Variant report

Variant	esv3440051
Chromosome Location	chr9:26892073-26892416
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:585)
CpG islands
(count:62)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:26892177-26893347	K562	blood:	n/a	n/a
2	ARID3A	chr9:26892213-26892999	HepG2	liver:	n/a	n/a
3	ATF1	chr9:26892115-26893225	K562	blood:	n/a	n/a
4	ATF2	chr9:26892013-26893122	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:26892198-26893098	GM12878	blood:	n/a	n/a
6	ATF3	chr9:26892257-26893018	A549	lung:	n/a	chr9:26892808-26892822
7	BACH1	chr9:26892276-26892919	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr9:26892270-26893005	GM12878	blood:	n/a	chr9:26892820-26892829
9	BCL3	chr9:26892108-26893104	A549	lung:	n/a	chr9:26892820-26892829
10	BCLAF1	chr9:26892105-26893182	GM12878	blood:	n/a	chr9:26892820-26892829
11	BCLAF1	chr9:26892196-26893074	GM12878	blood:	n/a	chr9:26892820-26892829
12	BHLHE40	chr9:26892236-26893061	K562	blood:	n/a	n/a
13	BHLHE40	chr9:26892227-26893079	HepG2	liver:	n/a	n/a
14	BHLHE40	chr9:26892210-26893289	GM12878	blood:	n/a	n/a
15	BRCA1	chr9:26892062-26892479	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr9:26892303-26892816	GM12878	blood:	n/a	n/a
17	BRCA1	chr9:26892305-26893025	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr9:26892240-26892960	K562	blood:	n/a	n/a
19	CEBPB	chr9:26892142-26892457	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:26892171-26893136	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:26892219-26893166	GM12878	blood:	n/a	n/a
22	CHD1	chr9:26892031-26893555	GM12878	blood:	n/a	n/a
23	CHD1	chr9:26891432-26893429	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr9:26892142-26893323	GM12878	blood:	n/a	n/a
25	CHD2	chr9:26892291-26892999	HepG2	liver:	n/a	n/a
26	CHD2	chr9:26892305-26893018	K562	blood:	n/a	n/a
27	CHD2	chr9:26892168-26893460	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr9:26892086-26893173	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr9:26892263-26893110	K562	blood:	n/a	n/a
30	CREB1	chr9:26892169-26893102	GM12878	blood:	n/a	n/a
31	CREB1	chr9:26892204-26893026	A549	lung:	n/a	n/a
32	CREB1	chr9:26892185-26893147	HepG2	liver:	n/a	n/a
33	CREB1	chr9:26892196-26893224	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr9:26892076-26893201	HepG2	liver:	n/a	n/a
35	CREB1	chr9:26891666-26893298	GM12878	blood:	n/a	n/a
36	CREB1	chr9:26892168-26893085	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr9:26892060-26892210	AG04450	lung:	n/a	n/a
38	CTCF	chr9:26892300-26892450	K562	blood:	n/a	n/a
39	CTCF	chr9:26892320-26892470	HPF	lung:	n/a	n/a
40	CTCF	chr9:26892266-26892553	GM12891	blood:	n/a	n/a
41	CTCF	chr9:26892320-26892470	NHEK	skin:	n/a	n/a
42	CTCF	chr9:26892290-26892517	NHEK	skin:	n/a	n/a
43	CTCF	chr9:26892320-26892470	HMEC	breast:	n/a	n/a
44	CTCF	chr9:26892340-26892490	GM12872	blood:	n/a	n/a
45	CTCF	chr9:26892320-26892470	HMF	breast:	n/a	n/a
46	CTCF	chr9:26892280-26892430	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr9:26892300-26892450	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr9:26892255-26892538	GM12892	blood:	n/a	n/a
49	CTCF	chr9:26892291-26892493	GM10248	blood:	n/a	n/a
50	CTCF	chr9:26892320-26892470	HCPEpiC	choroid plexus:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:26892069-26892119	NHDF-neo	bronchial:	n/a
2	chr9:26892069-26892119	NHDF-neo	bronchial:	n/a
3	chr9:26892069-26892119	NB4	blood:	n/a
4	chr9:26892069-26892119	NH-A	brain:	n/a
5	chr9:26892069-26892119	GM06990	blood:	n/a
6	chr9:26892069-26892119	MCF-7	breast:	n/a
7	chr9:26892069-26892119	CMK	blood:	n/a
8	chr9:26892069-26892119	RPTEC	kidney:	n/a
9	chr9:26892069-26892119	BJ	skin:	n/a
10	chr9:26892069-26892119	HRPEpiC	eye:	n/a
11	chr9:26892069-26892119	HUVEC	blood vessel:	n/a
12	chr9:26892069-26892119	AG04449	skin:	fetal
13	chr9:26892069-26892119	GM19239	blood:	n/a
14	chr9:26892069-26892119	HepG2	liver:	n/a
15	chr9:26892069-26892119	A549	lung:	n/a
16	chr9:26892069-26892119	ovcar-3	ovarian:	n/a
17	chr9:26892069-26892119	ECC-1	luminal epithelium:	n/a
18	chr9:26892069-26892119	HIPEpiC	eye:	n/a
19	chr9:26892069-26892119	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:26892069-26892119	Jurkat	blood:	n/a
21	chr9:26892069-26892119	HL-60	blood:	n/a
22	chr9:26892069-26892119	GM12892	blood:	n/a
23	chr9:26892069-26892119	Caco-2	colon:	n/a
24	chr9:26892069-26892119	HEK293	kidney:	embryo
25	chr9:26892069-26892119	NHBE	bronchial:	n/a
