Variant report

Variant	nsv1014219
Chromosome Location	chr4:8578779-8724531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2215)
CpG islands
(count:6350)
Chromatin interactive
region (count:101)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2215 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

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	chr4:8596088-8596524	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:8582336-8582809	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	BACH1	chr4:8689946-8690325	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:8686570-8686574	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr4:8579745-8580023	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8697209-8697485	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
12	BCL3	chr4:8579732-8579963	GM12878	blood:	n/a	n/a
13	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
14	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
16	BHLHE40	chr4:8689941-8690197	K562	blood:	n/a	n/a
17	BHLHE40	chr4:8586835-8587170	K562	blood:	n/a	n/a
18	BHLHE40	chr4:8599078-8599278	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8589655-8590092	K562	blood:	n/a	n/a
20	BHLHE40	chr4:8595611-8595677	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8593127-8593244	K562	blood:	n/a	n/a
22	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
24	BHLHE40	chr4:8582469-8582507	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8588537-8588647	K562	blood:	n/a	n/a
26	BHLHE40	chr4:8591224-8591267	GM12878	blood:	n/a	chr4:8591227-8591236
27	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
28	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
29	BHLHE40	chr4:8601384-8601739	K562	blood:	n/a	n/a
30	BHLHE40	chr4:8591090-8591396	K562	blood:	n/a	chr4:8591227-8591236
31	BHLHE40	chr4:8596119-8596493	K562	blood:	n/a	n/a
32	BHLHE40	chr4:8594327-8594941	K562	blood:	n/a	n/a
33	BRCA1	chr4:8601470-8601784	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr4:8609386-8609627	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr4:8609454-8609550	HepG2	liver:	n/a	n/a
36	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
37	CBX3	chr4:8582339-8582560	K562	blood:	n/a	n/a
38	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
39	CBX3	chr4:8582296-8582613	K562	blood:	n/a	n/a
40	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
41	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
42	CCNT2	chr4:8594231-8595394	K562	blood:	n/a	chr4:8594298-8594307 chr4:8595237-8595246
43	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
44	CCNT2	chr4:8706899-8707008	K562	blood:	n/a	n/a
45	CCNT2	chr4:8582433-8582494	K562	blood:	n/a	n/a
46	CCNT2	chr4:8689978-8690131	K562	blood:	n/a	n/a
47	CCNT2	chr4:8605790-8606066	K562	blood:	n/a	n/a
48	CCNT2	chr4:8589574-8589772	K562	blood:	n/a	n/a
49	CCNT2	chr4:8588768-8588840	K562	blood:	n/a	n/a
50	CCNT2	chr4:8593208-8593591	K562	blood:	n/a	chr4:8593575-8593584

