Variant report

Variant	esv3502788
Chromosome Location	chr4:98459061-98825579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:98607042-98607171	K562	blood:	n/a	n/a
2	BACH1	chr4:98577260-98577434	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:98508998-98509375	GM12878	blood:	n/a	n/a
4	CBX3	chr4:98618600-98618916	K562	blood:	n/a	n/a
5	CEBPB	chr4:98577196-98577821	HepG2	liver:	n/a	n/a
6	CEBPB	chr4:98646521-98646790	HepG2	liver:	n/a	chr4:98646627-98646638
7	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr4:98510992-98511342	MCF-7	breast:	n/a	n/a
9	CEBPB	chr4:98577269-98577808	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:98649287-98649587	HepG2	liver:	n/a	chr4:98649425-98649436 chr4:98649425-98649434
11	CEBPB	chr4:98778997-98779197	K562	blood:	n/a	chr4:98779056-98779067
12	CEBPB	chr4:98503368-98503620	HepG2	liver:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
13	CEBPB	chr4:98650615-98650904	IMR90	lung:	n/a	chr4:98650742-98650753 chr4:98650740-98650751 chr4:98650742-98650751
14	CEBPB	chr4:98577086-98577649	A549	lung:	n/a	n/a
15	CEBPB	chr4:98467897-98468197	IMR90	lung:	n/a	chr4:98468073-98468084
16	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
17	CEBPB	chr4:98664347-98664413	K562	blood:	n/a	chr4:98664382-98664393
18	CEBPB	chr4:98577188-98577535	A549	lung:	n/a	n/a
19	CEBPB	chr4:98577590-98577861	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:98795872-98796026	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:98766860-98767235	H1-hESC	embryonic stem cell:	n/a	chr4:98767092-98767109
22	CEBPB	chr4:98748818-98748844	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:98778907-98779234	IMR90	lung:	n/a	chr4:98779056-98779067
24	CEBPB	chr4:98664215-98664532	IMR90	lung:	n/a	chr4:98664382-98664393
25	CEBPB	chr4:98551808-98552192	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:98684928-98685150	HepG2	liver:	n/a	chr4:98685036-98685049 chr4:98685038-98685049 chr4:98684997-98685010 chr4:98685036-98685047
27	CEBPB	chr4:98778897-98779215	HepG2	liver:	n/a	chr4:98779056-98779067
28	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
29	CEBPB	chr4:98581138-98581275	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:98664241-98664530	HepG2	liver:	n/a	chr4:98664382-98664393
31	CEBPB	chr4:98510925-98511719	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:98511464-98511776	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
34	CEBPB	chr4:98675730-98675981	HepG2	liver:	n/a	chr4:98675830-98675841
35	CEBPB	chr4:98577212-98577826	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:98650603-98650914	HepG2	liver:	n/a	chr4:98650742-98650753 chr4:98650740-98650751 chr4:98650742-98650751
37	CEBPB	chr4:98503490-98503558	H1-hESC	embryonic stem cell:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
38	CEBPB	chr4:98467950-98468187	HepG2	liver:	n/a	chr4:98468073-98468084
39	CEBPB	chr4:98577187-98577805	A549	lung:	n/a	n/a
40	CEBPB	chr4:98586371-98586560	HepG2	liver:	n/a	chr4:98586497-98586508
41	CEBPB	chr4:98577066-98577631	MCF-7	breast:	n/a	n/a
42	CEBPB	chr4:98577169-98577759	HCT-116	colon:	n/a	n/a
43	CEBPB	chr4:98668425-98668529	A549	lung:	n/a	n/a
44	CEBPB	chr4:98577159-98577857	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:98664377-98664429	H1-hESC	embryonic stem cell:	n/a	chr4:98664382-98664393
46	CEBPB	chr4:98693338-98693594	HepG2	liver:	n/a	chr4:98693506-98693515 chr4:98693443-98693456
47	CEBPB	chr4:98577090-98577696	HCT-116	colon:	n/a	n/a
48	CEBPB	chr4:98577095-98577574	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:98586380-98586651	IMR90	lung:	n/a	chr4:98586497-98586508
