Variant report

Variant	nsv539607
Chromosome Location	chr8:51032883-51084279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 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	BATF	chr8:51057978-51058142	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:51038532-51038842	GM12878	blood:	n/a	chr8:51038771-51038792
3	CEBPB	chr8:51039822-51040220	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr8:51055553-51055690	HepG2	liver:	n/a	chr8:51055567-51055578
5	CEBPB	chr8:51054545-51054599	K562	blood:	n/a	chr8:51054559-51054572 chr8:51054561-51054572 chr8:51054561-51054572
6	CEBPB	chr8:51052112-51052647	Hela-S3	cervix:	n/a	chr8:51052494-51052505
7	CEBPB	chr8:51052157-51052994	IMR90	lung:	n/a	chr8:51052494-51052505
8	CEBPB	chr8:51056460-51056606	A549	lung:	n/a	n/a
9	CHD2	chr8:51039816-51040236	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr8:51066220-51066370	HAc	cerebellar:	n/a	n/a
11	CTCF	chr8:51066620-51066770	SAEC	small airway:	n/a	n/a
12	CTCF	chr8:51066300-51066450	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr8:51066420-51066570	RPTEC	kidney:	n/a	n/a
14	CTCF	chr8:51066640-51066790	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr8:51066300-51066450	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr8:51066645-51066760	LNCaP	prostate:	n/a	n/a
17	CTCF	chr8:51066673-51066748	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:51066271-51066464	GM12891	blood:	n/a	n/a
19	CTCF	chr8:51066300-51066450	AG09319	gingival:	n/a	n/a
20	CTCF	chr8:51066875-51066967	GM10248	blood:	n/a	n/a
21	CTCF	chr8:51066300-51066450	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr8:51066300-51066450	HCFaa	heart:	n/a	n/a
23	CTCF	chr8:51066300-51066450	SAEC	small airway:	n/a	n/a
24	CTCF	chr8:51066330-51066416	K562	blood:	n/a	n/a
25	CTCF	chr8:51066240-51066390	HVMF	connective:	n/a	n/a
26	CTCF	chr8:51066400-51066550	GM12872	blood:	n/a	n/a
27	CTCF	chr8:51066660-51066810	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:51066622-51066795	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:51066380-51066530	WI-38	lung:	n/a	n/a
30	CTCF	chr8:51066440-51066590	HCM	heart:	n/a	n/a
31	CTCF	chr8:51066620-51066770	GM12865	blood:	n/a	n/a
32	CTCF	chr8:51066627-51066793	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:51057635-51057735	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:51066632-51066707	GM13977	blood:	n/a	n/a
35	CTCF	chr8:51066709-51066762	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr8:51066320-51066409	GM13976	blood:	n/a	n/a
37	CTCF	chr8:51066256-51066528	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:51066620-51066770	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr8:51066240-51066390	GM12867	blood:	n/a	n/a
40	CTCF	chr8:51066640-51066790	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr8:51066256-51066495	Gliobla	brain:	n/a	n/a
42	CTCF	chr8:51066240-51066390	A549	lung:	n/a	n/a
43	CTCF	chr8:51066640-51066790	AG04449	skin:	n/a	n/a
44	CTCF	chr8:51066340-51066490	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr8:51066300-51066450	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr8:51066580-51066730	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr8:51049268-51049352	MCF-7	breast:	n/a	chr8:51049273-51049291 chr8:51049276-51049289
48	CTCF	chr8:51066240-51066390	RPTEC	kidney:	n/a	n/a
49	CTCF	chr8:51066240-51066530	HVMF	connective:	n/a	n/a
50	CTCF	chr8:51066320-51066470	HBMEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51039471-51039521	GM19239	blood:	n/a
2	chr8:51039471-51039521	SAEC	small airway:	n/a
3	chr8:51039471-51039521	AoSMC	blood vessel:	n/a
4	chr8:51039471-51039521	HCT-116	colon:	n/a
5	chr8:51039471-51039521	HMEC	breast:	n/a
6	chr8:51039471-51039521	ECC-1	luminal epithelium:	n/a
7	chr8:51039471-51039521	SK-N-MC	brain:	n/a
8	chr8:51039471-51039521	NB4	blood:	n/a
9	chr8:51039471-51039521	GM06990	blood:	n/a
10	chr8:51039471-51039521	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:51039471-51039521	HRE	kidney:	n/a
12	chr8:51039471-51039521	ProgFib	skin:	n/a
13	chr8:51039471-51039521	SK-N-SH_RA	brain:	n/a
14	chr8:51039471-51039521	AG10803	skin:	n/a
15	chr8:51039471-51039521	SKMC	muscle:	n/a
16	chr8:51039471-51039521	HEEpiC	esophagus:	n/a
17	chr8:51039471-51039521	GM12878	blood:	n/a
18	chr8:51039471-51039521	HEK293	kidney:	embryo
19	chr8:51039471-51039521	HNPCEpiC	eye:	n/a
20	chr8:51039471-51039521	T-47D	breast:	n/a
21	chr8:51039471-51039521	NHBE	bronchial:	n/a
22	chr8:51039471-51039521	GM12892	blood:	n/a
23	chr8:51039471-51039521	ovcar-3	ovarian:	n/a
24	chr8:51039471-51039521	GM12891	blood:	n/a
25	chr8:51039471-51039521	HL-60	blood:	n/a
