Variant report

Variant	nsv581878
Chromosome Location	chr2:51427174-51453079
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	BATF	chr2:51439527-51439799	GM12878	blood:	n/a	chr2:51439631-51439642
2	BHLHE40	chr2:51439638-51439779	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:51445259-51445582	HepG2	liver:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
4	CEBPB	chr2:51447009-51447209	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:51445272-51445575	A549	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
6	CEBPB	chr2:51430857-51430966	H1-hESC	embryonic stem cell:	n/a	chr2:51430918-51430929
7	CEBPB	chr2:51430799-51430988	HepG2	liver:	n/a	chr2:51430918-51430929
8	CEBPB	chr2:51445233-51445599	IMR90	lung:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
9	CEBPB	chr2:51445290-51445497	H1-hESC	embryonic stem cell:	n/a	chr2:51445408-51445419 chr2:51445407-51445420
10	CEBPB	chr2:51430897-51430932	A549	lung:	n/a	chr2:51430918-51430929
11	CTCF	chr2:51431722-51431746	GM20000	blood:	n/a	n/a
12	CUX1	chr2:51431162-51431168	GM12878	blood:	n/a	n/a
13	CUX1	chr2:51439433-51439440	GM12878	blood:	n/a	n/a
14	E2F4	chr2:51441537-51441615	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F6	chr2:51446529-51446947	H1-hESC	embryonic stem cell:	n/a	n/a
16	ELK1	chr2:51439695-51439800	GM12878	blood:	n/a	n/a
17	EP300	chr2:51439610-51439761	GM12878	blood:	n/a	n/a
18	EP300	chr2:51428389-51428781	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr2:51439535-51439862	GM12878	blood:	n/a	n/a
20	FAM48A	chr2:51442895-51442976	GM12878	blood:	n/a	n/a
21	FOS	chr2:51445386-51445425	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr2:51452525-51452815	MCF10A-Er-Src	breast:	n/a	chr2:51452715-51452724
23	FOS	chr2:51452587-51452811	MCF10A-Er-Src	breast:	n/a	chr2:51452715-51452724
24	FOS	chr2:51445303-51445492	MCF10A-Er-Src	breast:	n/a	chr2:51445336-51445345
25	FOS	chr2:51445328-51445440	MCF10A-Er-Src	breast:	n/a	chr2:51445336-51445345
26	FOS	chr2:51447794-51448467	HUVEC	blood vessel:	n/a	n/a
27	GATA3	chr2:51428499-51428638	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr2:51428309-51428840	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr2:51429118-51429248	SH-SY5Y	brain:	n/a	n/a
30	IKZF1	chr2:51435809-51435861	GM12878	blood:	n/a	n/a
31	JUN	chr2:51452542-51452905	HepG2	liver:	n/a	chr2:51452711-51452724 chr2:51452715-51452724
32	JUND	chr2:51452510-51452910	HepG2	liver:	n/a	chr2:51452715-51452724
33	JUND	chr2:51452448-51453022	GM12878	blood:	n/a	chr2:51452715-51452724
34	JUND	chr2:51452569-51453065	SK-N-SH	brain:	n/a	chr2:51452715-51452724
35	JUND	chr2:51452592-51452836	K562	blood:	n/a	chr2:51452715-51452724
36	MAFF	chr2:51436178-51436439	HepG2	liver:	n/a	n/a
37	MAFF	chr2:51447277-51447551	HepG2	liver:	n/a	chr2:51447414-51447428 chr2:51447415-51447433
38	MAFK	chr2:51451980-51452108	HepG2	liver:	n/a	n/a
39	MAFK	chr2:51436279-51436329	Hela-S3	cervix:	n/a	n/a
40	MAFK	chr2:51446725-51447010	IMR90	lung:	n/a	chr2:51446849-51446860 chr2:51446846-51446856 chr2:51446847-51446856
41	MAFK	chr2:51452907-51453115	HepG2	liver:	n/a	chr2:51452994-51453011
42	MAFK	chr2:51436133-51436386	IMR90	lung:	n/a	n/a
43	MAFK	chr2:51436181-51436408	HepG2	liver:	n/a	n/a
44	MAFK	chr2:51436146-51436463	HepG2	liver:	n/a	n/a
45	MAFK	chr2:51447254-51447578	HepG2	liver:	n/a	chr2:51447414-51447428 chr2:51447413-51447429 chr2:51447416-51447431 chr2:51447411-51447431
46	MAFK	chr2:51435777-51435924	HepG2	liver:	n/a	chr2:51435810-51435821 chr2:51435809-51435820 chr2:51435808-51435822 chr2:51435809-51435820 chr2:51435812-51435828 chr2:51435810-51435830 chr2:51435809-51435825 chr2:51435810-51435821
47	MAFK	chr2:51447257-51447594	HepG2	liver:	n/a	chr2:51447414-51447428 chr2:51447413-51447429 chr2:51447416-51447431 chr2:51447411-51447431
48	MAFK	chr2:51435724-51435906	IMR90	lung:	n/a	chr2:51435810-51435821 chr2:51435809-51435820 chr2:51435808-51435822 chr2:51435809-51435820 chr2:51435812-51435828 chr2:51435810-51435830 chr2:51435809-51435825 chr2:51435810-51435821
49	MAFK	chr2:51447250-51447589	IMR90	lung:	n/a	chr2:51447414-51447428 chr2:51447413-51447429 chr2:51447416-51447431 chr2:51447411-51447431
50	MAX	chr2:51446460-51446829	H1-hESC	embryonic stem cell:	n/a	chr2:51446714-51446723 chr2:51446715-51446722

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51446925-51446975	HepG2	liver:	n/a
2	chr2:51446925-51446975	K562	blood:	n/a
3	chr2:51446925-51446975	SK-N-SH	brain:	n/a
4	chr2:51446925-51446975	SAEC	small airway:	n/a
5	chr2:51446925-51446975	CMK	blood:	n/a
6	chr2:51446925-51446975	HAEpiC	amniotic membrane:	n/a
7	chr2:51446925-51446975	H1-hESC	embryonic stem cell:	embryo
8	chr2:51446925-51446975	HIPEpiC	eye:	n/a
