Variant report

Variant	nsv980178
Chromosome Location	chr4:3621331-3636820
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	ATF1	chr4:3622207-3622400	K562	blood:	n/a	n/a
2	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
3	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
4	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
6	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
7	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
8	CTCF	chr4:3621500-3621650	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr4:3621580-3621730	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr4:3621260-3621410	HVMF	connective:	n/a	n/a
11	CTCF	chr4:3621280-3621430	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:3621640-3621790	NB4	blood:	n/a	n/a
13	CTCF	chr4:3621200-3621350	HVMF	connective:	n/a	n/a
14	CTCF	chr4:3621400-3621550	A549	lung:	n/a	n/a
15	CTCF	chr4:3621620-3621770	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:3629970-3629976	K562	blood:	n/a	n/a
17	CUX1	chr4:3631334-3631484	K562	blood:	n/a	n/a
18	E2F4	chr4:3622097-3622427	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F6	chr4:3628166-3628626	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F6	chr4:3632546-3632710	K562	blood:	n/a	n/a
21	E2F6	chr4:3628336-3628473	K562	blood:	n/a	n/a
22	E2F6	chr4:3628073-3628656	H1-hESC	embryonic stem cell:	n/a	n/a
23	EGR1	chr4:3633533-3634208	MCF-7	breast:	n/a	chr4:3633835-3633844 chr4:3633835-3633846 chr4:3633829-3633851 chr4:3633835-3633845 chr4:3633834-3633847 chr4:3633834-3633847 chr4:3633836-3633845 chr4:3633833-3633847 chr4:3633835-3633845
24	EGR1	chr4:3633649-3633963	K562	blood:	n/a	chr4:3633835-3633844 chr4:3633835-3633846 chr4:3633829-3633851 chr4:3633835-3633845 chr4:3633834-3633847 chr4:3633834-3633847 chr4:3633836-3633845 chr4:3633833-3633847 chr4:3633835-3633845
25	EGR1	chr4:3625519-3626176	ECC-1	luminal epithelium:	n/a	chr4:3625915-3625925 chr4:3625976-3625998 chr4:3625915-3625926 chr4:3626024-3626039 chr4:3625914-3625927 chr4:3625909-3625931 chr4:3625914-3625927
26	EGR1	chr4:3625495-3626185	ECC-1	luminal epithelium:	n/a	chr4:3625915-3625925 chr4:3625976-3625998 chr4:3625915-3625926 chr4:3626024-3626039 chr4:3625914-3625927 chr4:3625909-3625931 chr4:3625914-3625927
27	EGR1	chr4:3625623-3626160	K562	blood:	n/a	chr4:3625915-3625925 chr4:3625976-3625998 chr4:3625915-3625926 chr4:3626024-3626039 chr4:3625914-3625927 chr4:3625909-3625931 chr4:3625914-3625927
28	EGR1	chr4:3633624-3633961	K562	blood:	n/a	chr4:3633835-3633844 chr4:3633835-3633846 chr4:3633829-3633851 chr4:3633835-3633845 chr4:3633834-3633847 chr4:3633834-3633847 chr4:3633836-3633845 chr4:3633833-3633847 chr4:3633835-3633845
29	EGR1	chr4:3633569-3634105	MCF-7	breast:	n/a	chr4:3633835-3633844 chr4:3633835-3633846 chr4:3633829-3633851 chr4:3633835-3633845 chr4:3633834-3633847 chr4:3633834-3633847 chr4:3633836-3633845 chr4:3633833-3633847 chr4:3633835-3633845
30	EGR1	chr4:3625716-3626099	K562	blood:	n/a	chr4:3625915-3625925 chr4:3625976-3625998 chr4:3625915-3625926 chr4:3626024-3626039 chr4:3625914-3625927 chr4:3625909-3625931 chr4:3625914-3625927
31	ELF1	chr4:3632541-3632762	K562	blood:	n/a	chr4:3632694-3632703 chr4:3632693-3632704 chr4:3632583-3632595 chr4:3632693-3632704 chr4:3632677-3632689
32	ELK1	chr4:3629229-3629372	Hela-S3	cervix:	n/a	n/a
33	EP300	chr4:3625291-3625869	ECC-1	luminal epithelium:	n/a	n/a
34	EP300	chr4:3635823-3635852	HepG2	liver:	n/a	n/a
35	EP300	chr4:3625263-3626233	ECC-1	luminal epithelium:	n/a	n/a
36	EP300	chr4:3622103-3622143	GM12878	blood:	n/a	n/a
37	EP300	chr4:3628677-3628679	GM12878	blood:	n/a	n/a
38	ESR1	chr4:3625438-3626094	ECC-1	luminal epithelium:	n/a	chr4:3625807-3625824
39	ESR1	chr4:3625397-3625964	ECC-1	luminal epithelium:	n/a	chr4:3625807-3625824
40	FOXA1	chr4:3636809-3637050	T-47D	breast:	n/a	chr4:3636915-3636930
41	FOXA1	chr4:3636804-3637027	HepG2	liver:	n/a	chr4:3636915-3636930
42	FOXA1	chr4:3636800-3637049	T-47D	breast:	n/a	chr4:3636915-3636930
43	GATA2	chr4:3621149-3621486	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr4:3621056-3621437	T-47D	breast:	n/a	n/a
45	GATA3	chr4:3621081-3621445	T-47D	breast:	n/a	n/a
46	GTF2F1	chr4:3625365-3625461	H1-hESC	embryonic stem cell:	n/a	n/a
47	HMGN3	chr4:3631471-3631611	K562	blood:	n/a	n/a
48	HMGN3	chr4:3635223-3635351	K562	blood:	n/a	n/a
49	IRF1	chr4:3621887-3622345	K562	blood:	n/a	n/a
50	IRF3	chr4:3624526-3624818	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3630746-3630796	ProgFib	skin:	n/a
2	chr4:3630746-3630796	ProgFib	skin:	n/a
3	chr4:3630746-3630796	SKMC	muscle:	n/a
4	chr4:3630603-3630653	IMR90	lung:	fetal
5	chr4:3630746-3630796	HepG2	liver:	n/a
6	chr4:3630603-3630653	PFSK-1	brain:	n/a
7	chr4:3630746-3630796	K562	blood:	n/a
8	chr4:3630603-3630653	HL-60	blood:	n/a
9	chr4:3630603-3630653	HCT-116	colon:	n/a
10	chr4:3630746-3630796	U87	brain:	n/a
11	chr4:3630603-3630653	LNCaP	prostate:	n/a
12	chr4:3630746-3630796	HRPEpiC	eye:	n/a
13	chr4:3630746-3630796	MCF-7	breast:	n/a
14	chr4:3630603-3630653	HRE	kidney:	n/a
15	chr4:3630746-3630796	Caco-2	colon:	n/a
16	chr4:3630603-3630653	HRCEpiC	kidney:	n/a
17	chr4:3630746-3630796	Jurkat	blood:	n/a
