Variant report

Variant	nsv879026
Chromosome Location	chr4:58041751-58098554
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	chr4:58057148-58057340	K562	blood:	n/a	n/a
2	ATF2	chr4:58057710-58058217	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:58050907-58050911	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:58060555-58060680	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:58057797-58057805	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:58085716-58085808	K562	blood:	n/a	n/a
7	BHLHE40	chr4:58057159-58057268	K562	blood:	n/a	n/a
8	CEBPB	chr4:58079996-58080196	H1-hESC	embryonic stem cell:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
9	CEBPB	chr4:58095296-58095615	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:58044971-58045291	HepG2	liver:	n/a	chr4:58045115-58045126
11	CEBPB	chr4:58079923-58080233	K562	blood:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
12	CEBPB	chr4:58063171-58063437	A549	lung:	n/a	n/a
13	CEBPB	chr4:58079932-58080295	IMR90	lung:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
14	CEBPB	chr4:58044941-58045259	IMR90	lung:	n/a	chr4:58045115-58045126
15	CEBPB	chr4:58079947-58080264	A549	lung:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
16	CEBPB	chr4:58059301-58059487	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:58079922-58080266	Hela-S3	cervix:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
18	CEBPB	chr4:58079925-58080294	HepG2	liver:	n/a	chr4:58080100-58080109 chr4:58080098-58080111 chr4:58080099-58080110 chr4:58080100-58080109 chr4:58080098-58080109 chr4:58080100-58080109 chr4:58080100-58080109 chr4:58080098-58080111
19	CEBPB	chr4:58095291-58095593	A549	lung:	n/a	n/a
20	CHD2	chr4:58086417-58086488	GM12878	blood:	n/a	n/a
21	CHD2	chr4:58057157-58057285	K562	blood:	n/a	n/a
22	CREB1	chr4:58057826-58058293	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr4:58057014-58058353	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr4:58057110-58057356	ProgFib	skin:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
25	CTCF	chr4:58057140-58057290	K562	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
26	CTCF	chr4:58057160-58057310	HRE	kidney:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
27	CTCF	chr4:58057160-58057310	SK-N-SH_RA	brain:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
28	CTCF	chr4:58077380-58077530	A549	lung:	n/a	n/a
29	CTCF	chr4:58060560-58060710	BJ	skin:	n/a	chr4:58060689-58060702 chr4:58060686-58060704
30	CTCF	chr4:58057160-58057310	HCPEpiC	choroid plexus:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
31	CTCF	chr4:58060640-58060790	GM12878	blood:	n/a	chr4:58060689-58060702 chr4:58060686-58060704
32	CTCF	chr4:58057160-58057310	HCT-116	colon:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
33	CTCF	chr4:58057160-58057310	Hela-S3	cervix:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
34	CTCF	chr4:58060640-58060790	HBMEC	blood vessel:	n/a	chr4:58060689-58060702 chr4:58060686-58060704
35	CTCF	chr4:58057120-58057270	K562	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
36	CTCF	chr4:58057114-58057357	GM19239	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
37	CTCF	chr4:58077400-58077550	HepG2	liver:	n/a	n/a
38	CTCF	chr4:58077720-58077870	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr4:58077450-58077558	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr4:58057160-58057310	HA-sp	spinal cord:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
41	CTCF	chr4:58057140-58057290	GM06990	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
42	CTCF	chr4:58057160-58057310	Caco-2	colon:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
43	CTCF	chr4:58057200-58057350	MCF-7	breast:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
44	CTCF	chr4:58077333-58077562	K562	blood:	n/a	n/a
45	CTCF	chr4:58077340-58077490	HFF	foreskin:	n/a	n/a
46	CTCF	chr4:58077443-58077555	ProgFib	skin:	n/a	n/a
47	CTCF	chr4:58057180-58057330	HBMEC	blood vessel:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
48	CTCF	chr4:58077400-58077550	GM12874	blood:	n/a	n/a
