Variant report

Variant	nsv878618
Chromosome Location	chr4:8579758-8641696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1662)
CpG islands
(count:3912)
Chromatin interactive
region (count:62)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8594303-8594474	K562	blood:	n/a	n/a
2	ARID3A	chr4:8596075-8596433	K562	blood:	n/a	n/a
3	ATF2	chr4:8582336-8582809	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:8596088-8596524	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:8601461-8601771	K562	blood:	n/a	n/a
6	BACH1	chr4:8582079-8582264	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:8579745-8580023	GM12878	blood:	n/a	n/a
8	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
9	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8579732-8579963	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:8596119-8596493	K562	blood:	n/a	n/a
13	BHLHE40	chr4:8591224-8591267	GM12878	blood:	n/a	chr4:8591227-8591236
14	BHLHE40	chr4:8595611-8595677	K562	blood:	n/a	n/a
15	BHLHE40	chr4:8601384-8601739	K562	blood:	n/a	n/a
16	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
17	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
18	BHLHE40	chr4:8594327-8594941	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8591090-8591396	K562	blood:	n/a	chr4:8591227-8591236
20	BHLHE40	chr4:8586835-8587170	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8582469-8582507	K562	blood:	n/a	n/a
22	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
23	BHLHE40	chr4:8593127-8593244	K562	blood:	n/a	n/a
24	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:8599078-8599278	K562	blood:	n/a	n/a
26	BHLHE40	chr4:8589655-8590092	K562	blood:	n/a	n/a
27	BHLHE40	chr4:8588537-8588647	K562	blood:	n/a	n/a
28	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
29	BRCA1	chr4:8609386-8609627	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr4:8609454-8609550	HepG2	liver:	n/a	n/a
31	BRCA1	chr4:8601470-8601784	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
33	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
34	CBX3	chr4:8582296-8582613	K562	blood:	n/a	n/a
35	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
36	CBX3	chr4:8582339-8582560	K562	blood:	n/a	n/a
37	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
38	CCNT2	chr4:8588768-8588840	K562	blood:	n/a	n/a
39	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
40	CCNT2	chr4:8605790-8606066	K562	blood:	n/a	n/a
41	CCNT2	chr4:8589574-8589772	K562	blood:	n/a	n/a
42	CCNT2	chr4:8582433-8582494	K562	blood:	n/a	n/a
43	CCNT2	chr4:8593208-8593591	K562	blood:	n/a	chr4:8593575-8593584
44	CCNT2	chr4:8594231-8595394	K562	blood:	n/a	chr4:8594298-8594307 chr4:8595237-8595246
45	CEBPB	chr4:8596146-8596755	K562	blood:	n/a	n/a
46	CEBPB	chr4:8596249-8596664	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:8596168-8596694	A549	lung:	n/a	n/a
48	CEBPB	chr4:8596168-8596681	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:8596268-8596675	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:8597461-8597467	K562	blood:	n/a	n/a

