Variant report

Variant	nsv878616
Chromosome Location	chr4:8566758-8669619
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1791)
CpG islands
(count:5503)
Chromatin interactive
region (count:89)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1791 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	ATF2	chr4:8582336-8582809	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:8569984-8570498	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr4:8601461-8601771	K562	blood:	n/a	n/a
7	BACH1	chr4:8582079-8582264	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr4:8610576-8611046	GM12878	blood:	n/a	n/a
9	BCL3	chr4:8612532-8612922	GM12878	blood:	n/a	n/a
10	BCL3	chr4:8579732-8579963	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8579745-8580023	GM12878	blood:	n/a	n/a
12	BCL3	chr4:8610662-8611065	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:8595611-8595677	K562	blood:	n/a	n/a
14	BHLHE40	chr4:8609413-8609700	HepG2	liver:	n/a	chr4:8609588-8609601
15	BHLHE40	chr4:8588537-8588647	K562	blood:	n/a	n/a
16	BHLHE40	chr4:8609354-8609763	K562	blood:	n/a	chr4:8609588-8609601
17	BHLHE40	chr4:8591224-8591267	GM12878	blood:	n/a	chr4:8591227-8591236
18	BHLHE40	chr4:8594327-8594941	K562	blood:	n/a	n/a
19	BHLHE40	chr4:8582469-8582507	K562	blood:	n/a	n/a
20	BHLHE40	chr4:8609534-8609694	A549	lung:	n/a	chr4:8609588-8609601
21	BHLHE40	chr4:8591090-8591396	K562	blood:	n/a	chr4:8591227-8591236
22	BHLHE40	chr4:8601384-8601739	K562	blood:	n/a	n/a
23	BHLHE40	chr4:8596119-8596493	K562	blood:	n/a	n/a
24	BHLHE40	chr4:8586835-8587170	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8589655-8590092	K562	blood:	n/a	n/a
26	BHLHE40	chr4:8609432-8609738	GM12878	blood:	n/a	chr4:8609588-8609601
27	BHLHE40	chr4:8610202-8610572	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:8593127-8593244	K562	blood:	n/a	n/a
29	BHLHE40	chr4:8599078-8599278	K562	blood:	n/a	n/a
30	BRCA1	chr4:8609386-8609627	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr4:8601470-8601784	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr4:8569877-8570345	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr4:8609454-8609550	HepG2	liver:	n/a	n/a
34	CBX3	chr4:8626547-8627016	K562	blood:	n/a	n/a
35	CBX3	chr4:8582339-8582560	K562	blood:	n/a	n/a
36	CBX3	chr4:8632192-8632581	K562	blood:	n/a	n/a
37	CBX3	chr4:8637918-8638194	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	CCNT2	chr4:8589574-8589772	K562	blood:	n/a	n/a
41	CCNT2	chr4:8593208-8593591	K562	blood:	n/a	chr4:8593575-8593584
42	CCNT2	chr4:8605790-8606066	K562	blood:	n/a	n/a
43	CCNT2	chr4:8594231-8595394	K562	blood:	n/a	chr4:8594298-8594307 chr4:8595237-8595246
44	CCNT2	chr4:8588768-8588840	K562	blood:	n/a	n/a
45	CCNT2	chr4:8609385-8609607	K562	blood:	n/a	chr4:8609415-8609424
46	CCNT2	chr4:8582433-8582494	K562	blood:	n/a	n/a
47	CEBPB	chr4:8596175-8596686	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:8596290-8596572	A549	lung:	n/a	n/a
49	CEBPB	chr4:8597367-8597593	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:8596410-8596636	K562	blood:	n/a	n/a

