Variant report

Variant	nsv429987
Chromosome Location	chr9:7522659-7619121
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	chr9:7536423-7536658	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:7562620-7562663	K562	blood:	n/a	n/a
3	CEBPB	chr9:7533406-7534152	A549	lung:	n/a	chr9:7533687-7533700 chr9:7533686-7533703
4	CEBPB	chr9:7545777-7546126	A549	lung:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
5	CEBPB	chr9:7578486-7578755	HepG2	liver:	n/a	chr9:7578623-7578634
6	CEBPB	chr9:7536464-7536727	H1-hESC	embryonic stem cell:	n/a	chr9:7536654-7536667 chr9:7536656-7536667 chr9:7536656-7536667 chr9:7536654-7536667
7	CEBPB	chr9:7545794-7546090	K562	blood:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
8	CEBPB	chr9:7545804-7546125	H1-hESC	embryonic stem cell:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
9	CEBPB	chr9:7545779-7546139	HepG2	liver:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
10	CEBPB	chr9:7542696-7542901	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:7608387-7608696	HepG2	liver:	n/a	chr9:7608538-7608549
12	CEBPB	chr9:7548909-7549114	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:7545781-7546113	Hela-S3	cervix:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
14	CEBPB	chr9:7548886-7549026	A549	lung:	n/a	n/a
15	CEBPB	chr9:7545763-7546136	IMR90	lung:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
16	CEBPB	chr9:7608413-7608697	A549	lung:	n/a	chr9:7608538-7608549
17	CEBPB	chr9:7578500-7578700	A549	lung:	n/a	chr9:7578623-7578634
18	CHD2	chr9:7592689-7592696	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr9:7549301-7549523	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr9:7536430-7536658	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:7536840-7536990	HVMF	connective:	n/a	n/a
22	CTCF	chr9:7592760-7592910	HRPEpiC	eye:	n/a	chr9:7592820-7592828
23	CTCF	chr9:7536460-7536610	GM12866	blood:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
24	CTCF	chr9:7592820-7592970	HUVEC	blood vessel:	n/a	chr9:7592820-7592828
25	CTCF	chr9:7536480-7536630	HRE	kidney:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
26	CTCF	chr9:7570164-7570444	Medullo	brain:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
27	CTCF	chr9:7570105-7570433	T-47D	breast:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
28	CTCF	chr9:7592740-7592890	HCFaa	heart:	n/a	chr9:7592820-7592828
29	CTCF	chr9:7536460-7536610	BJ	skin:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
30	CTCF	chr9:7536389-7536655	HUVEC	blood vessel:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
31	CTCF	chr9:7536432-7536638	GM13976	blood:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
32	CTCF	chr9:7592740-7592890	HFF	foreskin:	n/a	chr9:7592820-7592828
33	CTCF	chr9:7592740-7592890	GM12868	blood:	n/a	chr9:7592820-7592828
34	CTCF	chr9:7592780-7592930	HPF	lung:	n/a	chr9:7592820-7592828
35	CTCF	chr9:7536417-7536656	HepG2	liver:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
36	CTCF	chr9:7570231-7570385	H1-hESC	embryonic stem cell:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
37	CTCF	chr9:7593233-7593250	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:7592740-7592890	HBMEC	blood vessel:	n/a	chr9:7592820-7592828
39	CTCF	chr9:7570260-7570410	HRE	kidney:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
40	CTCF	chr9:7592700-7592850	GM12875	blood:	n/a	chr9:7592820-7592828
41	CTCF	chr9:7536403-7536667	MCF-7	breast:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
42	CTCF	chr9:7592760-7592910	GM12864	blood:	n/a	chr9:7592820-7592828
43	CTCF	chr9:7614060-7614210	GM12865	blood:	n/a	n/a
44	CTCF	chr9:7592780-7592930	Caco-2	colon:	n/a	chr9:7592820-7592828
45	CTCF	chr9:7536480-7536630	GM12872	blood:	n/a	chr9:7536518-7536539 chr9:7536524-7536540 chr9:7536523-7536541 chr9:7536528-7536536 chr9:7536575-7536588
46	CTCF	chr9:7570108-7570501	IMR90	lung:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
47	CTCF	chr9:7570076-7570451	A549	lung:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
48	CTCF	chr9:7570240-7570390	GM12864	blood:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
49	CTCF	chr9:7570239-7570388	MCF-7	breast:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
50	CTCF	chr9:7570240-7570390	HPAF	blood vessel:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:7543165-7543215	NB4	blood:	n/a
2	chr9:7543165-7543215	AG09319	gingival:	n/a
3	chr9:7543165-7543215	SAEC	small airway:	n/a
4	chr9:7543165-7543215	AG04450	lung:	fetal
5	chr9:7543165-7543215	HRPEpiC	eye:	n/a
6	chr9:7543165-7543215	LNCaP	prostate:	n/a
7	chr9:7543165-7543215	GM12878	blood:	n/a
8	chr9:7543165-7543215	Jurkat	blood:	n/a
9	chr9:7543165-7543215	PrEC	prostate:	n/a
10	chr9:7543165-7543215	PFSK-1	brain:	n/a
11	chr9:7543165-7543215	NT2-D1	testis:	n/a
12	chr9:7543165-7543215	U87	brain:	n/a
13	chr9:7543165-7543215	HCM	heart:	n/a
14	chr9:7543165-7543215	RPTEC	kidney:	n/a
15	chr9:7543165-7543215	HRCEpiC	kidney:	n/a
16	chr9:7543165-7543215	HAEpiC	amniotic membrane:	n/a
17	chr9:7543165-7543215	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:7543165-7543215	GM19239	blood:	n/a
