Variant report

Variant	esv2751278
Chromosome Location	chr14:46718250-47225891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1574)
CpG islands
(count:1161)
Chromatin interactive
region (count:23)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1574 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:47060393-47060753	HepG2	liver:	n/a	n/a
2	ATF1	chr14:47124636-47124919	K562	blood:	n/a	n/a
3	ATF2	chr14:46791299-46791687	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:47144126-47144310	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr14:46791312-46791676	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr14:46791333-46791636	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr14:46959550-46960028	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:47050460-47050552	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
10	CBX3	chr14:47128948-47129132	K562	blood:	n/a	n/a
11	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:47204885-47205091	A549	lung:	n/a	n/a
13	CEBPB	chr14:47007646-47007959	IMR90	lung:	n/a	chr14:47007809-47007820
14	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
15	CEBPB	chr14:47099640-47099928	HepG2	liver:	n/a	chr14:47099772-47099783
16	CEBPB	chr14:47052695-47053004	A549	lung:	n/a	chr14:47052838-47052849
17	CEBPB	chr14:47150385-47150700	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:47099568-47099959	MCF-7	breast:	n/a	chr14:47099772-47099783
19	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
20	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
21	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
22	CEBPB	chr14:47007631-47007991	HepG2	liver:	n/a	chr14:47007809-47007820
23	CEBPB	chr14:47150417-47150717	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:47217051-47217222	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:47052693-47053023	HepG2	liver:	n/a	chr14:47052838-47052849
26	CEBPB	chr14:47007725-47007946	H1-hESC	embryonic stem cell:	n/a	chr14:47007809-47007820
27	CEBPB	chr14:47191227-47191420	HepG2	liver:	n/a	chr14:47191326-47191337
28	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
29	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr14:47007729-47007887	K562	blood:	n/a	chr14:47007809-47007820
31	CEBPB	chr14:47163162-47163272	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr14:47099633-47099882	H1-hESC	embryonic stem cell:	n/a	chr14:47099772-47099783
35	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
36	CEBPB	chr14:47052769-47052969	H1-hESC	embryonic stem cell:	n/a	chr14:47052838-47052849
37	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
38	CEBPB	chr14:47079832-47080045	HepG2	liver:	n/a	chr14:47079944-47079955
39	CEBPB	chr14:47163064-47163185	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:46732453-46732625	HepG2	liver:	n/a	chr14:46732582-46732593 chr14:46732584-46732593
41	CEBPB	chr14:47007629-47007980	A549	lung:	n/a	chr14:47007809-47007820
42	CEBPB	chr14:47099591-47099933	ECC-1	luminal epithelium:	n/a	chr14:47099772-47099783
43	CEBPB	chr14:47150439-47150659	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
45	CEBPB	chr14:47191649-47191654	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr14:47099535-47099985	ECC-1	luminal epithelium:	n/a	chr14:47099772-47099783
47	CEBPB	chr14:47184168-47184434	HepG2	liver:	n/a	chr14:47184272-47184283
48	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
49	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr14:46959344-46959844	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:47096230-47096280	HMEC	breast:	n/a
2	chr14:47096230-47096280	U87	brain:	n/a
3	chr14:47096230-47096280	HMEC	breast:	n/a
4	chr14:47096230-47096280	U87	brain:	n/a
5	chr14:46791389-46791439	AG04450	lung:	fetal
6	chr14:47123088-47123138	BJ	skin:	n/a
7	chr14:47121158-47121208	BE2_C	brain:	n/a
8	chr14:47123088-47123138	HRCEpiC	kidney:	n/a
9	chr14:47120920-47120970	IMR90	lung:	fetal
10	chr14:47104140-47104190	NHDF-neo	bronchial:	n/a
11	chr14:46874779-46874829	HCT-116	colon:	n/a
12	chr14:47104140-47104190	SK-N-SH_RA	brain:	n/a
13	chr14:46791389-46791439	GM12891	blood:	n/a
14	chr14:47123088-47123138	ovcar-3	ovarian:	n/a
15	chr14:47121156-47121206	NHBE	bronchial:	n/a
