Variant report

Variant	nsv466334
Chromosome Location	chr9:27028947-27098940
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	ARID3A	chr9:27033859-27034180	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:27033873-27034153	K562	blood:	n/a	n/a
3	ARID3A	chr9:27054840-27055264	HepG2	liver:	n/a	n/a
4	BHLHE40	chr9:27033947-27034178	GM12878	blood:	n/a	n/a
5	CEBPB	chr9:27084920-27085120	A549	lung:	n/a	chr9:27084967-27084978
6	CEBPB	chr9:27080444-27081034	IMR90	lung:	n/a	chr9:27080622-27080633
7	CEBPB	chr9:27033872-27034187	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr9:27090352-27090555	HepG2	liver:	n/a	chr9:27090406-27090417
9	CEBPB	chr9:27084806-27085161	K562	blood:	n/a	chr9:27084967-27084978
10	CEBPB	chr9:27080503-27081125	K562	blood:	n/a	chr9:27080622-27080633
11	CEBPB	chr9:27080438-27080874	A549	lung:	n/a	chr9:27080622-27080633
12	CEBPB	chr9:27074093-27074412	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:27084807-27085146	IMR90	lung:	n/a	chr9:27084967-27084978
14	CEBPB	chr9:27080439-27081321	Hela-S3	cervix:	n/a	chr9:27080622-27080633
15	CEBPB	chr9:27085647-27085843	K562	blood:	n/a	chr9:27085735-27085746
16	CEBPB	chr9:27080501-27080763	A549	lung:	n/a	chr9:27080622-27080633
17	CEBPB	chr9:27094664-27094985	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:27084820-27085156	HepG2	liver:	n/a	chr9:27084967-27084978
19	CEBPB	chr9:27080493-27080836	ECC-1	luminal epithelium:	n/a	chr9:27080622-27080633
20	CEBPB	chr9:27087103-27087795	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:27090244-27091057	IMR90	lung:	n/a	chr9:27090406-27090417
22	CEBPB	chr9:27080439-27080817	A549	lung:	n/a	chr9:27080622-27080633
23	CEBPB	chr9:27088892-27089700	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:27090310-27090528	A549	lung:	n/a	chr9:27090406-27090417
25	CEBPB	chr9:27086452-27086787	IMR90	lung:	n/a	n/a
26	CEBPB	chr9:27080478-27080797	H1-hESC	embryonic stem cell:	n/a	chr9:27080622-27080633
27	CEBPB	chr9:27080465-27081128	HepG2	liver:	n/a	chr9:27080622-27080633
28	CHD1	chr9:27033812-27034364	IMR90	lung:	n/a	n/a
29	CTCF	chr9:27033900-27034050	HRE	kidney:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
30	CTCF	chr9:27033900-27034050	HA-sp	spinal cord:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
31	CTCF	chr9:27033900-27034050	HFF-Myc	foreskin:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
32	CTCF	chr9:27033900-27034050	Caco-2	colon:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
33	CTCF	chr9:27033844-27034108	SK-N-SH_RA	brain:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
34	CTCF	chr9:27033766-27034139	MCF-7	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
35	CTCF	chr9:27033940-27034090	HPAF	blood vessel:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
36	CTCF	chr9:27033662-27033710	GM13977	blood:	n/a	n/a
37	CTCF	chr9:27033920-27034070	HEK293	kidney:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
38	CTCF	chr9:27033860-27034010	NHEK	skin:	n/a	n/a
39	CTCF	chr9:27033880-27034030	GM12867	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
40	CTCF	chr9:27033900-27034050	HCM	heart:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
41	CTCF	chr9:27033920-27034070	GM06990	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
42	CTCF	chr9:27033940-27034090	HCPEpiC	choroid plexus:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
43	CTCF	chr9:27033802-27034063	A549	lung:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
44	CTCF	chr9:27033878-27034120	K562	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
45	CTCF	chr9:27033940-27034090	AG10803	skin:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
46	CTCF	chr9:27033940-27034090	HMF	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
47	CTCF	chr9:27087620-27087770	AG04449	skin:	n/a	n/a
48	CTCF	chr9:27033920-27034070	HMF	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
49	CTCF	chr9:27033920-27034070	HRE	kidney:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
50	CTCF	chr9:27033880-27034030	HepG2	liver:	n/a	chr9:27034004-27034017 chr9:27034003-27034024

No.	Distal block	Cell Line	Cell type
1	chr9:27044880..27046633-chr9:27052693..27055070,2	MCF-7	breast:
2	chr9:27033573..27034169-chr9:27165385..27166023,2	MCF-7	breast:
3	chr9:27033695..27036371-chr9:27569729..27572536,2	K562	blood:
4	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
5	chr9:27033902..27034442-chr9:27247489..27248319,2	MCF-7	breast:
6	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:
7	chr9:27044880..27046633-chr9:27052693..27055070,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IFT74	hsa-miR-16-5p	chr9:27062759-27062780

