Variant report

Variant	esv3380878
Chromosome Location	chr14:77687159-77687735
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	chr14:77687164..77689503-chr14:77690310..77692436,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NGB-3	chr14:77687547-77688021	NONHSAT037966
2	lnc-NGB-3	chr14:77686604-77687262	NONHSAT037966

Extended variants
information (count: 62 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:62 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77447506	chr14:77687206-77687207	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs117549925	chr14:77687210-77687211	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs116946248	chr14:77687212-77687213	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs111943938	chr14:77687224-77687225	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs112118487	chr14:77687225-77687226	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs112492642	chr14:77687226-77687227	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs141755835	chr14:77687230-77687231	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572706779	chr14:77687235-77687236	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs112887912	chr14:77687242-77687243	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs113679213	chr14:77687243-77687244	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs113144799	chr14:77687244-77687245	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs374240569	chr14:77687257-77687258	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs190762907	chr14:77687259-77687260	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs200646212	chr14:77687263-77687264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61991631	chr14:77687267-77687268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563784749	chr14:77687274-77687275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs430041	chr14:77687275-77687276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545708551	chr14:77687277-77687278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs454484	chr14:77687282-77687283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191795540	chr14:77687293-77687294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183043193	chr14:77687295-77687296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577293713	chr14:77687301-77687302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564291665	chr14:77687313-77687314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563057274	chr14:77687317-77687318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188074140	chr14:77687322-77687323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543100450	chr14:77687334-77687335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375979142	chr14:77687347-77687348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549489312	chr14:77687361-77687362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112811134	chr14:77687374-77687375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561402217	chr14:77687381-77687382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529048838	chr14:77687393-77687394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549172249	chr14:77687396-77687397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528870498	chr14:77687400-77687401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546982594	chr14:77687407-77687408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559379883	chr14:77687415-77687416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182134721	chr14:77687417-77687418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528436201	chr14:77687441-77687442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547793886	chr14:77687442-77687443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539858485	chr14:77687450-77687451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550271354	chr14:77687454-77687455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186727614	chr14:77687493-77687494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192598635	chr14:77687496-77687497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184910987	chr14:77687508-77687509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188544517	chr14:77687514-77687515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193035243	chr14:77687545-77687546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184791798	chr14:77687550-77687551	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs189736068	chr14:77687555-77687556	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs180910919	chr14:77687561-77687562	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs570138703	chr14:77687575-77687576	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs535632603	chr14:77687579-77687580	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77654200-77709400	Weak transcription	Esophagus	oesophagus
2	chr14:77680200-77688000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr14:77685000-77687400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr14:77685000-77692800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:77685200-77690800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:77685400-77692600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:77685600-77688000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr14:77686000-77688200	Weak transcription	Fetal Brain Female	brain
9	chr14:77686200-77687200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr14:77686400-77687400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr14:77686400-77712400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:77686600-77687200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr14:77686600-77688800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr14:77686600-77689600	Weak transcription	Fetal Brain Male	brain
15	chr14:77686600-77690200	Weak transcription	Spleen	Spleen
16	chr14:77686600-77691800	Weak transcription	Fetal Intestine Small	intestine
17	chr14:77686800-77687200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr14:77686800-77687200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr14:77686800-77687200	Enhancers	K562	blood
20	chr14:77687000-77687200	Enhancers	Gastric	stomach
21	chr14:77687000-77688000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr14:77687000-77688000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr14:77687000-77688200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr14:77687000-77688200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr14:77687000-77688600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr14:77687000-77688600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr14:77687000-77690000	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr14:77687000-77691400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr14:77687000-77692000	Weak transcription	Brain Angular Gyrus	brain
30	chr14:77687000-77697000	Weak transcription	Brain Substantia Nigra	brain
31	chr14:77687000-77697200	Weak transcription	Brain Anterior Caudate	brain
32	chr14:77687000-77697800	Weak transcription	Pancreas	Pancrea
33	chr14:77687200-77688200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr14:77687200-77688400	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr14:77687200-77689000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:77687200-77692400	Weak transcription	Gastric	stomach
37	chr14:77687400-77687800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr14:77687400-77687800	Weak transcription	H1 Cell Line	embryonic stem cell

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