Variant report

Variant	esv3431883
Chromosome Location	chr4:3618554-3637152
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	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
8	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
9	CTCF	chr4:3621400-3621550	A549	lung:	n/a	n/a
10	CTCF	chr4:3629970-3629976	K562	blood:	n/a	n/a
11	CTCF	chr4:3621620-3621770	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:3619474-3619496	GM20000	blood:	n/a	n/a
13	CTCF	chr4:3621500-3621650	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr4:3621200-3621350	HVMF	connective:	n/a	n/a
15	CTCF	chr4:3621280-3621430	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:3621580-3621730	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr4:3621640-3621790	NB4	blood:	n/a	n/a
18	CTCF	chr4:3621260-3621410	HVMF	connective:	n/a	n/a
19	CUX1	chr4:3631334-3631484	K562	blood:	n/a	n/a
20	E2F4	chr4:3620613-3620843	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr4:3622097-3622427	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F6	chr4:3628336-3628473	K562	blood:	n/a	n/a
23	E2F6	chr4:3628073-3628656	H1-hESC	embryonic stem cell:	n/a	n/a
24	E2F6	chr4:3632546-3632710	K562	blood:	n/a	n/a
25	E2F6	chr4:3628166-3628626	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr4:3625716-3626099	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
28	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
29	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
30	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
31	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
32	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
33	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
34	ELF1	chr4:3632541-3632762	K562	blood:	n/a	chr4:3632694-3632703 chr4:3632693-3632704 chr4:3632583-3632595 chr4:3632693-3632704 chr4:3632677-3632689
35	ELK1	chr4:3629229-3629372	Hela-S3	cervix:	n/a	n/a
36	EP300	chr4:3635823-3635852	HepG2	liver:	n/a	n/a
37	EP300	chr4:3628677-3628679	GM12878	blood:	n/a	n/a
38	EP300	chr4:3625291-3625869	ECC-1	luminal epithelium:	n/a	n/a
39	EP300	chr4:3622103-3622143	GM12878	blood:	n/a	n/a
40	EP300	chr4:3625263-3626233	ECC-1	luminal epithelium:	n/a	n/a
41	ESR1	chr4:3625438-3626094	ECC-1	luminal epithelium:	n/a	chr4:3625807-3625824
42	ESR1	chr4:3625397-3625964	ECC-1	luminal epithelium:	n/a	chr4:3625807-3625824
43	FOXA1	chr4:3636800-3637049	T-47D	breast:	n/a	chr4:3636915-3636930
44	FOXA1	chr4:3636804-3637027	HepG2	liver:	n/a	chr4:3636915-3636930
45	FOXA1	chr4:3636809-3637050	T-47D	breast:	n/a	chr4:3636915-3636930
46	GATA2	chr4:3621149-3621486	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr4:3621081-3621445	T-47D	breast:	n/a	n/a
48	GATA3	chr4:3621056-3621437	T-47D	breast:	n/a	n/a
49	GTF2F1	chr4:3625365-3625461	H1-hESC	embryonic stem cell:	n/a	n/a
50	HMGN3	chr4:3635223-3635351	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3630746-3630796	HRPEpiC	eye:	n/a
2	chr4:3630746-3630796	Jurkat	blood:	n/a
3	chr4:3630746-3630796	HAEpiC	amniotic membrane:	n/a
4	chr4:3630603-3630653	HEEpiC	esophagus:	n/a
5	chr4:3630603-3630653	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:3630603-3630653	K562	blood:	n/a
7	chr4:3630603-3630653	AG04450	lung:	fetal
8	chr4:3630603-3630653	SK-N-SH_RA	brain:	n/a
9	chr4:3630746-3630796	HCM	heart:	n/a
10	chr4:3630746-3630796	HIPEpiC	eye:	n/a
11	chr4:3630603-3630653	A549	lung:	n/a
12	chr4:3630746-3630796	SK-N-MC	brain:	n/a
13	chr4:3630603-3630653	NHBE	bronchial:	n/a
14	chr4:3630746-3630796	NHBE	bronchial:	n/a
15	chr4:3630746-3630796	AG09309	skin:	n/a
16	chr4:3630603-3630653	GM12892	blood:	n/a
17	chr4:3630603-3630653	GM19239	blood:	n/a
18	chr4:3630603-3630653	HRCEpiC	kidney:	n/a
19	chr4:3630603-3630653	HRE	kidney:	n/a
20	chr4:3630746-3630796	MCF10A-Er-Src	breast:	n/a
21	chr4:3630603-3630653	ProgFib	skin:	n/a
22	chr4:3630746-3630796	PFSK-1	brain:	n/a
23	chr4:3630746-3630796	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:3630746-3630796	NH-A	brain:	n/a
25	chr4:3630746-3630796	HEK293	kidney:	embryo
26	chr4:3630746-3630796	AG04450	lung:	fetal
27	chr4:3630746-3630796	RPTEC	kidney:	n/a
28	chr4:3630603-3630653	HUVEC	blood vessel:	n/a
29	chr4:3630746-3630796	NT2-D1	testis:	n/a
30	chr4:3630746-3630796	IMR90	lung:	fetal
31	chr4:3630603-3630653	RPTEC	kidney:	n/a
32	chr4:3630746-3630796	GM19239	blood:	n/a
33	chr4:3630603-3630653	MCF10A-Er-Src	breast:	n/a
34	chr4:3630746-3630796	HRE	kidney:	n/a
35	chr4:3630603-3630653	HCM	heart:	n/a
36	chr4:3630746-3630796	HCF	heart:	n/a
37	chr4:3630746-3630796	HRCEpiC	kidney:	n/a
38	chr4:3630603-3630653	H1-hESC	embryonic stem cell:	embryo
39	chr4:3630603-3630653	NB4	blood:	n/a
40	chr4:3630746-3630796	H1-hESC	embryonic stem cell:	embryo
41	chr4:3630746-3630796	HNPCEpiC	eye:	n/a
42	chr4:3630603-3630653	HEK293	kidney:	embryo
43	chr4:3630746-3630796	GM12878	blood:	n/a
44	chr4:3630603-3630653	PANC-1	pancreas:	n/a
45	chr4:3630603-3630653	BE2_C	brain:	n/a
46	chr4:3630746-3630796	SK-N-SH	brain:	n/a
47	chr4:3630603-3630653	BJ	skin:	n/a
48	chr4:3630603-3630653	SAEC	small airway:	n/a
49	chr4:3630746-3630796	A549	lung:	n/a
50	chr4:3630746-3630796	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
2	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
3	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
4	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
5	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
6	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
7	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
8	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
9	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
10	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
11	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
12	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
13	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
14	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
15	chr4:3621204..3623586-chr4:3624430..3626099,2	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
ENSG00000175920	chromatin interactions
ENSG00000250681	chromatin interactions

Extended variants