(count:5503 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8592328-8592378	NHBE	bronchial:	n/a
2	chr4:8578207-8578257	CMK	blood:	n/a
3	chr4:8594549-8594599	HCF	heart:	n/a
4	chr4:8603130-8603180	HCM	heart:	n/a
5	chr4:8603130-8603180	HL-60	blood:	n/a
6	chr4:8643068-8643118	AG10803	skin:	n/a
7	chr4:8666871-8666921	ovcar-3	ovarian:	n/a
8	chr4:8588716-8588766	HEK293	kidney:	embryo
9	chr4:8588858-8588908	MCF10A-Er-Src	breast:	n/a
10	chr4:8582227-8582277	HRE	kidney:	n/a
11	chr4:8585142-8585192	GM12891	blood:	n/a
12	chr4:8603130-8603180	BE2_C	brain:	n/a
13	chr4:8587077-8587127	HL-60	blood:	n/a
14	chr4:8592328-8592378	NHBE	bronchial:	n/a
15	chr4:8578207-8578257	CMK	blood:	n/a
16	chr4:8594549-8594599	HCF	heart:	n/a
17	chr4:8603130-8603180	HCM	heart:	n/a
18	chr4:8603130-8603180	HL-60	blood:	n/a
19	chr4:8643068-8643118	AG10803	skin:	n/a
20	chr4:8666871-8666921	ovcar-3	ovarian:	n/a
21	chr4:8588716-8588766	HEK293	kidney:	embryo
22	chr4:8588858-8588908	MCF10A-Er-Src	breast:	n/a
23	chr4:8582227-8582277	HRE	kidney:	n/a
24	chr4:8585142-8585192	GM12891	blood:	n/a
25	chr4:8603130-8603180	BE2_C	brain:	n/a
26	chr4:8587077-8587127	HL-60	blood:	n/a
27	chr4:8651225-8651275	GM19239	blood:	n/a
28	chr4:8617839-8617889	HRPEpiC	eye:	n/a
29	chr4:8621361-8621411	AG09319	gingival:	n/a
30	chr4:8648739-8648789	NB4	blood:	n/a
31	chr4:8588802-8588852	HRCEpiC	kidney:	n/a
32	chr4:8617839-8617889	GM12891	blood:	n/a
33	chr4:8643968-8644018	GM06990	blood:	n/a
34	chr4:8602556-8602606	BJ	skin:	n/a
35	chr4:8594514-8594564	NHDF-neo	bronchial:	n/a
36	chr4:8621226-8621276	PrEC	prostate:	n/a
37	chr4:8608235-8608285	AG10803	skin:	n/a
38	chr4:8608361-8608411	PFSK-1	brain:	n/a
39	chr4:8645833-8645883	BJ	skin:	n/a
40	chr4:8593933-8593983	PANC-1	pancreas:	n/a
41	chr4:8621266-8621316	SKMC	muscle:	n/a
42	chr4:8623002-8623052	HNPCEpiC	eye:	n/a
43	chr4:8617910-8617960	GM12892	blood:	n/a
44	chr4:8642313-8642363	HCM	heart:	n/a
45	chr4:8633794-8633844	HNPCEpiC	eye:	n/a
46	chr4:8643957-8644007	HCT-116	colon:	n/a
47	chr4:8581424-8581474	HCT-116	colon:	n/a
48	chr4:8588870-8588920	Caco-2	colon:	n/a
49	chr4:8594549-8594599	GM12891	blood:	n/a
50	chr4:8615996-8616046	H1-hESC	embryonic stem cell:	embryo

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:8429003..8431249-chr4:8585694..8587507,2	MCF-7	breast:
2	chr4:8562627..8565501-chr4:8586940..8588652,2	MCF-7	breast:
3	chr4:8468812..8470313-chr4:8589998..8592913,2	K562	blood:
4	chr4:8592274..8594245-chr4:8597755..8599882,2	MCF-7	breast:
5	chr4:8549627..8551396-chr4:8591821..8593935,2	MCF-7	breast:
6	chr4:8609002..8610016-chr4:8919155..8920078,6	MCF-7	breast:
7	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
8	chr4:8468552..8470312-chr4:8591413..8592935,2	K562	blood:
9	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
10	chr4:8667609..8668516-chr4:8887656..8888210,2	MCF-7	breast:
11	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
12	chr4:8590141..8592229-chr4:8594534..8596256,2	K562	blood:
13	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
14	chr4:8575279..8576809-chr4:8577990..8579555,2	K562	blood:
15	chr4:8568331..8569836-chr4:8571951..8573998,2	MCF-7	breast:
16	chr4:8573294..8576745-chr4:8580946..8583751,3	MCF-7	breast:
17	chr4:8657843..8659725-chr4:8665360..8667377,2	MCF-7	breast:
18	chr4:8617932..8619527-chr4:8918338..8920672,2	MCF-7	breast:
19	chr4:8595936..8597951-chr4:8606761..8608322,2	MCF-7	breast:
20	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
21	chr4:8470159..8471594-chr4:8587070..8589399,12	MCF-7	breast:
22	chr4:8470336..8471339-chr4:8588024..8588933,6	MCF-7	breast:
23	chr4:8600582..8603192-chr4:8603240..8605634,2	K562	blood:
24	chr4:8643957..8646441-chr4:8648684..8651421,2	MCF-7	breast:
25	chr4:8595995..8599950-chr4:8600230..8602284,3	K562	blood:
26	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
27	chr4:8639250..8640927-chr4:8642390..8645117,2	K562	blood:
28	chr4:8649453..8651448-chr4:8659369..8661380,2	MCF-7	breast:
29	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
30	chr4:8547587..8550346-chr4:8589117..8591927,3	MCF-7	breast:
31	chr4:8607464..8609784-chr4:8610863..8613633,2	MCF-7	breast:
32	chr4:8581776..8584128-chr4:8590195..8592685,3	K562	blood:
33	chr4:8646299..8649140-chr4:8652570..8655167,2	K562	blood:
34	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
35	chr4:8604553..8606540-chr4:8607081..8609786,2	MCF-7	breast:
36	chr4:8649831..8652641-chr4:8656604..8658458,2	K562	blood:
37	chr4:8595618..8598948-chr4:8601035..8605983,4	MCF-7	breast:
38	chr4:8641181..8642723-chr4:8648783..8650662,2	MCF-7	breast:
39	chr4:8657922..8660434-chr4:8662931..8664931,2	K562	blood:
40	chr4:8474144..8475116-chr4:8595899..8596574,2	MCF-7	breast:
41	chr4:8599492..8601366-chr4:8617273..8620008,2	K562	blood:
42	chr4:8582157..8584012-chr4:8592733..8594974,2	MCF-7	breast:
43	chr4:8527972..8528890-chr4:8587077..8587591,2	MCF-7	breast:
44	chr4:8575279..8576809-chr4:8577990..8579555,2	K562	blood:
45	chr4:8590424..8592185-chr4:8596876..8599266,2	K562	blood:
46	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
47	chr15:79417819..79418489-chr4:8588214..8588893,2	MCF-7	breast:
48	chr4:8470834..8472351-chr4:8587366..8589099,2	MCF-7	breast:
49	chr4:8649551..8650162-chr4:8919707..8920368,2	MCF-7	breast:
50	chr4:8474531..8475355-chr4:8595923..8596757,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR78-1	chr4:8582122-8582438	NONHSAT095110
2	lnc-GPR78-1	chr4:8584258-8584371	NR_045511
3	lnc-METTL19-6	chr4:8601180-8601688	NONHSAT095111
4	lnc-GPR78-1	chr4:8582122-8582251	NONHSAT095109
5	lnc-GPR78-1	chr4:8588781-8591750	NR_045511
6	lnc-GPR78-1	chr4:8581964-8582431	NR_045511
7	lnc-METTL19-6	chr4:8594561-8594648	NONHSAT095111
8	lnc-GPR78-1	chr4:8574460-8574576	NONHSAT095109

