Variant report

Variant	nsv1043473
Chromosome Location	chr13:48085526-48119960
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	chr13:48082466..48084126-chr13:48084171..48087051,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT15-3	chr13:48096508-48096529	XLOC_010386
2	lnc-NUDT15-3	chr13:48103786-48104202	XLOC_010386

Variant related genes	Relation type
CRY2	miRNA target sites
CSDA	miRNA target sites

Extended variants
information (count: 736 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:736 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17070253	chr13:48085526-48085527	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184375657	chr13:48085582-48085583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73183864	chr13:48085585-48085586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145675889	chr13:48085587-48085588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536375279	chr13:48085686-48085687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145351432	chr13:48085727-48085728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569883473	chr13:48085752-48085753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116142653	chr13:48085781-48085782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73183869	chr13:48086631-48086632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs79545290	chr13:48086645-48086646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540489719	chr13:48086648-48086649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9534665	chr13:48086656-48086657	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185607138	chr13:48086662-48086663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377562177	chr13:48086733-48086734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368846675	chr13:48086736-48086737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201528524	chr13:48086750-48086751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536918493	chr13:48086757-48086758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369928215	chr13:48086766-48086767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188451518	chr13:48086776-48086777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9534666	chr13:48086783-48086784	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116081751	chr13:48086797-48086798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180894308	chr13:48086805-48086806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547273421	chr13:48086845-48086846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370595192	chr13:48086861-48086862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533284202	chr13:48086867-48086868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568772496	chr13:48086877-48086878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535438269	chr13:48086965-48086966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557032224	chr13:48086973-48086974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148388161	chr13:48087003-48087004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539492371	chr13:48087010-48087011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187196438	chr13:48087050-48087051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs59266213	chr13:48087101-48087102	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs367972151	chr13:48087105-48087106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540060330	chr13:48087118-48087119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555241453	chr13:48087122-48087123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192131488	chr13:48087123-48087124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541804120	chr13:48087197-48087198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141999135	chr13:48087247-48087248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563368579	chr13:48087248-48087249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143296458	chr13:48087277-48087278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183501116	chr13:48087307-48087308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564432993	chr13:48087318-48087319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528637855	chr13:48087362-48087363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs57530506	chr13:48087438-48087439	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs145806419	chr13:48087451-48087452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529643580	chr13:48087462-48087463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551318414	chr13:48087631-48087632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568801608	chr13:48087642-48087643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577695751	chr13:48087662-48087663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539073969	chr13:48087704-48087705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian cancer	22355333	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48085000-48085800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr13:48086600-48087400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:48087200-48087400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr13:48087400-48089600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:48089600-48089800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:48089800-48097000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:48093600-48094400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr13:48093600-48094400	Enhancers	NHDF-Ad	bronchial
9	chr13:48093800-48094000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:48093800-48094400	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr13:48093800-48094600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:48094000-48094400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr13:48094000-48094400	Enhancers	Adipose Nuclei	Adipose
14	chr13:48094400-48094600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:48096200-48096600	Enhancers	Fetal Heart	heart
16	chr13:48097000-48097200	Enhancers	Right Atrium	heart
17	chr13:48098000-48098200	Enhancers	Right Atrium	heart
18	chr13:48098000-48099000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr13:48098400-48101000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:48098800-48099000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:48098800-48099400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr13:48101800-48102200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr13:48113200-48113800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr13:48113200-48114000	Enhancers	Fetal Heart	heart
25	chr13:48113400-48114200	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr13:48113600-48113800	Enhancers	HSMMtube	muscle
27	chr13:48114200-48114600	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr13:48114600-48114800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr13:48114800-48120200	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr13:48118000-48120400	Enhancers	Right Atrium	heart
31	chr13:48118000-48121000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr13:48118800-48119000	Enhancers	Left Ventricle	heart
33	chr13:48118800-48120600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:48119200-48120000	Weak transcription	Left Ventricle	heart
35	chr13:48119200-48120800	Enhancers	Adipose Nuclei	Adipose
36	chr13:48119200-48120800	Enhancers	Rectal Smooth Muscle	rectum
37	chr13:48119200-48120800	Enhancers	Stomach Smooth Muscle	stomach
38	chr13:48119200-48123000	Enhancers	Fetal Stomach	stomach
39	chr13:48119400-48119800	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr13:48119400-48121000	Enhancers	Fetal Muscle Leg	muscle
41	chr13:48119400-48121400	Enhancers	Colon Smooth Muscle	Colon
42	chr13:48119800-48120200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr13:48119800-48120800	Enhancers	Fetal Kidney	kidney

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