Variant report

Variant	nsv892860
Chromosome Location	chr9:26704385-26789940
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	chr9:26746311-26747148	GM12878	blood:	n/a	n/a
5	BACH1	chr9:26746447-26747018	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:26746185-26747145	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:26779130-26779354	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr9:26746522-26747086	HCT-116	colon:	n/a	n/a
9	CBX3	chr9:26746383-26747096	HCT-116	colon:	n/a	n/a
10	CEBPB	chr9:26772178-26772489	IMR90	lung:	n/a	chr9:26772321-26772332
11	CEBPB	chr9:26727899-26727940	H1-hESC	embryonic stem cell:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
12	CEBPB	chr9:26779098-26779379	A549	lung:	n/a	chr9:26779217-26779228
13	CEBPB	chr9:26727783-26728067	IMR90	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
14	CEBPB	chr9:26779131-26779393	HepG2	liver:	n/a	chr9:26779217-26779228
15	CEBPB	chr9:26772174-26772358	HepG2	liver:	n/a	chr9:26772321-26772332
16	CEBPB	chr9:26723563-26723907	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:26737005-26737170	A549	lung:	n/a	n/a
18	CEBPB	chr9:26727767-26728072	HepG2	liver:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
19	CEBPB	chr9:26779021-26779569	HCT-116	colon:	n/a	chr9:26779217-26779228
20	CEBPB	chr9:26723709-26723857	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:26747699-26748040	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr9:26727788-26728098	A549	lung:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
23	CEBPB	chr9:26746742-26746968	MCF-7	breast:	n/a	n/a
24	CEBPB	chr9:26723642-26723933	MCF-7	breast:	n/a	n/a
25	CEBPB	chr9:26727749-26728064	K562	blood:	n/a	chr9:26727923-26727936 chr9:26727923-26727934 chr9:26727923-26727936
26	CEBPB	chr9:26779040-26779491	Hela-S3	cervix:	n/a	chr9:26779217-26779228
27	CEBPB	chr9:26778913-26779621	HCT-116	colon:	n/a	chr9:26779217-26779228
28	CHD1	chr9:26746419-26746824	GM12878	blood:	n/a	n/a
29	CHD2	chr9:26748166-26748203	HepG2	liver:	n/a	n/a
30	CHD2	chr9:26746691-26747084	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:26723518-26723804	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr9:26723554-26723861	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr9:26723580-26723730	A549	lung:	n/a	n/a
34	CTCF	chr9:26723600-26723750	NHEK	skin:	n/a	n/a
35	CTCF	chr9:26744500-26744650	NHEK	skin:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
36	CTCF	chr9:26717480-26717630	BE2_C	brain:	n/a	n/a
37	CTCF	chr9:26723470-26723890	GM12878	blood:	n/a	n/a
38	CTCF	chr9:26723535-26723869	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr9:26723680-26723830	AG04450	lung:	n/a	n/a
40	CTCF	chr9:26744376-26744612	A549	lung:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
41	CTCF	chr9:26723547-26723827	GM19240	blood:	n/a	n/a
42	CTCF	chr9:26744500-26744650	GM12865	blood:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