16	chr14:47120795-47120845	SK-N-SH_RA	brain:	n/a
17	chr14:47121132-47121182	ECC-1	luminal epithelium:	n/a
18	chr14:47121033-47121083	HCPEpiC	choroid plexus:	n/a
19	chr14:47120845-47120895	HCPEpiC	choroid plexus:	n/a
20	chr14:47096230-47096280	BE2_C	brain:	n/a
21	chr14:47104140-47104190	HRCEpiC	kidney:	n/a
22	chr14:47120795-47120845	HRE	kidney:	n/a
23	chr14:47120920-47120970	NHDF-neo	bronchial:	n/a
24	chr14:47096230-47096280	HUVEC	blood vessel:	n/a
25	chr14:47120845-47120895	HRE	kidney:	n/a
26	chr14:47120920-47120970	NB4	blood:	n/a
27	chr14:46791389-46791439	HRCEpiC	kidney:	n/a
28	chr14:47120845-47120895	AG09319	gingival:	n/a
29	chr14:47120920-47120970	AoSMC	blood vessel:	n/a
30	chr14:47123088-47123138	AG09319	gingival:	n/a
31	chr14:46791389-46791439	SK-N-SH	brain:	n/a
32	chr14:47121117-47121167	PrEC	prostate:	n/a
33	chr14:47123298-47123348	HIPEpiC	eye:	n/a
34	chr14:47104140-47104190	SK-N-SH	brain:	n/a
35	chr14:46916080-46916130	AG10803	skin:	n/a
36	chr14:47120795-47120845	BE2_C	brain:	n/a
37	chr14:47104140-47104190	AG09309	skin:	n/a
38	chr14:47118100-47118150	LNCaP	prostate:	n/a
39	chr14:47120795-47120845	A549	lung:	n/a
40	chr14:47121002-47121052	T-47D	breast:	n/a
41	chr14:47120507-47120557	PANC-1	pancreas:	n/a
42	chr14:46916080-46916130	MCF10A-Er-Src	breast:	n/a
43	chr14:47121132-47121182	RPTEC	kidney:	n/a
44	chr14:47121156-47121206	Hepatocyte	liver:	n/a
45	chr14:47121002-47121052	GM12878	blood:	n/a
46	chr14:47120507-47120557	GM19239	blood:	n/a
47	chr14:47121002-47121052	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:47096230-47096280	ProgFib	skin:	n/a
49	chr14:47121002-47121052	SKMC	muscle:	n/a
50	chr14:47120507-47120557	HL-60	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
2	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:
3	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
4	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:
5	chr14:47110358..47111900-chr14:47112511..47115228,2	K562	blood:
6	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
7	chr14:47049935..47050932-chr14:48008149..48008898,3	MCF-7	breast:
8	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
9	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
10	chr14:47110358..47111900-chr14:47112511..47115228,2	K562	blood:
11	chr14:47049606..47051836-chr14:47067092..47069403,2	K562	blood:
12	chr14:47050439..47051198-chr14:48008059..48008561,2	MCF-7	breast:
13	chr14:47196544..47199011-chr14:47199972..47202196,2	K562	blood:
14	chr14:47050056..47050875-chr14:47509400..47510237,2	MCF-7	breast:
15	chr14:46517458..46517985-chr14:47049934..47050581,2	MCF-7	breast:
16	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
17	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
18	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
19	chr14:47049606..47051836-chr14:47067092..47069403,2	K562	blood:
20	chr14:47190435..47193179-chr14:47198084..47200809,2	MCF-7	breast:
21	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
22	chr14:47050051..47050804-chr14:48867648..48868551,2	MCF-7	breast:
23	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46959395-46959490	ENSG00000258700
2	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
3	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
4	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
5	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036679
6	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
7	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681
8	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036680
9	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
10	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
11	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
12	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
13	lnc-FANCM-6	chr14:46970510-46971026	ENSG00000258700
14	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036681
15	lnc-FANCM-6	chr14:46788016-46788064	ENSG00000258700
16	lnc-FANCM-6	chr14:46970510-46971104	NONHSAT036678
17	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
18	lnc-FANCM-6	chr14:46970510-46970814	ENSG00000258700
19	lnc-FANCM-6	chr14:46959395-46959490	NONHSAT036681
20	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680

