Variant report

Variant	esv3394966
Chromosome Location	chr6:165344187-165346735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 311 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532903310	chr6:165344207-165344208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377702575	chr6:165344213-165344214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551385986	chr6:165344234-165344235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566497256	chr6:165344278-165344279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200394005	chr6:165344295-165344296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375083394	chr6:165344297-165344298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146077529	chr6:165344301-165344302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61718399	chr6:165344308-165344309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9365817	chr6:165344317-165344318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60775618	chr6:165344322-165344323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191160004	chr6:165344340-165344341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13196801	chr6:165344350-165344351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555462553	chr6:165344373-165344374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567315317	chr6:165344379-165344380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369802768	chr6:165344380-165344381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141268115	chr6:165344381-165344382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9356304	chr6:165344387-165344388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146202974	chr6:165344406-165344407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577515471	chr6:165344445-165344446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183391113	chr6:165344456-165344457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs72569555	chr6:165344464-165344465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544833971	chr6:165344467-165344468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572424055	chr6:165344470-165344471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9459256	chr6:165344484-165344485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71026650	chr6:165344511-165344512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546253914	chr6:165344529-165344530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542718443	chr6:165344531-165344532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561440785	chr6:165344534-165344535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531763527	chr6:165344536-165344537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544026410	chr6:165344537-165344538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376693997	chr6:165344544-165344545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565519888	chr6:165344551-165344552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532839394	chr6:165344552-165344553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373942923	chr6:165344559-165344560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13197155	chr6:165344560-165344561	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs13212819	chr6:165344561-165344562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375656719	chr6:165344563-165344564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368083344	chr6:165344568-165344569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566316726	chr6:165344574-165344575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148435714	chr6:165344603-165344604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575310647	chr6:165344614-165344615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548763527	chr6:165344625-165344626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567360555	chr6:165344644-165344645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369634203	chr6:165344651-165344652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111066655	chr6:165344667-165344668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540864883	chr6:165344677-165344678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549558964	chr6:165344687-165344688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532814718	chr6:165344693-165344694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149977155	chr6:165344696-165344697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200837626	chr6:165344708-165344709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165333200-165346200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:165343200-165347400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:165346200-165346600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links