Variant report

Variant	nsv470015
Chromosome Location	chr4:8584879-8729638
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2068)
CpG islands
(count:5617)
Chromatin interactive
region (count:102)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2068 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8596075-8596433	K562	blood:	n/a	n/a
2	ARID3A	chr4:8594303-8594474	K562	blood:	n/a	n/a
3	ATF2	chr4:8596088-8596524	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:8601461-8601771	K562	blood:	n/a	n/a
5	BACH1	chr4:8689946-8690325	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:8686570-8686574	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
8	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
9	BCL3	chr4:8697209-8697485	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:8588537-8588647	K562	blood:	n/a	n/a
12	BHLHE40	chr4:8594327-8594941	K562	blood:	n/a	n/a
13	BHLHE40	chr4:8596119-8596493	K562	blood:	n/a	n/a
14	BHLHE40	chr4:8593127-8593244	K562	blood:	n/a	n/a
15	BHLHE40	chr4:8591224-8591267	GM12878	blood:	n/a	chr4:8591227-8591236
16	BHLHE40	chr4:8595611-8595677	K562	blood:	n/a	n/a
17	BHLHE40	chr4:8599078-8599278	K562	blood:	n/a	n/a
18	BHLHE40	chr4:8589655-8590092	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
20	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
21	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
22	BHLHE40	chr4:8586835-8587170	K562	blood:	n/a	n/a
23	BHLHE40	chr4:8689941-8690197	K562	blood:	n/a	n/a
24	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:8601384-8601739	K562	blood:	n/a	n/a
26	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
27	BHLHE40	chr4:8591090-8591396	K562	blood:	n/a	chr4:8591227-8591236
28	BRCA1	chr4:8601470-8601784	Hela-S3	cervix:	n/a	n/a
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	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
32	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
33	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
34	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
35	CCNT2	chr4:8689978-8690131	K562	blood:	n/a	n/a
36	CCNT2	chr4:8589574-8589772	K562	blood:	n/a	n/a
37	CCNT2	chr4:8706899-8707008	K562	blood:	n/a	n/a
38	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
39	CCNT2	chr4:8593208-8593591	K562	blood:	n/a	chr4:8593575-8593584
40	CCNT2	chr4:8605790-8606066	K562	blood:	n/a	n/a
41	CCNT2	chr4:8594231-8595394	K562	blood:	n/a	chr4:8594298-8594307 chr4:8595237-8595246
42	CCNT2	chr4:8588768-8588840	K562	blood:	n/a	n/a
43	CEBPB	chr4:8721400-8721748	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:8596149-8596681	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr4:8596168-8596681	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:8596268-8596675	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:8596290-8596572	A549	lung:	n/a	n/a
48	CEBPB	chr4:8595941-8596695	HCT-116	colon:	n/a	n/a
49	CEBPB	chr4:8721549-8721738	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:8596159-8596690	MCF-7	breast:	n/a	n/a

(count:5617 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8690035-8690085	GM12878	blood:	n/a
2	chr4:8651092-8651142	HCPEpiC	choroid plexus:	n/a
3	chr4:8594413-8594463	HIPEpiC	eye:	n/a
4	chr4:8607947-8607997	SK-N-SH	brain:	n/a
5	chr4:8687955-8688005	MCF10A-Er-Src	breast:	n/a
6	chr4:8690035-8690085	GM12878	blood:	n/a
7	chr4:8651092-8651142	HCPEpiC	choroid plexus:	n/a
8	chr4:8594413-8594463	HIPEpiC	eye:	n/a
9	chr4:8607947-8607997	SK-N-SH	brain:	n/a
10	chr4:8687955-8688005	MCF10A-Er-Src	breast:	n/a
11	chr4:8690489-8690539	ECC-1	luminal epithelium:	n/a
12	chr4:8621226-8621276	U87	brain:	n/a
13	chr4:8585142-8585192	HRE	kidney:	n/a
14	chr4:8696173-8696223	HCF	heart:	n/a
15	chr4:8594549-8594599	NHDF-neo	bronchial:	n/a
16	chr4:8646957-8647007	HMEC	breast:	n/a
17	chr4:8651855-8651905	HRE	kidney:	n/a
18	chr4:8692935-8692985	SK-N-MC	brain:	n/a
19	chr4:8588716-8588766	IMR90	lung:	fetal
20	chr4:8639337-8639387	GM19239	blood:	n/a
21	chr4:8603012-8603062	K562	blood:	n/a
22	chr4:8602619-8602669	AG09319	gingival:	n/a
23	chr4:8602619-8602669	U87	brain:	n/a
24	chr4:8692935-8692985	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:8651225-8651275	AG04450	lung:	fetal
26	chr4:8642776-8642826	IMR90	lung:	fetal
27	chr4:8702535-8702585	HCPEpiC	choroid plexus:	n/a
28	chr4:8594776-8594826	NH-A	brain:	n/a
29	chr4:8608003-8608053	HAEpiC	amniotic membrane:	n/a
30	chr4:8616045-8616095	NT2-D1	testis:	n/a
31	chr4:8727474-8727524	HCT-116	colon:	n/a
32	chr4:8603071-8603121	H1-hESC	embryonic stem cell:	embryo
33	chr4:8642306-8642356	ProgFib	skin:	n/a
34	chr4:8692828-8692878	PANC-1	pancreas:	n/a
35	chr4:8616045-8616095	ECC-1	luminal epithelium:	n/a
36	chr4:8692935-8692985	HEEpiC	esophagus:	n/a
37	chr4:8602594-8602644	BJ	skin:	n/a
38	chr4:8617910-8617960	A549	lung:	n/a
39	chr4:8693216-8693266	SK-N-SH_RA	brain:	n/a
40	chr4:8589313-8589363	BE2_C	brain:	n/a
41	chr4:8643068-8643118	NHDF-neo	bronchial:	n/a
42	chr4:8702475-8702525	RPTEC	kidney:	n/a
43	chr4:8639337-8639387	SK-N-SH_RA	brain:	n/a
44	chr4:8594857-8594907	GM06990	blood:	n/a
45	chr4:8651617-8651667	ovcar-3	ovarian:	n/a
46	chr4:8642313-8642363	AoSMC	blood vessel:	n/a
47	chr4:8648164-8648214	AG04449	skin:	fetal
48	chr4:8702279-8702329	HNPCEpiC	eye:	n/a
49	chr4:8642369-8642419	AG09309	skin:	n/a
50	chr4:8628157-8628207	ProgFib	skin:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:8527972..8528890-chr4:8587077..8587591,2	MCF-7	breast:
2	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
