Variant report

Variant	nsv971644
Chromosome Location	chr8:47826054-47842875
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	ATF2	chr8:47829248-47829745	GM12878	blood:	n/a	n/a
2	BATF	chr8:47829329-47829717	GM12878	blood:	n/a	n/a
3	BCL11A	chr8:47829368-47829677	GM12878	blood:	n/a	chr8:47829442-47829455 chr8:47829439-47829452 chr8:47829438-47829451
4	BCL11A	chr8:47829333-47829579	GM12878	blood:	n/a	chr8:47829442-47829455 chr8:47829439-47829452 chr8:47829438-47829451
5	BCLAF1	chr8:47829262-47829615	GM12878	blood:	n/a	chr8:47829442-47829455 chr8:47829439-47829452 chr8:47829438-47829451
6	BCLAF1	chr8:47829316-47829770	GM12878	blood:	n/a	chr8:47829442-47829455 chr8:47829439-47829452 chr8:47829438-47829451
7	BHLHE40	chr8:47829373-47829808	K562	blood:	n/a	chr8:47829733-47829749 chr8:47829460-47829476
8	BHLHE40	chr8:47829225-47829768	GM12878	blood:	n/a	chr8:47829733-47829749 chr8:47829460-47829476
9	BRCA1	chr8:47828421-47828499	GM12878	blood:	n/a	n/a
10	BRCA1	chr8:47829618-47829709	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:47829448-47829509	HepG2	liver:	n/a	n/a
12	CBX3	chr8:47829352-47829561	K562	blood:	n/a	n/a
13	CBX3	chr8:47829309-47829657	K562	blood:	n/a	n/a
14	CCNT2	chr8:47829318-47829747	K562	blood:	n/a	chr8:47829590-47829599
15	CEBPB	chr8:47836439-47836746	A549	lung:	n/a	chr8:47836561-47836574 chr8:47836561-47836574 chr8:47836561-47836572 chr8:47836563-47836574 chr8:47836561-47836574
16	CEBPB	chr8:47836466-47836725	IMR90	lung:	n/a	chr8:47836561-47836574 chr8:47836561-47836574 chr8:47836561-47836572 chr8:47836563-47836574 chr8:47836561-47836574
17	CEBPB	chr8:47840013-47840311	HepG2	liver:	n/a	chr8:47840180-47840193 chr8:47840182-47840193 chr8:47840180-47840191
18	CEBPB	chr8:47840011-47840310	A549	lung:	n/a	chr8:47840180-47840193 chr8:47840182-47840193 chr8:47840180-47840191
19	CEBPB	chr8:47842143-47842310	HepG2	liver:	n/a	chr8:47842227-47842238
20	CEBPB	chr8:47836450-47836703	HepG2	liver:	n/a	chr8:47836561-47836574 chr8:47836561-47836574 chr8:47836561-47836572 chr8:47836563-47836574 chr8:47836561-47836574
21	CHD1	chr8:47829414-47829837	GM12878	blood:	n/a	chr8:47829470-47829480
22	CHD2	chr8:47830491-47830577	GM12878	blood:	n/a	n/a
23	CHD2	chr8:47828614-47828616	GM12878	blood:	n/a	n/a
24	CHD2	chr8:47829464-47829469	HepG2	liver:	n/a	n/a
25	CHD2	chr8:47829320-47830021	GM12878	blood:	n/a	chr8:47829470-47829480
26	CREB1	chr8:47829272-47829874	GM12878	blood:	n/a	n/a
27	CREB1	chr8:47829308-47829550	A549	lung:	n/a	n/a
28	CTCF	chr8:47827911-47827929	GM10248	blood:	n/a	n/a
29	CTCF	chr8:47829320-47829470	HBMEC	blood vessel:	n/a	chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
30	CTCF	chr8:47829311-47829595	GM20000	blood:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
31	CTCF	chr8:47831880-47832030	GM12864	blood:	n/a	chr8:47831910-47831919 chr8:47831975-47831988
32	CTCF	chr8:47829380-47829530	GM12866	blood:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
33	CTCF	chr8:47829329-47829602	Fibrobl	skin:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
34	CTCF	chr8:47831932-47832013	MCF-7	breast:	n/a	chr8:47831975-47831988
35	CTCF	chr8:47829350-47829515	SK-N-SH_RA	brain:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
36	CTCF	chr8:47829216-47829845	HCT-116	colon:	n/a	chr8:47829729-47829742 chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
37	CTCF	chr8:47829360-47829510	GM12869	blood:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
38	CTCF	chr8:47829315-47829579	GM13976	blood:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
39	CTCF	chr8:47831938-47832029	GM19240	blood:	n/a	chr8:47831975-47831988
40	CTCF	chr8:47831800-47831950	MCF-7	breast:	n/a	chr8:47831910-47831919
41	CTCF	chr8:47829200-47829350	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr8:47829322-47829599	Gliobla	brain:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
43	CTCF	chr8:47829264-47829548	A549	lung:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
44	CTCF	chr8:47829390-47829522	HUVEC	blood vessel:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
45	CTCF	chr8:47829340-47829490	HPAF	blood vessel:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
46	CTCF	chr8:47831920-47832070	GM06990	blood:	n/a	chr8:47831975-47831988
47	CTCF	chr8:47829400-47829550	NHEK	skin:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
48	CTCF	chr8:47829400-47829550	HEK293	kidney:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
49	CTCF	chr8:47829261-47829605	T-47D	breast:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464
50	CTCF	chr8:47829309-47829685	K562	blood:	n/a	chr8:47829451-47829472 chr8:47829452-47829465 chr8:47829450-47829466 chr8:47829452-47829465 chr8:47829452-47829461 chr8:47829449-47829467 chr8:47829454-47829464

