Variant report

Variant	nsv539402
Chromosome Location	chr8:4631791-4685677
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:4668991-4669179	HepG2	liver:	n/a	chr8:4669056-4669067
2	CHD2	chr8:4644622-4644850	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr8:4654890-4654920	HepG2	liver:	n/a	n/a
4	CTCF	chr8:4644647-4644806	GM12891	blood:	n/a	n/a
5	CTCF	chr8:4644600-4644750	WERI-Rb-1	eye:	n/a	n/a
6	CTCF	chr8:4644680-4644748	Pancreas_OC	pancreas:	n/a	n/a
7	CTCF	chr8:4644646-4644815	A549	lung:	n/a	n/a
8	CTCF	chr8:4644580-4644730	A549	lung:	n/a	n/a
9	CTCF	chr8:4644647-4644651	HepG2	liver:	n/a	n/a
10	CTCF	chr8:4644591-4644910	K562	blood:	n/a	n/a
11	CTCF	chr8:4644551-4644864	K562	blood:	n/a	n/a
12	CTCF	chr8:4644640-4644790	GM12874	blood:	n/a	n/a
13	CTCF	chr8:4644620-4644770	RPTEC	kidney:	n/a	n/a
14	CTCF	chr8:4644680-4644830	GM12867	blood:	n/a	n/a
15	CTCF	chr8:4644640-4644790	HEK293	kidney:	n/a	n/a
16	CTCF	chr8:4644680-4644830	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr8:4644680-4644830	GM12871	blood:	n/a	n/a
18	CTCF	chr8:4644620-4644770	SAEC	small airway:	n/a	n/a
19	CTCF	chr8:4644625-4644807	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr8:4671759-4671827	ProgFib	skin:	n/a	n/a
21	CTCF	chr8:4644640-4644790	HepG2	liver:	n/a	n/a
22	CTCF	chr8:4644700-4644850	HRE	kidney:	n/a	n/a
23	CTCF	chr8:4644600-4644750	GM12872	blood:	n/a	n/a
24	CTCF	chr8:4644600-4644750	GM12873	blood:	n/a	n/a
25	CTCF	chr8:4644640-4644790	A549	lung:	n/a	n/a
26	CTCF	chr8:4644516-4644932	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:4644660-4644810	GM12866	blood:	n/a	n/a
28	CTCF	chr8:4650026-4650077	ProgFib	skin:	n/a	n/a
29	CTCF	chr8:4644660-4644810	GM12864	blood:	n/a	n/a
30	CTCF	chr8:4644700-4644850	GM12869	blood:	n/a	n/a
31	CTCF	chr8:4644640-4644790	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr8:4654887-4654940	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr8:4644640-4644790	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr8:4644597-4644867	HepG2	liver:	n/a	n/a
35	CTCF	chr8:4644700-4644850	GM12875	blood:	n/a	n/a
36	CTCF	chr8:4644652-4644813	HepG2	liver:	n/a	n/a
37	CTCF	chr8:4644660-4644810	GM12868	blood:	n/a	n/a
38	CTCF	chr8:4644647-4644794	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr8:4644584-4644870	K562	blood:	n/a	n/a
40	CTCF	chr8:4644620-4644770	NB4	blood:	n/a	n/a
41	CTCF	chr8:4644640-4644790	K562	blood:	n/a	n/a
42	CTCF	chr8:4644620-4644770	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr8:4644600-4644750	GM12864	blood:	n/a	n/a
