Variant report

Variant	nsv1015795
Chromosome Location	chr9:7540787-7701648
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	chr9:7562620-7562663	K562	blood:	n/a	n/a
2	BATF	chr9:7646803-7646970	GM12878	blood:	n/a	chr9:7646910-7646921
3	BATF	chr9:7646825-7646968	GM12878	blood:	n/a	chr9:7646910-7646921
4	BHLHE40	chr9:7657970-7658106	K562	blood:	n/a	chr9:7658052-7658073
5	BHLHE40	chr9:7656668-7657036	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:7578500-7578700	A549	lung:	n/a	chr9:7578623-7578634
7	CEBPB	chr9:7691005-7691230	HepG2	liver:	n/a	chr9:7691079-7691090
8	CEBPB	chr9:7548886-7549026	A549	lung:	n/a	n/a
9	CEBPB	chr9:7671973-7672082	K562	blood:	n/a	chr9:7671995-7672006
10	CEBPB	chr9:7635615-7635813	A549	lung:	n/a	n/a
11	CEBPB	chr9:7625413-7625638	HepG2	liver:	n/a	chr9:7625469-7625480
12	CEBPB	chr9:7545804-7546125	H1-hESC	embryonic stem cell:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
13	CEBPB	chr9:7542696-7542901	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr9:7608387-7608696	HepG2	liver:	n/a	chr9:7608538-7608549
15	CEBPB	chr9:7671864-7672143	HepG2	liver:	n/a	chr9:7671995-7672006
16	CEBPB	chr9:7545779-7546139	HepG2	liver:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
17	CEBPB	chr9:7671863-7672167	IMR90	lung:	n/a	chr9:7671995-7672006
18	CEBPB	chr9:7548909-7549114	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:7665957-7666290	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:7578486-7578755	HepG2	liver:	n/a	chr9:7578623-7578634
21	CEBPB	chr9:7653874-7654221	HepG2	liver:	n/a	chr9:7654041-7654054 chr9:7654043-7654052 chr9:7654041-7654052 chr9:7654043-7654054
22	CEBPB	chr9:7545794-7546090	K562	blood:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
23	CEBPB	chr9:7545781-7546113	Hela-S3	cervix:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
24	CEBPB	chr9:7545763-7546136	IMR90	lung:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
25	CEBPB	chr9:7608413-7608697	A549	lung:	n/a	chr9:7608538-7608549
26	CEBPB	chr9:7671880-7672164	A549	lung:	n/a	chr9:7671995-7672006
27	CEBPB	chr9:7653957-7654181	A549	lung:	n/a	chr9:7654041-7654054 chr9:7654043-7654052 chr9:7654041-7654052 chr9:7654043-7654054
28	CEBPB	chr9:7545777-7546126	A549	lung:	n/a	chr9:7545946-7545955 chr9:7545946-7545955 chr9:7545946-7545955
29	CHD2	chr9:7549301-7549523	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr9:7592689-7592696	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr9:7592720-7592870	GM12864	blood:	n/a	chr9:7592820-7592828
32	CTCF	chr9:7657863-7658108	H1-hESC	embryonic stem cell:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
33	CTCF	chr9:7570560-7570710	AG09319	gingival:	n/a	n/a
34	CTCF	chr9:7593160-7593310	RPTEC	kidney:	n/a	n/a
35	CTCF	chr9:7592700-7592850	HAc	cerebellar:	n/a	chr9:7592820-7592828
36	CTCF	chr9:7570260-7570410	MCF-7	breast:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
37	CTCF	chr9:7614100-7614250	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr9:7592780-7592930	HEK293	kidney:	n/a	chr9:7592820-7592828
39	CTCF	chr9:7657940-7658090	NB4	blood:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
40	CTCF	chr9:7570180-7570330	HEK293	kidney:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
41	CTCF	chr9:7657940-7658090	HCT-116	colon:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
42	CTCF	chr9:7657920-7658070	HMF	breast:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
43	CTCF	chr9:7570240-7570390	GM12872	blood:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
44	CTCF	chr9:7657900-7658050	HPAF	blood vessel:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
45	CTCF	chr9:7570620-7570770	NB4	blood:	n/a	n/a
46	CTCF	chr9:7657940-7658090	AG04449	skin:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009
47	CTCF	chr9:7592820-7592970	GM12873	blood:	n/a	chr9:7592820-7592828
48	CTCF	chr9:7570164-7570443	LNCaP	prostate:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
49	CTCF	chr9:7570240-7570390	AG04450	lung:	n/a	chr9:7570305-7570321 chr9:7570307-7570320 chr9:7570304-7570322 chr9:7570306-7570327 chr9:7570308-7570315
50	CTCF	chr9:7657898-7658107	GM12878	blood:	n/a	chr9:7657999-7658020 chr9:7658000-7658013 chr9:7657996-7658012 chr9:7657997-7658010 chr9:7657997-7658015 chr9:7658002-7658012 chr9:7657998-7658014 chr9:7657995-7658013 chr9:7658000-7658009

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:7543165-7543215	SK-N-SH	brain:	n/a
2	chr9:7543165-7543215	SK-N-SH	brain:	n/a
3	chr9:7543165-7543215	LNCaP	prostate:	n/a
4	chr9:7543165-7543215	Hela-S3	cervix:	n/a
5	chr9:7543165-7543215	HAEpiC	amniotic membrane:	n/a
6	chr9:7543165-7543215	AG09319	gingival:	n/a
7	chr9:7543165-7543215	AoSMC	blood vessel:	n/a
8	chr9:7543165-7543215	GM06990	blood:	n/a
9	chr9:7543165-7543215	NB4	blood:	n/a
10	chr9:7543165-7543215	SKMC	muscle:	n/a
11	chr9:7543165-7543215	BJ	skin:	n/a
12	chr9:7543165-7543215	AG04450	lung:	fetal
13	chr9:7543165-7543215	HNPCEpiC	eye:	n/a
14	chr9:7543165-7543215	AG10803	skin:	n/a
15	chr9:7543165-7543215	PFSK-1	brain:	n/a
16	chr9:7543165-7543215	GM12892	blood:	n/a
