Variant report

Variant	nsv1064445
Chromosome Location	chr18:65699694-65965746
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	chr18:65845401-65845751	HepG2	liver:	n/a	n/a
2	ATF2	chr18:65816013-65816483	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr18:65816079-65816448	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:65815072-65815334	H1-hESC	embryonic stem cell:	n/a	chr18:65815167-65815181
5	BACH1	chr18:65750379-65750688	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr18:65815062-65815155	K562	blood:	n/a	n/a
7	CEBPB	chr18:65782263-65782596	K562	blood:	n/a	chr18:65782418-65782427 chr18:65782416-65782429 chr18:65782417-65782428 chr18:65782418-65782427 chr18:65782418-65782427
8	CEBPB	chr18:65720566-65720903	HepG2	liver:	n/a	chr18:65720725-65720737
9	CEBPB	chr18:65700275-65700540	IMR90	lung:	n/a	chr18:65700399-65700408 chr18:65700397-65700408
10	CEBPB	chr18:65709646-65709896	A549	lung:	n/a	chr18:65709758-65709769
11	CEBPB	chr18:65700261-65700461	Hela-S3	cervix:	n/a	chr18:65700399-65700408 chr18:65700397-65700408
12	CEBPB	chr18:65845340-65845701	HepG2	liver:	n/a	chr18:65845351-65845363
13	CEBPB	chr18:65899601-65899801	HepG2	liver:	n/a	chr18:65899704-65899715
14	CEBPB	chr18:65748907-65749103	HepG2	liver:	n/a	n/a
15	CEBPB	chr18:65942945-65943241	HepG2	liver:	n/a	chr18:65943074-65943085
16	CEBPB	chr18:65803617-65803954	HepG2	liver:	n/a	chr18:65803781-65803792
17	CEBPB	chr18:65803621-65803935	IMR90	lung:	n/a	chr18:65803781-65803792
18	CEBPB	chr18:65709718-65709918	HepG2	liver:	n/a	chr18:65709758-65709769
19	CEBPB	chr18:65752628-65752702	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr18:65810273-65810579	K562	blood:	n/a	chr18:65810444-65810455 chr18:65810431-65810442
21	CEBPB	chr18:65701837-65702041	HepG2	liver:	n/a	chr18:65701980-65701991
22	CEBPB	chr18:65782251-65782599	A549	lung:	n/a	chr18:65782418-65782427 chr18:65782416-65782429 chr18:65782417-65782428 chr18:65782418-65782427 chr18:65782418-65782427
23	CEBPB	chr18:65782254-65782597	H1-hESC	embryonic stem cell:	n/a	chr18:65782418-65782427 chr18:65782416-65782429 chr18:65782417-65782428 chr18:65782418-65782427 chr18:65782418-65782427
24	CEBPB	chr18:65799862-65800068	HepG2	liver:	n/a	n/a
25	CEBPB	chr18:65817150-65817485	HepG2	liver:	n/a	chr18:65817299-65817310
26	CEBPB	chr18:65700250-65700487	HepG2	liver:	n/a	chr18:65700399-65700408 chr18:65700397-65700408
27	CEBPB	chr18:65914784-65914871	HepG2	liver:	n/a	n/a
28	CEBPB	chr18:65847726-65848252	IMR90	lung:	n/a	chr18:65847895-65847906
29	CEBPB	chr18:65807496-65807796	Hela-S3	cervix:	n/a	chr18:65807623-65807634 chr18:65807623-65807636
30	CEBPB	chr18:65724175-65724492	IMR90	lung:	n/a	n/a
31	CEBPB	chr18:65853300-65853676	ECC-1	luminal epithelium:	n/a	chr18:65853475-65853484 chr18:65853473-65853486 chr18:65853473-65853486 chr18:65853633-65853644 chr18:65853475-65853484 chr18:65853474-65853485 chr18:65853475-65853484
32	CEBPB	chr18:65934853-65935219	IMR90	lung:	n/a	n/a
33	CEBPB	chr18:65807481-65807802	IMR90	lung:	n/a	chr18:65807623-65807634 chr18:65807623-65807636
34	CEBPB	chr18:65853297-65853672	IMR90	lung:	n/a	chr18:65853475-65853484 chr18:65853473-65853486 chr18:65853473-65853486 chr18:65853633-65853644 chr18:65853475-65853484 chr18:65853474-65853485 chr18:65853475-65853484
35	CEBPB	chr18:65817155-65817469	IMR90	lung:	n/a	chr18:65817299-65817310
36	CEBPB	chr18:65764315-65764548	HepG2	liver:	n/a	chr18:65764401-65764412 chr18:65764399-65764410 chr18:65764399-65764412 chr18:65764401-65764412
37	CEBPB	chr18:65957312-65957504	HepG2	liver:	n/a	chr18:65957314-65957325 chr18:65957314-65957325
38	CEBPB	chr18:65789147-65789374	A549	lung:	n/a	chr18:65789221-65789234 chr18:65789223-65789232 chr18:65789221-65789232
39	CEBPB	chr18:65782253-65782566	Hela-S3	cervix:	n/a	chr18:65782418-65782427 chr18:65782416-65782429 chr18:65782417-65782428 chr18:65782418-65782427 chr18:65782418-65782427
40	CEBPB	chr18:65853307-65853627	H1-hESC	embryonic stem cell:	n/a	chr18:65853475-65853484 chr18:65853473-65853486 chr18:65853473-65853486 chr18:65853475-65853484 chr18:65853474-65853485 chr18:65853475-65853484
41	CEBPB	chr18:65810289-65810612	IMR90	lung:	n/a	chr18:65810444-65810455 chr18:65810431-65810442
42	CEBPB	chr18:65942834-65943277	IMR90	lung:	n/a	chr18:65943074-65943085
43	CEBPB	chr18:65789063-65789362	HepG2	liver:	n/a	chr18:65789221-65789234 chr18:65789223-65789232 chr18:65789221-65789232
44	CEBPB	chr18:65708741-65709031	IMR90	lung:	n/a	n/a
45	CEBPB	chr18:65847789-65848210	Hela-S3	cervix:	n/a	chr18:65847895-65847906
46	CEBPB	chr18:65789073-65789383	IMR90	lung:	n/a	chr18:65789221-65789234 chr18:65789223-65789232 chr18:65789221-65789232
47	CEBPB	chr18:65942882-65943264	Hela-S3	cervix:	n/a	chr18:65943074-65943085
48	CEBPB	chr18:65803616-65803947	A549	lung:	n/a	chr18:65803781-65803792
49	CEBPB	chr18:65842139-65842251	HepG2	liver:	n/a	n/a
