Variant report

Variant	nsv1044526
Chromosome Location	chr14:46727837-46975636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr14:46791312-46791676	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr14:46791333-46791636	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	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr14:46959344-46959844	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
8	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
9	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
10	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
11	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
13	CEBPB	chr14:46959392-46959846	MCF-7	breast:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
14	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr14:46959424-46959778	HepG2	liver:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
16	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr14:46959463-46959768	A549	lung:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
18	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
19	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
20	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
22	CEBPB	chr14:46732453-46732625	HepG2	liver:	n/a	chr14:46732582-46732593 chr14:46732584-46732593
23	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
24	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
25	CEBPB	chr14:46791324-46791680	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:46959438-46959906	H1-hESC	embryonic stem cell:	n/a	chr14:46959575-46959586 chr14:46959590-46959603
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	chr14:46813504-46813925	T-47D	breast:	n/a	n/a
31	CTCF	chr14:46813680-46813830	NB4	blood:	n/a	n/a
32	CTCF	chr14:46728818-46728961	LNCaP	prostate:	n/a	n/a
33	CTCF	chr14:46813638-46813842	GM10266	blood:	n/a	n/a
34	CTCF	chr14:46813680-46813830	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:46959773-46959837	GM19240	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
36	CTCF	chr14:46813640-46813790	BJ	skin:	n/a	n/a
37	CTCF	chr14:46728740-46728890	Caco-2	colon:	n/a	n/a
38	CTCF	chr14:46813662-46813804	K562	blood:	n/a	n/a
39	CTCF	chr14:46813680-46813830	GM06990	blood:	n/a	n/a
40	CTCF	chr14:46728700-46728973	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr14:46728817-46729002	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:46959725-46959908	MCF-7	breast:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
43	CTCF	chr14:46728740-46728890	GM12873	blood:	n/a	n/a
44	CTCF	chr14:46959740-46959868	GM10248	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
45	CTCF	chr14:46813680-46813830	GM12871	blood:	n/a	n/a
46	CTCF	chr14:46959760-46959910	HCPEpiC	choroid plexus:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834
47	CTCF	chr14:46813640-46813790	NHLF	lung:	n/a	n/a
48	CTCF	chr14:46785383-46785428	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr14:46813495-46814058	A549	lung:	n/a	n/a
50	CTCF	chr14:46959720-46959870	GM06990	blood:	n/a	chr14:46959811-46959829 chr14:46959814-46959827 chr14:46959812-46959828 chr14:46959813-46959834

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916528-46916578	GM06990	blood:	n/a
2	chr14:46916528-46916578	GM06990	blood:	n/a
3	chr14:46874779-46874829	CMK	blood:	n/a
4	chr14:46874779-46874829	ProgFib	skin:	n/a
5	chr14:46916528-46916578	RPTEC	kidney:	n/a
6	chr14:46874779-46874829	HNPCEpiC	eye:	n/a
7	chr14:46916528-46916578	U87	brain:	n/a
8	chr14:46916528-46916578	ProgFib	skin:	n/a
9	chr14:46874779-46874829	T-47D	breast:	n/a
10	chr14:46916528-46916578	H1-hESC	embryonic stem cell:	embryo
11	chr14:46791389-46791439	AG09319	gingival:	n/a
12	chr14:46874779-46874829	PFSK-1	brain:	n/a
13	chr14:46916080-46916130	PANC-1	pancreas:	n/a
14	chr14:46916080-46916130	IMR90	lung:	fetal
15	chr14:46791389-46791439	PFSK-1	brain:	n/a
16	chr14:46874779-46874829	SK-N-SH_RA	brain:	n/a
17	chr14:46916080-46916130	PrEC	prostate:	n/a
18	chr14:46916528-46916578	PANC-1	pancreas:	n/a
19	chr14:46916528-46916578	BE2_C	brain:	n/a
20	chr14:46916528-46916578	SKMC	muscle:	n/a
21	chr14:46874779-46874829	ovcar-3	ovarian:	n/a
22	chr14:46874779-46874829	NB4	blood:	n/a
23	chr14:46791389-46791439	Hela-S3	cervix:	n/a
24	chr14:46916080-46916130	GM12892	blood:	n/a
25	chr14:46791389-46791439	HL-60	blood:	n/a
26	chr14:46916080-46916130	Hepatocyte	liver:	n/a
27	chr14:46916528-46916578	Jurkat	blood:	n/a
28	chr14:46874779-46874829	MCF-7	breast:	n/a
29	chr14:46916528-46916578	NH-A	brain:	n/a
30	chr14:46791389-46791439	ProgFib	skin:	n/a
31	chr14:46874779-46874829	AG10803	skin:	n/a
32	chr14:46874779-46874829	NHBE	bronchial:	n/a
33	chr14:46916528-46916578	HEK293	kidney:	embryo
34	chr14:46916080-46916130	AG09319	gingival:	n/a
35	chr14:46874779-46874829	SAEC	small airway:	n/a
36	chr14:46916528-46916578	PFSK-1	brain:	n/a
37	chr14:46916528-46916578	NB4	blood:	n/a
38	chr14:46916080-46916130	Hela-S3	cervix:	n/a
39	chr14:46916080-46916130	ovcar-3	ovarian:	n/a
40	chr14:46874779-46874829	PANC-1	pancreas:	n/a
41	chr14:46916080-46916130	U87	brain:	n/a
42	chr14:46916528-46916578	HNPCEpiC	eye:	n/a
43	chr14:46916528-46916578	AG04450	lung:	fetal
44	chr14:46791389-46791439	PrEC	prostate:	n/a
45	chr14:46791389-46791439	HepG2	liver:	n/a
46	chr14:46791389-46791439	ECC-1	luminal epithelium:	n/a
47	chr14:46791389-46791439	CMK	blood:	n/a
48	chr14:46916080-46916130	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:46916080-46916130	GM12878	blood:	n/a
50	chr14:46874779-46874829	Hepatocyte	liver:	n/a

