Variant report

Variant	nsv831219
Chromosome Location	chr8:5917975-6108250
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:22)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:4919533..4920406-chr8:5997153..5998101,2	MCF-7	breast:
2	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
3	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
4	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
5	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
6	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
7	chr8:5933019..5936001-chr8:5936013..5938853,2	K562	blood:
8	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
9	chr8:6079332..6082540-chr8:6084426..6086508,3	K562	blood:
10	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
11	chr8:6106618..6108795-chr8:6113891..6116770,2	K562	blood:
12	chr8:5990205..5992800-chr8:5992973..5994775,2	K562	blood:
13	chr8:6084910..6087836-chr8:6095267..6098254,2	K562	blood:
14	chr8:5933019..5935981-chr8:5937353..5939270,2	K562	blood:
15	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
16	chr10:132324298..132325038-chr8:6023084..6023812,2	MCF-7	breast:
17	chr8:6079332..6082540-chr8:6084426..6086508,3	K562	blood:
18	chr8:6084910..6087836-chr8:6095267..6098254,2	K562	blood:
19	chr8:6040393..6043249-chr8:6044843..6046899,2	K562	blood:
20	chr8:4919838..4920394-chr8:5997449..5998189,2	K562	blood:
21	chr8:5917249..5917976-chr8:5997130..5997653,2	MCF-7	breast:
22	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-11	chr8:6082847-6083064	NONHSAT124769
2	lnc-ANGPT2-3	chr8:5957850-5957973	ENSG00000253880
3	lnc-ANGPT2-3	chr8:5923520-5923650	XLOC_006984

No data

Variant related genes	Relation type
ENSG00000253880	chromatin interactions
ACVR2A	miRNA target sites

Extended variants
information (count: 6628 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:6628 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575432419	chr8:5917980-5917981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11136966	chr8:5918026-5918027	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568763636	chr8:5918094-5918095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74649040	chr8:5918101-5918102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113125052	chr8:5918102-5918103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561260078	chr8:5918123-5918124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376106469	chr8:5918132-5918133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574711714	chr8:5918142-5918143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182482529	chr8:5918154-5918155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73508599	chr8:5918165-5918166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs532646948	chr8:5918207-5918208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376703918	chr8:5918225-5918226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185674344	chr8:5918256-5918257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114111226	chr8:5918268-5918269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531960135	chr8:5918306-5918307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs11779778	chr8:5918321-5918322	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568746289	chr8:5918322-5918323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535826158	chr8:5918355-5918356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76413689	chr8:5918358-5918359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566169732	chr8:5918396-5918397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13276759	chr8:5918413-5918414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs558256769	chr8:5918420-5918421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75913954	chr8:5918454-5918455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538057046	chr8:5918465-5918466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190084993	chr8:5918569-5918570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574682225	chr8:5918581-5918582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144784336	chr8:5918602-5918603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370432364	chr8:5918604-5918605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374475259	chr8:5918641-5918642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs66467124	chr8:5918674-5918675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs78726578	chr8:5918714-5918715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148570347	chr8:5918718-5918719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562994018	chr8:5918731-5918732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557701402	chr8:5918736-5918737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531777391	chr8:5918760-5918761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542412510	chr8:5918767-5918768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144270304	chr8:5918772-5918773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565696400	chr8:5918779-5918780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs375673459	chr8:5918783-5918784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4875691	chr8:5918789-5918790	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547717631	chr8:5918832-5918833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111741865	chr8:5918833-5918834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531999138	chr8:5918841-5918842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112635221	chr8:5918862-5918863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568939721	chr8:5918866-5918867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537599626	chr8:5918867-5918868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573077851	chr8:5918889-5918890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568207227	chr8:5918893-5918894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534065626	chr8:5918895-5918896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146098638	chr8:5918896-5918897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

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
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
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
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20688739	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5917200-5918000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:5917200-5919200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:5918000-5921000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:5921000-5921400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:5923200-5925200	Enhancers	Fetal Brain Male	brain
6	chr8:5923600-5923800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr8:5923600-5924000	Enhancers	Fetal Brain Female	brain
8	chr8:5929800-5930800	Enhancers	Fetal Heart	heart
9	chr8:5930800-5934200	Weak transcription	Fetal Heart	heart
10	chr8:5931400-5932600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:5932000-5932400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr8:5932000-5932400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr8:5932600-5935800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:5934000-5934200	Active TSS	Brain Hippocampus Middle	brain
15	chr8:5934200-5934400	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr8:5934200-5934600	Enhancers	Brain Anterior Caudate	brain
17	chr8:5934200-5934800	Enhancers	Fetal Heart	heart
18	chr8:5934400-5934600	Enhancers	Adipose Nuclei	Adipose
19	chr8:5934400-5934800	Enhancers	Fetal Brain Male	brain
20	chr8:5935800-5936800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:5936200-5936600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:5942800-5943200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr8:5949000-5949800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:5952600-5953000	Enhancers	Fetal Brain Female	brain
25	chr8:5952800-5954400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:5953000-5954000	Weak transcription	Fetal Brain Female	brain
27	chr8:5953400-5954200	Enhancers	Brain Substantia Nigra	brain
28	chr8:5953600-5954000	Enhancers	Brain Cingulate Gyrus	brain
29	chr8:5954000-5954200	Enhancers	Fetal Brain Male	brain
30	chr8:5954200-5954400	Enhancers	Fetal Brain Female	brain
31	chr8:5954200-5955400	Weak transcription	Fetal Brain Male	brain
32	chr8:5962200-5979000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:5973000-5973600	Enhancers	Brain Anterior Caudate	brain
34	chr8:5973000-5973800	Enhancers	Brain Hippocampus Middle	brain
35	chr8:5973000-5974000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr8:5973200-5973600	Enhancers	Brain Substantia Nigra	brain
37	chr8:5973600-5974200	Weak transcription	Brain Anterior Caudate	brain
38	chr8:5974200-5974400	Enhancers	Brain Anterior Caudate	brain
39	chr8:5979000-5979200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:5979000-5979200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr8:5979200-5983200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:5981400-5981800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:5981400-5981800	Enhancers	Brain Cingulate Gyrus	brain
44	chr8:5981600-5982000	Enhancers	Brain Hippocampus Middle	brain
45	chr8:5981600-5982000	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr8:5981800-5982000	Enhancers	Fetal Stomach	stomach
47	chr8:5982000-5984800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr8:5983200-5983400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:5983400-5991800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:5984800-5986200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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