Variant report

Variant	nsv1028775
Chromosome Location	chr8:9278695-9298658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9291262-9291958	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:9278878-9279410	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:9279045-9279235	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:9295186-9295259	K562	blood:	n/a	n/a
5	CEBPB	chr8:9278951-9279158	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:9293602-9293928	HepG2	liver:	n/a	chr8:9293763-9293774
7	CHD2	chr8:9279127-9279151	HepG2	liver:	n/a	n/a
8	CTCF	chr8:9290100-9290250	HepG2	liver:	n/a	n/a
9	CTCF	chr8:9290140-9290290	HCT-116	colon:	n/a	n/a
10	CTCF	chr8:9290120-9290270	BE2_C	brain:	n/a	n/a
11	CTCF	chr8:9290100-9290250	GM12875	blood:	n/a	n/a
12	CTCF	chr8:9290080-9290230	HCFaa	heart:	n/a	n/a
13	CTCF	chr8:9290080-9290230	GM12865	blood:	n/a	n/a
14	CTCF	chr8:9290120-9290270	HEK293	kidney:	n/a	n/a
15	CTCF	chr8:9290080-9290230	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr8:9290060-9290210	AG04450	lung:	n/a	n/a
17	CTCF	chr8:9290180-9290330	K562	blood:	n/a	n/a
18	CTCF	chr8:9290080-9290230	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr8:9290120-9290270	GM12873	blood:	n/a	n/a
20	CTCF	chr8:9290120-9290270	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr8:9290080-9290230	HMF	breast:	n/a	n/a
22	CTCF	chr8:9290080-9290230	BE2_C	brain:	n/a	n/a
23	CTCF	chr8:9290100-9290250	NHEK	skin:	n/a	n/a
24	CTCF	chr8:9290233-9290237	K562	blood:	n/a	n/a
25	CTCF	chr8:9294237-9294256	GM19240	blood:	n/a	n/a
26	CTCF	chr8:9294260-9294264	GM19240	blood:	n/a	n/a
27	CTCF	chr8:9290120-9290270	GM12864	blood:	n/a	n/a
28	CTCF	chr8:9290240-9290390	GM12866	blood:	n/a	n/a
29	CTCF	chr8:9290180-9290330	GM12872	blood:	n/a	n/a
30	CTCF	chr8:9290120-9290270	GM12871	blood:	n/a	n/a
31	CTCF	chr8:9290020-9290170	GM06990	blood:	n/a	n/a
32	CTCF	chr8:9290080-9290230	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr8:9290120-9290270	HRE	kidney:	n/a	n/a
34	CTCF	chr8:9290040-9290190	GM12866	blood:	n/a	n/a
35	CTCF	chr8:9290257-9290279	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr8:9290120-9290270	GM12874	blood:	n/a	n/a
37	CTCF	chr8:9290160-9290310	GM12873	blood:	n/a	n/a
38	CTCF	chr8:9290080-9290230	GM12872	blood:	n/a	n/a
39	CTCF	chr8:9290080-9290230	GM12864	blood:	n/a	n/a
40	CTCF	chr8:9290060-9290210	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr8:9290060-9290210	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:9290100-9290250	RPTEC	kidney:	n/a	n/a
43	CTCF	chr8:9290080-9290230	A549	lung:	n/a	n/a
44	CTCF	chr8:9290207-9290231	K562	blood:	n/a	n/a
45	CTCF	chr8:9290193-9290227	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr8:9290120-9290270	HVMF	connective:	n/a	n/a
