Variant report

Variant	nsv595423
Chromosome Location	chr4:131915585-132328214
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	chr4:131963666-131963672	K562	blood:	n/a	n/a
2	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
3	ATF3	chr4:132179544-132179772	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:132142159-132142343	K562	blood:	n/a	n/a
5	BACH1	chr4:132164565-132164579	K562	blood:	n/a	n/a
6	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
9	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
10	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
11	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
12	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
13	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
15	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:132128800-132129079	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:132178402-132178703	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:132082475-132082658	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
20	CBX3	chr4:131932433-131932625	K562	blood:	n/a	n/a
21	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
22	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
23	CEBPB	chr4:132046736-132046783	H1-hESC	embryonic stem cell:	n/a	chr4:132046763-132046774
24	CEBPB	chr4:131922292-131922532	IMR90	lung:	n/a	chr4:131922434-131922445
25	CEBPB	chr4:132046637-132046913	A549	lung:	n/a	chr4:132046763-132046774
26	CEBPB	chr4:132046639-132046932	IMR90	lung:	n/a	chr4:132046763-132046774
27	CEBPB	chr4:132184264-132184515	HepG2	liver:	n/a	chr4:132184363-132184376 chr4:132184363-132184374 chr4:132184365-132184376
28	CEBPB	chr4:132002295-132002597	Hela-S3	cervix:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426
29	CEBPB	chr4:132246621-132246930	K562	blood:	n/a	chr4:132246745-132246756
30	CEBPB	chr4:132046618-132046957	HepG2	liver:	n/a	chr4:132046763-132046774
31	CEBPB	chr4:131959580-131959858	IMR90	lung:	n/a	chr4:131959710-131959721 chr4:131959709-131959722
32	CEBPB	chr4:132092555-132092581	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:132002258-132002591	HepG2	liver:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426
34	CEBPB	chr4:132179496-132179815	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
35	CEBPB	chr4:132179525-132179882	H1-hESC	embryonic stem cell:	n/a	chr4:132179698-132179709
36	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267
37	CEBPB	chr4:132179607-132179807	HepG2	liver:	n/a	chr4:132179698-132179709
38	CEBPB	chr4:132110801-132111048	HepG2	liver:	n/a	chr4:132110945-132110956
39	CEBPB	chr4:132002372-132002565	A549	lung:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426
40	CEBPB	chr4:132002265-132002608	IMR90	lung:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426
41	CEBPB	chr4:131918512-131918725	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:132179537-132179884	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
43	CEBPB	chr4:132082393-132083000	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:132002292-132002529	H1-hESC	embryonic stem cell:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426
45	CEBPB	chr4:132123840-132124091	HepG2	liver:	n/a	chr4:132123973-132123984 chr4:132123975-132123986
46	CEBPB	chr4:132179571-132179733	A549	lung:	n/a	chr4:132179698-132179709
47	CEBPB	chr4:132246562-132246885	IMR90	lung:	n/a	chr4:132246745-132246756
48	CEBPB	chr4:132246573-132246902	HepG2	liver:	n/a	chr4:132246745-132246756
49	CEBPB	chr4:131922396-131922473	H1-hESC	embryonic stem cell:	n/a	chr4:131922434-131922445
50	CEBPB	chr4:132002251-132002587	K562	blood:	n/a	chr4:132002415-132002426 chr4:132002417-132002426 chr4:132002415-132002428 chr4:132002415-132002428 chr4:132002417-132002426 chr4:132002416-132002427 chr4:132002417-132002426 chr4:132002417-132002426

