Variant report

Variant	esv993737
Chromosome Location	chr4:618112-628837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:87)
CpG islands
(count:1098)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:87 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:618888-618908	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:623849-624084	HepG2	liver:	n/a	chr4:623964-623975
3	CHD2	chr4:618839-618975	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr4:621316-621357	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr4:618860-619010	HepG2	liver:	n/a	n/a
6	CTCF	chr4:618826-619035	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:618794-618986	K562	blood:	n/a	n/a
8	CTCF	chr4:618891-618972	K562	blood:	n/a	n/a
9	CTCF	chr4:618840-618990	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr4:628180-628330	WERI-Rb-1	eye:	n/a	chr4:628229-628247
11	CTCF	chr4:618912-618944	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:628141-628388	K562	blood:	n/a	chr4:628229-628247
13	CTCF	chr4:618820-618970	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr4:619920-620070	WERI-Rb-1	eye:	n/a	chr4:620031-620044
15	CTCF	chr4:623120-623270	GM12874	blood:	n/a	chr4:623175-623193
16	CTCF	chr4:618840-618990	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr4:618740-618890	HRE	kidney:	n/a	chr4:618772-618785 chr4:618786-618794
18	CTCF	chr4:618780-618930	WERI-Rb-1	eye:	n/a	chr4:618786-618794
19	CTCF	chr4:618754-619011	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
20	CTCF	chr4:628003-628071	H1-hESC	embryonic stem cell:	n/a	chr4:628052-628070 chr4:628055-628068
21	CTCF	chr4:628145-628346	HepG2	liver:	n/a	chr4:628229-628247
22	CTCF	chr4:628779-628837	GM20000	blood:	n/a	n/a
23	CTCF	chr4:627960-628110	WERI-Rb-1	eye:	n/a	chr4:628052-628070 chr4:628055-628068
24	CTCF	chr4:618699-619112	K562	blood:	n/a	chr4:618772-618785 chr4:618786-618794
25	CTCF	chr4:628144-628353	K562	blood:	n/a	chr4:628229-628247
26	CTCF	chr4:618869-618959	HepG2	liver:	n/a	n/a
27	CTCF	chr4:618840-618990	HepG2	liver:	n/a	n/a
28	CTCF	chr4:628140-628290	HepG2	liver:	n/a	chr4:628229-628247
29	CTCF	chr4:618820-618970	K562	blood:	n/a	n/a
30	CTCF	chr4:618974-618975	K562	blood:	n/a	n/a
31	CTCF	chr4:618880-619030	HRE	kidney:	n/a	n/a
32	CTCF	chr4:618735-619001	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
33	CTCF	chr4:628817-628980	Lung_OC	lung:	n/a	n/a
34	CTCF	chr4:618768-619128	H1-hESC	embryonic stem cell:	n/a	chr4:618772-618785 chr4:618786-618794
35	CTCF	chr4:628084-628374	K562	blood:	n/a	chr4:628229-628247
36	EBF1	chr4:619019-619131	GM12878	blood:	n/a	chr4:619099-619110
37	EGR1	chr4:619186-619431	K562	blood:	n/a	n/a
38	EGR1	chr4:619143-619455	K562	blood:	n/a	n/a
39	ELF1	chr4:621072-621300	K562	blood:	n/a	n/a
40	ESR1	chr4:618978-619401	ECC-1	luminal epithelium:	n/a	n/a
41	GABPA	chr4:618744-619078	H1-hESC	embryonic stem cell:	n/a	n/a
42	HMGN3	chr4:620665-620704	K562	blood:	n/a	n/a
43	KAP1	chr4:625376-625576	HEK293	kidney:	n/a	n/a
44	MAFK	chr4:619042-619412	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr4:618837-619779	ECC-1	luminal epithelium:	n/a	n/a
