Variant report

Variant	nsv968076
Chromosome Location	chr5:7992622-7994266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:7990734..7993974-chr5:8011834..8015550,5	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:66 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6864558	chr5:7992630-7992631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550408464	chr5:7992631-7992632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570649894	chr5:7992634-7992635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533206670	chr5:7992637-7992638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6863384	chr5:7992638-7992639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6863556	chr5:7992664-7992665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs535400591	chr5:7992681-7992682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554919605	chr5:7992711-7992712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6863763	chr5:7992846-7992847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537512826	chr5:7992854-7992855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181470985	chr5:7992864-7992865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6863902	chr5:7992886-7992887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs62356484	chr5:7992998-7992999	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs72718973	chr5:7993089-7993090	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs186208740	chr5:7993102-7993103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs58847619	chr5:7993202-7993203	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs190762339	chr5:7993208-7993209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528090642	chr5:7993221-7993222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs72718974	chr5:7993247-7993248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544290071	chr5:7993261-7993262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564194667	chr5:7993265-7993266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72718975	chr5:7993277-7993278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs148742364	chr5:7993361-7993362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373365751	chr5:7993366-7993367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7729780	chr5:7993372-7993373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566694690	chr5:7993429-7993430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577372610	chr5:7993446-7993447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373934934	chr5:7993489-7993490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529139798	chr5:7993511-7993512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7730131	chr5:7993616-7993617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs568433525	chr5:7993646-7993647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537097450	chr5:7993694-7993695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13182987	chr5:7993732-7993733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs182946910	chr5:7993738-7993739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375123272	chr5:7993767-7993768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59460608	chr5:7993785-7993786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs2102202	chr5:7993800-7993801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576873758	chr5:7993835-7993836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370431874	chr5:7993838-7993839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10036486	chr5:7993845-7993846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs536107469	chr5:7993897-7993898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555831659	chr5:7993898-7993899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575153022	chr5:7993899-7993900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540979391	chr5:7993921-7993922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2089032	chr5:7993925-7993926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs10042226	chr5:7993943-7993944	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs2089033	chr5:7993965-7993966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs2062797	chr5:7993966-7993967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs142697910	chr5:7994000-7994001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147018236	chr5:7994014-7994015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7991600-7996200	Weak transcription	Spleen	Spleen
2	chr5:7992800-7993000	Weak transcription	Ovary	ovary
3	chr5:7993000-7993200	Enhancers	Ovary	ovary
4	chr5:7993200-7994600	Weak transcription	Ovary	ovary

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