information (count: 1204 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560687446	chr4:3618572-3618573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531481680	chr4:3618587-3618588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548824766	chr4:3618594-3618595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141146548	chr4:3618616-3618617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574765029	chr4:3618652-3618653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575613331	chr4:3618666-3618667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112946341	chr4:3618667-3618668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540877492	chr4:3618678-3618679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs5855799	chr4:3618679-3618680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568681101	chr4:3618689-3618690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4259009	chr4:3618694-3618695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs5855798	chr4:3618727-3618728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534356397	chr4:3618728-3618729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557185998	chr4:3618736-3618737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147239079	chr4:3618760-3618761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571085238	chr4:3618761-3618762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs5855797	chr4:3618781-3618782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140803897	chr4:3618785-3618786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540110390	chr4:3618792-3618793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565563598	chr4:3618795-3618796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532703901	chr4:3618800-3618801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10937899	chr4:3618809-3618810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535554821	chr4:3618843-3618844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74544288	chr4:3618852-3618853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374610444	chr4:3618859-3618860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200140293	chr4:3618883-3618884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115774726	chr4:3618886-3618887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368430941	chr4:3618895-3618896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530352001	chr4:3618902-3618903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10937900	chr4:3618920-3618921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76075794	chr4:3618921-3618922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115853015	chr4:3618940-3618941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151091529	chr4:3618967-3618968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10937901	chr4:3618975-3618976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371864831	chr4:3618984-3618985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111216228	chr4:3619004-3619005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111065374	chr4:3619017-3619018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111064817	chr4:3619033-3619034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111203551	chr4:3619066-3619067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111216065	chr4:3619102-3619103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552296020	chr4:3619111-3619112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150409072	chr4:3619124-3619125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577106403	chr4:3619125-3619126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115077138	chr4:3619150-3619151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114401801	chr4:3619194-3619195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562348717	chr4:3619202-3619203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186590118	chr4:3619273-3619274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144281803	chr4:3619299-3619300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs71181306	chr4:3619304-3619305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548322515	chr4:3619320-3619321	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Ependymoma	20639864	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:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3615600-3619600	Enhancers	Fetal Brain Male	brain
2	chr4:3621400-3621800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:3621400-3621800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:3621800-3622200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:3621800-3622200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr4:3621800-3622200	Active TSS	Duodenum Mucosa	Duodenum
7	chr4:3621800-3622400	Active TSS	Osteobl	bone
8	chr4:3622000-3622400	Bivalent/Poised TSS	Stomach Mucosa	stomach
9	chr4:3622200-3622400	Flanking Active TSS	Duodenum Mucosa	Duodenum
10	chr4:3622200-3622800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:3624800-3625400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:3625000-3625400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:3625000-3628000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
14	chr4:3625200-3629400	ZNF genes & repeats	Fetal Brain Female	brain
15	chr4:3625400-3625600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:3625400-3625600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr4:3625400-3625600	Bivalent Enhancer	Placenta	Placenta
18	chr4:3625400-3626000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:3625400-3626000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:3625400-3626000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
21	chr4:3625400-3626000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:3625400-3626000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:3625400-3626000	Bivalent Enhancer	Brain Germinal Matrix	brain
24	chr4:3625400-3626000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr4:3625400-3626200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:3625400-3626200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr4:3625400-3626200	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr4:3625400-3626200	Bivalent Enhancer	Fetal Stomach	stomach
29	chr4:3625400-3626200	ZNF genes & repeats	Spleen	Spleen
30	chr4:3625400-3626400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
31	chr4:3625400-3626400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
32	chr4:3625400-3626400	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr4:3625400-3626800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:3625400-3626800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr4:3625400-3627000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:3625400-3627800	Enhancers	Fetal Brain Male	brain
37	chr4:3625600-3625800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:3625600-3625800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:3625600-3625800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:3625600-3626000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:3625600-3626000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr4:3625600-3626000	Enhancers	HSMM	muscle
43	chr4:3625600-3626000	Enhancers	Osteobl	bone
44	chr4:3625600-3626200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:3625600-3626600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr4:3625600-3626600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:3625800-3626000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:3625800-3626000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:3626000-3627400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:3626000-3628000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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