19	chr9:7543165-7543215	SK-N-SH_RA	brain:	n/a
20	chr9:7543165-7543215	A549	lung:	n/a
21	chr9:7543165-7543215	HepG2	liver:	n/a
22	chr9:7543165-7543215	MCF10A-Er-Src	breast:	n/a
23	chr9:7543165-7543215	SK-N-SH	brain:	n/a
24	chr9:7543165-7543215	HMEC	breast:	n/a
25	chr9:7543165-7543215	HCPEpiC	choroid plexus:	n/a
26	chr9:7543165-7543215	NHDF-neo	bronchial:	n/a
27	chr9:7543165-7543215	Caco-2	colon:	n/a
28	chr9:7543165-7543215	HEEpiC	esophagus:	n/a
29	chr9:7543165-7543215	HIPEpiC	eye:	n/a
30	chr9:7543165-7543215	Hela-S3	cervix:	n/a
31	chr9:7543165-7543215	GM12891	blood:	n/a
32	chr9:7543165-7543215	HCT-116	colon:	n/a
33	chr9:7543165-7543215	AoSMC	blood vessel:	n/a
34	chr9:7543165-7543215	BJ	skin:	n/a
35	chr9:7543165-7543215	ProgFib	skin:	n/a
36	chr9:7543165-7543215	NHBE	bronchial:	n/a
37	chr9:7543165-7543215	NH-A	brain:	n/a
38	chr9:7543165-7543215	H1-hESC	embryonic stem cell:	embryo
39	chr9:7543165-7543215	CMK	blood:	n/a
40	chr9:7543165-7543215	AG04449	skin:	fetal
41	chr9:7543165-7543215	IMR90	lung:	fetal
42	chr9:7543165-7543215	SK-N-MC	brain:	n/a
43	chr9:7543165-7543215	HEK293	kidney:	embryo
44	chr9:7543165-7543215	HCF	heart:	n/a
45	chr9:7543165-7543215	MCF-7	breast:	n/a
46	chr9:7543165-7543215	ovcar-3	ovarian:	n/a
47	chr9:7543165-7543215	AG10803	skin:	n/a
48	chr9:7543165-7543215	HL-60	blood:	n/a
49	chr9:7543165-7543215	K562	blood:	n/a
50	chr9:7543165-7543215	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:121484531..121485420-chr9:7590895..7591415,3	MCF-7	breast:
2	chr9:7569899..7570770-chr9:7827280..7828131,4	MCF-7	breast:
3	chr9:7569797..7570734-chr9:8895690..8896630,4	MCF-7	breast:
4	chr9:7052337..7053367-chr9:7536144..7537120,3	MCF-7	breast:
5	chr9:7526587..7529247-chr9:7794978..7796914,2	MCF-7	breast:
6	chr9:7592716..7593255-chr9:7844122..7844707,2	MCF-7	breast:
7	chr9:7401751..7402674-chr9:7535710..7536817,3	MCF-7	breast:
8	chr9:7570819..7572380-chr9:7577523..7579697,2	K562	blood:
9	chr9:7579179..7582103-chr9:7582391..7584856,2	K562	blood:
10	chr9:7592774..7593282-chr9:7827299..7827877,2	MCF-7	breast:
11	chr9:7570819..7572380-chr9:7577523..7579697,2	K562	blood:
12	chr9:7579179..7582103-chr9:7582391..7584856,2	K562	blood:
13	chr9:7569880..7570683-chr9:8895710..8896327,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000178654	TF binding region
ENSG00000178654	CpG island

Extended variants
information (count: 2549 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10511483	chr9:7522659-7522660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs144849637	chr9:7522663-7522664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572383288	chr9:7522678-7522679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148579081	chr9:7522690-7522691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563541551	chr9:7522723-7522724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570040277	chr9:7522737-7522738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530899749	chr9:7522738-7522739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565112581	chr9:7522771-7522772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10114142	chr9:7522823-7522824	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544378113	chr9:7522831-7522832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145033608	chr9:7522861-7522862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147552030	chr9:7522884-7522885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189287788	chr9:7522892-7522893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560388272	chr9:7522902-7522903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114496734	chr9:7522903-7522904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79753244	chr9:7522924-7522925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370965644	chr9:7522928-7522929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62532969	chr9:7522937-7522938	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs180839841	chr9:7522943-7522944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549563352	chr9:7522960-7522961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558021558	chr9:7522963-7522964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10114819	chr9:7522987-7522988	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs535608499	chr9:7523000-7523001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376722045	chr9:7523012-7523013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs36095850	chr9:7523044-7523045	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200209230	chr9:7523045-7523046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113639308	chr9:7523083-7523084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186584277	chr9:7523138-7523139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146161684	chr9:7523141-7523142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528947669	chr9:7523168-7523169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577117743	chr9:7523186-7523187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544605156	chr9:7523214-7523215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs111749769	