Variant report

Variant	nsv892858
Chromosome Location	chr9:26609613-26783463
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	ARID3A	chr9:26746655-26746928	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:26744401-26744755	HepG2	liver:	n/a	n/a
3	ATF1	chr9:26779126-26779512	K562	blood:	n/a	n/a
4	ATF2	chr9:26637055-26637518	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:26637101-26637510	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:26746311-26747148	GM12878	blood:	n/a	n/a
7	BACH1	chr9:26746447-26747018	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr9:26746185-26747145	GM12878	blood:	n/a	n/a
9	BRCA1	chr9:26779130-26779354	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr9:26746522-26747086	HCT-116	colon:	n/a	n/a
11	CBX3	chr9:26746383-26747096	HCT-116	colon:	n/a	n/a
12	CEBPB	chr9:26727783-26728067	IMR90	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
13	CEBPB	chr9:26723642-26723933	MCF-7	breast:	n/a	n/a
14	CEBPB	chr9:26778913-26779621	HCT-116	colon:	n/a	chr9:26779217-26779228
15	CEBPB	chr9:26779040-26779491	Hela-S3	cervix:	n/a	chr9:26779217-26779228
16	CEBPB	chr9:26779021-26779569	HCT-116	colon:	n/a	chr9:26779217-26779228
17	CEBPB	chr9:26772174-26772358	HepG2	liver:	n/a	chr9:26772321-26772332
18	CEBPB	chr9:26637102-26637435	H1-hESC	embryonic stem cell:	n/a	chr9:26637215-26637228
19	CEBPB	chr9:26685947-26686220	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:26779131-26779393	HepG2	liver:	n/a	chr9:26779217-26779228
21	CEBPB	chr9:26723709-26723857	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:26685951-26686224	A549	lung:	n/a	n/a
23	CEBPB	chr9:26685937-26686221	IMR90	lung:	n/a	n/a
24	CEBPB	chr9:26779098-26779379	A549	lung:	n/a	chr9:26779217-26779228
25	CEBPB	chr9:26727749-26728064	K562	blood:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
26	CEBPB	chr9:26684767-26684810	HepG2	liver:	n/a	chr9:26684786-26684797
27	CEBPB	chr9:26723563-26723907	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr9:26746742-26746968	MCF-7	breast:	n/a	n/a
29	CEBPB	chr9:26656235-26656535	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:26695601-26695779	HepG2	liver:	n/a	chr9:26695676-26695693 chr9:26695678-26695689
31	CEBPB	chr9:26747699-26748040	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr9:26727899-26727940	H1-hESC	embryonic stem cell:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
33	CEBPB	chr9:26727788-26728098	A549	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
34	CEBPB	chr9:26667005-26667349	HepG2	liver:	n/a	chr9:26667180-26667191 chr9:26667178-26667191 chr9:26667178-26667189 chr9:26667178-26667191
35	CEBPB	chr9:26772178-26772489	IMR90	lung:	n/a	chr9:26772321-26772332
36	CEBPB	chr9:26727767-26728072	HepG2	liver:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
37	CEBPB	chr9:26737005-26737170	A549	lung:	n/a	n/a
38	CHD1	chr9:26746419-26746824	GM12878	blood:	n/a	n/a
39	CHD2	chr9:26723518-26723804	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr9:26748166-26748203	HepG2	liver:	n/a	n/a
41	CHD2	chr9:26637151-26637458	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:26746691-26747084	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr9:26723554-26723861	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr9:26744453-26744748	ECC-1	luminal epithelium:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
45	CTCF	chr9:26744460-26744610	GM12873	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
46	CTCF	chr9:26613900-26614050	HAc	cerebellar:	n/a	n/a
47	CTCF	chr9:26744457-26744678	LNCaP	prostate:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
48	CTCF	chr9:26723620-26723770	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr9:26613929-26614158	GM12892	blood:	n/a	n/a
50	CTCF	chr9:26656400-26656550	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26722560-26722610	PFSK-1	brain:	n/a
2	chr9:26722560-26722610	H1-hESC	embryonic stem cell:	embryo
3	chr9:26722560-26722610	SK-N-MC	brain:	n/a
4	chr9:26722560-26722610	AG04449	skin:	fetal
5	chr9:26722560-26722610	SK-N-SH	brain:	n/a
6	chr9:26722560-26722610	K562	blood:	n/a
7	chr9:26761746-26761796	CMK	blood:	n/a
8	chr9:26761746-26761796	NH-A	brain:	n/a
9	chr9:26722560-26722610	CMK	blood:	n/a
10	chr9:26722560-26722610	AG04450	lung:	fetal
11	chr9:26761746-26761796	HL-60	blood:	n/a
12	chr9:26722560-26722610	LNCaP	prostate:	n/a
13	chr9:26722560-26722610	NHDF-neo	bronchial:	n/a
14	chr9:26722560-26722610	GM12892	blood:	n/a
15	chr9:26761746-26761796	K562	blood:	n/a
16	chr9:26761746-26761796	SK-N-SH_RA	brain:	n/a
17	chr9:26761746-26761796	HCF	heart:	n/a
18	chr9:26722560-26722610	Caco-2	colon:	n/a
19	chr9:26722560-26722610	MCF-7	breast:	n/a
20	chr9:26722560-26722610	RPTEC	kidney:	n/a
21	chr9:26761746-26761796	PFSK-1	brain:	n/a
22	chr9:26761746-26761796	IMR90	lung:	fetal
23	chr9:26761746-26761796	MCF-7	breast:	n/a
24	chr9:26761746-26761796	HRCEpiC	kidney:	n/a
25	chr9:26761746-26761796	AoSMC	blood vessel:	n/a
26	chr9:26722560-26722610	U87	brain:	n/a
27	chr9:26722560-26722610	Jurkat	blood:	n/a
28	chr9:26761746-26761796	PANC-1	pancreas:	n/a
29	chr9:26761746-26761796	HIPEpiC	eye:	n/a
30	chr9:26761746-26761796	AG09319	gingival:	n/a
31	chr9:26761746-26761796	ovcar-3	ovarian:	n/a
32	chr9:26761746-26761796	Caco-2	colon:	n/a