49	CTCF	chr4:58057140-58057290	GM12869	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
50	CTCF	chr4:58060460-58060610	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:58050932-58050982	HNPCEpiC	eye:	n/a
2	chr4:58059773-58059823	NHBE	bronchial:	n/a
3	chr4:58050932-58050982	HNPCEpiC	eye:	n/a
4	chr4:58059773-58059823	NHBE	bronchial:	n/a
5	chr4:58050932-58050982	HCF	heart:	n/a
6	chr4:58063449-58063499	ovcar-3	ovarian:	n/a
7	chr4:58086247-58086297	PANC-1	pancreas:	n/a
8	chr4:58059773-58059823	NH-A	brain:	n/a
9	chr4:58060773-58060823	NT2-D1	testis:	n/a
10	chr4:58058692-58058742	ECC-1	luminal epithelium:	n/a
11	chr4:58059773-58059823	GM12892	blood:	n/a
12	chr4:58061859-58061909	HIPEpiC	eye:	n/a
13	chr4:58058692-58058742	SK-N-SH_RA	brain:	n/a
14	chr4:58059773-58059823	HMEC	breast:	n/a
15	chr4:58058692-58058742	GM12892	blood:	n/a
16	chr4:58060609-58060659	SK-N-SH_RA	brain:	n/a
17	chr4:58060773-58060823	LNCaP	prostate:	n/a
18	chr4:58086247-58086297	HCPEpiC	choroid plexus:	n/a
19	chr4:58064691-58064741	PFSK-1	brain:	n/a
20	chr4:58059773-58059823	HUVEC	blood vessel:	n/a
21	chr4:58059773-58059823	SK-N-SH	brain:	n/a
22	chr4:58059773-58059823	LNCaP	prostate:	n/a
23	chr4:58060773-58060823	HCPEpiC	choroid plexus:	n/a
24	chr4:58063449-58063499	AG04450	lung:	fetal
25	chr4:58050932-58050982	RPTEC	kidney:	n/a
26	chr4:58064691-58064741	NHDF-neo	bronchial:	n/a
27	chr4:58058692-58058742	AG04449	skin:	fetal
28	chr4:58060609-58060659	RPTEC	kidney:	n/a
29	chr4:58064691-58064741	HCPEpiC	choroid plexus:	n/a
30	chr4:58061991-58062041	Caco-2	colon:	n/a
31	chr4:58059773-58059823	IMR90	lung:	fetal
32	chr4:58060609-58060659	AG09309	skin:	n/a
33	chr4:58058692-58058742	Jurkat	blood:	n/a
34	chr4:58060609-58060659	MCF-7	breast:	n/a
35	chr4:58061991-58062041	HRE	kidney:	n/a
36	chr4:58058692-58058742	HCF	heart:	n/a
37	chr4:58060773-58060823	HNPCEpiC	eye:	n/a
38	chr4:58058692-58058742	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:58086247-58086297	SK-N-SH	brain:	n/a
40	chr4:58058692-58058742	MCF10A-Er-Src	breast:	n/a
41	chr4:58060773-58060823	HRE	kidney:	n/a
42	chr4:58061991-58062041	ECC-1	luminal epithelium:	n/a
43	chr4:58064691-58064741	MCF10A-Er-Src	breast:	n/a
44	chr4:58063449-58063499	NHDF-neo	bronchial:	n/a
45	chr4:58060609-58060659	AG09319	gingival:	n/a
46	chr4:58061991-58062041	PFSK-1	brain:	n/a
47	chr4:58060609-58060659	NHBE	bronchial:	n/a
48	chr4:58059773-58059823	MCF-7	breast:	n/a
49	chr4:58059773-58059823	HIPEpiC	eye:	n/a
50	chr4:58061991-58062041	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:58056446..58057481-chr4:58169186..58169817,3	MCF-7	breast:
2	chr4:58047640..58050466-chr4:58055836..58057973,2	K562	blood:
3	chr4:58061801..58064588-chr4:58070107..58072268,2	K562	blood:
4	chr4:58029500..58030425-chr4:58077363..58078281,2	K562	blood:
5	chr4:58061801..58064588-chr4:58070107..58072268,2	K562	blood:
6	chr4:58047640..58050466-chr4:58055836..58057973,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR2B-1	chr4:58067952-58067986	XLOC_003547
2	lnc-POLR2B-1	chr4:58054431-58054485	XLOC_003547
3	lnc-POLR2B-1	chr4:58045310-58045551	XLOC_003547
4	lnc-POLR2B-1	chr4:58070644-58070759	ENSG00000245067.2
5	lnc-POLR2B-1	chr4:58071240-58071464	NONHSAT096544
6	lnc-POLR2B-1	chr4:58067299-58068163	XLOC_003547
7	lnc-POLR2B-1	chr4:58070644-58070740	NONHSAT096554
8	lnc-POLR2B-1	chr4:58070644-58070759	XLOC_003547
9	lnc-POLR2B-1	chr4:58067299-58067381	ENSG00000245067.2
10	lnc-POLR2B-1	chr4:58071240-58071676	XLOC_003547
11	lnc-POLR2B-1	chr4:58071240-58071676	ENSG00000245067.2
12	lnc-POLR2B-1	chr4:58069401-58069761	NONHSAT096554
13	lnc-POLR2B-1	chr4:58067299-58067986	ENSG00000245067.2
14	lnc-POLR2B-1	chr4:58070644-58070759	XLOC_003547
15	lnc-POLR2B-1	chr4:58067299-58067381	XLOC_003547
16	lnc-POLR2B-1	chr4:58067584-58067986	XLOC_003547
17	lnc-POLR2B-1	chr4:58070307-58070759	XLOC_003547
18	lnc-POLR2B-1	chr4:58045311-58045450	XLOC_003547
19	lnc-POLR2B-1	chr4:58054336-58054485	ENSG00000245067.2
20	lnc-POLR2B-1	chr4:58070644-58070759	ENSG00000245067.2
21	lnc-POLR2B-1	chr4:58045408-58045450	XLOC_003547
22	lnc-POLR2B-1	chr4:58071240-58071465	ENSG00000245067.2
23	lnc-POLR2B-1	chr4:58067299-58067381	XLOC_003547