50	CHD1	chr4:98522881-98522890	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98690072-98690122	GM06990	blood:	n/a
2	chr4:98479820-98479870	HRE	kidney:	n/a
3	chr4:98690072-98690122	AG04450	lung:	fetal
4	chr4:98690072-98690122	ovcar-3	ovarian:	n/a
5	chr4:98479820-98479870	HRCEpiC	kidney:	n/a
6	chr4:98690072-98690122	HNPCEpiC	eye:	n/a
7	chr4:98479820-98479870	HCPEpiC	choroid plexus:	n/a
8	chr4:98479820-98479870	Hela-S3	cervix:	n/a
9	chr4:98479820-98479870	SK-N-SH	brain:	n/a
10	chr4:98690072-98690122	SAEC	small airway:	n/a
11	chr4:98690072-98690122	ECC-1	luminal epithelium:	n/a
12	chr4:98690072-98690122	NH-A	brain:	n/a
13	chr4:98479820-98479870	NHBE	bronchial:	n/a
14	chr4:98479820-98479870	SAEC	small airway:	n/a
15	chr4:98690072-98690122	GM12878	blood:	n/a
16	chr4:98479820-98479870	HAEpiC	amniotic membrane:	n/a
17	chr4:98690072-98690122	NT2-D1	testis:	n/a
18	chr4:98479820-98479870	Jurkat	blood:	n/a
19	chr4:98690072-98690122	MCF10A-Er-Src	breast:	n/a
20	chr4:98690072-98690122	HRE	kidney:	n/a
21	chr4:98479820-98479870	SK-N-MC	brain:	n/a
22	chr4:98690072-98690122	NHBE	bronchial:	n/a
23	chr4:98690072-98690122	HMEC	breast:	n/a
24	chr4:98479820-98479870	Hepatocyte	liver:	n/a
25	chr4:98690072-98690122	A549	lung:	n/a
26	chr4:98479820-98479870	HNPCEpiC	eye:	n/a
27	chr4:98479820-98479870	NB4	blood:	n/a
28	chr4:98479820-98479870	HUVEC	blood vessel:	n/a
29	chr4:98690072-98690122	GM12891	blood:	n/a
30	chr4:98690072-98690122	K562	blood:	n/a
31	chr4:98690072-98690122	HCM	heart:	n/a
32	chr4:98690072-98690122	H1-hESC	embryonic stem cell:	embryo
33	chr4:98479820-98479870	NHDF-neo	bronchial:	n/a
34	chr4:98690072-98690122	LNCaP	prostate:	n/a
35	chr4:98690072-98690122	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:98690072-98690122	HIPEpiC	eye:	n/a
37	chr4:98479820-98479870	BE2_C	brain:	n/a
38	chr4:98479820-98479870	SKMC	muscle:	n/a
39	chr4:98690072-98690122	AG04449	skin:	fetal
40	chr4:98479820-98479870	AG04449	skin:	fetal
41	chr4:98690072-98690122	BE2_C	brain:	n/a
42	chr4:98479820-98479870	HEK293	kidney:	embryo
43	chr4:98479820-98479870	HL-60	blood:	n/a
44	chr4:98690072-98690122	Hepatocyte	liver:	n/a
45	chr4:98479820-98479870	AG09319	gingival:	n/a
46	chr4:98690072-98690122	HUVEC	blood vessel:	n/a
47	chr4:98479820-98479870	ECC-1	luminal epithelium:	n/a
48	chr4:98690072-98690122	MCF-7	breast:	n/a
49	chr4:98479820-98479870	T-47D	breast:	n/a
50	chr4:98690072-98690122	Jurkat	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
2	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
3	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
4	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:
5	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
6	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
7	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
8	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
9	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
10	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
11	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
12	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
13	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
14	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
15	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
16	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
17	chr4:97091475..97092009-chr4:98641981..98642501,2	MCF-7	breast:
18	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
19	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
20	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
21	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477
2	lnc-TSPAN5-3	chr4:98633850-98633965	NONHSAT097477

