Variant report

Variant	nsv1045700
Chromosome Location	chr14:63777124-63857536
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	ATF2	chr14:63850463-63850949	GM12878	blood:	n/a	n/a
2	BACH1	chr14:63855832-63855875	K562	blood:	n/a	n/a
3	BATF	chr14:63837832-63838034	GM12878	blood:	n/a	n/a
4	BATF	chr14:63837850-63838032	GM12878	blood:	n/a	n/a
5	BATF	chr14:63850478-63850694	GM12878	blood:	n/a	n/a
6	BCL3	chr14:63829154-63829566	GM12878	blood:	n/a	n/a
7	BCL3	chr14:63829151-63829554	GM12878	blood:	n/a	n/a
8	BCL3	chr14:63827695-63827949	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:63855463-63855787	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr14:63782321-63782360	GM12878	blood:	n/a	n/a
11	CEBPB	chr14:63798403-63798684	IMR90	lung:	n/a	n/a
12	CEBPB	chr14:63842544-63842804	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
13	CEBPB	chr14:63842418-63842898	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
14	CEBPB	chr14:63834999-63835300	A549	lung:	n/a	chr14:63835165-63835176
15	CEBPB	chr14:63845972-63846129	MCF-7	breast:	n/a	chr14:63846045-63846056
16	CEBPB	chr14:63826972-63827278	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:63790310-63790386	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:63842570-63842689	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
19	CEBPB	chr14:63809144-63809428	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:63842433-63843010	Hela-S3	cervix:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
21	CEBPB	chr14:63842579-63842902	K562	blood:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
22	CEBPB	chr14:63842449-63843004	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
23	CEBPB	chr14:63809186-63809476	A549	lung:	n/a	n/a
24	CEBPB	chr14:63835079-63835317	HepG2	liver:	n/a	chr14:63835165-63835176
25	CEBPB	chr14:63798468-63798578	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr14:63842540-63842810	H1-hESC	embryonic stem cell:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
27	CEBPB	chr14:63846009-63846069	HepG2	liver:	n/a	chr14:63846045-63846056
28	CEBPB	chr14:63842462-63842947	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
29	CEBPB	chr14:63842517-63842730	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
30	CEBPB	chr14:63842444-63843021	IMR90	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
31	CEBPB	chr14:63835034-63835323	IMR90	lung:	n/a	chr14:63835165-63835176
32	CEBPB	chr14:63798372-63798717	A549	lung:	n/a	n/a
33	CEBPB	chr14:63820978-63821201	HepG2	liver:	n/a	chr14:63821071-63821082
34	CEBPB	chr14:63842470-63842926	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
35	CEBPB	chr14:63835037-63835278	K562	blood:	n/a	chr14:63835165-63835176
36	CEBPB	chr14:63798489-63798718	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:63782893-63783093	A549	lung:	n/a	n/a
38	CHD2	chr14:63810023-63810048	HepG2	liver:	n/a	n/a
39	CHD2	chr14:63842557-63842804	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:63855550-63855774	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr14:63855608-63855801	A549	lung:	n/a	n/a
42	CTCF	chr14:63855660-63855810	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:63855640-63855790	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr14:63828588-63828851	H1-hESC	embryonic stem cell:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
45	CTCF	chr14:63834540-63834690	AG09309	skin:	n/a	n/a
46	CTCF	chr14:63828626-63828760	GM19238	blood:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
47	CTCF	chr14:63855583-63855859	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:63834540-63834690	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr14:63855604-63855830	GM13976	blood:	n/a	n/a
50	CTCF	chr14:63828660-63828810	GM06990	blood:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:63785287-63785337	HL-60	blood:	n/a
2	chr14:63784574-63784624	ovcar-3	ovarian:	n/a
3	chr14:63784394-63784444	SAEC	small airway:	n/a
4	chr14:63784394-63784444	HCF	heart:	n/a
5	chr14:63781994-63782044	MCF-7	breast:	n/a
6	chr14:63781994-63782044	SKMC	muscle:	n/a
7	chr14:63785334-63785384	HNPCEpiC	eye:	n/a
8	chr14:63784574-63784624	Hepatocyte	liver:	n/a
9	chr14:63784394-63784444	ovcar-3	ovarian:	n/a
10	chr14:63779694-63779744	HMEC	breast:	n/a
11	chr14:63785287-63785337	HMEC	breast:	n/a
12	chr14:63779694-63779744	HCM	heart:	n/a
13	chr14:63784394-63784444	NHBE	bronchial:	n/a
14	chr14:63785334-63785384	CMK	blood:	n/a
15	chr14:63784574-63784624	HEK293	kidney:	embryo
16	chr14:63785287-63785337	GM06990	blood:	n/a
17	chr14:63784394-63784444	PFSK-1	brain:	n/a
18	chr14:63785287-63785337	ProgFib	skin:	n/a
19	chr14:63784574-63784624	HEEpiC	esophagus:	n/a
20	chr14:63785287-63785337	SAEC	small airway:	n/a
21	chr14:63779694-63779744	HIPEpiC	eye:	n/a
22	chr14:63784574-63784624	U87	brain:	n/a
23	chr14:63785523-63785573	HCF	heart:	n/a
24	chr14:63785334-63785384	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:63779694-63779744	T-47D	breast:	n/a
26	chr14:63785287-63785337	AG10803	skin:	n/a
27	chr14:63785334-63785384	Hepatocyte	liver:	n/a
28	chr14:63784574-63784624	SAEC	small airway:	n/a
29	chr14:63785287-63785337	K562	blood:	n/a
30	chr14:63785287-63785337	NHDF-neo	bronchial:	n/a
31	chr14:63785334-63785384	PrEC	prostate:	n/a
32	chr14:63784394-63784444	HNPCEpiC	eye:	n/a
33	chr14:63779694-63779744	HCPEpiC	choroid plexus:	n/a