18	chr4:3630746-3630796	HIPEpiC	eye:	n/a
19	chr4:3630746-3630796	A549	lung:	n/a
20	chr4:3630746-3630796	HCT-116	colon:	n/a
21	chr4:3630603-3630653	AG09319	gingival:	n/a
22	chr4:3630746-3630796	HCM	heart:	n/a
23	chr4:3630746-3630796	BE2_C	brain:	n/a
24	chr4:3630746-3630796	HRE	kidney:	n/a
25	chr4:3630603-3630653	Hela-S3	cervix:	n/a
26	chr4:3630603-3630653	GM19239	blood:	n/a
27	chr4:3630746-3630796	Hepatocyte	liver:	n/a
28	chr4:3630603-3630653	A549	lung:	n/a
29	chr4:3630746-3630796	HMEC	breast:	n/a
30	chr4:3630603-3630653	MCF-7	breast:	n/a
31	chr4:3630746-3630796	SK-N-MC	brain:	n/a
32	chr4:3630603-3630653	ovcar-3	ovarian:	n/a
33	chr4:3630746-3630796	RPTEC	kidney:	n/a
34	chr4:3630746-3630796	PFSK-1	brain:	n/a
35	chr4:3630746-3630796	PANC-1	pancreas:	n/a
36	chr4:3630603-3630653	HNPCEpiC	eye:	n/a
37	chr4:3630746-3630796	HL-60	blood:	n/a
38	chr4:3630603-3630653	HepG2	liver:	n/a
39	chr4:3630746-3630796	HCF	heart:	n/a
40	chr4:3630603-3630653	HUVEC	blood vessel:	n/a
41	chr4:3630603-3630653	GM06990	blood:	n/a
42	chr4:3630746-3630796	AG04449	skin:	fetal
43	chr4:3630746-3630796	GM06990	blood:	n/a
44	chr4:3630746-3630796	AoSMC	blood vessel:	n/a
45	chr4:3630603-3630653	SK-N-MC	brain:	n/a
46	chr4:3630746-3630796	SK-N-SH_RA	brain:	n/a
47	chr4:3630603-3630653	HEK293	kidney:	embryo
48	chr4:3630746-3630796	MCF10A-Er-Src	breast:	n/a
49	chr4:3630746-3630796	HAEpiC	amniotic membrane:	n/a
50	chr4:3630603-3630653	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
2	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
3	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
4	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
5	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
6	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
7	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
8	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
9	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
10	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
11	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
12	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
13	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
14	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
2	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250681	CpG island
ENSG00000250681	chromatin interactions
ENSG00000175920	chromatin interactions

Extended variants
information (count: 1106 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557782660	chr4:3621401-3621402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186255088	chr4:3621453-3621454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536761586	chr4:3621485-3621486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556608273	chr4:3621487-3621488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4037430	chr4:3621493-3621494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573918777	chr4:3621517-3621518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542841892	chr4:3621530-3621531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189891159	chr4:3621534-3621535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369469302	chr4:3621561-3621562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4037432	chr4:3621562-3621563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559677312	chr4:3621570-3621571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112364704	chr4:3621586-3621587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10937902	chr4:3621602-3621603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4037433	chr4:3621627-3621628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565284769	chr4:3621628-3621629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146600482	chr4:3621631-3621632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551107399	chr4:3621657-3621658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561336357	chr4:3621676-3621677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530193620	chr4:3621682-3621683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28676715	chr4:3621693-3621694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565734847	chr4:3621720-3621721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534922607	chr4:3621723-3621724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4037434	chr4:3621728-3621729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551349305	chr4:3621779-3621780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2344297	chr4:3621810-3621811	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs55711895	chr4:3621814-3621815	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs56183463	chr4:3621819-3621820	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs397934513	chr4:3621822-3621823	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373198355	chr4:3621839-3621840	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs2344298	chr4:3621845-3621846	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs56287327	chr4:3621851-3621852	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs536622051	chr4:3621860-3621861	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs556517818	