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132300589-132300639	ovcar-3	ovarian:	n/a
2	chr4:132273830-132273880	MCF10A-Er-Src	breast:	n/a
3	chr4:132273830-132273880	HNPCEpiC	eye:	n/a
4	chr4:132273830-132273880	HCM	heart:	n/a
5	chr4:132300589-132300639	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:132273830-132273880	Caco-2	colon:	n/a
7	chr4:132273830-132273880	AG04450	lung:	fetal
8	chr4:132273830-132273880	RPTEC	kidney:	n/a
9	chr4:132300589-132300639	AG09319	gingival:	n/a
10	chr4:132300589-132300639	PFSK-1	brain:	n/a
11	chr4:132273830-132273880	Hepatocyte	liver:	n/a
12	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
13	chr4:132300589-132300639	SK-N-MC	brain:	n/a
14	chr4:132300589-132300639	HEK293	kidney:	embryo
15	chr4:132273830-132273880	GM06990	blood:	n/a
16	chr4:132300589-132300639	AG09309	skin:	n/a
17	chr4:132273830-132273880	SAEC	small airway:	n/a
18	chr4:132300589-132300639	GM06990	blood:	n/a
19	chr4:132273830-132273880	K562	blood:	n/a
20	chr4:132300589-132300639	MCF10A-Er-Src	breast:	n/a
21	chr4:132300589-132300639	LNCaP	prostate:	n/a
22	chr4:132300589-132300639	HMEC	breast:	n/a
23	chr4:132273830-132273880	NT2-D1	testis:	n/a
24	chr4:132273830-132273880	NHBE	bronchial:	n/a
25	chr4:132300589-132300639	SK-N-SH	brain:	n/a
26	chr4:132300589-132300639	HUVEC	blood vessel:	n/a
27	chr4:132300589-132300639	Jurkat	blood:	n/a
28	chr4:132300589-132300639	PANC-1	pancreas:	n/a
29	chr4:132273830-132273880	HL-60	blood:	n/a
30	chr4:132273830-132273880	BE2_C	brain:	n/a
31	chr4:132300589-132300639	BJ	skin:	n/a
32	chr4:132300589-132300639	SKMC	muscle:	n/a
33	chr4:132300589-132300639	HCPEpiC	choroid plexus:	n/a
34	chr4:132300589-132300639	HRPEpiC	eye:	n/a
35	chr4:132300589-132300639	RPTEC	kidney:	n/a
36	chr4:132273830-132273880	H1-hESC	embryonic stem cell:	embryo
37	chr4:132300589-132300639	HRCEpiC	kidney:	n/a
38	chr4:132273830-132273880	Hela-S3	cervix:	n/a
39	chr4:132300589-132300639	U87	brain:	n/a
40	chr4:132273830-132273880	NB4	blood:	n/a
41	chr4:132300589-132300639	HepG2	liver:	n/a
42	chr4:132300589-132300639	HAEpiC	amniotic membrane:	n/a
43	chr4:132300589-132300639	SAEC	small airway:	n/a
44	chr4:132300589-132300639	K562	blood:	n/a
45	chr4:132300589-132300639	Caco-2	colon:	n/a
46	chr4:132300589-132300639	NH-A	brain:	n/a
47	chr4:132273830-132273880	HEEpiC	esophagus:	n/a
48	chr4:132273830-132273880	IMR90	lung:	fetal
49	chr4:132300589-132300639	IMR90	lung:	fetal
50	chr4:132273830-132273880	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
2	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
3	chr4:132050225..132052503-chr4:132053839..132055546,2	MCF-7	breast:
4	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
5	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
6	chr4:88902738..88903615-chr4:132032553..132033450,2	MCF-7	breast:
7	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
8	chr4:132012841..132013396-chr4:132565892..132566443,2	MCF-7	breast:
9	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
10	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
11	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
12	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
13	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
14	chr2:52859439..52860286-chr4:132071047..132072003,2	MCF-7	breast:
15	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
16	chr4:132050225..132052503-chr4:132053839..132055546,2	MCF-7	breast:
17	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
18	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
19	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
20	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
21	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311
2	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1

Variant related genes	Relation type
RNU6-224P	TF binding region
ENSG00000250102	TF binding region
ENSG00000250213	TF binding region
RNU6-224P	CpG island
ENSG00000250102	CpG island
ENSG00000250213	CpG island

