Variant report

Variant	nsv1006128
Chromosome Location	chr2:185243887-185269058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:185103488..185105465-chr2:185244326..185245928,2	K562	blood:
2	chr2:185265120..185267657-chr2:185268029..185269760,2	K562	blood:
3	chr2:185267016..185267836-chr3:27870668..27871485,2	MCF-7	breast:
4	chr2:185065862..185068679-chr2:185266062..185268642,2	K562	blood:
5	chr2:185265120..185267657-chr2:185268029..185269760,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF804A-3	chr2:185244856-185245013	NONHSAT075951
2	lnc-ZNF804A-3	chr2:185246875-185247280	NONHSAT075951

No data

Extended variants
information (count: 69 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139251966	chr2:185244889-185244890	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs149390917	chr2:185244995-185244996	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs530830981	chr2:185245000-185245001	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs552179828	chr2:185245003-185245004	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs73035497	chr2:185246887-185246888	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs528113469	chr2:185246891-185246892	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs546311419	chr2:185246913-185246914	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs568135007	chr2:185246924-185246925	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs535242257	chr2:185246932-185246933	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs73035500	chr2:185247017-185247018	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182943234	chr2:185247056-185247057	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs539313281	chr2:185247075-185247076	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs557653019	chr2:185247078-185247079	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs573081936	chr2:185247125-185247126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs531710970	chr2:185247175-185247176	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs549374715	chr2:185247205-185247206	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs36012782	chr2:185247257-185247258	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs35492302	chr2:185251639-185251640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs35515524	chr2:185251641-185251642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552353464	chr2:185251645-185251646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368031056	chr2:185251674-185251675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571031986	chr2:185251704-185251705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528743345	chr2:185251722-185251723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370580686	chr2:185251724-185251725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547292123	chr2:185251742-185251743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35943580	chr2:185251751-185251752	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536236412	chr2:185251761-185251762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554645346	chr2:185251763-185251764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1596270	chr2:185251767-185251768	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs537146703	chr2:185251778-185251779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558744730	chr2:185251793-185251794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576983446	chr2:185251806-185251807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540940199	chr2:185251820-185251821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1596271	chr2:185251841-185251842	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187703407	chr2:185251842-185251843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573172609	chr2:185251912-185251913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1596272	chr2:185251975-185251976	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs563391798	chr2:185251979-185251980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1596273	chr2:185252018-185252019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs191331185	chr2:185252085-185252086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564492337	chr2:185252115-185252116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6751401	chr2:185252129-185252130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546910604	chr2:185252143-185252144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35371490	chr2:185252168-185252169	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs529660160	chr2:185252169-185252170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149639829	chr2:185252179-185252180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569678523	chr2:185252183-185252184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570588172	chr2:185259401-185259402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542418127	chr2:185259410-185259411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113992313	chr2:185259411-185259412	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Psychiatric disorder	20548289	CNVD
Psychosis	20048749	CNVD
Rectal cancer	20877625	CNVD
Schizophrenia	20548289	CNVD
anxiety disorder	20548289	CNVD
Autism	20548289	CNVD
Bipolar disorder	20548289	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:185251600-185252200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr2:185259400-185260000	Enhancers	Liver	Liver

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