Variant report

Variant	nsv821103
Chromosome Location	chr10:4857721-4858391
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4857664..4858243-chr10:4890593..4891221,2	MCF-7	breast:
2	chr10:4857632..4858594-chr10:4891971..4892610,3	K562	blood:
3	chr10:4857209..4858993-chr10:4874035..4875917,2	K562	blood:
4	chr10:4857556..4858565-chr10:4881032..4882202,10	MCF-7	breast:
5	chr10:4857251..4858256-chr10:4891548..4892484,4	MCF-7	breast:
6	chr10:4857671..4858400-chr10:5624407..5624994,2	K562	blood:
7	chr10:4857079..4859136-chr10:4895299..4898229,2	K562	blood:
8	chr10:4857628..4858745-chr10:4881174..4882066,5	MCF-7	breast:
9	chr10:4857646..4858298-chr10:5023972..5024754,3	MCF-7	breast:
10	chr10:4855444..4858431-chr10:5530481..5532071,2	MCF-7	breast:
11	chr10:4856147..4859117-chr10:5323721..5326556,2	K562	blood:
12	chr10:4857197..4858287-chr10:5475785..5476862,3	MCF-7	breast:
13	chr10:4856908..4859105-chr10:4868238..4871321,3	MCF-7	breast:
14	chr10:4857778..4858293-chr10:5425331..5426189,2	K562	blood:
15	chr10:4857887..4858608-chr10:5325585..5326522,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000165568	chromatin interactions

Extended variants
information (count: 36 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549406371	chr10:4857721-4857722	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200049472	chr10:4857727-4857728	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371122341	chr10:4857792-4857793	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77269601	chr10:4857794-4857795	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567501516	chr10:4857807-4857808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532051583	chr10:4857808-4857809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550169889	chr10:4857809-4857810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375387109	chr10:4857811-4857812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111398320	chr10:4857833-4857834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs71391977	chr10:4857884-4857885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11499182	chr10:4857887-4857888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111488752	chr10:4857904-4857905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553945285	chr10:4857917-4857918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566272506	chr10:4857918-4857919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533604433	chr10:4857919-4857920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555346608	chr10:4857922-4857923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs56094027	chr10:4857938-4857939	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs113284551	chr10:4857943-4857944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573529628	chr10:4857983-4857984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112147500	chr10:4857997-4857998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544511292	chr10:4858008-4858009	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561187035	chr10:4858014-4858015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556219258	chr10:4858027-4858028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577865377	chr10:4858028-4858029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545263508	chr10:4858029-4858030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112299575	chr10:4858053-4858054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375578878	chr10:4858057-4858058	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs368142579	chr10:4858107-4858108	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181892698	chr10:4858122-4858123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12764114	chr10:4858124-4858125	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191099564	chr10:4858141-4858142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543115030	chr10:4858268-4858269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12769532	chr10:4858328-4858329	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146281443	chr10:4858331-4858332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187790138	chr10:4858354-4858355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191335909	chr10:4858368-4858369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4853200-4857800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr10:4855400-4867400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:4855600-4862800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:4857200-4857800	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr10:4857200-4857800	Enhancers	Dnd41	blood
6	chr10:4857400-4857800	Enhancers	Primary B cells from peripheral blood	blood
7	chr10:4857400-4857800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr10:4857400-4857800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:4857400-4860600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:4857600-4857800	Active TSS	Monocytes-CD14+_RO01746	blood
11	chr10:4857600-4858400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr10:4857600-4858600	Weak transcription	A549	lung
13	chr10:4857600-4858600	Weak transcription	K562	blood
14	chr10:4857600-4868000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr10:4857800-4861800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr10:4857800-4862400	Weak transcription	Monocytes-CD14+_RO01746	blood

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