Variant report

Variant	esv2762824
Chromosome Location	chr9:105662920-105866457
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	BACH1	chr9:105800139-105800480	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr9:105732789-105732939	K562	blood:	n/a	n/a
3	CEBPB	chr9:105715318-105715459	A549	lung:	n/a	n/a
4	CEBPB	chr9:105776566-105776875	H1-hESC	embryonic stem cell:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
5	CEBPB	chr9:105707049-105707340	A549	lung:	n/a	chr9:105707185-105707196
6	CEBPB	chr9:105849411-105849629	HepG2	liver:	n/a	chr9:105849527-105849538
7	CEBPB	chr9:105765985-105766350	A549	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
8	CEBPB	chr9:105849361-105849706	IMR90	lung:	n/a	chr9:105849527-105849538
9	CEBPB	chr9:105776489-105777185	K562	blood:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
10	CEBPB	chr9:105663505-105663808	IMR90	lung:	n/a	n/a
11	CEBPB	chr9:105707036-105707335	IMR90	lung:	n/a	chr9:105707185-105707196
12	CEBPB	chr9:105707047-105707334	HepG2	liver:	n/a	chr9:105707185-105707196
13	CEBPB	chr9:105765986-105766361	HepG2	liver:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
14	CEBPB	chr9:105765984-105766352	IMR90	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
15	CEBPB	chr9:105763617-105763909	HepG2	liver:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
16	CEBPB	chr9:105802760-105803007	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:105716400-105716709	HepG2	liver:	n/a	chr9:105716559-105716570 chr9:105716561-105716572 chr9:105716561-105716572
18	CEBPB	chr9:105816725-105816945	HepG2	liver:	n/a	chr9:105816802-105816815 chr9:105816804-105816815 chr9:105816802-105816815 chr9:105816802-105816813 chr9:105816804-105816815
19	CEBPB	chr9:105776563-105777159	HepG2	liver:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
20	CEBPB	chr9:105671366-105671545	A549	lung:	n/a	n/a
21	CEBPB	chr9:105763606-105763848	A549	lung:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
22	CEBPB	chr9:105776565-105777146	IMR90	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
23	CEBPB	chr9:105763696-105763838	K562	blood:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
24	CEBPB	chr9:105848819-105848981	A549	lung:	n/a	n/a
25	CEBPB	chr9:105831139-105831163	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:105663619-105663820	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:105776625-105777150	A549	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
28	CEBPB	chr9:105766014-105766333	K562	blood:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
29	CEBPB	chr9:105716482-105716594	H1-hESC	embryonic stem cell:	n/a	chr9:105716559-105716570 chr9:105716561-105716572 chr9:105716561-105716572
30	CEBPB	chr9:105765994-105766337	H1-hESC	embryonic stem cell:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
31	CTCF	chr9:105840989-105841109	SK-N-SH_RA	brain:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
32	CTCF	chr9:105776881-105776940	LNCaP	prostate:	n/a	n/a
33	CTCF	chr9:105847214-105847286	GM20000	blood:	n/a	n/a
34	CTCF	chr9:105770040-105770190	GM12867	blood:	n/a	n/a
35	CTCF	chr9:105776918-105776999	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr9:105840920-105841070	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:105840980-105841130	HepG2	liver:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
38	CTCF	chr9:105840990-105841115	LNCaP	prostate:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
39	CTCF	chr9:105840880-105841030	BE2_C	brain:	n/a	n/a
40	CTCF	chr9:105729953-105729968	GM20000	blood:	n/a	n/a
41	CTCF	chr9:105840980-105841130	HRPEpiC	eye:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
42	CTCF	chr9:105841000-105841150	HEEpiC	esophagus:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
43	CTCF	chr9:105841020-105841170	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