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47829660-47829710	PANC-1	pancreas:	n/a
2	chr8:47829660-47829710	PANC-1	pancreas:	n/a
3	chr8:47829791-47829841	AG09309	skin:	n/a
4	chr8:47829791-47829841	ECC-1	luminal epithelium:	n/a
5	chr8:47829660-47829710	MCF-7	breast:	n/a
6	chr8:47829660-47829710	NB4	blood:	n/a
7	chr8:47829791-47829841	GM06990	blood:	n/a
8	chr8:47829660-47829710	ProgFib	skin:	n/a
9	chr8:47829660-47829710	SKMC	muscle:	n/a
10	chr8:47829660-47829710	HMEC	breast:	n/a
11	chr8:47829660-47829710	LNCaP	prostate:	n/a
12	chr8:47829660-47829710	GM19239	blood:	n/a
13	chr8:47829660-47829710	GM06990	blood:	n/a
14	chr8:47829660-47829710	HCPEpiC	choroid plexus:	n/a
15	chr8:47829791-47829841	AG04450	lung:	fetal
16	chr8:47829791-47829841	HEEpiC	esophagus:	n/a
17	chr8:47829791-47829841	Hela-S3	cervix:	n/a
18	chr8:47829660-47829710	NHDF-neo	bronchial:	n/a
19	chr8:47829791-47829841	HRCEpiC	kidney:	n/a
20	chr8:47829791-47829841	NB4	blood:	n/a
21	chr8:47829660-47829710	Caco-2	colon:	n/a
22	chr8:47829791-47829841	IMR90	lung:	fetal
23	chr8:47829791-47829841	HRE	kidney:	n/a
24	chr8:47829660-47829710	ovcar-3	ovarian:	n/a
25	chr8:47829660-47829710	HEK293	kidney:	embryo
26	chr8:47829791-47829841	CMK	blood:	n/a
27	chr8:47829791-47829841	H1-hESC	embryonic stem cell:	embryo
28	chr8:47829791-47829841	ProgFib	skin:	n/a
29	chr8:47829791-47829841	HAEpiC	amniotic membrane:	n/a
30	chr8:47829791-47829841	HepG2	liver:	n/a
31	chr8:47829660-47829710	HIPEpiC	eye:	n/a
32	chr8:47829660-47829710	NT2-D1	testis:	n/a
33	chr8:47829660-47829710	HCF	heart:	n/a
34	chr8:47829791-47829841	HEK293	kidney:	embryo
35	chr8:47829660-47829710	GM12891	blood:	n/a
36	chr8:47829660-47829710	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:47829791-47829841	U87	brain:	n/a
38	chr8:47829791-47829841	HCM	heart:	n/a
39	chr8:47829660-47829710	HRCEpiC	kidney:	n/a
40	chr8:47829791-47829841	GM12891	blood:	n/a
41	chr8:47829791-47829841	K562	blood:	n/a
42	chr8:47829660-47829710	HCM	heart:	n/a
43	chr8:47829660-47829710	ECC-1	luminal epithelium:	n/a
44	chr8:47829660-47829710	HCT-116	colon:	n/a
45	chr8:47829791-47829841	HL-60	blood:	n/a
46	chr8:47829660-47829710	SK-N-SH_RA	brain:	n/a
47	chr8:47829660-47829710	PrEC	prostate:	n/a
48	chr8:47829791-47829841	AG10803	skin:	n/a
49	chr8:47829791-47829841	SK-N-SH	brain:	n/a
50	chr8:47829791-47829841	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:47827930..47831126-chr8:47870805..47874048,3	K562	blood:
2	chr8:47829182..47829917-chr8:47868447..47869168,4	MCF-7	breast:
3	chr8:47619682..47620259-chr8:47831736..47832439,2	MCF-7	breast:
4	chr8:47829086..47829943-chr8:47868391..47869236,3	K562	blood:
5	chr8:47827930..47830534-chr8:47872091..47874048,2	K562	blood:
6	chr8:47828029..47830858-chr8:47832591..47835013,2	MCF-7	breast:
7	chr8:47828970..47829945-chr8:47868388..47869115,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-350F16.2.1-1	chr8:47841498-47842473	l_3587_chr8:47841497-47849870_testes
2	lnc-LINC00293-1	chr8:47834183-47834590	ENSG00000253745.1
3	lnc-LINC00293-1	chr8:47840258-47840454	ENSG00000253745.1
4	lnc-RP11-350F16.2.1-1	chr8:47842462-47842535	ENSG00000253782.1