9	chr2:51446925-51446975	GM19239	blood:	n/a
10	chr2:51446925-51446975	Hela-S3	cervix:	n/a
11	chr2:51446925-51446975	ProgFib	skin:	n/a
12	chr2:51446925-51446975	AG04450	lung:	fetal
13	chr2:51446925-51446975	GM06990	blood:	n/a
14	chr2:51446925-51446975	U87	brain:	n/a
15	chr2:51446925-51446975	ovcar-3	ovarian:	n/a
16	chr2:51446925-51446975	BJ	skin:	n/a
17	chr2:51446925-51446975	HCT-116	colon:	n/a
18	chr2:51446925-51446975	AoSMC	blood vessel:	n/a
19	chr2:51446925-51446975	AG09309	skin:	n/a
20	chr2:51446925-51446975	AG09319	gingival:	n/a
21	chr2:51446925-51446975	SK-N-MC	brain:	n/a
22	chr2:51446925-51446975	HCPEpiC	choroid plexus:	n/a
23	chr2:51446925-51446975	HL-60	blood:	n/a
24	chr2:51446925-51446975	GM12892	blood:	n/a
25	chr2:51446925-51446975	Jurkat	blood:	n/a
26	chr2:51446925-51446975	HUVEC	blood vessel:	n/a
27	chr2:51446925-51446975	PrEC	prostate:	n/a
28	chr2:51446925-51446975	PFSK-1	brain:	n/a
29	chr2:51446925-51446975	NH-A	brain:	n/a
30	chr2:51446925-51446975	BE2_C	brain:	n/a
31	chr2:51446925-51446975	HEEpiC	esophagus:	n/a
32	chr2:51446925-51446975	GM12878	blood:	n/a
33	chr2:51446925-51446975	NB4	blood:	n/a
34	chr2:51446925-51446975	SK-N-SH_RA	brain:	n/a
35	chr2:51446925-51446975	IMR90	lung:	fetal
36	chr2:51446925-51446975	Caco-2	colon:	n/a
37	chr2:51446925-51446975	HRCEpiC	kidney:	n/a
38	chr2:51446925-51446975	HPAEpiC	pulmonary alveolar:	n/a
39	chr2:51446925-51446975	HEK293	kidney:	embryo
40	chr2:51446925-51446975	GM12891	blood:	n/a
41	chr2:51446925-51446975	PANC-1	pancreas:	n/a
42	chr2:51446925-51446975	HRE	kidney:	n/a
43	chr2:51446925-51446975	T-47D	breast:	n/a
44	chr2:51446925-51446975	MCF10A-Er-Src	breast:	n/a
45	chr2:51446925-51446975	Hepatocyte	liver:	n/a
46	chr2:51446925-51446975	LNCaP	prostate:	n/a
47	chr2:51446925-51446975	A549	lung:	n/a
48	chr2:51446925-51446975	AG10803	skin:	n/a
49	chr2:51446925-51446975	HCF	heart:	n/a
50	chr2:51446925-51446975	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
2	chr2:51437981..51439669-chr2:51441644..51443887,2	K562	blood:
3	chr2:51450784..51453564-chr2:51456226..51459190,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-1	chr2:51430129-51430286	ENSG00000237374
2	lnc-NRXN1-1	chr2:51430129-51430299	ENSG00000237374
3	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
4	lnc-NRXN1-1	chr2:51429219-51429452	ENSG00000237374
5	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374
6	lnc-NRXN1-1	chr2:51448809-51448902	ENSG00000237374

Variant related genes	Relation type
ENSG00000237374	TF binding region
ENSG00000237374	CpG island

Extended variants
information (count: 591 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190457990	chr2:51429247-51429248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs41468948	chr2:51429262-51429263	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574664948	chr2:51429263-51429264	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs535784215	chr2:51429286-51429287	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs531341771	chr2:51429356-51429357	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs143733065	chr2:51429372-51429373	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs551437880	chr2:51429450-51429451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs566151419	chr2:51430220-51430221	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs10176094	chr2:51430278-51430279	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537147948	chr2:51435849-51435850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139941328	chr2:51435887-51435888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191290152	chr2:51435890-51435891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13419616	chr2:51435908-51435909	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs567397333	chr2:51435934-51435935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376127642	chr2:51435936-51435937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143375538	chr2:51435986-51435987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183485798	chr2:51435998-51435999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35941079	chr2:51436629-51436630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs567214385	chr2:51436635-51436636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140373425	chr2:51436662-51436663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555763682	chr2:51436666-51436667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573914380	chr2:51436671-51436672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34964547	chr2:51436672-51436673	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142813341	