Variant report

Variant	nsv1018636
Chromosome Location	chr9:2921825-3002862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:268)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:2982428-2982465	K562	blood:	n/a	n/a
2	CEBPB	chr9:2966474-2966653	HepG2	liver:	n/a	chr9:2966583-2966594
3	CEBPB	chr9:2963795-2964126	A549	lung:	n/a	chr9:2963958-2963969
4	CEBPB	chr9:2977783-2977971	HepG2	liver:	n/a	chr9:2977848-2977859
5	CEBPB	chr9:3001297-3001608	HepG2	liver:	n/a	n/a
6	CEBPB	chr9:2934167-2934358	HepG2	liver:	n/a	n/a
7	CEBPB	chr9:3001332-3001607	A549	lung:	n/a	n/a
8	CEBPB	chr9:3001349-3001549	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr9:2963823-2964031	H1-hESC	embryonic stem cell:	n/a	chr9:2963958-2963969
10	CEBPB	chr9:2963792-2964136	IMR90	lung:	n/a	chr9:2963958-2963969
11	CEBPB	chr9:2963816-2964129	Hela-S3	cervix:	n/a	chr9:2963958-2963969
12	CEBPB	chr9:2963795-2964137	HepG2	liver:	n/a	chr9:2963958-2963969
13	CEBPB	chr9:2963840-2964119	K562	blood:	n/a	chr9:2963958-2963969
14	CTCF	chr9:2991440-2991590	GM06990	blood:	n/a	n/a
15	CTCF	chr9:2991380-2991530	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr9:2991397-2991530	T-47D	breast:	n/a	n/a
17	CTCF	chr9:2991400-2991550	AG10803	skin:	n/a	n/a
18	CTCF	chr9:2969892-2969952	GM13976	blood:	n/a	n/a
19	CTCF	chr9:2955777-2955833	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:2955720-2955870	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr9:2991420-2991570	RPTEC	kidney:	n/a	n/a
22	CTCF	chr9:2991441-2991546	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr9:2991420-2991570	HEK293	kidney:	n/a	n/a
24	CTCF	chr9:2991422-2991551	LNCaP	prostate:	n/a	n/a
25	CTCF	chr9:2950391-2950414	GM10266	blood:	n/a	n/a
26	CTCF	chr9:2991460-2991610	AG04450	lung:	n/a	n/a
27	CTCF	chr9:2991420-2991570	Caco-2	colon:	n/a	n/a
28	CTCF	chr9:2955680-2955830	AG09309	skin:	n/a	n/a
29	CTCF	chr9:2991380-2991530	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:2991396-2991692	MCF-7	breast:	n/a	n/a
31	CTCF	chr9:2955799-2955860	HepG2	liver:	n/a	n/a
32	CTCF	chr9:2955672-2955967	GM12878	blood:	n/a	n/a
33	CTCF	chr9:2955740-2955890	AG04450	lung:	n/a	n/a
34	CTCF	chr9:2955720-2955870	NHEK	skin:	n/a	n/a
35	CTCF	chr9:2991400-2991550	HAc	cerebellar:	n/a	n/a
36	CTCF	chr9:2991400-2991550	AG04450	lung:	n/a	n/a
37	CTCF	chr9:2991458-2991528	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:2991400-2991550	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr9:2991440-2991590	Caco-2	colon:	n/a	n/a
40	CTCF	chr9:2991380-2991530	AG10803	skin:	n/a	n/a
41	CTCF	chr9:2955722-2955870	HepG2	liver:	n/a	n/a
42	CTCF	chr9:2955740-2955890	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr9:2955760-2955910	AG10803	skin:	n/a	n/a
44	CTCF	chr9:2961860-2962010	BE2_C	brain:	n/a	n/a
45	CTCF	chr9:2991440-2991590	HRE	kidney:	n/a	n/a
46	CTCF	chr9:2991308-2991621	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:2991400-2991550	AG09309	skin:	n/a	n/a
