Variant report

Variant	nsv1019671
Chromosome Location	chr8:89393818-89443392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:122)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:89434753-89434761	GM12878	blood:	n/a	n/a
2	CEBPB	chr8:89437147-89437622	MCF-7	breast:	n/a	n/a
3	CEBPB	chr8:89437192-89437527	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr8:89441602-89441631	Medullo	brain:	n/a	n/a
5	CTCF	chr8:89405680-89405830	HPF	lung:	n/a	n/a
6	CTCF	chr8:89437222-89437409	MCF-7	breast:	n/a	n/a
7	CTCF	chr8:89400500-89400650	MCF-7	breast:	n/a	n/a
8	CTCF	chr8:89401980-89402130	MCF-7	breast:	n/a	n/a
9	CTCF	chr8:89437242-89437386	MCF-7	breast:	n/a	n/a
10	CTCF	chr8:89437276-89437342	Fibrobl	skin:	n/a	n/a
11	CTCF	chr8:89437239-89437406	MCF-7	breast:	n/a	n/a
12	CTCF	chr8:89437304-89437335	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:89411957-89412044	ProgFib	skin:	n/a	n/a
14	CTCF	chr8:89437200-89437599	MCF-7	breast:	n/a	n/a
15	CTCF	chr8:89437227-89437408	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:89437230-89437419	MCF-7	breast:	n/a	n/a
17	E2F4	chr8:89437196-89437396	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr8:89414771-89414772	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr8:89397919-89398115	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr8:89400118-89400162	MCF10A-Er-Src	breast:	n/a	n/a
21	EP300	chr8:89407824-89408086	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr8:89427585-89428109	T-47D	breast:	n/a	chr8:89427624-89427634
23	EP300	chr8:89407750-89408275	MCF-7	breast:	n/a	chr8:89407757-89407766 chr8:89407753-89407767
24	EP300	chr8:89427609-89428284	MCF-7	breast:	n/a	chr8:89428222-89428232 chr8:89427624-89427634
25	EP300	chr8:89427477-89428260	MCF-7	breast:	n/a	chr8:89428222-89428232 chr8:89427624-89427634
26	FOS	chr8:89432765-89432946	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr8:89437102-89437447	MCF10A-Er-Src	breast:	n/a	chr8:89437228-89437235
28	FOS	chr8:89432712-89432943	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr8:89436991-89437447	MCF10A-Er-Src	breast:	n/a	chr8:89437228-89437235
30	FOS	chr8:89432740-89432983	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr8:89437042-89437532	MCF10A-Er-Src	breast:	n/a	chr8:89437228-89437235
32	FOS	chr8:89437021-89437495	MCF10A-Er-Src	breast:	n/a	chr8:89437228-89437235
33	FOSL1	chr8:89437011-89437559	HCT-116	colon:	n/a	chr8:89437228-89437235
34	FOSL2	chr8:89437034-89437536	MCF-7	breast:	n/a	chr8:89437228-89437235
35	FOXA1	chr8:89407856-89408128	T-47D	breast:	n/a	n/a
36	FOXA1	chr8:89427601-89428029	T-47D	breast:	n/a	chr8:89427621-89427633
37	FOXA1	chr8:89407841-89408141	T-47D	breast:	n/a	n/a
38	FOXA1	chr8:89427629-89428055	T-47D	breast:	n/a	n/a
39	GATA3	chr8:89427437-89428327	MCF-7	breast:	n/a	chr8:89427663-89427673 chr8:89427935-89427943
40	GATA3	chr8:89407801-89408239	MCF-7	breast:	n/a	n/a
41	GATA3	chr8:89407748-89408143	T-47D	breast:	n/a	chr8:89407755-89407765
42	GATA3	chr8:89427643-89428063	MCF-7	breast:	n/a	chr8:89427663-89427673 chr8:89427935-89427943
43	GATA3	chr8:89427601-89428182	MCF-7	breast:	n/a	chr8:89427663-89427673 chr8:89427935-89427943
44	GATA3	chr8:89407775-89408165	T-47D	breast:	n/a	n/a
45	GATA3	chr8:89407749-89408283	MCF-7	breast:	n/a	chr8:89407755-89407765
46	GATA3	chr8:89427527-89428086	T-47D	breast:	n/a	chr8:89427663-89427673 chr8:89427935-89427943
47	GATA3	chr8:89427596-89428073	T-47D	breast:	n/a	chr8:89427663-89427673 chr8:89427935-89427943
48	GATA3	chr8:89407837-89408154	MCF-7	breast:	n/a	n/a
49	GATA3	chr8:89430246-89431228	MCF-7	breast:	n/a	chr8:89431157-89431164
50	GATA3	chr8:89405751-89405870	SH-SY5Y	brain:	n/a	chr8:89405790-89405797 chr8:89405790-89405797 chr8:89405790-89405797

