Variant report

Variant	esv3362467
Chromosome Location	chr2:168418731-168421579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 192 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:192 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533343006	chr2:168418755-168418756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546792062	chr2:168418785-168418786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188460911	chr2:168418835-168418836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566600025	chr2:168418869-168418870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535658577	chr2:168418870-168418871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549128270	chr2:168418871-168418872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs57230846	chr2:168418973-168418974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199910055	chr2:168419001-168419002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558409289	chr2:168419082-168419083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192241108	chr2:168419141-168419142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533752401	chr2:168419142-168419143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71395293	chr2:168419159-168419160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113371016	chr2:168419174-168419175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80172011	chr2:168419175-168419176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60455696	chr2:168419176-168419177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553907390	chr2:168419201-168419202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371571720	chr2:168419312-168419313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200937770	chr2:168419355-168419356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11885819	chr2:168419386-168419387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111518893	chr2:168419442-168419443	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182994538	chr2:168419475-168419476	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576161617	chr2:168419483-168419484	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545007609	chr2:168419484-168419485	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565150311	chr2:168419485-168419486	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186713718	chr2:168419487-168419488	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541114160	chr2:168419504-168419505	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546928328	chr2:168419512-168419513	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560225221	chr2:168419515-168419516	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192388581	chr2:168419562-168419563	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560119005	chr2:168419571-168419572	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184724297	chr2:168419574-168419575	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569136855	chr2:168419585-168419586	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528292303	chr2:168419586-168419587	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551803911	chr2:168419595-168419596	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140759742	chr2:168419601-168419602	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564289919	chr2:168419612-168419613	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188782291	chr2:168419613-168419614	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533561152	chr2:168419617-168419618	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368840111	chr2:168419633-168419634	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553844142	chr2:168419655-168419656	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76360955	chr2:168419662-168419663	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536378796	chr2:168419669-168419670	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556275577	chr2:168419679-168419680	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs193194726	chr2:168419700-168419701	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184746194	chr2:168419723-168419724	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189953659	chr2:168419731-168419732	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79077107	chr2:168419734-168419735	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185168055	chr2:168419747-168419748	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79146122	chr2:168419762-168419763	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188361478	chr2:168419770-168419771	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

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
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	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
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	18414403	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neonatal seizures	20384724	CNVD
severe myoclonic epilepsy of infancy	18294202	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168415000-168420800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:168415600-168419400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:168415800-168420800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:168418400-168419400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:168419400-168421200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
6	chr2:168419600-168419800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:168420600-168421200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:168420800-168421000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
9	chr2:168420800-168421200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr2:168420800-168421200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:168421200-168421600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:168421200-168423200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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