48	CTCF	chr9:2991380-2991530	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr9:2991447-2991526	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:2991438-2991534	NHEK	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2933723-2933773	BE2_C	brain:	n/a
2	chr9:2933723-2933773	PANC-1	pancreas:	n/a
3	chr9:2933723-2933773	HAEpiC	amniotic membrane:	n/a
4	chr9:2933723-2933773	AG04450	lung:	fetal
5	chr9:2933859-2933909	GM12878	blood:	n/a
6	chr9:2933121-2933171	CMK	blood:	n/a
7	chr9:2933229-2933279	AoSMC	blood vessel:	n/a
8	chr9:2933229-2933279	PFSK-1	brain:	n/a
9	chr9:2933859-2933909	SK-N-SH	brain:	n/a
10	chr9:2933121-2933171	HCF	heart:	n/a
11	chr9:2933229-2933279	SKMC	muscle:	n/a
12	chr9:2933859-2933909	AG04449	skin:	fetal
13	chr9:2933121-2933171	PrEC	prostate:	n/a
14	chr9:2933859-2933909	HCF	heart:	n/a
15	chr9:2933723-2933773	PrEC	prostate:	n/a
16	chr9:2933121-2933171	AoSMC	blood vessel:	n/a
17	chr9:2933121-2933171	HRPEpiC	eye:	n/a
18	chr9:2933229-2933279	HMEC	breast:	n/a
19	chr9:2933121-2933171	T-47D	breast:	n/a
20	chr9:2933229-2933279	RPTEC	kidney:	n/a
21	chr9:2933229-2933279	AG10803	skin:	n/a
22	chr9:2933859-2933909	SAEC	small airway:	n/a
23	chr9:2933121-2933171	NT2-D1	testis:	n/a
24	chr9:2933723-2933773	NT2-D1	testis:	n/a
25	chr9:2933859-2933909	U87	brain:	n/a
26	chr9:2933859-2933909	HepG2	liver:	n/a
27	chr9:2933723-2933773	MCF-7	breast:	n/a
28	chr9:2933229-2933279	GM19239	blood:	n/a
29	chr9:2933121-2933171	HMEC	breast:	n/a
30	chr9:2933859-2933909	HNPCEpiC	eye:	n/a
31	chr9:2933723-2933773	AG09319	gingival:	n/a
32	chr9:2933229-2933279	HCM	heart:	n/a
33	chr9:2933859-2933909	AG09319	gingival:	n/a
34	chr9:2933229-2933279	ECC-1	luminal epithelium:	n/a
35	chr9:2933121-2933171	ECC-1	luminal epithelium:	n/a
36	chr9:2933859-2933909	AG04450	lung:	fetal
37	chr9:2933229-2933279	ProgFib	skin:	n/a
38	chr9:2933859-2933909	HL-60	blood:	n/a
39	chr9:2933121-2933171	GM19239	blood:	n/a
40	chr9:2933723-2933773	HL-60	blood:	n/a
41	chr9:2933121-2933171	AG09309	skin:	n/a
42	chr9:2933723-2933773	HEEpiC	esophagus:	n/a
43	chr9:2933859-2933909	NT2-D1	testis:	n/a
44	chr9:2933723-2933773	HCM	heart:	n/a
45	chr9:2933229-2933279	HNPCEpiC	eye:	n/a
46	chr9:2933229-2933279	HCF	heart:	n/a
47	chr9:2933121-2933171	PANC-1	pancreas:	n/a
48	chr9:2933121-2933171	HEK293	kidney:	embryo
49	chr9:2933229-2933279	Jurkat	blood:	n/a
50	chr9:2933859-2933909	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2937731..2940554-chr9:2963806..2965673,2	K562	blood:
2	chr9:2937731..2940554-chr9:2963806..2965673,2	K562	blood:
3	chr9:2859483..2860540-chr9:2991100..2991795,3	MCF-7	breast:
4	chr9:2993065..2995731-chr9:2996150..2997856,2	K562	blood:
5	chr9:2993065..2995731-chr9:2996150..2997856,2	K562	blood:
6	chr9:2991000..2991786-chr9:3181398..3182226,2	MCF-7	breast:
7	chr9:2872228..2873219-chr9:2989491..2990582,3	MCF-7	breast:
8	chr9:2857345..2858204-chr9:2991199..2991973,2	MCF-7	breast:

