Variant report

Variant	nsv892839
Chromosome Location	chr9:25750661-26050209
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	chr9:25964175-25964579	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr9:25964148-25964571	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr9:25876386-25876471	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr9:25830650-25830668	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr9:25761278-25761303	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:25917593-25918410	Hela-S3	cervix:	n/a	chr9:25918064-25918073 chr9:25918062-25918073 chr9:25918062-25918075 chr9:25918064-25918075 chr9:25918062-25918075 chr9:25918064-25918073 chr9:25918064-25918073 chr9:25918064-25918073
7	CEBPB	chr9:25763645-25763886	H1-hESC	embryonic stem cell:	n/a	chr9:25763776-25763787
8	CEBPB	chr9:25763626-25763962	IMR90	lung:	n/a	chr9:25763776-25763787
9	CEBPB	chr9:25783879-25784164	IMR90	lung:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
10	CEBPB	chr9:25848385-25848609	A549	lung:	n/a	chr9:25848536-25848547
11	CEBPB	chr9:25917894-25918212	A549	lung:	n/a	chr9:25918064-25918075 chr9:25918064-25918073 chr9:25918062-25918073 chr9:25918062-25918075 chr9:25918064-25918073 chr9:25918064-25918073 chr9:25918062-25918075 chr9:25918064-25918073
12	CEBPB	chr9:26033374-26033757	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr9:25892564-25892852	HepG2	liver:	n/a	chr9:25892682-25892693
14	CEBPB	chr9:25892638-25892790	IMR90	lung:	n/a	chr9:25892682-25892693
15	CEBPB	chr9:25761129-25761425	HepG2	liver:	n/a	chr9:25761277-25761288
16	CEBPB	chr9:25848391-25848698	IMR90	lung:	n/a	chr9:25848536-25848547
17	CEBPB	chr9:26043279-26043364	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:25892598-25892761	A549	lung:	n/a	chr9:25892682-25892693
19	CEBPB	chr9:26043027-26043292	HepG2	liver:	n/a	chr9:26043178-26043187 chr9:26043178-26043187 chr9:26043177-26043188 chr9:26043176-26043189 chr9:26043176-26043189 chr9:26043178-26043187 chr9:26043176-26043187 chr9:26043178-26043187
20	CEBPB	chr9:25917911-25918227	IMR90	lung:	n/a	chr9:25918064-25918073 chr9:25918062-25918073 chr9:25918062-25918075 chr9:25918064-25918075 chr9:25918062-25918075 chr9:25918064-25918073 chr9:25918064-25918073 chr9:25918064-25918073
21	CEBPB	chr9:25763598-25763944	HepG2	liver:	n/a	chr9:25763776-25763787
22	CEBPB	chr9:25827119-25827255	HepG2	liver:	n/a	chr9:25827176-25827187
23	CEBPB	chr9:25763654-25763950	A549	lung:	n/a	chr9:25763776-25763787
24	CEBPB	chr9:26038618-26038757	A549	lung:	n/a	n/a
25	CEBPB	chr9:25848509-25848579	H1-hESC	embryonic stem cell:	n/a	chr9:25848536-25848547
26	CEBPB	chr9:25783890-25784164	HepG2	liver:	n/a	chr9:25784053-25784064 chr9:25784055-25784064
27	CEBPB	chr9:25848401-25848676	HepG2	liver:	n/a	chr9:25848536-25848547
28	CEBPB	chr9:26038708-26038740	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:25861448-25861639	HepG2	liver:	n/a	chr9:25861567-25861578
30	CEBPB	chr9:26038647-26038850	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:25917881-25918235	HepG2	liver:	n/a	chr9:25918064-25918073 chr9:25918062-25918073 chr9:25918062-25918075 chr9:25918064-25918075 chr9:25918062-25918075 chr9:25918064-25918073 chr9:25918064-25918073 chr9:25918064-25918073
32	CTCF	chr9:25964216-25964577	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr9:25964280-25964430	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr9:25964216-25964453	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr9:25964320-25964470	HCT-116	colon:	n/a	n/a
36	CTCF	chr9:25964320-25964470	HVMF	connective:	n/a	n/a
37	CTCF	chr9:26002162-26002228	GM13976	blood:	n/a	n/a
38	CTCF	chr9:25964260-25964410	HCM	heart:	n/a	n/a
39	CTCF	chr9:25964224-25964503	NHEK	skin:	n/a	n/a
40	CTCF	chr9:25964300-25964450	HL-60	blood:	n/a	n/a
41	CTCF	chr9:25964300-25964450	GM12874	blood:	n/a	n/a
42	CTCF	chr9:25964189-25964572	ECC-1	luminal epithelium:	n/a	n/a
43	CTCF	chr9:25964260-25964410	HPF	lung:	n/a	n/a
44	CTCF	chr9:25964320-25964470	BJ	skin:	n/a	n/a
45	CTCF	chr9:25964280-25964430	HCFaa	heart:	n/a	n/a
46	CTCF	chr9:25964280-25964430	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr9:25964200-25964350	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr9:25964280-25964430	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:25964287-25964480	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:25772140-25772290	GM12872	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:25964124..25964728-chr9:26326171..26327079,3	MCF-7	breast:
2	chr9:25963971..25964744-chr9:26326247..26327016,2	MCF-7	breast:
3	chr9:25677479..25679226-chr9:25880720..25882284,2	MCF-7	breast:
4	chr9:25677137..25679533-chr9:25758553..25761140,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFT74-8	chr9:25774413-25774560	NONHSAT130502
2	lnc-IFT74-8	chr9:25770054-25770166	NONHSAT130502
3	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
4	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
5	lnc-IFT74-3	chr9:25798032-25798204	NONHSAT130503
6	lnc-IFT74-3	chr9:25798032-25798205	XLOC_007306
7	lnc-IFT74-8	chr9:25774413-25774614	ucscGeneNc_uc003zpy_2
8	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
