Variant report

Variant	esv2755175
Chromosome Location	chr4:58035372-58081172
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	chr4:58057159-58057268	K562	blood:	n/a	n/a
7	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
8	CEBPB	chr4:58040996-58041148	K562	blood:	n/a	chr4:58041092-58041105 chr4:58041093-58041104 chr4:58041092-58041103
9	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
10	CEBPB	chr4:58041042-58041155	HepG2	liver:	n/a	chr4:58041092-58041105 chr4:58041093-58041104 chr4:58041092-58041103
11	CEBPB	chr4:58063171-58063437	A549	lung:	n/a	n/a
12	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
13	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
14	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
15	CEBPB	chr4:58044941-58045259	IMR90	lung:	n/a	chr4:58045115-58045126
16	CEBPB	chr4:58059301-58059487	H1-hESC	embryonic stem cell:	n/a	n/a
17	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
18	CEBPB	chr4:58044971-58045291	HepG2	liver:	n/a	chr4:58045115-58045126
19	CHD2	chr4:58057157-58057285	K562	blood:	n/a	n/a
20	CHD2	chr4:58037081-58037168	K562	blood:	n/a	n/a
21	CREB1	chr4:58057826-58058293	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr4:58057014-58058353	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:58060460-58060610	A549	lung:	n/a	n/a
24	CTCF	chr4:58057160-58057310	HBMEC	blood vessel:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
25	CTCF	chr4:58057120-58057270	RPTEC	kidney:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
26	CTCF	chr4:58057160-58057310	GM12867	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
27	CTCF	chr4:58057180-58057330	HUVEC	blood vessel:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
28	CTCF	chr4:58057140-58057290	HVMF	connective:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
29	CTCF	chr4:58060600-58060750	HRPEpiC	eye:	n/a	chr4:58060689-58060702 chr4:58060686-58060704
30	CTCF	chr4:58077420-58077570	GM12872	blood:	n/a	n/a
31	CTCF	chr4:58057200-58057350	GM12868	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
32	CTCF	chr4:58060540-58060690	AG09309	skin:	n/a	n/a
33	CTCF	chr4:58077400-58077550	AG09319	gingival:	n/a	n/a
34	CTCF	chr4:58077398-58077567	GM12878	blood:	n/a	n/a
35	CTCF	chr4:58057096-58057332	A549	lung:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
36	CTCF	chr4:58077300-58077450	HRE	kidney:	n/a	n/a
37	CTCF	chr4:58048666-58048711	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:58077406-58077532	GM12891	blood:	n/a	n/a
39	CTCF	chr4:58069700-58069850	GM12867	blood:	n/a	n/a
40	CTCF	chr4:58057120-58057270	HRPEpiC	eye:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
41	CTCF	chr4:58060584-58060763	H1-hESC	embryonic stem cell:	n/a	chr4:58060689-58060702 chr4:58060686-58060704
42	CTCF	chr4:58057580-58057730	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr4:58077403-58077564	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:58057134-58057347	GM20000	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
45	CTCF	chr4:58077478-58077570	GM20000	blood:	n/a	n/a
46	CTCF	chr4:58057120-58057270	NHDF-neo	bronchial:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
47	CTCF	chr4:58077454-58077591	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:58057097-58057365	GM19240	blood:	n/a	chr4:58057229-58057247 chr4:58057232-58057245 chr4:58057231-58057252 chr4:58057230-58057246
49	CTCF	chr4:58048427-58048482	Fibrobl	skin:	n/a	n/a
50	CTCF	chr4:58060592-58060760	Fibrobl	skin:	n/a	chr4:58060689-58060702 chr4:58060686-58060704

