Variant report

Variant	nsv831505
Chromosome Location	chr9:9072216-9277320
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	CEBPB	chr9:9177863-9178135	HepG2	liver:	n/a	chr9:9177988-9177999
2	CEBPB	chr9:9184918-9185156	H1-hESC	embryonic stem cell:	n/a	chr9:9185056-9185069 chr9:9185058-9185069 chr9:9185058-9185067 chr9:9184998-9185011 chr9:9185056-9185067
3	CEBPB	chr9:9255418-9255716	HepG2	liver:	n/a	n/a
4	CEBPB	chr9:9174449-9174740	HepG2	liver:	n/a	chr9:9174591-9174600 chr9:9174590-9174601 chr9:9174656-9174669 chr9:9174589-9174602 chr9:9174589-9174600
5	CEBPB	chr9:9184992-9185148	IMR90	lung:	n/a	chr9:9185056-9185069 chr9:9185058-9185069 chr9:9185058-9185067 chr9:9184998-9185011 chr9:9185056-9185067
6	CEBPB	chr9:9219422-9219423	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:9097309-9097586	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr9:9191327-9191565	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:9174467-9174707	IMR90	lung:	n/a	chr9:9174591-9174600 chr9:9174590-9174601 chr9:9174656-9174669 chr9:9174589-9174602 chr9:9174589-9174600
10	CEBPB	chr9:9184906-9185209	HepG2	liver:	n/a	chr9:9185056-9185069 chr9:9185058-9185069 chr9:9185058-9185067 chr9:9184998-9185011 chr9:9185056-9185067
11	CEBPB	chr9:9162739-9163039	A549	lung:	n/a	n/a
12	CEBPB	chr9:9162786-9162996	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:9214265-9214465	HepG2	liver:	n/a	chr9:9214334-9214345
14	CEBPB	chr9:9177847-9178081	A549	lung:	n/a	chr9:9177988-9177999
15	CEBPB	chr9:9124942-9125086	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:9226676-9227019	HepG2	liver:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
17	CEBPB	chr9:9162739-9163026	IMR90	lung:	n/a	n/a
18	CEBPB	chr9:9226711-9226991	IMR90	lung:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
19	CEBPB	chr9:9226688-9226885	K562	blood:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
20	CEBPB	chr9:9162728-9163029	HepG2	liver:	n/a	n/a
21	CEBPB	chr9:9226707-9226943	A549	lung:	n/a	chr9:9226847-9226860 chr9:9226849-9226860 chr9:9226847-9226858
22	CTCF	chr9:9272828-9273086	GM12878	blood:	n/a	n/a
23	CTCF	chr9:9142030-9142310	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr9:9103876-9103932	Fibrobl	skin:	n/a	n/a
25	CTCF	chr9:9125540-9125690	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr9:9100479-9100522	K562	blood:	n/a	n/a
27	CTCF	chr9:9111980-9112130	GM12875	blood:	n/a	n/a
28	CTCF	chr9:9193713-9193786	GM10248	blood:	n/a	n/a
29	CTCF	chr9:9179580-9179730	AG10803	skin:	n/a	chr9:9179717-9179725
30	CTCF	chr9:9239680-9239830	WI-38	lung:	n/a	n/a
31	CTCF	chr9:9142160-9142310	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr9:9209942-9209998	Lung_OC	lung:	n/a	n/a
33	CTCF	chr9:9167565-9167588	Lung_OC	lung:	n/a	n/a
34	CTCF	chr9:9215100-9215250	HPF	lung:	n/a	n/a
35	CTCF	chr9:9133866-9133935	Lung_OC	lung:	n/a	n/a
36	CTCF	chr9:9142200-9142350	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr9:9126940-9126983	ProgFib	skin:	n/a	n/a
38	CTCF	chr9:9078440-9078590	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr9:9142185-9142330	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:9142206-9142328	Medullo	brain:	n/a	n/a
41	CTCF	chr9:9190557-9190582	LNCaP	prostate:	n/a	n/a
42	CTCF	chr9:9186301-9186336	GM12878	blood:	n/a	n/a
43	CTCF	chr9:9123240-9123390	NHLF	lung:	n/a	n/a
44	E2F4	chr9:9203843-9203929	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr9:9199402-9199663	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr9:9248595-9248706	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr9:9172070-9172270	MCF10A-Er-Src	breast:	n/a	chr9:9172074-9172083
48	E2F4	chr9:9083501-9083524	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr9:9220671-9220830	MCF10A-Er-Src	breast:	n/a	n/a
50	EP300	chr9:9250280-9250366	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:9091180-9091230	AG10803	skin:	n/a
2	chr9:9091180-9091230	PrEC	prostate:	n/a
3	chr9:9091180-9091230	GM06990	blood:	n/a
4	chr9:9091180-9091230	HRE	kidney:	n/a
5	chr9:9091180-9091230	ProgFib	skin:	n/a
6	chr9:9091180-9091230	NH-A	brain:	n/a
7	chr9:9091180-9091230	HNPCEpiC	eye:	n/a
8	chr9:9091180-9091230	NB4	blood:	n/a
9	chr9:9091180-9091230	AG09319	gingival:	n/a
10	chr9:9091180-9091230	LNCaP	prostate:	n/a
11	chr9:9091180-9091230	HEK293	kidney:	embryo
12	chr9:9091180-9091230	AoSMC	blood vessel:	n/a
13	chr9:9091180-9091230	NHDF-neo	bronchial:	n/a
14	chr9:9091180-9091230	PANC-1	pancreas:	n/a
15	chr9:9091180-9091230	BE2_C	brain:	n/a
16	chr9:9091180-9091230	K562	blood:	n/a
17	chr9:9091180-9091230	NHBE	bronchial:	n/a
18	chr9:9091180-9091230	AG04450	lung:	fetal
19	chr9:9091180-9091230	CMK	blood:	n/a
20	chr9:9091180-9091230	Hela-S3	cervix:	n/a
21	chr9:9091180-9091230	ECC-1	luminal epithelium:	n/a
22	chr9:9091180-9091230	HRCEpiC	kidney:	n/a
23	chr9:9091180-9091230	HMEC	breast:	n/a
24	chr9:9091180-9091230	Hepatocyte	liver:	n/a
25	chr9:9091180-9091230	HL-60	blood:	n/a
26	chr9:9091180-9091230	ovcar-3	ovarian:	n/a
