Variant report

Variant	esv2759989
Chromosome Location	chr14:46793652-46948526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:46847543-46847870	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:46874491-46874834	ECC-1	luminal epithelium:	n/a	n/a
3	CEBPB	chr14:46874231-46874599	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:46874424-46874880	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr14:46944327-46944520	HepG2	liver:	n/a	chr14:46944345-46944356
6	CEBPB	chr14:46874550-46874834	MCF-7	breast:	n/a	n/a
7	CEBPB	chr14:46817335-46817572	A549	lung:	n/a	n/a
8	CEBPB	chr14:46887921-46888002	K562	blood:	n/a	chr14:46887964-46887975
9	CEBPB	chr14:46889950-46890217	HepG2	liver:	n/a	chr14:46890121-46890134 chr14:46890122-46890133
10	CEBPB	chr14:46901890-46901905	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr14:46887890-46888142	HepG2	liver:	n/a	chr14:46887964-46887975
12	CEBPB	chr14:46922132-46922270	HepG2	liver:	n/a	chr14:46922172-46922183
13	CHD1	chr14:46921497-46921523	GM12878	blood:	n/a	n/a
14	CTCF	chr14:46813680-46813830	HFF	foreskin:	n/a	n/a
15	CTCF	chr14:46813640-46813790	BJ	skin:	n/a	n/a
16	CTCF	chr14:46921251-46921292	GM13976	blood:	n/a	n/a
17	CTCF	chr14:46813620-46813770	GM12872	blood:	n/a	n/a
18	CTCF	chr14:46813640-46813790	HL-60	blood:	n/a	n/a
19	CTCF	chr14:46813680-46813830	GM12875	blood:	n/a	n/a
20	CTCF	chr14:46813660-46813810	BE2_C	brain:	n/a	n/a
21	CTCF	chr14:46813560-46813710	AG04450	lung:	n/a	n/a
22	CTCF	chr14:46845284-46845313	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr14:46813660-46813810	HMEC	breast:	n/a	n/a
24	CTCF	chr14:46813657-46813850	GM10248	blood:	n/a	n/a
25	CTCF	chr14:46813627-46813873	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:46813660-46813810	HCM	heart:	n/a	n/a
27	CTCF	chr14:46794540-46794690	HepG2	liver:	n/a	n/a
28	CTCF	chr14:46813680-46813830	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr14:46813640-46813790	HCFaa	heart:	n/a	n/a
30	CTCF	chr14:46813660-46813810	HPF	lung:	n/a	n/a
31	CTCF	chr14:46813640-46813790	NHLF	lung:	n/a	n/a
32	CTCF	chr14:46813640-46813790	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr14:46813660-46813810	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr14:46813700-46813850	HMEC	breast:	n/a	n/a
35	CTCF	chr14:46813640-46813790	GM12870	blood:	n/a	n/a
36	CTCF	chr14:46813680-46813830	GM06990	blood:	n/a	n/a
37	CTCF	chr14:46813620-46813770	GM12874	blood:	n/a	n/a
38	CTCF	chr14:46813660-46813810	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr14:46813707-46813833	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr14:46813680-46813830	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr14:46908369-46908436	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:46813660-46813810	SAEC	small airway:	n/a	n/a
43	CTCF	chr14:46813720-46813870	HCT-116	colon:	n/a	n/a
44	CTCF	chr14:46813680-46813830	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr14:46813620-46813770	GM12865	blood:	n/a	n/a
46	CTCF	chr14:46813640-46813790	HEK293	kidney:	n/a	n/a
47	CTCF	chr14:46813680-46813830	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr14:46813660-46813810	AG09309	skin:	n/a	n/a
49	CTCF	chr14:46906330-46906348	GM10266	blood:	n/a	n/a
50	CTCF	chr14:46813620-46813770	GM12869	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46916080-46916130	SK-N-MC	brain:	n/a
2	chr14:46916528-46916578	BJ	skin:	n/a
3	chr14:46916528-46916578	SKMC	muscle:	n/a
4	chr14:46916080-46916130	AG04449	skin:	fetal
5	chr14:46916080-46916130	CMK	blood:	n/a
6	chr14:46874779-46874829	SAEC	small airway:	n/a
7	chr14:46874779-46874829	HRPEpiC	eye:	n/a
8	chr14:46874779-46874829	ProgFib	skin:	n/a
9	chr14:46874779-46874829	U87	brain:	n/a
10	chr14:46916080-46916130	SK-N-SH_RA	brain:	n/a
11	chr14:46916528-46916578	IMR90	lung:	fetal
12	chr14:46916528-46916578	GM12892	blood:	n/a
13	chr14:46874779-46874829	HNPCEpiC	eye:	n/a
14	chr14:46916528-46916578	SAEC	small airway:	n/a
15	chr14:46916528-46916578	Caco-2	colon:	n/a
16	chr14:46916528-46916578	HCT-116	colon:	n/a
17	chr14:46916528-46916578	T-47D	breast:	n/a
18	chr14:46916080-46916130	GM12878	blood:	n/a
19	chr14:46874779-46874829	ECC-1	luminal epithelium:	n/a
20	chr14:46916080-46916130	GM12892	blood:	n/a
21	chr14:46916528-46916578	NB4	blood:	n/a
22	chr14:46916080-46916130	GM19239	blood:	n/a
23	chr14:46916528-46916578	PANC-1	pancreas:	n/a
24	chr14:46916080-46916130	HNPCEpiC	eye:	n/a
25	chr14:46916528-46916578	A549	lung:	n/a
26	chr14:46916528-46916578	AG09319	gingival:	n/a
27	chr14:46916528-46916578	GM12878	blood:	n/a
28	chr14:46874779-46874829	K562	blood:	n/a
29	chr14:46874779-46874829	HCF	heart:	n/a
30	chr14:46916528-46916578	SK-N-SH_RA	brain:	n/a
31	chr14:46916528-46916578	RPTEC	kidney:	n/a
32	chr14:46916528-46916578	AG09309	skin:	n/a
33	chr14:46916080-46916130	NHDF-neo	bronchial:	n/a
34	chr14:46916080-46916130	HL-60	blood:	n/a
35	chr14:46874779-46874829	HMEC	breast:	n/a
36	chr14:46916528-46916578	AG10803	skin:	n/a
37	chr14:46916528-46916578	HCF	heart:	n/a
38	chr14:46916080-46916130	SAEC	small airway:	n/a
39	chr14:46874779-46874829	HEEpiC	esophagus:	n/a
40	chr14:46916528-46916578	PrEC	prostate:	n/a
41	chr14:46916080-46916130	GM06990	blood:	n/a
42	chr14:46916528-46916578	HEK293	kidney:	embryo
43	chr14:46874779-46874829	AoSMC	blood vessel:	n/a
44	chr14:46874779-46874829	RPTEC	kidney:	n/a
45	chr14:46916080-46916130	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:46916528-46916578	HIPEpiC	eye:	n/a
47	chr14:46916080-46916130	HRCEpiC	kidney:	n/a
48	chr14:46916528-46916578	NHDF-neo	bronchial:	n/a
49	chr14:46916080-46916130	HRPEpiC	eye:	n/a
50	chr14:46874779-46874829	BE2_C	brain:	n/a