47	CTCFL	chr8:9290117-9290261	K562	blood:	n/a	n/a
48	E2F6	chr8:9296077-9296307	K562	blood:	n/a	n/a
49	E2F6	chr8:9296022-9296383	K562	blood:	n/a	n/a
50	E2F6	chr8:9296082-9296337	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9278742-9278792	Hepatocyte	liver:	n/a
2	chr8:9278742-9278792	PANC-1	pancreas:	n/a
3	chr8:9278742-9278792	HCPEpiC	choroid plexus:	n/a
4	chr8:9278742-9278792	HRCEpiC	kidney:	n/a
5	chr8:9278742-9278792	HIPEpiC	eye:	n/a
6	chr8:9278742-9278792	NT2-D1	testis:	n/a
7	chr8:9278742-9278792	IMR90	lung:	fetal
8	chr8:9278742-9278792	PFSK-1	brain:	n/a
9	chr8:9278742-9278792	SAEC	small airway:	n/a
10	chr8:9278742-9278792	SKMC	muscle:	n/a
11	chr8:9278742-9278792	HepG2	liver:	n/a
12	chr8:9278742-9278792	AG04450	lung:	fetal
13	chr8:9278742-9278792	NH-A	brain:	n/a
14	chr8:9278742-9278792	GM12891	blood:	n/a
15	chr8:9278742-9278792	AoSMC	blood vessel:	n/a
16	chr8:9278742-9278792	Caco-2	colon:	n/a
17	chr8:9278742-9278792	ProgFib	skin:	n/a
18	chr8:9278742-9278792	LNCaP	prostate:	n/a
19	chr8:9278742-9278792	U87	brain:	n/a
20	chr8:9278742-9278792	H1-hESC	embryonic stem cell:	embryo
21	chr8:9278742-9278792	AG10803	skin:	n/a
22	chr8:9278742-9278792	CMK	blood:	n/a
23	chr8:9278742-9278792	MCF-7	breast:	n/a
24	chr8:9278742-9278792	HRPEpiC	eye:	n/a
25	chr8:9278742-9278792	K562	blood:	n/a
26	chr8:9278742-9278792	HEK293	kidney:	embryo
27	chr8:9278742-9278792	Hela-S3	cervix:	n/a
28	chr8:9278742-9278792	HEEpiC	esophagus:	n/a
29	chr8:9278742-9278792	SK-N-SH	brain:	n/a
30	chr8:9278742-9278792	GM12892	blood:	n/a
31	chr8:9278742-9278792	HRE	kidney:	n/a
32	chr8:9278742-9278792	T-47D	breast:	n/a
33	chr8:9278742-9278792	HCM	heart:	n/a
34	chr8:9278742-9278792	AG09309	skin:	n/a
35	chr8:9278742-9278792	HUVEC	blood vessel:	n/a
36	chr8:9278742-9278792	NHBE	bronchial:	n/a
37	chr8:9278742-9278792	PrEC	prostate:	n/a
38	chr8:9278742-9278792	BE2_C	brain:	n/a
39	chr8:9278742-9278792	HMEC	breast:	n/a
40	chr8:9278742-9278792	HL-60	blood:	n/a
41	chr8:9278742-9278792	GM12878	blood:	n/a
42	chr8:9278742-9278792	MCF10A-Er-Src	breast:	n/a
43	chr8:9278742-9278792	SK-N-SH_RA	brain:	n/a
44	chr8:9278742-9278792	GM06990	blood:	n/a
45	chr8:9278742-9278792	BJ	skin:	n/a
46	chr8:9278742-9278792	AG04449	skin:	fetal
47	chr8:9278742-9278792	NB4	blood:	n/a
48	chr8:9278742-9278792	NHDF-neo	bronchial:	n/a
49	chr8:9278742-9278792	SK-N-MC	brain:	n/a
50	chr8:9278742-9278792	HAEpiC	amniotic membrane:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3B-8	chr8:9280338-9281391	NONHSAT124954
2	lnc-PPP1R3B-4	chr8:9293542-9293715	ENSG00000254237
3	lnc-PPP1R3B-8	chr8:9282245-9282386	NONHSAT124954
4	lnc-PPP1R3B-8	chr8:9279664-9279765	NONHSAT124954