34	chr14:63784574-63784624	PFSK-1	brain:	n/a
35	chr14:63781994-63782044	H1-hESC	embryonic stem cell:	embryo
36	chr14:63781994-63782044	PFSK-1	brain:	n/a
37	chr14:63779694-63779744	AG09319	gingival:	n/a
38	chr14:63785523-63785573	NH-A	brain:	n/a
39	chr14:63785334-63785384	SK-N-SH_RA	brain:	n/a
40	chr14:63784394-63784444	NH-A	brain:	n/a
41	chr14:63784574-63784624	Hela-S3	cervix:	n/a
42	chr14:63785523-63785573	T-47D	breast:	n/a
43	chr14:63785523-63785573	SK-N-MC	brain:	n/a
44	chr14:63784394-63784444	HCPEpiC	choroid plexus:	n/a
45	chr14:63785334-63785384	AG09319	gingival:	n/a
46	chr14:63784574-63784624	HRE	kidney:	n/a
47	chr14:63785287-63785337	HRPEpiC	eye:	n/a
48	chr14:63781994-63782044	GM12878	blood:	n/a
49	chr14:63784574-63784624	Caco-2	colon:	n/a
50	chr14:63785287-63785337	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:63848595..63851169-chr14:64107183..64109145,2	K562	blood:
2	chr14:63836099..63836920-chr6:128541621..128542384,2	MCF-7	breast:
3	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
4	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
5	chr14:63855376..63858099-chr14:64105447..64108157,3	K562	blood:
6	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
7	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
8	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
9	chr14:63855376..63856976-chr14:64105685..64108470,2	K562	blood:
10	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
11	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
12	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
13	chr14:63855569..63857925-chr14:64009617..64011888,2	MCF-7	breast:
14	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
15	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
16	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
17	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
18	chr14:63784531..63787249-chr14:63793902..63795892,2	MCF-7	breast:
19	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
20	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
21	chr14:63855385..63856181-chr14:64010817..64012064,6	MCF-7	breast:
22	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
23	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
24	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:

Variant related genes	Relation type
GPHB5	TF binding region
GPHB5	CpG island
ENSG00000261242	chromatin interactions
ENSG00000140006	chromatin interactions
ENSG00000154001	chromatin interactions
ENSG00000179600	chromatin interactions

Extended variants
information (count: 2236 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2236 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539621324	chr14:63777139-63777140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181709341	chr14:63777143-63777144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139381506	chr14:63777146-63777147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185668465	chr14:63777147-63777148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1255570	chr14:63777152-63777153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs367716272	chr14:63777187-63777188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575463136	chr14:63777194-63777195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191625400	chr14:63777196-63777197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8008058	chr14:63777253-63777254	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs533094313	chr14:63777254-63777255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573244048	chr14:63777283-63777284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546709553	chr14:63777288-63777289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560237636	chr14:63777321-63777322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528884981	chr14:63777343-63777344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201123259	chr14:63777361-63777362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113142852	chr14:63777362-63777363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144347366	chr14:63777363-63777364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs57211440	chr14:63777365-63777366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2256072	chr14:63777366-63777367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200811528	chr14:63777367-63777368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548922171	chr14:63777389-63777390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569464652	chr14:63777398-63777399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538500547	chr14:63777403-63777404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1255571	chr14:63777408-63777409	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs571489989	chr14:63777442-63777443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534064664	chr14:63777446-63777447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1255572	chr14:63777462-63777463	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575683817	chr14:63777463-63777464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536267875	chr14:63777476-63777477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556494887	chr14:63777478-63777479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575478748	chr14:63777490-63777491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544480728	