Variant report

Variant	nsv892838
Chromosome Location	chr9:25743020-25825595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:25763645-25763886	H1-hESC	embryonic stem cell:	n/a	chr9:25763776-25763787
2	CEBPB	chr9:25783890-25784164	HepG2	liver:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
3	CEBPB	chr9:25783879-25784164	IMR90	lung:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
4	CEBPB	chr9:25761278-25761303	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr9:25761129-25761425	HepG2	liver:	n/a	chr9:25761277-25761288
6	CEBPB	chr9:25763654-25763950	A549	lung:	n/a	chr9:25763776-25763787
7	CEBPB	chr9:25748958-25749217	ECC-1	luminal epithelium:	n/a	chr9:25749030-25749041
8	CEBPB	chr9:25763598-25763944	HepG2	liver:	n/a	chr9:25763776-25763787
9	CEBPB	chr9:25763626-25763962	IMR90	lung:	n/a	chr9:25763776-25763787
10	CTCF	chr9:25769212-25769267	GM13976	blood:	n/a	n/a
11	CTCF	chr9:25769883-25769937	GM13976	blood:	n/a	n/a
12	CTCF	chr9:25812187-25812230	LNCaP	prostate:	n/a	n/a
13	CTCF	chr9:25772140-25772290	GM12872	blood:	n/a	n/a
14	E2F4	chr9:25796592-25796841	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr9:25804227-25804506	GM12878	blood:	n/a	n/a
16	EP300	chr9:25748755-25749311	ECC-1	luminal epithelium:	n/a	n/a
17	FOS	chr9:25780358-25780610	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr9:25755535-25755781	MCF10A-Er-Src	breast:	n/a	chr9:25755694-25755703
19	FOS	chr9:25820636-25820798	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr9:25755551-25755824	MCF10A-Er-Src	breast:	n/a	chr9:25755694-25755703
21	FOS	chr9:25780267-25780611	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr9:25755624-25755849	MCF10A-Er-Src	breast:	n/a	chr9:25755694-25755703
23	GATA2	chr9:25806953-25807459	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr9:25806992-25807415	SH-SY5Y	brain:	n/a	n/a
25	MAFK	chr9:25759496-25759706	HepG2	liver:	n/a	n/a
26	MAFK	chr9:25806682-25806683	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAZ	chr9:25779095-25779162	HepG2	liver:	n/a	n/a
28	MYC	chr9:25784940-25785067	MCF10A-Er-Src	breast:	n/a	n/a
29	NFIC	chr9:25748946-25749317	ECC-1	luminal epithelium:	n/a	n/a
30	NFIC	chr9:25748744-25749385	ECC-1	luminal epithelium:	n/a	n/a
31	NFYA	chr9:25812552-25812731	GM12878	blood:	n/a	n/a
32	NFYA	chr9:25796318-25796512	GM12878	blood:	n/a	n/a
33	NFYB	chr9:25807972-25808401	K562	blood:	n/a	n/a
34	POLR2A	chr9:25798894-25799045	GM12878	blood:	n/a	n/a
35	POLR2A	chr9:25782157-25782174	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr9:25748100-25748101	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr9:25798858-25799084	GM12878	blood:	n/a	n/a
38	POLR2A	chr9:25779780-25780203	H1-neurons	neurons:	n/a	n/a
39	POLR2A	chr9:25794102-25794114	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr9:25751624-25751757	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr9:25802998-25803060	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr9:25808440-25809003	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr9:25819962-25820101	GM12878	blood:	n/a	n/a
44	POLR2A	chr9:25808480-25809001	H1-neurons	neurons:	n/a	n/a
45	POLR2A	chr9:25754614-25754998	H1-neurons	neurons:	n/a	n/a
46	POLR2A	chr9:25786919-25786926	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr9:25813793-25813815	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr9:25798769-25799084	GM12892	blood:	n/a	n/a
49	POLR2A	chr9:25780917-25781056	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr9:25798920-25799032	GM12878	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:25677137..25679533-chr9:25758553..25761140,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
2	lnc-IFT74-8	chr9:25770414-25770615	NONHSAT130502
3	lnc-IFT74-8	chr9:25788032-25788204	ucscGeneNc_uc003zpy_2
4	lnc-IFT74-3	chr9:25798743-25798941	NONHSAT130503
5	lnc-IFT74-8	chr9:25770054-25770166	ucscGeneNc_uc003zpy_2
6	lnc-IFT74-3	chr9:25812619-25812963	XLOC_007306
7	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
8	lnc-IFT74-8	chr9:25788743-25788941	ucscGeneNc_uc003zpy_2
9	lnc-IFT74-3	chr9:25812619-25812966	NONHSAT130503
10	lnc-IFT74-3	chr9:25806693-25806736	XLOC_007306
11	lnc-IFT74-8	chr9:25774413-25774560	NONHSAT130502
12	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
13	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
14	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
15	lnc-IFT74-3	chr9:25784413-25784614	NONHSAT130503
16	lnc-IFT74-8	chr9:25770054-25770166	NONHSAT130502
17	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
18	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
19	lnc-IFT74-3	chr9:25784413-25784560	XLOC_007306
20	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
21	lnc-IFT74-3	chr9:25780414-25780615	NONHSAT130503
22	lnc-IFT74-3	chr9:25798032-25798204	NONHSAT130503
23	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
24	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
25	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
26	lnc-IFT74-8	chr9:25774413-25774614	ucscGeneNc_uc003zpy_2
27	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
28	lnc-IFT74-3	chr9:25780054-25780166	NONHSAT130503
29	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
30	lnc-IFT74-8	chr9:25770414-25770615	ucscGeneNc_uc003zpy_2
31	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
32	lnc-IFT74-8	chr9:25802619-25802963	ucscGeneNc_uc003zpy_2
33	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
34	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
35	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
36	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
37	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
38	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
39	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
40	lnc-IFT74-3	chr9:25798032-25798205	XLOC_007306
41	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
42	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
43	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306

