Variant report

Variant	nsv1032113
Chromosome Location	chr9:13861066-13923136
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	BRCA1	chr9:13901062-13901120	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr9:13900404-13900714	HepG2	liver:	n/a	n/a
3	CEBPB	chr9:13865929-13866231	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr9:13900456-13900737	A549	lung:	n/a	n/a
5	CEBPB	chr9:13873256-13873789	MCF-7	breast:	n/a	n/a
6	CTCF	chr9:13878166-13878218	GM20000	blood:	n/a	n/a
7	CTCF	chr9:13896880-13897030	GM12871	blood:	n/a	n/a
8	E2F4	chr9:13900286-13900722	MCF10A-Er-Src	breast:	n/a	chr9:13900631-13900640
9	E2F4	chr9:13873398-13873598	MCF10A-Er-Src	breast:	n/a	n/a
10	E2F4	chr9:13910261-13910390	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr9:13899756-13899938	MCF10A-Er-Src	breast:	n/a	n/a
12	EP300	chr9:13898948-13898977	Hela-S3	cervix:	n/a	n/a
13	EP300	chr9:13883971-13884234	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr9:13873367-13873912	MCF-7	breast:	n/a	n/a
15	FOS	chr9:13915656-13916308	MCF10A-Er-Src	breast:	n/a	chr9:13916120-13916132 chr9:13916122-13916130 chr9:13916118-13916129
16	FOS	chr9:13915959-13916307	MCF10A-Er-Src	breast:	n/a	chr9:13916120-13916132 chr9:13916122-13916130 chr9:13916118-13916129
17	FOS	chr9:13895867-13896443	MCF10A-Er-Src	breast:	n/a	chr9:13896209-13896220 chr9:13896270-13896280
18	FOS	chr9:13904819-13905019	HUVEC	blood vessel:	n/a	n/a
19	FOS	chr9:13904726-13905097	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr9:13873260-13873626	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr9:13900359-13900881	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr9:13873233-13873685	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr9:13901235-13901537	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr9:13865806-13866365	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr9:13895893-13896467	MCF10A-Er-Src	breast:	n/a	chr9:13896209-13896220 chr9:13896270-13896280
26	FOS	chr9:13904720-13905091	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr9:13900357-13900909	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr9:13900135-13900913	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr9:13865768-13866300	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr9:13868031-13868356	HUVEC	blood vessel:	n/a	chr9:13868222-13868233
31	FOS	chr9:13896020-13896367	HUVEC	blood vessel:	n/a	chr9:13896209-13896220 chr9:13896270-13896280
32	FOS	chr9:13900148-13900903	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr9:13896012-13896479	MCF10A-Er-Src	breast:	n/a	chr9:13896209-13896220 chr9:13896270-13896280
34	FOS	chr9:13915847-13916340	MCF10A-Er-Src	breast:	n/a	chr9:13916120-13916132 chr9:13916122-13916130 chr9:13916118-13916129
35	FOS	chr9:13904358-13905064	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr9:13873272-13873633	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr9:13865781-13866274	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr9:13901170-13901499	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr9:13873256-13873626	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr9:13896010-13896395	MCF10A-Er-Src	breast:	n/a	chr9:13896209-13896220 chr9:13896270-13896280
41	FOS	chr9:13915732-13916286	MCF10A-Er-Src	breast:	n/a	chr9:13916120-13916132 chr9:13916122-13916130 chr9:13916118-13916129
42	FOS	chr9:13865780-13866260	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr9:13868182-13868292	MCF10A-Er-Src	breast:	n/a	chr9:13868222-13868233
44	FOXA1	chr9:13919406-13919684	T-47D	breast:	n/a	n/a
45	FOXM1	chr9:13873213-13873830	MCF-7	breast:	n/a	n/a
46	GATA3	chr9:13917170-13917275	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr9:13873182-13874250	MCF-7	breast:	n/a	n/a
48	GATA3	chr9:13863645-13863871	T-47D	breast:	n/a	n/a
49	GATA3	chr9:13873167-13873890	MCF-7	breast:	n/a	n/a
50	GATA3	chr9:13873179-13873917	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13897073-13897123	RPTEC	kidney:	n/a
2	chr9:13897073-13897123	SKMC	muscle:	n/a
3	chr9:13897073-13897123	ECC-1	luminal epithelium:	n/a
4	chr9:13897073-13897123	PANC-1	pancreas:	n/a
5	chr9:13897073-13897123	HEEpiC	esophagus:	n/a
6	chr9:13897073-13897123	IMR90	lung:	fetal
7	chr9:13897073-13897123	HL-60	blood:	n/a
8	chr9:13897073-13897123	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:13897073-13897123	HCT-116	colon:	n/a
10	chr9:13897073-13897123	AG04450	lung:	fetal
11	chr9:13897073-13897123	LNCaP	prostate:	n/a
12	chr9:13897073-13897123	HAEpiC	amniotic membrane:	n/a
13	chr9:13897073-13897123	Hepatocyte	liver:	n/a
14	chr9:13897073-13897123	GM12878	blood:	n/a
15	chr9:13897073-13897123	AoSMC	blood vessel:	n/a
16	chr9:13897073-13897123	HCM	heart:	n/a
17	chr9:13897073-13897123	Caco-2	colon:	n/a
18	chr9:13897073-13897123	AG10803	skin:	n/a
19	chr9:13897073-13897123	NHDF-neo	bronchial:	n/a
20	chr9:13897073-13897123	ProgFib	skin:	n/a
