Variant report

Variant	nsv889931
Chromosome Location	chr8:3981876-4022811
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:4010079..4014350-chr8:4015920..4019883,4	K562	blood:
2	chr8:4010079..4014350-chr8:4015920..4018884,3	K562	blood:
3	chr8:4010079..4014350-chr8:4015920..4019883,4	K562	blood:
4	chr8:4010079..4014350-chr8:4015920..4018884,3	K562	blood:

Extended variants
information (count: 2345 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:2345 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1647326	chr8:3981876-3981877	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565757030	chr8:3981893-3981894	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs566570882	chr8:3981899-3981900	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs141116794	chr8:3981910-3981911	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs11998150	chr8:3981913-3981914	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs143135930	chr8:3981918-3981919	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs201767263	chr8:3981930-3981931	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs202012927	chr8:3981932-3981933	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs143216083	chr8:3981938-3981939	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs200107620	chr8:3981939-3981940	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs375833130	chr8:3981941-3981942	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs145470397	chr8:3981946-3981947	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs188365530	chr8:3981948-3981949	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs540772193	chr8:3981949-3981950	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs559367420	chr8:3981958-3981959	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs532864685	chr8:3981960-3981961	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs577648789	chr8:3981964-3981965	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs17404711	chr8:3981968-3981969	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148833279	chr8:3981975-3981976	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs143486644	chr8:3981977-3981978	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs549226441	chr8:3982030-3982031	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs561130677	chr8:3982046-3982047	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs373512805	chr8:3982047-3982048	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs112479612	chr8:3982048-3982049	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs546792161	chr8:3982053-3982054	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs181854976	chr8:3982055-3982056	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs539111474	chr8:3982069-3982070	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs551721155	chr8:3982082-3982083	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs569856371	chr8:3982084-3982085	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs537350806	chr8:3982085-3982086	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs187353321	chr8:3982090-3982091	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs13276808	chr8:3982105-3982106	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565672916	chr8:3982107-3982108	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs56003604	chr8:3982108-3982109	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs554638476	chr8:3982109-3982110	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs141744414	chr8:3982134-3982135	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs369823023	chr8:3982140-3982141	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs147091123	chr8:3982145-3982146	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs575388540	chr8:3982175-3982176	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs191801500	chr8:3982183-3982184	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs561590968	chr8:3982186-3982187	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs537227005	chr8:3982189-3982190	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs374939012	chr8:3982192-3982193	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs1647328	chr8:3982207-3982208	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs183627967	chr8:3982214-3982215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186986642	chr8:3982216-3982217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569868709	chr8:3982217-3982218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560260241	chr8:3982224-3982225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138513374	chr8:3982230-3982231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144111653	chr8:3982246-3982247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3980600-3983200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:3981400-3983400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:3981600-3982800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr8:3981600-3984400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:3981600-3984400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:3981600-3984600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:3981800-3982000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:3981800-3982200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr8:3981800-3984400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:3981800-3984600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:3981800-3993800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr8:3982000-3983000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr8:3982000-3984600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:3982200-3984400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr8:3982800-3984400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:3983000-3984200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:3983200-3983400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr8:3983200-3983600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:3983200-3983600	Enhancers	Fetal Kidney	kidney
20	chr8:3983400-3983800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr8:3983600-3984000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:3983800-3984200	Enhancers	Pancreas	Pancrea
23	chr8:3983800-3984800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:3984400-3985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr8:3984600-3985600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr8:3985400-3985600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:3985600-3985800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr8:3993800-3994800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:3993800-3994800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:3994000-3994600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr8:3994000-3994800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:3994000-3994800	Enhancers	Brain Germinal Matrix	brain
33	chr8:3994800-3999800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:3997000-3997200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:3999800-4000000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:4000000-4001200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr8:4001200-4001800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:4001400-4001600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:4001400-4001800	Enhancers	Fetal Lung	lung
40	chr8:4010800-4011000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr8:4010800-4011400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:4010800-4011400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:4010800-4011400	Enhancers	Fetal Muscle Leg	muscle
44	chr8:4011000-4011400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr8:4012800-4013400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr8:4012800-4013600	Enhancers	HUES48 Cell Line	embryonic stem cell

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