Variant report

Variant	nsv456292
Chromosome Location	chr14:46777209-46958836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:244)
Chromatin interactive
region (count:5)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
6	CEBPB	chr14:46784067-46784309	HepG2	liver:	n/a	chr14:46784195-46784206
7	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
8	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
11	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
12	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
13	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
14	CEBPB	chr14:46957289-46957481	HepG2	liver:	n/a	chr14:46957452-46957465 chr14:46957352-46957363 chr14:46957351-46957364
15	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
16	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr14:46785273-46785473	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:46791324-46791680	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
21	CHD2	chr14:46791309-46791730	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr14:46791285-46791675	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr14:46813680-46813830	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr14:46813620-46813770	GM12874	blood:	n/a	n/a
25	CTCF	chr14:46813620-46813770	GM12868	blood:	n/a	n/a
26	CTCF	chr14:46813680-46813830	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr14:46906330-46906348	GM10266	blood:	n/a	n/a
28	CTCF	chr14:46813720-46813870	HCT-116	colon:	n/a	n/a
29	CTCF	chr14:46813616-46813857	LNCaP	prostate:	n/a	n/a
30	CTCF	chr14:46813600-46813750	A549	lung:	n/a	n/a
31	CTCF	chr14:46813709-46813854	GM12891	blood:	n/a	n/a
32	CTCF	chr14:46813760-46813910	HVMF	connective:	n/a	n/a
33	CTCF	chr14:46794540-46794690	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:46813700-46813850	AG09309	skin:	n/a	n/a
35	CTCF	chr14:46868420-46868570	BE2_C	brain:	n/a	n/a
36	CTCF	chr14:46813680-46813839	GM12892	blood:	n/a	n/a
37	CTCF	chr14:46813676-46813855	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:46813660-46813810	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr14:46813640-46813790	GM12866	blood:	n/a	n/a
40	CTCF	chr14:46813668-46813823	GM19239	blood:	n/a	n/a
41	CTCF	chr14:46813680-46813830	GM12866	blood:	n/a	n/a
42	CTCF	chr14:46921251-46921292	GM13976	blood:	n/a	n/a
43	CTCF	chr14:46813638-46813842	GM10266	blood:	n/a	n/a
44	CTCF	chr14:46813605-46813879	GM12878	blood:	n/a	n/a
45	CTCF	chr14:46813640-46813790	BJ	skin:	n/a	n/a
46	CTCF	chr14:46813680-46813830	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr14:46813680-46813830	GM12878	blood:	n/a	n/a
48	CTCF	chr14:46813680-46813830	HepG2	liver:	n/a	n/a
49	CTCF	chr14:46813680-46813830	GM12868	blood:	n/a	n/a
50	CTCF	chr14:46813640-46813862	ProgFib	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46791389-46791439	MCF10A-Er-Src	breast:	n/a
2	chr14:46791389-46791439	GM12892	blood:	n/a
3	chr14:46874779-46874829	PFSK-1	brain:	n/a
4	chr14:46791389-46791439	ovcar-3	ovarian:	n/a
5	chr14:46916080-46916130	HAEpiC	amniotic membrane:	n/a
6	chr14:46916528-46916578	ECC-1	luminal epithelium:	n/a
7	chr14:46791389-46791439	Caco-2	colon:	n/a
8	chr14:46791389-46791439	HRPEpiC	eye:	n/a
9	chr14:46791389-46791439	NHDF-neo	bronchial:	n/a
10	chr14:46874779-46874829	NT2-D1	testis:	n/a
11	chr14:46916528-46916578	HCT-116	colon:	n/a
12	chr14:46916528-46916578	H1-hESC	embryonic stem cell:	embryo
13	chr14:46874779-46874829	AG09309	skin:	n/a
14	chr14:46791389-46791439	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:46916080-46916130	SKMC	muscle:	n/a
16	chr14:46916080-46916130	IMR90	lung:	fetal
17	chr14:46791389-46791439	SAEC	small airway:	n/a
18	chr14:46791389-46791439	PANC-1	pancreas:	n/a
19	chr14:46874779-46874829	PrEC	prostate:	n/a
20	chr14:46874779-46874829	HCPEpiC	choroid plexus:	n/a
21	chr14:46916528-46916578	HepG2	liver:	n/a
22	chr14:46916080-46916130	Hepatocyte	liver:	n/a
23	chr14:46791389-46791439	T-47D	breast:	n/a
24	chr14:46916528-46916578	GM12878	blood:	n/a
25	chr14:46791389-46791439	AG04450	lung:	fetal
26	chr14:46916528-46916578	Jurkat	blood:	n/a
27	chr14:46916080-46916130	HRPEpiC	eye:	n/a
28	chr14:46916528-46916578	HCM	heart:	n/a
29	chr14:46916528-46916578	HCF	heart:	n/a
30	chr14:46916080-46916130	GM06990	blood:	n/a
31	chr14:46916080-46916130	HepG2	liver:	n/a
32	chr14:46874779-46874829	Hela-S3	cervix:	n/a
33	chr14:46916528-46916578	HAEpiC	amniotic membrane:	n/a
34	chr14:46916528-46916578	NHBE	bronchial:	n/a
35	chr14:46791389-46791439	AG04449	skin:	fetal
36	chr14:46791389-46791439	NB4	blood:	n/a
37	chr14:46916080-46916130	Jurkat	blood:	n/a
38	chr14:46916528-46916578	HRCEpiC	kidney:	n/a
39	chr14:46874779-46874829	NB4	blood:	n/a
40	chr14:46874779-46874829	AG10803	skin:	n/a
41	chr14:46874779-46874829	CMK	blood:	n/a
42	chr14:46916528-46916578	AG10803	skin:	n/a
43	chr14:46916528-46916578	SK-N-MC	brain:	n/a
44	chr14:46791389-46791439	HMEC	breast:	n/a
45	chr14:46874779-46874829	AG04449	skin:	fetal
46	chr14:46916080-46916130	PFSK-1	brain:	n/a
47	chr14:46874779-46874829	HRCEpiC	kidney:	n/a
48	chr14:46916528-46916578	SKMC	muscle:	n/a
49	chr14:46916528-46916578	SAEC	small airway:	n/a
50	chr14:46916528-46916578	HL-60	blood:	n/a

