Variant report

Variant	nsv557998
Chromosome Location	chr12:30238868-30242303
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 122 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542968943	chr12:30238874-30238875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148173867	chr12:30238974-30238975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560802319	chr12:30239065-30239066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142006918	chr12:30239080-30239081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531665157	chr12:30239086-30239087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79419471	chr12:30239092-30239093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150255367	chr12:30239093-30239094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532166466	chr12:30239141-30239142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547419278	chr12:30239171-30239172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73086910	chr12:30239186-30239187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181800495	chr12:30239198-30239199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76034020	chr12:30239218-30239219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76038184	chr12:30239222-30239223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537179590	chr12:30239244-30239245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138897528	chr12:30239258-30239259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74549099	chr12:30239279-30239280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545536653	chr12:30239324-30239325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554179412	chr12:30239417-30239418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs16935373	chr12:30239419-30239420	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs149391161	chr12:30239496-30239497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566759045	chr12:30239503-30239504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560974078	chr12:30239532-30239533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74596629	chr12:30239550-30239551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543548507	chr12:30239551-30239552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185372564	chr12:30239601-30239602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565034797	chr12:30239641-30239642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147384406	chr12:30239648-30239649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190235596	chr12:30239671-30239672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79602880	chr12:30239719-30239720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573769283	chr12:30239720-30239721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139524292	chr12:30239726-30239727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548172888	chr12:30239732-30239733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569708912	chr12:30239775-30239776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537041076	chr12:30239777-30239778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79801052	chr12:30239819-30239820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570524323	chr12:30239826-30239827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143454943	chr12:30239829-30239830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554317252	chr12:30239856-30239857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571681429	chr12:30239891-30239892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147134699	chr12:30239902-30239903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11050641	chr12:30239929-30239930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79480252	chr12:30239989-30239990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554830161	chr12:30240004-30240005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182170177	chr12:30240006-30240007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185254858	chr12:30240062-30240063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565047006	chr12:30240119-30240120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200998801	chr12:30240144-30240145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139520931	chr12:30240145-30240146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199563746	chr12:30240146-30240147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112052935	chr12:30240147-30240148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	17133270	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30237800-30241400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr12:30239400-30242200	Enhancers	Muscle Satellite Cultured Cells	--
3	chr12:30239600-30240000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:30240000-30240400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr12:30240400-30240600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr12:30240600-30241400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:30241400-30241800	Enhancers	Rectal Smooth Muscle	rectum
8	chr12:30241400-30241800	Active TSS	Stomach Smooth Muscle	stomach
9	chr12:30241400-30242200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:30241600-30242000	Enhancers	HSMM	muscle
11	chr12:30241800-30243400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr12:30242200-30243400	Weak transcription	Muscle Satellite Cultured Cells	--

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