Variant report

Variant	nsv433218
Chromosome Location	chr4:28641062-28732481
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	BCL11A	chr4:28684526-28684791	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr4:28688187-28688716	HCT-116	colon:	n/a	n/a
3	CEBPB	chr4:28725885-28726210	Hela-S3	cervix:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
4	CEBPB	chr4:28676408-28676634	IMR90	lung:	n/a	n/a
5	CEBPB	chr4:28725875-28726235	A549	lung:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
6	CEBPB	chr4:28730328-28730676	MCF-7	breast:	n/a	n/a
7	CEBPB	chr4:28663372-28663685	HepG2	liver:	n/a	chr4:28663629-28663640 chr4:28663629-28663640 chr4:28663426-28663439 chr4:28663482-28663494 chr4:28663629-28663642
8	CEBPB	chr4:28641218-28641462	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:28730369-28730815	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:28711290-28711826	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr4:28711321-28711600	MCF-7	breast:	n/a	n/a
12	CEBPB	chr4:28721270-28721402	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:28725878-28726242	H1-hESC	embryonic stem cell:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
14	CEBPB	chr4:28689104-28689305	IMR90	lung:	n/a	chr4:28689150-28689161
15	CEBPB	chr4:28655343-28655667	HepG2	liver:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
16	CEBPB	chr4:28655386-28655554	H1-hESC	embryonic stem cell:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
17	CEBPB	chr4:28711314-28711622	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:28663440-28663693	A549	lung:	n/a	chr4:28663629-28663640 chr4:28663629-28663640 chr4:28663482-28663494 chr4:28663629-28663642
19	CEBPB	chr4:28730461-28730602	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr4:28641171-28641469	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:28655370-28655599	K562	blood:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
22	CEBPB	chr4:28689154-28689222	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:28725870-28726243	IMR90	lung:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
24	CEBPB	chr4:28725866-28726227	K562	blood:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
25	CEBPB	chr4:28725882-28726242	HepG2	liver:	n/a	chr4:28726053-28726064 chr4:28725937-28725949
26	CEBPB	chr4:28707505-28707745	A549	lung:	n/a	n/a
27	CEBPB	chr4:28655314-28655637	IMR90	lung:	n/a	chr4:28655487-28655498 chr4:28655485-28655496 chr4:28655487-28655496 chr4:28655485-28655498
28	CEBPB	chr4:28666584-28666603	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:28666175-28666318	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:28689052-28689245	H1-hESC	embryonic stem cell:	n/a	chr4:28689150-28689161
31	CHD2	chr4:28684477-28684861	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:28688298-28688477	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:28732020-28732170	HFF	foreskin:	n/a	n/a
34	CTCF	chr4:28688400-28688550	GM12875	blood:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
35	CTCF	chr4:28688380-28688530	HEEpiC	esophagus:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
36	CTCF	chr4:28732040-28732190	HMF	breast:	n/a	n/a
37	CTCF	chr4:28688312-28688577	A549	lung:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
38	CTCF	chr4:28688380-28688530	BE2_C	brain:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
39	CTCF	chr4:28688374-28688498	GM10248	blood:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
40	CTCF	chr4:28688360-28688510	HCPEpiC	choroid plexus:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
41	CTCF	chr4:28688309-28688548	GM19238	blood:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
42	CTCF	chr4:28688358-28688531	K562	blood:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
43	CTCF	chr4:28688127-28688698	HCT-116	colon:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
44	CTCF	chr4:28688340-28688490	MCF-7	breast:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
45	CTCF	chr4:28688277-28688574	Fibrobl	skin:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
46	CTCF	chr4:28688243-28688639	IMR90	lung:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
47	CTCF	chr4:28688380-28688530	GM12865	blood:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
48	CTCF	chr4:28688320-28688470	HVMF	connective:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
49	CTCF	chr4:28688360-28688510	RPTEC	kidney:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449
50	CTCF	chr4:28688380-28688530	HAc	cerebellar:	n/a	chr4:28688434-28688450 chr4:28688433-28688451 chr4:28688435-28688456 chr4:28688436-28688449

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:28725306-28725356	U87	brain:	n/a
2	chr4:28725306-28725356	A549	lung:	n/a
3	chr4:28725306-28725356	SAEC	small airway:	n/a
4	chr4:28725306-28725356	HUVEC	blood vessel:	n/a
5	chr4:28725306-28725356	IMR90	lung:	fetal
6	chr4:28725306-28725356	HNPCEpiC	eye:	n/a
7	chr4:28725306-28725356	HEK293	kidney:	embryo
8	chr4:28725306-28725356	NHBE	bronchial:	n/a
9	chr4:28725306-28725356	HAEpiC	amniotic membrane:	n/a
10	chr4:28725306-28725356	ProgFib	skin:	n/a
11	chr4:28725306-28725356	CMK	blood:	n/a
12	chr4:28725306-28725356	AoSMC	blood vessel:	n/a
13	chr4:28725306-28725356	HCF	heart:	n/a
14	chr4:28725306-28725356	Hela-S3	cervix:	n/a
15	chr4:28725306-28725356	NH-A	brain:	n/a
16	chr4:28725306-28725356	AG04450	lung:	fetal
