Variant report

Variant	esv2761411
Chromosome Location	chr14:46716963-46996307
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	chr14:46791299-46791687	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr14:46791333-46791636	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:46791312-46791676	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr14:46959550-46960028	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
8	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
10	CEBPB	chr14:46959344-46959844	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
11	CEBPB	chr14:46959438-46959906	H1-hESC	embryonic stem cell:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
12	CEBPB	chr14:46791324-46791680	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
14	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
16	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
17	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
18	CEBPB	chr14:46732453-46732625	HepG2	liver:	n/a	chr14:46732582-46732593 chr14:46732584-46732593
19	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
21	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
22	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
24	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
25	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
26	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
27	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
28	CHD2	chr14:46791309-46791730	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr14:46791285-46791675	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr14:46959700-46959850	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
31	CTCF	chr14:46813571-46813886	T-47D	breast:	n/a	n/a
32	CTCF	chr14:46813533-46813920	HepG2	liver:	n/a	n/a
33	CTCF	chr14:46813640-46813790	HEK293	kidney:	n/a	n/a
34	CTCF	chr14:46719400-46719550	HPAF	blood vessel:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
35	CTCF	chr14:46719380-46719530	MCF-7	breast:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
36	CTCF	chr14:46813680-46813830	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr14:46959720-46959870	NB4	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
38	CTCF	chr14:46813640-46813790	HCFaa	heart:	n/a	n/a
39	CTCF	chr14:46813495-46814058	A549	lung:	n/a	n/a
40	CTCF	chr14:46719400-46719550	Caco-2	colon:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
41	CTCF	chr14:46959760-46959910	HCPEpiC	choroid plexus:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
42	CTCF	chr14:46813680-46813830	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr14:46959740-46959890	GM12866	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
44	CTCF	chr14:46719389-46719547	HepG2	liver:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
45	CTCF	chr14:46959780-46959930	A549	lung:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
46	CTCF	chr14:46719382-46719563	MCF-7	breast:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
47	CTCF	chr14:46728818-46728961	LNCaP	prostate:	n/a	n/a
48	CTCF	chr14:46719371-46719601	LNCaP	prostate:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
49	CTCF	chr14:46845284-46845313	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr14:46719400-46719550	K562	blood:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	IMR90	lung:	fetal
2	chr14:46916528-46916578	AG09319	gingival:	n/a
3	chr14:46916528-46916578	Jurkat	blood:	n/a
4	chr14:46874779-46874829	GM06990	blood:	n/a
5	chr14:46916080-46916130	CMK	blood:	n/a
6	chr14:46916080-46916130	NH-A	brain:	n/a
7	chr14:46874779-46874829	HCPEpiC	choroid plexus:	n/a
8	chr14:46916528-46916578	MCF10A-Er-Src	breast:	n/a
9	chr14:46916080-46916130	NT2-D1	testis:	n/a
10	chr14:46791389-46791439	SK-N-SH	brain:	n/a
11	chr14:46916528-46916578	NHBE	bronchial:	n/a
12	chr14:46916080-46916130	HCF	heart:	n/a
13	chr14:46874779-46874829	Hepatocyte	liver:	n/a
14	chr14:46791389-46791439	AG09309	skin:	n/a
15	chr14:46916528-46916578	LNCaP	prostate:	n/a
16	chr14:46916080-46916130	NHDF-neo	bronchial:	n/a
17	chr14:46791389-46791439	T-47D	breast:	n/a
18	chr14:46916080-46916130	HRPEpiC	eye:	n/a
19	chr14:46916528-46916578	HEEpiC	esophagus:	n/a
20	chr14:46916528-46916578	A549	lung:	n/a
21	chr14:46916080-46916130	AG09309	skin:	n/a
22	chr14:46916080-46916130	PFSK-1	brain:	n/a
23	chr14:46874779-46874829	NHDF-neo	bronchial:	n/a
24	chr14:46791389-46791439	HCM	heart:	n/a
25	chr14:46916080-46916130	K562	blood:	n/a
26	chr14:46874779-46874829	MCF10A-Er-Src	breast:	n/a
27	chr14:46791389-46791439	K562	blood:	n/a
28	chr14:46916528-46916578	ECC-1	luminal epithelium:	n/a
29	chr14:46791389-46791439	U87	brain:	n/a
30	chr14:46874779-46874829	AG04449	skin:	fetal
31	chr14:46791389-46791439	NT2-D1	testis:	n/a
32	chr14:46874779-46874829	HRE	kidney:	n/a
33	chr14:46916528-46916578	AG04449	skin:	fetal
34	chr14:46874779-46874829	MCF-7	breast:	n/a
35	chr14:46874779-46874829	LNCaP	prostate:	n/a
36	chr14:46916528-46916578	U87	brain:	n/a
37	chr14:46916080-46916130	AG04449	skin:	fetal
38	chr14:46791389-46791439	AoSMC	blood vessel:	n/a
39	chr14:46916080-46916130	HNPCEpiC	eye:	n/a
40	chr14:46874779-46874829	SK-N-SH_RA	brain:	n/a
41	chr14:46874779-46874829	ovcar-3	ovarian:	n/a
42	chr14:46916528-46916578	HMEC	breast:	n/a
43	chr14:46874779-46874829	HNPCEpiC	eye:	n/a
44	chr14:46916528-46916578	Hepatocyte	liver:	n/a
45	chr14:46874779-46874829	SK-N-MC	brain:	n/a
46	chr14:46791389-46791439	Caco-2	colon:	n/a
47	chr14:46916080-46916130	GM12891	blood:	n/a
48	chr14:46874779-46874829	HRCEpiC	kidney:	n/a
49	chr14:46916528-46916578	AG09309	skin:	n/a
50	chr14:46916528-46916578	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
2	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
3	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
4	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:
5	chr14:46984156..46986673-chr14:46987478..46989928,2	K562	blood:
6	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
7	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
8	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
9	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
10	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:

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

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

Extended variants
information (count: 4669 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4669 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527688297	chr14:46716984-46716985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547630496	chr14:46716998-46716999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189894393	chr14:46717007-46717008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533263861	chr14:46717036-46717037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371173737	chr14:46717037-46717038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572198648	chr14:46717066-46717067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541017404	chr14:46717121-46717122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76265294	chr14:46717190-46717191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139832887	chr14:46717229-46717230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59376903	chr14:46717268-46717269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561216874	chr14:46717269-46717270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530073788	chr14:46717288-46717289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550214193	chr14:46717289-46717290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181588354	chr14:46717340-46717341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575941483	chr14:46717378-46717379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186312248	chr14:46717440-46717441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556563680	chr14:46717464-46717465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575092619	chr14:46717470-46717471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541990027	chr14:46717559-46717560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143160835	chr14:46717598-46717599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541373460	chr14:46717614-46717615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541508440	chr14:46717619-46717620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572167383	chr14:46717628-46717629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545883599	chr14:46717645-46717646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564649499	chr14:46717683-46717684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146886484	chr14:46717686-46717687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189942137	chr14:46717760-46717761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561146566	chr14:46717814-46717815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182213101	chr14:46717824-46717825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529950653	chr14:46717833-46717834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs8013513	chr14:46717838-46717839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564586403	chr14:46717859-46717860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569783669	chr14:46717878-46717879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184946254	chr14:46717882-46717883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551167115	chr14:46717932-46717933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569765633	chr14:46717948-46717949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149002951	chr14:46717977-46717978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536607389	chr14:46718004-46718005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143772314	chr14:46718017-46718018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115497119	chr14:46718069-46718070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs151077462	chr14:46718077-46718078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554085770	chr14:46718100-46718101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572302577	chr14:46718197-46718198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374257900	chr14:46718207-46718208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs546018748	chr14:46718231-46718232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557957757	chr14:46718236-46718237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17737767	chr14:46718257-46718258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140995434	chr14:46718314-46718315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146641521	chr14:46718342-46718343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79409812	chr14:46718362-46718363	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46715000-46718000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:46716400-46717000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr14:46716600-46717000	Enhancers	Colon Smooth Muscle	Colon
4	chr14:46717200-46718400	Enhancers	Fetal Heart	heart
5	chr14:46717800-46718000	Enhancers	Fetal Brain Female	brain
6	chr14:46719400-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:46719600-46720000	Enhancers	Fetal Brain Female	brain
8	chr14:46720200-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr14:46725000-46725600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:46725200-46725600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:46725200-46725600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr14:46725600-46725800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr14:46725600-46726000	Enhancers	Primary hematopoietic stem cells	blood
14	chr14:46725600-46726000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:46725600-46726000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:46725800-46740400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr14:46728800-46729000	Enhancers	Fetal Kidney	kidney
18	chr14:46728800-46729200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:46729800-46730200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:46729800-46730400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr14:46730400-46730800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:46730400-46731600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr14:46731600-46733000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr14:46740400-46740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr14:46740600-46748200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr14:46748200-46749600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr14:46748400-46749200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr14:46748800-46749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr14:46749400-46749800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr14:46775400-46775800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr14:46775400-46776000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr14:46780200-46780400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr14:46780800-46781200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr14:46781000-46781200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:46785600-46790400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr14:46785600-46790600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr14:46788200-46788600	Active TSS	Left Ventricle	heart
40	chr14:46790400-46790600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr14:46790400-46790800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
42	chr14:46790400-46791000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr14:46790400-46792400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr14:46790400-46792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:46790400-46792800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr14:46790400-46795200	Enhancers	Primary hematopoietic stem cells	blood
47	chr14:46790600-46795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr14:46790800-46791000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
49	chr14:46790800-46791000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
50	chr14:46790800-46791200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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