44	CTCF	chr8:4644540-4644690	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr8:4644640-4644790	GM12872	blood:	n/a	n/a
46	CTCF	chr8:4644600-4644750	HEK293	kidney:	n/a	n/a
47	CTCF	chr8:4644672-4644761	GM13977	blood:	n/a	n/a
48	CTCF	chr8:4644660-4644810	GM12869	blood:	n/a	n/a
49	CTCF	chr8:4644642-4644821	K562	blood:	n/a	n/a
50	CTCF	chr8:4644587-4644847	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:4644719-4644769	A549	lung:	n/a
2	chr8:4644719-4644769	AG04450	lung:	fetal
3	chr8:4637584-4637634	A549	lung:	n/a
4	chr8:4637584-4637634	AG10803	skin:	n/a
5	chr8:4637584-4637634	GM12878	blood:	n/a
6	chr8:4644739-4644789	SAEC	small airway:	n/a
7	chr8:4637584-4637634	MCF-7	breast:	n/a
8	chr8:4644739-4644789	Jurkat	blood:	n/a
9	chr8:4644719-4644769	HUVEC	blood vessel:	n/a
10	chr8:4637584-4637634	RPTEC	kidney:	n/a
11	chr8:4644719-4644769	Caco-2	colon:	n/a
12	chr8:4644719-4644769	ProgFib	skin:	n/a
13	chr8:4644739-4644789	AG04450	lung:	fetal
14	chr8:4644719-4644769	RPTEC	kidney:	n/a
15	chr8:4637584-4637634	GM12891	blood:	n/a
16	chr8:4644719-4644769	HCF	heart:	n/a
17	chr8:4644719-4644769	PFSK-1	brain:	n/a
18	chr8:4637584-4637634	HEK293	kidney:	embryo
19	chr8:4644719-4644769	H1-hESC	embryonic stem cell:	embryo
20	chr8:4644719-4644769	SKMC	muscle:	n/a
21	chr8:4637584-4637634	NH-A	brain:	n/a
22	chr8:4637584-4637634	Hela-S3	cervix:	n/a
23	chr8:4644739-4644789	HRE	kidney:	n/a
24	chr8:4644739-4644789	HIPEpiC	eye:	n/a
25	chr8:4644739-4644789	IMR90	lung:	fetal
26	chr8:4637584-4637634	HRE	kidney:	n/a
27	chr8:4644719-4644769	NHDF-neo	bronchial:	n/a
28	chr8:4644739-4644789	LNCaP	prostate:	n/a
29	chr8:4637584-4637634	HCT-116	colon:	n/a
30	chr8:4637584-4637634	NB4	blood:	n/a
31	chr8:4637584-4637634	U87	brain:	n/a
32	chr8:4644739-4644789	ECC-1	luminal epithelium:	n/a
33	chr8:4644739-4644789	T-47D	breast:	n/a
34	chr8:4644739-4644789	HRPEpiC	eye:	n/a
35	chr8:4644739-4644789	CMK	blood:	n/a
36	chr8:4644739-4644789	GM12891	blood:	n/a
37	chr8:4644739-4644789	GM06990	blood:	n/a
38	chr8:4637584-4637634	H1-hESC	embryonic stem cell:	embryo
39	chr8:4637584-4637634	HAEpiC	amniotic membrane:	n/a
40	chr8:4644719-4644769	NT2-D1	testis:	n/a
41	chr8:4637584-4637634	Hepatocyte	liver:	n/a
42	chr8:4644719-4644769	Hela-S3	cervix:	n/a
43	chr8:4644719-4644769	SK-N-SH	brain:	n/a
44	chr8:4637584-4637634	AG09309	skin:	n/a
45	chr8:4644739-4644789	PFSK-1	brain:	n/a
46	chr8:4637584-4637634	HNPCEpiC	eye:	n/a
47	chr8:4644739-4644789	BJ	skin:	n/a
48	chr8:4637584-4637634	HRCEpiC	kidney:	n/a
49	chr8:4644739-4644789	HMEC	breast:	n/a
50	chr8:4644739-4644789	HAEpiC	amniotic membrane:	n/a

