Variant report

Variant	nsv594932
Chromosome Location	chr4:98425582-98595080
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:479)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:98577260-98577434	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr4:98508998-98509375	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:98577095-98577574	MCF-7	breast:	n/a	n/a
4	CEBPB	chr4:98577086-98577649	A549	lung:	n/a	n/a
5	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
6	CEBPB	chr4:98586380-98586651	IMR90	lung:	n/a	chr4:98586497-98586508
7	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
8	CEBPB	chr4:98426805-98427085	A549	lung:	n/a	chr4:98426906-98426915 chr4:98426904-98426915 chr4:98426905-98426916
9	CEBPB	chr4:98577590-98577861	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:98577066-98577631	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
12	CEBPB	chr4:98511464-98511776	MCF-7	breast:	n/a	n/a
13	CEBPB	chr4:98426750-98427060	HepG2	liver:	n/a	chr4:98426906-98426915 chr4:98426904-98426915 chr4:98426905-98426916
14	CEBPB	chr4:98577188-98577535	A549	lung:	n/a	n/a
15	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:98581138-98581275	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:98577212-98577826	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:98510925-98511719	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:98577196-98577821	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:98577187-98577805	A549	lung:	n/a	n/a
21	CEBPB	chr4:98467897-98468197	IMR90	lung:	n/a	chr4:98468073-98468084
22	CEBPB	chr4:98577159-98577857	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:98551808-98552192	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:98577169-98577759	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:98577269-98577808	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:98503368-98503620	HepG2	liver:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
27	CEBPB	chr4:98586371-98586560	HepG2	liver:	n/a	chr4:98586497-98586508
28	CEBPB	chr4:98467950-98468187	HepG2	liver:	n/a	chr4:98468073-98468084
29	CEBPB	chr4:98503490-98503558	H1-hESC	embryonic stem cell:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
30	CEBPB	chr4:98577090-98577696	HCT-116	colon:	n/a	n/a
31	CEBPB	chr4:98510992-98511342	MCF-7	breast:	n/a	n/a
32	CHD1	chr4:98522881-98522890	GM12878	blood:	n/a	n/a
33	CTCF	chr4:98470260-98470410	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr4:98470220-98470370	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr4:98437060-98437210	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr4:98470260-98470410	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr4:98470200-98470350	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr4:98487508-98487591	LNCaP	prostate:	n/a	n/a
39	CTCF	chr4:98470340-98470490	RPTEC	kidney:	n/a	n/a
40	CTCF	chr4:98470287-98470384	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr4:98470244-98470434	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:98470220-98470370	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:98470240-98470390	HMF	breast:	n/a	n/a
44	CTCF	chr4:98470220-98470370	HMEC	breast:	n/a	n/a
45	CTCF	chr4:98470260-98470410	HMEC	breast:	n/a	n/a
46	CTCF	chr4:98470280-98470430	HCT-116	colon:	n/a	n/a
47	CTCF	chr4:98470220-98470370	BE2_C	brain:	n/a	n/a
48	CTCF	chr4:98450689-98450738	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr4:98470220-98470370	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr4:98470200-98470350	HA-sp	spinal cord:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98479820-98479870	SKMC	muscle:	n/a
2	chr4:98479820-98479870	ECC-1	luminal epithelium:	n/a
3	chr4:98479820-98479870	GM06990	blood:	n/a
4	chr4:98479820-98479870	MCF-7	breast:	n/a
5	chr4:98479820-98479870	Caco-2	colon:	n/a
6	chr4:98479820-98479870	HNPCEpiC	eye:	n/a
7	chr4:98479820-98479870	T-47D	breast:	n/a
8	chr4:98479820-98479870	NB4	blood:	n/a
9	chr4:98479820-98479870	HepG2	liver:	n/a
10	chr4:98479820-98479870	HEEpiC	esophagus:	n/a
11	chr4:98479820-98479870	ProgFib	skin:	n/a
12	chr4:98479820-98479870	SK-N-SH	brain:	n/a
13	chr4:98479820-98479870	HL-60	blood:	n/a
14	chr4:98479820-98479870	BJ	skin:	n/a
15	chr4:98479820-98479870	NHDF-neo	bronchial:	n/a
16	chr4:98479820-98479870	PANC-1	pancreas:	n/a
17	chr4:98479820-98479870	SK-N-SH_RA	brain:	n/a
18	chr4:98479820-98479870	PrEC	prostate:	n/a
19	chr4:98479820-98479870	HEK293	kidney:	embryo
20	chr4:98479820-98479870	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:98479820-98479870	HRE	kidney:	n/a
22	chr4:98479820-98479870	HCM	heart:	n/a
23	chr4:98479820-98479870	Hepatocyte	liver:	n/a
24	chr4:98479820-98479870	K562	blood:	n/a
25	chr4:98479820-98479870	HMEC	breast:	n/a
26	chr4:98479820-98479870	AG04449	skin:	fetal
27	chr4:98479820-98479870	HUVEC	blood vessel:	n/a
28	chr4:98479820-98479870	ovcar-3	ovarian:	n/a
29	chr4:98479820-98479870	SK-N-MC	brain:	n/a
30	chr4:98479820-98479870	HCF	heart:	n/a
31	chr4:98479820-98479870	NH-A	brain:	n/a
32	chr4:98479820-98479870	LNCaP	prostate:	n/a
33	chr4:98479820-98479870	AG09319	gingival:	n/a
34	chr4:98479820-98479870	HCPEpiC	choroid plexus:	n/a
35	chr4:98479820-98479870	A549	lung:	n/a
36	chr4:98479820-98479870	NT2-D1	testis:	n/a
37	chr4:98479820-98479870	CMK	blood:	n/a
38	chr4:98479820-98479870	AoSMC	blood vessel:	n/a
39	chr4:98479820-98479870	H1-hESC	embryonic stem cell:	embryo
40	chr4:98479820-98479870	SAEC	small airway:	n/a
41	chr4:98479820-98479870	AG10803	skin:	n/a
42	chr4:98479820-98479870	NHBE	bronchial:	n/a
43	chr4:98479820-98479870	HRCEpiC	kidney:	n/a
44	chr4:98479820-98479870	IMR90	lung:	fetal
45	chr4:98479820-98479870	AG04450	lung:	fetal
46	chr4:98479820-98479870	Hela-S3	cervix:	n/a
47	chr4:98479820-98479870	HCT-116	colon:	n/a
48	chr4:98479820-98479870	MCF10A-Er-Src	breast:	n/a
49	chr4:98479820-98479870	RPTEC	kidney:	n/a
50	chr4:98479820-98479870	GM12892	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
2	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
3	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
4	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
5	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
6	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
7	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
8	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
9	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
10	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
11	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:
12	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
