Variant report

Variant	nsv1013446
Chromosome Location	chr3:25176609-25221334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:25197045-25198071	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:25197041-25198078	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr3:25197196-25197507	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr3:25197656-25197929	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:25198190-25198515	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:25190883-25191148	HepG2	liver:	n/a	chr3:25191030-25191041
7	CEBPB	chr3:25212341-25212643	H1-hESC	embryonic stem cell:	n/a	chr3:25212458-25212469
8	CEBPB	chr3:25197180-25197958	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:25212333-25212577	HepG2	liver:	n/a	chr3:25212458-25212469
10	CEBPB	chr3:25212335-25212578	A549	lung:	n/a	chr3:25212458-25212469
11	CHD1	chr3:25198524-25198662	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr3:25197113-25198328	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr3:25197161-25198097	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr3:25197106-25197973	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr3:25215965-25215967	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:25219060-25219210	GM12878	blood:	n/a	n/a
17	CTCF	chr3:25215896-25215964	MCF-7	breast:	n/a	n/a
18	CTCF	chr3:25191636-25191696	Lung_OC	lung:	n/a	n/a
19	E2F4	chr3:25198307-25198506	MCF10A-Er-Src	breast:	n/a	n/a
20	ELK1	chr3:25193084-25193106	GM12878	blood:	n/a	n/a
21	ELK1	chr3:25193135-25193245	Hela-S3	cervix:	n/a	n/a
22	EP300	chr3:25212538-25213287	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
23	EP300	chr3:25197082-25197497	SK-N-SH_RA	brain:	n/a	chr3:25197174-25197183
24	EP300	chr3:25212226-25214085	SK-N-SH	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213452-25213462 chr3:25213136-25213150 chr3:25212704-25212714
25	EP300	chr3:25212547-25213299	SK-N-SH_RA	brain:	n/a	chr3:25213135-25213149 chr3:25213137-25213151 chr3:25213138-25213152 chr3:25213136-25213150 chr3:25212704-25212714
26	EP300	chr3:25198224-25198547	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr3:25197025-25198012	H1-hESC	embryonic stem cell:	n/a	chr3:25197174-25197183
28	EP300	chr3:25197051-25197488	SK-N-SH_RA	brain:	n/a	chr3:25197174-25197183
29	EP300	chr3:25197453-25198623	SK-N-SH	brain:	n/a	n/a
30	EP300	chr3:25213543-25213823	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr3:25197194-25197539	H1-hESC	embryonic stem cell:	n/a	n/a
32	EP300	chr3:25200974-25201312	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr3:25194737-25195080	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr3:25213501-25213811	SK-N-SH_RA	brain:	n/a	n/a
35	FAM48A	chr3:25177839-25177917	GM12878	blood:	n/a	n/a
36	FOS	chr3:25184962-25185067	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr3:25198285-25198512	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:25184936-25185069	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:25198183-25198567	MCF10A-Er-Src	breast:	n/a	chr3:25198504-25198513
40	FOS	chr3:25198130-25198588	HUVEC	blood vessel:	n/a	chr3:25198504-25198513
41	FOS	chr3:25192689-25193476	HUVEC	blood vessel:	n/a	chr3:25193201-25193210
42	FOS	chr3:25198191-25198491	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:25184914-25185072	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:25184926-25185056	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:25198208-25198523	MCF10A-Er-Src	breast:	n/a	chr3:25198504-25198513