(count:6350 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8593665-8593715	AG09319	gingival:	n/a
2	chr4:8588802-8588852	GM19239	blood:	n/a
3	chr4:8696173-8696223	AG04449	skin:	fetal
4	chr4:8582300-8582350	T-47D	breast:	n/a
5	chr4:8594857-8594907	NHDF-neo	bronchial:	n/a
6	chr4:8588858-8588908	NB4	blood:	n/a
7	chr4:8593665-8593715	AG09319	gingival:	n/a
8	chr4:8588802-8588852	GM19239	blood:	n/a
9	chr4:8696173-8696223	AG04449	skin:	fetal
10	chr4:8582300-8582350	T-47D	breast:	n/a
11	chr4:8594857-8594907	NHDF-neo	bronchial:	n/a
12	chr4:8588858-8588908	NB4	blood:	n/a
13	chr4:8620162-8620212	HepG2	liver:	n/a
14	chr4:8582101-8582151	LNCaP	prostate:	n/a
15	chr4:8692854-8692904	MCF10A-Er-Src	breast:	n/a
16	chr4:8608361-8608411	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:8648164-8648214	HIPEpiC	eye:	n/a
18	chr4:8582565-8582615	SK-N-MC	brain:	n/a
19	chr4:8588802-8588852	HepG2	liver:	n/a
20	chr4:8643813-8643863	Hepatocyte	liver:	n/a
21	chr4:8582565-8582615	U87	brain:	n/a
22	chr4:8666871-8666921	Hela-S3	cervix:	n/a
23	chr4:8609594-8609644	AG04449	skin:	fetal
24	chr4:8643068-8643118	HCT-116	colon:	n/a
25	chr4:8687039-8687089	HCF	heart:	n/a
26	chr4:8642369-8642419	ovcar-3	ovarian:	n/a
27	chr4:8582300-8582350	NB4	blood:	n/a
28	chr4:8602619-8602669	PANC-1	pancreas:	n/a
29	chr4:8633794-8633844	HRCEpiC	kidney:	n/a
30	chr4:8628157-8628207	GM12891	blood:	n/a
31	chr4:8702535-8702585	NT2-D1	testis:	n/a
32	chr4:8620162-8620212	HMEC	breast:	n/a
33	chr4:8692854-8692904	HCM	heart:	n/a
34	chr4:8588929-8588979	HEK293	kidney:	embryo
35	chr4:8609706-8609756	U87	brain:	n/a
36	chr4:8693216-8693266	AG04450	lung:	fetal
37	chr4:8582249-8582299	A549	lung:	n/a
38	chr4:8645833-8645883	HCF	heart:	n/a
39	chr4:8585142-8585192	HUVEC	blood vessel:	n/a
40	chr4:8645949-8645999	PFSK-1	brain:	n/a
41	chr4:8605881-8605931	HepG2	liver:	n/a
42	chr4:8646016-8646066	HepG2	liver:	n/a
43	chr4:8616045-8616095	HEEpiC	esophagus:	n/a
44	chr4:8594514-8594564	PANC-1	pancreas:	n/a
45	chr4:8594857-8594907	HEK293	kidney:	embryo
46	chr4:8602594-8602644	SK-N-SH	brain:	n/a
47	chr4:8643968-8644018	Caco-2	colon:	n/a
48	chr4:8643813-8643863	NHDF-neo	bronchial:	n/a
49	chr4:8582227-8582277	AG04449	skin:	fetal
50	chr4:8692935-8692985	HUVEC	blood vessel:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:8649551..8650162-chr4:8919707..8920368,2	MCF-7	breast:
2	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
3	chr4:8595963..8596810-chr4:8919438..8920172,2	MCF-7	breast:
4	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
5	chr4:8587258..8589695-chr4:8592259..8593843,2	K562	blood:
6	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
7	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
8	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
9	chr4:8677416..8680217-chr4:8770931..8773550,2	K562	blood:
10	chr4:8582036..8584128-chr4:8589824..8592478,3	K562	blood:
11	chr4:8649831..8652641-chr4:8656604..8658458,2	K562	blood:
12	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
13	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
14	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
15	chr4:8682718..8684639-chr4:8704262..8707197,2	MCF-7	breast:
16	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:
17	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
18	chr4:8657922..8660434-chr4:8662931..8664931,2	K562	blood:
19	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
20	chr4:8599492..8601366-chr4:8617273..8620008,2	K562	blood:
21	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
22	chr4:8527972..8528890-chr4:8587077..8587591,2	MCF-7	breast:
23	chr4:8470834..8472351-chr4:8587366..8589099,2	MCF-7	breast:
24	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
25	chr4:8693492..8696360-chr4:8722183..8724152,2	MCF-7	breast:
26	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
27	chr4:8657922..8660434-chr4:8662931..8664931,2	K562	blood:
28	chr4:8470272..8471640-chr4:8595955..8596822,5	MCF-7	breast:
29	chr4:8689647..8690533-chr4:8887295..8888077,4	K562	blood:
30	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
31	chr4:8609002..8610016-chr4:8919155..8920078,6	MCF-7	breast:
32	chr4:8474144..8475116-chr4:8595899..8596574,2	MCF-7	breast:
33	chr4:8550386..8551492-chr4:8588111..8588948,4	MCF-7	breast:
34	chr4:8575279..8576809-chr4:8577990..8579555,2	K562	blood:
35	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
36	chr4:8581776..8584128-chr4:8590195..8592685,3	K562	blood:
37	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:
38	chr4:8562627..8565501-chr4:8586940..8588652,2	MCF-7	breast:
39	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
40	chr15:79417819..79418489-chr4:8588214..8588893,2	MCF-7	breast:
41	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
42	chr4:8582157..8584012-chr4:8592733..8594974,2	MCF-7	breast:
43	chr4:8468552..8470312-chr4:8591413..8592935,2	K562	blood:
44	chr4:8586944..8588877-chr4:8595919..8597857,2	MCF-7	breast:
45	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
46	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
47	chr4:8468812..8470313-chr4:8589998..8592913,2	K562	blood:
48	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
49	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
50	chr4:8609226..8610032-chr4:8887698..8888205,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
CPZ	TF binding region
GPR78	TF binding region
CPZ	CpG island
GPR78	CpG island
ENSG00000250915	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000155269	chromatin interactions
ENSG00000109625	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000205959	chromatin interactions
GAK	miRNA target sites
GADD45A	miRNA target sites
GABRB3	miRNA target sites

