Variant report

Variant	nsv1016445
Chromosome Location	chr4:131946375-132350324
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	chr4:132347383-132348003	GM12878	blood:	n/a	n/a
3	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
4	ATF2	chr4:132347459-132347932	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	chr4:132164565-132164579	K562	blood:	n/a	n/a
8	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:132150946-132150962	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:132347572-132347877	GM12878	blood:	n/a	n/a
11	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
12	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
13	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
14	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
15	BATF	chr4:132347469-132347900	GM12878	blood:	n/a	n/a
16	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
17	BCL11A	chr4:132178410-132178696	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:132347442-132347953	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:132178348-132178643	GM12878	blood:	n/a	chr4:132178369-132178378
21	BCL11A	chr4:132347576-132347893	GM12878	blood:	n/a	n/a
22	BCL3	chr4:132347488-132347811	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:132347567-132347910	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:132347460-132347821	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	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
30	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
31	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
32	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
33	CEBPB	chr4:132179571-132179733	A549	lung:	n/a	chr4:132179698-132179709
34	CEBPB	chr4:131959580-131959858	IMR90	lung:	n/a	chr4:131959710-131959721 chr4:131959709-131959722
35	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
36	CEBPB	chr4:132179496-132179815	ECC-1	luminal epithelium:	n/a	chr4:132179698-132179709
37	CEBPB	chr4:132110801-132111048	HepG2	liver:	n/a	chr4:132110945-132110956
38	CEBPB	chr4:132246573-132246902	HepG2	liver:	n/a	chr4:132246745-132246756
39	CEBPB	chr4:132046736-132046783	H1-hESC	embryonic stem cell:	n/a	chr4:132046763-132046774
40	CEBPB	chr4:132179525-132179882	H1-hESC	embryonic stem cell:	n/a	chr4:132179698-132179709
41	CEBPB	chr4:132082393-132083000	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:131959563-131959894	HepG2	liver:	n/a	chr4:131959710-131959721 chr4:131959709-131959722
43	CEBPB	chr4:132110833-132110991	H1-hESC	embryonic stem cell:	n/a	chr4:132110945-132110956
44	CEBPB	chr4:132179607-132179807	HepG2	liver:	n/a	chr4:132179698-132179709
45	CEBPB	chr4:131992954-131993141	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:132316111-132316328	HepG2	liver:	n/a	chr4:132316170-132316181 chr4:132316241-132316252 chr4:132316170-132316183 chr4:132316241-132316254 chr4:132316241-132316254
47	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
48	CEBPB	chr4:132334422-132334633	K562	blood:	n/a	chr4:132334512-132334525 chr4:132334513-132334524 chr4:132334514-132334523 chr4:132334512-132334525 chr4:132334512-132334523
49	CEBPB	chr4:132046618-132046957	HepG2	liver:	n/a	chr4:132046763-132046774
50	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132273830-132273880	MCF-7	breast:	n/a
2	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
3	chr4:132300589-132300639	NHDF-neo	bronchial:	n/a
4	chr4:132300589-132300639	Hela-S3	cervix:	n/a
5	chr4:132273830-132273880	LNCaP	prostate:	n/a
6	chr4:132300589-132300639	GM12878	blood:	n/a
7	chr4:132300589-132300639	ovcar-3	ovarian:	n/a
8	chr4:132300589-132300639	HAEpiC	amniotic membrane:	n/a
9	chr4:132273830-132273880	HCF	heart:	n/a
10	chr4:132300589-132300639	HCT-116	colon:	n/a
11	chr4:132273830-132273880	HepG2	liver:	n/a
12	chr4:132300589-132300639	T-47D	breast:	n/a
13	chr4:132273830-132273880	CMK	blood:	n/a
14	chr4:132300589-132300639	K562	blood:	n/a
15	chr4:132273830-132273880	NH-A	brain:	n/a
16	chr4:132273830-132273880	HAEpiC	amniotic membrane:	n/a
17	chr4:132273830-132273880	AG09319	gingival:	n/a
18	chr4:132273830-132273880	HEK293	kidney:	embryo
19	chr4:132273830-132273880	HEEpiC	esophagus:	n/a
20	chr4:132273830-132273880	PrEC	prostate:	n/a
21	chr4:132273830-132273880	NB4	blood:	n/a
22	chr4:132273830-132273880	GM06990	blood:	n/a
23	chr4:132273830-132273880	BE2_C	brain:	n/a
24	chr4:132300589-132300639	SK-N-SH_RA	brain:	n/a
25	chr4:132273830-132273880	SK-N-MC	brain:	n/a
26	chr4:132273830-132273880	Caco-2	colon:	n/a
27	chr4:132273830-132273880	Jurkat	blood:	n/a
28	chr4:132273830-132273880	PFSK-1	brain:	n/a
29	chr4:132273830-132273880	HRCEpiC	kidney:	n/a
30	chr4:132300589-132300639	AG09309	skin:	n/a
31	chr4:132300589-132300639	ProgFib	skin:	n/a
32	chr4:132300589-132300639	HRE	kidney:	n/a
33	chr4:132300589-132300639	IMR90	lung:	fetal
34	chr4:132300589-132300639	RPTEC	kidney:	n/a
35	chr4:132300589-132300639	SKMC	muscle:	n/a
36	chr4:132300589-132300639	ECC-1	luminal epithelium:	n/a
37	chr4:132300589-132300639	HCM	heart:	n/a
