Variant report

Variant	nsv1050269
Chromosome Location	chr14:46527381-46936207
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:889)
CpG islands
(count:246)
Chromatin interactive
region (count:10)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:889 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	BACH1	chr14:46559473-46559585	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:46791333-46791636	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:46791312-46791676	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:46624384-46624661	A549	lung:	n/a	n/a
7	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr14:46673638-46673846	HepG2	liver:	n/a	chr14:46673736-46673749 chr14:46673736-46673747 chr14:46673736-46673749
9	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
11	CEBPB	chr14:46559908-46560222	IMR90	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
12	CEBPB	chr14:46791324-46791680	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
14	CEBPB	chr14:46669191-46669427	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:46587638-46587921	HepG2	liver:	n/a	chr14:46587769-46587780
16	CEBPB	chr14:46624371-46624707	IMR90	lung:	n/a	n/a
17	CEBPB	chr14:46688925-46689144	IMR90	lung:	n/a	chr14:46689036-46689047
18	CEBPB	chr14:46547984-46548190	HepG2	liver:	n/a	chr14:46548062-46548073
19	CEBPB	chr14:46624379-46624686	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr14:46624367-46624581	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:46688915-46689127	HepG2	liver:	n/a	chr14:46689036-46689047
23	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
24	CEBPB	chr14:46629835-46630166	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr14:46629938-46630176	A549	lung:	n/a	n/a
28	CEBPB	chr14:46559949-46560242	HepG2	liver:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
29	CEBPB	chr14:46658833-46659107	HepG2	liver:	n/a	chr14:46658963-46658974
30	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
31	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
32	CEBPB	chr14:46559920-46560194	A549	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
33	CEBPB	chr14:46732453-46732625	HepG2	liver:	n/a	chr14:46732582-46732593 chr14:46732584-46732593
34	CEBPB	chr14:46615814-46615966	K562	blood:	n/a	n/a
35	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
36	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
37	CEBPB	chr14:46705042-46705302	IMR90	lung:	n/a	n/a
38	CEBPB	chr14:46560063-46560127	K562	blood:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
39	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
40	CHD2	chr14:46791309-46791730	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr14:46791285-46791675	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr14:46813680-46813830	GM12873	blood:	n/a	n/a
43	CTCF	chr14:46719380-46719530	AoAF	blood vessel:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
44	CTCF	chr14:46631636-46631706	LNCaP	prostate:	n/a	n/a
45	CTCF	chr14:46813760-46813910	HVMF	connective:	n/a	n/a
46	CTCF	chr14:46719360-46719510	Caco-2	colon:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
47	CTCF	chr14:46813696-46813698	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr14:46719420-46719570	HVMF	connective:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
49	CTCF	chr14:46719420-46719570	HUVEC	blood vessel:	n/a	chr14:46719475-46719491 chr14:46719476-46719497 chr14:46719474-46719492
50	CTCF	chr14:46813680-46813830	HCPEpiC	choroid plexus:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46791389-46791439	PrEC	prostate:	n/a
2	chr14:46791389-46791439	T-47D	breast:	n/a
3	chr14:46791389-46791439	PrEC	prostate:	n/a
4	chr14:46791389-46791439	T-47D	breast:	n/a
5	chr14:46874779-46874829	NB4	blood:	n/a
6	chr14:46916080-46916130	ovcar-3	ovarian:	n/a
7	chr14:46916080-46916130	ECC-1	luminal epithelium:	n/a
8	chr14:46791389-46791439	HCPEpiC	choroid plexus:	n/a
9	chr14:46916080-46916130	HUVEC	blood vessel:	n/a
10	chr14:46916528-46916578	NHBE	bronchial:	n/a
11	chr14:46791389-46791439	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:46916080-46916130	GM12892	blood:	n/a
13	chr14:46791389-46791439	AG10803	skin:	n/a
14	chr14:46874779-46874829	HNPCEpiC	eye:	n/a
15	chr14:46874779-46874829	PrEC	prostate:	n/a
16	chr14:46874779-46874829	HRE	kidney:	n/a
17	chr14:46916080-46916130	PANC-1	pancreas:	n/a
18	chr14:46791389-46791439	HMEC	breast:	n/a
19	chr14:46874779-46874829	HCF	heart:	n/a
20	chr14:46916528-46916578	HRPEpiC	eye:	n/a
21	chr14:46791389-46791439	HRCEpiC	kidney:	n/a
22	chr14:46874779-46874829	IMR90	lung:	fetal
23	chr14:46916528-46916578	HEEpiC	esophagus:	n/a
24	chr14:46874779-46874829	MCF-7	breast:	n/a
25	chr14:46791389-46791439	PANC-1	pancreas:	n/a
26	chr14:46874779-46874829	A549	lung:	n/a
27	chr14:46916528-46916578	AG04449	skin:	fetal
28	chr14:46874779-46874829	HPAEpiC	pulmonary alveolar:	n/a
29	chr14:46916080-46916130	RPTEC	kidney:	n/a
30	chr14:46874779-46874829	HCPEpiC	choroid plexus:	n/a
31	chr14:46791389-46791439	GM12891	blood:	n/a
32	chr14:46791389-46791439	HCT-116	colon:	n/a
33	chr14:46874779-46874829	ProgFib	skin:	n/a
34	chr14:46916528-46916578	U87	brain:	n/a
35	chr14:46916528-46916578	Hepatocyte	liver:	n/a
36	chr14:46791389-46791439	SK-N-SH_RA	brain:	n/a
37	chr14:46916080-46916130	NT2-D1	testis:	n/a
38	chr14:46874779-46874829	T-47D	breast:	n/a
39	chr14:46874779-46874829	AoSMC	blood vessel:	n/a
40	chr14:46791389-46791439	HIPEpiC	eye:	n/a
41	chr14:46874779-46874829	AG04450	lung:	fetal
42	chr14:46791389-46791439	MCF10A-Er-Src	breast:	n/a
43	chr14:46916528-46916578	RPTEC	kidney:	n/a
44	chr14:46916528-46916578	Hela-S3	cervix:	n/a
45	chr14:46916080-46916130	AG04449	skin:	fetal
46	chr14:46874779-46874829	SAEC	small airway:	n/a
47	chr14:46916528-46916578	PFSK-1	brain:	n/a
48	chr14:46874779-46874829	HRPEpiC	eye:	n/a
49	chr14:46916528-46916578	Jurkat	blood:	n/a
50	chr14:46874779-46874829	MCF10A-Er-Src	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46557288..46558270-chr17:53789584..53790485,2	MCF-7	breast:
2	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
3	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:
4	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
5	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
6	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:
7	chr14:46538407..46539085-chr4:43195045..43195862,2	MCF-7	breast:
8	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
9	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
10	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
2	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036678
3	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
4	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
5	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
6	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036679
7	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
8	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
9	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036679
10	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
11	lnc-FANCM-6	chr14:46788016-46788064	ENSG00000258700
12	lnc-FANCM-6	chr14:46533362-46533419	ENSG00000258700
13	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036678
14	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036678
15	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
16	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036679
17	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700
18	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700

