Variant report

Variant	nsv829855
Chromosome Location	chr4:8604879-8729607
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1258)
CpG islands
(count:3969)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:8689946-8690325	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:8686570-8686574	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
4	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
5	BCL3	chr4:8697209-8697485	GM12878	blood:	n/a	n/a
6	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:8689941-8690197	K562	blood:	n/a	n/a
8	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
9	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
10	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
11	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
13	BRCA1	chr4:8609454-8609550	HepG2	liver:	n/a	n/a
14	BRCA1	chr4:8609386-8609627	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
16	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
17	CBX3	chr4:8637870-8638277	K562	blood:	n/a	n/a
18	CBX3	chr4:8637918-8638194	K562	blood:	n/a	n/a
19	CCNT2	chr4:8706899-8707008	K562	blood:	n/a	n/a
20	CCNT2	chr4:8605790-8606066	K562	blood:	n/a	n/a
21	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
22	CCNT2	chr4:8689978-8690131	K562	blood:	n/a	n/a
23	CEBPB	chr4:8721549-8721738	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:8721400-8721748	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:8689931-8690213	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:8721337-8721861	MCF-7	breast:	n/a	n/a
27	CEBPB	chr4:8689005-8689157	A549	lung:	n/a	n/a
28	CHD2	chr4:8609474-8609658	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr4:8609419-8609693	H1-hESC	embryonic stem cell:	n/a	chr4:8609458-8609468
30	CHD2	chr4:8609527-8609681	K562	blood:	n/a	n/a
31	CHD2	chr4:8646212-8646412	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:8677074-8677417	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr4:8677230-8677272	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr4:8689813-8689859	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr4:8677108-8677533	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:8608820-8608970	AG04450	lung:	n/a	n/a
37	CTCF	chr4:8609440-8609590	HFF-Myc	foreskin:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
38	CTCF	chr4:8689960-8690110	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr4:8609290-8609740	K562	blood:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
40	CTCF	chr4:8622432-8622526	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr4:8679796-8679834	K562	blood:	n/a	n/a
42	CTCF	chr4:8609460-8609610	SK-N-SH_RA	brain:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
43	CTCF	chr4:8637963-8638240	GM10266	blood:	n/a	chr4:8638075-8638088 chr4:8638075-8638088 chr4:8638073-8638091 chr4:8638076-8638086 chr4:8638079-8638088 chr4:8638074-8638090
44	CTCF	chr4:8689944-8690208	LNCaP	prostate:	n/a	n/a
45	CTCF	chr4:8609397-8609644	Kidney_OC	kidney:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
46	CTCF	chr4:8609420-8609570	HA-sp	spinal cord:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
47	CTCF	chr4:8689968-8690193	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:8689960-8690189	A549	lung:	n/a	n/a
49	CTCF	chr4:8609440-8609590	AG09309	skin:	n/a	chr4:8609521-8609534 chr4:8609518-8609536 chr4:8609520-8609541
50	CTCF	chr4:8689980-8690130	NHLF	lung:	n/a	n/a

