Variant report

Variant	nsv960265
Chromosome Location	chr18:14984974-14991119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 139 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:139 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551043585	chr18:14985006-14985007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189505905	chr18:14985011-14985012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570906503	chr18:14985012-14985013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561424734	chr18:14985050-14985051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530563981	chr18:14985055-14985056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191659588	chr18:14985074-14985075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569450504	chr18:14985089-14985090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533030123	chr18:14985105-14985106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7245302	chr18:14985107-14985108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566808003	chr18:14985112-14985113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143219410	chr18:14985130-14985131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548531927	chr18:14985141-14985142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549248328	chr18:14985147-14985148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184613540	chr18:14985167-14985168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538346157	chr18:14985183-14985184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557821809	chr18:14985205-14985206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577987967	chr18:14985220-14985221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534191585	chr18:14985299-14985300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554026760	chr18:14985309-14985310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567168497	chr18:14985318-14985319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188915983	chr18:14985331-14985332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542809183	chr18:14985332-14985333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562779712	chr18:14985357-14985358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575205733	chr18:14985398-14985399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377081848	chr18:14985409-14985410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150893033	chr18:14985490-14985491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182056325	chr18:14985493-14985494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139423162	chr18:14985507-14985508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546650230	chr18:14985526-14985527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560465476	chr18:14985527-14985528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529245720	chr18:14985533-14985534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549158557	chr18:14985538-14985539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569078082	chr18:14985546-14985547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534891489	chr18:14985558-14985559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553021646	chr18:14985675-14985676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373917779	chr18:14985686-14985687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551867354	chr18:14985687-14985688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571682757	chr18:14985688-14985689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534175342	chr18:14985727-14985728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577753511	chr18:14985783-14985784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377704369	chr18:14985806-14985807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371017737	chr18:14985823-14985824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145214392	chr18:14985824-14985825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557487765	chr18:14985830-14985831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187173425	chr18:14985900-14985901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140066050	chr18:14986038-14986039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576595728	chr18:14986067-14986068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545308985	chr18:14986071-14986072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189570830	chr18:14986085-14986086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577714028	chr18:14986148-14986149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14977800-14985400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:14978000-14985600	Weak transcription	Osteobl	bone
3	chr18:14980200-14985400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr18:14985400-14985600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:14985400-14985800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr18:14985400-14988400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr18:14985600-14985800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr18:14985600-14985800	Enhancers	Osteobl	bone
9	chr18:14985600-14986000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr18:14985800-14986200	Weak transcription	Osteobl	bone
11	chr18:14986200-14986800	Enhancers	Osteobl	bone
12	chr18:14986400-14986600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr18:14986400-14986800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr18:14986600-14987000	Enhancers	Adipose Nuclei	Adipose

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