Variant related genes	Relation type
ENSG00000253745	TF binding region
ENSG00000253745	CpG island
ENSG00000253745	chromatin interactions

Extended variants
information (count: 658 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531282254	chr8:47826087-47826088	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536107145	chr8:47826089-47826090	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190222687	chr8:47826113-47826114	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561685362	chr8:47826124-47826125	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571088317	chr8:47826200-47826201	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181312566	chr8:47826226-47826227	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185385121	chr8:47826240-47826241	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189800931	chr8:47826244-47826245	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4872967	chr8:47826282-47826283	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs4872966	chr8:47826311-47826312	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs180721308	chr8:47826318-47826319	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569845537	chr8:47826324-47826325	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537313837	chr8:47826327-47826328	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555374183	chr8:47826360-47826361	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149369356	chr8:47826370-47826371	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544025647	chr8:47826422-47826423	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535029433	chr8:47826483-47826484	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146333725	chr8:47826521-47826522	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578162578	chr8:47826556-47826557	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139647547	chr8:47826638-47826639	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529874544	chr8:47826641-47826642	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs60279139	chr8:47826642-47826643	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575758065	chr8:47826663-47826664	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543277456	chr8:47826712-47826713	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12546396	chr8:47826713-47826714	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573623574	chr8:47826726-47826727	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545691388	chr8:47826758-47826759	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573566508	chr8:47826797-47826798	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540655608	chr8:47826801-47826802	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116298298	chr8:47826817-47826818	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565511772	chr8:47826886-47826887	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142954097	chr8:47826892-47826893	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551073939	chr8:47826958-47826959	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115340185	chr8:47826998-47826999	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371738644	chr8:47827011-47827012	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375917731	chr8:47827123-47827124	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs884703	chr8:47827130-47827131	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs567481296	chr8:47827148-47827149	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534992167	chr8:47827166-47827167	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547061481	chr8:47827331-47827332	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114502135	chr8:47827341-47827342	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62538768	chr8:47827344-47827345	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112351449	chr8:47827353-47827354	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575760825	chr8:47827360-47827361	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536480988	chr8:47827374-47827375	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187437829	chr8:47827410-47827411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573249529	chr8:47827411-47827412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372405354	chr8:47827447-47827448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540616189	chr8:47827451-47827452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs867896	chr8:47827459-47827460	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	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
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47821400-47829200	Weak transcription	Right Atrium	heart
2	chr8:47822600-47827400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:47824200-47826400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:47826400-47826800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr8:47826800-47827200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
6	chr8:47826800-47829200	Enhancers	Primary B cells from peripheral blood	blood
7	chr8:47827800-47828600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:47828000-47834200	Enhancers	Spleen	Spleen
9	chr8:47828200-47828600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr8:47828200-47829200	Enhancers	GM12878-XiMat	blood
11	chr8:47828200-47829600	Enhancers	Primary B cells from cord blood	blood
12	chr8:47828400-47828600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
13	chr8:47828400-47828800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr8:47828600-47829000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:47828600-47829200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr8:47828600-47829200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr8:47828800-47829000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr8:47828800-47829200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr8:47828800-47829200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr8:47828800-47829200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr8:47828800-47829200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:47828800-47829200	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr8:47828800-47829200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr8:47828800-47829400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr8:47828800-47829400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr8:47828800-47829400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:47828800-47830400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr8:47829000-47829200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:47829000-47830400	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr8:47829200-47829400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr8:47829200-47829400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr8:47829200-47829400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:47829200-47829400	Enhancers	Adipose Nuclei	Adipose
34	chr8:47829200-47829400	Flanking Active TSS	Colonic Mucosa	Colon
35	chr8:47829200-47829400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr8:47829200-47829400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
37	chr8:47829200-47829400	Enhancers	HepG2	liver
38	chr8:47829200-47829600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr8:47829200-47829600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr8:47829200-47829800	Enhancers	Liver	Liver
41	chr8:47829200-47829800	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr8:47829200-47829800	Active TSS	GM12878-XiMat	blood
43	chr8:47829200-47830000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:47829200-47830000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
45	chr8:47829200-47830000	Active TSS	Primary hematopoietic stem cells	blood
46	chr8:47829200-47830000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr8:47829200-47830000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr8:47829200-47830000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:47829200-47830000	Active TSS	Brain Anterior Caudate	brain
50	chr8:47829200-47830000	Active TSS	Brain Hippocampus Middle	brain

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