27	chr9:9091180-9091230	NT2-D1	testis:	n/a
28	chr9:9091180-9091230	SAEC	small airway:	n/a
29	chr9:9091180-9091230	HCF	heart:	n/a
30	chr9:9091180-9091230	RPTEC	kidney:	n/a
31	chr9:9091180-9091230	MCF-7	breast:	n/a
32	chr9:9091180-9091230	T-47D	breast:	n/a
33	chr9:9091180-9091230	IMR90	lung:	fetal
34	chr9:9091180-9091230	SK-N-SH_RA	brain:	n/a
35	chr9:9091180-9091230	SK-N-SH	brain:	n/a
36	chr9:9091180-9091230	Jurkat	blood:	n/a
37	chr9:9091180-9091230	SKMC	muscle:	n/a
38	chr9:9091180-9091230	AG04449	skin:	fetal
39	chr9:9091180-9091230	MCF10A-Er-Src	breast:	n/a
40	chr9:9091180-9091230	HCM	heart:	n/a
41	chr9:9091180-9091230	GM12878	blood:	n/a
42	chr9:9091180-9091230	HEEpiC	esophagus:	n/a
43	chr9:9091180-9091230	HCPEpiC	choroid plexus:	n/a
44	chr9:9091180-9091230	HIPEpiC	eye:	n/a
45	chr9:9091180-9091230	GM12891	blood:	n/a
46	chr9:9091180-9091230	AG09309	skin:	n/a
47	chr9:9091180-9091230	HepG2	liver:	n/a
48	chr9:9091180-9091230	HUVEC	blood vessel:	n/a
49	chr9:9091180-9091230	H1-hESC	embryonic stem cell:	embryo
50	chr9:9091180-9091230	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:56434264..56436145-chr9:9090873..9092394,2	K562	blood:
2	chr9:9179702..9181500-chr9:9182795..9185230,2	K562	blood:
3	chr12:56435690..56436195-chr9:9090395..9091395,2	HCT-116	colon:
4	chr12:56435572..56436393-chr9:9090873..9091393,3	MCF-7	breast:
5	chr9:9128289..9130655-chr9:9131606..9133901,2	K562	blood:
6	chr9:9128289..9130655-chr9:9131606..9133901,2	K562	blood:
7	chr12:56434645..56437118-chr9:9089375..9092373,2	K562	blood:
8	chr12:56435752..56436286-chr9:9090373..9090875,2	MCF-7	breast:
9	chr9:9179702..9181500-chr9:9182795..9185230,2	K562	blood:

Variant related genes	Relation type
RPS26P3	TF binding region
RPS26P3	CpG island
ENSG00000257449	chromatin interactions
ENSG00000197728	chromatin interactions

Extended variants
information (count: 3157 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3157 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73641209	chr9:9077603-9077604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs324475	chr9:9077607-9077608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs574037323	chr9:9077689-9077690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541482717	chr9:9077758-9077759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543732969	chr9:9077801-9077802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs377724433	chr9:9077826-9077827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140207189	chr9:9077834-9077835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146969601	chr9:9077857-9077858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545331534	chr9:9077858-9077859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563564976	chr9:9077894-9077895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530566780	chr9:9077905-9077906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564811760	chr9:9077918-9077919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs137897690	chr9:9077942-9077943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141993882	chr9:9077970-9077971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79563006	chr9:9077992-9077993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541415849	chr9:9077997-9077998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76865358	chr9:9078013-9078014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561865979	chr9:9078016-9078017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539601219	chr9:9078034-9078035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12238667	chr9:9078128-9078129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs569996280	chr9:9078133-9078134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541259674	chr9:9078195-9078196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183731468	chr9:9078196-9078197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555494941	chr9:9078201-9078202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567624344	chr9:9078205-9078206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534812882	chr9:9078207-9078208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553392297	chr9:9078220-9078221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs324476	chr9:9078244-9078245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs117769545	chr9:9078285-9078286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557320571	chr9:9078286-9078287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575593748	chr9:9078308-9078309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188444518	chr9:9078315-9078316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146105954	chr9:9078326-9078327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528039827	chr9:9078334-9078335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533131077	chr9:9078336-9078337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564981351	