No data

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

Extended variants
information (count: 4462 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4462 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530741618	chr14:46527630-46527631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142660286	chr14:46527686-46527687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541437445	chr14:46527749-46527750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190361654	chr14:46527751-46527752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146066443	chr14:46527791-46527792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377120334	chr14:46527793-46527794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533472843	chr14:46527813-46527814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77550519	chr14:46527828-46527829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550145737	chr14:46527832-46527833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182081048	chr14:46527835-46527836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543916626	chr14:46527845-46527846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577522147	chr14:46527899-46527900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548871535	chr14:46527911-46527912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35325224	chr14:46527915-46527916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199903838	chr14:46527954-46527955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567573456	chr14:46528008-46528009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114829703	chr14:46528046-46528047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185100240	chr14:46528064-46528065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115553694	chr14:46528069-46528070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1011865	chr14:46528078-46528079	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556615715	chr14:46528088-46528089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188942466	chr14:46528183-46528184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537259475	chr14:46528194-46528195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555650253	chr14:46528201-46528202	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs117207252	chr14:46528203-46528204	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs534965551	chr14:46528235-46528236	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs553371924	chr14:46528244-46528245	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs199879933	chr14:46528317-46528318	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs370758229	chr14:46528356-46528357	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs111692886	chr14:46528413-46528414	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs578066591	chr14:46528442-46528443	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs563031113	chr14:46528443-46528444	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545554249	chr14:46528445-46528446	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs563789125	chr14:46528454-46528455	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs148278760	chr14:46528490-46528491	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs146897704	chr14:46528526-46528527	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs139268091	chr14:46528527-46528528	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560882575	chr14:46528557-46528558	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528427791	chr14:46528573-46528574	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs546577210	chr14:46528574-46528575	Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs564565375	chr14:46528614-46528615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs181353925	chr14:46528647-46528648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs185529074	chr14:46528659-46528660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs568630645	chr14:46528679-46528680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535919955	chr14:46528680-46528681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs73233919	chr14:46528695-46528696	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs114071999	chr14:46528697-46528698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs143177053	chr14:46528699-46528700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553375744	chr14:46528701-46528702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs1983747	chr14:46528754-46528755	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Breast cancer	21364760	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46527600-46528200	Enhancers	GM12878-XiMat	blood
2	chr14:46528200-46528600	Flanking Active TSS	GM12878-XiMat	blood
3	chr14:46533000-46533600	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr14:46560400-46562200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:46560600-46561400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:46563000-46563600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:46576600-46576800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:46581800-46582200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:46581800-46582200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:46592200-46592800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr14:46592200-46592800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr14:46592200-46592800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr14:46592400-46592800	Enhancers	H1 Cell Line	embryonic stem cell
14	chr14:46592400-46592800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:46592400-46593000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr14:46592400-46593000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr14:46605000-46605400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:46605200-46607400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr14:46605200-46607400	Enhancers	HUVEC	blood vessel
20	chr14:46605400-46606000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:46605600-46606400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:46605800-46607800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:46607400-46609000	Weak transcription	HUVEC	blood vessel
24	chr14:46609000-46609800	Enhancers	HUVEC	blood vessel
25	chr14:46616200-46617200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr14:46616800-46617200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr14:46616800-46617200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:46616800-46617200	Enhancers	Brain Germinal Matrix	brain
29	chr14:46625400-46626000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:46665400-46665800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr14:46666400-46667200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr14:46666400-46667600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr14:46666400-46667800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:46666800-46667400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr14:46667000-46667400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr14:46674000-46674800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:46674400-46674800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:46703000-46704200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:46703200-46704200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr14:46711600-46712600	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr14:46714800-46715000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:46714800-46715200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:46715000-46718000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr14:46716400-46717000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr14:46716600-46717000	Enhancers	Colon Smooth Muscle	Colon
46	chr14:46717200-46718400	Enhancers	Fetal Heart	heart
47	chr14:46717800-46718000	Enhancers	Fetal Brain Female	brain
48	chr14:46719400-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:46719600-46720000	Enhancers	Fetal Brain Female	brain
50	chr14:46720200-46721200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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