Variant report

Variant	esv2761502
Chromosome Location	chr9:14757877-14827373
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	ARID3A	chr9:14768583-14768889	K562	blood:	n/a	n/a
2	ATF1	chr9:14779539-14779966	K562	blood:	n/a	n/a
3	ATF1	chr9:14797561-14797747	K562	blood:	n/a	n/a
4	ATF3	chr9:14779743-14779981	K562	blood:	n/a	n/a
5	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:14779512-14779982	K562	blood:	n/a	n/a
8	BHLHE40	chr9:14770538-14770679	K562	blood:	n/a	n/a
9	CEBPB	chr9:14782745-14783078	MCF-7	breast:	n/a	n/a
10	CEBPB	chr9:14799044-14799407	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
11	CEBPB	chr9:14782789-14783062	MCF-7	breast:	n/a	n/a
12	CEBPB	chr9:14782802-14783000	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:14799087-14799406	A549	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
14	CEBPB	chr9:14782726-14783009	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr9:14799090-14799366	MCF-7	breast:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
16	CEBPB	chr9:14777093-14777293	A549	lung:	n/a	chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135
17	CEBPB	chr9:14799070-14799407	IMR90	lung:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
18	CEBPB	chr9:14799051-14799431	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
19	CEBPB	chr9:14779694-14779938	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
20	CEBPB	chr9:14799112-14799348	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
21	CEBPB	chr9:14799137-14799326	Hela-S3	cervix:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
22	CEBPB	chr9:14799005-14799390	HepG2	liver:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
23	CEBPB	chr9:14799109-14799362	H1-hESC	embryonic stem cell:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
24	CEBPB	chr9:14779747-14779985	A549	lung:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
25	CEBPB	chr9:14799060-14799419	K562	blood:	n/a	chr9:14799312-14799325 chr9:14799234-14799245
26	CEBPB	chr9:14779678-14780012	HepG2	liver:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
27	CEBPB	chr9:14779706-14780011	K562	blood:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
28	CEBPB	chr9:14779753-14779973	MCF-7	breast:	n/a	chr9:14779847-14779860 chr9:14779848-14779859 chr9:14779847-14779858
29	CEBPB	chr9:14777095-14777393	HepG2	liver:	n/a	chr9:14777345-14777356 chr9:14777261-14777272 chr9:14777124-14777135 chr9:14777124-14777135 chr9:14777345-14777356
30	CEBPD	chr9:14799130-14799332	HepG2	liver:	n/a	n/a
31	CHD2	chr9:14818253-14818267	GM12878	blood:	n/a	n/a
32	CTCF	chr9:14769300-14769450	AG09319	gingival:	n/a	n/a
33	CTCF	chr9:14769280-14769430	BE2_C	brain:	n/a	n/a
34	CTCF	chr9:14769320-14769470	GM12865	blood:	n/a	n/a
35	CTCF	chr9:14769280-14769430	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr9:14768614-14768810	GM10248	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
37	CTCF	chr9:14768530-14768895	T-47D	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
38	CTCF	chr9:14768600-14768750	BE2_C	brain:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
39	CTCF	chr9:14768620-14768770	HCPEpiC	choroid plexus:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
40	CTCF	chr9:14769300-14769450	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr9:14768640-14768790	GM12865	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
42	CTCF	chr9:14768518-14768874	MCF-7	breast:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
43	CTCF	chr9:14768620-14768770	GM12874	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
44	CTCF	chr9:14769352-14769454	HepG2	liver:	n/a	n/a
45	CTCF	chr9:14768640-14768790	GM12873	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
46	CTCF	chr9:14768640-14768790	HRPEpiC	eye:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
47	CTCF	chr9:14768596-14768730	GM19240	blood:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714
48	CTCF	chr9:14769280-14769430	GM06990	blood:	n/a	n/a
49	CTCF	chr9:14769300-14769450	HMF	breast:	n/a	n/a
50	CTCF	chr9:14768620-14768770	SK-N-SH_RA	brain:	n/a	chr9:14768698-14768716 chr9:14768699-14768715 chr9:14768693-14768714

No.	Distal block	Cell Line	Cell type
1	chr9:14441846..14442823-chr9:14768420..14769609,5	MCF-7	breast:
2	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
3	chr4:48089025..48089740-chr9:14788684..14789184,2	MCF-7	breast:
4	chr9:14778874..14780922-chr9:14784330..14786333,2	K562	blood:
5	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
6	chr9:14465013..14466518-chr9:14768250..14769873,6	MCF-7	breast:
7	chr9:14692712..14694901-chr9:14767288..14769707,2	MCF-7	breast:
8	chr9:14693065..14694740-chr9:14764446..14767133,2	MCF-7	breast:
9	chr9:14785127..14787393-chr9:14791653..14793787,2	MCF-7	breast:
10	chr9:14616185..14616937-chr9:14768483..14769168,4	MCF-7	breast:
11	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
12	chr9:14678774..14681640-chr9:14758881..14761517,2	MCF-7	breast:

