Variant report

Variant	nsv984331
Chromosome Location	chr16:35146912-35148868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 93 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556312419	chr16:35146914-35146915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs574546547	chr16:35146934-35146935	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs368179813	chr16:35146940-35146941	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs543249060	chr16:35146942-35146943	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs75955607	chr16:35146947-35146948	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs528669994	chr16:35146964-35146965	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs189205396	chr16:35146969-35146970	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs553681509	chr16:35146972-35146973	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs565533389	chr16:35146973-35146974	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs571621027	chr16:35146982-35146983	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs200259218	chr16:35146989-35146990	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs190950014	chr16:35147007-35147008	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs7203289	chr16:35147008-35147009	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550526423	chr16:35147021-35147022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs562651723	chr16:35147035-35147036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs62059139	chr16:35147040-35147041	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs548271987	chr16:35147047-35147048	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs539051609	chr16:35147059-35147060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs533730594	chr16:35147060-35147061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs536081278	chr16:35147061-35147062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs182477380	chr16:35147075-35147076	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs557475537	chr16:35147087-35147088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs554473904	chr16:35147108-35147109	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs186762271	chr16:35147110-35147111	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs529604428	chr16:35147122-35147123	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs191267123	chr16:35147123-35147124	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs184254134	chr16:35147128-35147129	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs573413870	chr16:35147132-35147133	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs368115777	chr16:35147136-35147137	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs540444648	chr16:35147156-35147157	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs565588007	chr16:35147182-35147183	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs577424586	chr16:35147216-35147217	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs544203105	chr16:35147217-35147218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs562588964	chr16:35147224-35147225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs375908077	chr16:35147229-35147230	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs530026475	chr16:35147238-35147239	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs7185498	chr16:35147254-35147255	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs560358689	chr16:35147291-35147292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs76431249	chr16:35147301-35147302	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs187839210	chr16:35147339-35147340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs75723622	chr16:35147376-35147377	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs570729817	chr16:35147384-35147385	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs140327973	chr16:35147452-35147453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs550091561	chr16:35147454-35147455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs193188450	chr16:35147457-35147458	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs535421438	chr16:35147470-35147471	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs551243975	chr16:35147529-35147530	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs149926018	chr16:35147545-35147546	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs185080783	chr16:35147546-35147547	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs558837213	chr16:35147547-35147548	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:35139800-35148400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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