Variant report

Variant	nsv559099
Chromosome Location	chr12:59969179-59970132
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10747847	chr12:59969179-59969180	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576801556	chr12:59969202-59969203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80107517	chr12:59969235-59969236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560881872	chr12:59969252-59969253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146982901	chr12:59969263-59969264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542872616	chr12:59969269-59969270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs137998756	chr12:59969285-59969286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs10747848	chr12:59969312-59969313	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10747849	chr12:59969332-59969333	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs61936275	chr12:59969334-59969335	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79164747	chr12:59969366-59969367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377675291	chr12:59969400-59969401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547469875	chr12:59969424-59969425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187394138	chr12:59969472-59969473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536561914	chr12:59969473-59969474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10783988	chr12:59969474-59969475	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs386763465	chr12:59969482-59969483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10783989	chr12:59969483-59969484	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148199921	chr12:59969502-59969503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576855285	chr12:59969522-59969523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541068325	chr12:59969533-59969534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552702744	chr12:59969595-59969596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368677903	chr12:59969596-59969597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542933999	chr12:59969677-59969678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561223565	chr12:59969708-59969709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553584785	chr12:59969719-59969720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34331285	chr12:59969739-59969740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60632928	chr12:59969765-59969766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543599470	chr12:59969779-59969780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565421545	chr12:59969844-59969845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532505370	chr12:59969853-59969854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547831943	chr12:59969859-59969860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112952238	chr12:59969873-59969874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34616470	chr12:59969874-59969875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11173088	chr12:59969901-59969902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530090797	chr12:59969920-59969921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6581255	chr12:59969968-59969969	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182858559	chr12:59969984-59969985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141479884	chr12:59970053-59970054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs74095610	chr12:59970126-59970127	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs6581256	chr12:59970132-59970133	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59961800-59970600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:59968200-59969200	Enhancers	Hela-S3	cervix
3	chr12:59968600-59970600	Weak transcription	Dnd41	blood
4	chr12:59968800-59969200	Weak transcription	Primary T cells from cord blood	blood
5	chr12:59969000-59970600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr12:59969000-59970800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr12:59969200-59971800	Enhancers	Primary T cells from cord blood	blood
8	chr12:59969400-59969600	Enhancers	Fetal Thymus	thymus
9	chr12:59969600-59969800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr12:59969600-59970200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:59969800-59972200	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:59970000-59971200	Weak transcription	Fetal Thymus	thymus

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