3	chr4:8428794..8430882-chr4:8596413..8599395,2	MCF-7	breast:
4	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
5	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
6	chr4:8649551..8650162-chr4:8919707..8920368,2	MCF-7	breast:
7	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
8	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
9	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
10	chr4:8727792..8729635-chr4:8777761..8780174,2	MCF-7	breast:
11	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
12	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
13	chr4:8586944..8588877-chr4:8595919..8597857,2	MCF-7	breast:
14	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
15	chr4:8550386..8551492-chr4:8588111..8588948,4	MCF-7	breast:
16	chr4:8429003..8431249-chr4:8585694..8587507,2	MCF-7	breast:
17	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:
18	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
19	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
20	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
21	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
22	chr4:8728690..8730772-chr4:10106539..10108201,2	K562	blood:
23	chr4:8470159..8471594-chr4:8587070..8589399,12	MCF-7	breast:
24	chr4:8548872..8549469-chr4:8586632..8587168,2	MCF-7	breast:
25	chr4:8689949..8690495-chr4:8884145..8884993,2	MCF-7	breast:
26	chr4:8578448..8580242-chr4:8586074..8587928,2	K562	blood:
27	chr15:79417819..79418489-chr4:8588214..8588893,2	MCF-7	breast:
28	chr4:8581776..8584128-chr4:8590195..8592685,3	K562	blood:
29	chr4:8609226..8610032-chr4:8887698..8888205,2	MCF-7	breast:
30	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
31	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
32	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
33	chr4:8587258..8589695-chr4:8592259..8593843,2	K562	blood:
34	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
35	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
36	chr4:8594040..8595789-chr4:8608077..8610422,2	MCF-7	breast:
37	chr4:8715458..8718338-chr4:8719661..8722261,4	MCF-7	breast:
38	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
39	chr4:8468812..8470313-chr4:8589998..8592913,2	K562	blood:
40	chr4:8582036..8584128-chr4:8589824..8592478,3	K562	blood:
41	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
42	chr4:8592274..8594245-chr4:8597755..8599882,2	MCF-7	breast:
43	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
44	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
45	chr4:8596740..8598589-chr4:8600076..8602284,2	K562	blood:
46	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
47	chr4:8654425..8657330-chr7:61967859..61969474,2	MCF-7	breast:
48	chr4:8677416..8680217-chr4:8770931..8773550,2	K562	blood:
49	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:
50	chr4:8549627..8551396-chr4:8591821..8593935,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-METTL19-6	chr4:8601180-8601688	NONHSAT095111
2	lnc-METTL19-6	chr4:8594561-8594648	NONHSAT095111
3	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
ENSG00000071127	chromatin interactions
ENSG00000250915	chromatin interactions
ENSG00000155269	chromatin interactions
ENSG00000155275	chromatin interactions
ENSG00000087008	chromatin interactions
GAK	miRNA target sites

Extended variants
information (count: 7004 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7004 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4235272	chr4:8584879-8584880	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562374997	chr4:8584884-8584885	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs550735100	chr4:8584890-8584891	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs6843979	chr4:8584927-8584928	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs564593892	chr4:8584942-8584943	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs544548198	chr4:8584946-8584947	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs371054221	chr4:8584949-8584950	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs551351818	chr4:8584950-8584951	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562853007	chr4:8584962-8584963	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs141386831	chr4:8584972-8584973	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs116398660	chr4:8584988-8584989	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs180888112	chr4:8585047-8585048	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs200006217	chr4:8585089-8585090	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs397881455	chr4:8585090-8585091	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs150795879	chr4:8585120-8585121	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185480896	chr4:8585133-8585134	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7686776	chr4:8585143-8585144	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs535111450	chr4:8585158-8585159	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs550539919	chr4:8585162-8585163	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs569018274	chr4:8585168-8585169	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs539520825	chr4:8585170-8585171	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs546940148	chr4:8585183-8585184	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs4235273	chr4:8585197-8585198	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs567088771	chr4:8585198-8585199	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs191032993	chr4:8585211-8585212	