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:58061859-58061909	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:58060773-58060823	LNCaP	prostate:	n/a
3	chr4:58061859-58061909	GM12892	blood:	n/a
4	chr4:58060609-58060659	IMR90	lung:	fetal
5	chr4:58063449-58063499	SKMC	muscle:	n/a
6	chr4:58050932-58050982	HEEpiC	esophagus:	n/a
7	chr4:58050932-58050982	HepG2	liver:	n/a
8	chr4:58039421-58039471	SK-N-MC	brain:	n/a
9	chr4:58061859-58061909	CMK	blood:	n/a
10	chr4:58061859-58061909	HUVEC	blood vessel:	n/a
11	chr4:58061991-58062041	ovcar-3	ovarian:	n/a
12	chr4:58050932-58050982	AoSMC	blood vessel:	n/a
13	chr4:58039421-58039471	Jurkat	blood:	n/a
14	chr4:58060773-58060823	BE2_C	brain:	n/a
15	chr4:58058692-58058742	AG04450	lung:	fetal
16	chr4:58061991-58062041	HCT-116	colon:	n/a
17	chr4:58035366-58035416	NT2-D1	testis:	n/a
18	chr4:58050932-58050982	HCF	heart:	n/a
19	chr4:58063449-58063499	LNCaP	prostate:	n/a
20	chr4:58060609-58060659	HCF	heart:	n/a
21	chr4:58039421-58039471	PANC-1	pancreas:	n/a
22	chr4:58059773-58059823	NH-A	brain:	n/a
23	chr4:58039421-58039471	BJ	skin:	n/a
24	chr4:58061859-58061909	K562	blood:	n/a
25	chr4:58061859-58061909	HEK293	kidney:	embryo
26	chr4:58035366-58035416	GM12878	blood:	n/a
27	chr4:58059773-58059823	AG04450	lung:	fetal
28	chr4:58035366-58035416	Jurkat	blood:	n/a
29	chr4:58064691-58064741	Hela-S3	cervix:	n/a
30	chr4:58061859-58061909	HNPCEpiC	eye:	n/a
31	chr4:58059773-58059823	BE2_C	brain:	n/a
32	chr4:58061991-58062041	IMR90	lung:	fetal
33	chr4:58061859-58061909	PrEC	prostate:	n/a
34	chr4:58064691-58064741	HCT-116	colon:	n/a
35	chr4:58060773-58060823	NHDF-neo	bronchial:	n/a
36	chr4:58064691-58064741	ovcar-3	ovarian:	n/a
37	chr4:58035366-58035416	HEK293	kidney:	embryo
38	chr4:58064691-58064741	LNCaP	prostate:	n/a
39	chr4:58050932-58050982	HCPEpiC	choroid plexus:	n/a
40	chr4:58060773-58060823	AG10803	skin:	n/a
41	chr4:58050932-58050982	Hela-S3	cervix:	n/a
42	chr4:58050932-58050982	NHDF-neo	bronchial:	n/a
43	chr4:58050932-58050982	MCF10A-Er-Src	breast:	n/a
44	chr4:58061991-58062041	HepG2	liver:	n/a
45	chr4:58039421-58039471	NT2-D1	testis:	n/a
46	chr4:58060773-58060823	HCT-116	colon:	n/a
47	chr4:58061859-58061909	T-47D	breast:	n/a
48	chr4:58061859-58061909	AG04450	lung:	fetal
49	chr4:58039421-58039471	SK-N-SH	brain:	n/a
50	chr4:58058692-58058742	HAEpiC	amniotic membrane:	n/a

