Variant report

Variant	nsv902018
Chromosome Location	chr14:63786658-63884984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr14:63865575-63865812	GM12878	blood:	n/a	chr14:63865706-63865717
4	BATF	chr14:63865499-63865864	GM12878	blood:	n/a	chr14:63865706-63865717
5	BATF	chr14:63850478-63850694	GM12878	blood:	n/a	n/a
6	BATF	chr14:63884387-63884649	GM12878	blood:	n/a	n/a
7	BATF	chr14:63884758-63885075	GM12878	blood:	n/a	n/a
8	BATF	chr14:63867907-63868096	GM12878	blood:	n/a	chr14:63868005-63868016
9	BATF	chr14:63837832-63838034	GM12878	blood:	n/a	n/a
10	BATF	chr14:63837850-63838032	GM12878	blood:	n/a	n/a
11	BCL3	chr14:63827695-63827949	GM12878	blood:	n/a	n/a
12	BCL3	chr14:63829151-63829554	GM12878	blood:	n/a	n/a
13	BCL3	chr14:63829154-63829566	GM12878	blood:	n/a	n/a
14	BRCA1	chr14:63855463-63855787	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:63842517-63842730	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
16	CEBPB	chr14:63798489-63798718	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:63842449-63843004	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
18	CEBPB	chr14:63842418-63842898	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
19	CEBPB	chr14:63820978-63821201	HepG2	liver:	n/a	chr14:63821071-63821082
20	CEBPB	chr14:63845972-63846129	MCF-7	breast:	n/a	chr14:63846045-63846056
21	CEBPB	chr14:63842462-63842947	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
22	CEBPB	chr14:63809144-63809428	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:63809186-63809476	A549	lung:	n/a	n/a
24	CEBPB	chr14:63834999-63835300	A549	lung:	n/a	chr14:63835165-63835176
25	CEBPB	chr14:63835037-63835278	K562	blood:	n/a	chr14:63835165-63835176
26	CEBPB	chr14:63846009-63846069	HepG2	liver:	n/a	chr14:63846045-63846056
27	CEBPB	chr14:63842444-63843021	IMR90	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
28	CEBPB	chr14:63842570-63842689	HepG2	liver:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
29	CEBPB	chr14:63798403-63798684	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:63842433-63843010	Hela-S3	cervix:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
31	CEBPB	chr14:63790310-63790386	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:63835034-63835323	IMR90	lung:	n/a	chr14:63835165-63835176
33	CEBPB	chr14:63798372-63798717	A549	lung:	n/a	n/a
34	CEBPB	chr14:63842544-63842804	MCF-7	breast:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
35	CEBPB	chr14:63826972-63827278	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:63842470-63842926	A549	lung:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
37	CEBPB	chr14:63842579-63842902	K562	blood:	n/a	chr14:63842637-63842648 chr14:63842657-63842668 chr14:63842871-63842882
38	CEBPB	chr14:63842540-63842810	H1-hESC	embryonic stem cell:	n/a	chr14:63842637-63842648 chr14:63842657-63842668
39	CEBPB	chr14:63835079-63835317	HepG2	liver:	n/a	chr14:63835165-63835176
40	CEBPB	chr14:63798468-63798578	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr14:63810023-63810048	HepG2	liver:	n/a	n/a
42	CHD2	chr14:63855550-63855774	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr14:63842557-63842804	Hela-S3	cervix:	n/a	n/a
44	CREB1	chr14:63855608-63855801	A549	lung:	n/a	n/a
45	CTCF	chr14:63855590-63855871	A549	lung:	n/a	n/a
46	CTCF	chr14:63828518-63828913	MCF-7	breast:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728
47	CTCF	chr14:63855581-63855848	GM13977	blood:	n/a	n/a
48	CTCF	chr14:63838500-63838650	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr14:63855640-63855790	HepG2	liver:	n/a	n/a
50	CTCF	chr14:63828640-63828790	GM12873	blood:	n/a	chr14:63828705-63828723 chr14:63828710-63828718 chr14:63828707-63828728

