Variant report

Variant	nsv892093
Chromosome Location	chr9:3613712-3696874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 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	chr9:3689736-3689800	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr9:3656318-3656576	GM12878	blood:	n/a	n/a
3	BATF	chr9:3656298-3656558	GM12878	blood:	n/a	n/a
4	BATF	chr9:3631375-3631642	GM12878	blood:	n/a	n/a
5	BCL3	chr9:3651345-3651710	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:3648954-3649126	K562	blood:	n/a	n/a
7	BHLHE40	chr9:3661642-3661842	K562	blood:	n/a	n/a
8	BHLHE40	chr9:3651100-3651575	GM12878	blood:	n/a	n/a
9	CEBPB	chr9:3618064-3618264	HepG2	liver:	n/a	chr9:3618137-3618148
10	CEBPB	chr9:3667037-3667287	A549	lung:	n/a	chr9:3667147-3667158
11	CEBPB	chr9:3649161-3649459	IMR90	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
12	CEBPB	chr9:3633690-3633806	K562	blood:	n/a	n/a
13	CEBPB	chr9:3667020-3667258	K562	blood:	n/a	chr9:3667147-3667158
14	CEBPB	chr9:3642733-3642933	HepG2	liver:	n/a	chr9:3642822-3642833
15	CEBPB	chr9:3649175-3649477	K562	blood:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
16	CEBPB	chr9:3651301-3651734	GM12878	blood:	n/a	n/a
17	CEBPB	chr9:3667066-3667291	H1-hESC	embryonic stem cell:	n/a	chr9:3667147-3667158
18	CEBPB	chr9:3671067-3671327	HepG2	liver:	n/a	n/a
19	CEBPB	chr9:3649224-3649451	Hela-S3	cervix:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
20	CEBPB	chr9:3649165-3649500	HepG2	liver:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
21	CEBPB	chr9:3649628-3649648	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr9:3649158-3649446	A549	lung:	n/a	chr9:3649331-3649344 chr9:3649332-3649343
23	CEBPB	chr9:3650762-3650973	HepG2	liver:	n/a	chr9:3650859-3650872 chr9:3650856-3650873 chr9:3650859-3650870
24	CEBPB	chr9:3642748-3642878	K562	blood:	n/a	chr9:3642822-3642833
25	CEBPB	chr9:3633564-3633808	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:3667017-3667275	HepG2	liver:	n/a	chr9:3667147-3667158
27	CEBPB	chr9:3671154-3671354	A549	lung:	n/a	n/a
28	CEBPB	chr9:3667036-3667296	IMR90	lung:	n/a	chr9:3667147-3667158
29	CHD1	chr9:3651104-3651525	GM12878	blood:	n/a	n/a
30	CHD2	chr9:3651207-3651583	GM12878	blood:	n/a	n/a
31	CTCF	chr9:3652374-3652449	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr9:3647667-3648061	GM12878	blood:	n/a	n/a
33	CTCF	chr9:3647760-3647910	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:3647678-3647995	K562	blood:	n/a	n/a
35	CTCF	chr9:3647800-3647950	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr9:3647781-3647916	GM10266	blood:	n/a	n/a
37	CTCF	chr9:3647780-3647922	GM12878	blood:	n/a	n/a
38	CTCF	chr9:3647818-3647910	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:3647660-3647810	BE2_C	brain:	n/a	n/a
40	CTCF	chr9:3618279-3618341	GM20000	blood:	n/a	n/a
