Variant report

Variant	nsv570455
Chromosome Location	chr15:92577382-92579182
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	chr15:92578004..92579721-chr15:92585811..92587645,2	K562	blood:
2	chr15:92574683..92576781-chr15:92577494..92579219,2	MCF-7	breast:

Extended variants
information (count: 85 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13329180	chr15:92577382-92577383	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs186318061	chr15:92577390-92577391	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs149539131	chr15:92577391-92577392	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs115164564	chr15:92577401-92577402	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs541118049	chr15:92577408-92577409	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs377715231	chr15:92577425-92577426	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs533322841	chr15:92577426-92577427	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs540912394	chr15:92577427-92577428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs543776092	chr15:92577428-92577429	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs555371938	chr15:92577440-92577441	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs573813203	chr15:92577444-92577445	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs540882942	chr15:92577452-92577453	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs548218442	chr15:92577483-92577484	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs561661177	chr15:92577500-92577501	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs552720489	chr15:92577507-92577508	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs562283681	chr15:92577510-92577511	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs527388782	chr15:92577572-92577573	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs142108989	chr15:92577578-92577579	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs113310751	chr15:92577588-92577589	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs60178869	chr15:92577589-92577590	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs143180394	chr15:92577600-92577601	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs148253987	chr15:92577601-92577602	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs539584085	chr15:92577653-92577654	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs191078829	chr15:92577660-92577661	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs569961086	chr15:92577678-92577679	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs535382142	chr15:92577680-92577681	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs182109415	chr15:92577685-92577686	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs572061909	chr15:92577691-92577692	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs187782386	chr15:92577712-92577713	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs192901007	chr15:92577748-92577749	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs577700993	chr15:92577776-92577777	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs544023550	chr15:92577795-92577796	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs59528323	chr15:92577796-92577797	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574318879	chr15:92577888-92577889	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs530418505	chr15:92577894-92577895	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs542914482	chr15:92577954-92577955	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs62008567	chr15:92577963-92577964	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs56274903	chr15:92577964-92577965	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs117420852	chr15:92577974-92577975	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs62008568	chr15:92577984-92577985	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs79708696	chr15:92577991-92577992	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs368410322	chr15:92577993-92577994	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs371872096	chr15:92578013-92578014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28656147	chr15:92578057-92578058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs28538166	chr15:92578063-92578064	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs532663644	chr15:92578100-92578101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76395857	chr15:92578101-92578102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28502579	chr15:92578109-92578110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs534731968	chr15:92578119-92578120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557710431	chr15:92578171-92578172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Epilepsy	19486360	CNVD
Acute myeloid leukemia	17237825	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92570600-92578000	Enhancers	Right Atrium	heart
2	chr15:92571000-92578000	Enhancers	Brain Hippocampus Middle	brain
3	chr15:92572200-92581000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:92573000-92578000	Enhancers	Brain Cingulate Gyrus	brain
5	chr15:92573200-92577800	Enhancers	Brain Substantia Nigra	brain
6	chr15:92573800-92579400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr15:92574200-92580600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr15:92574200-92585800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr15:92574600-92579400	Enhancers	Left Ventricle	heart
10	chr15:92574800-92580600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr15:92574800-92585800	Weak transcription	Pancreas	Pancrea
12	chr15:92575000-92580400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr15:92575000-92580600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr15:92575000-92580600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr15:92575200-92578000	Enhancers	Primary T cells fromperipheralblood	blood
16	chr15:92575200-92578200	Enhancers	Right Ventricle	heart
17	chr15:92575400-92580400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr15:92575400-92580800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr15:92575600-92584000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr15:92575800-92577400	Enhancers	Brain Angular Gyrus	brain
21	chr15:92575800-92584400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr15:92576000-92583800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr15:92576400-92577800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:92576400-92578000	Enhancers	Spleen	Spleen
25	chr15:92576400-92578200	Enhancers	Fetal Heart	heart
26	chr15:92576600-92577400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:92576600-92577400	Enhancers	Brain Anterior Caudate	brain
28	chr15:92576600-92577400	Enhancers	Fetal Lung	lung
29	chr15:92576600-92577600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr15:92576600-92577800	Enhancers	Fetal Brain Male	brain
31	chr15:92576600-92577800	Enhancers	Ovary	ovary
32	chr15:92576600-92578000	Enhancers	Aorta	Aorta
33	chr15:92576600-92578000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr15:92576600-92578000	Enhancers	Lung	lung
35	chr15:92576800-92577400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr15:92576800-92577800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr15:92576800-92580000	Weak transcription	Adipose Nuclei	Adipose
38	chr15:92576800-92580200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:92577000-92577800	Weak transcription	Esophagus	oesophagus
40	chr15:92577000-92578200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr15:92577000-92579000	Weak transcription	Stomach Smooth Muscle	stomach
42	chr15:92577000-92580400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr15:92577000-92586600	Weak transcription	Primary hematopoietic stem cells	blood
44	chr15:92577200-92577400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr15:92577200-92578400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:92577200-92578800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:92577200-92580200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:92577400-92577800	Weak transcription	Brain Angular Gyrus	brain
49	chr15:92577400-92578200	Enhancers	Colonic Mucosa	Colon
50	chr15:92577400-92580800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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