Extended variants
information (count: 2699 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2699 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1392617	chr4:131915585-131915586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553858503	chr4:131916604-131916605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574784881	chr4:131916719-131916720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577036456	chr4:131916754-131916755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111660731	chr4:131916771-131916772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536924095	chr4:131916785-131916786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576185746	chr4:131916799-131916800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563686299	chr4:131916869-131916870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557812204	chr4:131916934-131916935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11941696	chr4:131916948-131916949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555382536	chr4:131916973-131916974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572060101	chr4:131916978-131916979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541047003	chr4:131916991-131916992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537846777	chr4:131917044-131917045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545546934	chr4:131917123-131917124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191378416	chr4:131917290-131917291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182798171	chr4:131917365-131917366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543578256	chr4:131917391-131917392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115688090	chr4:131917392-131917393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529506806	chr4:131917396-131917397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549615571	chr4:131917407-131917408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149972987	chr4:131917424-131917425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527252343	chr4:131917425-131917426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188662476	chr4:131917470-131917471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570497620	chr4:131917474-131917475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539498485	chr4:131917539-131917540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561840837	chr4:131917553-131917554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192054759	chr4:131917597-131917598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535294270	chr4:131917598-131917599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145249811	chr4:131917600-131917601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189760191	chr4:131918208-131918209	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs543179589	chr4:131918221-131918222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs372161909	chr4:131918314-131918315	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs573525768	chr4:131918351-131918352	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs572764126	chr4:131918352-131918353	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs140714465	chr4:131918392-131918393	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs184563305	chr4:131918616-131918617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563328915	chr4:131918630-131918631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528958128	chr4:131918631-131918632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150074909	chr4:131918638-131918639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565527170	chr4:131918664-131918665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs386679565	chr4:131918667-131918668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138480974	chr4:131918669-131918670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149280908	chr4:131918689-131918690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537419899	chr4:131918694-131918695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539855305	chr4:131918776-131918777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557065397	chr4:131918855-131918856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574009145	chr4:131918878-131918879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147373420	chr4:131918897-131918898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs138159535	chr4:131918905-131918906	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Thoracic aortic aneurysm	21092924	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
Breast cancer	16272173	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
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
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:188 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131915200-131915600	Enhancers	Fetal Kidney	kidney
2	chr4:131916600-131917600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:131918200-131918400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:131918600-131919400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:131918800-131919200	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:131919000-131919800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:131919800-131923400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:131922200-131924000	Enhancers	HUVEC	blood vessel
9	chr4:131922600-131924200	Enhancers	NHEK	skin
10	chr4:131923400-131924000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:131931400-131932800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:131932000-131933000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:131932000-131933600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:131932800-131933600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:131933000-131933400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:131933400-131933600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:131933400-131933600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:131933400-131933800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:131933400-131933800	Enhancers	H1 Cell Line	embryonic stem cell
20	chr4:131933400-131933800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr4:131933400-131933800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:131933400-131935200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:131933400-131935400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr4:131933400-131935800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:131933600-131934000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
26	chr4:131933600-131934800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:131933600-131935000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:131933600-131935000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:131933800-131934800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:131933800-131934800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:131933800-131935000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr4:131933800-131935000	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr4:131934400-131935200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr4:131934800-131935000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:131934800-131935800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:131935000-131935200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr4:131935000-131935200	Enhancers	H9 Cell Line	embryonic stem cell
38	chr4:131935000-131935200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:131935000-131935400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:131935000-131935600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:131935200-131935400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
42	chr4:131935200-131935600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr4:131940000-131940800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:131949400-131949800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:131959800-131960600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:131972200-131972600	Enhancers	Fetal Heart	heart
47	chr4:131982400-131983000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:131982400-131983200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:131982400-131983400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:131982600-131983400	ZNF genes & repeats	Dnd41	blood

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