9	lnc-IFT74-8	chr9:25788032-25788204	ucscGeneNc_uc003zpy_2
10	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
11	lnc-IFT74-3	chr9:25780414-25780615	NONHSAT130503
12	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
13	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
14	lnc-IFT74-3	chr9:25812619-25812942	XLOC_007306
15	lnc-IFT74-3	chr9:25780054-25780166	NONHSAT130503
16	lnc-IFT74-3	chr9:25798743-25798941	NONHSAT130503
17	lnc-IFT74-3	chr9:25784413-25784614	NONHSAT130503
18	lnc-IFT74-8	chr9:25770054-25770166	ucscGeneNc_uc003zpy_2
19	lnc-IFT74-8	chr9:25802619-25802963	ucscGeneNc_uc003zpy_2
20	lnc-IFT74-3	chr9:25806594-25806736	XLOC_007306
21	lnc-IFT74-3	chr9:25780075-25780166	XLOC_007306
22	lnc-IFT74-3	chr9:25812619-25812966	NONHSAT130503
23	lnc-IFT74-8	chr9:25770414-25770615	ucscGeneNc_uc003zpy_2
24	lnc-IFT74-7	chr9:25937910-25938432	NONHSAT130507
25	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
26	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
27	lnc-IFT74-8	chr9:25770414-25770615	NONHSAT130502
28	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
29	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
30	lnc-IFT74-3	chr9:25780414-25780615	XLOC_007306
31	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
32	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
33	lnc-IFT74-8	chr9:25788743-25788941	ucscGeneNc_uc003zpy_2
34	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
35	lnc-IFT74-3	chr9:25784413-25784614	XLOC_007306
36	lnc-IFT74-3	chr9:25798743-25798941	XLOC_007306
37	lnc-IFT74-3	chr9:25806693-25806736	XLOC_007306
38	lnc-IFT74-3	chr9:25804154-25804257	XLOC_007306
39	lnc-IFT74-3	chr9:25784413-25784560	XLOC_007306
40	lnc-IFT74-3	chr9:25802427-25802517	XLOC_007306
41	lnc-IFT74-3	chr9:25798032-25798204	XLOC_007306
42	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
43	lnc-IFT74-3	chr9:25780054-25780166	XLOC_007306
44	lnc-IFT74-3	chr9:25812619-25812963	XLOC_007306

Variant related genes	Relation type
ENSG00000236306	TF binding region
ENSG00000270683	TF binding region
ENSG00000198680	chromatin interactions
ARID5B	miRNA target sites
FBXW7	miRNA target sites
PRPF38B	miRNA target sites
PDE4D	miRNA target sites
DEPDC1	miRNA target sites
RNF182	miRNA target sites
FAM49B	miRNA target sites

Extended variants
information (count: 3327 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3327 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543282410	chr9:25752000-25752001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532507341	chr9:25752013-25752014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544632313	chr9:25752088-25752089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183584396	chr9:25752144-25752145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562941183	chr9:25752153-25752154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530240501	chr9:25752166-25752167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572106382	chr9:25752175-25752176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548479660	chr9:25752192-25752193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567100693	chr9:25752239-25752240	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527884817	chr9:25752282-25752283	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1231362	chr9:25752310-25752311	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191033863	chr9:25752317-25752318	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1231363	chr9:25752318-25752319	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs62531875	chr9:25752373-25752374	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146767998	chr9:25752377-25752378	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140331189	chr9:25752388-25752389	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536389920	chr9:25752389-25752390	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180769455	chr9:25752391-25752392	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs572943590	chr9:25752414-25752415	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs540060642	chr9:25752437-25752438	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558855155	chr9:25752446-25752447	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs73644586	chr9:25752492-25752493	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs544593834	chr9:25752513-25752514	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs118185318	chr9:25752529-25752530	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs185262903	chr9:25752530-25752531	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142630764	chr9:25752535-25752536	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370090348	chr9:25752537-25752538	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs560393083	chr9:25752581-25752582	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs199581759	chr9:25752582-25752583	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs527854063	chr9:25752606-25752607	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552377970	chr9:25752639-25752640	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34455010	chr9:25752640-25752641	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531918372	