No data

Variant related genes	Relation type
CARM1P1	TF binding region
ENSG00000221450	TF binding region
CARM1P1	CpG island
ENSG00000221450	CpG island
ENSG00000236511	chromatin interactions

Extended variants
information (count: 2224 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2224 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4013197	chr9:2921825-2921826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201746758	chr9:2921828-2921829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577384599	chr9:2921835-2921836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559082774	chr9:2921843-2921844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528586110	chr9:2921877-2921878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541242375	chr9:2921941-2921942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147289425	chr9:2921989-2921990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551950122	chr9:2922003-2922004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182303781	chr9:2922006-2922007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115696043	chr9:2922016-2922017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562949963	chr9:2922044-2922045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531977732	chr9:2922067-2922068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377144122	chr9:2922074-2922075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545535340	chr9:2922130-2922131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200709937	chr9:2922144-2922145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371745946	chr9:2922145-2922146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188186203	chr9:2922146-2922147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143057271	chr9:2922176-2922177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs985009	chr9:2922193-2922194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144736354	chr9:2922211-2922212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7024329	chr9:2922216-2922217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530716988	chr9:2922253-2922254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142824336	chr9:2922256-2922257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78750110	chr9:2922267-2922268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570102329	chr9:2922298-2922299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539016997	chr9:2922301-2922302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570611865	chr9:2922313-2922314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559120259	chr9:2922330-2922331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539661774	chr9:2922336-2922337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375532774	chr9:2922344-2922345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78624445	chr9:2922351-2922352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs985010	chr9:2922370-2922371	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs151218495	chr9:2922433-2922434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569829731	chr9:2922446-2922447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574931790	chr9:2922447-2922448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543755128	chr9:2922459-2922460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191380127	chr9:2922478-2922479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183635143	chr9:2922481-2922482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188221466	chr9:2922486-2922487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370361017	chr9:2922543-2922544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192169962	chr9:2922551-2922552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139376053	chr9:2922583-2922584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183285839	chr9:2922586-2922587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541861719	chr9:2922587-2922588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535775386	chr9:2922593-2922594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77052049	chr9:2922603-2922604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530715788	chr9:2922628-2922629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550925458	chr9:2922733-2922734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570734872	chr9:2922747-2922748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533233962	chr9:2922785-2922786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Ovarian cancer	22355333	CNVD
Autism	20808228	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2920800-2922200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:2922200-2922400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:2922400-2922800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:2922800-2924000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:2923000-2923400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:2924000-2924200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:2924000-2924200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr9:2924000-2924400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:2924000-2924600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:2924000-2924600	Enhancers	Stomach Mucosa	stomach
11	chr9:2927800-2928400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr9:2927800-2928400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr9:2927800-2928800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr9:2928000-2928400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr9:2928200-2929000	Enhancers	Fetal Brain Male	brain
16	chr9:2933200-2935200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:2933600-2934600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:2935000-2935200	Enhancers	Fetal Muscle Trunk	muscle
19	chr9:2942000-2943200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr9:2943200-2944400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:2944400-2946200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr9:2944800-2946200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:2946200-2949400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:2946200-2949400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:2949200-2957600	Weak transcription	Fetal Brain Male	brain
26	chr9:2949400-2950000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:2949400-2950000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:2955600-2955800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:2957600-2958400	Enhancers	Fetal Brain Male	brain
30	chr9:2957600-2958600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:2958000-2958400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr9:2958000-2958600	Enhancers	Adipose Nuclei	Adipose
33	chr9:2958000-2958600	Enhancers	NHDF-Ad	bronchial
34	chr9:2958200-2958600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:2958400-2963000	Weak transcription	Fetal Brain Male	brain
36	chr9:2958600-2960800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:2958600-2961600	Weak transcription	NHDF-Ad	bronchial
38	chr9:2960800-2963600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:2961600-2969000	Enhancers	NHDF-Ad	bronchial
40	chr9:2962200-2963200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr9:2962200-2963200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:2962200-2963200	Enhancers	NHEK	skin
43	chr9:2962400-2962600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:2962600-2962800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:2962600-2964000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:2962800-2966600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr9:2963000-2963600	Enhancers	Fetal Brain Male	brain
48	chr9:2963200-2963400	Enhancers	Fetal Stomach	stomach
49	chr9:2963200-2968000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:2963400-2963600	Enhancers	Fetal Brain Female	brain

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