17	chr9:7543165-7543215	HIPEpiC	eye:	n/a
18	chr9:7543165-7543215	ECC-1	luminal epithelium:	n/a
19	chr9:7543165-7543215	K562	blood:	n/a
20	chr9:7543165-7543215	U87	brain:	n/a
21	chr9:7543165-7543215	Hepatocyte	liver:	n/a
22	chr9:7543165-7543215	HRE	kidney:	n/a
23	chr9:7543165-7543215	IMR90	lung:	fetal
24	chr9:7543165-7543215	RPTEC	kidney:	n/a
25	chr9:7543165-7543215	GM19239	blood:	n/a
26	chr9:7543165-7543215	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:7543165-7543215	HEK293	kidney:	embryo
28	chr9:7543165-7543215	NH-A	brain:	n/a
29	chr9:7543165-7543215	GM12891	blood:	n/a
30	chr9:7543165-7543215	HRCEpiC	kidney:	n/a
31	chr9:7543165-7543215	SAEC	small airway:	n/a
32	chr9:7543165-7543215	NT2-D1	testis:	n/a
33	chr9:7543165-7543215	SK-N-SH_RA	brain:	n/a
34	chr9:7543165-7543215	HCPEpiC	choroid plexus:	n/a
35	chr9:7543165-7543215	Caco-2	colon:	n/a
36	chr9:7543165-7543215	NHDF-neo	bronchial:	n/a
37	chr9:7543165-7543215	SK-N-MC	brain:	n/a
38	chr9:7543165-7543215	MCF-7	breast:	n/a
39	chr9:7543165-7543215	HUVEC	blood vessel:	n/a
40	chr9:7543165-7543215	GM12878	blood:	n/a
41	chr9:7543165-7543215	HCF	heart:	n/a
42	chr9:7543165-7543215	HepG2	liver:	n/a
43	chr9:7543165-7543215	MCF10A-Er-Src	breast:	n/a
44	chr9:7543165-7543215	AG09309	skin:	n/a
45	chr9:7543165-7543215	A549	lung:	n/a
46	chr9:7543165-7543215	AG04449	skin:	fetal
47	chr9:7543165-7543215	HEEpiC	esophagus:	n/a
48	chr9:7543165-7543215	ovcar-3	ovarian:	n/a
49	chr9:7543165-7543215	Jurkat	blood:	n/a
50	chr9:7543165-7543215	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:7592716..7593255-chr9:7844122..7844707,2	MCF-7	breast:
2	chr9:7634427..7636382-chr9:7637356..7639690,2	K562	blood:
3	chr9:7579179..7582103-chr9:7582391..7584856,2	K562	blood:
4	chr9:7570819..7572380-chr9:7577523..7579697,2	K562	blood:
5	chr1:121484531..121485420-chr9:7590895..7591415,3	MCF-7	breast:
6	chr9:7570819..7572380-chr9:7577523..7579697,2	K562	blood:
7	chr9:7579179..7582103-chr9:7582391..7584856,2	K562	blood:
8	chr9:7569797..7570734-chr9:8895690..8896630,4	MCF-7	breast:
9	chr9:7569899..7570770-chr9:7827280..7828131,4	MCF-7	breast:
10	chr9:7569880..7570683-chr9:8895710..8896327,2	MCF-7	breast:
11	chr9:7634427..7636382-chr9:7637356..7639690,2	K562	blood:
12	chr9:7592774..7593282-chr9:7827299..7827877,2	MCF-7	breast:

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

Extended variants
information (count: 4822 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:4822 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566607940	chr9:7540796-7540797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566540693	chr9:7540797-7540798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561602818	chr9:7540827-7540828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147908765	chr9:7540829-7540830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200905000	chr9:7540852-7540853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374809911	chr9:7540853-7540854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34484136	chr9:7540854-7540855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376947162	chr9:7540859-7540860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10976376	chr9:7540863-7540864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190559624	chr9:7540875-7540876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533457751	chr9:7540884-7540885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552122391	chr9:7540888-7540889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544435745	chr9:7540894-7540895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574455031	chr9:7540909-7540910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10976377	chr9:7540912-7540913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10976378	chr9:7540930-7540931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181866220	chr9:7541109-7541110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553837866	chr9:7541127-7541128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572161440	chr9:7541140-7541141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554565793	chr9:7541188-7541189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545928845	chr9:7541190-7541191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564081034	chr9:7541205-7541206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139280608	chr9:7541212-7541213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186842172	chr9:7541230-7541231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs10976379	chr9:7541249-7541250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34188515	chr9:7541253-7541254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75242314	chr9:7541282-7541283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529181388	chr9:7541287-7541288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7849878	chr9:7541338-7541339	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150038863	chr9:7541391-7541392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78924510	chr9:7541397-7541398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145375765	