26	chr9:26892069-26892119	HAEpiC	amniotic membrane:	n/a
27	chr9:26892069-26892119	NT2-D1	testis:	n/a
28	chr9:26892069-26892119	PANC-1	pancreas:	n/a
29	chr9:26892069-26892119	T-47D	breast:	n/a
30	chr9:26892069-26892119	HCT-116	colon:	n/a
31	chr9:26892069-26892119	SK-N-SH	brain:	n/a
32	chr9:26892069-26892119	Hela-S3	cervix:	n/a
33	chr9:26892069-26892119	U87	brain:	n/a
34	chr9:26892069-26892119	SK-N-SH_RA	brain:	n/a
35	chr9:26892069-26892119	BE2_C	brain:	n/a
36	chr9:26892069-26892119	AG10803	skin:	n/a
37	chr9:26892069-26892119	IMR90	lung:	fetal
38	chr9:26892069-26892119	SAEC	small airway:	n/a
39	chr9:26892069-26892119	HRCEpiC	kidney:	n/a
40	chr9:26892069-26892119	MCF10A-Er-Src	breast:	n/a
41	chr9:26892069-26892119	LNCaP	prostate:	n/a
42	chr9:26892069-26892119	HNPCEpiC	eye:	n/a
43	chr9:26892069-26892119	SK-N-MC	brain:	n/a
44	chr9:26892069-26892119	HCM	heart:	n/a
45	chr9:26892069-26892119	HMEC	breast:	n/a
46	chr9:26892069-26892119	GM12891	blood:	n/a
47	chr9:26892069-26892119	HCPEpiC	choroid plexus:	n/a
48	chr9:26892069-26892119	H1-hESC	embryonic stem cell:	embryo
49	chr9:26892069-26892119	AG04450	lung:	fetal
50	chr9:26892069-26892119	AG09319	gingival:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:26886338..26888156-chr9:26890310..26892766,2	MCF-7	breast:
2	chr9:26890972..26893985-chr9:26945405..26948624,3	MCF-7	breast:
3	chr9:26889862..26894629-chr9:26953159..26958871,9	K562	blood:
4	chr9:26891902..26893962-chr9:26955453..26958235,3	MCF-7	breast:
5	chr9:26891080..26894676-chr9:26945695..26949113,9	K562	blood:
6	chr9:26891080..26895841-chr9:26945501..26948974,8	K562	blood:
7	chr9:26891939..26894308-chr9:26895080..26897868,2	K562	blood:
8	chr9:26891289..26894164-chr9:26921199..26924471,3	MCF-7	breast:
9	chr9:26886474..26888568-chr9:26890678..26892880,3	MCF-7	breast:
10	chr12:39299074..39299955-chr9:26892301..26892993,2	Hela-S3	cervix:
11	chr9:26890425..26894629-chr9:26953159..26958312,6	K562	blood:
12	chr1:45195949..45196852-chr9:26892311..26892847,2	HCT-116	colon:
13	chr9:26892381..26894407-chr9:26894414..26897617,3	MCF-7	breast:
14	chr9:26890555..26892142-chr9:26919709..26921210,2	MCF-7	breast:
15	chr9:26886311..26888299-chr9:26891061..26892871,2	K562	blood:
16	chr9:26890485..26893190-chr9:26945159..26948755,7	MCF-7	breast:

No data

Variant related genes	Relation type
CAAP1	TF binding region
RN7SL100P	TF binding region
CAAP1	CpG island
RN7SL100P	CpG island
ENSG00000240306	chromatin interactions
ENSG00000120159	chromatin interactions
ENSG00000137055	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000096872	chromatin interactions
ENSG00000139117	chromatin interactions
ENSG00000234676	chromatin interactions

Extended variants
information (count: 31 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117832419	chr9:26892073-26892074	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs375458023	chr9:26892077-26892078	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs575214817	chr9:26892081-26892082	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs555243587	chr9:26892089-26892090	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs573640754	chr9:26892095-26892096	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs181081159	chr9:26892120-26892121	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs533475323	chr9:26892131-26892132	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs138901050	chr9:26892134-26892135	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs186319170	chr9:26892135-26892136	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs7860830	chr9:26892137-26892138	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544793652	chr9:26892146-26892147	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs563879903	chr9:26892151-26892152	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs575913972	chr9:26892152-26892153	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs543300508	chr9:26892158-26892159	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs200922414	chr9:26892182-26892183	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs191265248	chr9:26892183-26892184	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs527868063	chr9:26892199-26892200	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs546948722	chr9:26892214-26892215	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs565169101	chr9:26892218-26892219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs115704734	