Variant report

Variant	nsv885951
Chromosome Location	chr6:57761561-58144557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:611)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:57996881-57996935	K562	blood:	n/a	n/a
2	ATF3	chr6:58142472-58142715	K562	blood:	n/a	n/a
3	ATF3	chr6:58142478-58142721	A549	lung:	n/a	n/a
4	ATF3	chr6:58141691-58142004	K562	blood:	n/a	n/a
5	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
6	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
7	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
9	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
10	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
11	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
12	CTCF	chr6:57880380-57880530	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr6:57903826-57904041	GM13977	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
14	CTCF	chr6:57903680-57903830	HEK293	kidney:	n/a	n/a
15	CTCF	chr6:57903680-57903830	BJ	skin:	n/a	n/a
16	CTCF	chr6:57811475-57811593	GM12891	blood:	n/a	n/a
17	CTCF	chr6:57811529-57811590	HepG2	liver:	n/a	n/a
18	CTCF	chr6:57903820-57904035	Hela-S3	cervix:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
19	CTCF	chr6:57812094-57812195	Medullo	brain:	n/a	n/a
20	CTCF	chr6:58142480-58142630	HEK293	kidney:	n/a	n/a
21	CTCF	chr6:57811193-57811206	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr6:57811400-57811550	WERI-Rb-1	eye:	n/a	chr6:57811427-57811440
23	CTCF	chr6:57903805-57904023	GM12878	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
24	CTCF	chr6:57903787-57904046	MCF-7	breast:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
25	CTCF	chr6:57767031-57767102	ProgFib	skin:	n/a	n/a
26	CTCF	chr6:58047077-58047104	Lung_OC	lung:	n/a	n/a
27	CTCF	chr6:57766987-57767126	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr6:58032301-58032319	HepG2	liver:	n/a	n/a
29	CTCF	chr6:57903834-57903968	NHEK	skin:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
30	CTCF	chr6:57767015-57767160	HepG2	liver:	n/a	n/a
31	CTCF	chr6:57811420-57811570	A549	lung:	n/a	chr6:57811427-57811440
32	CTCF	chr6:57792874-57792950	LNCaP	prostate:	n/a	n/a
33	CTCF	chr6:57766927-57767194	LNCaP	prostate:	n/a	n/a
34	CTCF	chr6:57903680-57903830	GM12870	blood:	n/a	n/a
35	CTCF	chr6:57903680-57903830	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr6:58032451-58032505	GM10266	blood:	n/a	n/a
37	CTCF	chr6:57903819-57903974	A549	lung:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
38	CTCF	chr6:58021630-58021707	Medullo	brain:	n/a	n/a
39	CTCF	chr6:57983763-57983815	GM20000	blood:	n/a	n/a
40	CTCF	chr6:57801044-57801048	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:57811442-57811630	NHEK	skin:	n/a	n/a
42	CTCF	chr6:57800930-57801041	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:57811153-57811192	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr6:57903680-57903830	GM12873	blood:	n/a	n/a
45	CTCF	chr6:57800926-57800927	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:57811506-57811607	GM13977	blood:	n/a	n/a
47	CTCF	chr6:57964797-57964883	GM10248	blood:	n/a	n/a
48	CTCF	chr6:57766931-57767201	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:57811430-57811663	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:57767000-57767150	NHEK	skin:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58141890-58141940	MCF10A-Er-Src	breast:	n/a
2	chr6:58141890-58141940	MCF10A-Er-Src	breast:	n/a
3	chr6:57970592-57970642	HNPCEpiC	eye:	n/a
4	chr6:57912662-57912712	HCT-116	colon:	n/a
5	chr6:58142044-58142094	RPTEC	kidney:	n/a
6	chr6:57970666-57970716	GM19239	blood:	n/a
7	chr6:58141890-58141940	NHBE	bronchial:	n/a
8	chr6:58142044-58142094	K562	blood:	n/a
9	chr6:57972721-57972771	GM12878	blood:	n/a
10	chr6:57972721-57972771	HL-60	blood:	n/a
11	chr6:57972721-57972771	SAEC	small airway:	n/a
12	chr6:58001971-58002021	SKMC	muscle:	n/a
13	chr6:57912662-57912712	HRE	kidney:	n/a
14	chr6:58001971-58002021	NH-A	brain:	n/a
15	chr6:57970666-57970716	ECC-1	luminal epithelium:	n/a
16	chr6:58142044-58142094	PFSK-1	brain:	n/a
17	chr6:57972721-57972771	ECC-1	luminal epithelium:	n/a
18	chr6:57972721-57972771	GM12892	blood:	n/a
19	chr6:57972721-57972771	HRPEpiC	eye:	n/a
20	chr6:57912662-57912712	Caco-2	colon:	n/a
21	chr6:57912662-57912712	SKMC	muscle:	n/a
22	chr6:57972223-57972273	SK-N-MC	brain:	n/a
23	chr6:57972349-57972399	BJ	skin:	n/a
24	chr6:57972721-57972771	AG09309	skin:	n/a
25	chr6:57972349-57972399	IMR90	lung:	fetal
26	chr6:57972349-57972399	RPTEC	kidney:	n/a
27	chr6:57972721-57972771	HRCEpiC	kidney:	n/a
28	chr6:58142044-58142094	GM12892	blood:	n/a
29	chr6:57912662-57912712	HEEpiC	esophagus:	n/a
30	chr6:57912662-57912712	HEK293	kidney:	embryo
31	chr6:57970666-57970716	GM12892	blood:	n/a
32	chr6:58142044-58142094	HRPEpiC	eye:	n/a
33	chr6:57972680-57972730	K562	blood:	n/a
34	chr6:58142044-58142094	HCPEpiC	choroid plexus:	n/a
35	chr6:57972680-57972730	HL-60	blood:	n/a
36	chr6:58001971-58002021	NB4	blood:	n/a
37	chr6:57972349-57972399	HCF	heart:	n/a
38	chr6:57970592-57970642	T-47D	breast:	n/a
39	chr6:58141890-58141940	HRCEpiC	kidney:	n/a
40	chr6:58001971-58002021	PFSK-1	brain:	n/a
41	chr6:57970592-57970642	AG04449	skin:	fetal
42	chr6:57972349-57972399	NB4	blood:	n/a
43	chr6:58142044-58142094	HL-60	blood:	n/a
44	chr6:57972680-57972730	BJ	skin:	n/a
45	chr6:57972680-57972730	HCF	heart:	n/a
46	chr6:58141890-58141940	K562	blood:	n/a
47	chr6:58141890-58141940	LNCaP	prostate:	n/a
48	chr6:57912662-57912712	NH-A	brain:	n/a
49	chr6:58001971-58002021	K562	blood:	n/a
50	chr6:57972349-57972399	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-15	chr6:57793932-57794280	NONHSAT113301
2	lnc-BAG2-11	chr6:57798854-57798915	NONHSAT113302
3	lnc-BAG2-11	chr6:57799352-57799604	NONHSAT113302