17	chr4:28725306-28725356	AG04449	skin:	fetal
18	chr4:28725306-28725356	PFSK-1	brain:	n/a
19	chr4:28725306-28725356	HIPEpiC	eye:	n/a
20	chr4:28725306-28725356	BE2_C	brain:	n/a
21	chr4:28725306-28725356	GM06990	blood:	n/a
22	chr4:28725306-28725356	HCPEpiC	choroid plexus:	n/a
23	chr4:28725306-28725356	NB4	blood:	n/a
24	chr4:28725306-28725356	LNCaP	prostate:	n/a
25	chr4:28725306-28725356	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:28725306-28725356	PANC-1	pancreas:	n/a
27	chr4:28725306-28725356	Hepatocyte	liver:	n/a
28	chr4:28725306-28725356	GM12891	blood:	n/a
29	chr4:28725306-28725356	Caco-2	colon:	n/a
30	chr4:28725306-28725356	AG09319	gingival:	n/a
31	chr4:28725306-28725356	GM12892	blood:	n/a
32	chr4:28725306-28725356	T-47D	breast:	n/a
33	chr4:28725306-28725356	HCM	heart:	n/a
34	chr4:28725306-28725356	RPTEC	kidney:	n/a
35	chr4:28725306-28725356	HRCEpiC	kidney:	n/a
36	chr4:28725306-28725356	MCF-7	breast:	n/a
37	chr4:28725306-28725356	HepG2	liver:	n/a
38	chr4:28725306-28725356	SKMC	muscle:	n/a
39	chr4:28725306-28725356	HEEpiC	esophagus:	n/a
40	chr4:28725306-28725356	K562	blood:	n/a
41	chr4:28725306-28725356	AG09309	skin:	n/a
42	chr4:28725306-28725356	HMEC	breast:	n/a
43	chr4:28725306-28725356	BJ	skin:	n/a
44	chr4:28725306-28725356	AG10803	skin:	n/a
45	chr4:28725306-28725356	MCF10A-Er-Src	breast:	n/a
46	chr4:28725306-28725356	ovcar-3	ovarian:	n/a
47	chr4:28725306-28725356	H1-hESC	embryonic stem cell:	embryo
48	chr4:28725306-28725356	GM12878	blood:	n/a
49	chr4:28725306-28725356	GM19239	blood:	n/a
50	chr4:28725306-28725356	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:28690061..28692565-chr4:28693804..28695877,2	K562	blood:
2	chr4:28642172..28644284-chr4:28671364..28674142,2	MCF-7	breast:
3	chr4:28666962..28669631-chr4:28671140..28674094,2	K562	blood:
4	chr4:28642172..28644284-chr4:28671364..28674142,2	MCF-7	breast:
5	chr4:28699826..28702524-chr4:28704115..28706351,2	MCF-7	breast:
6	chr4:28464145..28465046-chr4:28688173..28688894,2	MCF-7	breast:
7	chr4:28654800..28656998-chr4:28661413..28663386,2	MCF-7	breast:
8	chr2:19310340..19311108-chr4:28646906..28647846,2	MCF-7	breast:
9	chr4:28690061..28692565-chr4:28693804..28695877,2	K562	blood:
10	chr4:28654800..28656998-chr4:28661413..28663386,2	MCF-7	breast:
11	chr4:28712094..28713787-chr4:28714088..28715942,2	MCF-7	breast:
12	chr4:28699826..28702524-chr4:28704115..28706351,2	MCF-7	breast:
13	chr4:28683044..28685145-chr4:28691951..28693893,2	K562	blood:
14	chr4:28683044..28685145-chr4:28691951..28693893,2	K562	blood:
15	chr4:28666962..28669631-chr4:28671140..28674094,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STIM2-8	chr4:28712820-28713094	NONHSAT095914

Variant related genes	Relation type
RN7SL101P	TF binding region
RN7SL101P	CpG island
ENSG00000243548	chromatin interactions

Extended variants
information (count: 1184 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6831370	chr4:28641062-28641063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12501442	chr4:28641096-28641097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs190258936	chr4:28641110-28641111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113734369	chr4:28641166-28641167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552947463	chr4:28641179-28641180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544460487	chr4:28641234-28641235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182023686	chr4:28641239-28641240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529928586	chr4:28641266-28641267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140354887	chr4:28641330-28641331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566217865	chr4:28641341-28641342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528553707	chr4:28641342-28641343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551802172	chr4:28641415-28641416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571588299	chr4:28641422-28641423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368004303	chr4:28641448-28641449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185916713	chr4:28641467-28641468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557666663	chr4:28641479-28641480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73133376	chr4:28641585-28641586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs144214136	chr4:28641594-28641595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149793448	chr4:28655809-28655810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552558087	chr4:28655811-28655812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75480502	chr4:28655816-28655817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79372107	chr4:28655820-28655821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561268492	chr4:28655827-28655828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370541812	chr4:28655833-28655834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544190817	chr4:28655841-28655842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59017482	chr4:28655873-28655874	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188561338	chr4:28655914-28655915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540490319	chr4:28655923-28655924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs386672879	chr4:28656016-28656017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67012534	