Variant report

Variant	nsv871859
Chromosome Location	chr1:80752283-80908148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:384)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:80883213-80883325	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:80784561-80784761	A549	lung:	n/a	n/a
3	CEBPB	chr1:80858254-80858574	A549	lung:	n/a	n/a
4	CEBPB	chr1:80818747-80819048	HepG2	liver:	n/a	chr1:80818857-80818868
5	CEBPB	chr1:80840772-80841661	IMR90	lung:	n/a	chr1:80840946-80840957
6	CEBPB	chr1:80758555-80758803	HepG2	liver:	n/a	chr1:80758663-80758674 chr1:80758661-80758672 chr1:80758661-80758674
7	CEBPB	chr1:80858020-80858759	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:80840764-80841890	Hela-S3	cervix:	n/a	chr1:80840946-80840957
9	CEBPB	chr1:80846904-80847143	K562	blood:	n/a	chr1:80847004-80847015
10	CEBPB	chr1:80784586-80784803	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:80858137-80858634	A549	lung:	n/a	n/a
12	CEBPB	chr1:80858164-80858591	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:80846825-80847141	Hela-S3	cervix:	n/a	chr1:80847004-80847015
14	CEBPB	chr1:80758562-80758804	K562	blood:	n/a	chr1:80758663-80758674 chr1:80758661-80758672 chr1:80758661-80758674
15	CEBPB	chr1:80784526-80784853	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:80858095-80858832	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:80758590-80758834	IMR90	lung:	n/a	chr1:80758663-80758674 chr1:80758661-80758672 chr1:80758661-80758674
18	CEBPB	chr1:80818721-80819051	Hela-S3	cervix:	n/a	chr1:80818857-80818868
19	CEBPB	chr1:80798417-80798682	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:80846876-80847176	IMR90	lung:	n/a	chr1:80847004-80847015
21	CEBPB	chr1:80858289-80858669	A549	lung:	n/a	n/a
22	CEBPB	chr1:80840786-80841111	HepG2	liver:	n/a	chr1:80840946-80840957
23	CEBPB	chr1:80871572-80871772	HepG2	liver:	n/a	chr1:80871641-80871652
24	CEBPB	chr1:80840795-80841063	A549	lung:	n/a	chr1:80840946-80840957
25	CTCF	chr1:80907480-80907630	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr1:80907380-80907530	A549	lung:	n/a	n/a
27	CTCF	chr1:80907500-80907650	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr1:80907440-80907590	BE2_C	brain:	n/a	n/a
29	CTCF	chr1:80907479-80907584	HepG2	liver:	n/a	n/a
30	CTCF	chr1:80907487-80907613	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:80907500-80907650	HPF	lung:	n/a	n/a
32	CTCF	chr1:80907480-80907630	HMF	breast:	n/a	n/a
33	CTCF	chr1:80907392-80907640	T-47D	breast:	n/a	n/a
34	CTCF	chr1:80907420-80907570	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr1:80907505-80907645	GM12878	blood:	n/a	n/a
36	CTCF	chr1:80907474-80907597	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:80817964-80818025	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr1:80829610-80829697	GM10248	blood:	n/a	n/a
39	CTCF	chr1:80907460-80907610	HCT-116	colon:	n/a	n/a
40	CTCF	chr1:80907500-80907650	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:80907460-80907610	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr1:80907520-80907670	HMEC	breast:	n/a	n/a
43	CTCF	chr1:80907440-80907590	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr1:80907480-80907630	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:80907420-80907570	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:80907480-80907630	HMEC	breast:	n/a	n/a
47	CTCF	chr1:80907480-80907630	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr1:80907460-80907610	RPTEC	kidney:	n/a	n/a
49	CTCF	chr1:80791630-80791694	ProgFib	skin:	n/a	n/a
50	CTCF	chr1:80889857-80889948	Hela-S3	cervix:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:80908006..80910063-chr1:80913147..80915791,2	K562	blood:
2	chr1:80784427..80786663-chr1:80792675..80794437,2	K562	blood:
3	chr1:80754826..80757744-chr1:80760526..80762840,2	K562	blood:
4	chr1:80879820..80881703-chr1:80888899..80891310,2	MCF-7	breast:
5	chr1:80380861..80381772-chr1:80785065..80785571,2	K562	blood:
6	chr1:80879820..80881703-chr1:80888899..80891310,2	MCF-7	breast:
7	chr1:80754826..80757744-chr1:80760526..80762840,2	K562	blood:
8	chr1:80784427..80786663-chr1:80792675..80794437,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004113
2	lnc-ELTD1-7	chr1:80839049-80839443	XLOC_000882
3	lnc-ELTD1-13	chr1:80822563-80822636	NONHSAT004108
4	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004113
5	lnc-LPHN2-10	chr1:80884836-80885114	l_76_chr1:80879560-80885114_adrenal
6	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004110
7	lnc-LPHN2-10	chr1:80879561-80879674	l_76_chr1:80879560-80885114_adrenal
8	lnc-LPHN2-10	chr1:80882498-80882626	l_76_chr1:80879560-80885114_adrenal
9	lnc-LPHN2-10	chr1:80879557-80879674	NONHSAT004113
10	lnc-LPHN2-10	chr1:80774028-80774215	NONHSAT004109
11	lnc-LPHN2-10	chr1:80884836-80885061	NONHSAT004109
12	lnc-LPHN2-10	chr1:80778862-80778909	NONHSAT004109
13	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004109
14	lnc-LPHN2-10	chr1:80774028-80774215	NONHSAT004110
15	lnc-ELTD1-13	chr1:80773251-80773525	NONHSAT004108
16	lnc-LPHN2-10	chr1:80882498-80882626	NONHSAT004110
17	lnc-ELTD1-7	chr1:80840122-80840306	XLOC_000882