44	CTCF	chr9:105840988-105841121	SK-N-SH_RA	brain:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
45	CTCF	chr9:105717599-105717636	Lung_OC	lung:	n/a	n/a
46	CTCF	chr9:105841000-105841150	HMF	breast:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
47	CTCF	chr9:105829780-105829785	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr9:105840980-105841130	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
49	CTCF	chr9:105747084-105747155	GM13976	blood:	n/a	n/a
50	CTCF	chr9:105859580-105859730	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:105764606-105764656	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:105764606-105764656	HNPCEpiC	eye:	n/a
3	chr9:105764606-105764656	HepG2	liver:	n/a
4	chr9:105764606-105764656	HCT-116	colon:	n/a
5	chr9:105764606-105764656	MCF-7	breast:	n/a
6	chr9:105764606-105764656	NHBE	bronchial:	n/a
7	chr9:105764606-105764656	SK-N-MC	brain:	n/a
8	chr9:105764606-105764656	AG09309	skin:	n/a
9	chr9:105764606-105764656	AG04450	lung:	fetal
10	chr9:105764606-105764656	HCM	heart:	n/a
11	chr9:105764606-105764656	A549	lung:	n/a
12	chr9:105764606-105764656	SK-N-SH_RA	brain:	n/a
13	chr9:105764606-105764656	HUVEC	blood vessel:	n/a
14	chr9:105764606-105764656	NH-A	brain:	n/a
15	chr9:105764606-105764656	GM06990	blood:	n/a
16	chr9:105764606-105764656	ECC-1	luminal epithelium:	n/a
17	chr9:105764606-105764656	NB4	blood:	n/a
18	chr9:105764606-105764656	IMR90	lung:	fetal
19	chr9:105764606-105764656	T-47D	breast:	n/a
20	chr9:105764606-105764656	PANC-1	pancreas:	n/a
21	chr9:105764606-105764656	AG10803	skin:	n/a
22	chr9:105764606-105764656	HCPEpiC	choroid plexus:	n/a
23	chr9:105764606-105764656	AG09319	gingival:	n/a
24	chr9:105764606-105764656	LNCaP	prostate:	n/a
25	chr9:105764606-105764656	NHDF-neo	bronchial:	n/a
26	chr9:105764606-105764656	AG04449	skin:	fetal
27	chr9:105764606-105764656	H1-hESC	embryonic stem cell:	embryo
28	chr9:105764606-105764656	HEEpiC	esophagus:	n/a
29	chr9:105764606-105764656	PrEC	prostate:	n/a
30	chr9:105764606-105764656	HAEpiC	amniotic membrane:	n/a
31	chr9:105764606-105764656	ProgFib	skin:	n/a
32	chr9:105764606-105764656	MCF10A-Er-Src	breast:	n/a
33	chr9:105764606-105764656	SKMC	muscle:	n/a
34	chr9:105764606-105764656	K562	blood:	n/a
35	chr9:105764606-105764656	HRPEpiC	eye:	n/a
36	chr9:105764606-105764656	HIPEpiC	eye:	n/a
37	chr9:105764606-105764656	AoSMC	blood vessel:	n/a
38	chr9:105764606-105764656	SAEC	small airway:	n/a
39	chr9:105764606-105764656	Caco-2	colon:	n/a
40	chr9:105764606-105764656	HL-60	blood:	n/a
41	chr9:105764606-105764656	HRE	kidney:	n/a
42	chr9:105764606-105764656	HEK293	kidney:	embryo
43	chr9:105764606-105764656	GM12892	blood:	n/a
44	chr9:105764606-105764656	CMK	blood:	n/a
45	chr9:105764606-105764656	HCF	heart:	n/a
46	chr9:105764606-105764656	Hepatocyte	liver:	n/a
47	chr9:105764606-105764656	ovcar-3	ovarian:	n/a
48	chr9:105764606-105764656	BE2_C	brain:	n/a
49	chr9:105764606-105764656	SK-N-SH	brain:	n/a
50	chr9:105764606-105764656	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:105754455..105757293-chr9:105759259..105760916,2	K562	blood:
2	chr9:105776596..105779117-chr9:105802439..105805135,2	MCF-7	breast:
3	chr9:105776596..105779117-chr9:105802439..105805135,2	MCF-7	breast:
4	chr9:105754455..105757293-chr9:105759259..105760916,2	K562	blood:
5	chr9:105671845..105674344-chr9:105674742..105677700,2	MCF-7	breast:
6	chr6:27862961..27863907-chr9:105815485..105816300,2	K562	blood:
7	chr9:105864792..105866771-chr9:107507159..107509861,2	K562	blood:
8	chr10:16933551..16934193-chr9:105772591..105773111,2	HCT-116	colon:
9	chr9:105671845..105674344-chr9:105674742..105677700,2	MCF-7	breast:
10	chr3:28772851..28773583-chr9:105771894..105772469,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYLC2-2	chr9:105774341-105774379	NONHSAT133770
2	lnc-CYLC2-2	chr9:105780607-105780770	NONHSAT133770
3	lnc-CYLC2-3	chr9:105684856-105685526	NONHSAT133769

