Variant report

Variant	esv34850
Chromosome Location	chr4:131920334-132351655
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	ATF2	chr4:132347459-132347932	GM12878	blood:	n/a	n/a
4	ATF2	chr4:132347383-132348003	GM12878	blood:	n/a	n/a
5	ATF3	chr4:132179544-132179772	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:132142159-132142343	K562	blood:	n/a	n/a
7	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:132164565-132164579	K562	blood:	n/a	n/a
10	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
11	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
12	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
13	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
14	BATF	chr4:132347469-132347900	GM12878	blood:	n/a	n/a
15	BATF	chr4:132347572-132347877	GM12878	blood:	n/a	n/a
16	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
17	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
18	BCL11A	chr4:132347442-132347953	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:132347576-132347893	GM12878	blood:	n/a	n/a
22	BCL3	chr4:132347488-132347811	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:132347460-132347821	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:132347567-132347910	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:132347604-132347811	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:132128800-132129079	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:132178402-132178703	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:132082475-132082658	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr4:131932433-131932625	K562	blood:	n/a	n/a
30	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
31	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
32	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
33	CEBPB	chr4:132092555-132092581	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:131959563-131959894	HepG2	liver:	n/a	chr4:131959710-131959721 chr4:131959709-131959722
35	CEBPB	chr4:132179607-132179807	HepG2	liver:	n/a	chr4:132179698-132179709
36	CEBPB	chr4:132046639-132046932	IMR90	lung:	n/a	chr4:132046763-132046774
37	CEBPB	chr4:132046736-132046783	H1-hESC	embryonic stem cell:	n/a	chr4:132046763-132046774
38	CEBPB	chr4:132334417-132334650	HepG2	liver:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
39	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
40	CEBPB	chr4:131922292-131922532	IMR90	lung:	n/a	chr4:131922434-131922445
41	CEBPB	chr4:131959580-131959858	IMR90	lung:	n/a	chr4:131959710-131959721 chr4:131959709-131959722
42	CEBPB	chr4:132110801-132111048	HepG2	liver:	n/a	chr4:132110945-132110956
43	CEBPB	chr4:132316111-132316328	HepG2	liver:	n/a	chr4:132316170-132316181 chr4:132316241-132316252 chr4:132316170-132316183 chr4:132316241-132316254 chr4:132316241-132316254
44	CEBPB	chr4:132046618-132046957	HepG2	liver:	n/a	chr4:132046763-132046774
45	CEBPB	chr4:132184264-132184515	HepG2	liver:	n/a	chr4:132184363-132184376 chr4:132184363-132184374 chr4:132184365-132184376
46	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
47	CEBPB	chr4:132179537-132179884	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
48	CEBPB	chr4:132082393-132083000	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:132110833-132110991	H1-hESC	embryonic stem cell:	n/a	chr4:132110945-132110956
50	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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132300589-132300639	IMR90	lung:	fetal
2	chr4:132300589-132300639	Hela-S3	cervix:	n/a
3	chr4:132300589-132300639	GM06990	blood:	n/a
4	chr4:132300589-132300639	BE2_C	brain:	n/a
5	chr4:132273830-132273880	NH-A	brain:	n/a
6	chr4:132273830-132273880	A549	lung:	n/a
7	chr4:132273830-132273880	PrEC	prostate:	n/a
8	chr4:132300589-132300639	Hepatocyte	liver:	n/a
9	chr4:132273830-132273880	MCF10A-Er-Src	breast:	n/a
10	chr4:132273830-132273880	IMR90	lung:	fetal
11	chr4:132273830-132273880	AG04449	skin:	fetal
12	chr4:132273830-132273880	ECC-1	luminal epithelium:	n/a
13	chr4:132300589-132300639	NHDF-neo	bronchial:	n/a
14	chr4:132273830-132273880	HRE	kidney:	n/a
15	chr4:132300589-132300639	NH-A	brain:	n/a
16	chr4:132273830-132273880	AG09309	skin:	n/a
17	chr4:132300589-132300639	HUVEC	blood vessel:	n/a
18	chr4:132273830-132273880	NB4	blood:	n/a
19	chr4:132300589-132300639	GM12878	blood:	n/a
20	chr4:132300589-132300639	HCM	heart:	n/a
21	chr4:132300589-132300639	AoSMC	blood vessel:	n/a
22	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
23	chr4:132300589-132300639	SKMC	muscle:	n/a
24	chr4:132273830-132273880	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:132273830-132273880	GM12891	blood:	n/a
26	chr4:132273830-132273880	AoSMC	blood vessel:	n/a
27	chr4:132273830-132273880	Jurkat	blood:	n/a
28	chr4:132300589-132300639	PFSK-1	brain:	n/a
29	chr4:132300589-132300639	SK-N-SH	brain:	n/a
30	chr4:132300589-132300639	ovcar-3	ovarian:	n/a
31	chr4:132273830-132273880	HRPEpiC	eye:	n/a
32	chr4:132300589-132300639	GM19239	blood:	n/a
33	chr4:132300589-132300639	AG09319	gingival:	n/a
34	chr4:132300589-132300639	Caco-2	colon:	n/a
35	chr4:132300589-132300639	A549	lung:	n/a
36	chr4:132273830-132273880	Hepatocyte	liver:	n/a
37	chr4:132300589-132300639	LNCaP	prostate:	n/a
38	chr4:132273830-132273880	BJ	skin:	n/a
39	chr4:132273830-132273880	Caco-2	colon:	n/a
40	chr4:132300589-132300639	AG04450	lung:	fetal
41	chr4:132273830-132273880	SK-N-MC	brain:	n/a
42	chr4:132300589-132300639	SAEC	small airway:	n/a
43	chr4:132300589-132300639	MCF-7	breast:	n/a
44	chr4:132273830-132273880	LNCaP	prostate:	n/a
45	chr4:132300589-132300639	NB4	blood:	n/a
46	chr4:132300589-132300639	SK-N-MC	brain:	n/a
47	chr4:132273830-132273880	ovcar-3	ovarian:	n/a
48	chr4:132273830-132273880	RPTEC	kidney:	n/a
49	chr4:132273830-132273880	GM12878	blood:	n/a
50	chr4:132273830-132273880	HEK293	kidney:	embryo