(count:3912 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8621226-8621276	HCM	heart:	n/a
2	chr4:8581650-8581700	HL-60	blood:	n/a
3	chr4:8594857-8594907	A549	lung:	n/a
4	chr4:8619939-8619989	GM12891	blood:	n/a
5	chr4:8592328-8592378	AG09319	gingival:	n/a
6	chr4:8617738-8617788	SK-N-SH_RA	brain:	n/a
7	chr4:8593507-8593557	A549	lung:	n/a
8	chr4:8593507-8593557	PANC-1	pancreas:	n/a
9	chr4:8621226-8621276	HCM	heart:	n/a
10	chr4:8581650-8581700	HL-60	blood:	n/a
11	chr4:8594857-8594907	A549	lung:	n/a
12	chr4:8619939-8619989	GM12891	blood:	n/a
13	chr4:8592328-8592378	AG09319	gingival:	n/a
14	chr4:8617738-8617788	SK-N-SH_RA	brain:	n/a
15	chr4:8593507-8593557	A549	lung:	n/a
16	chr4:8593507-8593557	PANC-1	pancreas:	n/a
17	chr4:8621266-8621316	LNCaP	prostate:	n/a
18	chr4:8594514-8594564	SKMC	muscle:	n/a
19	chr4:8583937-8583987	SK-N-MC	brain:	n/a
20	chr4:8588870-8588920	Hela-S3	cervix:	n/a
21	chr4:8594776-8594826	PFSK-1	brain:	n/a
22	chr4:8602594-8602644	RPTEC	kidney:	n/a
23	chr4:8639337-8639387	NH-A	brain:	n/a
24	chr4:8640896-8640946	AoSMC	blood vessel:	n/a
25	chr4:8609401-8609451	GM12891	blood:	n/a
26	chr4:8585142-8585192	A549	lung:	n/a
27	chr4:8608361-8608411	LNCaP	prostate:	n/a
28	chr4:8608361-8608411	T-47D	breast:	n/a
29	chr4:8621361-8621411	PANC-1	pancreas:	n/a
30	chr4:8583363-8583413	HCPEpiC	choroid plexus:	n/a
31	chr4:8585142-8585192	H1-hESC	embryonic stem cell:	embryo
32	chr4:8605881-8605931	Jurkat	blood:	n/a
33	chr4:8594549-8594599	AG10803	skin:	n/a
34	chr4:8594413-8594463	SAEC	small airway:	n/a
35	chr4:8617738-8617788	HMEC	breast:	n/a
36	chr4:8597048-8597098	BJ	skin:	n/a
37	chr4:8620162-8620212	HL-60	blood:	n/a
38	chr4:8602619-8602669	U87	brain:	n/a
39	chr4:8616045-8616095	NT2-D1	testis:	n/a
40	chr4:8582227-8582277	PANC-1	pancreas:	n/a
41	chr4:8621361-8621411	HRPEpiC	eye:	n/a
42	chr4:8594857-8594907	HNPCEpiC	eye:	n/a
43	chr4:8616045-8616095	PrEC	prostate:	n/a
44	chr4:8617738-8617788	AG04449	skin:	fetal
45	chr4:8609706-8609756	HRE	kidney:	n/a
46	chr4:8585142-8585192	NT2-D1	testis:	n/a
47	chr4:8588929-8588979	A549	lung:	n/a
48	chr4:8587077-8587127	AG04450	lung:	fetal
49	chr4:8582227-8582277	HepG2	liver:	n/a
50	chr4:8585142-8585192	Hepatocyte	liver:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8550386..8551492-chr4:8588111..8588948,4	MCF-7	breast:
2	chr4:8429003..8431249-chr4:8585694..8587507,2	MCF-7	breast:
3	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
4	chr4:8581776..8584128-chr4:8590195..8592685,3	K562	blood:
5	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
6	chr4:8470336..8471339-chr4:8588024..8588933,6	MCF-7	breast:
7	chr4:8470170..8471110-chr4:8595421..8596838,7	MCF-7	breast:
8	chr4:8594040..8595789-chr4:8608077..8610422,2	MCF-7	breast:
9	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
10	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
11	chr4:8595618..8598948-chr4:8601035..8605983,4	MCF-7	breast:
12	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
13	chr4:8562627..8565501-chr4:8586940..8588652,2	MCF-7	breast:
14	chr4:8470474..8471083-chr4:8586784..8587611,2	MCF-7	breast:
15	chr4:8474531..8475355-chr4:8595923..8596757,2	MCF-7	breast:
16	chr4:8474144..8475116-chr4:8595899..8596574,2	MCF-7	breast:
17	chr4:8590141..8592229-chr4:8594534..8596256,2	K562	blood:
18	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
19	chr15:79417819..79418489-chr4:8588214..8588893,2	MCF-7	breast:
20	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
21	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
22	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
23	chr4:8468552..8470312-chr4:8591413..8592935,2	K562	blood:
24	chr4:8586944..8588877-chr4:8595919..8597857,2	MCF-7	breast:
25	chr4:8507896..8508408-chr4:8595816..8596778,2	MCF-7	breast:
26	chr4:8582157..8584012-chr4:8592733..8594974,2	MCF-7	breast:
27	chr4:8595963..8596810-chr4:8919438..8920172,2	MCF-7	breast:
28	chr4:8582157..8584012-chr4:8592733..8594974,2	MCF-7	breast:
29	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
30	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
31	chr4:8599492..8601366-chr4:8617273..8620008,2	K562	blood:
32	chr4:8549627..8551396-chr4:8591821..8593935,2	MCF-7	breast:
33	chr4:8428794..8430882-chr4:8596413..8599395,2	MCF-7	breast:
34	chr4:8470834..8472351-chr4:8587366..8589099,2	MCF-7	breast:
35	chr4:8470225..8471528-chr4:8595848..8597093,11	K562	blood:
36	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
37	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
38	chr4:8578448..8580242-chr4:8586074..8587928,2	K562	blood:
39	chr4:8587258..8589695-chr4:8592259..8593843,2	K562	blood:
40	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
41	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
42	chr4:8609226..8610032-chr4:8887698..8888205,2	MCF-7	breast:
43	chr1:7246479..7246979-chr4:8580772..8581329,2	MCF-7	breast:
44	chr4:8470159..8471594-chr4:8587070..8589399,12	MCF-7	breast:
45	chr4:8592274..8594245-chr4:8597755..8599882,2	MCF-7	breast:
46	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
47	chr4:8547587..8550346-chr4:8589117..8591927,3	MCF-7	breast:
48	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:
49	chr4:8587258..8589695-chr4:8592259..8593843,2	K562	blood:
50	chr4:8592274..8594245-chr4:8597755..8599882,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL19-6	chr4:8601180-8601688	NONHSAT095111
2	lnc-GPR78-1	chr4:8582122-8582438	NONHSAT095110
3	lnc-METTL19-6	chr4:8594561-8594648	NONHSAT095111
4	lnc-GPR78-1	chr4:8582122-8582251	NONHSAT095109
5	lnc-GPR78-1	chr4:8584258-8584371	NR_045511
6	lnc-GPR78-1	chr4:8581964-8582431	NR_045511
7	lnc-GPR78-1	chr4:8588781-8591750	NR_045511