41	CTCF	chr9:3674380-3674530	BE2_C	brain:	n/a	n/a
42	CTCF	chr9:3647880-3648030	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr9:3647834-3647901	GM13976	blood:	n/a	n/a
44	CTCF	chr9:3647827-3647918	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr9:3647778-3647918	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr9:3651540-3651655	GM12878	blood:	n/a	n/a
47	CTCF	chr9:3647820-3647970	GM12869	blood:	n/a	n/a
48	CTCF	chr9:3647795-3647894	K562	blood:	n/a	n/a
49	CTCF	chr9:3647760-3647910	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:3651540-3651690	GM12878	blood:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:3690355..3691926-chr9:3696454..3698344,2	MCF-7	breast:
2	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:
3	chr9:3684957..3686893-chr9:3690032..3691953,2	MCF-7	breast:
4	chr13:45496976..45497802-chr9:3627604..3628338,2	Hela-S3	cervix:
5	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
6	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
7	chr9:3526287..3529194-chr9:3646038..3648964,2	K562	blood:
8	chr9:3649975..3652712-chr9:3654160..3655972,2	K562	blood:
9	chr9:3632578..3635092-chr9:3639764..3642505,2	MCF-7	breast:
10	chr9:3605941..3608408-chr9:3657516..3659534,2	K562	blood:
11	chr9:3690355..3691926-chr9:3696454..3698344,2	MCF-7	breast:
12	chr9:3526118..3527672-chr9:3696360..3698362,2	MCF-7	breast:
13	chr9:3655163..3657660-chr9:3672402..3674386,2	K562	blood:
14	chr9:3525115..3527683-chr9:3647759..3649608,2	MCF-7	breast:
15	chr9:3684957..3686893-chr9:3690032..3691953,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV2-3	chr9:3671477-3671634	ENSG00000232104.2
2	lnc-GLIS3-1	chr9:3684076-3684459	ENSG00000226669.2
3	lnc-GLIS3-3	chr9:3679335-3679626	NONHSAT130032
4	lnc-GLIS3-3	chr9:3674076-3674459	NONHSAT130032
5	lnc-KCNV2-3	chr9:3668086-3668408	ENSG00000232104
6	lnc-SLC1A1-4	chr9:3691504-3691814	ENSG00000235326
7	lnc-SLC1A1-5	chr9:3647754-3648338	ENSG00000237359
8	lnc-SLC1A1-5	chr9:3647335-3647477	ENSG00000237359
9	lnc-GLIS3-1	chr9:3689335-3689626	XLOC_007633
10	lnc-SLC1A1-4	chr9:3690837-3690959	ENSG00000235326
11	lnc-SLC1A1-12	chr9:3680837-3680959	NONHSAT130030
12	lnc-SLC1A1-12	chr9:3681504-3681814	NONHSAT130030
13	lnc-SLC1A1-12	chr9:3656974-3658408	l_3729_chr9:3656973-3664950_testes
14	lnc-SLC1A1-12	chr9:3661474-3661660	l_3729_chr9:3656973-3664950_testes
15	lnc-GLIS3-1	chr9:3684076-3684459	XLOC_007633
16	lnc-SLC1A1-13	chr9:3637335-3637477	NONHSAT130028
17	lnc-SLC1A1-13	chr9:3637754-3638338	NONHSAT130028
18	lnc-SLC1A1-12	chr9:3664411-3665024	l_3729_chr9:3656973-3664950_testes
19	lnc-SLC1A1-4	chr9:3674546-3674648	ENSG00000235326
20	lnc-KCNV2-3	chr9:3671477-3671624	ENSG00000232104
21	lnc-KCNV2-3	chr9:3671474-3671646	ENSG00000232104
22	lnc-GLIS3-1	chr9:3689332-3689626	ENSG00000226669.2
23	lnc-SLC1A1-12	chr9:3664546-3664648	NONHSAT130030