(count:3969 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8621266-8621316	NHDF-neo	bronchial:	n/a
2	chr4:8651451-8651501	NHBE	bronchial:	n/a
3	chr4:8617839-8617889	HRCEpiC	kidney:	n/a
4	chr4:8643068-8643118	HEK293	kidney:	embryo
5	chr4:8621266-8621316	NHDF-neo	bronchial:	n/a
6	chr4:8651451-8651501	NHBE	bronchial:	n/a
7	chr4:8617839-8617889	HRCEpiC	kidney:	n/a
8	chr4:8643068-8643118	HEK293	kidney:	embryo
9	chr4:8651617-8651667	AG04449	skin:	fetal
10	chr4:8692828-8692878	CMK	blood:	n/a
11	chr4:8642776-8642826	A549	lung:	n/a
12	chr4:8643029-8643079	Hela-S3	cervix:	n/a
13	chr4:8651617-8651667	PFSK-1	brain:	n/a
14	chr4:8640896-8640946	HMEC	breast:	n/a
15	chr4:8619939-8619989	ovcar-3	ovarian:	n/a
16	chr4:8643218-8643268	HNPCEpiC	eye:	n/a
17	chr4:8642776-8642826	HAEpiC	amniotic membrane:	n/a
18	chr4:8645833-8645883	PFSK-1	brain:	n/a
19	chr4:8651092-8651142	BE2_C	brain:	n/a
20	chr4:8616045-8616095	ovcar-3	ovarian:	n/a
21	chr4:8687955-8688005	K562	blood:	n/a
22	chr4:8642776-8642826	AG09309	skin:	n/a
23	chr4:8643068-8643118	Hepatocyte	liver:	n/a
24	chr4:8639337-8639387	ProgFib	skin:	n/a
25	chr4:8643068-8643118	Caco-2	colon:	n/a
26	chr4:8645833-8645883	HRPEpiC	eye:	n/a
27	chr4:8666871-8666921	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:8608361-8608411	HRPEpiC	eye:	n/a
29	chr4:8651617-8651667	PrEC	prostate:	n/a
30	chr4:8692828-8692878	Hepatocyte	liver:	n/a
31	chr4:8615996-8616046	Jurkat	blood:	n/a
32	chr4:8646016-8646066	HIPEpiC	eye:	n/a
33	chr4:8690489-8690539	A549	lung:	n/a
34	chr4:8702475-8702525	Caco-2	colon:	n/a
35	chr4:8617738-8617788	ProgFib	skin:	n/a
36	chr4:8619939-8619989	SKMC	muscle:	n/a
37	chr4:8643068-8643118	SK-N-MC	brain:	n/a
38	chr4:8690035-8690085	HEK293	kidney:	embryo
39	chr4:8651092-8651142	GM12891	blood:	n/a
40	chr4:8607947-8607997	HL-60	blood:	n/a
41	chr4:8690489-8690539	GM19239	blood:	n/a
42	chr4:8648468-8648518	HIPEpiC	eye:	n/a
43	chr4:8619939-8619989	AG10803	skin:	n/a
44	chr4:8642776-8642826	PrEC	prostate:	n/a
45	chr4:8609594-8609644	NHDF-neo	bronchial:	n/a
46	chr4:8621226-8621276	PANC-1	pancreas:	n/a
47	chr4:8642306-8642356	SK-N-SH	brain:	n/a
48	chr4:8623002-8623052	AG04450	lung:	fetal
49	chr4:8702397-8702447	ProgFib	skin:	n/a
50	chr4:8696173-8696223	HEEpiC	esophagus:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
2	chr4:8715458..8718338-chr4:8719661..8722261,4	MCF-7	breast:
3	chr4:8654425..8657330-chr7:61967859..61969474,2	MCF-7	breast:
4	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:
5	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
6	chr4:8727792..8729635-chr4:8777761..8780174,2	MCF-7	breast:
7	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
8	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
9	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
10	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
11	chr4:8693492..8696360-chr4:8722183..8724152,2	MCF-7	breast:
12	chr4:8693492..8696360-chr4:8722183..8724152,2	MCF-7	breast:
13	chr4:8701567..8704524-chr4:8729204..8732158,2	K562	blood:
14	chr4:8657922..8660434-chr4:8662931..8664931,2	K562	blood:
15	chr4:8720313..8722738-chr4:8763583..8766332,2	MCF-7	breast:
16	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
17	chr4:8682718..8684639-chr4:8704262..8707197,2	MCF-7	breast:
18	chr4:8648999..8649710-chr4:8883912..8884471,2	MCF-7	breast:
19	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
20	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
21	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
22	chr4:8723681..8726595-chr4:8727045..8729022,2	MCF-7	breast:
23	chr4:8715458..8718338-chr4:8719661..8722261,4	MCF-7	breast:
24	chr4:8728690..8730772-chr4:10106539..10108201,2	K562	blood:
25	chr4:8690025..8690993-chr4:8919534..8920174,2	MCF-7	breast:
26	chr4:8709795..8712592-chr4:8714328..8716618,2	MCF-7	breast:
27	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
28	chr4:8594040..8595789-chr4:8608077..8610422,2	MCF-7	breast:
29	chr4:8609002..8610016-chr4:8919155..8920078,6	MCF-7	breast:
30	chr4:8689949..8690495-chr4:8884145..8884993,2	MCF-7	breast:
31	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
32	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
33	chr4:8682718..8684639-chr4:8704262..8707197,2	MCF-7	breast:
34	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
35	chr4:8722609..8725304-chr4:8746886..8749545,2	MCF-7	breast:
36	chr4:8649831..8652641-chr4:8656604..8658458,2	K562	blood:
37	chr4:8709795..8712592-chr4:8714328..8716618,2	MCF-7	breast:
38	chr4:8689272..8690551-chr4:8887541..8888216,4	MCF-7	breast:
39	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
40	chr4:8657922..8660434-chr4:8662931..8664931,2	K562	blood:
41	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
42	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
43	chr4:8472717..8474725-chr4:8621251..8624026,2	K562	blood:
44	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
45	chr4:8707817..8709520-chr4:8713049..8714741,2	MCF-7	breast:
46	chr4:8689647..8690533-chr4:8887295..8888077,4	K562	blood:
47	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
48	chr4:8709792..8713378-chr4:8726638..8730577,3	K562	blood:
49	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
50	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:

