Variant report

Variant	nsv1051059
Chromosome Location	chr9:105643281-105863176
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	CCNT2	chr9:105654934-105655131	K562	blood:	n/a	n/a
4	CEBPB	chr9:105707049-105707340	A549	lung:	n/a	chr9:105707185-105707196
5	CEBPB	chr9:105715318-105715459	A549	lung:	n/a	n/a
6	CEBPB	chr9:105765986-105766361	HepG2	liver:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
7	CEBPB	chr9:105763696-105763838	K562	blood:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
8	CEBPB	chr9:105716482-105716594	H1-hESC	embryonic stem cell:	n/a	chr9:105716559-105716570 chr9:105716561-105716572 chr9:105716561-105716572
9	CEBPB	chr9:105766014-105766333	K562	blood:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
10	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
11	CEBPB	chr9:105816725-105816945	HepG2	liver:	n/a	chr9:105816802-105816815 chr9:105816804-105816815 chr9:105816802-105816815 chr9:105816802-105816813 chr9:105816804-105816815
12	CEBPB	chr9:105765985-105766350	A549	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
13	CEBPB	chr9:105802760-105803007	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:105707036-105707335	IMR90	lung:	n/a	chr9:105707185-105707196
15	CEBPB	chr9:105671366-105671545	A549	lung:	n/a	n/a
16	CEBPB	chr9:105763617-105763909	HepG2	liver:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
17	CEBPB	chr9:105655038-105655340	HepG2	liver:	n/a	chr9:105655174-105655185 chr9:105655173-105655190 chr9:105655174-105655185 chr9:105655174-105655187 chr9:105655174-105655187 chr9:105655175-105655186 chr9:105655174-105655187
18	CEBPB	chr9:105849411-105849629	HepG2	liver:	n/a	chr9:105849527-105849538
19	CEBPB	chr9:105663505-105663808	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:105776563-105777159	HepG2	liver:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
21	CEBPB	chr9:105707047-105707334	HepG2	liver:	n/a	chr9:105707185-105707196
22	CEBPB	chr9:105776625-105777150	A549	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
23	CEBPB	chr9:105663619-105663820	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:105763606-105763848	A549	lung:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
25	CEBPB	chr9:105776566-105776875	H1-hESC	embryonic stem cell:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
26	CEBPB	chr9:105776489-105777185	K562	blood:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
27	CEBPB	chr9:105831139-105831163	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr9:105716400-105716709	HepG2	liver:	n/a	chr9:105716559-105716570 chr9:105716561-105716572 chr9:105716561-105716572
29	CEBPB	chr9:105849361-105849706	IMR90	lung:	n/a	chr9:105849527-105849538
30	CEBPB	chr9:105848819-105848981	A549	lung:	n/a	n/a
31	CEBPB	chr9:105776565-105777146	IMR90	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
32	CEBPB	chr9:105765984-105766352	IMR90	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
33	CTCF	chr9:105776881-105776940	LNCaP	prostate:	n/a	n/a
34	CTCF	chr9:105770040-105770190	GM12867	blood:	n/a	n/a
35	CTCF	chr9:105840980-105841130	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
36	CTCF	chr9:105651120-105651270	GM12865	blood:	n/a	n/a
37	CTCF	chr9:105841020-105841170	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
