Variant report

Variant	esv2757947
Chromosome Location	chr4:104179925-104342395
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:104227844-104228137	HepG2	liver:	n/a	n/a
2	BACH1	chr4:104321608-104321927	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:104266900-104266909	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:104321623-104321858	GM12878	blood:	n/a	chr4:104321771-104321782
5	BHLHE40	chr4:104321687-104321948	K562	blood:	n/a	n/a
6	BHLHE40	chr4:104185099-104185243	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:104228861-104229061	HepG2	liver:	n/a	n/a
8	BHLHE40	chr4:104321736-104321854	HepG2	liver:	n/a	n/a
9	CBX3	chr4:104281133-104281404	K562	blood:	n/a	n/a
10	CBX3	chr4:104281096-104281352	K562	blood:	n/a	n/a
11	CEBPB	chr4:104219134-104219376	K562	blood:	n/a	chr4:104219276-104219287
12	CEBPB	chr4:104219128-104219366	HepG2	liver:	n/a	chr4:104219276-104219287
13	CEBPB	chr4:104219116-104219412	IMR90	lung:	n/a	chr4:104219276-104219287
14	CEBPB	chr4:104271810-104272041	A549	lung:	n/a	chr4:104271930-104271941
15	CEBPB	chr4:104269838-104270035	HepG2	liver:	n/a	chr4:104269963-104269974
16	CEBPB	chr4:104271815-104272039	Hela-S3	cervix:	n/a	chr4:104271930-104271941
17	CEBPB	chr4:104219117-104219359	K562	blood:	n/a	chr4:104219276-104219287
18	CEBPB	chr4:104252950-104253036	HepG2	liver:	n/a	chr4:104253004-104253015
19	CEBPB	chr4:104328268-104328562	HepG2	liver:	n/a	chr4:104328385-104328396
20	CEBPB	chr4:104271857-104272028	H1-hESC	embryonic stem cell:	n/a	chr4:104271930-104271941
21	CEBPB	chr4:104271788-104272061	HepG2	liver:	n/a	chr4:104271930-104271941
22	CEBPB	chr4:104219154-104219355	A549	lung:	n/a	chr4:104219276-104219287
23	CEBPB	chr4:104256109-104256232	K562	blood:	n/a	n/a
24	CEBPB	chr4:104275063-104275203	HepG2	liver:	n/a	chr4:104275091-104275102
25	CEBPB	chr4:104321803-104322048	HepG2	liver:	n/a	chr4:104321934-104321945
26	CEBPB	chr4:104328273-104328473	A549	lung:	n/a	chr4:104328385-104328396
27	CHD2	chr4:104277715-104277724	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:104271728-104271768	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:104228023-104228347	HepG2	liver:	n/a	n/a
30	CTCF	chr4:104286560-104286710	SAEC	small airway:	n/a	n/a
31	CTCF	chr4:104242900-104243050	NHLF	lung:	n/a	n/a
32	CTCF	chr4:104286540-104286690	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr4:104336340-104336490	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr4:104268974-104268984	K562	blood:	n/a	n/a
35	CTCF	chr4:104336344-104336377	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:104336300-104336450	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:104286568-104286660	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:104239820-104239970	GM12869	blood:	n/a	n/a
39	CTCF	chr4:104300280-104300430	GM06990	blood:	n/a	n/a
40	CTCF	chr4:104336260-104336410	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:104286548-104286657	Medullo	brain:	n/a	n/a
42	CTCF	chr4:104336320-104336419	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:104336260-104336410	SAEC	small airway:	n/a	n/a
44	CTCF	chr4:104286589-104286626	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:104283080-104283230	Caco-2	colon:	n/a	n/a
46	CTCF	chr4:104286524-104286590	GM10248	blood:	n/a	n/a
47	CTCF	chr4:104336320-104336470	GM12873	blood:	n/a	n/a
48	CTCF	chr4:104286540-104286690	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:104341735-104341843	Fibrobl	skin:	n/a	n/a
50	CTCF	chr4:104286480-104286630	HEEpiC	esophagus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:104227316-104227366	ECC-1	luminal epithelium:	n/a
