Variant report

Variant	nsv879565
Chromosome Location	chr4:92142966-92251839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:287)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:92177249-92177619	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:92177198-92177597	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:92177316-92177515	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:92191483-92191539	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:92246684-92246980	GM12878	blood:	n/a	n/a
6	BATF	chr4:92246616-92246958	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:92177222-92177529	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr4:92177273-92177559	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr4:92223302-92223415	GM12878	blood:	n/a	n/a
10	CEBPB	chr4:92148021-92148389	Hela-S3	cervix:	n/a	chr4:92148264-92148277
11	CEBPB	chr4:92148015-92148366	HepG2	liver:	n/a	chr4:92148264-92148277
12	CEBPB	chr4:92148030-92148354	H1-hESC	embryonic stem cell:	n/a	chr4:92148264-92148277
13	CEBPB	chr4:92148719-92148746	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr4:92177264-92177553	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:92148031-92148396	K562	blood:	n/a	chr4:92148264-92148277
16	CEBPB	chr4:92147997-92148383	A549	lung:	n/a	chr4:92148264-92148277
17	CEBPB	chr4:92148597-92148798	A549	lung:	n/a	chr4:92148629-92148642
18	CEBPB	chr4:92181253-92181489	HepG2	liver:	n/a	chr4:92181364-92181375
19	CEBPB	chr4:92148019-92148382	IMR90	lung:	n/a	chr4:92148264-92148277
20	CHD1	chr4:92143874-92143897	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr4:92223402-92223554	GM12878	blood:	n/a	n/a
22	CHD2	chr4:92177261-92177681	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr4:92160583-92160590	GM10266	blood:	n/a	n/a
24	CTCF	chr4:92160485-92160575	GM10266	blood:	n/a	n/a
25	CTCF	chr4:92185520-92185670	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr4:92160187-92160271	GM13976	blood:	n/a	n/a
27	CTCF	chr4:92236120-92236270	HVMF	connective:	n/a	n/a
28	CTCF	chr4:92237937-92237962	GM20000	blood:	n/a	n/a
29	CTCF	chr4:92160278-92160299	GM13976	blood:	n/a	n/a
30	CTCF	chr4:92247480-92247630	GM12874	blood:	n/a	n/a
31	CTCF	chr4:92160532-92160614	GM13977	blood:	n/a	n/a
32	CTCF	chr4:92143320-92143470	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr4:92224307-92224326	GM10266	blood:	n/a	n/a
34	CTCF	chr4:92247623-92247698	GM13976	blood:	n/a	n/a
35	CTCF	chr4:92196766-92196816	GM10248	blood:	n/a	n/a
36	CTCF	chr4:92165532-92165567	GM10248	blood:	n/a	n/a
37	CUX1	chr4:92153200-92153271	GM12878	blood:	n/a	n/a
38	CUX1	chr4:92217982-92218053	GM12878	blood:	n/a	n/a
39	E2F4	chr4:92210264-92210314	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr4:92225103-92225323	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr4:92158345-92158585	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr4:92188793-92188993	GM12878	blood:	n/a	n/a
43	EP300	chr4:92246505-92247133	SK-N-SH	brain:	n/a	chr4:92246526-92246533 chr4:92246898-92246912
44	EP300	chr4:92177209-92177582	H1-hESC	embryonic stem cell:	n/a	n/a
45	EP300	chr4:92246540-92246754	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr4:92223445-92223554	GM12878	blood:	n/a	n/a
47	EP300	chr4:92229381-92229386	K562	blood:	n/a	n/a
48	EP300	chr4:92188777-92188977	GM12878	blood:	n/a	n/a
49	EP300	chr4:92210232-92210450	GM12878	blood:	n/a	n/a
50	EP300	chr4:92223291-92223465	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92189705-92189755	A549	lung:	n/a
2	chr4:92189705-92189755	HMEC	breast:	n/a
3	chr4:92189705-92189755	BE2_C	brain:	n/a
4	chr4:92189705-92189755	ECC-1	luminal epithelium:	n/a
5	chr4:92189705-92189755	HCM	heart:	n/a
6	chr4:92189705-92189755	HIPEpiC	eye:	n/a
7	chr4:92189705-92189755	AG09319	gingival:	n/a
8	chr4:92189705-92189755	GM12891	blood:	n/a
9	chr4:92189705-92189755	BJ	skin:	n/a
10	chr4:92189705-92189755	GM12878	blood:	n/a
11	chr4:92189705-92189755	SK-N-MC	brain:	n/a
12	chr4:92189705-92189755	HL-60	blood:	n/a
13	chr4:92189705-92189755	GM06990	blood:	n/a
14	chr4:92189705-92189755	GM12892	blood:	n/a
15	chr4:92189705-92189755	PANC-1	pancreas:	n/a
16	chr4:92189705-92189755	HAEpiC	amniotic membrane:	n/a
17	chr4:92189705-92189755	NHDF-neo	bronchial:	n/a
18	chr4:92189705-92189755	HEK293	kidney:	embryo
19	chr4:92189705-92189755	GM19239	blood:	n/a
20	chr4:92189705-92189755	SK-N-SH	brain:	n/a
21	chr4:92189705-92189755	Caco-2	colon:	n/a
22	chr4:92189705-92189755	HEEpiC	esophagus:	n/a
23	chr4:92189705-92189755	IMR90	lung:	fetal
24	chr4:92189705-92189755	MCF-7	breast:	n/a
25	chr4:92189705-92189755	AG04449	skin:	fetal
26	chr4:92189705-92189755	Jurkat	blood:	n/a
27	chr4:92189705-92189755	HRPEpiC	eye:	n/a
28	chr4:92189705-92189755	NHBE	bronchial:	n/a
29	chr4:92189705-92189755	CMK	blood:	n/a
30	chr4:92189705-92189755	SAEC	small airway:	n/a
31	chr4:92189705-92189755	NB4	blood:	n/a
32	chr4:92189705-92189755	SKMC	muscle:	n/a
33	chr4:92189705-92189755	HCT-116	colon:	n/a
34	chr4:92189705-92189755	PrEC	prostate:	n/a
35	chr4:92189705-92189755	AG04450	lung:	fetal
36	chr4:92189705-92189755	HCPEpiC	choroid plexus:	n/a
37	chr4:92189705-92189755	HepG2	liver:	n/a
38	chr4:92189705-92189755	AG10803	skin:	n/a
39	chr4:92189705-92189755	AG09309	skin:	n/a
40	chr4:92189705-92189755	MCF10A-Er-Src	breast:	n/a
41	chr4:92189705-92189755	HNPCEpiC	eye:	n/a
42	chr4:92189705-92189755	HCF	heart:	n/a
43	chr4:92189705-92189755	T-47D	breast:	n/a
44	chr4:92189705-92189755	HUVEC	blood vessel:	n/a
45	chr4:92189705-92189755	HRCEpiC	kidney:	n/a
46	chr4:92189705-92189755	Hela-S3	cervix:	n/a
47	chr4:92189705-92189755	ProgFib	skin:	n/a
48	chr4:92189705-92189755	U87	brain:	n/a
49	chr4:92189705-92189755	NH-A	brain:	n/a
50	chr4:92189705-92189755	LNCaP	prostate:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:92176022..92178505-chr4:92180113..92182729,2	K562	blood:
2	chr4:92228930..92230474-chr4:92239556..92242007,2	K562	blood:
3	chr4:92249209..92252138-chr4:92252795..92255607,2	MCF-7	breast:
4	chr4:92228930..92230474-chr4:92239556..92242007,2	K562	blood:
5	chr4:92176022..92178505-chr4:92180113..92182729,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000249049	TF binding region
ENSG00000249049	CpG island

Extended variants
