Variant report

Variant	nsv615037
Chromosome Location	chr9:105756213-105884764
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	CEBPB	chr9:105776489-105777185	K562	blood:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
3	CEBPB	chr9:105765986-105766361	HepG2	liver:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
4	CEBPB	chr9:105763606-105763848	A549	lung:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
5	CEBPB	chr9:105802760-105803007	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr9:105763696-105763838	K562	blood:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
7	CEBPB	chr9:105816725-105816945	HepG2	liver:	n/a	chr9:105816802-105816815 chr9:105816804-105816815 chr9:105816802-105816815 chr9:105816802-105816813 chr9:105816804-105816815
8	CEBPB	chr9:105765985-105766350	A549	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
9	CEBPB	chr9:105831139-105831163	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr9:105776565-105777146	IMR90	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
11	CEBPB	chr9:105849361-105849706	IMR90	lung:	n/a	chr9:105849527-105849538
12	CEBPB	chr9:105776566-105776875	H1-hESC	embryonic stem cell:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
13	CEBPB	chr9:105776625-105777150	A549	lung:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
14	CEBPB	chr9:105867168-105867437	HepG2	liver:	n/a	chr9:105867316-105867329 chr9:105867316-105867327 chr9:105867317-105867328
15	CEBPB	chr9:105766014-105766333	K562	blood:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
16	CEBPB	chr9:105849411-105849629	HepG2	liver:	n/a	chr9:105849527-105849538
17	CEBPB	chr9:105776563-105777159	HepG2	liver:	n/a	chr9:105776765-105776776 chr9:105776716-105776727
18	CEBPB	chr9:105763617-105763909	HepG2	liver:	n/a	chr9:105763745-105763756 chr9:105763746-105763757 chr9:105763745-105763758
19	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
20	CEBPB	chr9:105848819-105848981	A549	lung:	n/a	n/a
21	CEBPB	chr9:105765984-105766352	IMR90	lung:	n/a	chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766167-105766176 chr9:105766165-105766176 chr9:105766165-105766178
22	CTCF	chr9:105840880-105841030	BE2_C	brain:	n/a	n/a
23	CTCF	chr9:105840990-105841115	LNCaP	prostate:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
24	CTCF	chr9:105841020-105841170	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
25	CTCF	chr9:105840920-105841070	MCF-7	breast:	n/a	n/a
26	CTCF	chr9:105829780-105829785	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr9:105840898-105841178	GM12878	blood:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
28	CTCF	chr9:105770040-105770190	GM12867	blood:	n/a	n/a
29	CTCF	chr9:105841000-105841150	HEEpiC	esophagus:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
30	CTCF	chr9:105840980-105841130	HepG2	liver:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
31	CTCF	chr9:105859580-105859730	SAEC	small airway:	n/a	n/a
32	CTCF	chr9:105840980-105841130	HPAF	blood vessel:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
33	CTCF	chr9:105776881-105776940	LNCaP	prostate:	n/a	n/a
34	CTCF	chr9:105840989-105841109	SK-N-SH_RA	brain:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
35	CTCF	chr9:105840980-105841130	HRPEpiC	eye:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
36	CTCF	chr9:105847214-105847286	GM20000	blood:	n/a	n/a
37	CTCF	chr9:105841000-105841150	HMF	breast:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
38	CTCF	chr9:105840980-105841130	HRE	kidney:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
39	CTCF	chr9:105840988-105841121	SK-N-SH_RA	brain:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
40	CTCF	chr9:105840940-105841090	BE2_C	brain:	n/a	chr9:105841057-105841078 chr9:105841055-105841073
41	CTCF	chr9:105811900-105812050	GM12869	blood:	n/a	n/a
42	CTCF	chr9:105776918-105776999	Spleen_OC	spleen:	n/a	n/a
43	E2F4	chr9:105870109-105870536	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr9:105803442-105803654	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr9:105864148-105864370	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr9:105800354-105800356	MCF10A-Er-Src	breast:	n/a	n/a
47	EP300	chr9:105776659-105776798	HepG2	liver:	n/a	n/a
48	FAM48A	chr9:105884611-105884727	GM12878	blood:	n/a	n/a
49	FOS	chr9:105799310-105799574	MCF10A-Er-Src	breast:	n/a	chr9:105799419-105799426 chr9:105799417-105799426
50	FOS	chr9:105800112-105800493	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:105764606-105764656	HIPEpiC	eye:	n/a
2	chr9:105764606-105764656	Caco-2	colon:	n/a
3	chr9:105764606-105764656	IMR90	lung:	fetal
4	chr9:105764606-105764656	SAEC	small airway:	n/a
5	chr9:105764606-105764656	HRE	kidney:	n/a
6	chr9:105764606-105764656	HCF	heart:	n/a
7	chr9:105764606-105764656	HNPCEpiC	eye:	n/a
8	chr9:105764606-105764656	HAEpiC	amniotic membrane:	n/a
9	chr9:105764606-105764656	MCF-7	breast:	n/a
10	chr9:105764606-105764656	K562	blood:	n/a
11	chr9:105764606-105764656	SK-N-SH_RA	brain:	n/a
12	chr9:105764606-105764656	HL-60	blood:	n/a
13	chr9:105764606-105764656	GM12891	blood:	n/a
14	chr9:105764606-105764656	SK-N-SH	brain:	n/a
15	chr9:105764606-105764656	AoSMC	blood vessel:	n/a
16	chr9:105764606-105764656	AG09309	skin:	n/a
17	chr9:105764606-105764656	HEK293	kidney:	embryo
18	chr9:105764606-105764656	NB4	blood:	n/a
19	chr9:105764606-105764656	HCT-116	colon:	n/a
20	chr9:105764606-105764656	AG04449	skin:	fetal
21	chr9:105764606-105764656	AG10803	skin:	n/a
22	chr9:105764606-105764656	HRPEpiC	eye:	n/a
23	chr9:105764606-105764656	BE2_C	brain:	n/a
24	chr9:105764606-105764656	AG09319	gingival:	n/a
25	chr9:105764606-105764656	PrEC	prostate:	n/a
26	chr9:105764606-105764656	Jurkat	blood:	n/a
27	chr9:105764606-105764656	U87	brain:	n/a
28	chr9:105764606-105764656	BJ	skin:	n/a
29	chr9:105764606-105764656	GM06990	blood:	n/a
30	chr9:105764606-105764656	A549	lung:	n/a
31	chr9:105764606-105764656	RPTEC	kidney:	n/a
32	chr9:105764606-105764656	SK-N-MC	brain:	n/a
33	chr9:105764606-105764656	HEEpiC	esophagus:	n/a
34	chr9:105764606-105764656	CMK	blood:	n/a
35	chr9:105764606-105764656	HUVEC	blood vessel:	n/a
36	chr9:105764606-105764656	MCF10A-Er-Src	breast:	n/a
37	chr9:105764606-105764656	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:105764606-105764656	GM19239	blood:	n/a
39	chr9:105764606-105764656	AG04450	lung:	fetal
40	chr9:105764606-105764656	GM12878	blood:	n/a
41	chr9:105764606-105764656	HCM	heart:	n/a
42	chr9:105764606-105764656	HCPEpiC	choroid plexus:	n/a
43	chr9:105764606-105764656	SKMC	muscle:	n/a
44	chr9:105764606-105764656	NHBE	bronchial:	n/a
45	chr9:105764606-105764656	NT2-D1	testis:	n/a
46	chr9:105764606-105764656	ovcar-3	ovarian:	n/a
47	chr9:105764606-105764656	LNCaP	prostate:	n/a
48	chr9:105764606-105764656	ProgFib	skin:	n/a
49	chr9:105764606-105764656	HepG2	liver:	n/a
50	chr9:105764606-105764656	T-47D	breast:	n/a