chr9:25752666-25752667	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1231364	chr9:25752686-25752687	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs73644587	chr9:25752694-25752695	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535870569	chr9:25752732-25752733	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1231365	chr9:25752734-25752735	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs190075250	chr9:25752771-25752772	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533959246	chr9:25752773-25752774	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561828430	chr9:25754800-25754801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529047513	chr9:25754808-25754809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181685012	chr9:25754816-25754817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185408169	chr9:25754829-25754830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533093440	chr9:25754839-25754840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17369639	chr9:25754840-25754841	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569762920	chr9:25754877-25754878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537457400	chr9:25754883-25754884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555537879	chr9:25754922-25754923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567768988	chr9:25754925-25754926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369479440	chr9:25754926-25754927	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Cancer	22183965	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
Adenoid cystic carcinoma	18332873	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
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	21811587	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:139 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:25752000-25752200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr9:25752000-25752400	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr9:25752200-25752600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:25752400-25752600	Enhancers	Colon Smooth Muscle	Colon
5	chr9:25752400-25752800	Enhancers	Brain Angular Gyrus	brain
6	chr9:25752400-25752800	Active TSS	Brain Cingulate Gyrus	brain
7	chr9:25752400-25752800	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr9:25752400-25752800	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr9:25752400-25752800	Active TSS	Ovary	ovary
10	chr9:25752600-25752800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr9:25754800-25755600	Enhancers	Fetal Stomach	stomach
12	chr9:25756200-25756800	Enhancers	Fetal Brain Male	brain
13	chr9:25758000-25758200	Enhancers	Gastric	stomach
14	chr9:25763600-25764000	ZNF genes & repeats	Pancreas	Pancrea
15	chr9:25764000-25764400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr9:25773800-25774400	Enhancers	Fetal Stomach	stomach
17	chr9:25798800-25799000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:25802400-25803400	Enhancers	Stomach Mucosa	stomach
19	chr9:25803000-25803400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr9:25803200-25805600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:25803400-25804000	Weak transcription	Stomach Mucosa	stomach
22	chr9:25803400-25807000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr9:25804200-25804400	Enhancers	Stomach Mucosa	stomach
24	chr9:25804400-25805600	Enhancers	Fetal Lung	lung
25	chr9:25805800-25806400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr9:25807000-25807200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr9:25837200-25837600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr9:25844600-25844800	Enhancers	Lung	lung
29	chr9:25844800-25845200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:25844800-25845200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:25844800-25845200	Flanking Active TSS	Lung	lung
32	chr9:25846400-25847000	Enhancers	Ovary	ovary
33	chr9:25846400-25847200	Enhancers	Adipose Nuclei	Adipose
34	chr9:25851600-25854000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr9:25853800-25854400	Enhancers	Hela-S3	cervix
36	chr9:25862800-25864400	Enhancers	HUVEC	blood vessel
37	chr9:25864400-25865000	Flanking Active TSS	HUVEC	blood vessel
38	chr9:25864600-25865200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr9:25865000-25865600	Enhancers	HUVEC	blood vessel
40	chr9:25865800-25866200	Active TSS	Fetal Heart	heart
41	chr9:25875800-25883600	Weak transcription	HUVEC	blood vessel
42	chr9:25876200-25877200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:25883600-25884800	Enhancers	HUVEC	blood vessel
44	chr9:25889400-25889800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr9:25891600-25892200	Enhancers	Fetal Muscle Leg	muscle
46	chr9:25891800-25892200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:25892200-25892600	Enhancers	Fetal Brain Male	brain
48	chr9:25904200-25904600	Active TSS	Fetal Heart	heart
49	chr9:25904400-25905000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr9:25914800-25915000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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