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:63872285-63872335	HPAEpiC	pulmonary alveolar:	n/a
2	chr14:63872285-63872335	HEEpiC	esophagus:	n/a
3	chr14:63872285-63872335	CMK	blood:	n/a
4	chr14:63872285-63872335	AG09319	gingival:	n/a
5	chr14:63872285-63872335	AG10803	skin:	n/a
6	chr14:63872285-63872335	GM12891	blood:	n/a
7	chr14:63872285-63872335	NHBE	bronchial:	n/a
8	chr14:63872285-63872335	A549	lung:	n/a
9	chr14:63872285-63872335	H1-hESC	embryonic stem cell:	embryo
10	chr14:63872285-63872335	HCM	heart:	n/a
11	chr14:63872285-63872335	Hepatocyte	liver:	n/a
12	chr14:63872285-63872335	Caco-2	colon:	n/a
13	chr14:63872285-63872335	NB4	blood:	n/a
14	chr14:63872285-63872335	GM12892	blood:	n/a
15	chr14:63872285-63872335	GM19239	blood:	n/a
16	chr14:63872285-63872335	HRCEpiC	kidney:	n/a
17	chr14:63872285-63872335	GM06990	blood:	n/a
18	chr14:63872285-63872335	PANC-1	pancreas:	n/a
19	chr14:63872285-63872335	HNPCEpiC	eye:	n/a
20	chr14:63872285-63872335	AoSMC	blood vessel:	n/a
21	chr14:63872285-63872335	HCPEpiC	choroid plexus:	n/a
22	chr14:63872285-63872335	AG09309	skin:	n/a
23	chr14:63872285-63872335	HUVEC	blood vessel:	n/a
24	chr14:63872285-63872335	LNCaP	prostate:	n/a
25	chr14:63872285-63872335	ProgFib	skin:	n/a
26	chr14:63872285-63872335	HL-60	blood:	n/a
27	chr14:63872285-63872335	T-47D	breast:	n/a
28	chr14:63872285-63872335	PrEC	prostate:	n/a
29	chr14:63872285-63872335	SK-N-MC	brain:	n/a
30	chr14:63872285-63872335	PFSK-1	brain:	n/a
31	chr14:63872285-63872335	HCF	heart:	n/a
32	chr14:63872285-63872335	SK-N-SH	brain:	n/a
33	chr14:63872285-63872335	BJ	skin:	n/a
34	chr14:63872285-63872335	AG04450	lung:	fetal
35	chr14:63872285-63872335	SKMC	muscle:	n/a
36	chr14:63872285-63872335	NHDF-neo	bronchial:	n/a
37	chr14:63872285-63872335	NH-A	brain:	n/a
38	chr14:63872285-63872335	HEK293	kidney:	embryo
39	chr14:63872285-63872335	HCT-116	colon:	n/a
40	chr14:63872285-63872335	HepG2	liver:	n/a
41	chr14:63872285-63872335	HMEC	breast:	n/a
42	chr14:63872285-63872335	SK-N-SH_RA	brain:	n/a
43	chr14:63872285-63872335	HRE	kidney:	n/a
44	chr14:63872285-63872335	ECC-1	luminal epithelium:	n/a
45	chr14:63872285-63872335	Jurkat	blood:	n/a
46	chr14:63872285-63872335	AG04449	skin:	fetal
47	chr14:63872285-63872335	HRPEpiC	eye:	n/a
48	chr14:63872285-63872335	K562	blood:	n/a
49	chr14:63872285-63872335	SAEC	small airway:	n/a
50	chr14:63872285-63872335	BE2_C	brain:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
2	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
3	chr14:63855569..63857925-chr14:64009617..64011888,2	MCF-7	breast:
4	chr14:63866982..63869213-chr14:64008832..64010696,2	MCF-7	breast:
5	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
6	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
7	chr14:63807896..63809809-chr14:63818163..63820932,2	MCF-7	breast:
8	chr14:63855385..63856181-chr14:64010817..64012064,6	MCF-7	breast:
9	chr14:63855376..63856976-chr14:64105685..64108470,2	K562	blood:
10	chr14:63881053..63883432-chr14:63886290..63888118,2	K562	blood:
11	chr14:63876148..63878726-chr14:63887830..63889791,2	MCF-7	breast:
12	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
13	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
14	chr14:63855793..63857430-chr14:63857511..63859200,2	MCF-7	breast:
15	chr14:63830891..63833406-chr14:63833743..63835753,2	K562	blood:
16	chr14:63857974..63860690-chr14:63917148..63919988,2	MCF-7	breast:
17	chr14:63836099..63836920-chr6:128541621..128542384,2	MCF-7	breast:
18	chr14:63792244..63793991-chr14:63822346..63825319,2	MCF-7	breast:
19	chr14:63884387..63889474-chr14:63890982..63895061,6	MCF-7	breast:
20	chr14:63848595..63851169-chr14:64107183..64109145,2	K562	blood:
21	chr14:63873643..63876759-chr14:63877495..63879586,3	MCF-7	breast:
22	chr14:63873643..63876759-chr14:63877495..63879586,3	MCF-7	breast:
23	chr14:63816228..63817986-chr14:63819817..63821976,2	MCF-7	breast:
24	chr14:63784531..63787249-chr14:63793902..63795892,2	MCF-7	breast:
25	chr14:63881965..63883896-chr14:63890081..63891991,2	K562	blood:
26	chr14:63858881..63861162-chr14:64008688..64011612,2	MCF-7	breast:
27	chr14:63855376..63858099-chr14:64105447..64108157,3	K562	blood:
28	chr14:63881511..63883896-chr14:63890081..63891913,2	K562	blood:
29	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
30	chr14:63837297..63838980-chr14:63840657..63842212,2	MCF-7	breast:
31	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
32	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
33	chr14:63855657..63857190-chr14:63857945..63860225,2	K562	blood:
34	chr14:63833848..63836637-chr14:63841701..63844309,2	MCF-7	breast:
35	chr14:63823098..63825061-chr14:63826857..63829778,2	MCF-7	breast:
36	chr14:63883493..63885324-chr14:63895629..63897308,2	MCF-7	breast:

