Variant report

Variant	esv3450681
Chromosome Location	chr15:33344627-33344819
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144663247	chr15:33344642-33344643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572779237	chr15:33344664-33344665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs35573301	chr15:33344675-33344676	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558668400	chr15:33344676-33344677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577274621	chr15:33344681-33344682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34508278	chr15:33344697-33344698	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs563096730	chr15:33344698-33344699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560037240	chr15:33344726-33344727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571999082	chr15:33344746-33344747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543459596	chr15:33344755-33344756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375986535	chr15:33344767-33344768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190045658	chr15:33344786-33344787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	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
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33324000-33356800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr15:33332200-33355200	Weak transcription	Gastric	stomach
3	chr15:33335400-33347600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:33337000-33352000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:33337000-33358000	Weak transcription	Colonic Mucosa	Colon
6	chr15:33337600-33345000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:33337600-33356800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:33337800-33356800	Weak transcription	HSMMtube	muscle
9	chr15:33338800-33355200	Weak transcription	HSMM	muscle
10	chr15:33341600-33345400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:33341800-33348000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:33342200-33348000	Weak transcription	NHLF	lung
13	chr15:33344000-33345200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:33344000-33345200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:33344000-33345400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:33344000-33356800	Weak transcription	Esophagus	oesophagus
17	chr15:33344000-33356800	Weak transcription	Lung	lung
18	chr15:33344200-33349800	Weak transcription	Placenta	Placenta

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