chr4:3621881-3621882	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs73081108	chr4:3621885-3621886	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs573437450	chr4:3621891-3621892	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs73204973	chr4:3621906-3621907	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs2344299	chr4:3621913-3621914	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs535934789	chr4:3621925-3621926	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs553576450	chr4:3621926-3621927	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs35651444	chr4:3621928-3621929	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs140148317	chr4:3621954-3621955	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs68120314	chr4:3621956-3621957	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs368859649	chr4:3621989-3621990	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs545691493	chr4:3622009-3622010	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs565402400	chr4:3622010-3622011	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs35864857	chr4:3622034-3622035	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs575730407	chr4:3622057-3622058	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs544644790	chr4:3622065-3622066	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73792556	chr4:3622066-3622067	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs73792557	chr4:3622068-3622069	Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
Urothelial carcinoma	21177765	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
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3621400-3621800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:3621400-3621800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr4:3621800-3622200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:3621800-3622200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr4:3621800-3622200	Active TSS	Duodenum Mucosa	Duodenum
6	chr4:3621800-3622400	Active TSS	Osteobl	bone
7	chr4:3622000-3622400	Bivalent/Poised TSS	Stomach Mucosa	stomach
8	chr4:3622200-3622400	Flanking Active TSS	Duodenum Mucosa	Duodenum
9	chr4:3622200-3622800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr4:3624800-3625400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:3625000-3625400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:3625000-3628000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
13	chr4:3625200-3629400	ZNF genes & repeats	Fetal Brain Female	brain
14	chr4:3625400-3625600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr4:3625400-3625600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr4:3625400-3625600	Bivalent Enhancer	Placenta	Placenta
17	chr4:3625400-3626000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:3625400-3626000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:3625400-3626000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
20	chr4:3625400-3626000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:3625400-3626000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:3625400-3626000	Bivalent Enhancer	Brain Germinal Matrix	brain
23	chr4:3625400-3626000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr4:3625400-3626200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:3625400-3626200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr4:3625400-3626200	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr4:3625400-3626200	Bivalent Enhancer	Fetal Stomach	stomach
28	chr4:3625400-3626200	ZNF genes & repeats	Spleen	Spleen
29	chr4:3625400-3626400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr4:3625400-3626400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr4:3625400-3626400	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr4:3625400-3626800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:3625400-3626800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:3625400-3627000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:3625400-3627800	Enhancers	Fetal Brain Male	brain
36	chr4:3625600-3625800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:3625600-3625800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:3625600-3625800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:3625600-3626000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:3625600-3626000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:3625600-3626000	Enhancers	HSMM	muscle
42	chr4:3625600-3626000	Enhancers	Osteobl	bone
43	chr4:3625600-3626200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:3625600-3626600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
45	chr4:3625600-3626600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:3625800-3626000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:3625800-3626000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:3626000-3627400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:3626000-3628000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:3626800-3627000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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