No data

Variant related genes	Relation type
LINC00871	TF binding region
RPL10L	TF binding region
LINC00871	CpG island
RPL10L	CpG island

Extended variants
information (count: 10210 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:10210 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17737767	chr14:46718257-46718258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140995434	chr14:46718314-46718315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146641521	chr14:46718342-46718343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79409812	chr14:46718362-46718363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191026323	chr14:46718365-46718366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559652200	chr14:46719434-46719435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144168798	chr14:46719473-46719474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144548523	chr14:46719483-46719484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544828663	chr14:46719484-46719485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191690664	chr14:46719488-46719489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554889134	chr14:46719501-46719502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563508308	chr14:46719537-46719538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117231030	chr14:46719600-46719601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183840769	chr14:46719609-46719610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567051492	chr14:46719634-46719635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188216289	chr14:46719647-46719648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370111039	chr14:46719688-46719689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148443994	chr14:46719701-46719702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79920166	chr14:46719714-46719715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200153017	chr14:46719746-46719747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538719433	chr14:46719749-46719750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142548306	chr14:46719754-46719755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551826129	chr14:46719762-46719763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570226009	chr14:46719783-46719784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537271611	chr14:46719876-46719877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73242262	chr14:46719916-46719917	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574197198	chr14:46719955-46719956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12587915	chr14:46719997-46719998	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553405636	chr14:46720072-46720073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533144241	chr14:46720120-46720121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139853285	chr14:46720172-46720173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558619173	chr14:46720236-46720237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563482785	chr14:46720247-46720248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143201376	chr14:46720306-46720307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs193279273	chr14:46720344-46720345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560618034	chr14:46720354-46720355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79283753	chr14:46720380-46720381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185536741	chr14:46720392-46720393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577340077	chr14:46720398-46720399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564526908	chr14:46720432-46720433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532056131	chr14:46720453-46720454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552026566	chr14:46720455-46720456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570286961	chr14:46720517-46720518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367895656	chr14:46720530-46720531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558671109	chr14:46720532-46720533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537616572	chr14:46720572-46720573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151133857	chr14:46720588-46720589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139421928	chr14:46720617-46720618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372517448	chr14:46720624-46720625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190395706	chr14:46720633-46720634	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46717200-46718400	Enhancers	Fetal Heart	heart
2	chr14:46719400-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:46719600-46720000	Enhancers	Fetal Brain Female	brain
4	chr14:46720200-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:46725000-46725600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:46725200-46725600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr14:46725200-46725600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:46725600-46725800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr14:46725600-46726000	Enhancers	Primary hematopoietic stem cells	blood
10	chr14:46725600-46726000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr14:46725600-46726000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:46725800-46740400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr14:46728800-46729000	Enhancers	Fetal Kidney	kidney
14	chr14:46728800-46729200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:46729800-46730200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:46729800-46730400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:46730400-46730800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr14:46730400-46731600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:46731600-46733000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:46740400-46740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr14:46740600-46748200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr14:46748200-46749600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:46748400-46749200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr14:46748800-46749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr14:46749400-46749800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr14:46775400-46775800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr14:46775400-46776000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr14:46780200-46780400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:46780800-46781200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:46781000-46781200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:46785600-46790400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:46785600-46790600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:46788200-46788600	Active TSS	Left Ventricle	heart
36	chr14:46790400-46790600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr14:46790400-46790800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
38	chr14:46790400-46791000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
39	chr14:46790400-46792400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:46790400-46792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:46790400-46792800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
42	chr14:46790400-46795200	Enhancers	Primary hematopoietic stem cells	blood
43	chr14:46790600-46795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:46790800-46791000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr14:46790800-46791000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
46	chr14:46790800-46791200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:46790800-46791600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
48	chr14:46790800-46792000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr14:46790800-46792800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
50	chr14:46791000-46791200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell

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