Variant report

Variant	esv3481250
Chromosome Location	chr8:120645679-120646200
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551340860	chr8:120645746-120645747	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372384536	chr8:120645787-120645788	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543219489	chr8:120645828-120645829	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs561378674	chr8:120645856-120645857	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532046020	chr8:120645880-120645881	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550195628	chr8:120645955-120645956	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182668896	chr8:120645982-120645983	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567462420	chr8:120646022-120646023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113433714	chr8:120646059-120646060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111682060	chr8:120646100-120646101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547604558	chr8:120646103-120646104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566187104	chr8:120646145-120646146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536026168	chr8:120646151-120646152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377693265	chr8:120646186-120646187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557440164	chr8:120646193-120646194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186378361	chr8:120646194-120646195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1865292	chr8:120646196-120646197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120619200-120648000	Weak transcription	Brain Angular Gyrus	brain
2	chr8:120627800-120649200	Weak transcription	NHLF	lung
3	chr8:120633400-120647800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr8:120634800-120650000	Weak transcription	Primary T cells from cord blood	blood
5	chr8:120635400-120649200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:120635400-120649400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:120635800-120647200	Weak transcription	Placenta	Placenta
8	chr8:120635800-120648600	Weak transcription	Osteobl	bone
9	chr8:120639200-120647200	Weak transcription	Brain Anterior Caudate	brain
10	chr8:120639200-120647200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:120639200-120647400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:120639400-120647000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr8:120641800-120647200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:120642200-120646600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr8:120644000-120645800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:120644000-120646400	Enhancers	Fetal Thymus	thymus
17	chr8:120644600-120649400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr8:120645200-120645800	Enhancers	Brain Cingulate Gyrus	brain
19	chr8:120645200-120650600	Enhancers	Brain Hippocampus Middle	brain
20	chr8:120645400-120645800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr8:120645400-120645800	Enhancers	Adipose Nuclei	Adipose
22	chr8:120645400-120645800	Enhancers	Brain Substantia Nigra	brain
23	chr8:120645400-120645800	Flanking Active TSS	Fetal Lung	lung
24	chr8:120645400-120645800	Enhancers	GM12878-XiMat	blood
25	chr8:120645400-120646000	Genic enhancers	NHDF-Ad	bronchial
26	chr8:120645600-120645800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:120645600-120645800	Enhancers	Liver	Liver
28	chr8:120645600-120647200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:120645600-120649600	Weak transcription	Thymus	Thymus
30	chr8:120645800-120647000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:120645800-120647000	Weak transcription	Adipose Nuclei	Adipose
32	chr8:120645800-120647200	Weak transcription	Liver	Liver
33	chr8:120645800-120647200	Weak transcription	Brain Substantia Nigra	brain
34	chr8:120645800-120647200	Weak transcription	Fetal Lung	lung
35	chr8:120645800-120647600	Weak transcription	Brain Cingulate Gyrus	brain
36	chr8:120645800-120647800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:120645800-120649400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr8:120645800-120650400	Weak transcription	GM12878-XiMat	blood
39	chr8:120646000-120646600	Weak transcription	NHDF-Ad	bronchial
40	chr8:120646200-120649200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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