Variant report

Variant	nsv1015918
Chromosome Location	chr8:122317724-122339722
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:122336290..122338351-chr8:122338998..122341730,2	MCF-7	breast:
2	chr8:122314614..122316625-chr8:122317794..122319472,2	MCF-7	breast:
3	chr17:59652019..59652612-chr8:122328178..122329036,2	MCF-7	breast:
4	chr8:122336290..122338351-chr8:122338998..122341730,2	MCF-7	breast:

Extended variants
information (count: 641 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143723225	chr8:122317748-122317749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534068507	chr8:122317753-122317754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558612145	chr8:122317787-122317788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539266073	chr8:122317801-122317802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553187901	chr8:122317850-122317851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566820206	chr8:122317882-122317883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35516464	chr8:122317912-122317913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535840050	chr8:122317919-122317920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555830667	chr8:122317928-122317929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575787048	chr8:122317937-122317938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146807695	chr8:122317983-122317984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79802362	chr8:122318009-122318010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578090594	chr8:122318135-122318136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368094713	chr8:122318165-122318166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560908101	chr8:122318168-122318169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369126697	chr8:122318184-122318185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561088349	chr8:122318200-122318201	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10956015	chr8:122318257-122318258	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560834676	chr8:122318292-122318293	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376644590	chr8:122318380-122318381	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62528351	chr8:122318382-122318383	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7843647	chr8:122318464-122318465	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs563249596	chr8:122318473-122318474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530440145	chr8:122318485-122318486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150390654	chr8:122318514-122318515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564030203	chr8:122318522-122318523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7843884	chr8:122318550-122318551	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs7844118	chr8:122318595-122318596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546517847	chr8:122318601-122318602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182702466	chr8:122318602-122318603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535775933	chr8:122318612-122318613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10110068	chr8:122318620-122318621	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554651630	chr8:122318631-122318632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73326410	chr8:122318663-122318664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs11783052	chr8:122318694-122318695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10098524	chr8:122318827-122318828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138394613	chr8:122318873-122318874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200650807	chr8:122318877-122318878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71308638	chr8:122318895-122318896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11787361	chr8:122318906-122318907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10956016	chr8:122318917-122318918	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs375926963	chr8:122318918-122318919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534390146	chr8:122318972-122318973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553975906	chr8:122318980-122318981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs57014002	chr8:122319022-122319023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573920980	chr8:122319033-122319034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537867133	chr8:122319062-122319063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11776971	chr8:122319077-122319078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs186701918	chr8:122319083-122319084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372420711	chr8:122319105-122319106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Burkitt''s lymphoma	20823134	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122313600-122318000	Weak transcription	Fetal Intestine Large	intestine
2	chr8:122318000-122318600	Enhancers	Fetal Intestine Large	intestine
3	chr8:122318000-122318800	Enhancers	Fetal Lung	lung
4	chr8:122318200-122318400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:122318800-122319600	Weak transcription	Fetal Lung	lung
6	chr8:122319600-122319800	Enhancers	Fetal Lung	lung
7	chr8:122322200-122330200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:122326200-122326800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr8:122326400-122326800	Active TSS	Gastric	stomach
10	chr8:122326800-122327000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:122326800-122327000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:122326800-122327200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:122327000-122328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr8:122327000-122328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:122327200-122330400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:122328000-122328800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:122328000-122330800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:122328200-122328600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:122328600-122329200	Enhancers	Primary hematopoietic stem cells	blood
20	chr8:122328800-122329800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr8:122329200-122329600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr8:122329600-122330800	Enhancers	Primary hematopoietic stem cells	blood
23	chr8:122329800-122330800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:122329800-122331000	Enhancers	Fetal Kidney	kidney
25	chr8:122329800-122332000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr8:122329800-122332200	Enhancers	HUVEC	blood vessel
27	chr8:122330200-122330800	Enhancers	HepG2	liver
28	chr8:122330200-122331000	Enhancers	NHEK	skin
29	chr8:122330200-122331000	Enhancers	Osteobl	bone
30	chr8:122330200-122331400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:122330400-122330800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:122330400-122330800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:122330400-122330800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr8:122330400-122330800	Enhancers	Hela-S3	cervix
35	chr8:122330400-122330800	Enhancers	NHLF	lung
36	chr8:122330400-122331000	Enhancers	Duodenum Mucosa	Duodenum
37	chr8:122330400-122331000	Enhancers	NH-A	brain
38	chr8:122330400-122331400	Enhancers	HMEC	breast
39	chr8:122330400-122331400	Enhancers	HSMM	muscle
40	chr8:122330800-122333600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:122330800-122333800	Weak transcription	NHLF	lung
42	chr8:122330800-122334400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:122330800-122335000	Weak transcription	Hela-S3	cervix
44	chr8:122330800-122335400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr8:122331000-122334200	Weak transcription	Osteobl	bone
46	chr8:122331000-122334600	Weak transcription	NH-A	brain
47	chr8:122331000-122334600	Weak transcription	NHEK	skin
48	chr8:122331400-122334600	Weak transcription	HMEC	breast
49	chr8:122331400-122334800	Weak transcription	HSMM	muscle
50	chr8:122331400-122335400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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