No data

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

Extended variants
information (count: 5593 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5593 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7682211	chr4:8566758-8566759	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140754418	chr4:8566817-8566818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557348338	chr4:8566835-8566836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572428950	chr4:8566844-8566845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376760319	chr4:8566845-8566846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550613773	chr4:8566849-8566850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539462302	chr4:8566852-8566853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34092784	chr4:8566855-8566856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558152189	chr4:8566889-8566890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568934174	chr4:8566899-8566900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540688080	chr4:8566928-8566929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28789398	chr4:8566939-8566940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574526865	chr4:8566979-8566980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188837071	chr4:8566984-8566985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576925153	chr4:8567024-8567025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370358818	chr4:8567106-8567107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530805761	chr4:8567167-8567168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374850071	chr4:8567203-8567204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564127067	chr4:8567204-8567205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543507877	chr4:8567207-8567208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529858069	chr4:8567229-8567230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551759981	chr4:8567234-8567235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13108246	chr4:8567305-8567306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs181569005	chr4:8567306-8567307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185317108	chr4:8567310-8567311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs115195089	chr4:8567387-8567388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535655346	chr4:8567433-8567434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147542807	chr4:8567461-8567462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535810815	chr4:8567471-8567472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569468752	chr4:8567503-8567504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534548940	chr4:8567505-8567506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540090100	chr4:8567508-8567509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558190746	chr4:8567525-8567526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566871110	chr4:8567553-8567554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373533048	chr4:8567594-8567595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4504233	chr4:8567600-8567601	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555885477	chr4:8567613-8567614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574048004	chr4:8567663-8567664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190071398	chr4:8567674-8567675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374587150	chr4:8567701-8567702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181593932	chr4:8567702-8567703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148578147	chr4:8567727-8567728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545684533	chr4:8567741-8567742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142930082	chr4:8567744-8567745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372332514	chr4:8567775-8567776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs6831061	chr4:8567787-8567788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539973932	chr4:8567788-8567789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531905366	chr4:8567798-8567799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550408983	chr4:8567802-8567803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561643367	chr4:8567844-8567845	Weak transcription Enhancers	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:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8549400-8568400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:8562800-8568400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr4:8563000-8568000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr4:8563000-8568000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:8563000-8568200	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr4:8563000-8568400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:8563400-8568000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:8563600-8568200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr4:8564000-8569000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr4:8564200-8568400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:8564200-8568600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr4:8564200-8569000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:8565800-8567400	Weak transcription	Placenta	Placenta
14	chr4:8566400-8566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:8566400-8566800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:8566800-8569200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:8566800-8569400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:8567400-8568400	Enhancers	Placenta	Placenta
19	chr4:8568000-8568800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:8568000-8569600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:8568000-8569800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:8568000-8571000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:8568200-8568800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:8568200-8569800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:8568400-8569000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:8568400-8569400	Weak transcription	Placenta	Placenta
27	chr4:8568400-8569600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:8568400-8569800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:8568400-8570800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:8568600-8570600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr4:8568800-8569400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:8568800-8573800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:8569000-8570000	Enhancers	Placenta Amnion	Placenta Amnion
34	chr4:8569000-8570200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr4:8569000-8570400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:8569200-8570400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr4:8569200-8570800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:8569400-8569600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:8569400-8570000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:8569400-8577600	Enhancers	Placenta	Placenta
41	chr4:8569600-8569800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr4:8569600-8570400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:8569600-8570400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr4:8569600-8579000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:8569800-8570000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:8569800-8570200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr4:8569800-8570200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr4:8569800-8570600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:8569800-8570800	Enhancers	HSMMtube	muscle
50	chr4:8569800-8572600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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