46	FOSL2	chr3:25198062-25198596	SK-N-SH	brain:	n/a	chr3:25198504-25198513
47	GATA2	chr3:25206713-25207182	SH-SY5Y	brain:	n/a	n/a
48	GATA2	chr3:25212562-25213261	SH-SY5Y	brain:	n/a	n/a
49	GATA2	chr3:25192936-25193343	HUVEC	blood vessel:	n/a	n/a
50	GATA2	chr3:25194789-25195363	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:25197710-25197760	H1-hESC	embryonic stem cell:	embryo
2	chr3:25197710-25197760	IMR90	lung:	fetal
3	chr3:25197710-25197760	HMEC	breast:	n/a
4	chr3:25197710-25197760	HRCEpiC	kidney:	n/a
5	chr3:25197710-25197760	LNCaP	prostate:	n/a
6	chr3:25197710-25197760	MCF10A-Er-Src	breast:	n/a
7	chr3:25197710-25197760	HepG2	liver:	n/a
8	chr3:25215914-25215964	HAEpiC	amniotic membrane:	n/a
9	chr3:25215914-25215964	HepG2	liver:	n/a
10	chr3:25197710-25197760	AG10803	skin:	n/a
11	chr3:25197710-25197760	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:25215914-25215964	SK-N-SH_RA	brain:	n/a
13	chr3:25215914-25215964	GM12878	blood:	n/a
14	chr3:25215914-25215964	ovcar-3	ovarian:	n/a
15	chr3:25215914-25215964	Caco-2	colon:	n/a
16	chr3:25215914-25215964	HNPCEpiC	eye:	n/a
17	chr3:25197710-25197760	HEEpiC	esophagus:	n/a
18	chr3:25215914-25215964	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:25215914-25215964	HCPEpiC	choroid plexus:	n/a
20	chr3:25215914-25215964	PrEC	prostate:	n/a
21	chr3:25215914-25215964	CMK	blood:	n/a
22	chr3:25215914-25215964	NHBE	bronchial:	n/a
23	chr3:25215914-25215964	AG09319	gingival:	n/a
24	chr3:25197710-25197760	Caco-2	colon:	n/a
25	chr3:25197710-25197760	K562	blood:	n/a
26	chr3:25215914-25215964	T-47D	breast:	n/a
27	chr3:25197710-25197760	AG09309	skin:	n/a
28	chr3:25215914-25215964	PANC-1	pancreas:	n/a
29	chr3:25215914-25215964	GM12892	blood:	n/a
30	chr3:25215914-25215964	NT2-D1	testis:	n/a
31	chr3:25215914-25215964	HCM	heart:	n/a
32	chr3:25197710-25197760	ovcar-3	ovarian:	n/a
33	chr3:25215914-25215964	HMEC	breast:	n/a
34	chr3:25197710-25197760	NH-A	brain:	n/a
35	chr3:25197710-25197760	Hela-S3	cervix:	n/a
36	chr3:25215914-25215964	HIPEpiC	eye:	n/a
37	chr3:25197710-25197760	U87	brain:	n/a
38	chr3:25215914-25215964	BJ	skin:	n/a
39	chr3:25215914-25215964	Hela-S3	cervix:	n/a
40	chr3:25215914-25215964	GM12891	blood:	n/a
41	chr3:25197710-25197760	NB4	blood:	n/a
42	chr3:25215914-25215964	HRPEpiC	eye:	n/a
43	chr3:25215914-25215964	ECC-1	luminal epithelium:	n/a
44	chr3:25215914-25215964	MCF-7	breast:	n/a
45	chr3:25215914-25215964	SK-N-SH	brain:	n/a
46	chr3:25197710-25197760	AG04449	skin:	fetal
47	chr3:25197710-25197760	NT2-D1	testis:	n/a
48	chr3:25215914-25215964	HCT-116	colon:	n/a
49	chr3:25215914-25215964	HEK293	kidney:	embryo
50	chr3:25215914-25215964	AG04449	skin:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:25173033..25175213-chr3:25183319..25185736,2	MCF-7	breast:
2	chr3:25162001..25164779-chr3:25173824..25178190,3	K562	blood:
3	chr3:25187342..25189876-chr3:25191897..25194177,2	MCF-7	breast:
4	chr3:25201532..25204868-chr3:25206067..25208834,3	K562	blood:
5	chr3:25187342..25189876-chr3:25191897..25194177,2	MCF-7	breast:
6	chr3:25200008..25202995-chr3:25206457..25208830,2	MCF-7	breast:
7	chr3:25200008..25202995-chr3:25206457..25208830,2	MCF-7	breast:
8	chr3:25201532..25204868-chr3:25206067..25208834,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RARB-1	chr3:25215610-25215796	ENSG00000237838