2	chr4:104227316-104227366	AG09309	skin:	n/a
3	chr4:104239655-104239705	AG04449	skin:	fetal
4	chr4:104227316-104227366	HMEC	breast:	n/a
5	chr4:104227316-104227366	MCF10A-Er-Src	breast:	n/a
6	chr4:104227316-104227366	GM06990	blood:	n/a
7	chr4:104227316-104227366	U87	brain:	n/a
8	chr4:104239655-104239705	LNCaP	prostate:	n/a
9	chr4:104227316-104227366	SK-N-SH_RA	brain:	n/a
10	chr4:104239655-104239705	CMK	blood:	n/a
11	chr4:104227316-104227366	PANC-1	pancreas:	n/a
12	chr4:104239655-104239705	ECC-1	luminal epithelium:	n/a
13	chr4:104227316-104227366	HEEpiC	esophagus:	n/a
14	chr4:104239655-104239705	MCF10A-Er-Src	breast:	n/a
15	chr4:104227316-104227366	AG10803	skin:	n/a
16	chr4:104227316-104227366	PFSK-1	brain:	n/a
17	chr4:104227316-104227366	GM12891	blood:	n/a
18	chr4:104239655-104239705	Hela-S3	cervix:	n/a
19	chr4:104239655-104239705	T-47D	breast:	n/a
20	chr4:104239655-104239705	GM19239	blood:	n/a
21	chr4:104227316-104227366	HCT-116	colon:	n/a
22	chr4:104227316-104227366	HRPEpiC	eye:	n/a
23	chr4:104227316-104227366	A549	lung:	n/a
24	chr4:104227316-104227366	LNCaP	prostate:	n/a
25	chr4:104227316-104227366	BE2_C	brain:	n/a
26	chr4:104227316-104227366	HepG2	liver:	n/a
27	chr4:104239655-104239705	AG10803	skin:	n/a
28	chr4:104239655-104239705	GM12878	blood:	n/a
29	chr4:104239655-104239705	HepG2	liver:	n/a
30	chr4:104239655-104239705	HUVEC	blood vessel:	n/a
31	chr4:104239655-104239705	HCPEpiC	choroid plexus:	n/a
32	chr4:104239655-104239705	Jurkat	blood:	n/a
33	chr4:104227316-104227366	HIPEpiC	eye:	n/a
34	chr4:104239655-104239705	HRCEpiC	kidney:	n/a
35	chr4:104227316-104227366	SKMC	muscle:	n/a
36	chr4:104227316-104227366	NHBE	bronchial:	n/a
37	chr4:104227316-104227366	AG04450	lung:	fetal
38	chr4:104227316-104227366	HEK293	kidney:	embryo
39	chr4:104239655-104239705	SK-N-MC	brain:	n/a
40	chr4:104239655-104239705	NB4	blood:	n/a
41	chr4:104239655-104239705	HMEC	breast:	n/a
42	chr4:104239655-104239705	ProgFib	skin:	n/a
43	chr4:104227316-104227366	HAEpiC	amniotic membrane:	n/a
44	chr4:104227316-104227366	Hepatocyte	liver:	n/a
45	chr4:104239655-104239705	AG04450	lung:	fetal
46	chr4:104227316-104227366	HNPCEpiC	eye:	n/a
47	chr4:104239655-104239705	HNPCEpiC	eye:	n/a
48	chr4:104239655-104239705	BJ	skin:	n/a
49	chr4:104227316-104227366	HCF	heart:	n/a
50	chr4:104227316-104227366	RPTEC	kidney:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:104333746..104335920-chr4:104344875..104346775,2	MCF-7	breast:
2	chr4:104180046..104181574-chr4:104181582..104183273,2	K562	blood:
3	chr4:104246786..104248754-chr4:104256476..104258038,2	K562	blood:
4	chr4:104322090..104323891-chr4:104326352..104329222,2	MCF-7	breast:
5	chr4:104117492..104119427-chr4:104178040..104180048,2	K562	blood:
6	chr4:104246786..104248754-chr4:104256476..104258038,2	K562	blood:
7	chr4:104243719..104245643-chr4:104247001..104248713,2	K562	blood:
8	chr4:104213569..104215673-chr4:104223134..104225892,2	MCF-7	breast:
9	chr4:104250850..104252961-chr4:104254841..104257774,2	K562	blood:
10	chr4:104181685..104183408-chr4:104209717..104212156,2	K562	blood:
11	chr4:104322090..104323891-chr4:104326352..104329222,2	MCF-7	breast:
12	chr4:104213569..104215673-chr4:104223134..104225892,2	MCF-7	breast:
13	chr4:104180046..104181574-chr4:104181582..104183273,2	K562	blood:
14	chr4:104250850..104252961-chr4:104254841..104257774,2	K562	blood:
15	chr4:104181685..104183408-chr4:104209717..104212156,2	K562	blood:
16	chr4:104243719..104245643-chr4:104247001..104248713,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CISD2-3	chr4:104298160-104298332	ENSG00000248740

