Variant report

Variant	nsv608055
Chromosome Location	chr7:102277589-102358137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2140)
CpG islands
(count:856)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2140 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102339769-102340073	K562	blood:	n/a	n/a
2	ATF1	chr7:102339824-102340183	K562	blood:	n/a	n/a
3	ATF2	chr7:102353714-102354151	GM12878	blood:	n/a	n/a
4	ATF2	chr7:102353660-102354116	GM12878	blood:	n/a	n/a
5	ATF3	chr7:102312022-102312401	A549	lung:	n/a	chr7:102312144-102312152
6	ATF3	chr7:102312099-102312242	K562	blood:	n/a	chr7:102312144-102312152
7	BATF	chr7:102355431-102355796	GM12878	blood:	n/a	n/a
8	BATF	chr7:102291963-102292217	GM12878	blood:	n/a	n/a
9	BATF	chr7:102356182-102356563	GM12878	blood:	n/a	n/a
10	BATF	chr7:102356109-102356632	GM12878	blood:	n/a	n/a
11	BATF	chr7:102310540-102311004	GM12878	blood:	n/a	n/a
12	BATF	chr7:102311459-102312701	GM12878	blood:	n/a	n/a
13	BATF	chr7:102353557-102354555	GM12878	blood:	n/a	n/a
14	BATF	chr7:102278880-102279149	GM12878	blood:	n/a	n/a
15	BATF	chr7:102353721-102354553	GM12878	blood:	n/a	n/a
16	BATF	chr7:102305017-102305524	GM12878	blood:	n/a	n/a
17	BATF	chr7:102306478-102306740	GM12878	blood:	n/a	n/a
18	BATF	chr7:102285771-102286300	GM12878	blood:	n/a	chr7:102286082-102286093
19	BATF	chr7:102278828-102279089	GM12878	blood:	n/a	n/a
20	BATF	chr7:102352581-102352892	GM12878	blood:	n/a	n/a
21	BATF	chr7:102330287-102330744	GM12878	blood:	n/a	n/a
22	BATF	chr7:102312293-102312492	GM12878	blood:	n/a	n/a
23	BATF	chr7:102329824-102330101	GM12878	blood:	n/a	n/a
24	BATF	chr7:102313151-102313476	GM12878	blood:	n/a	n/a
25	BATF	chr7:102284765-102285178	GM12878	blood:	n/a	n/a
26	BATF	chr7:102310144-102310402	GM12878	blood:	n/a	n/a
27	BATF	chr7:102286810-102287040	GM12878	blood:	n/a	n/a
28	BATF	chr7:102285752-102286469	GM12878	blood:	n/a	chr7:102286082-102286093
29	BATF	chr7:102313180-102313439	GM12878	blood:	n/a	n/a
30	BATF	chr7:102352630-102352884	GM12878	blood:	n/a	n/a
31	BATF	chr7:102355536-102355847	GM12878	blood:	n/a	n/a
32	BATF	chr7:102293584-102293766	GM12878	blood:	n/a	n/a
33	BATF	chr7:102284603-102285287	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:102291566-102291715	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:102306495-102306740	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:102278940-102279146	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:102285818-102286298	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:102305036-102305578	GM12878	blood:	n/a	chr7:102305424-102305433
39	BCL11A	chr7:102352587-102352904	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:102285737-102286323	GM12878	blood:	n/a	n/a
41	BCL11A	chr7:102353630-102354526	GM12878	blood:	n/a	n/a
42	BCL11A	chr7:102311468-102312674	GM12878	blood:	n/a	chr7:102312277-102312290
43	BCL11A	chr7:102355571-102355806	GM12878	blood:	n/a	n/a
44	BCL11A	chr7:102304517-102304823	GM12878	blood:	n/a	n/a
45	BCL11A	chr7:102301177-102301426	GM12878	blood:	n/a	n/a
46	BCL11A	chr7:102352667-102352857	GM12878	blood:	n/a	n/a
47	BCL11A	chr7:102353677-102354018	GM12878	blood:	n/a	n/a
48	BCL11A	chr7:102330382-102330951	GM12878	blood:	n/a	chr7:102330751-102330764
49	BCL11A	chr7:102312275-102312544	GM12878	blood:	n/a	chr7:102312277-102312290
50	BCL11A	chr7:102298598-102298785	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102313412-102313462	NB4	blood:	n/a
2	chr7:102279588-102279638	SK-N-SH_RA	brain:	n/a
3	chr7:102313412-102313462	NB4	blood:	n/a
4	chr7:102279588-102279638	SK-N-SH_RA	brain:	n/a
5	chr7:102332458-102332508	T-47D	breast:	n/a
6	chr7:102332458-102332508	HCT-116	colon:	n/a
7	chr7:102312200-102312250	NHDF-neo	bronchial:	n/a
8	chr7:102332458-102332508	SKMC	muscle:	n/a
9	chr7:102313412-102313462	H1-hESC	embryonic stem cell:	embryo
10	chr7:102313412-102313462	HNPCEpiC	eye:	n/a
11	chr7:102312200-102312250	Hepatocyte	liver:	n/a
12	chr7:102312318-102312368	MCF10A-Er-Src	breast:	n/a
13	chr7:102329146-102329196	HAEpiC	amniotic membrane:	n/a
14	chr7:102329146-102329196	Caco-2	colon:	n/a
15	chr7:102312315-102312365	SAEC	small airway:	n/a
16	chr7:102312315-102312365	SKMC	muscle:	n/a
17	chr7:102312318-102312368	GM06990	blood:	n/a
18	chr7:102279588-102279638	GM06990	blood:	n/a
19	chr7:102312308-102312358	NHBE	bronchial:	n/a
20	chr7:102311965-102312015	PFSK-1	brain:	n/a
21	chr7:102332458-102332508	GM12891	blood:	n/a
22	chr7:102312308-102312358	HCT-116	colon:	n/a
23	chr7:102308061-102308111	NH-A	brain:	n/a
24	chr7:102313389-102313439	HEEpiC	esophagus:	n/a
25	chr7:102313389-102313439	SK-N-SH	brain:	n/a
26	chr7:102313389-102313439	BJ	skin:	n/a
27	chr7:102279588-102279638	K562	blood:	n/a
28	chr7:102313412-102313462	SKMC	muscle:	n/a
29	chr7:102330635-102330685	PFSK-1	brain:	n/a