24	lnc-POLR2B-1	chr4:58071240-58071627	XLOC_003547
25	lnc-POLR2B-1	chr4:58069674-58069736	XLOC_003547
26	lnc-POLR2B-1	chr4:58071240-58071590	XLOC_003547

Variant related genes	Relation type
IGFBP7-AS1	TF binding region
IGFBP7-AS1	CpG island
UNC119B	miRNA target sites
TMX3	miRNA target sites
INSIG2	miRNA target sites
INSIG1	miRNA target sites
RBM12B	miRNA target sites
HAUS3	miRNA target sites
SPATS2	miRNA target sites

Extended variants
information (count: 2199 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2199 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4412045	chr4:58041751-58041752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372770196	chr4:58041764-58041765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531899288	chr4:58041773-58041774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537400348	chr4:58041790-58041791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149674593	chr4:58041906-58041907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183130027	chr4:58041913-58041914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185830648	chr4:58041967-58041968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4470700	chr4:58042029-58042030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568560840	chr4:58042034-58042035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189755783	chr4:58042040-58042041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535189830	chr4:58042076-58042077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147741868	chr4:58042135-58042136	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs79243194	chr4:58042162-58042163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs557184206	chr4:58042178-58042179	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565750381	chr4:58042256-58042257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542890678	chr4:58042259-58042260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553181427	chr4:58042287-58042288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573208025	chr4:58042320-58042321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539567921	chr4:58042342-58042343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370692582	chr4:58042343-58042344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182486463	chr4:58042476-58042477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187862585	chr4:58042573-58042574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565158343	chr4:58042619-58042620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557452133	chr4:58042660-58042661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142666018	chr4:58042692-58042693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs193214208	chr4:58042720-58042721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545916008	chr4:58042738-58042739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560687799	chr4:58042792-58042793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34378112	chr4:58042811-58042812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571888123	chr4:58042815-58042816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148349181	chr4:58042918-58042919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549201879	chr4:58042921-58042922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113981082	chr4:58042936-58042937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555591122	chr4:58042962-58042963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528660144	chr4:58042973-58042974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551793397	chr4:58042981-58042982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374846940	chr4:58043004-58043005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571870193	chr4:58043024-58043025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183891549	chr4:58043041-58043042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554376506	chr4:58043052-58043053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557322950	chr4:58043071-58043072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567790288	