Variant report

Variant	nsv830107
Chromosome Location	chr4:147452434-147635720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147558227-147558300	HepG2	liver:	n/a	n/a
2	ATF2	chr4:147558048-147558348	H1-hESC	embryonic stem cell:	n/a	chr4:147558317-147558331
3	ATF3	chr4:147466340-147466550	K562	blood:	n/a	n/a
4	ATF3	chr4:147466307-147466599	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:147554984-147555098	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:147482036-147482054	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr4:147558034-147558061	K562	blood:	n/a	n/a
8	CBX3	chr4:147466278-147466653	K562	blood:	n/a	n/a
9	CCNT2	chr4:147521683-147521740	K562	blood:	n/a	n/a
10	CEBPB	chr4:147619331-147619531	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:147506281-147506298	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:147610925-147611158	A549	lung:	n/a	chr4:147611067-147611078
13	CEBPB	chr4:147595663-147595937	IMR90	lung:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
14	CEBPB	chr4:147596345-147596690	K562	blood:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
15	CEBPB	chr4:147610968-147611231	HepG2	liver:	n/a	chr4:147611067-147611078
16	CEBPB	chr4:147507126-147507589	A549	lung:	n/a	chr4:147507399-147507410
17	CEBPB	chr4:147507184-147507598	IMR90	lung:	n/a	chr4:147507399-147507410
18	CEBPB	chr4:147596338-147596672	A549	lung:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
19	CEBPB	chr4:147507186-147507586	K562	blood:	n/a	chr4:147507399-147507410
20	CEBPB	chr4:147507165-147507539	ECC-1	luminal epithelium:	n/a	chr4:147507399-147507410
21	CEBPB	chr4:147507214-147507592	A549	lung:	n/a	chr4:147507399-147507410
22	CEBPB	chr4:147507263-147507489	HepG2	liver:	n/a	chr4:147507399-147507410
23	CEBPB	chr4:147595673-147595958	HepG2	liver:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
24	CEBPB	chr4:147507203-147507592	H1-hESC	embryonic stem cell:	n/a	chr4:147507399-147507410
25	CEBPB	chr4:147596427-147596671	H1-hESC	embryonic stem cell:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
26	CEBPB	chr4:147507232-147507552	MCF-7	breast:	n/a	chr4:147507399-147507410
27	CEBPB	chr4:147507214-147507595	HepG2	liver:	n/a	chr4:147507399-147507410
28	CEBPB	chr4:147507084-147507636	HCT-116	colon:	n/a	chr4:147507399-147507410
29	CEBPB	chr4:147596336-147596711	HepG2	liver:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
30	CEBPB	chr4:147619350-147619516	K562	blood:	n/a	n/a
31	CEBPB	chr4:147596352-147596700	IMR90	lung:	n/a	chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596516-147596527 chr4:147596518-147596527 chr4:147596518-147596527 chr4:147596516-147596529 chr4:147596518-147596527 chr4:147596518-147596529
32	CEBPB	chr4:147507253-147507575	ECC-1	luminal epithelium:	n/a	chr4:147507399-147507410
33	CEBPB	chr4:147506211-147506419	IMR90	lung:	n/a	chr4:147506301-147506312
34	CEBPB	chr4:147534765-147534922	K562	blood:	n/a	n/a
35	CEBPB	chr4:147506834-147507624	Hela-S3	cervix:	n/a	chr4:147507399-147507410
36	CEBPB	chr4:147522770-147522821	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:147506262-147506371	K562	blood:	n/a	chr4:147506301-147506312
38	CEBPB	chr4:147507202-147507574	MCF-7	breast:	n/a	chr4:147507399-147507410
39	CEBPB	chr4:147595644-147595933	Hela-S3	cervix:	n/a	chr4:147595791-147595808 chr4:147595793-147595804 chr4:147595757-147595770 chr4:147595792-147595805
40	CEBPB	chr4:147506179-147506450	HepG2	liver:	n/a	chr4:147506301-147506312
41	CHD1	chr4:147568761-147569083	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:147560154-147560352	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr4:147569671-147569802	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr4:147576502-147576844	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr4:147569561-147569855	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:147466364-147466613	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr4:147559720-147560281	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:147504263-147504266	GM12878	blood:	n/a	n/a
49	CHD2	chr4:147471573-147471652	K562	blood:	n/a	n/a
50	CHD2	chr4:147561612-147561851	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147577630-147577680	AG09309	skin:	n/a
2	chr4:147569938-147569988	ovcar-3	ovarian:	n/a
3	chr4:147560282-147560332	SAEC	small airway:	n/a
4	chr4:147560286-147560336	HAEpiC	amniotic membrane:	n/a
5	chr4:147577630-147577680	AG09309	skin:	n/a
6	chr4:147569938-147569988	ovcar-3	ovarian:	n/a
7	chr4:147560282-147560332	SAEC	small airway:	n/a
8	chr4:147560286-147560336	HAEpiC	amniotic membrane:	n/a
9	chr4:147554144-147554194	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:147558435-147558485	ProgFib	skin:	n/a
11	chr4:147561669-147561719	HEEpiC	esophagus:	n/a
12	chr4:147558435-147558485	PANC-1	pancreas:	n/a
13	chr4:147554144-147554194	PANC-1	pancreas:	n/a
14	chr4:147558089-147558139	CMK	blood:	n/a
15	chr4:147558435-147558485	A549	lung:	n/a
16	chr4:147559648-147559698	Hepatocyte	liver:	n/a
17	chr4:147561203-147561253	H1-hESC	embryonic stem cell:	embryo
18	chr4:147561203-147561253	NHDF-neo	bronchial:	n/a
19	chr4:147560286-147560336	Hela-S3	cervix:	n/a
20	chr4:147579200-147579250	NB4	blood:	n/a
21	chr4:147561900-147561950	A549	lung:	n/a
22	chr4:147577630-147577680	HCM	heart:	n/a
23	chr4:147569938-147569988	RPTEC	kidney:	n/a
24	chr4:147569185-147569235	T-47D	breast:	n/a
25	chr4:147576227-147576277	MCF10A-Er-Src	breast:	n/a