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

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

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

Extended variants
information (count: 1722 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1722 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571655326	chr4:58035374-58035375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537323239	chr4:58035448-58035449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557359983	chr4:58035449-58035450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573966493	chr4:58035497-58035498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536620951	chr4:58035516-58035517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553506114	chr4:58035521-58035522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183840135	chr4:58035566-58035567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4412050	chr4:58035586-58035587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545263345	chr4:58035596-58035597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34384712	chr4:58035624-58035625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34850768	chr4:58035631-58035632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558870464	chr4:58035639-58035640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558779657	chr4:58035674-58035675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs73818699	chr4:58035675-58035676	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs111968474	chr4:58035703-58035704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544161071	chr4:58035705-58035706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561210862	chr4:58035732-58035733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78181345	chr4:58035733-58035734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372286832	chr4:58035784-58035785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539804871	chr4:58035799-58035800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112738353	chr4:58035834-58035835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7696751	chr4:58035857-58035858	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs139241246	chr4:58035888-58035889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571734130	chr4:58035909-58035910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187934836	chr4:58036019-58036020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551012394	chr4:58036046-58036047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567901788	chr4:58036083-58036084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575274001	chr4:58036122-58036123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191252963	chr4:58036147-58036148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4273531	chr4:58036155-58036156	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs11133488	chr4:58036217-58036218	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs116636760	chr4:58036220-58036221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558818543	chr4:58036247-58036248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575362236	chr4:58036251-58036252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112861032	chr4:58036253-58036254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111798645	chr4:58036264-58036265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375969088	chr4:58036297-58036298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76661749	chr4:58036324-58036325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149877804	chr4:58036343-58036344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144894963	chr4:58036344-58036345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372327452	chr4:58036373-58036374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559698746	chr4:58036394-58036395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532111829	chr4:58036431-58036432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572114855	chr4:58036476-58036477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562576139	chr4:58036505-58036506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572833848	chr4:58036518-58036519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371449309	chr4:58036520-58036521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62308338	chr4:58036562-58036563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551113734	chr4:58036580-58036581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142983180	chr4:58036637-58036638	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:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:58034600-58035600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr4:58034600-58035600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:58034600-58036000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:58034600-58036000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:58034600-58036000	Enhancers	Brain Substantia Nigra	brain
6	chr4:58034600-58036200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:58034600-58036200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr4:58034600-58036600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:58034800-58035400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:58034800-58035400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr4:58034800-58035400	Enhancers	HSMMtube	muscle
12	chr4:58034800-58035800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:58034800-58035800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:58034800-58036000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:58034800-58036000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:58034800-58036000	Enhancers	Fetal Muscle Leg	muscle
17	chr4:58035000-58035800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:58035200-58035400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:58035200-58035800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr4:58035200-58036000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:58035200-58038000	Weak transcription	Fetal Heart	heart
22	chr4:58035800-58036000	Enhancers	Brain Cingulate Gyrus	brain
23	chr4:58038000-58038600	Enhancers	Fetal Heart	heart
24	chr4:58038200-58038600	Enhancers	HSMMtube	muscle
25	chr4:58038600-58047000	Weak transcription	Fetal Heart	heart
26	chr4:58039800-58040200	Enhancers	K562	blood
27	chr4:58040000-58044200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:58047000-58047400	Enhancers	Fetal Heart	heart
29	chr4:58047000-58047400	Enhancers	Fetal Muscle Leg	muscle
30	chr4:58047400-58048400	Weak transcription	Fetal Heart	heart
31	chr4:58047400-58059600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:58047800-58048600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr4:58047800-58049000	Enhancers	Fetal Muscle Leg	muscle
34	chr4:58047800-58049000	Enhancers	HSMMtube	muscle
35	chr4:58047800-58049200	Enhancers	Brain Substantia Nigra	brain
36	chr4:58047800-58049400	Enhancers	Brain Hippocampus Middle	brain
37	chr4:58048000-58048600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr4:58048000-58048800	Enhancers	Spleen	Spleen
39	chr4:58048000-58049000	Enhancers	Brain Anterior Caudate	brain
40	chr4:58048000-58049800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr4:58048200-58049000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:58048200-58049000	Enhancers	Brain Angular Gyrus	brain
43	chr4:58048400-58048600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:58048400-58048600	Enhancers	Brain Cingulate Gyrus	brain
45	chr4:58048400-58048600	Enhancers	Brain Germinal Matrix	brain
46	chr4:58048400-58048800	Enhancers	Fetal Muscle Trunk	muscle
47	chr4:58048400-58048800	Enhancers	Left Ventricle	heart
48	chr4:58048400-58048800	Enhancers	Right Ventricle	heart
49	chr4:58048400-58049000	Enhancers	Fetal Heart	heart
50	chr4:58048400-58049000	Enhancers	HSMM	muscle

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