chr2:51436709-51436710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs151029481	chr2:51436715-51436716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186451316	chr2:51436733-51436734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140925013	chr2:51436738-51436739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150227993	chr2:51436743-51436744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56880304	chr2:51436752-51436753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560955246	chr2:51436784-51436785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13411241	chr2:51436799-51436800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556593187	chr2:51438810-51438811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1468895	chr2:51438822-51438823	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs543652301	chr2:51438826-51438827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565138160	chr2:51438832-51438833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567183136	chr2:51438883-51438884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532724114	chr2:51438891-51438892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541698109	chr2:51438895-51438896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559507312	chr2:51438909-51438910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142270647	chr2:51438923-51438924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529959317	chr2:51438971-51438972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530054716	chr2:51438972-51438973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76351527	chr2:51438985-51438986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568384424	chr2:51439619-51439620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543790211	chr2:51439623-51439624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535384563	chr2:51439624-51439625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550192554	chr2:51439656-51439657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570502559	chr2:51439674-51439675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs1468898	chr2:51439688-51439689	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs539164716	chr2:51439740-51439741	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Bladder cancer	21909424	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51435800-51436000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:51436600-51436800	Enhancers	Pancreas	Pancrea
3	chr2:51438800-51439000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:51439600-51439800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:51440800-51441600	Enhancers	NH-A	brain
6	chr2:51441600-51445600	Weak transcription	NH-A	brain
7	chr2:51443800-51444200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:51445600-51447400	Enhancers	NH-A	brain
9	chr2:51446200-51448000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr2:51446400-51446800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:51446400-51448000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:51446400-51448000	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:51446400-51448200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr2:51446400-51448200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr2:51446600-51447000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:51446600-51448200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr2:51446600-51448200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:51446800-51447200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr2:51446800-51447800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:51446800-51448000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr2:51447000-51447400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:51447200-51448000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:51447600-51448000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr2:51447600-51448000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr2:51447800-51448200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr2:51448000-51448200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:51448000-51452200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:51450400-51450600	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr2:51450600-51451200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr2:51451200-51453200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr2:51451800-51452600	Enhancers	Adipose Nuclei	Adipose
32	chr2:51452200-51453000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:51452400-51452800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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