Variant report

Variant	nsv436173
Chromosome Location	chr13:91662320-91665263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:91661017..91663555-chr13:91999766..92002181,2	K562	blood:
2	chr13:91660431..91663097-chr13:91765114..91768066,3	K562	blood:

Variant related genes	Relation type
ENSG00000215417	chromatin interactions

Extended variants
information (count: 65 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:65 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371922267	chr13:91662369-91662370	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs374740294	chr13:91662371-91662372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs9583858	chr13:91662376-91662377	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141796187	chr13:91662381-91662382	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139235408	chr13:91662384-91662385	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149248031	chr13:91662503-91662504	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144437937	chr13:91662516-91662517	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148441038	chr13:91662529-91662530	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs115554985	chr13:91662535-91662536	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532036035	chr13:91662578-91662579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552844312	chr13:91662580-91662581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571038933	chr13:91662588-91662589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531868202	chr13:91662632-91662633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186297434	chr13:91662715-91662716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376890517	chr13:91662717-91662718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534839684	chr13:91662735-91662736	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs74103373	chr13:91662752-91662753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535487336	chr13:91662782-91662783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs5805679	chr13:91662803-91662804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34533171	chr13:91662804-91662805	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs72514916	chr13:91662805-91662806	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs397721154	chr13:91662809-91662810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377524864	chr13:91662810-91662811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs369346614	chr13:91662811-91662812	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373087681	chr13:91662812-91662813	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs5005996	chr13:91662813-91662814	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs536208810	chr13:91662818-91662819	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565680624	chr13:91662861-91662862	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552813129	chr13:91662863-91662864	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs570886304	chr13:91662924-91662925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539335365	chr13:91662940-91662941	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557559376	chr13:91662948-91662949	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189470781	chr13:91662970-91662971	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543569742	chr13:91663009-91663010	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555180574	chr13:91663010-91663011	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs9515872	chr13:91663024-91663025	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372711424	chr13:91663031-91663032	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540716133	chr13:91663058-91663059	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs146009613	chr13:91663060-91663061	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528026322	chr13:91663110-91663111	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs180754285	chr13:91663122-91663123	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185369620	chr13:91663123-91663124	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139925794	chr13:91663132-91663133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568212121	chr13:91663134-91663135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538479523	chr13:91663145-91663146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370043078	chr13:91663159-91663160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550306668	chr13:91663161-91663162	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562089828	chr13:91663173-91663174	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529380864	chr13:91663182-91663183	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558328223	chr13:91663208-91663209	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:0 , 50 per page) page:

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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