Variant report

Variant	nsv892331
Chromosome Location	chr9:10923290-11012562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:10959847-10960172	A549	lung:	n/a	chr9:10959996-10960007
2	CEBPB	chr9:10959931-10960102	HepG2	liver:	n/a	chr9:10959996-10960007
3	CEBPB	chr9:10957932-10958241	H1-hESC	embryonic stem cell:	n/a	chr9:10958059-10958070
4	CEBPB	chr9:10937715-10937998	HepG2	liver:	n/a	chr9:10937875-10937886
5	CEBPB	chr9:10997740-10997983	HepG2	liver:	n/a	chr9:10997888-10997899
6	CEBPB	chr9:10978428-10978694	HepG2	liver:	n/a	chr9:10978574-10978585
7	CEBPB	chr9:10929200-10929413	HepG2	liver:	n/a	chr9:10929234-10929247 chr9:10929234-10929245 chr9:10929234-10929247 chr9:10929293-10929304
8	CEBPB	chr9:10957899-10958248	IMR90	lung:	n/a	chr9:10958059-10958070
9	CEBPB	chr9:10957871-10958258	HepG2	liver:	n/a	chr9:10958059-10958070
10	CEBPB	chr9:10937740-10938007	IMR90	lung:	n/a	chr9:10937875-10937886
11	CEBPB	chr9:10928603-10928846	HepG2	liver:	n/a	chr9:10928719-10928730
12	CEBPB	chr9:10978471-10978631	A549	lung:	n/a	chr9:10978574-10978585
13	CEBPB	chr9:10957928-10958232	A549	lung:	n/a	chr9:10958059-10958070
14	CEBPB	chr9:10997736-10998005	A549	lung:	n/a	chr9:10997888-10997899
15	CTCF	chr9:10964233-10964354	Lung_OC	lung:	n/a	n/a
16	CTCF	chr9:10983863-10983874	GM10248	blood:	n/a	n/a
17	CTCF	chr9:11009607-11009644	GM10248	blood:	n/a	n/a
18	CTCF	chr9:10966906-10966970	GM10266	blood:	n/a	n/a
19	CTCF	chr9:10986506-10986511	LNCaP	prostate:	n/a	n/a
20	CTCF	chr9:10986479-10986499	LNCaP	prostate:	n/a	n/a
21	E2F4	chr9:10930979-10931276	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr9:10939940-10940085	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr9:10940398-10940605	GM12878	blood:	n/a	chr9:10940517-10940528
24	EBF1	chr9:10959316-10959484	GM12878	blood:	n/a	chr9:10959442-10959453
25	ELK1	chr9:10984050-10984097	GM12878	blood:	n/a	n/a
26	EP300	chr9:10988018-10988161	GM12878	blood:	n/a	n/a
27	FOS	chr9:10955477-10955737	MCF10A-Er-Src	breast:	n/a	chr9:10955598-10955605 chr9:10955597-10955606 chr9:10955598-10955606 chr9:10955598-10955607
28	FOS	chr9:10931014-10931264	MCF10A-Er-Src	breast:	n/a	n/a
29	FOXA1	chr9:10957912-10958238	HepG2	liver:	n/a	n/a
30	FOXA2	chr9:10957940-10958200	HepG2	liver:	n/a	n/a
31	GATA3	chr9:10928832-10928970	SH-SY5Y	brain:	n/a	chr9:10928957-10928964 chr9:10928957-10928967 chr9:10928957-10928964 chr9:10928955-10928965 chr9:10928952-10928968 chr9:10928957-10928964
32	JUN	chr9:10983542-10983586	H1-hESC	embryonic stem cell:	n/a	n/a
33	JUND	chr9:10962849-10963137	HepG2	liver:	n/a	chr9:10962988-10962999
34	JUND	chr9:10925059-10925235	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr9:10959577-10959843	HepG2	liver:	n/a	chr9:10959686-10959697
36	NFYA	chr9:10927518-10927775	GM12878	blood:	n/a	n/a
37	NFYA	chr9:10936920-10937274	GM12878	blood:	n/a	n/a
38	NFYB	chr9:10959675-10959848	GM12878	blood:	n/a	n/a
39	NFYB	chr9:10983990-10984160	GM12878	blood:	n/a	n/a
40	POLR2A	chr9:11007376-11007961	K562	blood:	n/a	n/a
41	POLR2A	chr9:10947418-10947491	A549	lung:	n/a	n/a
42	POLR2A	chr9:11006132-11006971	K562	blood:	n/a	n/a
43	POLR2A	chr9:11001543-11002015	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr9:10959073-10959259	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr9:10934162-10934184	A549	lung:	n/a	n/a
46	POLR2A	chr9:10930675-10930690	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr9:10947218-10947414	A549	lung:	n/a	n/a
48	POLR2A	chr9:10971817-10971819	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr9:11011146-11012585	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr9:11011937-11011991	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10966083-10966133	NH-A	brain:	n/a
2	chr9:10966083-10966133	T-47D	breast:	n/a
3	chr9:10966083-10966133	GM12892	blood:	n/a
4	chr9:10966083-10966133	H1-hESC	embryonic stem cell:	embryo
5	chr9:10966083-10966133	RPTEC	kidney:	n/a
6	chr9:10966083-10966133	ovcar-3	ovarian:	n/a
7	chr9:10966083-10966133	HUVEC	blood vessel:	n/a
8	chr9:10966083-10966133	Hepatocyte	liver:	n/a
9	chr9:10966083-10966133	NHDF-neo	bronchial:	n/a
10	chr9:10966083-10966133	HCT-116	colon:	n/a
11	chr9:10966083-10966133	Caco-2	colon:	n/a
12	chr9:10966083-10966133	IMR90	lung:	fetal
13	chr9:10966083-10966133	BJ	skin:	n/a
14	chr9:10966083-10966133	HCPEpiC	choroid plexus:	n/a
15	chr9:10966083-10966133	AoSMC	blood vessel:	n/a
16	chr9:10966083-10966133	MCF10A-Er-Src	breast:	n/a
17	chr9:10966083-10966133	CMK	blood:	n/a