30	chr7:102312200-102312250	HMEC	breast:	n/a
31	chr7:102313389-102313439	HCF	heart:	n/a
32	chr7:102329146-102329196	AG04450	lung:	fetal
33	chr7:102313389-102313439	T-47D	breast:	n/a
34	chr7:102311965-102312015	AG04450	lung:	fetal
35	chr7:102279588-102279638	MCF10A-Er-Src	breast:	n/a
36	chr7:102329146-102329196	SKMC	muscle:	n/a
37	chr7:102312315-102312365	AoSMC	blood vessel:	n/a
38	chr7:102312315-102312365	HRE	kidney:	n/a
39	chr7:102311965-102312015	HCT-116	colon:	n/a
40	chr7:102312308-102312358	AoSMC	blood vessel:	n/a
41	chr7:102332458-102332508	AG09309	skin:	n/a
42	chr7:102332458-102332508	GM12892	blood:	n/a
43	chr7:102312331-102312381	GM12892	blood:	n/a
44	chr7:102308061-102308111	H1-hESC	embryonic stem cell:	embryo
45	chr7:102313389-102313439	HL-60	blood:	n/a
46	chr7:102312200-102312250	HepG2	liver:	n/a
47	chr7:102327236-102327286	AG09319	gingival:	n/a
48	chr7:102313412-102313462	GM12878	blood:	n/a
49	chr7:102327236-102327286	AG09309	skin:	n/a
50	chr7:102313412-102313462	MCF-7	breast:	n/a

No data

Variant related genes	Relation type
ENSG00000205236	TF binding region
ENSG00000228049	TF binding region
UPK3BL	TF binding region
POLR2J2	TF binding region
RASA4DP	TF binding region
SPDYE2B	TF binding region
ENSG00000205236	CpG island
ENSG00000228049	CpG island
UPK3BL	CpG island
POLR2J2	CpG island
RASA4DP	CpG island
SPDYE2B	CpG island

Extended variants
information (count: 1024 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1024 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1063549	chr7:102277589-102277590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1140582	chr7:102277601-102277602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74655384	chr7:102277612-102277613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370720520	chr7:102277620-102277621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs60135736	chr7:102277632-102277633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551892399	chr7:102277698-102277699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112626569	chr7:102277709-102277710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371572799	chr7:102277832-102277833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142575422	chr7:102277851-102277852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375006180	chr7:102277852-102277853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563835601	chr7:102278158-102278159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528102961	chr7:102278206-102278207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546541055	chr7:102278389-102278390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376077958	chr7:102278516-102278517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201457495	chr7:102278617-102278618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62483475	chr7:102278673-102278674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200677151	chr7:102278755-102278756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199891539	chr7:102278765-102278766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373132016	chr7:102278782-102278783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568285815	chr7:102278854-102278855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376028359	chr7:102278899-102278900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371536244	chr7:102278903-102278904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374729230	chr7:102279004-102279005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377724042	chr7:102279039-102279040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371050293	chr7:102279070-102279071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550512570	chr7:102279151-102279152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569115113	chr7:102279363-102279364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539643531	chr7:102279397-102279398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559124523	chr7:102279436-102279437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570944966	chr7:102279460-102279461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534721876	chr7:102279478-102279479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553300722	chr7:102279508-102279509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575032898	chr7:102279543-102279544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201129776	chr7:102279581-102279582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs56365279	chr7:102279621-102279622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542467611	chr7:102279701-102279702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557221804	chr7:102279741-102279742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200036333	