No data

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

Extended variants
information (count: 2189 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2189 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7636453	chr3:25176609-25176610	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570471189	chr3:25176616-25176617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539493103	chr3:25176632-25176633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552813164	chr3:25176637-25176638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572957818	chr3:25176663-25176664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371778229	chr3:25176693-25176694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191894688	chr3:25176694-25176695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575191887	chr3:25176718-25176719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544188788	chr3:25176726-25176727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564094572	chr3:25176747-25176748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184186385	chr3:25176749-25176750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533179893	chr3:25176815-25176816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188851214	chr3:25176817-25176818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375785283	chr3:25176823-25176824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143710593	chr3:25176836-25176837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191733903	chr3:25176842-25176843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146773394	chr3:25176843-25176844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532002633	chr3:25176845-25176846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552105385	chr3:25176897-25176898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140452012	chr3:25176914-25176915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559635470	chr3:25176925-25176926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539454816	chr3:25176939-25176940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182902645	chr3:25176946-25176947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs997309	chr3:25176954-25176955	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535633090	chr3:25176956-25176957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548296896	chr3:25176986-25176987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2062485	chr3:25176988-25176989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575102779	chr3:25177044-25177045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4386457	chr3:25177050-25177051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs58405464	chr3:25177060-25177061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186967346	chr3:25177094-25177095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540298467	chr3:25177095-25177096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2062486	chr3:25177101-25177102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs574090734	chr3:25177134-25177135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61640000	chr3:25177146-25177147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562892989	chr3:25177159-25177160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78991919	chr3:25177195-25177196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552066690	chr3:25177235-25177236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565610262	chr3:25177259-25177260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532933559	chr3:25177289-25177290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546323835	chr3:25177291-25177292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115693758	chr3:25177294-25177295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191862363	chr3:25177298-25177299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4312625	chr3:25177378-25177379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76065565	chr3:25177435-25177436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67672853	chr3:25177436-25177437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568680111	chr3:25177441-25177442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9871379	chr3:25177454-25177455	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557610531	chr3:25177461-25177462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528018652	chr3:25177462-25177463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25175800-25184200	Weak transcription	Fetal Lung	lung
2	chr3:25179200-25179600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:25179200-25179600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:25180800-25181000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:25184200-25185000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:25184200-25185000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:25184200-25186200	Enhancers	Fetal Lung	lung
8	chr3:25184600-25185000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:25184600-25185200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr3:25184600-25185200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:25184600-25185400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:25184600-25185400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr3:25184600-25185400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:25184600-25185600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:25184600-25187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr3:25184800-25185000	Enhancers	Fetal Stomach	stomach
17	chr3:25184800-25185200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:25184800-25185400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr3:25185000-25186200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr3:25185200-25186000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr3:25185200-25186400	Weak transcription	Fetal Stomach	stomach
22	chr3:25185600-25192200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr3:25186000-25186800	Enhancers	Colon Smooth Muscle	Colon
24	chr3:25186200-25186400	Flanking Active TSS	Fetal Lung	lung
25	chr3:25186200-25186600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:25186200-25186800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr3:25186400-25186600	Enhancers	Fetal Lung	lung
28	chr3:25186600-25186800	Flanking Active TSS	Fetal Lung	lung
29	chr3:25186600-25191800	Weak transcription	Fetal Stomach	stomach
30	chr3:25186800-25187000	Enhancers	Fetal Lung	lung
31	chr3:25187400-25191000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:25190000-25190400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr3:25190000-25190600	Enhancers	Fetal Heart	heart
34	chr3:25190000-25191800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:25190400-25190600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:25190400-25190800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr3:25190600-25192000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:25190600-25194400	Weak transcription	Fetal Heart	heart
39	chr3:25190800-25191000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr3:25190800-25193000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:25191000-25191400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:25191000-25194400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr3:25191400-25194600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:25191400-25195200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr3:25191800-25192600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr3:25191800-25192800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr3:25191800-25192800	Enhancers	Right Atrium	heart
48	chr3:25191800-25193200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr3:25191800-25193200	Enhancers	Fetal Muscle Leg	muscle
50	chr3:25191800-25193400	Enhancers	Fetal Stomach	stomach

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