Variant related genes	Relation type
FREM1	TF binding region
ENSG00000164946	chromatin interactions
ENSG00000175893	chromatin interactions

Extended variants
information (count: 3588 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:3588 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7864052	chr9:14757877-14757878	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543125440	chr9:14757885-14757886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529903773	chr9:14757891-14757892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561764423	chr9:14757916-14757917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148116255	chr9:14757935-14757936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560210334	chr9:14757965-14757966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115519525	chr9:14758021-14758022	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189297966	chr9:14758028-14758029	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142820956	chr9:14758037-14758038	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527931761	chr9:14758044-14758045	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146091908	chr9:14758050-14758051	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182138488	chr9:14758071-14758072	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539942161	chr9:14758117-14758118	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550275639	chr9:14758145-14758146	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570098213	chr9:14758149-14758150	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139942047	chr9:14758151-14758152	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187669185	chr9:14758160-14758161	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572381286	chr9:14758166-14758167	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112728192	chr9:14758169-14758170	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557956685	chr9:14758171-14758172	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150804982	chr9:14758214-14758215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375068569	chr9:14758217-14758218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10810234	chr9:14758222-14758223	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7040337	chr9:14758228-14758229	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs114037290	chr9:14758233-14758234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542216402	chr9:14758257-14758258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191002944	chr9:14758262-14758263	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528002296	chr9:14758301-14758302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377015684	chr9:14758334-14758335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541333944	chr9:14758382-14758383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564729148	chr9:14758383-14758384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533348335	chr9:14758441-14758442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76793813	chr9:14758490-14758491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139183507	chr9:14758540-14758541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367612654	chr9:14758569-14758570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7026234	chr9:14758578-14758579	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7026238	chr9:14758587-14758588	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534948075	chr9:14758595-14758596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567829524	chr9:14758665-14758666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35084046	chr9:14758685-14758686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557754367	chr9:14758686-14758687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571462132	chr9:14758695-14758696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs149881806	chr9:14758703-14758704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370024484	chr9:14758758-14758759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531286405	chr9:14758759-14758760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556970915	chr9:14758772-14758773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114100191	chr9:14758784-14758785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542279309	chr9:14758787-14758788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144870120	chr9:14758888-14758889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572728508	chr9:14758902-14758903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	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
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14730800-14764400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:14748800-14775600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:14748800-14775800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr9:14748800-14790000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:14752200-14759400	Strong transcription	HepG2	liver
7	chr9:14752800-14759800	Weak transcription	Fetal Heart	heart
8	chr9:14752800-14775800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:14755400-14768400	Weak transcription	Colon Smooth Muscle	Colon
10	chr9:14755600-14759800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr9:14755600-14765200	Weak transcription	Adipose Nuclei	Adipose
12	chr9:14755800-14758000	Weak transcription	Aorta	Aorta
13	chr9:14755800-14759600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr9:14755800-14766000	Weak transcription	Fetal Intestine Large	intestine
15	chr9:14755800-14775600	Weak transcription	Fetal Stomach	stomach
16	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
17	chr9:14756200-14759600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr9:14756400-14766400	Weak transcription	Fetal Muscle Leg	muscle
19	chr9:14757000-14759400	Strong transcription	Fetal Lung	lung
20	chr9:14757000-14771800	Strong transcription	Fetal Kidney	kidney
21	chr9:14757600-14758000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr9:14758000-14758200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:14758000-14758400	Strong transcription	Aorta	Aorta
24	chr9:14758200-14766400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr9:14758400-14793400	Weak transcription	Aorta	Aorta
26	chr9:14759400-14759600	Weak transcription	Fetal Lung	lung
27	chr9:14759400-14765800	Weak transcription	HepG2	liver
28	chr9:14759600-14759800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr9:14759600-14760000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr9:14759600-14760800	Strong transcription	Fetal Lung	lung
31	chr9:14759800-14760000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr9:14759800-14760200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:14759800-14760400	Enhancers	Fetal Heart	heart
34	chr9:14760000-14760600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr9:14760000-14775200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:14760200-14760800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr9:14760600-14761400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr9:14760800-14761800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:14760800-14763000	Weak transcription	Fetal Lung	lung
40	chr9:14761400-14763000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr9:14761800-14762200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:14762200-14762600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:14762600-14763800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr9:14763000-14763200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr9:14763000-14770800	Strong transcription	Fetal Lung	lung
46	chr9:14763800-14764200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr9:14764200-14764400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:14764400-14764800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr9:14764400-14765200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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