46	MAX	chr4:618140-618245	NB4	blood:	n/a	n/a
47	MAX	chr4:618870-619756	ECC-1	luminal epithelium:	n/a	n/a
48	MYC	chr4:618289-618301	MCF-7	breast:	n/a	n/a
49	NFIC	chr4:618808-619891	ECC-1	luminal epithelium:	n/a	n/a
50	NFIC	chr4:618843-619815	ECC-1	luminal epithelium:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:622887-622937	MCF10A-Er-Src	breast:	n/a
2	chr4:618114-618164	A549	lung:	n/a
3	chr4:619314-619364	SK-N-SH_RA	brain:	n/a
4	chr4:618204-618254	HRPEpiC	eye:	n/a
5	chr4:618114-618164	SAEC	small airway:	n/a
6	chr4:618204-618254	GM12878	blood:	n/a
7	chr4:618332-618382	HCPEpiC	choroid plexus:	n/a
8	chr4:618549-618599	HNPCEpiC	eye:	n/a
9	chr4:618753-618803	ProgFib	skin:	n/a
10	chr4:619865-619915	HRPEpiC	eye:	n/a
11	chr4:622887-622937	NH-A	brain:	n/a
12	chr4:618114-618164	SK-N-MC	brain:	n/a
13	chr4:619272-619322	NHBE	bronchial:	n/a
14	chr4:619635-619685	HRPEpiC	eye:	n/a
15	chr4:622887-622937	Hela-S3	cervix:	n/a
16	chr4:618753-618803	HEEpiC	esophagus:	n/a
17	chr4:618497-618547	HEK293	kidney:	embryo
18	chr4:622887-622937	GM06990	blood:	n/a
19	chr4:618204-618254	HEEpiC	esophagus:	n/a
20	chr4:619167-619217	MCF10A-Er-Src	breast:	n/a
21	chr4:628649-628699	HUVEC	blood vessel:	n/a
22	chr4:619865-619915	A549	lung:	n/a
23	chr4:619635-619685	AG09309	skin:	n/a
24	chr4:619392-619442	AG09309	skin:	n/a
25	chr4:618332-618382	SK-N-SH_RA	brain:	n/a
26	chr4:619392-619442	GM12891	blood:	n/a
27	chr4:619314-619364	LNCaP	prostate:	n/a
28	chr4:622887-622937	SKMC	muscle:	n/a
29	chr4:619659-619709	T-47D	breast:	n/a
30	chr4:619865-619915	GM06990	blood:	n/a
31	chr4:619162-619212	AoSMC	blood vessel:	n/a
32	chr4:618204-618254	CMK	blood:	n/a
33	chr4:628649-628699	GM19239	blood:	n/a
34	chr4:618753-618803	RPTEC	kidney:	n/a
35	chr4:619635-619685	Hepatocyte	liver:	n/a
36	chr4:622887-622937	GM19239	blood:	n/a
37	chr4:619392-619442	ProgFib	skin:	n/a
38	chr4:628649-628699	HRCEpiC	kidney:	n/a
39	chr4:619392-619442	SK-N-SH	brain:	n/a
40	chr4:619167-619217	ProgFib	skin:	n/a
41	chr4:621306-621356	ECC-1	luminal epithelium:	n/a
42	chr4:621306-621356	BJ	skin:	n/a
43	chr4:618497-618547	SK-N-SH	brain:	n/a
44	chr4:618332-618382	NB4	blood:	n/a
45	chr4:619865-619915	NH-A	brain:	n/a
46	chr4:619314-619364	RPTEC	kidney:	n/a
47	chr4:618204-618254	NHDF-neo	bronchial:	n/a
48	chr4:619865-619915	HL-60	blood:	n/a
49	chr4:619272-619322	LNCaP	prostate:	n/a
50	chr4:618549-618599	K562	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
2	chr4:492359..493966-chr4:619634..621403,2	K562	blood:
3	chr4:624127..625792-chr4:659574..661910,2	K562	blood:
4	chr4:615876..617771-chr4:628086..630978,3	K562	blood:
5	chr4:618337..620311-chr4:627716..629406,2	MCF-7	breast:
6	chr4:611669..613220-chr4:626593..629173,2	MCF-7	breast:
7	chr4:626004..628523-chr4:666543..668678,2	K562	blood:
8	chr4:627338..629172-chr4:662112..664476,2	MCF-7	breast:
9	chr4:626527..629135-chr4:629423..631548,2	MCF-7	breast:
10	chr4:619501..622132-chr4:622263..626030,4	MCF-7	breast:
11	chr4:623895..625703-chr4:641254..643295,2	K562	blood:
12	chr4:619437..623881-chr4:666212..669300,4	MCF-7	breast:

No data

Variant related genes	Relation type
PDE6B	TF binding region
PDE6B	CpG island
ENSG00000133256	chromatin interactions
ENSG00000174227	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000182903	chromatin interactions
ENSG00000169020	chromatin interactions

Extended variants
information (count: 589 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535289323	chr4:618140-618141	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs188568146	chr4:618188-618189	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs374883233	chr4:618192-618193	Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191813455	chr4:618202-618203	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs77031975	chr4:618242-618243	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs183607530	chr4:618285-618286	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149039703	chr4:618291-618292	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576072140	chr4:618295-618296	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs543178212	chr4:618311-618312	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs138097749	chr4:618322-618323	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs376931724	chr4:618323-618324	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs189640817	chr4:618330-618331	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550012871	chr4:618343-618344	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs71602485	chr4:618359-618360	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs548807502	chr4:618392-618393	Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs560723219	chr4:618407-618408	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs187607896	chr4:618414-618415	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs552536741	chr4:618434-618435	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs539006371	chr4:618464-618465	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs201097535	chr4:618466-618467	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs10027392	chr4:618477-618478	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs369240625	chr4:618478-618479	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs538315596	chr4:618487-618488	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs549979257	chr4:618529-618530	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs568231689	chr4:618534-618535	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs76343285	chr4:618544-618545	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs189894605	chr4:618549-618550	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs9998776	chr4:618579-618580	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373422319	chr4:618585-618586	Enhancers Genic enhancers ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs181434166	chr4:618623-618624	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs557711341	chr4:618625-618626	Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs575917272	chr4:618650-618651	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543418855	chr4:618666-618667	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561723477	chr4:618667-618668	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs9998967	chr4:618720-618721	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs9998968	chr4:618728-618729	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs185917202	chr4:618729-618730	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs115359246	chr4:618733-618734	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs552622986	chr4:618737-618738	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs564824529	chr4:618743-618744	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs555117939	chr4:618750-618751	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs531573526	chr4:618753-618754	Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs550160336	chr4:618786-618787	Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs147090420	chr4:618789-618790	Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs529386359	chr4:618793-618794	Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs370113051	chr4:618799-618800	Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs565566292	chr4:618823-618824	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs73056568	chr4:618842-618843	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555367998	chr4:618891-618892	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs141673012	chr4:618893-618894	Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
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
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:615800-618200	Enhancers	Brain Substantia Nigra	brain
2	chr4:616200-618200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:616200-618400	Enhancers	Brain Angular Gyrus	brain
4	chr4:616800-624200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:617000-618200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr4:617200-618200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr4:617200-619800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:617600-619600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:617600-619800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:617600-620000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr4:617600-620200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:617600-620200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:617800-618200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:618000-618400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:618000-619800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:618200-618400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:618200-618400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:618200-618400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr4:618200-618800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr4:618200-618800	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr4:618200-619200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:618200-619200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:618200-619200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:618200-619200	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:618200-619600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:618200-619600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:618400-619200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:618400-619200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr4:618600-619200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:618800-620000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr4:619000-619400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr4:619200-620200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr4:619200-624000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:619600-620000	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:619600-626000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:619800-621400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:620000-621200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr4:620000-622800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:620200-620400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:620600-620800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:620800-621000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:621200-621400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:621200-621400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr4:621400-621800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:621800-624000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:622000-624200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr4:622200-623000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr4:622800-623000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:623000-623200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:623000-625000	Enhancers	Fetal Muscle Leg	muscle

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