Variant report

Variant	esv3336900
Chromosome Location	chr12:40641397-40641583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56277949	chr12:40641419-40641420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568004362	chr12:40641420-40641421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540613675	chr12:40641437-40641438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2952713	chr12:40641467-40641468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201370158	chr12:40641470-40641471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202115776	chr12:40641473-40641474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200483913	chr12:40641475-40641476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201341969	chr12:40641477-40641478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557466724	chr12:40641478-40641479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28417544	chr12:40641499-40641500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376172638	chr12:40641506-40641507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368194392	chr12:40641508-40641509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372014800	chr12:40641509-40641510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374749891	chr12:40641511-40641512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11175723	chr12:40641563-40641564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71078235	chr12:40641564-40641565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40619400-40644400	Weak transcription	Gastric	stomach
2	chr12:40619600-40661000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:40619600-40678400	Weak transcription	Right Ventricle	heart
4	chr12:40619800-40658800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr12:40620400-40644200	Weak transcription	Brain Angular Gyrus	brain
6	chr12:40620800-40644200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:40620800-40648000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr12:40620800-40659200	Weak transcription	Brain Anterior Caudate	brain
9	chr12:40620800-40704200	Weak transcription	Esophagus	oesophagus
10	chr12:40621000-40643800	Weak transcription	Stomach Smooth Muscle	stomach
11	chr12:40621000-40659800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:40621000-40661200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:40622800-40661000	Weak transcription	Colon Smooth Muscle	Colon
14	chr12:40622800-40708800	Weak transcription	Left Ventricle	heart
15	chr12:40630600-40643600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:40630600-40669400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr12:40630600-40686400	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr12:40631200-40646600	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr12:40632000-40655200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr12:40632000-40656000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:40633200-40643800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:40633400-40646600	Weak transcription	Ovary	ovary
23	chr12:40633400-40654200	Weak transcription	Aorta	Aorta
24	chr12:40635000-40647400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:40635000-40647400	Weak transcription	Lung	lung
26	chr12:40635200-40648200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr12:40636200-40648000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:40636200-40648200	Weak transcription	NHDF-Ad	bronchial
29	chr12:40636400-40643600	Weak transcription	Adipose Nuclei	Adipose
30	chr12:40637400-40647200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:40638200-40641800	Weak transcription	Primary B cells from cord blood	blood
32	chr12:40639600-40643600	Weak transcription	Liver	Liver
33	chr12:40640200-40680400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr12:40640600-40727400	Weak transcription	Spleen	Spleen
35	chr12:40640600-40768200	Weak transcription	Pancreas	Pancrea
36	chr12:40640800-40641800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:40640800-40641800	Weak transcription	A549	lung
38	chr12:40640800-40642400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr12:40641200-40662800	Weak transcription	Brain Cingulate Gyrus	brain

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