38	CTCF	chr9:105776918-105776999	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr9:105651240-105651390	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr9:105729953-105729968	GM20000	blood:	n/a	n/a
41	CTCF	chr9:105847214-105847286	GM20000	blood:	n/a	n/a
42	CTCF	chr9:105840990-105841115	LNCaP	prostate:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
43	CTCF	chr9:105840980-105841130	HRPEpiC	eye:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
44	CTCF	chr9:105840989-105841109	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	chr9:105747084-105747155	GM13976	blood:	n/a	n/a
47	CTCF	chr9:105840920-105841070	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:105811900-105812050	GM12869	blood:	n/a	n/a
49	CTCF	chr9:105754978-105755001	GM13977	blood:	n/a	n/a
50	CTCF	chr9:105829780-105829785	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:105764606-105764656	NHBE	bronchial:	n/a
2	chr9:105764606-105764656	GM12891	blood:	n/a
3	chr9:105764606-105764656	NT2-D1	testis:	n/a
4	chr9:105764606-105764656	Jurkat	blood:	n/a
5	chr9:105764606-105764656	HCM	heart:	n/a
6	chr9:105764606-105764656	HRE	kidney:	n/a
7	chr9:105764606-105764656	HUVEC	blood vessel:	n/a
8	chr9:105764606-105764656	ECC-1	luminal epithelium:	n/a
9	chr9:105764606-105764656	ovcar-3	ovarian:	n/a
10	chr9:105764606-105764656	A549	lung:	n/a
11	chr9:105764606-105764656	GM12892	blood:	n/a
12	chr9:105764606-105764656	MCF-7	breast:	n/a
13	chr9:105764606-105764656	HRCEpiC	kidney:	n/a
14	chr9:105764606-105764656	GM06990	blood:	n/a
15	chr9:105764606-105764656	HAEpiC	amniotic membrane:	n/a
16	chr9:105764606-105764656	AG09309	skin:	n/a
17	chr9:105764606-105764656	AG09319	gingival:	n/a
18	chr9:105764606-105764656	Hepatocyte	liver:	n/a
19	chr9:105764606-105764656	CMK	blood:	n/a
20	chr9:105764606-105764656	HEEpiC	esophagus:	n/a
21	chr9:105764606-105764656	BJ	skin:	n/a
22	chr9:105764606-105764656	HepG2	liver:	n/a
23	chr9:105764606-105764656	HL-60	blood:	n/a
24	chr9:105764606-105764656	HMEC	breast:	n/a
25	chr9:105764606-105764656	ProgFib	skin:	n/a
26	chr9:105764606-105764656	HRPEpiC	eye:	n/a
27	chr9:105764606-105764656	NHDF-neo	bronchial:	n/a
28	chr9:105764606-105764656	GM12878	blood:	n/a
29	chr9:105764606-105764656	NB4	blood:	n/a
30	chr9:105764606-105764656	HPAEpiC	pulmonary alveolar:	n/a
31	chr9:105764606-105764656	SK-N-SH	brain:	n/a
32	chr9:105764606-105764656	IMR90	lung:	fetal
33	chr9:105764606-105764656	Caco-2	colon:	n/a
34	chr9:105764606-105764656	AG04450	lung:	fetal
35	chr9:105764606-105764656	PFSK-1	brain:	n/a
36	chr9:105764606-105764656	SKMC	muscle:	n/a
37	chr9:105764606-105764656	HCF	heart:	n/a
38	chr9:105764606-105764656	AoSMC	blood vessel:	n/a
39	chr9:105764606-105764656	HCT-116	colon:	n/a
40	chr9:105764606-105764656	T-47D	breast:	n/a
41	chr9:105764606-105764656	BE2_C	brain:	n/a
42	chr9:105764606-105764656	K562	blood:	n/a
43	chr9:105764606-105764656	SAEC	small airway:	n/a
44	chr9:105764606-105764656	HIPEpiC	eye:	n/a
45	chr9:105764606-105764656	Hela-S3	cervix:	n/a
46	chr9:105764606-105764656	U87	brain:	n/a
47	chr9:105764606-105764656	PrEC	prostate:	n/a
48	chr9:105764606-105764656	LNCaP	prostate:	n/a
49	chr9:105764606-105764656	AG04449	skin:	fetal
50	chr9:105764606-105764656	HEK293	kidney:	embryo