No data

Variant related genes	Relation type
ENSG00000266033	TF binding region
ENSG00000225598	TF binding region

Extended variants
information (count: 2708 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2708 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1342860	chr1:80752283-80752284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547430223	chr1:80752296-80752297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551576539	chr1:80752300-80752301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556162836	chr1:80752343-80752344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138960733	chr1:80752345-80752346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77739294	chr1:80752367-80752368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557332921	chr1:80752395-80752396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1342861	chr1:80752404-80752405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533327306	chr1:80752405-80752406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572599793	chr1:80752415-80752416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75450156	chr1:80752421-80752422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181458209	chr1:80752537-80752538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545243360	chr1:80752548-80752549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185821974	chr1:80752580-80752581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575781776	chr1:80752593-80752594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544491792	chr1:80752600-80752601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190246496	chr1:80752622-80752623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528821470	chr1:80752626-80752627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548587899	chr1:80752632-80752633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559157622	chr1:80752678-80752679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4650455	chr1:80752686-80752687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116195297	chr1:80752703-80752704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72673653	chr1:80752717-80752718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537290666	chr1:80752742-80752743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113546657	chr1:80752747-80752748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542716660	chr1:80752801-80752802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562467477	chr1:80752840-80752841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569928474	chr1:80752874-80752875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180980803	chr1:80752883-80752884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74522212	chr1:80752905-80752906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4650456	chr1:80752915-80752916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185755960	chr1:80752916-80752917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566780218	chr1:80752930-80752931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190273863	chr1:80752943-80752944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558823447	chr1:80753002-80753003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527530077	chr1:80753042-80753043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575787821	chr1:80753062-80753063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368181954	chr1:80753083-80753084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554811402	chr1:80753101-80753102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574816662	chr1:80753181-80753182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181400360	chr1:80753196-80753197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559286746	chr1:80753259-80753260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78230392	chr1:80753300-80753301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148392536	chr1:80753424-80753425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545086156	chr1:80753425-80753426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76035371	chr1:80753439-80753440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12087702	chr1:80753442-80753443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs530218151	chr1:80753451-80753452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530683438	chr1:80753452-80753453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550809379	chr1:80753525-80753526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80745000-80758800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:80758800-80759000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:80759000-80761400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:80761200-80762400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:80761400-80761800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:80765000-80765400	Enhancers	Fetal Brain Male	brain
7	chr1:80771200-80771800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr1:80771400-80771800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:80771600-80772000	Enhancers	Fetal Brain Male	brain
10	chr1:80771800-80776600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:80776400-80776800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:80776600-80777000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr1:80776600-80777400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr1:80787600-80790000	Weak transcription	Hela-S3	cervix
15	chr1:80796600-80796800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:80796800-80804600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:80804600-80805200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:80825200-80826800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr1:80825400-80825800	Enhancers	Colon Smooth Muscle	Colon
20	chr1:80829600-80830000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:80829800-80830200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:80829800-80830200	Enhancers	HMEC	breast
23	chr1:80831200-80831800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr1:80831400-80832400	Enhancers	Fetal Lung	lung
25	chr1:80832200-80840000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:80839000-80843000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:80839200-80842000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:80839400-80840800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:80840000-80840800	Enhancers	HSMMtube	muscle
30	chr1:80840000-80841000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:80840000-80842000	Enhancers	HMEC	breast
32	chr1:80840600-80841800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:80840600-80841800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:80840600-80842400	Enhancers	Fetal Heart	heart
35	chr1:80840600-80842800	Enhancers	Hela-S3	cervix
36	chr1:80840800-80841400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:80840800-80841600	Weak transcription	HSMMtube	muscle
38	chr1:80840800-80842000	Enhancers	NHEK	skin
39	chr1:80841000-80841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:80841400-80842000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr1:80841400-80842200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:80841600-80842000	Enhancers	HSMMtube	muscle
43	chr1:80842000-80846200	Weak transcription	HMEC	breast
44	chr1:80842200-80842600	Enhancers	Placenta Amnion	Placenta Amnion
45	chr1:80842200-80843000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:80850800-80851800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr1:80851000-80851600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:80851000-80851800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:80851200-80851800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:80854000-80854600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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