Variant report

Variant	nsv971864
Chromosome Location	chr10:56824788-56849175
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	chr10:56848923..56849830-chr22:31212899..31213539,2	MCF-7	breast:

Extended variants
information (count: 405 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3858273	chr10:56824889-56824890	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78536933	chr10:56824894-56824895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11004721	chr10:56824909-56824910	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543259275	chr10:56824948-56824949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553613469	chr10:56825083-56825084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181361307	chr10:56825142-56825143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573485462	chr10:56825153-56825154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4472838	chr10:56825154-56825155	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs565172773	chr10:56825209-56825210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185574899	chr10:56825216-56825217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190726071	chr10:56825274-56825275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148963478	chr10:56825291-56825292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142858820	chr10:56825308-56825309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs80228685	chr10:56825319-56825320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546507852	chr10:56825345-56825346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3905359	chr10:56825358-56825359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370984419	chr10:56825382-56825383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532346258	chr10:56825511-56825512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116070109	chr10:56825526-56825527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568823923	chr10:56825609-56825610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140995740	chr10:56825613-56825614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182865667	chr10:56825638-56825639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75044201	chr10:56825715-56825716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202172010	chr10:56825726-56825727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536832357	chr10:56825733-56825734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565323197	chr10:56840420-56840421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534344499	chr10:56840470-56840471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557428825	chr10:56840494-56840495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372529289	chr10:56840504-56840505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577707790	chr10:56840525-56840526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571004778	chr10:56840535-56840536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190585155	chr10:56840548-56840549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373922374	chr10:56840564-56840565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576599792	chr10:56840578-56840579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542503863	chr10:56840584-56840585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2250764	chr10:56840593-56840594	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs572446386	chr10:56840600-56840601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140703759	chr10:56840627-56840628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183451502	chr10:56840628-56840629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374774594	chr10:56840632-56840633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74879474	chr10:56840646-56840647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377554803	chr10:56840653-56840654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533228566	chr10:56840654-56840655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1573227	chr10:56840690-56840691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370335599	chr10:56840717-56840718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75134975	chr10:56840733-56840734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10825457	chr10:56840738-56840739	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs10437360	chr10:56840745-56840746	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565684697	chr10:56840755-56840756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145647706	chr10:56840761-56840762	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
small cell lung cancer	17426248	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56824000-56825800	Enhancers	HepG2	liver
2	chr10:56840400-56841000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr10:56840800-56841200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:56841000-56841200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:56841200-56849000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:56847200-56847600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr10:56849000-56849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr10:56849000-56849200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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