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

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

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

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

Extended variants
information (count: 1381 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1381 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563088192	chr9:105645209-105645210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542424002	chr9:105645228-105645229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563537492	chr9:105645245-105645246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576684557	chr9:105645301-105645302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544782148	chr9:105645305-105645306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150299131	chr9:105645321-105645322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527337762	chr9:105645359-105645360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558579672	chr9:105645401-105645402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs137963652	chr9:105645406-105645407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560876302	chr9:105645411-105645412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190294831	chr9:105645501-105645502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529923672	chr9:105645510-105645511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549636460	chr9:105645558-105645559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191503273	chr9:105645575-105645576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10820298	chr9:105645592-105645593	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554117317	chr9:105645807-105645808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1418779	chr9:105645826-105645827	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs536970784	chr9:105645896-105645897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575045028	chr9:105646005-105646006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199891024	chr9:105646017-105646018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545577191	chr9:105646020-105646021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564877813	chr9:105646080-105646081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572085452	chr9:105646140-105646141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143547625	chr9:105646190-105646191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115584316	chr9:105646215-105646216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188126558	chr9:105646252-105646253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111636853	chr9:105646265-105646266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77741083	chr9:105646275-105646276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542392094	chr9:105646313-105646314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180977593	chr9:105646333-105646334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79246985	chr9:105646337-105646338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560613750	chr9:105646350-105646351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554097796	chr9:105646376-105646377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147186811	chr9:105646414-105646415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547881061	chr9:105646446-105646447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373038888	chr9:105646487-105646488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373874478	chr9:105646518-105646519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376591920	chr9:105646545-105646546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536611809	chr9:105646601-105646602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545934493	chr9:105646629-105646630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187286415	chr9:105646650-105646651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138861509	chr9:105646659-105646660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142881706	chr9:105646702-105646703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs531569750	chr9:105646728-105646729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2027549	chr9:105646746-105646747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs117952066	chr9:105646773-105646774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190283020	chr9:105646781-105646782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182452739	chr9:105646805-105646806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117610160	chr9:105646846-105646847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536863068	chr9:105646921-105646922	Weak transcription Enhancers	n/a	n/a	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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:105645200-105645600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr9:105645800-105646800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:105646000-105648200	Enhancers	Fetal Heart	heart
4	chr9:105646400-105648600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr9:105648200-105650000	Weak transcription	Fetal Heart	heart
6	chr9:105650000-105650200	Active TSS	Fetal Heart	heart
7	chr9:105650200-105650400	Flanking Active TSS	Fetal Heart	heart
8	chr9:105650400-105656400	Weak transcription	Fetal Heart	heart
9	chr9:105654400-105655600	Enhancers	Fetal Intestine Small	intestine
10	chr9:105655600-105659400	Weak transcription	Fetal Intestine Small	intestine
11	chr9:105656400-105656600	Enhancers	Fetal Heart	heart
12	chr9:105656600-105657400	Weak transcription	Fetal Heart	heart
13	chr9:105657400-105657800	Enhancers	Fetal Heart	heart
14	chr9:105659400-105659800	Enhancers	Fetal Intestine Small	intestine
15	chr9:105676400-105676800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr9:105680400-105680600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:105694600-105695000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:105694800-105695200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr9:105695000-105695400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr9:105705000-105709400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr9:105747400-105748000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:105747400-105749200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr9:105747600-105747800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr9:105747800-105748600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr9:105747800-105748800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr9:105747800-105749200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr9:105748000-105748200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr9:105748400-105749200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr9:105748400-105749200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr9:105748600-105749200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr9:105748600-105749200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr9:105748800-105749000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr9:105748800-105749400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr9:105799400-105800600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:105799400-105800600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr9:105799600-105800600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr9:105799600-105800600	Enhancers	Left Ventricle	heart
38	chr9:105799800-105800800	Enhancers	Right Ventricle	heart
39	chr9:105799800-105801200	Enhancers	Fetal Heart	heart
40	chr9:105799800-105801400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:105800000-105800400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr9:105800000-105800600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr9:105800000-105800800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:105800000-105800800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:105800200-105800400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:105800200-105800400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr9:105800200-105800600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr9:105800400-105801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:105800400-105802400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr9:105800600-105802600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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