Variant report

Variant	esv1810156
Chromosome Location	chr5:12800877-12820064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:12272244..12273131-chr5:12803955..12804598,2	MCF-7	breast:
2	chr5:12810723..12813220-chr5:12814346..12816159,2	MCF-7	breast:
3	chr5:12794344..12796084-chr5:12809073..12810960,2	MCF-7	breast:
4	chr5:12815455..12818211-chr5:12818393..12820982,3	MCF-7	breast:
5	chr5:12790107..12792363-chr5:12800379..12802802,3	MCF-7	breast:
6	chr5:12810723..12813220-chr5:12814346..12816159,2	MCF-7	breast:
7	chr5:12660866..12661403-chr5:12804029..12804604,2	MCF-7	breast:
8	chr5:12815455..12818211-chr5:12818393..12820982,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIO-4	chr5:12804316-12804475	ENSG00000248131
2	lnc-TRIO-4	chr5:12805052-12805295	NONHSAT100514
3	lnc-TRIO-4	chr5:12805052-12805295	NONHSAT100511

No data

Variant related genes	Relation type
ENSG00000249053	chromatin interactions
PURA	miRNA target sites

Extended variants
information (count: 93 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs33932985	chr5:12804331-12804332	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs551245544	chr5:12804366-12804367	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs185056468	chr5:12804377-12804378	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs569927318	chr5:12804394-12804395	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs537313252	chr5:12804409-12804410	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs111688761	chr5:12804423-12804424	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs189393032	chr5:12804433-12804434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs146430528	chr5:12804445-12804446	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs71595891	chr5:12804451-12804452	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs374139878	chr5:12804452-12804453	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs552936755	chr5:12804455-12804456	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs72022493	chr5:12804469-12804470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs373860776	chr5:12804470-12804471	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs111757928	chr5:12804471-12804472	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs538744549	chr5:12804472-12804473	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs376029276	chr5:12805073-12805074	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs554271754	chr5:12805099-12805100	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs554743924	chr5:12805153-12805154	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs113958175	chr5:12805171-12805172	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs540937215	chr5:12805282-12805283	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs144450041	chr5:12809089-12809090	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148395243	chr5:12809134-12809135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377589033	chr5:12809145-12809146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547801356	chr5:12809174-12809175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566048017	chr5:12809221-12809222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190294956	chr5:12809263-12809264	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551848383	chr5:12809290-12809291	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142564573	chr5:12809331-12809332	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs34760755	chr5:12809373-12809374	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs397884177	chr5:12809377-12809378	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201527933	chr5:12809378-12809379	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs199622821	chr5:12809379-12809380	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113930400	chr5:12809382-12809383	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537163754	chr5:12809387-12809388	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111947202	chr5:12809402-12809403	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs4582272	chr5:12809403-12809404	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567943558	chr5:12809450-12809451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543486288	chr5:12809474-12809475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140399760	chr5:12809565-12809566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557434162	chr5:12809598-12809599	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192870497	chr5:12809631-12809632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144852405	chr5:12809649-12809650	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147926281	chr5:12809701-12809702	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557793778	chr5:12809708-12809709	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571987310	chr5:12809710-12809711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs199784731	chr5:12809712-12809713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184990939	chr5:12809714-12809715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562243118	chr5:12809715-12809716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559687880	chr5:12809726-12809727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368334465	chr5:12809731-12809732	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No data

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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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