Variant report

Variant	nsv1031952
Chromosome Location	chr8:4638594-4691865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:4691580-4691808	HepG2	liver:	n/a	n/a
2	BHLHE40	chr8:4691724-4691748	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
4	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
6	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
7	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr8:4691440-4691590	NHLF	lung:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
9	CTCF	chr8:4691520-4691670	NHDF-neo	bronchial:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
10	CTCF	chr8:4691500-4691650	SAEC	small airway:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
11	CTCF	chr8:4691480-4691630	AG04449	skin:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
12	CTCF	chr8:4691460-4691610	GM12871	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
13	CTCF	chr8:4691448-4691686	Spleen_OC	spleen:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
14	CTCF	chr8:4644700-4644850	Caco-2	colon:	n/a	n/a
15	CTCF	chr8:4691500-4691650	HUVEC	blood vessel:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
16	CTCF	chr8:4671759-4671827	ProgFib	skin:	n/a	n/a
17	CTCF	chr8:4644680-4644830	GM12867	blood:	n/a	n/a
18	CTCF	chr8:4691459-4691507	GM19238	blood:	n/a	n/a
19	CTCF	chr8:4691510-4691627	GM20000	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
20	CTCF	chr8:4691480-4691630	WERI-Rb-1	eye:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
21	CTCF	chr8:4691440-4691590	GM12878	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
22	CTCF	chr8:4691468-4691633	MCF-7	breast:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
23	CTCF	chr8:4691480-4691630	BJ	skin:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
24	CTCF	chr8:4691520-4691670	MCF-7	breast:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
25	CTCF	chr8:4691384-4691641	SK-N-SH_RA	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
26	CTCF	chr8:4691420-4691570	GM12866	blood:	n/a	n/a
27	CTCF	chr8:4691360-4691510	HAc	cerebellar:	n/a	n/a
28	CTCF	chr8:4691456-4691687	GM13977	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
29	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
31	CTCF	chr8:4644600-4644750	SAEC	small airway:	n/a	n/a
32	CTCF	chr8:4644620-4644770	GM12872	blood:	n/a	n/a
33	CTCF	chr8:4691460-4691610	HL-60	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
34	CTCF	chr8:4691500-4691650	GM12868	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
35	CTCF	chr8:4644620-4644770	RPTEC	kidney:	n/a	n/a
36	CTCF	chr8:4691462-4691663	LNCaP	prostate:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
37	CTCF	chr8:4691500-4691650	GM12865	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
38	CTCF	chr8:4691479-4691485	A549	lung:	n/a	n/a
39	CTCF	chr8:4691500-4691650	HA-sp	spinal cord:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
40	CTCF	chr8:4644640-4644790	GM12865	blood:	n/a	n/a
41	CTCF	chr8:4691440-4691590	GM12869	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
42	CTCF	chr8:4644680-4644830	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr8:4644660-4644810	HepG2	liver:	n/a	n/a
44	CTCF	chr8:4690820-4690970	GM12872	blood:	n/a	n/a
45	CTCF	chr8:4691380-4691530	A549	lung:	n/a	n/a
46	CTCF	chr8:4691520-4691670	GM12870	blood:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
47	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
48	CTCF	chr8:4691480-4691630	HPF	lung:	n/a	chr8:4691557-4691578 chr8:4691555-4691573
49	CTCF	chr8:4644647-4644651	HepG2	liver:	n/a	n/a
50	CTCF	chr8:4691407-4691709	Medullo	brain:	n/a	chr8:4691557-4691578 chr8:4691555-4691573

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4644739-4644789	SK-N-SH	brain:	n/a
2	chr8:4644739-4644789	HCF	heart:	n/a
3	chr8:4644719-4644769	NT2-D1	testis:	n/a
4	chr8:4644719-4644769	BJ	skin:	n/a
5	chr8:4644739-4644789	AG09319	gingival:	n/a
6	chr8:4644739-4644789	HEEpiC	esophagus:	n/a
7	chr8:4644719-4644769	PANC-1	pancreas:	n/a
8	chr8:4644719-4644769	RPTEC	kidney:	n/a
9	chr8:4644719-4644769	NB4	blood:	n/a
10	chr8:4644739-4644789	RPTEC	kidney:	n/a
11	chr8:4644739-4644789	SK-N-MC	brain:	n/a
12	chr8:4644739-4644789	HMEC	breast:	n/a
13	chr8:4644739-4644789	HRE	kidney:	n/a
14	chr8:4644719-4644769	HUVEC	blood vessel:	n/a
15	chr8:4644739-4644789	NT2-D1	testis:	n/a
16	chr8:4644739-4644789	PANC-1	pancreas:	n/a
17	chr8:4644719-4644769	CMK	blood:	n/a
18	chr8:4644739-4644789	ProgFib	skin:	n/a
19	chr8:4644739-4644789	HCPEpiC	choroid plexus:	n/a
20	chr8:4644719-4644769	NHDF-neo	bronchial:	n/a
21	chr8:4644719-4644769	NHBE	bronchial:	n/a
22	chr8:4644719-4644769	AG04449	skin:	fetal
23	chr8:4644719-4644769	SKMC	muscle:	n/a
24	chr8:4644719-4644769	HepG2	liver:	n/a
25	chr8:4644739-4644789	HRPEpiC	eye:	n/a
26	chr8:4644719-4644769	ProgFib	skin:	n/a
27	chr8:4644739-4644789	HCM	heart:	n/a
28	chr8:4644719-4644769	H1-hESC	embryonic stem cell:	embryo
29	chr8:4644719-4644769	HEK293	kidney:	embryo
30	chr8:4644739-4644789	HL-60	blood:	n/a
31	chr8:4644719-4644769	A549	lung:	n/a
32	chr8:4644739-4644789	NHBE	bronchial:	n/a
33	chr8:4644739-4644789	HRCEpiC	kidney:	n/a
34	chr8:4644719-4644769	HIPEpiC	eye:	n/a
35	chr8:4644719-4644769	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:4644719-4644769	HNPCEpiC	eye:	n/a
37	chr8:4644739-4644789	HUVEC	blood vessel:	n/a
38	chr8:4644739-4644789	HAEpiC	amniotic membrane:	n/a
39	chr8:4644719-4644769	PrEC	prostate:	n/a
40	chr8:4644739-4644789	SKMC	muscle:	n/a
41	chr8:4644739-4644789	GM12878	blood:	n/a
42	chr8:4644739-4644789	ovcar-3	ovarian:	n/a
43	chr8:4644739-4644789	NHDF-neo	bronchial:	n/a
44	chr8:4644719-4644769	SK-N-MC	brain:	n/a
45	chr8:4644739-4644789	CMK	blood:	n/a
46	chr8:4644719-4644769	ECC-1	luminal epithelium:	n/a
47	chr8:4644719-4644769	MCF10A-Er-Src	breast:	n/a
48	chr8:4644739-4644789	U87	brain:	n/a
49	chr8:4644739-4644789	IMR90	lung:	fetal
50	chr8:4644719-4644769	Hepatocyte	liver:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCPH1-7	chr8:4644854-4646106	NONHSAT124751