No data

Variant related genes	Relation type
CPZ	TF binding region
CPZ	CpG island
ENSG00000109625	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000250915	chromatin interactions

Extended variants
information (count: 5692 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5692 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151278104	chr4:8604890-8604891	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs73088292	chr4:8604924-8604925	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs368762890	chr4:8604926-8604927	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs74661807	chr4:8604929-8604930	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs537505117	chr4:8604969-8604970	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs150428663	chr4:8604975-8604976	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs578088633	chr4:8604978-8604979	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs3756167	chr4:8604991-8604992	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs145216836	chr4:8604995-8604996	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs572431636	chr4:8604996-8604997	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs3756166	chr4:8604999-8605000	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs371868139	chr4:8605012-8605013	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552083113	chr4:8605020-8605021	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540323310	chr4:8605064-8605065	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376524297	chr4:8605077-8605078	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369799850	chr4:8605078-8605079	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75552046	chr4:8605081-8605082	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574050946	chr4:8605127-8605128	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4235275	chr4:8605143-8605144	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78235890	chr4:8605157-8605158	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141202790	chr4:8605272-8605273	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560185997	chr4:8605276-8605277	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184251874	chr4:8605312-8605313	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76340726	chr4:8605320-8605321	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188089279	chr4:8605337-8605338	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4621412	chr4:8605338-8605339	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537568670	chr4:8605362-8605363	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549430345	chr4:8605389-8605390	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386671390	chr4:8605404-8605405	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2241068	chr4:8605406-8605407	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112879863	chr4:8605409-8605410	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180903916	chr4:8605433-8605434	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572661562	chr4:8605438-8605439	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2241067	chr4:8605442-8605443	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs373049901	chr4:8605467-8605468	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58825861	chr4:8605472-8605473	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77204838	chr4:8605475-8605476	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4441741	chr4:8605483-8605484	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577818090	chr4:8605497-8605498	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371197224	chr4:8605498-8605499	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376289233	chr4:8605513-8605514	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145179295	chr4:8605525-8605526	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185470550	chr4:8605547-8605548	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571198233	chr4:8605601-8605602	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560564009	chr4:8605629-8605630	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531191959	chr4:8605636-8605637	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549875484	chr4:8605637-8605638	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201458208	chr4:8605672-8605673	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571251410	chr4:8605683-8605684	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116765715	chr4:8605684-8605685	Strong transcription Weak transcription Enhancers	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:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8596000-8622800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:8596000-8623200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:8596200-8609000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:8597600-8618400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:8598800-8609000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:8599600-8616000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:8599800-8609000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:8600600-8605800	Strong transcription	Placenta Amnion	Placenta Amnion
10	chr4:8600800-8608400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
11	chr4:8601200-8611400	Weak transcription	Spleen	Spleen
12	chr4:8601400-8609000	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr4:8601400-8616000	Weak transcription	HSMMtube	muscle
14	chr4:8601600-8609600	Strong transcription	Ovary	ovary
15	chr4:8601600-8620200	Weak transcription	NHDF-Ad	bronchial
16	chr4:8601800-8617000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:8601800-8622000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:8602400-8608600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:8602600-8605400	Weak transcription	HSMM	muscle
20	chr4:8603000-8607000	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr4:8603000-8607400	Weak transcription	NHLF	lung
22	chr4:8603200-8609200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:8603200-8615400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:8604000-8608200	Strong transcription	Placenta	Placenta
25	chr4:8604800-8605000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:8604800-8607200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:8604800-8608600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr4:8605400-8605800	Enhancers	Gastric	stomach
29	chr4:8605600-8606000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:8605800-8607600	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr4:8605800-8612000	Weak transcription	Gastric	stomach
32	chr4:8606000-8609000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:8606800-8615400	Weak transcription	Osteobl	bone
34	chr4:8607000-8607800	Strong transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:8607200-8607600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:8607600-8608000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:8607600-8608000	Strong transcription	Placenta Amnion	Placenta Amnion
38	chr4:8607800-8616000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr4:8608000-8610200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:8608000-8613000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr4:8608200-8610400	Genic enhancers	Placenta	Placenta
42	chr4:8608400-8614200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr4:8608600-8609000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr4:8609000-8609200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:8609000-8609200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
46	chr4:8609000-8609200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:8609000-8609400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
48	chr4:8609000-8609600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:8609000-8610200	Genic enhancers	H1 Cell Line	embryonic stem cell
50	chr4:8609200-8609400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell

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