21	chr9:13897073-13897123	SK-N-MC	brain:	n/a
22	chr9:13897073-13897123	MCF-7	breast:	n/a
23	chr9:13897073-13897123	K562	blood:	n/a
24	chr9:13897073-13897123	GM12892	blood:	n/a
25	chr9:13897073-13897123	AG09309	skin:	n/a
26	chr9:13897073-13897123	Hela-S3	cervix:	n/a
27	chr9:13897073-13897123	HEK293	kidney:	embryo
28	chr9:13897073-13897123	H1-hESC	embryonic stem cell:	embryo
29	chr9:13897073-13897123	HMEC	breast:	n/a
30	chr9:13897073-13897123	AG09319	gingival:	n/a
31	chr9:13897073-13897123	MCF10A-Er-Src	breast:	n/a
32	chr9:13897073-13897123	GM06990	blood:	n/a
33	chr9:13897073-13897123	GM19239	blood:	n/a
34	chr9:13897073-13897123	HepG2	liver:	n/a
35	chr9:13897073-13897123	GM12891	blood:	n/a
36	chr9:13897073-13897123	SK-N-SH_RA	brain:	n/a
37	chr9:13897073-13897123	HRPEpiC	eye:	n/a
38	chr9:13897073-13897123	PFSK-1	brain:	n/a
39	chr9:13897073-13897123	HUVEC	blood vessel:	n/a
40	chr9:13897073-13897123	BJ	skin:	n/a
41	chr9:13897073-13897123	NB4	blood:	n/a
42	chr9:13897073-13897123	HRE	kidney:	n/a
43	chr9:13897073-13897123	SAEC	small airway:	n/a
44	chr9:13897073-13897123	HIPEpiC	eye:	n/a
45	chr9:13897073-13897123	CMK	blood:	n/a
46	chr9:13897073-13897123	AG04449	skin:	fetal
47	chr9:13897073-13897123	NT2-D1	testis:	n/a
48	chr9:13897073-13897123	Jurkat	blood:	n/a
49	chr9:13897073-13897123	SK-N-SH	brain:	n/a
50	chr9:13897073-13897123	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:13896594..13899401-chr9:13941918..13943557,2	K562	blood:
2	chr9:13876520..13879167-chr9:14313329..14315109,2	MCF-7	breast:
3	chr18:35921755..35922326-chr9:13895279..13896053,2	MCF-7	breast:

Variant related genes	Relation type
LINC00583	TF binding region
LINC00583	CpG island
ENSG00000147862	chromatin interactions

Extended variants
information (count: 3366 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3366 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552253874	chr9:13861077-13861078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190699508	chr9:13861083-13861084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117081918	chr9:13861084-13861085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557621836	chr9:13861094-13861095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574262221	chr9:13861144-13861145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548030423	chr9:13861145-13861146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577278561	chr9:13861164-13861165	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536999339	chr9:13861218-13861219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180764160	chr9:13861220-13861221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553377885	chr9:13861227-13861228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146937661	chr9:13861230-13861231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545025479	chr9:13861236-13861237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565059078	chr9:13861288-13861289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575370079	chr9:13861296-13861297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544280775	chr9:13861327-13861328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560797551	chr9:13861348-13861349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs16931040	chr9:13861380-13861381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546883217	chr9:13861386-13861387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560142627	chr9:13861409-13861410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532156771	chr9:13861417-13861418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs16931045	chr9:13861427-13861428	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs144778986	chr9:13861441-13861442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373435393	chr9:13861450-13861451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550443327	chr9:13861463-13861464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563584573	chr9:13861483-13861484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377454009	chr9:13861499-13861500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537966087	chr9:13861570-13861571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs59556338	chr9:13861574-13861575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs397941985	chr9:13861576-13861577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548302100	chr9:13861577-13861578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28565455	chr9:13861582-13861583	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553630937	chr9:13861583-13861584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148551386	chr9:13861595-13861596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58928986	chr9:13861596-13861597	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560443465	