chr9:26892219-26892220	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs376246843	chr9:26892229-26892230	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs3739550	chr9:26892301-26892302	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs569464792	chr9:26892311-26892312	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs536839798	chr9:26892319-26892320	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs548812964	chr9:26892323-26892324	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs372929881	chr9:26892332-26892333	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs567398633	chr9:26892335-26892336	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs75519737	chr9:26892338-26892339	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs552901982	chr9:26892345-26892346	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs577590099	chr9:26892394-26892395	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs538682075	chr9:26892398-26892399	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	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
Epilepsy	22083797	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26883200-26892200	Weak transcription	Spleen	Spleen
2	chr9:26883400-26892200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:26888200-26893600	Active TSS	K562	blood
4	chr9:26890000-26893000	Active TSS	Hela-S3	cervix
5	chr9:26890200-26893400	Active TSS	Psoas Muscle	Psoas
6	chr9:26890200-26893600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr9:26890400-26894400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr9:26890600-26893000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:26890600-26893200	Active TSS	Fetal Intestine Large	intestine
10	chr9:26890600-26893200	Active TSS	A549	lung
11	chr9:26890600-26893600	Active TSS	Fetal Intestine Small	intestine
12	chr9:26890600-26893600	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr9:26890800-26892400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:26890800-26893000	Active TSS	Fetal Kidney	kidney
15	chr9:26890800-26893000	Active TSS	GM12878-XiMat	blood
16	chr9:26890800-26893200	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr9:26890800-26893200	Active TSS	Colonic Mucosa	Colon
18	chr9:26890800-26893200	Active TSS	Duodenum Mucosa	Duodenum
19	chr9:26890800-26893600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:26890800-26893600	Active TSS	HSMM	muscle
21	chr9:26891000-26892200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:26891000-26892400	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr9:26891000-26893000	Active TSS	Muscle Satellite Cultured Cells	--
24	chr9:26891000-26893000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:26891000-26893200	Active TSS	Aorta	Aorta
26	chr9:26891000-26893200	Active TSS	Fetal Stomach	stomach
27	chr9:26891000-26893200	Active TSS	Right Ventricle	heart
28	chr9:26891000-26893200	Active TSS	Thymus	Thymus
29	chr9:26891000-26893200	Active TSS	HSMMtube	muscle
30	chr9:26891000-26893400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr9:26891000-26893400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:26891000-26893400	Active TSS	Right Atrium	heart
33	chr9:26891000-26893600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr9:26891200-26892200	Flanking Active TSS	Primary T cells from cord blood	blood
35	chr9:26891200-26892600	Active TSS	Skeletal Muscle Female	skeletal muscle
36	chr9:26891200-26893000	Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr9:26891200-26893000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:26891200-26893000	Active TSS	Dnd41	blood
39	chr9:26891200-26893000	Active TSS	HMEC	breast
40	chr9:26891200-26893000	Active TSS	NHDF-Ad	bronchial
41	chr9:26891200-26893000	Active TSS	NHEK	skin
42	chr9:26891200-26893200	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr9:26891200-26893200	Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr9:26891200-26893200	Active TSS	Fetal Thymus	thymus
45	chr9:26891200-26893200	Active TSS	Rectal Mucosa Donor 31	rectum
46	chr9:26891200-26893400	Active TSS	H1 Cell Line	embryonic stem cell
47	chr9:26891200-26893400	Active TSS	Fetal Heart	heart
48	chr9:26891200-26893600	Active TSS	Brain Anterior Caudate	brain
49	chr9:26891200-26893600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr9:26891400-26892200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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