26	chr8:51039471-51039521	LNCaP	prostate:	n/a
27	chr8:51039471-51039521	IMR90	lung:	fetal
28	chr8:51039471-51039521	Hepatocyte	liver:	n/a
29	chr8:51039471-51039521	PrEC	prostate:	n/a
30	chr8:51039471-51039521	PANC-1	pancreas:	n/a
31	chr8:51039471-51039521	NT2-D1	testis:	n/a
32	chr8:51039471-51039521	SK-N-SH	brain:	n/a
33	chr8:51039471-51039521	BJ	skin:	n/a
34	chr8:51039471-51039521	HCPEpiC	choroid plexus:	n/a
35	chr8:51039471-51039521	HCM	heart:	n/a
36	chr8:51039471-51039521	HRCEpiC	kidney:	n/a
37	chr8:51039471-51039521	RPTEC	kidney:	n/a
38	chr8:51039471-51039521	NHDF-neo	bronchial:	n/a
39	chr8:51039471-51039521	CMK	blood:	n/a
40	chr8:51039471-51039521	AG04450	lung:	fetal
41	chr8:51039471-51039521	Caco-2	colon:	n/a
42	chr8:51039471-51039521	HAEpiC	amniotic membrane:	n/a
43	chr8:51039471-51039521	NH-A	brain:	n/a
44	chr8:51039471-51039521	AG09319	gingival:	n/a
45	chr8:51039471-51039521	Jurkat	blood:	n/a
46	chr8:51039471-51039521	HUVEC	blood vessel:	n/a
47	chr8:51039471-51039521	A549	lung:	n/a
48	chr8:51039471-51039521	AG09309	skin:	n/a
49	chr8:51039471-51039521	AG04449	skin:	fetal
50	chr8:51039471-51039521	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:
2	chr8:51030711..51032424-chr8:51036929..51039858,2	MCF-7	breast:
3	chr8:51050537..51053146-chr8:51056966..51059260,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-14	chr8:51076059-51076529	NONHSAT126523

No data

Variant related genes	Relation type
SNTG1	TF binding region
SNTG1	CpG island

Extended variants
information (count: 1097 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185686353	chr8:51032898-51032899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115777709	chr8:51032905-51032906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373337898	chr8:51032946-51032947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375347343	chr8:51032948-51032949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369725902	chr8:51032952-51032953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138358327	chr8:51032984-51032985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527658760	chr8:51032987-51032988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113217895	chr8:51033062-51033063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371142217	chr8:51033068-51033069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191685214	chr8:51033114-51033115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545766247	chr8:51033142-51033143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112884979	chr8:51033146-51033147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs5891349	chr8:51033149-51033150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398007745	chr8:51033151-51033152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs55646551	chr8:51033155-51033156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531644967	chr8:51033186-51033187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550050705	chr8:51033196-51033197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568626941	chr8:51033214-51033215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149271373	chr8:51033225-51033226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548047446	chr8:51033226-51033227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566348173	chr8:51033243-51033244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183927242	chr8:51033244-51033245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188722285	chr8:51033247-51033248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557746839	chr8:51033249-51033250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569672639	chr8:51033259-51033260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537148126	chr8:51033265-51033266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555211370	chr8:51033329-51033330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573766328	chr8:51033333-51033334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540899063	chr8:51033350-51033351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552773171	chr8:51033351-51033352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577482266	chr8:51033364-51033365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544904243	chr8:51033365-51033366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7005973	chr8:51033423-51033424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs111863740	chr8:51033483-51033484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192425080	chr8:51033511-51033512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs203617	chr8:51033517-51033518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562069692	