Variant report

Variant	nsv613757
Chromosome Location	chr9:21289923-21316649
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	ATF2	chr9:21295176-21295511	GM12878	blood:	n/a	n/a
2	BCL11A	chr9:21294961-21295244	GM12878	blood:	n/a	n/a
3	BCL11A	chr9:21295273-21295487	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:21295247-21295511	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:21295038-21295518	GM12878	blood:	n/a	n/a
6	CBX3	chr9:21294177-21294800	HCT-116	colon:	n/a	n/a
7	CBX3	chr9:21294159-21294859	HCT-116	colon:	n/a	n/a
8	CEBPB	chr9:21294131-21294913	HCT-116	colon:	n/a	n/a
9	CEBPB	chr9:21294087-21295054	HCT-116	colon:	n/a	chr9:21294973-21294984
10	CEBPB	chr9:21314055-21314593	A549	lung:	n/a	chr9:21314308-21314319
11	CEBPB	chr9:21294292-21294892	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:21308602-21308919	A549	lung:	n/a	n/a
13	CEBPB	chr9:21314059-21314587	IMR90	lung:	n/a	chr9:21314308-21314319
14	CEBPB	chr9:21314073-21314585	HepG2	liver:	n/a	chr9:21314308-21314319
15	CEBPB	chr9:21314148-21314498	Hela-S3	cervix:	n/a	chr9:21314308-21314319
16	CEBPB	chr9:21308626-21308922	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:21316276-21316754	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:21308634-21308922	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr9:21308598-21308918	HepG2	liver:	n/a	n/a
20	CHD2	chr9:21294296-21294681	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr9:21295023-21295452	GM12878	blood:	n/a	n/a
22	CTCF	chr9:21289780-21289930	HFF	foreskin:	n/a	n/a
23	CTCF	chr9:21306574-21306627	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:21302450-21302489	GM10266	blood:	n/a	n/a
25	CTCF	chr9:21300767-21300841	GM20000	blood:	n/a	n/a
26	CUX1	chr9:21295238-21295438	GM12878	blood:	n/a	n/a
27	E2F4	chr9:21306957-21307157	MCF10A-Er-Src	breast:	n/a	n/a
28	EBF1	chr9:21296293-21296300	GM12878	blood:	n/a	n/a
29	EBF1	chr9:21295018-21295535	GM12878	blood:	n/a	n/a
30	EBF1	chr9:21294348-21294561	GM12878	blood:	n/a	n/a
31	EP300	chr9:21294977-21295571	GM12878	blood:	n/a	chr9:21295183-21295197
32	EP300	chr9:21294891-21295540	GM12878	blood:	n/a	chr9:21295183-21295197
33	EP300	chr9:21294307-21294789	Hela-S3	cervix:	n/a	chr9:21294431-21294440 chr9:21294715-21294729
34	EP300	chr9:21294963-21295587	GM12878	blood:	n/a	chr9:21295183-21295197
35	FAM48A	chr9:21309956-21309990	GM12878	blood:	n/a	n/a
36	FOS	chr9:21294288-21294891	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
37	FOS	chr9:21294256-21294636	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
38	FOS	chr9:21294312-21294611	HUVEC	blood vessel:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
39	FOS	chr9:21294290-21294669	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
40	FOS	chr9:21294286-21294878	MCF10A-Er-Src	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
41	FOSL1	chr9:21294030-21294995	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
42	FOSL1	chr9:21293304-21293875	HCT-116	colon:	n/a	chr9:21293625-21293633 chr9:21293625-21293633 chr9:21293626-21293633
43	FOSL1	chr9:21294149-21294790	HCT-116	colon:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
44	FOSL2	chr9:21294329-21294604	HepG2	liver:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
45	FOSL2	chr9:21294261-21294651	MCF-7	breast:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438
46	GATA2	chr9:21289874-21290218	SH-SY5Y	brain:	n/a	chr9:21290053-21290063 chr9:21290053-21290062 chr9:21290050-21290066
47	GATA3	chr9:21289924-21290166	T-47D	breast:	n/a	chr9:21290053-21290063 chr9:21290053-21290062 chr9:21290054-21290062 chr9:21290050-21290066
48	IKZF1	chr9:21295093-21295574	GM12878	blood:	n/a	n/a
49	JUN	chr9:21294282-21294452	HepG2	liver:	n/a	chr9:21294431-21294440 chr9:21294431-21294438
50	JUN	chr9:21294272-21294882	Hela-S3	cervix:	n/a	chr9:21294485-21294496 chr9:21294431-21294440 chr9:21294431-21294438