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

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
ENSG00000250102	TF binding region
ENSG00000250213	TF binding region
RNU6-224P	TF binding region
ENSG00000250102	CpG island
ENSG00000250213	CpG island
RNU6-224P	CpG island

Extended variants
information (count: 2745 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2745 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12647096	chr4:131920334-131920335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537310599	chr4:131920370-131920371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180988495	chr4:131920378-131920379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552339082	chr4:131920421-131920422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs137970567	chr4:131920459-131920460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143632660	chr4:131920486-131920487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548750281	chr4:131920491-131920492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147185647	chr4:131920537-131920538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138655361	chr4:131920633-131920634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149332831	chr4:131920648-131920649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144589386	chr4:131920667-131920668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148729525	chr4:131920674-131920675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558334740	chr4:131920693-131920694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373464859	chr4:131920833-131920834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575282711	chr4:131920834-131920835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577339362	chr4:131920888-131920889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368111716	chr4:131920913-131920914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10684440	chr4:131920936-131920937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367749002	chr4:131920939-131920940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372140174	chr4:131920941-131920942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376798639	chr4:131920942-131920943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368315255	chr4:131920950-131920951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143576856	chr4:131920974-131920975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186109916	chr4:131921009-131921010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146334854	chr4:131921046-131921047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546357117	chr4:131921102-131921103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139568722	chr4:131921136-131921137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560465655	chr4:131921138-131921139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190587753	chr4:131921187-131921188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1392618	chr4:131921222-131921223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552559567	chr4:131921260-131921261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144422582	chr4:131921333-131921334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376342737	chr4:131921346-131921347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183367889	chr4:131921393-131921394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548323579	chr4:131921407-131921408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186226906	chr4:131921474-131921475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146596002	chr4:131921501-131921502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547638912	chr4:131921527-131921528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571145327	chr4:131921553-131921554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190779043	chr4:131921569-131921570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546191873	chr4:131921588-131921589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10033260	chr4:131921602-131921603	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558503224	chr4:131921669-131921670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575196410	chr4:131921717-131921718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139860079	chr4:131921747-131921748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554712805	chr4:131921805-131921806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574636468	chr4:131921841-131921842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149864924	chr4:131921848-131921849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560451899	chr4:131921895-131921896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370331927	chr4:131921911-131921912	Weak transcription	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:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131919800-131923400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:131922200-131924000	Enhancers	HUVEC	blood vessel
3	chr4:131922600-131924200	Enhancers	NHEK	skin
4	chr4:131923400-131924000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:131931400-131932800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:131932000-131933000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:131932000-131933600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr4:131932800-131933600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:131933000-131933400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr4:131933400-131933600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:131933400-131933600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:131933400-131933800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:131933400-131933800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:131933400-131933800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr4:131933400-131933800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:131933400-131935200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:131933400-131935400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr4:131933400-131935800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:131933600-131934000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
20	chr4:131933600-131934800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:131933600-131935000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr4:131933600-131935000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:131933800-131934800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:131933800-131934800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr4:131933800-131935000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr4:131933800-131935000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr4:131934400-131935200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
28	chr4:131934800-131935000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:131934800-131935800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:131935000-131935200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr4:131935000-131935200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr4:131935000-131935200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:131935000-131935400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:131935000-131935600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:131935200-131935400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
36	chr4:131935200-131935600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr4:131940000-131940800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:131949400-131949800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:131959800-131960600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr4:131972200-131972600	Enhancers	Fetal Heart	heart
41	chr4:131982400-131983000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:131982400-131983200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:131982400-131983400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:131982600-131983400	ZNF genes & repeats	Dnd41	blood
45	chr4:131982600-131986400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr4:131983000-131985000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:131983400-131985000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:131985000-131985800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:131985000-131986400	ZNF genes & repeats	Dnd41	blood
50	chr4:131985000-131986800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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