No data

Variant related genes	Relation type
ENSG00000254237	TF binding region
ENSG00000254237	CpG island

Extended variants
information (count: 719 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571560900	chr8:9278698-9278699	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs537381230	chr8:9278702-9278703	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs557173623	chr8:9278703-9278704	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185807024	chr8:9278711-9278712	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs372227329	chr8:9278730-9278731	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs146125243	chr8:9278743-9278744	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs138622322	chr8:9278794-9278795	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140664554	chr8:9278809-9278810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190659439	chr8:9278813-9278814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182519229	chr8:9278871-9278872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564180435	chr8:9278880-9278881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533430830	chr8:9278893-9278894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543734984	chr8:9278917-9278918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs13279136	chr8:9278946-9278947	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs529454316	chr8:9278961-9278962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549318931	chr8:9278965-9278966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79900195	chr8:9278976-9278977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528218605	chr8:9279000-9279001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187030177	chr8:9279010-9279011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571294757	chr8:9279026-9279027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535699004	chr8:9279029-9279030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557261136	chr8:9279034-9279035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568215999	chr8:9279061-9279062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567460199	chr8:9279085-9279086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375580225	chr8:9279097-9279098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368539721	chr8:9279101-9279102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190882478	chr8:9279111-9279112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182637336	chr8:9279254-9279255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534841473	chr8:9279285-9279286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376389219	chr8:9279301-9279302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149297935	chr8:9279303-9279304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555412840	chr8:9279308-9279309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577586695	chr8:9279329-9279330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543426111	chr8:9279352-9279353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563597308	chr8:9279427-9279428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188954360	chr8:9279451-9279452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574252229	chr8:9279453-9279454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535280819	chr8:9279458-9279459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116693656	chr8:9279480-9279481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369924921	chr8:9279487-9279488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193063612	chr8:9279506-9279507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs58555622	chr8:9279536-9279537	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530479379	chr8:9279537-9279538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550600709	chr8:9279547-9279548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13281098	chr8:9279553-9279554	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs536194845	chr8:9279577-9279578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115993882	chr8:9279582-9279583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374845785	chr8:9279600-9279601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556794841	chr8:9279605-9279606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538467868	chr8:9279606-9279607	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:136)

Disease	PMID	Source
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
Prostate cancer	16573809	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
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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9277200-9280000	Enhancers	HepG2	liver
2	chr8:9277800-9279600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr8:9278000-9278800	Enhancers	Fetal Stomach	stomach
4	chr8:9278200-9278800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr8:9278200-9278800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:9278200-9278800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:9278200-9278800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:9278200-9278800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:9278200-9279000	Enhancers	Primary hematopoietic stem cells	blood
10	chr8:9278200-9279000	Enhancers	Liver	Liver
11	chr8:9278400-9278800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr8:9278600-9279000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:9278600-9279600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:9278800-9279200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:9279600-9279800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:9287000-9287200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:9287200-9288200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:9288200-9289400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:9288400-9289000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr8:9288600-9289400	Enhancers	Brain Germinal Matrix	brain
21	chr8:9288600-9289600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:9288800-9289200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:9288800-9289400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr8:9288800-9289800	Enhancers	Fetal Brain Female	brain
25	chr8:9288800-9290200	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:9289000-9290000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:9289000-9290200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:9289400-9293600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr8:9290200-9291800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:9290200-9296000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:9291000-9292200	Enhancers	HepG2	liver
32	chr8:9291800-9292000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:9291800-9292200	Enhancers	Fetal Intestine Small	intestine
34	chr8:9292000-9292200	Enhancers	Fetal Intestine Large	intestine
35	chr8:9292200-9293200	Weak transcription	Fetal Intestine Small	intestine
36	chr8:9292200-9293400	Weak transcription	Fetal Intestine Large	intestine
37	chr8:9292200-9293800	Weak transcription	HepG2	liver
38	chr8:9293200-9294200	Enhancers	Fetal Intestine Small	intestine
39	chr8:9293400-9293800	Enhancers	Duodenum Mucosa	Duodenum
40	chr8:9293400-9294200	Enhancers	Fetal Intestine Large	intestine
41	chr8:9293600-9293800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:9293800-9294000	Enhancers	HepG2	liver
43	chr8:9295800-9296400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:9296000-9296200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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