(count:5 , 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	chr14:46878574..46881068-chr14:46881642..46884417,2	K562	blood:
5	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46907384-46907453	ENSG00000258700
2	lnc-FANCM-6	chr14:46916512-46916578	ENSG00000258700
3	lnc-FANCM-6	chr14:46940562-46940714	ENSG00000258700
4	lnc-FANCM-6	chr14:46919111-46919157	ENSG00000258700
5	lnc-FANCM-6	chr14:46940564-46940714	ENSG00000258700
6	lnc-FANCM-6	chr14:46788016-46788064	ENSG00000258700
7	lnc-FANCM-6	chr14:46915388-46915429	ENSG00000258700
8	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036680
9	lnc-FANCM-6	chr14:46907384-46907453	NONHSAT036678
10	lnc-FANCM-6	chr14:46919111-46919157	NONHSAT036678
11	lnc-FANCM-6	chr14:46940562-46940714	NONHSAT036681

No data

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

Extended variants
information (count: 2993 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553248699	chr14:46780201-46780202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577763135	chr14:46780214-46780215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138302659	chr14:46780239-46780240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72670504	chr14:46780319-46780320	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575111499	chr14:46780321-46780322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187229732	chr14:46780327-46780328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562236351	chr14:46780363-46780364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114329249	chr14:46780371-46780372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529152827	chr14:46780397-46780398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186242032	chr14:46780815-46780816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577794601	chr14:46780827-46780828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545230464	chr14:46780839-46780840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531872448	chr14:46780849-46780850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199729530	chr14:46780890-46780891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs115781895	chr14:46780930-46780931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531078575	chr14:46780968-46780969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542607694	chr14:46780976-46780977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561342451	chr14:46781020-46781021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377281826	chr14:46781022-46781023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528370131	chr14:46781028-46781029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551840108	chr14:46781118-46781119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571605975	chr14:46781129-46781130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150606922	chr14:46781148-46781149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550841677	chr14:46781190-46781191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12147827	chr14:46781200-46781201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145187880	chr14:46784865-46784866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76470894	chr14:46784871-46784872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540979730	chr14:46784889-46784890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368173405	chr14:46784890-46784891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs386777129	chr14:46784897-46784898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114869045	chr14:46784936-46784937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560978324	chr14:46784956-46784957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564826873	chr14:46785134-46785135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2415951	chr14:46785207-46785208	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550398542	chr14:46785217-46785218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561995888	chr14:46785231-46785232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181882734	chr14:46785232-46785233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs72670510	chr14:46785268-46785269	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs375116284	chr14:46785272-46785273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530409705	chr14:46785309-46785310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565758354	chr14:46785328-46785329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539476879	chr14:46785331-46785332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544222024	chr14:46785350-46785351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569975510	chr14:46785375-46785376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536848926	chr14:46785386-46785387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186272694	chr14:46785390-46785391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113782553	chr14:46785392-46785393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567328529	chr14:46785399-46785400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140682421	chr14:46785415-46785416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555034920	chr14:46785423-46785424	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:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46780200-46780400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr14:46780800-46781200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:46781000-46781200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:46784800-46785600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:46785600-46790400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:46785600-46790600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:46788200-46788600	Active TSS	Left Ventricle	heart
9	chr14:46790400-46790600	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr14:46790400-46790800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr14:46790400-46791000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr14:46790400-46792400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:46790400-46792600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:46790400-46792800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
15	chr14:46790400-46795200	Enhancers	Primary hematopoietic stem cells	blood
16	chr14:46790600-46795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:46790800-46791000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
18	chr14:46790800-46791000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
19	chr14:46790800-46791200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:46790800-46791600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
21	chr14:46790800-46792000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr14:46790800-46792800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr14:46791000-46791200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
24	chr14:46791000-46791400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr14:46791000-46791400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr14:46791000-46791600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr14:46791200-46791600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:46791200-46791600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
29	chr14:46791200-46791800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr14:46791200-46792000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr14:46791200-46792400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr14:46791200-46792800	Enhancers	Fetal Kidney	kidney
33	chr14:46791400-46791600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr14:46791400-46791800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr14:46791600-46791800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
36	chr14:46791600-46791800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
37	chr14:46791600-46792000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
38	chr14:46791600-46792200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr14:46791600-46792200	Enhancers	HUVEC	blood vessel
40	chr14:46791600-46792400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
41	chr14:46791600-46792800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:46791800-46792000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr14:46791800-46792600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
44	chr14:46791800-46792600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
45	chr14:46791800-46792800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
46	chr14:46792000-46792200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
47	chr14:46792000-46792200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr14:46792000-46792800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
49	chr14:46792000-46792800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr14:46792000-46792800	Enhancers	Fetal Lung	lung

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