Variant related genes	Relation type
IFNA20P	TF binding region
IFNA5	TF binding region

Extended variants
information (count: 726 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4978092	chr9:21289923-21289924	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539509666	chr9:21289953-21289954	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs552955626	chr9:21289975-21289976	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs186575924	chr9:21289981-21289982	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs145278950	chr9:21289990-21289991	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs147647712	chr9:21290007-21290008	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs375174218	chr9:21290029-21290030	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs142305063	chr9:21290090-21290091	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs191796191	chr9:21290101-21290102	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs76752328	chr9:21290139-21290140	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs532254302	chr9:21290183-21290184	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs116979632	chr9:21290186-21290187	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs200901569	chr9:21290196-21290197	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs528052473	chr9:21290204-21290205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183191224	chr9:21290277-21290278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144605628	chr9:21290280-21290281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534183310	chr9:21290281-21290282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145732007	chr9:21290293-21290294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550763814	chr9:21290316-21290317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570267869	chr9:21290350-21290351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200607966	chr9:21290351-21290352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs72691699	chr9:21290367-21290368	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553016680	chr9:21290368-21290369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539734179	chr9:21290416-21290417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572936739	chr9:21290487-21290488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371266435	chr9:21290500-21290501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535820781	chr9:21290510-21290511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375566640	chr9:21290511-21290512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557977353	chr9:21290590-21290591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143710121	chr9:21290601-21290602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575884100	chr9:21290628-21290629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148128939	chr9:21290638-21290639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558386505	chr9:21290671-21290672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs578196380	chr9:21290756-21290757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187075380	chr9:21290789-21290790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559472918	chr9:21290790-21290791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528100996	chr9:21290792-21290793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577151777	chr9:21290836-21290837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369818342	chr9:21290945-21290946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541802302	chr9:21290949-21290950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141357351	chr9:21290958-21290959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527790954	chr9:21290970-21290971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112567982	chr9:21290978-21290979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547872667	chr9:21290980-21290981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566688712	chr9:21290981-21290982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114918211	chr9:21291010-21291011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550435773	chr9:21291018-21291019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs202148261	chr9:21291051-21291052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570327758	chr9:21291055-21291056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145146820	chr9:21291075-21291076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:21289600-21290200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:21289800-21290200	Bivalent Enhancer	Dnd41	blood
5	chr9:21290200-21294400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr9:21290200-21294800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:21293600-21294400	Enhancers	GM12878-XiMat	blood
8	chr9:21293600-21295200	Enhancers	HMEC	breast
9	chr9:21293800-21295400	Enhancers	Hela-S3	cervix
10	chr9:21294000-21295400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr9:21294200-21295000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:21294200-21295000	Enhancers	NHEK	skin
13	chr9:21294200-21295200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:21294400-21294800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:21294400-21294800	Bivalent Enhancer	A549	lung
16	chr9:21294400-21295200	Flanking Active TSS	GM12878-XiMat	blood
17	chr9:21294400-21295400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:21294400-21296800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr9:21294400-21297000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr9:21294600-21295600	Bivalent Enhancer	Primary B cells from cord blood	blood
21	chr9:21294800-21296600	Enhancers	Primary hematopoietic stem cells	blood
22	chr9:21294800-21296600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr9:21294800-21296800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr9:21294800-21296800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:21295000-21296400	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr9:21295200-21295800	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr9:21295200-21296000	Enhancers	GM12878-XiMat	blood
28	chr9:21295400-21295600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:21295400-21295800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:21295400-21295800	Enhancers	Primary B cells from peripheral blood	blood
31	chr9:21295800-21296200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:21296000-21296400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr9:21296000-21296400	Enhancers	Fetal Muscle Trunk	muscle
34	chr9:21296200-21296400	Enhancers	Esophagus	oesophagus
35	chr9:21296200-21296400	Bivalent Enhancer	Small Intestine	intestine
36	chr9:21296600-21296800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr9:21304800-21305400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr9:21308800-21309000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:21308800-21309200	Enhancers	Brain Substantia Nigra	brain
40	chr9:21309000-21312000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:21309200-21309600	Weak transcription	Brain Substantia Nigra	brain
42	chr9:21309600-21309800	Enhancers	Brain Substantia Nigra	brain
43	chr9:21309800-21322600	Weak transcription	Brain Substantia Nigra	brain
44	chr9:21310400-21311800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr9:21310800-21311400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr9:21311400-21311600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:21311600-21312000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:21311800-21312200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:21311800-21313000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:21311800-21313600	Enhancers	Cortex derived primary cultured neurospheres	brain

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