No data

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

Extended variants
information (count: 3112 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3112 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542174400	chr14:63786999-63787000	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs186438413	chr14:63787115-63787116	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs8006562	chr14:63787140-63787141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1266713	chr14:63787171-63787172	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs150576313	chr14:63787184-63787185	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs59456872	chr14:63787215-63787216	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs551991263	chr14:63787233-63787234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs180819411	chr14:63787240-63787241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534335709	chr14:63787257-63787258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs139625940	chr14:63787357-63787358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs375150710	chr14:63787473-63787474	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145899524	chr14:63787475-63787476	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs61079739	chr14:63787477-63787478	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs71425337	chr14:63787483-63787484	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs5029911	chr14:63787491-63787492	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs1964832	chr14:63787501-63787502	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201314414	chr14:63787502-63787503	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1268645	chr14:63787519-63787520	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1964833	chr14:63787553-63787554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558125517	chr14:63787561-63787562	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs576914096	chr14:63787565-63787566	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs143524916	chr14:63787576-63787577	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555452239	chr14:63788991-63788992	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568973989	chr14:63789044-63789045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537868815	chr14:63789081-63789082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563303337	chr14:63789094-63789095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191794679	chr14:63789110-63789111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182133228	chr14:63789137-63789138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12587804	chr14:63789182-63789183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546069297	chr14:63789210-63789211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10137202	chr14:63789238-63789239	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs542003420	chr14:63789276-63789277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186861080	chr14:63789333-63789334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530601699	chr14:63789384-63789385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552159159	chr14:63789386-63789387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368763362	chr14:63789397-63789398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544259932	chr14:63789413-63789414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564099612	chr14:63789434-63789435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146917769	chr14:63789492-63789493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs578005914	chr14:63789546-63789547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371709750	chr14:63789557-63789558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139221992	chr14:63789596-63789597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529463737	chr14:63789618-63789619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373727137	chr14:63789619-63789620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548412191	chr14:63789656-63789657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367869891	chr14:63789684-63789685	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569035394	chr14:63789761-63789762	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs537930302	chr14:63789822-63789823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557903300	chr14:63789832-63789833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571611880	chr14:63789870-63789871	Enhancers	n/a	n/a	Overlapped CNVs	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:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63789000-63790800	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr14:63789200-63790200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:63789200-63790400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:63789400-63790200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:63789400-63790200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr14:63789600-63790000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr14:63789800-63790400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr14:63790000-63790400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr14:63790000-63790400	Enhancers	Fetal Muscle Leg	muscle
10	chr14:63790000-63790600	Enhancers	Fetal Brain Male	brain
11	chr14:63793400-63794400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr14:63795000-63797200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr14:63797200-63799600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:63799600-63799800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:63799800-63800000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:63800000-63800200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr14:63800200-63800600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr14:63800200-63801000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:63801000-63801400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:63801400-63801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:63801600-63801800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:63801800-63802000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:63802000-63802600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr14:63806800-63807400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:63808800-63809400	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr14:63809000-63809600	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr14:63809000-63809600	Enhancers	A549	lung
28	chr14:63809000-63809800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr14:63809000-63811600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:63809400-63809600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr14:63809400-63809800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr14:63809400-63810000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr14:63809800-63812000	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr14:63810000-63811000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:63810200-63811400	Enhancers	HUVEC	blood vessel
36	chr14:63810600-63811400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr14:63811000-63811400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr14:63811200-63811600	Enhancers	Fetal Muscle Leg	muscle
39	chr14:63811600-63811800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr14:63811800-63812000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr14:63812000-63812200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr14:63812000-63813200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr14:63812200-63813000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:63813000-63813200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr14:63813200-63814400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:63815800-63816400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr14:63821000-63821800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr14:63821600-63830400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:63826800-63827200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:63826800-63847600	Weak transcription	Left Ventricle	heart

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