chr9:13861602-13861603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575233186	chr9:13861606-13861607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113547007	chr9:13861612-13861613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201596109	chr9:13861613-13861614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561007262	chr9:13861623-13861624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532636097	chr9:13861629-13861630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1410019	chr9:13861802-13861803	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560414056	chr9:13861837-13861838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565853298	chr9:13861867-13861868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28564078	chr9:13861892-13861893	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs80173647	chr9:13861895-13861896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562515314	chr9:13861921-13861922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531323090	chr9:13861943-13861944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190882401	chr9:13861944-13861945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73415097	chr9:13861945-13861946	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs530336285	chr9:13862002-13862003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13852000-13871000	Weak transcription	Right Ventricle	heart
2	chr9:13856400-13862600	Weak transcription	Left Ventricle	heart
3	chr9:13857600-13863000	Weak transcription	HSMM	muscle
4	chr9:13857800-13862000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr9:13858200-13862600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:13858800-13861800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:13858800-13862200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:13859400-13862600	Weak transcription	Fetal Heart	heart
9	chr9:13860000-13861600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr9:13860000-13862000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr9:13860000-13862200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr9:13860200-13861600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:13860200-13861600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr9:13860200-13862000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr9:13860200-13862400	Enhancers	Fetal Lung	lung
16	chr9:13860200-13864400	Enhancers	Adipose Nuclei	Adipose
17	chr9:13860400-13863200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr9:13860600-13861800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr9:13860600-13861800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr9:13860600-13864000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:13860800-13861800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:13860800-13864600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:13861000-13861200	Enhancers	Fetal Kidney	kidney
24	chr9:13861000-13861200	Enhancers	Psoas Muscle	Psoas
25	chr9:13861000-13861400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr9:13861000-13861600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr9:13861000-13861600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr9:13861000-13862000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr9:13861000-13863600	Enhancers	Fetal Muscle Leg	muscle
30	chr9:13861200-13861400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr9:13861200-13861600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:13861200-13861600	Enhancers	Fetal Stomach	stomach
33	chr9:13861400-13862000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr9:13861400-13862400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr9:13861400-13862600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr9:13861400-13862600	Weak transcription	Psoas Muscle	Psoas
37	chr9:13861600-13862600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr9:13861600-13862600	Weak transcription	Fetal Stomach	stomach
39	chr9:13861600-13863200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr9:13861800-13862200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:13861800-13862800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr9:13861800-13862800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr9:13862000-13862400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:13862000-13862400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr9:13862000-13863000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr9:13862000-13864400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr9:13862200-13862600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr9:13862200-13862600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr9:13862200-13865000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr9:13862400-13862600	Flanking Active TSS	Fetal Lung	lung

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