(count:6 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 4391 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4391 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1953924	chr14:46727845-46727846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184500020	chr14:46727879-46727880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144798362	chr14:46727884-46727885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138632016	chr14:46727903-46727904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs871605	chr14:46727916-46727917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs3037601	chr14:46727942-46727943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs33987850	chr14:46727943-46727944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369115867	chr14:46727945-46727946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2415949	chr14:46727946-46727947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575703506	chr14:46727948-46727949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573346871	chr14:46727949-46727950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189358694	chr14:46727957-46727958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs66897914	chr14:46727960-46727961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs565184515	chr14:46727975-46727976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578001197	chr14:46727998-46727999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs893636	chr14:46728004-46728005	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571874257	chr14:46728021-46728022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs712425	chr14:46728057-46728058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs562524130	chr14:46728068-46728069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs8003040	chr14:46728083-46728084	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs141735390	chr14:46728121-46728122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117516702	chr14:46728125-46728126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568919635	chr14:46728139-46728140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527449202	chr14:46728208-46728209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566527884	chr14:46728218-46728219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534334856	chr14:46728230-46728231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552371132	chr14:46728258-46728259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555311170	chr14:46728262-46728263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150757789	chr14:46728268-46728269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs137971376	chr14:46728286-46728287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537924823	chr14:46728287-46728288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs858882	chr14:46728306-46728307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs182065338	chr14:46728324-46728325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535482864	chr14:46728348-46728349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554922790	chr14:46728375-46728376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs858883	chr14:46728380-46728381	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs540441343	chr14:46728390-46728391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559118908	chr14:46728402-46728403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549562464	chr14:46728449-46728450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs8003557	chr14:46728486-46728487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377385681	chr14:46728487-46728488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544299348	chr14:46728543-46728544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370150992	chr14:46728544-46728545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs858884	chr14:46728554-46728555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs858885	chr14:46728593-46728594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557418592	chr14:46728601-46728602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186401287	chr14:46728618-46728619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552222523	chr14:46728652-46728653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190865746	chr14:46728723-46728724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181605124	chr14:46728736-46728737	Weak transcription	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:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46725800-46740400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:46728800-46729000	Enhancers	Fetal Kidney	kidney
3	chr14:46728800-46729200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:46729800-46730200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:46729800-46730400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr14:46730400-46730800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr14:46730400-46731600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr14:46731600-46733000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:46740400-46740600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:46740600-46748200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr14:46748200-46749600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:46748400-46749200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr14:46748800-46749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:46749400-46749800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr14:46775400-46775800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr14:46775400-46776000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr14:46780200-46780400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:46780800-46781200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr14:46781000-46781200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:46785600-46790400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:46785600-46790600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:46788200-46788600	Active TSS	Left Ventricle	heart
25	chr14:46790400-46790600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr14:46790400-46790800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr14:46790400-46791000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
28	chr14:46790400-46792400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:46790400-46792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:46790400-46792800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
31	chr14:46790400-46795200	Enhancers	Primary hematopoietic stem cells	blood
32	chr14:46790600-46795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:46790800-46791000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr14:46790800-46791000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr14:46790800-46791200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr14:46790800-46791600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
37	chr14:46790800-46792000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr14:46790800-46792800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
39	chr14:46791000-46791200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
40	chr14:46791000-46791400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
41	chr14:46791000-46791400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr14:46791000-46791600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
43	chr14:46791200-46791600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:46791200-46791600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr14:46791200-46791800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:46791200-46792000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr14:46791200-46792400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr14:46791200-46792800	Enhancers	Fetal Kidney	kidney
49	chr14:46791400-46791600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr14:46791400-46791800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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