Variant report

Variant	esv3396811
Chromosome Location	chr8:1390581-1391028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535650311	chr8:1390586-1390587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs6985404	chr8:1390604-1390605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7002906	chr8:1390641-1390642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555894816	chr8:1390653-1390654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575772068	chr8:1390663-1390664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544844242	chr8:1390664-1390665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373451162	chr8:1390669-1390670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6985546	chr8:1390674-1390675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111589931	chr8:1390702-1390703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112564022	chr8:1390710-1390711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558041889	chr8:1390716-1390717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577210862	chr8:1390717-1390718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7004157	chr8:1390722-1390723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10089488	chr8:1390727-1390728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7004173	chr8:1390744-1390745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371014770	chr8:1390755-1390756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529015836	chr8:1390756-1390757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542370459	chr8:1390763-1390764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10089511	chr8:1390770-1390771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182491638	chr8:1390774-1390775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531407693	chr8:1390777-1390778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188355966	chr8:1390780-1390781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571608087	chr8:1390790-1390791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533360951	chr8:1390803-1390804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547044840	chr8:1390808-1390809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566767641	chr8:1390823-1390824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535917175	chr8:1390829-1390830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555584529	chr8:1390840-1390841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6989849	chr8:1390861-1390862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569394518	chr8:1390896-1390897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556237459	chr8:1390900-1390901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538091366	chr8:1390914-1390915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62485586	chr8:1390928-1390929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs577947781	chr8:1390929-1390930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533532820	chr8:1390935-1390936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368379414	chr8:1390947-1390948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112107651	chr8:1390981-1390982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573575757	chr8:1391002-1391003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10108209	chr8:1391018-1391019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1388000-1397800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:1388000-1402000	Weak transcription	Brain Cingulate Gyrus	brain

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