Variant related genes	Relation type
PAICSP4	TF binding region
PAICSP4	CpG island

Extended variants
information (count: 2593 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2593 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17071320	chr8:4638594-4638595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147878208	chr8:4638598-4638599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73179606	chr8:4638665-4638666	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs372157219	chr8:4638678-4638679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554667299	chr8:4638691-4638692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566826689	chr8:4638695-4638696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10503282	chr8:4638706-4638707	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs559124338	chr8:4638711-4638712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577403356	chr8:4638712-4638713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544861006	chr8:4638751-4638752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367666570	chr8:4638759-4638760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568375645	chr8:4638765-4638766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541803469	chr8:4638768-4638769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542469751	chr8:4638773-4638774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559907478	chr8:4638775-4638776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17071321	chr8:4638836-4638837	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs545370065	chr8:4638837-4638838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563872447	chr8:4638840-4638841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184070075	chr8:4638849-4638850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549754338	chr8:4638862-4638863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554441896	chr8:4638894-4638895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141718646	chr8:4638901-4638902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574277124	chr8:4638904-4638905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529180875	chr8:4638936-4638937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73179609	chr8:4638939-4638940	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs543385332	chr8:4638971-4638972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565960293	chr8:4638985-4638986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150169812	chr8:4639019-4639020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56191817	chr8:4639028-4639029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571005553	chr8:4639039-4639040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188626584	chr8:4639047-4639048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556490107	chr8:4639062-4639063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574942088	chr8:4639082-4639083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542180135	chr8:4639093-4639094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554476776	chr8:4639101-4639102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532431539	chr8:4639134-4639135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572387144	chr8:4639136-4639137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545432480	chr8:4639165-4639166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563734146	chr8:4639174-4639175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368937916	chr8:4639189-4639190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531305986	chr8:4639194-4639195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs193196821	chr8:4639197-4639198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112074901	chr8:4639202-4639203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561758541	chr8:4639242-4639243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529117728	chr8:4639247-4639248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547262307	chr8:4639253-4639254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559728201	chr8:4639262-4639263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10081503	chr8:4639285-4639286	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs552609506	chr8:4639287-4639288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570818767	chr8:4639301-4639302	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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4631600-4638800	Weak transcription	Brain Angular Gyrus	brain
2	chr8:4636600-4639000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:4637000-4638600	Enhancers	Fetal Kidney	kidney
4	chr8:4637000-4639000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr8:4637200-4639000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:4637600-4638800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:4638000-4639000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:4638000-4639200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:4638000-4639600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:4638400-4639000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:4638800-4639400	Enhancers	Brain Angular Gyrus	brain
12	chr8:4639000-4640800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:4639000-4641000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr8:4639200-4639400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:4639400-4640600	Weak transcription	Brain Angular Gyrus	brain
16	chr8:4639600-4639800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:4639600-4639800	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:4640600-4640800	Enhancers	Brain Angular Gyrus	brain
19	chr8:4640800-4641400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:4641000-4641200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:4641000-4641400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:4644400-4645000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:4644600-4644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:4653200-4654000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr8:4653200-4654400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr8:4653800-4654200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr8:4654200-4654600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:4658400-4670600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:4668000-4668200	Enhancers	Fetal Brain Male	brain
30	chr8:4668200-4669600	Weak transcription	Fetal Brain Male	brain
31	chr8:4669400-4669800	Active TSS	Brain Angular Gyrus	brain
32	chr8:4669400-4670000	Active TSS	Brain Substantia Nigra	brain
33	chr8:4669600-4670000	Enhancers	Fetal Brain Male	brain
34	chr8:4670000-4671600	Weak transcription	Fetal Brain Male	brain
35	chr8:4671600-4672000	Enhancers	Fetal Brain Male	brain
36	chr8:4681200-4693800	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr8:4684600-4685200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr8:4684800-4685200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:4685000-4685200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:4685800-4686000	Enhancers	HUES48 Cell Line	embryonic stem cell

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