chr9:7523217-7523218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144356442	chr9:7523270-7523271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373145959	chr9:7523275-7523276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541951235	chr9:7523279-7523280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190944883	chr9:7523283-7523284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374558030	chr9:7523285-7523286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377549584	chr9:7523314-7523315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527923249	chr9:7523345-7523346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542727971	chr9:7523358-7523359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552594604	chr9:7523365-7523366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4237168	chr9:7523369-7523370	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs72693190	chr9:7523392-7523393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528302947	chr9:7523400-7523401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549762939	chr9:7523410-7523411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568131687	chr9:7523423-7523424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535521158	chr9:7523438-7523439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551640712	chr9:7523506-7523507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75741523	chr9:7523514-7523515	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	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
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
Developmental delay	21147756	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
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7520000-7522800	Weak transcription	Fetal Lung	lung
2	chr9:7522800-7523200	Enhancers	Fetal Brain Male	brain
3	chr9:7522800-7523400	Enhancers	Fetal Lung	lung
4	chr9:7523000-7523800	Enhancers	Fetal Heart	heart
5	chr9:7523200-7524000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:7523600-7523800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr9:7523600-7524000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:7530400-7530800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr9:7532000-7532600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr9:7534000-7535600	Enhancers	Dnd41	blood
11	chr9:7534600-7534800	Enhancers	Fetal Thymus	thymus
12	chr9:7534600-7535000	Enhancers	Fetal Lung	lung
13	chr9:7534600-7535000	Enhancers	Fetal Muscle Leg	muscle
14	chr9:7534800-7535000	Enhancers	Right Atrium	heart
15	chr9:7535000-7542800	Weak transcription	Fetal Lung	lung
16	chr9:7536200-7537000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:7536200-7537000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:7536600-7536800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr9:7536600-7537000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr9:7536600-7537000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr9:7536600-7537000	Enhancers	Fetal Thymus	thymus
22	chr9:7536800-7537200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:7537000-7541800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr9:7537000-7542200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr9:7537000-7542200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr9:7537000-7542200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr9:7537200-7543000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:7540800-7549000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:7541600-7544000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr9:7541800-7542000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr9:7541800-7543400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr9:7542000-7542200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:7542000-7542800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr9:7542000-7543600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:7542200-7542800	Enhancers	Brain Hippocampus Middle	brain
36	chr9:7542200-7543000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:7542200-7543000	Enhancers	Fetal Muscle Leg	muscle
38	chr9:7542200-7543200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr9:7542200-7543200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr9:7542200-7543400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr9:7542200-7543400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr9:7542200-7543600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr9:7542200-7543600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr9:7542200-7543800	Enhancers	Brain Anterior Caudate	brain
45	chr9:7542400-7542800	Enhancers	Brain Substantia Nigra	brain
46	chr9:7542400-7543200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr9:7542400-7543200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr9:7542400-7543400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr9:7542400-7543800	Enhancers	Brain Cingulate Gyrus	brain
50	chr9:7542600-7542800	Enhancers	Brain Angular Gyrus	brain

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