chr7:102279886-102279887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575478540	chr7:102279887-102279888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200773626	chr7:102279925-102279926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545965553	chr7:102280025-102280026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563854273	chr7:102280038-102280039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146507062	chr7:102280102-102280103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139231776	chr7:102280250-102280251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75817495	chr7:102280356-102280357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55865673	chr7:102280405-102280406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78965459	chr7:102280415-102280416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs56277901	chr7:102280429-102280430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs56348740	chr7:102280432-102280433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528162226	chr7:102280698-102280699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102260200-102286200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:102267200-102278000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:102267800-102278400	Weak transcription	Fetal Muscle Leg	muscle
4	chr7:102273200-102281200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:102273200-102281200	Weak transcription	Fetal Thymus	thymus
6	chr7:102275000-102281200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:102275000-102281800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:102275000-102283800	Weak transcription	Lung	lung
9	chr7:102275600-102284000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:102281800-102282400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr7:102282400-102284400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:102286200-102286400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:102301600-102310200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:102303400-102305400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:102303600-102305400	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr7:102303600-102305400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr7:102303600-102311800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr7:102303800-102305400	Weak transcription	Liver	Liver
19	chr7:102303800-102305400	Weak transcription	Brain Anterior Caudate	brain
20	chr7:102303800-102305400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr7:102303800-102308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:102304000-102311800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr7:102304000-102311800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:102304200-102311800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr7:102304200-102311800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr7:102304200-102311800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr7:102304200-102311800	Weak transcription	Adipose Nuclei	Adipose
28	chr7:102304200-102311800	Weak transcription	Fetal Muscle Leg	muscle
29	chr7:102304200-102311800	Weak transcription	Fetal Stomach	stomach
30	chr7:102304200-102311800	Weak transcription	Thymus	Thymus
31	chr7:102304400-102308400	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr7:102304600-102306800	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:102304600-102307000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:102305400-102306000	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr7:102305400-102306000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr7:102305400-102306000	Strong transcription	Liver	Liver
37	chr7:102305400-102306000	Strong transcription	Brain Anterior Caudate	brain
38	chr7:102305400-102306000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr7:102305400-102306000	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr7:102306000-102308200	Weak transcription	Liver	Liver
41	chr7:102306000-102308400	Weak transcription	Brain Anterior Caudate	brain
42	chr7:102306000-102310000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr7:102306000-102311800	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr7:102306000-102311800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:102306000-102311800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr7:102308200-102308400	Enhancers	Liver	Liver
47	chr7:102308200-102308600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:102311800-102312200	Active TSS	H9 Cell Line	embryonic stem cell
49	chr7:102311800-102312200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:102311800-102312200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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