Variant report

Variant	esv3364655
Chromosome Location	chr13:69485633-69485797
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377326634	chr13:69485645-69485646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201506227	chr13:69485648-69485649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199837029	chr13:69485656-69485657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61951409	chr13:69485657-69485658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370005653	chr13:69485658-69485659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148707520	chr13:69485667-69485668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142354954	chr13:69485671-69485672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544834552	chr13:69485672-69485673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372232912	chr13:69485677-69485678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192815071	chr13:69485679-69485680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375547033	chr13:69485683-69485684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369326488	chr13:69485687-69485688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532963377	chr13:69485688-69485689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28853699	chr13:69485699-69485700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184164283	chr13:69485705-69485706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368935290	chr13:69485707-69485708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200621169	chr13:69485710-69485711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs61951410	chr13:69485711-69485712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201347519	chr13:69485716-69485717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200754255	chr13:69485727-69485728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs28812886	chr13:69485729-69485730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200881622	chr13:69485730-69485731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs28890616	chr13:69485733-69485734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376076591	chr13:69485735-69485736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs28870139	chr13:69485739-69485740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9592575	chr13:69485741-69485742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369346171	chr13:69485747-69485748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200036060	chr13:69485750-69485751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35675402	chr13:69485751-69485752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376194726	chr13:69485752-69485753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9599347	chr13:69485753-69485754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373565193	chr13:69485761-69485762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71113369	chr13:69485762-69485763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371980915	chr13:69485763-69485764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9599348	chr13:69485769-69485770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28888161	chr13:69485771-69485772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9592577	chr13:69485777-69485778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9592578	chr13:69485781-69485782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376752768	chr13:69485782-69485783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575419290	chr13:69485785-69485786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186979405	chr13:69485795-69485796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69483400-69486800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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