No data

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

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

No data

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

Extended variants
information (count: 2599 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2599 , 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	rs549083107	chr8:4631803-4631804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536835707	chr8:4631823-4631824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567455942	chr8:4631830-4631831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556506599	chr8:4631836-4631837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150967220	chr8:4631847-4631848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183143997	chr8:4631851-4631852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576647052	chr8:4631872-4631873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140547616	chr8:4631880-4631881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77045365	chr8:4631882-4631883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17419398	chr8:4631905-4631906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs187581220	chr8:4631914-4631915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554581463	chr8:4631917-4631918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573019039	chr8:4631931-4631932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540317755	chr8:4631954-4631955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564941177	chr8:4631963-4631964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192053901	chr8:4631965-4631966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544200111	chr8:4631970-4631971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565167658	chr8:4631971-4631972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541485502	chr8:4631982-4631983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529931670	chr8:4632002-4632003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546918646	chr8:4632005-4632006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59018211	chr8:4632025-4632026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560943779	chr8:4632044-4632045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528604311	chr8:4632061-4632062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546651812	chr8:4632063-4632064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184193747	chr8:4632081-4632082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188106502	chr8:4632082-4632083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539196533	chr8:4632099-4632100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10105707	chr8:4632105-4632106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs117129617	chr8:4632130-4632131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542787369	chr8:4632133-4632134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562565689	chr8:4632138-4632139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536940315	chr8:4632150-4632151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192491299	chr8:4632151-4632152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572835990	chr8:4632153-4632154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145744155	chr8:4632183-4632184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558592267	chr8:4632207-4632208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551262713	chr8:4632216-4632217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544431410	chr8:4632222-4632223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562522527	chr8:4632265-4632266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574439632	chr8:4632278-4632279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576839326	chr8:4632280-4632281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560959698	chr8:4632283-4632284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138418924	chr8:4632291-4632292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546802369	chr8:4632292-4632293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374387125	chr8:4632300-4632301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184467571	chr8:4632316-4632317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143023392	chr8:4632324-4632325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551200756	chr8:4632339-4632340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59550804	chr8:4632346-4632347	Enhancers Weak transcription	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:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:4630800-4637000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:4631200-4632400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:4631600-4638800	Weak transcription	Brain Angular Gyrus	brain
4	chr8:4632200-4632600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr8:4635800-4636800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:4636000-4636200	Enhancers	Fetal Kidney	kidney
7	chr8:4636200-4637000	Weak transcription	Fetal Kidney	kidney
8	chr8:4636600-4639000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:4636800-4638000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:4637000-4637800	Enhancers	Rectal Smooth Muscle	rectum
11	chr8:4637000-4638000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:4637000-4638000	Enhancers	Brain Cingulate Gyrus	brain
13	chr8:4637000-4638600	Enhancers	Fetal Kidney	kidney
14	chr8:4637000-4639000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr8:4637200-4637600	Enhancers	Fetal Brain Female	brain
16	chr8:4637200-4637800	Enhancers	Fetal Brain Male	brain
17	chr8:4637200-4638000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr8:4637200-4638000	Enhancers	Colon Smooth Muscle	Colon
19	chr8:4637200-4639000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:4637400-4638000	Enhancers	Fetal Stomach	stomach
21	chr8:4637600-4638800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:4638000-4638400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:4638000-4639000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr8:4638000-4639200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:4638000-4639600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr8:4638400-4639000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:4638800-4639400	Enhancers	Brain Angular Gyrus	brain
28	chr8:4639000-4640800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:4639000-4641000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:4639200-4639400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:4639400-4640600	Weak transcription	Brain Angular Gyrus	brain
32	chr8:4639600-4639800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:4639600-4639800	Enhancers	Brain Cingulate Gyrus	brain
34	chr8:4640600-4640800	Enhancers	Brain Angular Gyrus	brain
35	chr8:4640800-4641400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:4641000-4641200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:4641000-4641400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:4644400-4645000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr8:4644600-4644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:4653200-4654000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:4653200-4654400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:4653800-4654200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr8:4654200-4654600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:4658400-4670600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:4668000-4668200	Enhancers	Fetal Brain Male	brain
46	chr8:4668200-4669600	Weak transcription	Fetal Brain Male	brain
47	chr8:4669400-4669800	Active TSS	Brain Angular Gyrus	brain
48	chr8:4669400-4670000	Active TSS	Brain Substantia Nigra	brain
49	chr8:4669600-4670000	Enhancers	Fetal Brain Male	brain
50	chr8:4670000-4671600	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links