50	CEBPB	chr18:65810301-65810569	A549	lung:	n/a	chr18:65810444-65810455 chr18:65810431-65810442

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:65183072..65183789-chr18:65819833..65820407,2	MCF-7	breast:
2	chr18:65829262..65829762-chrX:11551081..11551794,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMX3-2	chr18:65930736-65931225	NONHSAT059732
2	lnc-CCDC102B-5	chr18:65773447-65773611	ENSG00000264869.1
3	lnc-CCDC102B-5	chr18:65780867-65780920	ENSG00000264869.1
4	lnc-TMX3-2	chr18:65930736-65930840	ENSG00000264699.1
5	lnc-CCDC102B-5	chr18:65781528-65781614	ENSG00000264869.1
6	lnc-TMX3-2	chr18:65927518-65927611	ENSG00000264699.1
7	lnc-TMX3-2	chr18:65932041-65932064	ENSG00000264699.1
8	lnc-CCDC102B-5	chr18:65769353-65769392	ENSG00000264869.1
9	lnc-TMX3-2	chr18:65928862-65928907	ENSG00000264699.1
10	lnc-TMX3-2	chr18:65907358-65907379	NONHSAT059730
11	lnc-TMX3-2	chr18:65930736-65931225	NONHSAT059730
12	lnc-TMX3-2	chr18:65925576-65925802	ENSG00000264699.1
13	lnc-TMX3-2	chr18:65928862-65928907	NONHSAT059732
14	lnc-TMX3-2	chr18:65927519-65927611	NONHSAT059732
15	lnc-TMX3-2	chr18:65928862-65928907	NONHSAT059730

Variant related genes	Relation type
ENSG00000260747	TF binding region
ENSG00000264699	TF binding region
ENSG00000264869	TF binding region
ENSG00000265533	chromatin interactions

Extended variants
information (count: 5219 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:5219 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557288524	chr18:65699743-65699744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372968297	chr18:65699767-65699768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7228699	chr18:65699784-65699785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371420644	chr18:65699785-65699786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564817659	chr18:65699814-65699815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549110022	chr18:65699830-65699831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573330964	chr18:65699884-65699885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1464190	chr18:65699920-65699921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs183516577	chr18:65699936-65699937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145970878	chr18:65699949-65699950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185994120	chr18:65699999-65700000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369506693	chr18:65700082-65700083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569522908	chr18:65700183-65700184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368913476	chr18:65700202-65700203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530570442	chr18:65700208-65700209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190356931	chr18:65700251-65700252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542258162	chr18:65700283-65700284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139844207	chr18:65700301-65700302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182622682	chr18:65700308-65700309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115750081	chr18:65700316-65700317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143209390	chr18:65700341-65700342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571472649	chr18:65700392-65700393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535208465	chr18:65700410-65700411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117551811	chr18:65700431-65700432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200387539	chr18:65700462-65700463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371549372	chr18:65700463-65700464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556973582	chr18:65700468-65700469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs3053854	chr18:65700477-65700478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376349812	chr18:65700478-65700479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200370464	chr18:65700479-65700480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575410263	chr18:65700510-65700511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10503124	chr18:65700555-65700556	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186953362	chr18:65700569-65700570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539539576	chr18:65700570-65700571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544170127	chr18:65700586-65700587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139426813	chr18:65700724-65700725	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190788742	chr18:65700785-65700786	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150058226	chr18:65700808-65700809	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557531718	chr18:65700819-65700820	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145389609	chr18:65700857-65700858	