No data

Variant related genes	Relation type
ENSG00000270213	TF binding region
RBBP4P3	TF binding region
ENSG00000262828	TF binding region
ENSG00000270213	CpG island
RBBP4P3	CpG island
ENSG00000262828	CpG island

Extended variants
information (count: 1700 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367955687	chr6:57766406-57766407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376189068	chr6:57766438-57766439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs58051839	chr6:57766471-57766472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539415708	chr6:57766472-57766473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553361322	chr6:57766481-57766482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558440005	chr6:57766512-57766513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368169089	chr6:57766546-57766547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573414400	chr6:57766560-57766561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573387539	chr6:57766565-57766566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs3000259	chr6:57766566-57766567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535632768	chr6:57766574-57766575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540869739	chr6:57766630-57766631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73463057	chr6:57766636-57766637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555672794	chr6:57766649-57766650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574620035	chr6:57766661-57766662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112035981	chr6:57766674-57766675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541925797	chr6:57766697-57766698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373891805	chr6:57766716-57766717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189071539	chr6:57766735-57766736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575325867	chr6:57766736-57766737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545774999	chr6:57766742-57766743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6918012	chr6:57766746-57766747	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528368933	chr6:57766749-57766750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546811714	chr6:57766754-57766755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71695096	chr6:57766765-57766766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs5015050	chr6:57766794-57766795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140448508	chr6:57766825-57766826	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs377580411	chr6:57766928-57766929	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs529028458	chr6:57766940-57766941	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs550678794	chr6:57766951-57766952	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs568972003	chr6:57766973-57766974	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191981676	chr6:57766999-57767000	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185688019	chr6:57767048-57767049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567194702	chr6:57767074-57767075	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs150293240	chr6:57767075-57767076	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs555956428	chr6:57767079-57767080	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574305159	chr6:57767105-57767106	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs538406100	chr6:57767119-57767120	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185886451	chr6:57767405-57767406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529064999	chr6:57767412-57767413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575852364	chr6:57767478-57767479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562692097	chr6:57767516-57767517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372765711	chr6:57767543-57767544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533242733	chr6:57767574-57767575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9476310	chr6:57767576-57767577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566732497	chr6:57767649-57767650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534170719	chr6:57767668-57767669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564505564	chr6:57767705-57767706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370027363	chr6:57767727-57767728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537096551	chr6:57767813-57767814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57766400-57766800	Enhancers	Brain Cingulate Gyrus	brain
2	chr6:57766400-57766800	Enhancers	Brain Hippocampus Middle	brain
3	chr6:57766600-57767000	Enhancers	Fetal Brain Male	brain
4	chr6:57766800-57767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr6:57766800-57767200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:57767400-57768400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:57768400-57768800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:57768400-57769200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:57768400-57769200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr6:57789800-57790400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:57790000-57790600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:57808400-57808800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr6:57808800-57810400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:57810400-57812000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr6:57810400-57812000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:57810600-57811400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:57810600-57812000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:57810600-57812000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr6:57811200-57812000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:57832800-57833600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:57833600-57838600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:57835000-57835400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr6:57835000-57835600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr6:57835000-57835600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr6:57835000-57835600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:57835000-57836000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr6:57835400-57836000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:57835400-57849000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr6:57835600-57838800	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:57835600-57838800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:57836000-57838800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:57838600-57839400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:57838600-57839600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:57838800-57839000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr6:57838800-57839200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr6:57838800-57839400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr6:57842800-57843000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:57843000-57843200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:57843200-57846400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:57845200-57848000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:57846200-57846600	Enhancers	Fetal Intestine Large	intestine
42	chr6:57846400-57847200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:57846600-57846800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:57846600-57849200	Weak transcription	Fetal Intestine Large	intestine
45	chr6:57846800-57847200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:57846800-57848000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr6:57847000-57849000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr6:57847200-57849000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:57848000-57850800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr6:57849000-57849400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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