No data

Variant related genes	Relation type
ENSG00000226669	TF binding region
ENSG00000232104	TF binding region
ENSG00000235326	TF binding region
ENSG00000237359	TF binding region
ENSG00000232104	chromatin interactions
ENSG00000080298	chromatin interactions
KLF4	miRNA target sites

Extended variants
information (count: 3104 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:3104 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12685801	chr9:3613712-3613713	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576842689	chr9:3613717-3613718	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550500945	chr9:3613781-3613782	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545728278	chr9:3613808-3613809	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565547956	chr9:3613831-3613832	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527887598	chr9:3613868-3613869	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142289431	chr9:3613869-3613870	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373436815	chr9:3613870-3613871	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs36112795	chr9:3613895-3613896	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547633328	chr9:3613910-3613911	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181675009	chr9:3613911-3613912	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529751228	chr9:3613945-3613946	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377187367	chr9:3613971-3613972	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569297342	chr9:3613974-3613975	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538212413	chr9:3614007-3614008	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562455588	chr9:3614031-3614032	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145265638	chr9:3614046-3614047	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185919786	chr9:3614080-3614081	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs62522479	chr9:3614082-3614083	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536785555	chr9:3614143-3614144	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143256752	chr9:3614210-3614211	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62522480	chr9:3614215-3614216	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs536333263	chr9:3614216-3614217	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7031679	chr9:3614227-3614228	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs556346194	chr9:3614229-3614230	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576524515	chr9:3614231-3614232	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545372531	chr9:3614239-3614240	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138199979	chr9:3614284-3614285	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575534558	chr9:3614319-3614320	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192342196	chr9:3614342-3614343	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184050395	chr9:3614353-3614354	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529833617	chr9:3614394-3614395	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189031332	chr9:3614406-3614407	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143681950	chr9:3614516-3614517	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369290199	chr9:3614527-3614528	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115869976	chr9:3614529-3614530	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376023408	chr9:3614559-3614560	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62522481	chr9:3614566-3614567	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs117856096	chr9:3614579-3614580	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190883310	chr9:3614626-3614627	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568177379	chr9:3614630-3614631	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533386981	chr9:3614638-3614639	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556695571	chr9:3614653-3614654	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570121981	chr9:3614667-3614668	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374234287	chr9:3614676-3614677	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570315912	chr9:3614698-3614699	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376279721	chr9:3614763-3614764	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572729172	chr9:3614766-3614767	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541348658	chr9:3614767-3614768	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182141467	chr9:3614794-3614795	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3600800-3620400	Weak transcription	Ovary	ovary
2	chr9:3606400-3640400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr9:3611600-3628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr9:3613600-3619600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr9:3619600-3625600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:3619800-3620000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:3621400-3629600	Weak transcription	Brain Substantia Nigra	brain
8	chr9:3621800-3627800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:3622600-3626200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr9:3622800-3626000	Weak transcription	Pancreas	Pancrea
11	chr9:3623800-3625800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
12	chr9:3624000-3624800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:3624000-3626200	Weak transcription	Spleen	Spleen
14	chr9:3624000-3629800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr9:3624200-3627000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr9:3624800-3626400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:3625600-3626400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr9:3625800-3626000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
19	chr9:3626000-3626800	ZNF genes & repeats	Pancreas	Pancrea
20	chr9:3626000-3629400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr9:3626200-3626800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:3626200-3626800	ZNF genes & repeats	Spleen	Spleen
23	chr9:3626400-3627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:3626400-3629400	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr9:3626800-3627600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr9:3627000-3627400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr9:3627800-3628800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:3627800-3629800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:3628000-3630000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr9:3628000-3630000	Enhancers	Osteobl	bone
31	chr9:3628200-3629800	Enhancers	Adipose Nuclei	Adipose
32	chr9:3628200-3630000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:3628800-3629200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr9:3629000-3630000	Enhancers	Stomach Smooth Muscle	stomach
35	chr9:3629200-3629400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:3629400-3629600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr9:3629400-3630000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr9:3629600-3630000	Enhancers	Brain Substantia Nigra	brain
39	chr9:3629800-3630000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr9:3632200-3633600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr9:3644400-3644600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr9:3644800-3646000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr9:3645600-3647200	Enhancers	Brain Hippocampus Middle	brain
44	chr9:3645600-3647400	Enhancers	Fetal Brain Male	brain
45	chr9:3645800-3647000	Enhancers	Brain Anterior Caudate	brain
46	chr9:3645800-3647000	Enhancers	Fetal Brain Female	brain
47	chr9:3645800-3647400	Enhancers	Brain Substantia Nigra	brain
48	chr9:3646000-3646600	Enhancers	Brain Angular Gyrus	brain
49	chr9:3646000-3646800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr9:3646000-3646800	Enhancers	Cortex derived primary cultured neurospheres	brain

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