43	CTCF	chr9:26748540-26748690	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr9:26744840-26744990	GM12868	blood:	n/a	n/a
45	CTCF	chr9:26723520-26723670	WI-38	lung:	n/a	n/a
46	CTCF	chr9:26744480-26744630	HEK293	kidney:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
47	CTCF	chr9:26723380-26723530	HFF	foreskin:	n/a	n/a
48	CTCF	chr9:26723600-26723750	GM12874	blood:	n/a	n/a
49	CTCF	chr9:26744500-26744650	WI-38	lung:	n/a	chr9:26744556-26744574 chr9:26744559-26744568 chr9:26744559-26744572 chr9:26744561-26744571
50	CTCF	chr9:26717520-26717670	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26722560-26722610	HRE	kidney:	n/a
2	chr9:26722560-26722610	HRCEpiC	kidney:	n/a
3	chr9:26722560-26722610	HEK293	kidney:	embryo
4	chr9:26722560-26722610	LNCaP	prostate:	n/a
5	chr9:26722560-26722610	AG09309	skin:	n/a
6	chr9:26761746-26761796	AoSMC	blood vessel:	n/a
7	chr9:26761746-26761796	AG09309	skin:	n/a
8	chr9:26722560-26722610	AG09319	gingival:	n/a
9	chr9:26722560-26722610	PrEC	prostate:	n/a
10	chr9:26761746-26761796	Hela-S3	cervix:	n/a
11	chr9:26761746-26761796	HCM	heart:	n/a
12	chr9:26722560-26722610	HMEC	breast:	n/a
13	chr9:26761746-26761796	HRPEpiC	eye:	n/a
14	chr9:26722560-26722610	SK-N-SH_RA	brain:	n/a
15	chr9:26761746-26761796	Caco-2	colon:	n/a
16	chr9:26722560-26722610	Hepatocyte	liver:	n/a
17	chr9:26722560-26722610	ECC-1	luminal epithelium:	n/a
18	chr9:26722560-26722610	GM12878	blood:	n/a
19	chr9:26761746-26761796	GM12892	blood:	n/a
20	chr9:26761746-26761796	T-47D	breast:	n/a
21	chr9:26722560-26722610	HepG2	liver:	n/a
22	chr9:26722560-26722610	GM06990	blood:	n/a
23	chr9:26761746-26761796	GM19239	blood:	n/a
24	chr9:26761746-26761796	IMR90	lung:	fetal
25	chr9:26722560-26722610	NB4	blood:	n/a
26	chr9:26722560-26722610	H1-hESC	embryonic stem cell:	embryo
27	chr9:26722560-26722610	HEEpiC	esophagus:	n/a
28	chr9:26722560-26722610	SK-N-SH	brain:	n/a
29	chr9:26722560-26722610	GM19239	blood:	n/a
30	chr9:26722560-26722610	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:26761746-26761796	NHBE	bronchial:	n/a
32	chr9:26722560-26722610	CMK	blood:	n/a
33	chr9:26761746-26761796	AG09319	gingival:	n/a
34	chr9:26722560-26722610	HAEpiC	amniotic membrane:	n/a
35	chr9:26722560-26722610	GM12892	blood:	n/a
36	chr9:26761746-26761796	HRCEpiC	kidney:	n/a
37	chr9:26722560-26722610	NHBE	bronchial:	n/a
38	chr9:26722560-26722610	SAEC	small airway:	n/a
39	chr9:26761746-26761796	ovcar-3	ovarian:	n/a
40	chr9:26722560-26722610	MCF10A-Er-Src	breast:	n/a
41	chr9:26761746-26761796	SK-N-MC	brain:	n/a
42	chr9:26761746-26761796	HepG2	liver:	n/a
43	chr9:26761746-26761796	K562	blood:	n/a
44	chr9:26761746-26761796	PrEC	prostate:	n/a
45	chr9:26761746-26761796	SK-N-SH	brain:	n/a
46	chr9:26761746-26761796	H1-hESC	embryonic stem cell:	embryo
47	chr9:26761746-26761796	AG10803	skin:	n/a
48	chr9:26761746-26761796	HUVEC	blood vessel:	n/a
49	chr9:26722560-26722610	NH-A	brain:	n/a
50	chr9:26722560-26722610	NHDF-neo	bronchial:	n/a

