Variant report

Variant	nsv8383
Chromosome Location	chr8:119926155-119934422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:119927571..119930099-chr8:119939839..119941774,2	MCF-7	breast:
2	chr8:119424882..119426911-chr8:119926050..119928623,2	MCF-7	breast:
3	chr8:119921054..119923444-chr8:119928585..119930805,2	MCF-7	breast:
4	chr8:119918824..119921066-chr8:119925326..119927068,2	MCF-7	breast:
5	chr8:119921061..119923064-chr8:119931822..119933473,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164761	chromatin interactions

Extended variants
information (count: 309 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138502219	chr8:119926179-119926180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553952043	chr8:119926215-119926216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74872066	chr8:119926220-119926221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575269868	chr8:119926263-119926264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545809701	chr8:119926272-119926273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538411066	chr8:119926273-119926274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573832925	chr8:119926344-119926345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564113446	chr8:119926345-119926346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190900268	chr8:119926364-119926365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539008885	chr8:119926368-119926369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546870849	chr8:119926372-119926373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142940668	chr8:119926404-119926405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556525112	chr8:119926421-119926422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182434293	chr8:119926423-119926424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558972308	chr8:119926447-119926448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550537134	chr8:119926457-119926458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570113922	chr8:119926469-119926470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146127594	chr8:119926512-119926513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552261870	chr8:119926516-119926517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373615261	chr8:119926521-119926522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570465901	chr8:119926523-119926524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11997782	chr8:119926553-119926554	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs115493545	chr8:119926561-119926562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562406198	chr8:119926578-119926579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575063432	chr8:119926601-119926602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536023526	chr8:119926618-119926619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77356647	chr8:119926653-119926654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575286657	chr8:119926658-119926659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545876706	chr8:119926666-119926667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148212522	chr8:119926695-119926696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572850315	chr8:119926705-119926706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114476496	chr8:119926729-119926730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61073261	chr8:119926783-119926784	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35671926	chr8:119926789-119926790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185760473	chr8:119926824-119926825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550749382	chr8:119926852-119926853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574933748	chr8:119926882-119926883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191209431	chr8:119926904-119926905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372819580	chr8:119926922-119926923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576009120	chr8:119926952-119926953	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73709377	chr8:119926953-119926954	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs372126462	chr8:119926970-119926971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4876868	chr8:119926989-119926990	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs574013352	chr8:119926991-119926992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61694778	chr8:119927007-119927008	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs534681576	chr8:119927049-119927050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78925611	chr8:119927100-119927101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564834838	chr8:119927130-119927131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527431719	chr8:119927168-119927169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187148163	chr8:119927171-119927172	Enhancers 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
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	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

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119918600-119926600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:119920600-119929200	Enhancers	HSMM	muscle
3	chr8:119921000-119927000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:119921200-119927200	Enhancers	NHDF-Ad	bronchial
5	chr8:119921200-119929000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr8:119921400-119927000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr8:119921600-119926800	Enhancers	HSMMtube	muscle
8	chr8:119921800-119927000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:119921800-119927000	Enhancers	Osteobl	bone
10	chr8:119922000-119926800	Enhancers	NHLF	lung
11	chr8:119922400-119927000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:119923200-119926400	Weak transcription	NHEK	skin
13	chr8:119923600-119928200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:119924800-119926800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:119925200-119929200	Enhancers	Hela-S3	cervix
16	chr8:119925600-119926200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:119925600-119926400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:119925600-119926600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:119925800-119926200	Weak transcription	HMEC	breast
20	chr8:119925800-119926600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:119925800-119927000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr8:119926000-119926400	Weak transcription	NH-A	brain
23	chr8:119926000-119927200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:119926200-119927000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:119926200-119927000	Enhancers	HMEC	breast
26	chr8:119926400-119926800	Enhancers	NH-A	brain
27	chr8:119926400-119927000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:119926400-119927200	Enhancers	NHEK	skin
29	chr8:119926600-119927000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:119926600-119927200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:119926600-119927400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:119926800-119928400	Weak transcription	HSMMtube	muscle
33	chr8:119926800-119928400	Weak transcription	NH-A	brain
34	chr8:119926800-119928800	Weak transcription	NHLF	lung
35	chr8:119926800-119934600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr8:119927000-119927600	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr8:119927000-119928400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr8:119927000-119928600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:119927000-119928600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:119927000-119928600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:119927000-119928800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:119927000-119928800	Weak transcription	HMEC	breast
43	chr8:119927000-119935400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:119927000-119935600	Weak transcription	Osteobl	bone
45	chr8:119927200-119928600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:119927200-119928600	Weak transcription	NHDF-Ad	bronchial
47	chr8:119927200-119928800	Weak transcription	NHEK	skin
48	chr8:119927200-119936400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr8:119927400-119927800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:119927400-119941400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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