13	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2301 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2301 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2865798	chr4:98425582-98425583	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548978039	chr4:98425699-98425700	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567238415	chr4:98425709-98425710	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535291461	chr4:98425737-98425738	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74715055	chr4:98425773-98425774	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184592871	chr4:98425816-98425817	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs552750796	chr4:98425867-98425868	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs572211720	chr4:98425934-98425935	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs548113871	chr4:98425957-98425958	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs114065254	chr4:98425984-98425985	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs188487895	chr4:98425999-98426000	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs557305405	chr4:98426002-98426003	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575575801	chr4:98426003-98426004	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569477480	chr4:98426077-98426078	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149588164	chr4:98426086-98426087	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554926975	chr4:98426091-98426092	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191847135	chr4:98426137-98426138	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536725942	chr4:98426194-98426195	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540828536	chr4:98426195-98426196	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565520313	chr4:98426212-98426213	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536873680	chr4:98426213-98426214	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533045820	chr4:98426221-98426222	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562319998	chr4:98426328-98426329	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144068891	chr4:98426336-98426337	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541339076	chr4:98426338-98426339	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77353957	chr4:98426352-98426353	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367802249	chr4:98426389-98426390	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530390978	chr4:98426408-98426409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548971571	chr4:98426434-98426435	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs567175320	chr4:98426435-98426436	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12643594	chr4:98426448-98426449	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs570463262	chr4:98426461-98426462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184320166	chr4:98426496-98426497	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs529858797	chr4:98426573-98426574	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs367992461	chr4:98426614-98426615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571141105	chr4:98426615-98426616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188944740	chr4:98426662-98426663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72887273	chr4:98426667-98426668	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs569344594	chr4:98426727-98426728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536207263	chr4:98426732-98426733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148660481	chr4:98426823-98426824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553001509	chr4:98426905-98426906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144374047	chr4:98426936-98426937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79058619	chr4:98426949-98426950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182223411	chr4:98426964-98426965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371079687	chr4:98426983-98426984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544805281	chr4:98427025-98427026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548230980	chr4:98427053-98427054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563196370	chr4:98427069-98427070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs67016390	chr4:98427103-98427104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98420600-98425600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:98421000-98425600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:98421000-98426000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:98422200-98425600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:98422400-98428600	Weak transcription	HMEC	breast
6	chr4:98425200-98427000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:98425400-98425600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:98425400-98426800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:98425400-98426800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:98425600-98425800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr4:98425600-98426600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr4:98425600-98426800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:98425600-98427000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:98425800-98426200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr4:98425800-98426200	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr4:98425800-98426400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr4:98425800-98426400	Enhancers	A549	lung
18	chr4:98425800-98427000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:98426000-98426600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr4:98426000-98426600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:98426000-98427400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:98426000-98427400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr4:98426200-98426600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr4:98426400-98428600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:98426600-98427400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr4:98426600-98427400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:98426600-98428800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr4:98427000-98428600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr4:98427400-98428600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:98427400-98429000	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr4:98427400-98429800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr4:98428600-98428800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:98428600-98428800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr4:98428600-98429200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr4:98428600-98429200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:98428600-98429200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr4:98428600-98429400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:98428600-98429400	Enhancers	HMEC	breast
39	chr4:98428600-98429800	Enhancers	HUVEC	blood vessel
40	chr4:98428800-98429200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr4:98428800-98429200	Enhancers	NH-A	brain
42	chr4:98429000-98429200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr4:98429200-98430000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr4:98430000-98430600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr4:98432000-98432800	Enhancers	Dnd41	blood
46	chr4:98437000-98437600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:98446000-98446600	Enhancers	HUVEC	blood vessel
48	chr4:98446400-98446800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:98446600-98447000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:98446600-98447000	Flanking Active TSS	HUVEC	blood vessel

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