38	chr4:132300589-132300639	HIPEpiC	eye:	n/a
39	chr4:132300589-132300639	Jurkat	blood:	n/a
40	chr4:132273830-132273880	SK-N-SH	brain:	n/a
41	chr4:132273830-132273880	U87	brain:	n/a
42	chr4:132273830-132273880	HIPEpiC	eye:	n/a
43	chr4:132273830-132273880	ECC-1	luminal epithelium:	n/a
44	chr4:132300589-132300639	HCPEpiC	choroid plexus:	n/a
45	chr4:132273830-132273880	IMR90	lung:	fetal
46	chr4:132300589-132300639	SK-N-MC	brain:	n/a
47	chr4:132273830-132273880	Hepatocyte	liver:	n/a
48	chr4:132273830-132273880	HMEC	breast:	n/a
49	chr4:132300589-132300639	HUVEC	blood vessel:	n/a
50	chr4:132300589-132300639	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
2	chr4:132012841..132013396-chr4:132565892..132566443,2	MCF-7	breast:
3	chr4:88902738..88903615-chr4:132032553..132033450,2	MCF-7	breast:
4	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
5	chr4:132050225..132052503-chr4:132053839..132055546,2	MCF-7	breast:
6	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
7	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
8	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
9	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
10	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
11	chr4:131949917..131952007-chr4:131958103..131960574,2	K562	blood:
12	chr4:131991641..131994380-chr4:131997829..132000348,2	MCF-7	breast:
13	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
14	chr4:132122573..132124807-chr4:132127097..132129962,3	MCF-7	breast:
15	chr2:52859439..52860286-chr4:132071047..132072003,2	MCF-7	breast:
16	chr4:132149758..132152174-chr4:132152925..132155789,2	MCF-7	breast:
17	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:
18	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
19	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
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
ENSG00000250213	TF binding region
ENSG00000250102	TF binding region
RNU6-224P	TF binding region
ENSG00000250213	CpG island
ENSG00000250102	CpG island
RNU6-224P	CpG island

Extended variants
information (count: 2405 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2405 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558474721	chr4:131949411-131949412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17051135	chr4:131949420-131949421	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530548817	chr4:131949452-131949453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17051136	chr4:131949457-131949458	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs567352879	chr4:131949458-131949459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188335418	chr4:131949466-131949467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370630253	chr4:131949475-131949476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17051137	chr4:131949500-131949501	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs546811414	chr4:131949507-131949508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151263950	chr4:131949646-131949647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572414533	chr4:131949696-131949697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538513689	chr4:131949718-131949719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140553534	chr4:131949771-131949772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569087476	chr4:131949781-131949782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541060622	chr4:131959889-131959890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564508370	chr4:131959918-131959919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199962458	chr4:131959967-131959968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397878768	chr4:131959981-131959982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533423728	chr4:131960011-131960012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369743532	chr4:131960071-131960072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188748914	chr4:131960088-131960089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181949407	chr4:131960206-131960207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549595311	chr4:131960310-131960311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566240709	chr4:131960311-131960312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115612650	chr4:131960322-131960323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574909108	chr4:131960344-131960345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547041197	chr4:131960355-131960356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570131749	chr4:131960370-131960371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539121622	chr4:131960424-131960425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374606032	chr4:131960499-131960500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571043469	chr4:131960501-131960502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17051140	chr4:131960512-131960513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575765444	