Variant report

Variant	nsv603177
Chromosome Location	chr6:55828425-55832258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 143 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2843540	chr6:55828425-55828426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564707201	chr6:55828458-55828459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140095516	chr6:55828510-55828511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371876366	chr6:55828549-55828550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187328184	chr6:55828608-55828609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78487168	chr6:55828626-55828627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568000732	chr6:55828650-55828651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143714554	chr6:55828672-55828673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566486150	chr6:55828688-55828689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528761265	chr6:55828694-55828695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552125730	chr6:55828706-55828707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2745745	chr6:55828727-55828728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537689743	chr6:55828735-55828736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146324497	chr6:55828738-55828739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567702679	chr6:55828763-55828764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114354554	chr6:55828797-55828798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192287861	chr6:55828867-55828868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113412070	chr6:55828967-55828968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111475327	chr6:55828989-55828990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544880421	chr6:55829063-55829064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139256451	chr6:55829066-55829067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553034750	chr6:55829218-55829219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566314867	chr6:55829239-55829240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535444913	chr6:55829266-55829267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62405040	chr6:55829290-55829291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181008061	chr6:55829388-55829389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145431549	chr6:55829410-55829411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149218288	chr6:55829411-55829412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184930174	chr6:55829416-55829417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144850003	chr6:55829463-55829464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2843541	chr6:55829499-55829500	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552089096	chr6:55829569-55829570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77624413	chr6:55829570-55829571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557550772	chr6:55829579-55829580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147925226	chr6:55829596-55829597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6904423	chr6:55829626-55829627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs577520227	chr6:55829633-55829634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368640440	chr6:55829664-55829665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112937751	chr6:55829668-55829669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190119536	chr6:55829720-55829721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559813863	chr6:55829782-55829783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4354151	chr6:55829788-55829789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182434694	chr6:55829808-55829809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528613702	chr6:55829821-55829822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141714026	chr6:55829856-55829857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2009726	chr6:55829863-55829864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188725739	chr6:55829900-55829901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558425446	chr6:55829933-55829934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35798372	chr6:55829937-55829938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575448672	chr6:55829938-55829939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55823600-55828600	Weak transcription	Fetal Lung	lung
2	chr6:55828200-55828600	Enhancers	Fetal Stomach	stomach
3	chr6:55828400-55833800	Weak transcription	Colon Smooth Muscle	Colon
4	chr6:55828600-55829200	Enhancers	Fetal Lung	lung
5	chr6:55828600-55833400	Weak transcription	Fetal Stomach	stomach
6	chr6:55829200-55833800	Weak transcription	Fetal Lung	lung

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