chr8:51033535-51033536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182250913	chr8:51033551-51033552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186818297	chr8:51033594-51033595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547639714	chr8:51033634-51033635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559995909	chr8:51033691-51033692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565867404	chr8:51033758-51033759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557993791	chr8:51033795-51033796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59840040	chr8:51033838-51033839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552150374	chr8:51033909-51033910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191617953	chr8:51033913-51033914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111634417	chr8:51033965-51033966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557266225	chr8:51034007-51034008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549044695	chr8:51034017-51034018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7839718	chr8:51034018-51034019	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51018400-51039600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:51031400-51034800	Weak transcription	Brain Germinal Matrix	brain
3	chr8:51031600-51038800	Weak transcription	Osteobl	bone
4	chr8:51032200-51046600	Weak transcription	Fetal Brain Male	brain
5	chr8:51034600-51035200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:51034600-51035200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:51034600-51038200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:51034800-51035200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr8:51034800-51037800	Enhancers	Brain Germinal Matrix	brain
10	chr8:51035000-51035600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr8:51037400-51039000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr8:51037800-51046800	Weak transcription	Brain Germinal Matrix	brain
13	chr8:51038000-51047600	Weak transcription	Right Atrium	heart
14	chr8:51038200-51038600	Enhancers	Spleen	Spleen
15	chr8:51038200-51038800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:51038200-51038800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:51038200-51040400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:51038400-51038600	Enhancers	Fetal Intestine Large	intestine
19	chr8:51038400-51039000	Enhancers	NH-A	brain
20	chr8:51038600-51039400	Weak transcription	Fetal Intestine Large	intestine
21	chr8:51038800-51040000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:51038800-51040400	Enhancers	Osteobl	bone
23	chr8:51039000-51039400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:51039000-51039800	Weak transcription	NH-A	brain
25	chr8:51039200-51040000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:51039400-51039800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr8:51039400-51040200	Enhancers	Fetal Intestine Large	intestine
28	chr8:51039400-51040600	Enhancers	Hela-S3	cervix
29	chr8:51039400-51040800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr8:51039600-51040200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:51039600-51040600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:51039600-51040600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr8:51039600-51040600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:51039800-51040600	Enhancers	Adipose Nuclei	Adipose
35	chr8:51039800-51040600	Enhancers	NH-A	brain
36	chr8:51039800-51040800	Enhancers	Rectal Smooth Muscle	rectum
37	chr8:51040000-51040200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr8:51040000-51040600	Enhancers	Colon Smooth Muscle	Colon
39	chr8:51040000-51040800	Enhancers	NHLF	lung
40	chr8:51040600-51040800	Weak transcription	NH-A	brain
41	chr8:51040600-51048400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr8:51045400-51045800	ZNF genes & repeats	Brain Substantia Nigra	brain
43	chr8:51045800-51047200	Weak transcription	Brain Substantia Nigra	brain
44	chr8:51046000-51046800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr8:51046200-51047000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:51046200-51048200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:51046600-51047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:51046600-51047600	Enhancers	Fetal Brain Female	brain
49	chr8:51046600-51047800	Enhancers	Fetal Brain Male	brain
50	chr8:51046600-51048000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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