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17078468	chr18:65700858-65700859	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1356479	chr18:65700885-65700886	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1356474	chr18:65700902-65700903	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114274457	chr18:65700911-65700912	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182641488	chr18:65700997-65700998	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs80282005	chr18:65701001-65701002	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17078469	chr18:65701008-65701009	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535482528	chr18:65701039-65701040	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74887751	chr18:65701074-65701075	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs578200295	chr18:65701098-65701099	Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Burkitt''s lymphoma	18698080	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Testicular germ cell tumor	18059402	CNVD
Glioblastoma	21080181	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Colorectal cancer	16912164	CNVD
Intracranial aneurysm	16715129	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Gastric cancer	22539939	CNVD
Ovarian cancer	20844748	CNVD
Squamous cell cancer	20885788	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	21811587	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:363 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:65698800-65700200	Weak transcription	NHDF-Ad	bronchial
2	chr18:65700200-65701000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr18:65700200-65701400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr18:65700200-65701600	Enhancers	NHEK	skin
5	chr18:65700200-65702600	Enhancers	NHDF-Ad	bronchial
6	chr18:65700400-65700600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr18:65700400-65701000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr18:65700400-65701400	Enhancers	HMEC	breast
9	chr18:65700400-65702400	Enhancers	NHLF	lung
10	chr18:65700600-65700800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr18:65700600-65701600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr18:65700800-65701000	Enhancers	Aorta	Aorta
13	chr18:65700800-65701200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr18:65700800-65701400	Enhancers	Fetal Lung	lung
15	chr18:65700800-65701800	Enhancers	Fetal Stomach	stomach
16	chr18:65701000-65701600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr18:65701200-65701600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr18:65701400-65701600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr18:65701400-65703000	Weak transcription	Fetal Lung	lung
20	chr18:65701600-65703200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:65701600-65703400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr18:65701800-65702200	Weak transcription	Fetal Stomach	stomach
23	chr18:65701800-65703000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr18:65702200-65704800	Enhancers	Fetal Stomach	stomach
25	chr18:65702400-65703600	Weak transcription	NHLF	lung
26	chr18:65703000-65703600	Enhancers	Ovary	ovary
27	chr18:65703000-65703800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr18:65703000-65703800	Enhancers	Fetal Lung	lung
29	chr18:65703600-65703800	Enhancers	NHLF	lung
30	chr18:65704000-65708200	Weak transcription	Aorta	Aorta
31	chr18:65708000-65708400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr18:65708000-65709400	Enhancers	HSMM	muscle
33	chr18:65708200-65708400	ZNF genes & repeats	Aorta	Aorta
34	chr18:65718000-65719400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr18:65718200-65718400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr18:65718400-65718800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr18:65718400-65719000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr18:65718400-65719200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr18:65718400-65719200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr18:65718400-65719400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr18:65718800-65719200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr18:65719000-65719400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr18:65724000-65724800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr18:65733000-65733400	ZNF genes & repeats	NHDF-Ad	bronchial
45	chr18:65742800-65745000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr18:65743400-65744800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr18:65744800-65750200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr18:65745000-65746000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr18:65746000-65746400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:65746400-65750200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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