chr4:58043080-58043081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536726970	chr4:58043102-58043103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149255667	chr4:58043137-58043138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188560916	chr4:58043166-58043167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573096518	chr4:58043167-58043168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10212768	chr4:58043182-58043183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184834849	chr4:58043206-58043207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576296197	chr4:58043210-58043211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188662701	chr4:58043216-58043217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:58038600-58047000	Weak transcription	Fetal Heart	heart
2	chr4:58040000-58044200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:58047000-58047400	Enhancers	Fetal Heart	heart
4	chr4:58047000-58047400	Enhancers	Fetal Muscle Leg	muscle
5	chr4:58047400-58048400	Weak transcription	Fetal Heart	heart
6	chr4:58047400-58059600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:58047800-58048600	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr4:58047800-58049000	Enhancers	Fetal Muscle Leg	muscle
9	chr4:58047800-58049000	Enhancers	HSMMtube	muscle
10	chr4:58047800-58049200	Enhancers	Brain Substantia Nigra	brain
11	chr4:58047800-58049400	Enhancers	Brain Hippocampus Middle	brain
12	chr4:58048000-58048600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:58048000-58048800	Enhancers	Spleen	Spleen
14	chr4:58048000-58049000	Enhancers	Brain Anterior Caudate	brain
15	chr4:58048000-58049800	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr4:58048200-58049000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:58048200-58049000	Enhancers	Brain Angular Gyrus	brain
18	chr4:58048400-58048600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:58048400-58048600	Enhancers	Brain Cingulate Gyrus	brain
20	chr4:58048400-58048600	Enhancers	Brain Germinal Matrix	brain
21	chr4:58048400-58048800	Enhancers	Fetal Muscle Trunk	muscle
22	chr4:58048400-58048800	Enhancers	Left Ventricle	heart
23	chr4:58048400-58048800	Enhancers	Right Ventricle	heart
24	chr4:58048400-58049000	Enhancers	Fetal Heart	heart
25	chr4:58048400-58049000	Enhancers	HSMM	muscle
26	chr4:58048600-58049000	Flanking Active TSS	Brain Cingulate Gyrus	brain
27	chr4:58048600-58049000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
28	chr4:58048600-58049800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:58048600-58059600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:58048800-58050600	Weak transcription	Fetal Muscle Trunk	muscle
31	chr4:58049000-58049200	Enhancers	Brain Cingulate Gyrus	brain
32	chr4:58049000-58049200	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr4:58049000-58050400	Weak transcription	Fetal Muscle Leg	muscle
34	chr4:58049000-58050600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:58049000-58050600	Weak transcription	Brain Anterior Caudate	brain
36	chr4:58049000-58059400	Weak transcription	Brain Angular Gyrus	brain
37	chr4:58049200-58050000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr4:58049200-58050400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr4:58049200-58059200	Weak transcription	Brain Substantia Nigra	brain
40	chr4:58049400-58050400	Weak transcription	Brain Hippocampus Middle	brain
41	chr4:58049800-58050200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr4:58049800-58051000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:58050000-58050200	Enhancers	Brain Cingulate Gyrus	brain
44	chr4:58050200-58050800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr4:58050200-58054200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:58050400-58050600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:58050400-58050600	Enhancers	Fetal Muscle Leg	muscle
48	chr4:58050400-58050800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:58050400-58051200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:58050400-58051400	Enhancers	Brain Germinal Matrix	brain

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