No data

Variant related genes	Relation type
CPZ	TF binding region
GPR78	TF binding region
CPZ	CpG island
GPR78	CpG island
ENSG00000109625	chromatin interactions
ENSG00000155269	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000205959	chromatin interactions
GADD45A	miRNA target sites
GAK	miRNA target sites
GABRB3	miRNA target sites

Extended variants
information (count: 3484 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3484 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1282	chr4:8579758-8579759	Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576307987	chr4:8579817-8579818	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs543683347	chr4:8579831-8579832	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564764424	chr4:8579867-8579868	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576790955	chr4:8579868-8579869	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540597668	chr4:8579870-8579871	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs2286999	chr4:8579871-8579872	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs529701832	chr4:8579876-8579877	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs548415283	chr4:8579885-8579886	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376548734	chr4:8579890-8579891	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531143036	chr4:8579891-8579892	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs535117974	chr4:8579892-8579893	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552849335	chr4:8579897-8579898	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs145913567	chr4:8579907-8579908	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs375177825	chr4:8579926-8579927	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535018810	chr4:8579943-8579944	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs114342755	chr4:8579945-8579946	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs115143712	chr4:8579972-8579973	Bivalent Enhancer Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535947312	chr4:8580041-8580042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554835430	chr4:8580049-8580050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567192276	chr4:8580050-8580051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558837537	chr4:8580077-8580078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577018250	chr4:8580083-8580084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2286998	chr4:8580087-8580088	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs372842293	chr4:8580125-8580126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114634891	chr4:8580132-8580133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138466314	chr4:8580164-8580165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2286997	chr4:8580169-8580170	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs560022263	chr4:8580187-8580188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531155804	chr4:8580196-8580197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77789199	chr4:8580224-8580225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574588616	chr4:8580282-8580283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564808463	chr4:8580321-8580322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375616141	chr4:8580329-8580330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528783626	chr4:8580332-8580333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547061077	chr4:8580336-8580337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371995657	chr4:8580348-8580349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535990887	chr4:8580370-8580371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551071253	chr4:8580377-8580378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149620264	chr4:8580386-8580387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537255590	chr4:8580432-8580433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558428362	chr4:8580436-8580437	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143322281	chr4:8580451-8580452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373537002	chr4:8580474-8580475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74808234	chr4:8580499-8580500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552583242	chr4:8580533-8580534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148222011	chr4:8580547-8580548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541396170	chr4:8580584-8580585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555996518	chr4:8580596-8580597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150752196	chr4:8580628-8580629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8574400-8582400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr4:8577600-8579800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:8577600-8580800	Weak transcription	Placenta	Placenta
5	chr4:8577600-8581400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:8577600-8582000	Weak transcription	Ovary	ovary
7	chr4:8578400-8579800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:8578600-8581800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:8578600-8582200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:8579000-8580000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:8579000-8580600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:8579400-8579800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr4:8579600-8580000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
14	chr4:8579800-8580000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:8579800-8580000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:8579800-8580000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:8579800-8580000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr4:8579800-8580000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:8580000-8581200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:8580000-8581200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr4:8580000-8581600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:8580600-8581400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:8580800-8582200	Enhancers	Placenta	Placenta
24	chr4:8581000-8581400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
25	chr4:8581000-8581400	Bivalent Enhancer	HSMMtube	muscle
26	chr4:8581000-8581600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
27	chr4:8581000-8581600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr4:8581200-8581400	Enhancers	H9 Cell Line	embryonic stem cell
29	chr4:8581200-8581400	Bivalent Enhancer	Right Ventricle	heart
30	chr4:8581200-8581600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr4:8581200-8581600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr4:8581200-8581600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
33	chr4:8581200-8581600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
34	chr4:8581200-8582200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:8581400-8581600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr4:8581400-8581800	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr4:8581400-8581800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:8581400-8581800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:8581400-8582000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:8581400-8582200	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr4:8581400-8582800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:8581400-8583000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
43	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
44	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
47	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
48	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
49	chr4:8581600-8582000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
50	chr4:8581600-8582000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell

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