(count:5 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 2212 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2212 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184942516	chr14:46793680-46793681	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562195054	chr14:46793722-46793723	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141621117	chr14:46793724-46793725	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541388293	chr14:46793726-46793727	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559913222	chr14:46793736-46793737	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192073883	chr14:46793748-46793749	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28634866	chr14:46793782-46793783	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs565612420	chr14:46793797-46793798	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563239225	chr14:46793824-46793825	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147037060	chr14:46793852-46793853	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551205961	chr14:46793875-46793876	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs11846677	chr14:46793917-46793918	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551901229	chr14:46793929-46793930	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536767026	chr14:46793930-46793931	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182299433	chr14:46793947-46793948	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566738906	chr14:46793988-46793989	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576092804	chr14:46794032-46794033	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs4506807	chr14:46794059-46794060	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs186972365	chr14:46794126-46794127	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558573797	chr14:46794147-46794148	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17659488	chr14:46794184-46794185	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs138255676	chr14:46794185-46794186	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567962031	chr14:46794223-46794224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142338054	chr14:46794244-46794245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150383499	chr14:46794274-46794275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560226673	chr14:46794277-46794278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571936126	chr14:46794390-46794391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545830639	chr14:46794415-46794416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572001921	chr14:46794444-46794445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532872725	chr14:46794471-46794472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367779861	chr14:46794480-46794481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551168451	chr14:46794508-46794509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563053273	chr14:46794510-46794511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530353939	chr14:46794511-46794512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548386218	chr14:46794590-46794591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78740482	chr14:46794594-46794595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527643580	chr14:46794647-46794648	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11851560	chr14:46794666-46794667	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs570375746	chr14:46794723-46794724	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537769495	chr14:46794724-46794725	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556064559	chr14:46794728-46794729	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138077679	chr14:46794823-46794824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535679649	chr14:46794830-46794831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111963749	chr14:46794841-46794842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36115206	chr14:46794886-46794887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572109380	chr14:46794959-46794960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112712587	chr14:46794995-46794996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557757880	chr14:46795027-46795028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576136039	chr14:46795059-46795060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544906867	chr14:46795116-46795117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46790400-46795200	Enhancers	Primary hematopoietic stem cells	blood
2	chr14:46790600-46795400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr14:46793200-46794200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:46793400-46797400	Weak transcription	Ovary	ovary
5	chr14:46794200-46795600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:46794600-46794800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr14:46794600-46794800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr14:46795200-46796800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr14:46795600-46797200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:46797200-46797400	Enhancers	Primary hematopoietic stem cells	blood
11	chr14:46797200-46798200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:46797200-46798400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:46797400-46797600	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr14:46797400-46797800	Enhancers	Ovary	ovary
15	chr14:46797600-46798000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr14:46797600-46798200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr14:46799200-46799400	Enhancers	Fetal Kidney	kidney
18	chr14:46813000-46814000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:46813600-46814000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr14:46814800-46815800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr14:46818800-46821200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:46836800-46838000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr14:46837400-46839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:46837600-46838200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:46838000-46838800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr14:46838200-46838800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:46838800-46839000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr14:46838800-46839800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:46844800-46845000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr14:46845600-46847600	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr14:46846200-46846400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
32	chr14:46846200-46846800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:46846200-46846800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr14:46846200-46847200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr14:46846200-46847200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr14:46846400-46846800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:46846400-46847200	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr14:46846400-46847200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:46846400-46847200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr14:46846600-46850800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr14:46846800-46848000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr14:46847200-46847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr14:46847200-46850400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr14:46847200-46850400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr14:46847600-46847800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr14:46847600-46850400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr14:46847800-46850800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr14:46850400-46851000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr14:46850400-46851400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr14:46850400-46851600	Enhancers	HUES6 Cell Line	embryonic stem cell

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