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs183511066	chr4:8585249-8585250	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs149925002	chr4:8585306-8585307	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs544322583	chr4:8585364-8585365	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs116748443	chr4:8585371-8585372	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs577747474	chr4:8585403-8585404	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs545113627	chr4:8585459-8585460	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs560184755	chr4:8585489-8585490	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs528273295	chr4:8585490-8585491	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs28625495	chr4:8585517-8585518	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs543719219	chr4:8585543-8585544	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561871980	chr4:8585562-8585563	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs9683869	chr4:8585665-8585666	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187467055	chr4:8585675-8585676	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs57246320	chr4:8585678-8585679	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs146339234	chr4:8585681-8585682	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs190698963	chr4:8585706-8585707	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551526139	chr4:8585740-8585741	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566528447	chr4:8585751-8585752	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10006769	chr4:8585762-8585763	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9684826	chr4:8585772-8585773	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs567912916	chr4:8585795-8585796	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs28612558	chr4:8585867-8585868	Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs139584966	chr4:8585874-8585875	Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10662031	chr4:8585949-8585950	Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs33916570	chr4:8585950-8585951	Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	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:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8583600-8588800	Weak transcription	Spleen	Spleen
3	chr4:8584000-8585200	Flanking Active TSS	Placenta	Placenta
4	chr4:8584200-8586600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:8584400-8587400	Weak transcription	Esophagus	oesophagus
6	chr4:8584600-8587200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:8584600-8593800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:8584800-8586200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:8585200-8585400	Active TSS	Placenta	Placenta
10	chr4:8585400-8585600	Flanking Active TSS	Placenta	Placenta
11	chr4:8585600-8585800	Active TSS	Placenta	Placenta
12	chr4:8585800-8586000	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
13	chr4:8585800-8586600	Transcr. at gene 5' and 3'	Placenta	Placenta
14	chr4:8586000-8586200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:8586000-8586200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr4:8586200-8589000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:8586400-8586800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:8586400-8586800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr4:8586600-8587000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
20	chr4:8586600-8587000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:8586600-8587200	Genic enhancers	Placenta	Placenta
22	chr4:8586800-8587000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:8586800-8587600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:8586800-8591800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:8587000-8587600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:8587000-8588000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:8587000-8588400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr4:8587000-8588400	Enhancers	HSMM	muscle
29	chr4:8587200-8587400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr4:8587200-8588200	Transcr. at gene 5' and 3'	Placenta	Placenta
31	chr4:8587200-8588400	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr4:8587200-8588400	Bivalent Enhancer	Fetal Stomach	stomach
33	chr4:8587200-8588800	Enhancers	HSMMtube	muscle
34	chr4:8587200-8590200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:8587400-8587600	Enhancers	Esophagus	oesophagus
36	chr4:8587600-8588400	Bivalent Enhancer	Fetal Lung	lung
37	chr4:8587600-8588800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:8587600-8593400	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr4:8588000-8588600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:8588200-8590000	Genic enhancers	Placenta	Placenta
41	chr4:8588400-8588600	Enhancers	Fetal Kidney	kidney
42	chr4:8588600-8588800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
43	chr4:8588600-8589000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr4:8588600-8591200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:8588800-8589200	ZNF genes & repeats	Spleen	Spleen
46	chr4:8588800-8591400	Weak transcription	Fetal Kidney	kidney
47	chr4:8588800-8594000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:8589000-8591200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:8589200-8590000	Enhancers	K562	blood
50	chr4:8589200-8593800	Weak transcription	Spleen	Spleen

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