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89434982-89435032	ovcar-3	ovarian:	n/a
2	chr8:89434982-89435032	HEEpiC	esophagus:	n/a
3	chr8:89437704-89437754	SKMC	muscle:	n/a
4	chr8:89434982-89435032	SK-N-SH	brain:	n/a
5	chr8:89434982-89435032	LNCaP	prostate:	n/a
6	chr8:89437704-89437754	Hepatocyte	liver:	n/a
7	chr8:89437704-89437754	CMK	blood:	n/a
8	chr8:89437704-89437754	HUVEC	blood vessel:	n/a
9	chr8:89434982-89435032	HCM	heart:	n/a
10	chr8:89434982-89435032	T-47D	breast:	n/a
11	chr8:89434982-89435032	Caco-2	colon:	n/a
12	chr8:89437704-89437754	NB4	blood:	n/a
13	chr8:89437704-89437754	Jurkat	blood:	n/a
14	chr8:89434982-89435032	PFSK-1	brain:	n/a
15	chr8:89434982-89435032	AG09319	gingival:	n/a
16	chr8:89434982-89435032	HNPCEpiC	eye:	n/a
17	chr8:89434982-89435032	HCPEpiC	choroid plexus:	n/a
18	chr8:89434982-89435032	H1-hESC	embryonic stem cell:	embryo
19	chr8:89437704-89437754	Caco-2	colon:	n/a
20	chr8:89437704-89437754	AoSMC	blood vessel:	n/a
21	chr8:89437704-89437754	HCF	heart:	n/a
22	chr8:89437704-89437754	HepG2	liver:	n/a
23	chr8:89437704-89437754	NH-A	brain:	n/a
24	chr8:89437704-89437754	HRPEpiC	eye:	n/a
25	chr8:89434982-89435032	GM12891	blood:	n/a
26	chr8:89437704-89437754	GM12891	blood:	n/a
27	chr8:89437704-89437754	HCM	heart:	n/a
28	chr8:89437704-89437754	HCPEpiC	choroid plexus:	n/a
29	chr8:89437704-89437754	GM06990	blood:	n/a
30	chr8:89434982-89435032	Hepatocyte	liver:	n/a
31	chr8:89437704-89437754	HL-60	blood:	n/a
32	chr8:89437704-89437754	Hela-S3	cervix:	n/a
33	chr8:89437704-89437754	RPTEC	kidney:	n/a
34	chr8:89437704-89437754	HMEC	breast:	n/a
35	chr8:89437704-89437754	IMR90	lung:	fetal
36	chr8:89434982-89435032	BE2_C	brain:	n/a
37	chr8:89434982-89435032	PrEC	prostate:	n/a
38	chr8:89434982-89435032	A549	lung:	n/a
39	chr8:89434982-89435032	HEK293	kidney:	embryo
40	chr8:89434982-89435032	RPTEC	kidney:	n/a
41	chr8:89437704-89437754	ovcar-3	ovarian:	n/a
42	chr8:89434982-89435032	MCF-7	breast:	n/a
43	chr8:89434982-89435032	AG04450	lung:	fetal
44	chr8:89437704-89437754	AG09319	gingival:	n/a
45	chr8:89434982-89435032	HRE	kidney:	n/a
46	chr8:89437704-89437754	A549	lung:	n/a
47	chr8:89437704-89437754	AG04449	skin:	fetal
48	chr8:89434982-89435032	NHBE	bronchial:	n/a
49	chr8:89437704-89437754	HEEpiC	esophagus:	n/a
50	chr8:89434982-89435032	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr8:89340837..89341409-chr8:89437211..89438075,2	MCF-7	breast:
2	chr8:89425784..89429285-chr8:89429819..89432091,4	MCF-7	breast:
3	chr8:89018606..89019180-chr8:89440797..89441298,2	MCF-7	breast:
4	chr2:55102932..55103433-chr8:89431868..89432368,2	MCF-7	breast:
5	chr8:89425784..89429285-chr8:89429819..89432091,4	MCF-7	breast:
6	chr8:89422414..89424969-chr8:89426442..89428598,2	MCF-7	breast:
7	chr8:89418881..89421418-chr8:89427304..89430285,2	MCF-7	breast:
8	chr8:89415801..89418475-chr8:89422424..89424654,2	MCF-7	breast:
9	chr8:89415801..89418475-chr8:89422424..89424654,2	MCF-7	breast:
10	chr8:89432818..89434615-chr8:89434769..89436302,2	MCF-7	breast:
11	chr8:89432818..89434615-chr8:89434769..89436302,2	MCF-7	breast:
12	chr8:89409309..89411257-chr8:89436132..89438369,2	MCF-7	breast:
13	chr8:89409309..89411257-chr8:89436132..89438369,2	MCF-7	breast:
14	chr8:89418881..89421418-chr8:89427304..89430285,2	MCF-7	breast:
15	chr8:89418361..89420652-chr8:89426081..89428403,2	MCF-7	breast:
16	chr8:89428683..89430712-chr8:89432742..89436681,3	MCF-7	breast:
17	chr8:89422414..89424969-chr8:89426442..89428598,2	MCF-7	breast:
18	chr8:89397259..89399282-chr8:89402381..89405145,2	MCF-7	breast:
19	chr8:89418361..89420652-chr8:89426081..89428403,2	MCF-7	breast:
20	chr8:89389126..89391030-chr8:89391049..89394104,3	MCF-7	breast:
21	chr8:89428683..89430712-chr8:89432742..89436681,3	MCF-7	breast:
22	chr8:89397259..89399282-chr8:89402381..89405145,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MMP16-2	chr8:89426140-89426343	NONHSAT127593