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

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
ENSG00000229830	CpG island
CYLC2	CpG island

Extended variants
information (count: 414 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1417704	chr9:105756213-105756214	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs558709183	chr9:105756784-105756785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs79653623	chr9:105756883-105756884	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375011930	chr9:105756919-105756920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs535048710	chr9:105756931-105756932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs137955352	chr9:105756956-105756957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs574747467	chr9:105756975-105756976	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs537259253	chr9:105757060-105757061	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs557101411	chr9:105757150-105757151	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs369495597	chr9:105757163-105757164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545865450	chr9:105757173-105757174	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs149593670	chr9:105757194-105757195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs182141847	chr9:105757216-105757217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149455307	chr9:105757259-105757260	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs10739861	chr9:105757558-105757559	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139420249	chr9:105757595-105757596	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs369916189	chr9:105757613-105757614	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs373802579	chr9:105757623-105757624	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs16922390	chr9:105768172-105768173	Inactive region	miRNA target site	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539659993	chr9:105769996-105769997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs947187	chr9:105770038-105770039	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs139746330	chr9:105770062-105770063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs16922403	chr9:105770068-105770069	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs184591698	chr9:105770069-105770070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575228673	chr9:105770072-105770073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558608972	chr9:105770073-105770074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188512988	chr9:105770124-105770125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557449459	chr9:105770135-105770136	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs143024686	chr9:105770140-105770141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs181282705	chr9:105770156-105770157	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs947186	chr9:105770158-105770159	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573453457	chr9:105770163-105770164	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185911033	chr9:105771207-105771208	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs562556562	chr9:105771230-105771231	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs567862373	chr9:105774353-105774354	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs77031137	chr9:105780607-105780608	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs117142631	chr9:105780616-105780617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs13291989	chr9:105780618-105780619	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs116397477	chr9:105780635-105780636	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs182596440	chr9:105780647-105780648	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs533114905	chr9:105780656-105780657	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs186720241	chr9:105780670-105780671	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs370930452	chr9:105780686-105780687	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs566370432	chr9:105780698-105780699	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs142981694	chr9:105780712-105780713	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs530518329	chr9:105780717-105780718	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs548687660	chr9:105780721-105780722	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs568276540	chr9:105780731-105780732	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs10820341	chr9:105780762-105780763	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs557319777	chr9:105780768-105780769	Inactive region	lncRNA	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	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:105799400-105800600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr9:105799400-105800600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr9:105799600-105800600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr9:105799600-105800600	Enhancers	Left Ventricle	heart
5	chr9:105799800-105800800	Enhancers	Right Ventricle	heart
6	chr9:105799800-105801200	Enhancers	Fetal Heart	heart
7	chr9:105799800-105801400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:105800000-105800400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr9:105800000-105800600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr9:105800000-105800800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:105800000-105800800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:105800200-105800400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:105800200-105800400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:105800200-105800600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:105800400-105801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr9:105800400-105802400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr9:105800600-105802600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr9:105800600-105803400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr9:105801000-105801200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:105801400-105802400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:105802200-105803600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr9:105802400-105802600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr9:105802400-105804800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr9:105802600-105802800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr9:105802600-105803000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr9:105802600-105803000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr9:105803000-105804000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:105803400-105804000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr9:105804000-105804600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr9:105804400-105805600	Enhancers	HepG2	liver
31	chr9:105804600-105804800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr9:105814200-105814400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:105824600-105825800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:105837000-105837400	Enhancers	Brain Germinal Matrix	brain
35	chr9:105866600-105866800	Enhancers	Gastric	stomach

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