Variant report

Variant	nsv826687
Chromosome Location	chr13:67219612-67220893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560993229	chr13:67219674-67219675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558553192	chr13:67219750-67219751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34894862	chr13:67219773-67219774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546810323	chr13:67219818-67219819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78171502	chr13:67219878-67219879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141068447	chr13:67219896-67219897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551554560	chr13:67219922-67219923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565158565	chr13:67219944-67219945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530869272	chr13:67219959-67219960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550594756	chr13:67219982-67219983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567300643	chr13:67219992-67219993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35768687	chr13:67220044-67220045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570338944	chr13:67220159-67220160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552759784	chr13:67220174-67220175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9564326	chr13:67220179-67220180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149848631	chr13:67220186-67220187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532529281	chr13:67220219-67220220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9564327	chr13:67220253-67220254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538811532	chr13:67220289-67220290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74095617	chr13:67220420-67220421	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs117573991	chr13:67220437-67220438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181301428	chr13:67220458-67220459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377355258	chr13:67220463-67220464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554527463	chr13:67220488-67220489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574455692	chr13:67220545-67220546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112557627	chr13:67220607-67220608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560335901	chr13:67220661-67220662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532646475	chr13:67220765-67220766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs111984770	chr13:67220800-67220801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs964381	chr13:67220803-67220804	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145262761	chr13:67220891-67220892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67215800-67221200	Weak transcription	Brain Substantia Nigra	brain
2	chr13:67219000-67220200	Enhancers	Primary B cells from peripheral blood	blood
3	chr13:67219400-67221000	Weak transcription	Brain Hippocampus Middle	brain
4	chr13:67219600-67221400	Enhancers	Primary B cells from cord blood	blood
5	chr13:67220200-67221000	Weak transcription	Primary B cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links