information (count: 1104 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1104 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190273334	chr4:92143606-92143607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150959130	chr4:92143633-92143634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12509942	chr4:92143658-92143659	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs529859811	chr4:92143669-92143670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549700747	chr4:92143684-92143685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570178936	chr4:92143691-92143692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539115497	chr4:92143777-92143778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559027850	chr4:92143823-92143824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566050419	chr4:92143887-92143888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs180899438	chr4:92143933-92143934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184908138	chr4:92143958-92143959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368229907	chr4:92144076-92144077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575022540	chr4:92144096-92144097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190260052	chr4:92144137-92144138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560814376	chr4:92144164-92144165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528106661	chr4:92144165-92144166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs57497886	chr4:92144203-92144204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397699011	chr4:92144210-92144211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576858925	chr4:92144285-92144286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12506868	chr4:92144381-92144382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182509487	chr4:92144397-92144398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544667712	chr4:92144417-92144418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4491986	chr4:92144469-92144470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs527248649	chr4:92144476-92144477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116259394	chr4:92144497-92144498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201804747	chr4:92144521-92144522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561278518	chr4:92144551-92144552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72875137	chr4:92144562-92144563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs549977257	chr4:92144563-92144564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569852160	chr4:92144629-92144630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532670339	chr4:92144698-92144699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552656130	chr4:92144725-92144726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140757216	chr4:92144727-92144728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535058386	chr4:92144739-92144740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560776929	chr4:92144871-92144872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59066405	chr4:92144941-92144942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537326974	chr4:92144976-92144977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552273608	chr4:92145011-92145012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564649212	chr4:92145015-92145016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369045378	chr4:92145036-92145037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11730949	chr4:92145041-92145042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185985544	chr4:92145058-92145059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72875138	chr4:92145081-92145082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558191374	chr4:92145099-92145100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571800922	chr4:92145118-92145119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200205225	chr4:92145145-92145146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541068302	chr4:92145156-92145157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191783984	chr4:92145198-92145199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34962423	chr4:92145209-92145210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574832884	chr4:92145210-92145211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
lymphocytic leukemia	21291569	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92143600-92143800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:92143800-92145400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:92145400-92145800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:92145800-92146800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr4:92146800-92147000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:92147000-92147600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:92154000-92154200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr4:92154000-92154600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:92154000-92154800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr4:92154200-92154800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr4:92154200-92154800	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr4:92154200-92155400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr4:92155400-92155600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:92164400-92164800	Enhancers	Stomach Mucosa	stomach
15	chr4:92177800-92178600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
16	chr4:92178600-92179000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr4:92179000-92179200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:92188000-92190600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:92188200-92189600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr4:92188200-92190000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:92188600-92189600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:92188600-92190000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:92188600-92190800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:92188600-92191000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:92188800-92189000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:92188800-92189600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:92189000-92189200	Enhancers	Fetal Intestine Large	intestine
28	chr4:92189000-92189400	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr4:92189000-92190400	Enhancers	Stomach Mucosa	stomach
30	chr4:92189000-92190600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr4:92189200-92190200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:92189200-92190200	Weak transcription	Fetal Intestine Large	intestine
33	chr4:92189200-92190400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:92189600-92190000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:92189600-92190600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr4:92190000-92190200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:92190000-92190400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr4:92190000-92190400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr4:92190000-92190400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr4:92190200-92190600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:92190200-92190600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:92190200-92190600	Enhancers	Fetal Intestine Large	intestine
43	chr4:92190200-92191000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr4:92190400-92190800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr4:92190400-92192000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:92190600-92191000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr4:92190600-92191200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:92190800-92191000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:92190800-92191200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr4:92191000-92191400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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