33	chr9:26761746-26761796	BJ	skin:	n/a
34	chr9:26722560-26722610	PrEC	prostate:	n/a
35	chr9:26761746-26761796	ECC-1	luminal epithelium:	n/a
36	chr9:26722560-26722610	GM12878	blood:	n/a
37	chr9:26722560-26722610	T-47D	breast:	n/a
38	chr9:26722560-26722610	HEEpiC	esophagus:	n/a
39	chr9:26761746-26761796	HepG2	liver:	n/a
40	chr9:26722560-26722610	HCM	heart:	n/a
41	chr9:26722560-26722610	HCPEpiC	choroid plexus:	n/a
42	chr9:26722560-26722610	HRPEpiC	eye:	n/a
43	chr9:26761746-26761796	SKMC	muscle:	n/a
44	chr9:26722560-26722610	HPAEpiC	pulmonary alveolar:	n/a
45	chr9:26761746-26761796	GM06990	blood:	n/a
46	chr9:26722560-26722610	GM19239	blood:	n/a
47	chr9:26761746-26761796	U87	brain:	n/a
48	chr9:26722560-26722610	HRE	kidney:	n/a
49	chr9:26761746-26761796	H1-hESC	embryonic stem cell:	embryo
50	chr9:26761746-26761796	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:26744169..26744992-chr9:26856156..26857045,4	MCF-7	breast:
2	chr9:26722378..26723174-chr9:26856170..26856819,2	MCF-7	breast:
3	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
4	chr9:26744529..26745078-chr9:26976174..26976879,2	K562	blood:
5	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
6	chr9:26744400..26745094-chr9:26856160..26856966,3	MCF-7	breast:
7	chr9:26758275..26760056-chr9:26761242..26763572,2	K562	blood:
8	chr9:26744400..26745007-chr9:26975049..26975918,2	MCF-7	breast:
9	chr9:26762229..26764985-chr9:26768189..26769709,2	MCF-7	breast:
10	chr9:26745009..26745599-chr9:26856133..26856633,2	MCF-7	breast:
11	chr9:26762229..26764985-chr9:26768189..26769709,2	MCF-7	breast:
12	chr9:26751819..26753348-chr9:26754776..26757194,2	MCF-7	breast:
13	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:
14	chr9:26697199..26699954-chr9:26703852..26705743,2	K562	blood:
15	chr9:26723206..26723920-chr9:26975181..26975897,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf82-3	chr9:26642695-26644593	NONHSAT130585
2	lnc-C9orf82-1	chr9:26716406-26716605	XLOC_007661
3	lnc-C9orf82-1	chr9:26718906-26718917	XLOC_007661

Variant related genes	Relation type
ENSG00000266429	TF binding region
ENSG00000254261	TF binding region
ENSG00000266429	CpG island
ENSG00000254261	CpG island
ENSG00000096872	chromatin interactions

Extended variants
information (count: 4245 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:4245 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561256384	chr9:26613835-26613836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367858548	chr9:26613852-26613853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191405092	chr9:26613855-26613856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147369654	chr9:26613865-26613866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559534872	chr9:26613872-26613873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532972748	chr9:26613895-26613896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147984128	chr9:26613926-26613927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563725408	chr9:26613927-26613928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528824114	chr9:26613928-26613929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530938058	chr9:26613950-26613951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549360779	chr9:26613980-26613981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143466056	chr9:26614161-26614162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs577771109	chr9:26614230-26614231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs545183692	chr9:26614238-26614239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs563785270	chr9:26614286-26614287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs377668942	chr9:26614310-26614311	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201645244	chr9:26614314-26614315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs530997519	chr9:26614322-26614323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs146251322	chr9:26614323-26614324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs113742282	chr9:26614371-26614372	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528473845	chr9:26614405-26614406	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs139273104	chr9:26614426-26614427	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183113310	chr9:26614438-26614439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs12555809	chr9:26614446-26614447	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550736872	chr9:26614463-26614464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs7035373	chr9:26614473-26614474	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs116644499	chr9:26614807-26614808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188603315	chr9:26614812-26614813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543191974	chr9:26614835-26614836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561179677	chr9:26614841-26614842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10812428	chr9:26614847-26614848	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