26	chr4:147557774-147557824	NHDF-neo	bronchial:	n/a
27	chr4:147560286-147560336	ECC-1	luminal epithelium:	n/a
28	chr4:147558239-147558289	A549	lung:	n/a
29	chr4:147554210-147554260	HMEC	breast:	n/a
30	chr4:147554527-147554577	AoSMC	blood vessel:	n/a
31	chr4:147579200-147579250	HRE	kidney:	n/a
32	chr4:147557859-147557909	GM12892	blood:	n/a
33	chr4:147558089-147558139	PANC-1	pancreas:	n/a
34	chr4:147559648-147559698	GM12891	blood:	n/a
35	chr4:147558544-147558594	IMR90	lung:	fetal
36	chr4:147561203-147561253	HCM	heart:	n/a
37	chr4:147579200-147579250	T-47D	breast:	n/a
38	chr4:147560770-147560820	PANC-1	pancreas:	n/a
39	chr4:147576547-147576597	GM12892	blood:	n/a
40	chr4:147554527-147554577	PFSK-1	brain:	n/a
41	chr4:147575999-147576049	HCM	heart:	n/a
42	chr4:147569185-147569235	ovcar-3	ovarian:	n/a
43	chr4:147576547-147576597	HCF	heart:	n/a
44	chr4:147561669-147561719	HNPCEpiC	eye:	n/a
45	chr4:147556288-147556338	PFSK-1	brain:	n/a
46	chr4:147554210-147554260	Caco-2	colon:	n/a
47	chr4:147557774-147557824	HMEC	breast:	n/a
48	chr4:147560126-147560176	GM19239	blood:	n/a
49	chr4:147561900-147561950	AoSMC	blood vessel:	n/a
50	chr4:147554144-147554194	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:147569955..147572256-chr4:147575383..147578342,2	K562	blood:
2	chr4:147263663..147264500-chr4:147465865..147466846,2	MCF-7	breast:
3	chr4:147534574..147536794-chr4:147536840..147539665,2	MCF-7	breast:
4	chr4:147569383..147571342-chr4:147575306..147577219,2	MCF-7	breast:
5	chr4:147488323..147490035-chr4:147830960..147833079,2	MCF-7	breast:
6	chr4:147569383..147571342-chr4:147575306..147577219,2	MCF-7	breast:
7	chr4:147444230..147446047-chr4:147464429..147467416,2	K562	blood:
8	chr4:147503963..147504700-chr4:147820617..147821516,3	MCF-7	breast:
9	chr4:147570143..147572498-chr4:147573319..147574831,2	K562	blood:
10	chr4:147534574..147536794-chr4:147536840..147539665,2	MCF-7	breast:
11	chr1:149223777..149224378-chr4:147501200..147501718,2	HCT-116	colon:
12	chr4:147603707..147604442-chr5:15685536..15686251,2	MCF-7	breast:
13	chr4:147570143..147572498-chr4:147573319..147574831,2	K562	blood:
14	chr4:147569955..147572256-chr4:147575383..147578342,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC10A7-3	chr4:147628339-147628340	NONHSAT098674
2	lnc-SLC10A7-3	chr4:147628637-147628703	NONHSAT098674

No.	miRNA target gene	miRNA name	Chromosome Location
1	POU4F2	hsa-miR-23a-3p	chr4:147562409-147562430
2	POU4F2	hsa-miR-214-3p	chr4:147562574-147562580
3	POU4F2	hsa-miR-23a-3p	chr4:147562120-147562140
4	POU4F2	hsa-miR-214-3p	chr4:147562560-147562581
5	POU4F2	hsa-miR-23a-3p	chr4:147562062-147562069
6	POU4F2	hsa-miR-23a-3p	chr4:147562049-147562069

Variant related genes	Relation type
POU4F2	TF binding region
ENSG00000264323	TF binding region
RNU1-44P	TF binding region
POU4F2	CpG island
ENSG00000264323	CpG island
RNU1-44P	CpG island
ENSG00000206737	chromatin interactions

Extended variants
information (count: 1471 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114789795	chr4:147466606-147466607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543525197	chr4:147466614-147466615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564080920	chr4:147466625-147466626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531387775	chr4:147466634-147466635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551293253	chr4:147466659-147466660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564836380	chr4:147466681-147466682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182189730	chr4:147466685-147466686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373069465	chr4:147466772-147466773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74417288	chr4:147466783-147466784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs62326903	chr4:147466789-147466790	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs550588643	chr4:147466837-147466838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549573871	chr4:147466852-147466853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568984407	chr4:147466862-147466863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371579414	chr4:147466882-147466883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147890964	chr4:147466900-147466901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528618086	chr4:147466938-147466939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2102252	chr4:147466990-147466991	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565220376	chr4:147468643-147468644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543694779	chr4:147468661-147468662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532444701	chr4:147468688-147468689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115959243	chr4:147468721-147468722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368398051	chr4:147468762-147468763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559181578	chr4:147468771-147468772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147023008	chr4:147468803-147468804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550601061	chr4:147468831-147468832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191537291	chr4:147468871-147468872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138090652	chr4:147468885-147468886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531133813	chr4:147468915-147468916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576372763	