chr9:7541401-7541402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189675274	chr9:7541445-7541446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375585192	chr9:7541451-7541452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115942094	chr9:7541469-7541470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112441031	chr9:7541471-7541472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10976380	chr9:7541473-7541474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553799220	chr9:7541533-7541534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75195623	chr9:7541536-7541537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111786044	chr9:7541569-7541570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539122767	chr9:7541592-7541593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113718983	chr9:7541649-7541650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567542872	chr9:7541651-7541652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78429587	chr9:7541684-7541685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12347473	chr9:7541694-7541695	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149191543	chr9:7541695-7541696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs145179133	chr9:7541696-7541697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181041754	chr9:7541745-7541746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540977038	chr9:7541748-7541749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146873659	chr9:7541771-7541772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7535000-7542800	Weak transcription	Fetal Lung	lung
2	chr9:7537000-7541800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr9:7537000-7542200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr9:7537000-7542200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:7537000-7542200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr9:7537200-7543000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr9:7540800-7549000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:7541600-7544000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr9:7541800-7542000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:7541800-7543400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr9:7542000-7542200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:7542000-7542800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr9:7542000-7543600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:7542200-7542800	Enhancers	Brain Hippocampus Middle	brain
15	chr9:7542200-7543000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:7542200-7543000	Enhancers	Fetal Muscle Leg	muscle
17	chr9:7542200-7543200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr9:7542200-7543200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr9:7542200-7543400	Enhancers	H9 Cell Line	embryonic stem cell
20	chr9:7542200-7543400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr9:7542200-7543600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:7542200-7543600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr9:7542200-7543800	Enhancers	Brain Anterior Caudate	brain
24	chr9:7542400-7542800	Enhancers	Brain Substantia Nigra	brain
25	chr9:7542400-7543200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr9:7542400-7543200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr9:7542400-7543400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr9:7542400-7543800	Enhancers	Brain Cingulate Gyrus	brain
29	chr9:7542600-7542800	Enhancers	Brain Angular Gyrus	brain
30	chr9:7542600-7543000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr9:7542600-7543000	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr9:7542800-7543000	Enhancers	Fetal Lung	lung
33	chr9:7542800-7543200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr9:7542800-7543200	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr9:7542800-7543200	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr9:7542800-7543200	Flanking Active TSS	Brain Substantia Nigra	brain
37	chr9:7543000-7543200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:7543000-7543200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr9:7543000-7543200	Enhancers	Fetal Brain Female	brain
40	chr9:7543000-7544000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:7543000-7548800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr9:7543200-7543400	Enhancers	Brain Angular Gyrus	brain
43	chr9:7543200-7543600	Enhancers	Brain Hippocampus Middle	brain
44	chr9:7543200-7543800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr9:7543200-7543800	Enhancers	Brain Substantia Nigra	brain
46	chr9:7543200-7548800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr9:7543200-7548800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr9:7543400-7543600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr9:7543400-7544600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr9:7543400-7548000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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