Extended variants
information (count: 7142 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7142 , 50 per page) page: 1 2 3 4 5 6 7 ... 143

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181573184	chr4:8578781-8578782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79677500	chr4:8578789-8578790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554305105	chr4:8578792-8578793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572443068	chr4:8578793-8578794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536541998	chr4:8578817-8578818	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs528941983	chr4:8578869-8578870	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs111502453	chr4:8578873-8578874	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs186020024	chr4:8578894-8578895	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs573692678	chr4:8578905-8578906	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs543764205	chr4:8578906-8578907	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs6447883	chr4:8578923-8578924	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs377076447	chr4:8578952-8578953	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs115386576	chr4:8578975-8578976	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs544885802	chr4:8578994-8578995	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs560386490	chr4:8579006-8579007	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs201196102	chr4:8579012-8579013	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs140538109	chr4:8579019-8579020	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs142153015	chr4:8579063-8579064	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs371517401	chr4:8579087-8579088	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs561134141	chr4:8579100-8579101	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs531232374	chr4:8579119-8579120	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs549705730	chr4:8579121-8579122	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs151067499	chr4:8579135-8579136	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs6838103	chr4:8579149-8579150	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114559205	chr4:8579163-8579164	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs6838127	chr4:8579193-8579194	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs140968428	chr4:8579214-8579215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560021715	chr4:8579221-8579222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554856731	chr4:8579257-8579258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58594803	chr4:8579259-8579260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7665929	chr4:8579329-8579330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190091472	chr4:8579354-8579355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552215375	chr4:8579355-8579356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114024004	chr4:8579362-8579363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35424665	chr4:8579367-8579368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146801674	chr4:8579377-8579378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562026324	chr4:8579411-8579412	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs554044589	chr4:8579423-8579424	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs572286800	chr4:8579430-8579431	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs556140376	chr4:8579441-8579442	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs561172751	chr4:8579450-8579451	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs181283132	chr4:8579460-8579461	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs140498748	chr4:8579507-8579508	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs529417930	chr4:8579523-8579524	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs564891128	chr4:8579528-8579529	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs550697875	chr4:8579529-8579530	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs186010060	chr4:8579573-8579574	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs77405593	chr4:8579583-8579584	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs75157371	chr4:8579589-8579590	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs548327464	chr4:8579605-8579606	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:937 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8569600-8579000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
3	chr4:8574400-8582400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr4:8577600-8579000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:8577600-8579800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:8577600-8580800	Weak transcription	Placenta	Placenta
7	chr4:8577600-8581400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:8577600-8582000	Weak transcription	Ovary	ovary
9	chr4:8578400-8579800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr4:8578600-8581800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:8578600-8582200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:8578800-8579000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
13	chr4:8578800-8579200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr4:8579000-8580000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:8579000-8580600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:8579400-8579800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr4:8579600-8580000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
18	chr4:8579800-8580000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:8579800-8580000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:8579800-8580000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:8579800-8580000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr4:8579800-8580000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:8580000-8581200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:8580000-8581200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr4:8580000-8581600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:8580600-8581400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:8580800-8582200	Enhancers	Placenta	Placenta
28	chr4:8581000-8581400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
29	chr4:8581000-8581400	Bivalent Enhancer	HSMMtube	muscle
30	chr4:8581000-8581600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr4:8581000-8581600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr4:8581200-8581400	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:8581200-8581400	Bivalent Enhancer	Right Ventricle	heart
34	chr4:8581200-8581600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr4:8581200-8581600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:8581200-8581600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
37	chr4:8581200-8581600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
38	chr4:8581200-8582200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:8581400-8581600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr4:8581400-8581800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr4:8581400-8581800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:8581400-8581800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:8581400-8582000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:8581400-8582200	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr4:8581400-8582800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr4:8581400-8583000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
47	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
48	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
49	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:8581600-8581800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell

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