chr4:131960521-131960522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535281056	chr4:131960525-131960526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555581172	chr4:131960568-131960569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565258341	chr4:131960598-131960599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572856573	chr4:131972212-131972213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183068514	chr4:131972213-131972214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs574292230	chr4:131972216-131972217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538675069	chr4:131972220-131972221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558363425	chr4:131972243-131972244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs202223920	chr4:131972307-131972308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13145260	chr4:131972377-131972378	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561147990	chr4:131972404-131972405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563175760	chr4:131972414-131972415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560393709	chr4:131972432-131972433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540160052	chr4:131972460-131972461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531847060	chr4:131972506-131972507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527614555	chr4:131972511-131972512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560044302	chr4:131972519-131972520	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:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:131949400-131949800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:131959800-131960600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:131972200-131972600	Enhancers	Fetal Heart	heart
4	chr4:131982400-131983000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:131982400-131983200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:131982400-131983400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:131982600-131983400	ZNF genes & repeats	Dnd41	blood
8	chr4:131982600-131986400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr4:131983000-131985000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:131983400-131985000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:131985000-131985800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:131985000-131986400	ZNF genes & repeats	Dnd41	blood
13	chr4:131985000-131986800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:131985200-131985400	ZNF genes & repeats	Pancreas	Pancrea
15	chr4:131985800-131987800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:131986600-131986800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:132005200-132005400	Enhancers	Dnd41	blood
18	chr4:132005200-132006400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:132005400-132005800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:132005400-132005800	Flanking Active TSS	Dnd41	blood
21	chr4:132005400-132005800	Active TSS	GM12878-XiMat	blood
22	chr4:132005600-132006400	Enhancers	Liver	Liver
23	chr4:132006400-132007800	Weak transcription	Liver	Liver
24	chr4:132007800-132008000	Enhancers	Liver	Liver
25	chr4:132008000-132008400	Weak transcription	Liver	Liver
26	chr4:132008400-132008800	Enhancers	Liver	Liver
27	chr4:132020000-132020600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:132020200-132020400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:132020400-132020800	Enhancers	Pancreas	Pancrea
30	chr4:132020400-132023400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:132023200-132024000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:132023400-132024000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:132033800-132034400	Enhancers	Pancreas	Pancrea
34	chr4:132036400-132036600	Enhancers	Pancreas	Pancrea
35	chr4:132037800-132040600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:132038800-132040400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:132039600-132040600	Enhancers	Dnd41	blood
38	chr4:132044000-132044400	Active TSS	A549	lung
39	chr4:132052000-132052400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:132056800-132057800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:132057000-132057600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:132069000-132069200	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:132069200-132070000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr4:132070000-132070400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:132070400-132070600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:132070600-132071000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:132070600-132071000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:132082400-132083000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:132082400-132083000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:132082800-132083000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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