No data

Variant related genes	Relation type
ENSG00000248740	TF binding region
ENSG00000248740	CpG island
ENSG00000248740	chromatin interactions

Extended variants
information (count: 3827 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3827 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557463345	chr4:104179950-104179951	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs17033498	chr4:104179961-104179962	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs534585134	chr4:104179998-104179999	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs116669405	chr4:104180045-104180046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566377670	chr4:104180103-104180104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182494972	chr4:104180164-104180165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574997349	chr4:104180172-104180173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542311404	chr4:104180174-104180175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563896452	chr4:104180189-104180190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144835595	chr4:104180190-104180191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576225431	chr4:104180192-104180193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113340595	chr4:104180209-104180210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555973779	chr4:104180225-104180226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573722647	chr4:104180273-104180274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188013762	chr4:104180277-104180278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559456117	chr4:104180323-104180324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148566845	chr4:104180324-104180325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191499504	chr4:104180341-104180342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544929888	chr4:104180383-104180384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183273624	chr4:104180456-104180457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530717660	chr4:104180493-104180494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28553985	chr4:104180511-104180512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187898225	chr4:104180564-104180565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376545916	chr4:104180568-104180569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546215679	chr4:104180585-104180586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201882372	chr4:104180586-104180587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191985681	chr4:104180594-104180595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546584073	chr4:104180618-104180619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571110318	chr4:104180650-104180651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533727368	chr4:104180675-104180676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145576026	chr4:104180692-104180693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566087792	chr4:104180700-104180701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569946960	chr4:104180769-104180770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528118858	chr4:104180808-104180809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs184684451	chr4:104180829-104180830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189552566	chr4:104180836-104180837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116111250	chr4:104180861-104180862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540224679	chr4:104180868-104180869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367863481	chr4:104180891-104180892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370511588	chr4:104180904-104180905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534770084	chr4:104180942-104180943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561304907	chr4:104180966-104180967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553337574	chr4:104180974-104180975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192966183	chr4:104180986-104180987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs58265700	chr4:104180991-104180992	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540961881	chr4:104181081-104181082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184258007	chr4:104181094-104181095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556959990	chr4:104181102-104181103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189318164	chr4:104181105-104181106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11732717	chr4:104181116-104181117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:315 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:104177200-104180000	Active TSS	K562	blood
2	chr4:104178800-104180400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr4:104179000-104183000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr4:104179200-104180200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:104179400-104181000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:104179600-104180000	Enhancers	HepG2	liver
7	chr4:104179800-104180200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:104179800-104180600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:104180200-104180400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:104180400-104180800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:104180600-104181000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:104180800-104183000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr4:104181000-104183200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:104183000-104183400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:104183000-104183600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:104183200-104183600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:104189600-104193800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:104192600-104192800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:104192600-104193000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr4:104192800-104193000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:104192800-104200800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr4:104193000-104193400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr4:104193000-104194400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:104193000-104194400	Enhancers	HMEC	breast
25	chr4:104193000-104194600	Enhancers	Gastric	stomach
26	chr4:104193400-104193800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr4:104193400-104194200	Enhancers	Pancreas	Pancrea
28	chr4:104193800-104194200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
29	chr4:104194200-104194600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr4:104194400-104194600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
31	chr4:104194600-104202600	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr4:104197800-104198200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:104197800-104198200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:104198000-104198200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:104209400-104229400	Weak transcription	Right Atrium	heart
36	chr4:104210200-104210600	Enhancers	Muscle Satellite Cultured Cells	--
37	chr4:104213400-104214400	Enhancers	HMEC	breast
38	chr4:104213600-104213800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:104214200-104214600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:104214600-104214800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr4:104214800-104223800	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr4:104215000-104216800	Enhancers	HepG2	liver
43	chr4:104215400-104216000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:104215800-104216800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:104216000-104220200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:104220200-104220400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:104220400-104224000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:104223800-104224800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr4:104223800-104224800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr4:104223800-104224800	Enhancers	HUES64 Cell Line	embryonic stem cell

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