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CYLC2	hsa-miR-26b-5p	chr9:105768164-105768186

Variant related genes	Relation type
ENSG00000234269	TF binding region
ENSG00000229830	TF binding region
CYLC2	TF binding region
ENSG00000234269	CpG island
ENSG00000229830	CpG island
CYLC2	CpG island

Extended variants
information (count: 809 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139752991	chr9:105676407-105676408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs7875851	chr9:105676435-105676436	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs181370503	chr9:105676439-105676440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369833501	chr9:105676462-105676463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558474858	chr9:105676477-105676478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532884334	chr9:105676491-105676492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371566964	chr9:105676508-105676509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34945964	chr9:105676516-105676517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374444655	chr9:105676553-105676554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143734484	chr9:105676562-105676563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574912874	chr9:105676622-105676623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186512279	chr9:105676640-105676641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76809512	chr9:105676651-105676652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563226351	chr9:105676697-105676698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146844406	chr9:105676702-105676703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545837819	chr9:105676715-105676716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559358762	chr9:105676730-105676731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528430736	chr9:105676736-105676737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79551133	chr9:105676746-105676747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548482750	chr9:105676761-105676762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192972590	chr9:105680409-105680410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573813630	chr9:105680429-105680430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540658077	chr9:105680468-105680469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76089840	chr9:105680489-105680490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149331440	chr9:105680491-105680492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533727343	chr9:105680503-105680504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371404499	chr9:105680558-105680559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544704142	chr9:105680569-105680570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367767981	chr9:105681591-105681592	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs540633524	chr9:105681592-105681593	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553851061	chr9:105681596-105681597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574290589	chr9:105681607-105681608	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs557319515	chr9:105681650-105681651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542935122	chr9:105681651-105681652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs184914899	chr9:105681653-105681654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574461632	chr9:105683200-105683201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs183317524	chr9:105683250-105683251	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs188006957	chr9:105683301-105683302	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs7037875	chr9:105683337-105683338	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs529964133	chr9:105683364-105683365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs545775279	chr9:105683367-105683368	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs376245862	chr9:105683376-105683377	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs559688718	chr9:105683395-105683396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10820309	chr9:105683398-105683399	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs193276195	chr9:105683516-105683517	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561906809	chr9:105683551-105683552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs185042417	chr9:105683552-105683553	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549635473	chr9:105683554-105683555	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549862180	chr9:105683622-105683623	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569758686	chr9:105683651-105683652	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:105676400-105676800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr9:105680400-105680600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:105694600-105695000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr9:105694800-105695200	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr9:105695000-105695400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:105705000-105709400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:105747400-105748000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr9:105747400-105749200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:105747600-105747800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr9:105747800-105748600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr9:105747800-105748800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:105747800-105749200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr9:105748000-105748200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr9:105748400-105749200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr9:105748400-105749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:105748600-105749200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:105748600-105749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr9:105748800-105749000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr9:105748800-105749400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr9:105799400-105800600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr9:105799400-105800600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr9:105799600-105800600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr9:105799600-105800600	Enhancers	Left Ventricle	heart
24	chr9:105799800-105800800	Enhancers	Right Ventricle	heart
25	chr9:105799800-105801200	Enhancers	Fetal Heart	heart
26	chr9:105799800-105801400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:105800000-105800400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr9:105800000-105800600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr9:105800000-105800800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr9:105800000-105800800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:105800200-105800400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr9:105800200-105800400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:105800200-105800600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr9:105800400-105801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:105800400-105802400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr9:105800600-105802600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr9:105800600-105803400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr9:105801000-105801200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr9:105801400-105802400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:105802200-105803600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr9:105802400-105802600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:105802400-105804800	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr9:105802600-105802800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr9:105802600-105803000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr9:105802600-105803000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:105803000-105804000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr9:105803400-105804000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr9:105804000-105804600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr9:105804400-105805600	Enhancers	HepG2	liver
50	chr9:105804600-105804800	Enhancers	HUES6 Cell Line	embryonic stem cell

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