No data

Variant related genes	Relation type
STPG2	TF binding region
ENSG00000254044	TF binding region
STPG2	CpG island
ENSG00000254044	CpG island

Extended variants
information (count: 4087 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4087 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35714120	chr4:98465844-98465845	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565901885	chr4:98465878-98465879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183123686	chr4:98465918-98465919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs3864228	chr4:98465938-98465939	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544339594	chr4:98465986-98465987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548288896	chr4:98466010-98466011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369501037	chr4:98466103-98466104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536190337	chr4:98466116-98466117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567577026	chr4:98466167-98466168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187864777	chr4:98466219-98466220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs651769	chr4:98466229-98466230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148344975	chr4:98466233-98466234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577921022	chr4:98466266-98466267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569505247	chr4:98466272-98466273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2036965	chr4:98466292-98466293	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557536476	chr4:98466293-98466294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575698390	chr4:98466434-98466435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543042884	chr4:98466448-98466449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs960450	chr4:98466559-98466560	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs573454974	chr4:98466565-98466566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141593916	chr4:98466607-98466608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565439652	chr4:98466610-98466611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532573368	chr4:98466613-98466614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150487045	chr4:98466617-98466618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571161866	chr4:98466619-98466620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563085783	chr4:98466648-98466649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535370145	chr4:98466683-98466684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs113324894	chr4:98466684-98466685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138462644	chr4:98466692-98466693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142764904	chr4:98466711-98466712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567164351	chr4:98466748-98466749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56211207	chr4:98466776-98466777	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116068197	chr4:98466856-98466857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535548359	chr4:98466857-98466858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111268278	chr4:98466902-98466903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538876083	chr4:98466948-98466949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557475606	chr4:98467161-98467162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs58996528	chr4:98467212-98467213	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs536369502	chr4:98467218-98467219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76146684	chr4:98467246-98467247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192698498	chr4:98467289-98467290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11297109	chr4:98467291-98467292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540878064	chr4:98467328-98467329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146047812	chr4:98467395-98467396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577015227	chr4:98467412-98467413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544428742	chr4:98467446-98467447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114709932	chr4:98467486-98467487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564186429	chr4:98467502-98467503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374203395	chr4:98467508-98467509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10011487	chr4:98467521-98467522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98465800-98466400	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr4:98465800-98466600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:98465800-98466800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr4:98465800-98467000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:98466000-98466600	Enhancers	H1 Cell Line	embryonic stem cell
6	chr4:98466000-98466600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:98466000-98466800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:98466000-98467200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:98466200-98466800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:98466200-98466800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:98466800-98478600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr4:98470600-98472800	Enhancers	Dnd41	blood
13	chr4:98478400-98480000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:98478400-98481400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:98478600-98479800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:98478600-98480200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:98478600-98480600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:98478600-98480800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:98478600-98481400	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr4:98478800-98480000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:98478800-98480000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr4:98479000-98481200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr4:98479600-98480000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr4:98481600-98483800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr4:98486600-98487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr4:98495000-98495800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:98495200-98495600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:98495200-98495600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr4:98506400-98507000	Enhancers	Dnd41	blood
30	chr4:98508800-98509000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:98509000-98509400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:98509400-98510600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:98510600-98511600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:98510800-98511200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:98510800-98511600	Enhancers	HMEC	breast
36	chr4:98514200-98514800	ZNF genes & repeats	Pancreas	Pancrea
37	chr4:98514400-98515000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:98548600-98549400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:98548800-98549200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr4:98548800-98549400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:98548800-98549400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:98549200-98549400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr4:98549400-98552800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr4:98551600-98552800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:98552800-98553000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:98552800-98553000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:98553000-98553800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:98553000-98554000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr4:98553800-98554800	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr4:98553800-98555400	Active TSS	HUES6 Cell Line	embryonic stem cell

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