32	rs142295439	chr9:26614863-26614864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565596398	chr9:26614871-26614872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192836239	chr9:26614888-26614889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75624983	chr9:26614923-26614924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs151244593	chr9:26614926-26614927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554987290	chr9:26614943-26614944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530227330	chr9:26614976-26614977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557171429	chr9:26615074-26615075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567207304	chr9:26615082-26615083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141890244	chr9:26615107-26615108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552665905	chr9:26615108-26615109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76081970	chr9:26615149-26615150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13286676	chr9:26615220-26615221	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs182959071	chr9:26615237-26615238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374550965	chr9:26615293-26615294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368788962	chr9:26615306-26615307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555062338	chr9:26615355-26615356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376706703	chr9:26615373-26615374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573229306	chr9:26615385-26615386	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
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
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
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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26613800-26614000	Enhancers	Lung	lung
2	chr9:26614800-26615400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:26615200-26615800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr9:26615200-26616000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr9:26615200-26616000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr9:26615400-26620600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr9:26620000-26621400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:26620400-26621200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:26620600-26621200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:26620800-26621000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:26620800-26621200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr9:26620800-26621200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr9:26624000-26624800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:26635600-26639200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:26636200-26636600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr9:26636200-26636600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:26636200-26637000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:26636200-26638200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:26636400-26638200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
20	chr9:26636400-26638200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:26636400-26638400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
22	chr9:26636600-26636800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
23	chr9:26636600-26637000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:26636600-26637200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr9:26636600-26637400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr9:26636600-26637400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr9:26636600-26637600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr9:26636600-26637800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr9:26636800-26637200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
30	chr9:26636800-26637200	Enhancers	Brain Germinal Matrix	brain
31	chr9:26636800-26637800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
32	chr9:26636800-26638200	Enhancers	H9 Cell Line	embryonic stem cell
33	chr9:26637200-26637400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr9:26637400-26638000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
35	chr9:26637600-26637800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr9:26637600-26638000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr9:26637800-26638000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr9:26637800-26638200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
39	chr9:26638000-26638200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
40	chr9:26638400-26640400	Enhancers	Fetal Lung	lung
41	chr9:26640400-26641200	Weak transcription	Fetal Lung	lung
42	chr9:26641200-26641400	Enhancers	Fetal Lung	lung
43	chr9:26641800-26642600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr9:26642000-26642400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr9:26642200-26642400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr9:26642400-26642600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr9:26649800-26650400	Enhancers	Brain Substantia Nigra	brain
48	chr9:26650200-26650800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr9:26656000-26656200	Enhancers	Brain Cingulate Gyrus	brain
50	chr9:26656000-26656400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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