chr14:63777503-63777504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1268643	chr14:63777505-63777506	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs147281145	chr14:63777513-63777514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540381953	chr14:63777525-63777526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9671807	chr14:63777532-63777533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182368606	chr14:63777551-63777552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1255573	chr14:63777560-63777561	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548723900	chr14:63777603-63777604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1255574	chr14:63777621-63777622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140680947	chr14:63777652-63777653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551647209	chr14:63777690-63777691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571564267	chr14:63777708-63777709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534137830	chr14:63777711-63777712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547553620	chr14:63777726-63777727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144642232	chr14:63777800-63777801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536729343	chr14:63777805-63777806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147838770	chr14:63777825-63777826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs111730502	chr14:63777879-63777880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1255575	chr14:63777906-63777907	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22737080	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63772600-63777200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:63777200-63779000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr14:63779600-63780400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:63779800-63780000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr14:63779800-63780200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:63780000-63780400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:63784200-63784600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:63789000-63790800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:63789200-63790200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:63789200-63790400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:63789400-63790200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr14:63789400-63790200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr14:63789600-63790000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:63789800-63790400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr14:63790000-63790400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr14:63790000-63790400	Enhancers	Fetal Muscle Leg	muscle
17	chr14:63790000-63790600	Enhancers	Fetal Brain Male	brain
18	chr14:63793400-63794400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:63795000-63797200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:63797200-63799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:63799600-63799800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:63799800-63800000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:63800000-63800200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr14:63800200-63800600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr14:63800200-63801000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:63801000-63801400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:63801400-63801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:63801600-63801800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:63801800-63802000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:63802000-63802600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:63806800-63807400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:63808800-63809400	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr14:63809000-63809600	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr14:63809000-63809600	Enhancers	A549	lung
35	chr14:63809000-63809800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:63809000-63811600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr14:63809400-63809600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:63809400-63809800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr14:63809400-63810000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr14:63809800-63812000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr14:63810000-63811000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:63810200-63811400	Enhancers	HUVEC	blood vessel
43	chr14:63810600-63811400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr14:63811000-63811400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr14:63811200-63811600	Enhancers	Fetal Muscle Leg	muscle
46	chr14:63811600-63811800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr14:63811800-63812000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:63812000-63812200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:63812000-63813200	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr14:63812200-63813000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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