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

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

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

Extended variants
information (count: 2353 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12115568	chr9:26706212-26706213	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137996631	chr9:26706221-26706222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149476126	chr9:26706249-26706250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550799415	chr9:26706270-26706271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10115168	chr9:26706278-26706279	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560128916	chr9:26708014-26708015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371497218	chr9:26708015-26708016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374937252	chr9:26708019-26708020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73425876	chr9:26708056-26708057	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145633379	chr9:26708074-26708075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528287152	chr9:26708130-26708131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549926144	chr9:26708162-26708163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367790816	chr9:26708182-26708183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531008156	chr9:26708242-26708243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116683557	chr9:26708273-26708274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548069217	chr9:26708302-26708303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566307566	chr9:26708310-26708311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs114353451	chr9:26708355-26708356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34251528	chr9:26708387-26708388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569471178	chr9:26708389-26708390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577036293	chr9:26708416-26708417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537894519	chr9:26708482-26708483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555896639	chr9:26708517-26708518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116467031	chr9:26708556-26708557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115866571	chr9:26708578-26708579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554012660	chr9:26708580-26708581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534560509	chr9:26712013-26712014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545119289	chr9:26712053-26712054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563219947	chr9:26712075-26712076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530591710	chr9:26712109-26712110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542276460	chr9:26712112-26712113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371414562	chr9:26712174-26712175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560816952	chr9:26712249-26712250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143699365	chr9:26712269-26712270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546907273	chr9:26712300-26712301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146829184	chr9:26712342-26712343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34836868	chr9:26712486-26712487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532323424	chr9:26712488-26712489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550717108	chr9:26712523-26712524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562166370	chr9:26712553-26712554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187414006	chr9:26712571-26712572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536703807	chr9:26712615-26712616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190679805	chr9:26712639-26712640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139605179	chr9:26712664-26712665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116152820	chr9:26712710-26712711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115036309	chr9:26712732-26712733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116648447	chr9:26712781-26712782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538068772	chr9:26712788-26712789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs36002225	chr9:26713011-26713012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11790418	chr9:26713012-26713013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26706200-26706400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:26708000-26708400	Enhancers	Small Intestine	intestine
3	chr9:26708000-26708400	Enhancers	Stomach Mucosa	stomach
4	chr9:26708200-26708600	Enhancers	Duodenum Mucosa	Duodenum
5	chr9:26712000-26712800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:26713000-26714800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:26715000-26715200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:26715200-26716400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr9:26715200-26720400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:26715800-26716400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:26718600-26719000	Active TSS	Aorta	Aorta
12	chr9:26720400-26720600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr9:26720600-26726600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr9:26721600-26723400	Enhancers	Brain Germinal Matrix	brain
15	chr9:26722200-26723000	Enhancers	Fetal Lung	lung
16	chr9:26722200-26723600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:26722200-26723800	Enhancers	Duodenum Mucosa	Duodenum
18	chr9:26722400-26723000	Enhancers	Fetal Brain Female	brain
19	chr9:26722400-26723400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr9:26722600-26722800	Enhancers	Fetal Stomach	stomach
21	chr9:26722600-26723000	Bivalent Enhancer	Brain Hippocampus Middle	brain
22	chr9:26722800-26723000	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr9:26722800-26723200	Enhancers	Brain Anterior Caudate	brain
24	chr9:26722800-26723600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr9:26723000-26723400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr9:26723000-26723400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:26723000-26723400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr9:26723000-26723800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
29	chr9:26723000-26723800	Active TSS	Fetal Brain Female	brain
30	chr9:26723000-26724000	Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr9:26723200-26723400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:26723200-26723600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr9:26723200-26723600	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr9:26723200-26723600	Active TSS	Fetal Kidney	kidney
35	chr9:26723200-26723800	Active TSS	Brain Anterior Caudate	brain
36	chr9:26723200-26723800	Active TSS	Brain Inferior Temporal Lobe	brain
37	chr9:26723400-26723600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr9:26723400-26723600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr9:26723400-26723600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:26723400-26723800	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr9:26723400-26723800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr9:26723400-26723800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:26723400-26723800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:26723400-26723800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr9:26723400-26723800	Active TSS	Brain Germinal Matrix	brain
46	chr9:26723400-26723800	Flanking Bivalent TSS/Enh	A549	lung
47	chr9:26723400-26724000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr9:26723400-26724000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr9:26723600-26723800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:26723600-26723800	Active TSS	HUES6 Cell Line	embryonic stem cell

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