Variant report

Variant	nsv981151
Chromosome Location	chr6:58617575-58680055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3914656	chr6:58617592-58617593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115791572	chr6:58617609-58617610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3914655	chr6:58617625-58617626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141722561	chr6:58617627-58617628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372100749	chr6:58617666-58617667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540702854	chr6:58617667-58617668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553184683	chr6:58617679-58617680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4092498	chr6:58617704-58617705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs13201728	chr6:58617714-58617715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541990083	chr6:58617749-58617750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs71568742	chr6:58617750-58617751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564012310	chr6:58617753-58617754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs202096942	chr6:58668603-58668604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs549583725	chr6:58668615-58668616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs145450275	chr6:58668616-58668617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs532305507	chr6:58668634-58668635	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs547265613	chr6:58668678-58668679	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs201968751	chr6:58668692-58668693	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs565715596	chr6:58668704-58668705	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs533982994	chr6:58668710-58668711	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs144978141	chr6:58668711-58668712	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148667836	chr6:58668758-58668759	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs553648322	chr6:58668759-58668760	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs537115978	chr6:58668819-58668820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs12196943	chr6:58668835-58668836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs185582684	chr6:58668839-58668840	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs536327755	chr6:58668860-58668861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs111967371	chr6:58668866-58668867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs553389886	chr6:58668908-58668909	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs574819671	chr6:58668951-58668952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs541870920	chr6:58668962-58668963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs140076213	chr6:58668966-58668967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs376791840	chr6:58668967-58668968	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs545875092	chr6:58668987-58668988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs188625629	chr6:58668988-58668989	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs181522867	chr6:58668989-58668990	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs369953481	chr6:58669012-58669013	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs146452669	chr6:58669022-58669023	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs373524992	chr6:58669023-58669024	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs544947641	chr6:58669029-58669030	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs529952983	chr6:58669031-58669032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs185949494	chr6:58669045-58669046	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs569600265	chr6:58669078-58669079	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs191198805	chr6:58669080-58669081	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs552281190	chr6:58669105-58669106	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs571106713	chr6:58669106-58669107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs201552929	chr6:58669107-58669108	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs558421932	chr6:58669120-58669121	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs553494512	chr6:58669135-58669136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs111297745	chr6:58669149-58669150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:58614800-58617800	Enhancers	NHEK	skin
2	chr6:58668600-58669200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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