18	chr9:10966083-10966133	HepG2	liver:	n/a
19	chr9:10966083-10966133	U87	brain:	n/a
20	chr9:10966083-10966133	AG04449	skin:	fetal
21	chr9:10966083-10966133	HNPCEpiC	eye:	n/a
22	chr9:10966083-10966133	GM12878	blood:	n/a
23	chr9:10966083-10966133	GM12891	blood:	n/a
24	chr9:10966083-10966133	AG09309	skin:	n/a
25	chr9:10966083-10966133	AG04450	lung:	fetal
26	chr9:10966083-10966133	BE2_C	brain:	n/a
27	chr9:10966083-10966133	AG10803	skin:	n/a
28	chr9:10966083-10966133	SK-N-SH_RA	brain:	n/a
29	chr9:10966083-10966133	Jurkat	blood:	n/a
30	chr9:10966083-10966133	MCF-7	breast:	n/a
31	chr9:10966083-10966133	GM19239	blood:	n/a
32	chr9:10966083-10966133	SK-N-SH	brain:	n/a
33	chr9:10966083-10966133	ECC-1	luminal epithelium:	n/a
34	chr9:10966083-10966133	NT2-D1	testis:	n/a
35	chr9:10966083-10966133	HRE	kidney:	n/a
36	chr9:10966083-10966133	PANC-1	pancreas:	n/a
37	chr9:10966083-10966133	SAEC	small airway:	n/a
38	chr9:10966083-10966133	A549	lung:	n/a
39	chr9:10966083-10966133	HMEC	breast:	n/a
40	chr9:10966083-10966133	PFSK-1	brain:	n/a
41	chr9:10966083-10966133	GM06990	blood:	n/a
42	chr9:10966083-10966133	NHBE	bronchial:	n/a
43	chr9:10966083-10966133	HCM	heart:	n/a
44	chr9:10966083-10966133	HCF	heart:	n/a
45	chr9:10966083-10966133	AG09319	gingival:	n/a
46	chr9:10966083-10966133	SK-N-MC	brain:	n/a
47	chr9:10966083-10966133	HEEpiC	esophagus:	n/a
48	chr9:10966083-10966133	LNCaP	prostate:	n/a
49	chr9:10966083-10966133	Hela-S3	cervix:	n/a
50	chr9:10966083-10966133	K562	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-7	chr9:10958410-10958540	NONHSAT130207
2	lnc-PTPRD-7	chr9:10948366-10948481	NONHSAT130207

Variant related genes	Relation type
ENSG00000270372	TF binding region
ENSG00000234146	TF binding region
ENSG00000270372	CpG island
ENSG00000234146	CpG island

Extended variants
information (count: 1147 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1536997	chr9:10923290-10923291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190594744	chr9:10923309-10923310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117000648	chr9:10923333-10923334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs71501081	chr9:10923337-10923338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563210071	chr9:10923367-10923368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182771788	chr9:10923383-10923384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113781131	chr9:10923401-10923402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140448553	chr9:10923405-10923406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528372778	chr9:10923412-10923413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551652903	chr9:10923413-10923414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565081691	chr9:10923447-10923448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35760327	chr9:10923490-10923491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530687743	chr9:10923502-10923503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191799108	chr9:10923503-10923504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567640278	chr9:10923524-10923525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530150794	chr9:10923594-10923595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143595257	chr9:10923597-10923598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556160491	chr9:10923600-10923601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148041882	chr9:10923631-10923632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538956261	chr9:10923643-10923644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558791403	chr9:10923666-10923667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569130861	chr9:10923707-10923708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538029167	chr9:10923714-10923715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557052652	chr9:10923722-10923723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140810427	chr9:10923724-10923725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542654244	chr9:10923749-10923750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568777978	chr9:10923751-10923752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562385342	chr9:10923762-10923763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552696635	chr9:10923781-10923782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184038040	chr9:10923788-10923789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187746579	