Variant related genes	Relation type
ENSG00000254396	TF binding region

Extended variants
information (count: 2900 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:2900 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7390085	chr9:27028947-27028948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557711028	chr9:27028964-27028965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376199698	chr9:27028978-27028979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574361807	chr9:27028989-27028990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189713026	chr9:27028990-27028991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553309366	chr9:27029043-27029044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571708471	chr9:27029051-27029052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374241230	chr9:27029054-27029055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138659883	chr9:27029055-27029056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377639405	chr9:27029072-27029073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200353043	chr9:27029078-27029079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376870332	chr9:27029080-27029081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370456819	chr9:27029081-27029082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373619388	chr9:27029092-27029093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73436090	chr9:27029105-27029106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs370411235	chr9:27029141-27029142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564062962	chr9:27029158-27029159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367961135	chr9:27029216-27029217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531914678	chr9:27029247-27029248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543628680	chr9:27029248-27029249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562285828	chr9:27029314-27029315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549347352	chr9:27029335-27029336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529572800	chr9:27029337-27029338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548113094	chr9:27029340-27029341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs397941774	chr9:27029350-27029351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181347749	chr9:27029384-27029385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185196058	chr9:27029408-27029409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368080481	chr9:27029409-27029410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551836219	chr9:27029410-27029411	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568031562	chr9:27029458-27029459	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570079210	chr9:27029505-27029506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537573262	chr9:27029516-27029517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528355530	chr9:27029528-27029529	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112179676	chr9:27029536-27029537	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189206315	chr9:27029544-27029545	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113969825	chr9:27029603-27029604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571695853	chr9:27029606-27029607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181890445	chr9:27029613-27029614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10812515	chr9:27029639-27029640	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs10967672	chr9:27029686-27029687	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149639372	chr9:27029701-27029702	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562218113	chr9:27029726-27029727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529559925	chr9:27029748-27029749	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186578091	chr9:27029758-27029759	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557919094	chr9:27029762-27029763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76006619	chr9:27029776-27029777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533338239	chr9:27029787-27029788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191040926	chr9:27029811-27029812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73436096	chr9:27029823-27029824	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs530868004	chr9:27029875-27029876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
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
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
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26957200-27040000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr9:26985200-27063800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr9:26991800-27058000	Weak transcription	NHDF-Ad	bronchial
4	chr9:27009800-27070000	Weak transcription	Psoas Muscle	Psoas
5	chr9:27011200-27037400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr9:27012000-27048800	Weak transcription	HepG2	liver
7	chr9:27014400-27060800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr9:27014400-27068200	Weak transcription	Fetal Heart	heart
9	chr9:27018400-27065200	Weak transcription	Osteobl	bone
10	chr9:27018600-27029400	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr9:27019200-27061800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr9:27022600-27036200	Weak transcription	NHEK	skin
13	chr9:27024400-27029400	Weak transcription	Esophagus	oesophagus
14	chr9:27024400-27047200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr9:27024400-27053800	Weak transcription	Lung	lung
16	chr9:27024400-27082600	Weak transcription	Gastric	stomach
17	chr9:27024600-27029400	Weak transcription	Ovary	ovary
18	chr9:27024600-27031800	Weak transcription	Small Intestine	intestine
19	chr9:27024600-27036200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:27024600-27036400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr9:27024600-27037400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr9:27024600-27037600	Weak transcription	HSMMtube	muscle
23	chr9:27024600-27044800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:27024600-27048600	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr9:27024600-27048800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr9:27024600-27049200	Weak transcription	Colon Smooth Muscle	Colon
27	chr9:27024600-27053400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr9:27024600-27054400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr9:27024600-27056400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr9:27024600-27058800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr9:27024600-27059600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:27024600-27061000	Weak transcription	Dnd41	blood
33	chr9:27024600-27061400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr9:27024600-27061800	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr9:27024600-27064400	Weak transcription	Colonic Mucosa	Colon
36	chr9:27024600-27075800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr9:27024600-27078600	Weak transcription	Aorta	Aorta
38	chr9:27024600-27079000	Weak transcription	Pancreas	Pancrea
39	chr9:27024600-27082400	Weak transcription	Primary T cells from cord blood	blood
40	chr9:27024600-27083400	Weak transcription	Left Ventricle	heart
41	chr9:27024600-27085000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr9:27024600-27086800	Weak transcription	Right Ventricle	heart
43	chr9:27024800-27029000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:27024800-27029400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:27024800-27029800	Weak transcription	Brain Germinal Matrix	brain
46	chr9:27024800-27031200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr9:27024800-27031600	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr9:27024800-27033400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr9:27024800-27033600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr9:27024800-27034600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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