No data

Variant related genes	Relation type
ENSG00000236306	TF binding region
ENSG00000198680	chromatin interactions
FBXW7	miRNA target sites
ARID5B	miRNA target sites
PRPF38B	miRNA target sites
FAM49B	miRNA target sites
RNF182	miRNA target sites
DEPDC1	miRNA target sites
PDE4D	miRNA target sites

Extended variants
information (count: 704 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10491876	chr9:25743020-25743021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374714074	chr9:25743035-25743036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558318773	chr9:25743041-25743042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186270120	chr9:25743043-25743044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575436348	chr9:25743045-25743046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549013589	chr9:25743053-25743054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544040767	chr9:25743083-25743084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562733079	chr9:25743084-25743085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs721672	chr9:25743092-25743093	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs16909712	chr9:25743105-25743106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs721671	chr9:25743121-25743122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139882449	chr9:25743122-25743123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527638692	chr9:25743133-25743134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552551460	chr9:25743143-25743144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529136725	chr9:25743171-25743172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183402015	chr9:25743199-25743200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145125811	chr9:25743200-25743201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531853017	chr9:25743233-25743234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28665975	chr9:25743242-25743243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550856642	chr9:25743260-25743261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568349158	chr9:25743268-25743269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535737524	chr9:25743298-25743299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs73644585	chr9:25743306-25743307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147598548	chr9:25743316-25743317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76190937	chr9:25743349-25743350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533511217	chr9:25743406-25743407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558536885	chr9:25743422-25743423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576844409	chr9:25743432-25743433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28499196	chr9:25743436-25743437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186678211	chr9:25743450-25743451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75677802	chr9:25743474-25743475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs398096335	chr9:25743481-25743482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556078231	chr9:25743496-25743497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113162271	chr9:25743507-25743508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377524552	chr9:25743517-25743518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542048547	chr9:25743523-25743524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192747888	chr9:25743525-25743526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114787909	chr9:25743542-25743543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs56331477	chr9:25743575-25743576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150450157	chr9:25743585-25743586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142694487	chr9:25743586-25743587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182712511	chr9:25743610-25743611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375416996	chr9:25743635-25743636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10812306	chr9:25743652-25743653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531695946	chr9:25743654-25743655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55936606	chr9:25743659-25743660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374125152	chr9:25743660-25743661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367768463	chr9:25743678-25743679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371248775	chr9:25743689-25743690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529396694	chr9:25743695-25743696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Adenoid cystic carcinoma	18332873	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25741600-25743400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr9:25743400-25744000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:25747400-25747600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:25752000-25752200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr9:25752000-25752400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr9:25752200-25752600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr9:25752400-25752600	Enhancers	Colon Smooth Muscle	Colon
8	chr9:25752400-25752800	Enhancers	Brain Angular Gyrus	brain
9	chr9:25752400-25752800	Active TSS	Brain Cingulate Gyrus	brain
10	chr9:25752400-25752800	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr9:25752400-25752800	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr9:25752400-25752800	Active TSS	Ovary	ovary
13	chr9:25752600-25752800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:25754800-25755600	Enhancers	Fetal Stomach	stomach
15	chr9:25756200-25756800	Enhancers	Fetal Brain Male	brain
16	chr9:25758000-25758200	Enhancers	Gastric	stomach
17	chr9:25763600-25764000	ZNF genes & repeats	Pancreas	Pancrea
18	chr9:25764000-25764400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr9:25773800-25774400	Enhancers	Fetal Stomach	stomach
20	chr9:25798800-25799000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:25802400-25803400	Enhancers	Stomach Mucosa	stomach
22	chr9:25803000-25803400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:25803200-25805600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:25803400-25804000	Weak transcription	Stomach Mucosa	stomach
25	chr9:25803400-25807000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr9:25804200-25804400	Enhancers	Stomach Mucosa	stomach
27	chr9:25804400-25805600	Enhancers	Fetal Lung	lung
28	chr9:25805800-25806400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr9:25807000-25807200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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