chr9:10923793-10923794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545335500	chr9:10923796-10923797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150431459	chr9:10923816-10923817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530761528	chr9:10923842-10923843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544412810	chr9:10923868-10923869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10959370	chr9:10923969-10923970	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34938669	chr9:10923994-10923995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138348627	chr9:10924005-10924006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368429981	chr9:10924014-10924015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547031466	chr9:10924022-10924023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117973701	chr9:10924035-10924036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368326720	chr9:10924037-10924038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532345347	chr9:10924042-10924043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552480988	chr9:10924056-10924057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143912046	chr9:10924073-10924074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538089219	chr9:10924074-10924075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372542149	chr9:10924081-10924082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568592866	chr9:10924118-10924119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146436928	chr9:10924133-10924134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192672452	chr9:10924149-10924150	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	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
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10921400-10924800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr9:10921600-10924000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr9:10921600-10924200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:10921800-10924000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:10922000-10924800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr9:10922600-10923600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:10923000-10923400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr9:10923400-10924800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:10923600-10924200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:10923800-10924000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr9:10928200-10928800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:10928400-10928800	Enhancers	Fetal Heart	heart
13	chr9:10937400-10947200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:10947000-10947400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:10947200-10947400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:10947200-10947400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:10953400-10954000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:10953400-10954000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:10953600-10954000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:10953600-10954000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr9:10953600-10954000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:10953600-10954000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr9:10954000-10954200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr9:10954000-10954200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr9:10954000-10955200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr9:10954000-10956000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr9:10954000-10956000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr9:10955200-10957000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr9:10956000-10956400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:10956000-10956400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr9:10956000-10956800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr9:10956000-10957000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr9:10956000-10957200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr9:10999600-11000000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr9:10999600-11000000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr9:11000000-11002600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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