs549476934	chr2:184079866-184079867	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs369296475	chr2:184079876-184079877	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs138134207	chr2:184080006-184080007	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs189126216	chr2:184080012-184080013	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs181874005	chr2:184080018-184080019	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs566903950	chr2:184080032-184080033	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs142627474	chr2:184080053-184080054	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs558548953	chr2:184080081-184080082	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs575150576	chr2:184080143-184080144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544158690	chr2:184080156-184080157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146065996	chr2:184080169-184080170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139706150	chr2:184080178-184080179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185011339	chr2:184080258-184080259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1462528	chr2:184080371-184080372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574147557	chr2:184080420-184080421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77043053	chr2:184080473-184080474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559518743	chr2:184080533-184080534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551401699	chr2:184080567-184080568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149768352	chr2:184080578-184080579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144755636	chr2:184080611-184080612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565538853	chr2:184080644-184080645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530832145	chr2:184080666-184080667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550903560	chr2:184080747-184080748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs567767670	chr2:184080748-184080749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373670388	chr2:184080755-184080756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10183020	chr2:184080772-184080773	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546860504	chr2:184080829-184080830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566658653	chr2:184080834-184080835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188264670	chr2:184080912-184080913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558603061	chr2:184080928-184080929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180721169	chr2:184080950-184080951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17757979	chr2:184080968-184080969	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs554135139	chr2:184080997-184080998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574240754	chr2:184081019-184081020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367674758	chr2:184081030-184081031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114030094	chr2:184081058-184081059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs16824171	chr2:184081074-184081075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185978759	chr2:184081075-184081076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189740239	chr2:184081143-184081144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148534029	chr2:184081200-184081201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531194005	chr2:184081211-184081212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544656721	chr2:184081230-184081231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184050400-184091600	Weak transcription	Psoas Muscle	Psoas
2	chr2:184062800-184080600	Weak transcription	K562	blood
3	chr2:184072200-184082800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:184072600-184094000	Weak transcription	HSMM	muscle
5	chr2:184073000-184084600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:184074800-184080600	Weak transcription	A549	lung
7	chr2:184077200-184080000	Weak transcription	Primary T cells from cord blood	blood
8	chr2:184078000-184080000	Enhancers	GM12878-XiMat	blood
9	chr2:184080600-184081000	Enhancers	HUVEC	blood vessel
10	chr2:184080600-184081200	Enhancers	K562	blood
11	chr2:184080800-184081000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr2:184082400-184091400	Weak transcription	Primary T cells from cord blood	blood

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