chr4:147468930-147468931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113451878	chr4:147469225-147469226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188587909	chr4:147469260-147469261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77906097	chr4:147469297-147469298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192385396	chr4:147469311-147469312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139551050	chr4:147469370-147469371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3059768	chr4:147469372-147469373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143138566	chr4:147469391-147469392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs576960501	chr4:147469447-147469448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545807533	chr4:147469454-147469455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559262561	chr4:147469477-147469478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148212125	chr4:147469511-147469512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541884152	chr4:147469521-147469522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562161457	chr4:147469525-147469526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs6829633	chr4:147469546-147469547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1474039	chr4:147469559-147469560	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs570854194	chr4:147469579-147469580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538103199	chr4:147469604-147469605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564435666	chr4:147469633-147469634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533193030	chr4:147469641-147469642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141665518	chr4:147469667-147469668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566810241	chr4:147469695-147469696	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147466600-147467000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:147468600-147469000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:147469200-147469800	Enhancers	HSMMtube	muscle
4	chr4:147472000-147474000	Enhancers	Fetal Heart	heart
5	chr4:147473400-147473800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:147473400-147473800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr4:147481200-147481400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr4:147481400-147489400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr4:147485800-147486200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:147486000-147486400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr4:147488200-147489400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:147488400-147488800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:147488400-147489000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:147488400-147489000	Enhancers	NHEK	skin
15	chr4:147488400-147489400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:147488600-147488800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr4:147488600-147488800	Flanking Active TSS	A549	lung
18	chr4:147488600-147489000	Enhancers	HMEC	breast
19	chr4:147488800-147489000	Enhancers	A549	lung
20	chr4:147494200-147494400	Enhancers	Fetal Heart	heart
21	chr4:147494400-147494800	Flanking Active TSS	Fetal Heart	heart
22	chr4:147494800-147495800	Enhancers	Fetal Heart	heart
23	chr4:147497800-147498200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:147498000-147498600	Enhancers	Fetal Stomach	stomach
25	chr4:147498200-147499000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:147506400-147506800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:147506600-147507600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr4:147506600-147508600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:147506800-147507200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:147506800-147508600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr4:147507000-147507400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:147507000-147507400	Enhancers	Fetal Heart	heart
33	chr4:147507000-147507600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr4:147507000-147507800	Enhancers	Hela-S3	cervix
35	chr4:147507000-147508600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr4:147507200-147507600	Enhancers	Adipose Nuclei	Adipose
37	chr4:147507200-147507600	Enhancers	HSMMtube	muscle
38	chr4:147507200-147508600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:147507200-147508600	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr4:147524600-147525200	Enhancers	H9 Cell Line	embryonic stem cell
41	chr4:147553800-147554000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
42	chr4:147553800-147554000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:147554000-147554200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
44	chr4:147554000-147554200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr4:147554000-147554200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr4:147554000-147554200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
47	chr4:147554000-147554200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:147554000-147554200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
49	chr4:147554000-147554200	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:147554000-147554400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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