chr4:28656017-28656018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545946144	chr4:28656062-28656063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562570906	chr4:28656124-28656125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs57767930	chr4:28656165-28656166	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548169302	chr4:28656167-28656168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73807356	chr4:28656189-28656190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs527555355	chr4:28656204-28656205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16880880	chr4:28656246-28656247	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570661068	chr4:28656249-28656250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539245178	chr4:28656254-28656255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558665718	chr4:28656255-28656256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557806553	chr4:28656258-28656259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568969589	chr4:28656303-28656304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147886607	chr4:28656318-28656319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571539300	chr4:28656382-28656383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs554919443	chr4:28656446-28656447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534114949	chr4:28656479-28656480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191676174	chr4:28656494-28656495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540953619	chr4:28656547-28656548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs16880882	chr4:28656565-28656566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs183768807	chr4:28656586-28656587	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28623800-28641200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:28632800-28641400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:28641200-28641400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:28641400-28641600	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr4:28655800-28656400	Enhancers	HMEC	breast
6	chr4:28655800-28656600	Enhancers	HUVEC	blood vessel
7	chr4:28656000-28656600	Enhancers	NHEK	skin
8	chr4:28661600-28662200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:28669600-28669800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:28673200-28674000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr4:28673400-28673800	Enhancers	Placenta Amnion	Placenta Amnion
12	chr4:28673800-28674800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr4:28675000-28675200	Enhancers	Placenta Amnion	Placenta Amnion
14	chr4:28676800-28677000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:28678200-28678800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:28678600-28679200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:28678800-28682000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:28679200-28679600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:28679200-28679800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:28679400-28680000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:28679600-28679800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:28679600-28679800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:28679600-28680400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:28679800-28680000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:28680000-28681600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr4:28680000-28682600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:28680400-28681800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:28681600-28684400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:28681600-28684400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:28681800-28684000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:28682000-28682800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:28682000-28682800	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:28682200-28682800	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr4:28682200-28684400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:28682200-28685400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:28682400-28682800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr4:28682400-28684200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:28682600-28683200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:28682800-28683800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr4:28682800-28683800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:28682800-28684800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:28682800-28685200	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr4:28683000-28683200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr4:28683200-28684400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr4:28683200-28685000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:28683800-28684200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr4:28683800-28684200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:28684000-28684200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr4:28684000-28684800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:28684200-28684600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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