No data

Variant related genes	Relation type
RNA5SP272	TF binding region
RNA5SP272	CpG island

Extended variants
information (count: 1202 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374365340	chr8:89393824-89393825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554616165	chr8:89393920-89393921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71526936	chr8:89393952-89393953	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs528430585	chr8:89393987-89393988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371575258	chr8:89394004-89394005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543551118	chr8:89394054-89394055	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565328881	chr8:89394093-89394094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577403931	chr8:89394122-89394123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189609757	chr8:89394211-89394212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75145948	chr8:89394233-89394234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530345289	chr8:89394245-89394246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548136196	chr8:89394400-89394401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542996515	chr8:89394434-89394435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28417952	chr8:89394517-89394518	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs76199562	chr8:89394525-89394526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571338203	chr8:89394527-89394528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200917970	chr8:89394568-89394569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143606596	chr8:89394574-89394575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75967672	chr8:89394577-89394578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62525778	chr8:89394585-89394586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200104476	chr8:89394591-89394592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62525780	chr8:89394594-89394595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202247428	chr8:89394609-89394610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558750576	chr8:89394620-89394621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554602293	chr8:89394627-89394628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577016882	chr8:89394629-89394630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576148126	chr8:89394638-89394639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536732455	chr8:89394646-89394647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141435871	chr8:89394655-89394656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372589541	chr8:89394666-89394667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558649834	chr8:89394671-89394672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148566335	chr8:89394675-89394676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200488130	chr8:89394677-89394678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576888034	chr8:89394683-89394684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113434176	chr8:89394686-89394687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140202576	chr8:89394690-89394691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560937750	chr8:89394697-89394698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546962449	chr8:89394705-89394706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541373982	chr8:89394734-89394735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368161933	chr8:89394745-89394746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112801847	chr8:89394753-89394754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567953466	chr8:89394791-89394792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138646884	chr8:89394912-89394913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144145660	chr8:89394936-89394937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542161117	chr8:89394953-89394954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs180862674	chr8:89394955-89394956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147313188	chr8:89395014-89395015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111529753	chr8:89395024-89395025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568952205	chr8:89395028-89395029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186150301	chr8:89395050-89395051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89380600-89394800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:89393000-89395000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr8:89394800-89395000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr8:89395000-89405400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr8:89405400-89405800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:89405400-89405800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr8:89405400-89406000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:89411200-89411600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:89411200-89411600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:89426600-89427000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr8:89426600-89427000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr8:89426600-89427000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:89426600-89427200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:89426600-89427200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr8:89427000-89428600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr8:89427200-89432800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:89427200-89434000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr8:89427600-89428400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr8:89428600-89429000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:89430800-89431000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:89432600-89433800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:89432600-89435000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr8:89432600-89435200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:89432600-89435200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:89432800-89433000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr8:89432800-89433000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:89432800-89435000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:89433000-89433800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:89433000-89437400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:89433800-89435200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr8:89433800-89436600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:89434000-89435200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:89434400-89435200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:89434800-89435200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr8:89434800-89435200	Active TSS	Aorta	Aorta
36	chr8:89435000-89435200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr8:89435000-89436800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr8:89435000-89436800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr8:89435200-89436200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr8:89435200-89436600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr8:89435200-89436800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:89435200-89436800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr8:89435200-89437000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr8:89435200-89437400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr8:89435200-89438000	Weak transcription	Aorta	Aorta
46	chr8:89436200-89438400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:89436600-89436800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr8:89436600-89437200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr8:89436600-89437400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:89436800-89437200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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