chr9:9078377-9078378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533379579	chr9:9078402-9078403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563844616	chr9:9078416-9078417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138656641	chr9:9078434-9078435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181258282	chr9:9078451-9078452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550115766	chr9:9078456-9078457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535546259	chr9:9078457-9078458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531133675	chr9:9078465-9078466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549607483	chr9:9078469-9078470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567562215	chr9:9078516-9078517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535007950	chr9:9078541-9078542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185021143	chr9:9078547-9078548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553238130	chr9:9078551-9078552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190242820	chr9:9078567-9078568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538869783	chr9:9078589-9078590	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Disorders of sex development	21048976	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21080181	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
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	21251322	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:9077600-9080200	Enhancers	Fetal Heart	heart
2	chr9:9086400-9087000	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr9:9096800-9097200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:9096800-9097400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr9:9096800-9097400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr9:9096800-9097400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:9097000-9097200	Enhancers	Fetal Brain Female	brain
8	chr9:9097000-9097400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:9097000-9097400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr9:9097000-9097800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr9:9097200-9097400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr9:9097400-9104400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:9097400-9104600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr9:9098400-9098800	Weak transcription	Fetal Brain Female	brain
15	chr9:9098600-9099600	Enhancers	Fetal Brain Male	brain
16	chr9:9099000-9099400	Enhancers	Fetal Brain Female	brain
17	chr9:9099200-9100800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:9099400-9099600	Flanking Active TSS	Fetal Brain Female	brain
19	chr9:9099600-9099800	Active TSS	Fetal Brain Female	brain
20	chr9:9099600-9100400	Weak transcription	Fetal Brain Male	brain
21	chr9:9099800-9101400	Weak transcription	Fetal Brain Female	brain
22	chr9:9100400-9102400	Enhancers	Fetal Brain Male	brain
23	chr9:9100800-9101400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:9101400-9102000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr9:9101400-9103000	Enhancers	Fetal Brain Female	brain
26	chr9:9102000-9102800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:9102800-9103400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:9103400-9104400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:9104400-9105400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr9:9104400-9105600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:9104600-9104800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:9104800-9108600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr9:9105000-9106000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:9105400-9105800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:9105400-9107600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr9:9105600-9105800	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:9105600-9106800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr9:9105800-9108400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr9:9105800-9108600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr9:9106000-9108800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr9:9106800-9107200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:9107600-9107800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr9:9107800-9108200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:9107800-9108200	Enhancers	Placenta Amnion	Placenta Amnion
45	chr9:9108200-9108600	Enhancers	Fetal Heart	heart
46	chr9:9108200-9108600	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr9:9108200-9109000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr9:9108400-9109200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr9:9108400-9109600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr9:9108600-9109200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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