Variant report

Variant	nsv1023726
Chromosome Location	chr9:1288053-1386203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:186)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:186 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
2	BHLHE40	chr9:1329191-1329209	GM12878	blood:	n/a	n/a
3	CEBPB	chr9:1321802-1322099	IMR90	lung:	n/a	chr9:1321967-1321978 chr9:1321966-1321979 chr9:1321966-1321979 chr9:1321966-1321977 chr9:1321966-1321979 chr9:1322004-1322017
4	CEBPB	chr9:1383860-1384144	A549	lung:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
5	CEBPB	chr9:1383819-1384236	HepG2	liver:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
6	CEBPB	chr9:1337163-1337564	MCF-7	breast:	n/a	n/a
7	CEBPB	chr9:1320743-1320979	HepG2	liver:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
8	CEBPB	chr9:1320828-1321012	A549	lung:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
9	CEBPB	chr9:1321822-1322145	HepG2	liver:	n/a	chr9:1321967-1321978 chr9:1321966-1321979 chr9:1321966-1321979 chr9:1321966-1321977 chr9:1321966-1321979 chr9:1322004-1322017
10	CEBPB	chr9:1321875-1322061	K562	blood:	n/a	chr9:1321967-1321978 chr9:1321966-1321979 chr9:1321966-1321979 chr9:1321966-1321977 chr9:1321966-1321979 chr9:1322004-1322017
11	CEBPB	chr9:1321798-1322094	A549	lung:	n/a	chr9:1321967-1321978 chr9:1321966-1321979 chr9:1321966-1321979 chr9:1321966-1321977 chr9:1321966-1321979 chr9:1322004-1322017
12	CTCF	chr9:1319693-1319720	MCF-7	breast:	n/a	n/a
13	CTCF	chr9:1365380-1365530	AG09319	gingival:	n/a	n/a
14	CTCF	chr9:1337360-1337510	GM12865	blood:	n/a	n/a
15	CTCF	chr9:1337355-1337630	MCF-7	breast:	n/a	n/a
16	CTCF	chr9:1337400-1337550	HEK293	kidney:	n/a	n/a
17	CTCF	chr9:1337219-1337724	MCF-7	breast:	n/a	n/a
18	CTCF	chr9:1337400-1337550	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr9:1337360-1337510	RPTEC	kidney:	n/a	n/a
20	CTCF	chr9:1337420-1337570	HMF	breast:	n/a	n/a
21	CTCF	chr9:1337340-1337490	NHEK	skin:	n/a	n/a
22	CTCF	chr9:1365280-1365430	HFF	foreskin:	n/a	n/a
23	CTCF	chr9:1365265-1365449	IMR90	lung:	n/a	n/a
24	CTCF	chr9:1337420-1337570	AG04449	skin:	n/a	n/a
25	CTCF	chr9:1312083-1312130	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr9:1337480-1337630	AG10803	skin:	n/a	n/a
27	CTCF	chr9:1337400-1337550	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr9:1337440-1337590	SAEC	small airway:	n/a	n/a
29	CTCF	chr9:1337420-1337570	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr9:1333087-1333159	GM10248	blood:	n/a	n/a
31	CTCF	chr9:1337380-1337530	SAEC	small airway:	n/a	n/a
32	CTCF	chr9:1337440-1337590	GM12878	blood:	n/a	n/a
33	CTCF	chr9:1382980-1383130	GM12871	blood:	n/a	n/a
34	CTCF	chr9:1337440-1337590	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr9:1337420-1337570	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr9:1337400-1337550	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:1337480-1337630	BE2_C	brain:	n/a	n/a
38	CTCF	chr9:1337320-1337470	HVMF	connective:	n/a	n/a
39	CTCF	chr9:1337380-1337530	AG09319	gingival:	n/a	n/a
40	CTCF	chr9:1337360-1337510	GM06990	blood:	n/a	n/a
41	CTCF	chr9:1337368-1337612	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:1337440-1337590	HFF	foreskin:	n/a	n/a
43	CTCF	chr9:1337318-1337634	GM12878	blood:	n/a	n/a
44	CTCF	chr9:1337340-1337490	BJ	skin:	n/a	n/a
45	CTCF	chr9:1337428-1337547	Fibrobl	skin:	n/a	n/a
46	CTCF	chr9:1337400-1337550	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr9:1337400-1337550	AG04449	skin:	n/a	n/a
48	CTCF	chr9:1337440-1337590	GM12874	blood:	n/a	n/a
49	CTCF	chr9:1337260-1337410	HFF	foreskin:	n/a	n/a
50	CTCF	chr9:1365360-1365510	AG10803	skin:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:1100620..1101481-chr9:1337009..1337893,4	MCF-7	breast:
2	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
3	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:
4	chr9:1017828..1018465-chr9:1337011..1337699,2	MCF-7	breast:
5	chr9:1100638..1101499-chr9:1337048..1337780,3	MCF-7	breast:
6	chr9:1049884..1051008-chr9:1336243..1337579,9	MCF-7	breast:
7	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
8	chr9:1049884..1050964-chr9:1336243..1337456,4	MCF-7	breast:
9	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
10	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
11	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:

(count:39 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRT2-4	chr9:1288277-1288431	l_3725_chr9:1288276-1302899_breast
2	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
3	lnc-DMRT2-2	chr9:1299313-1299412	NONHSAT129967
4	lnc-DMRT2-6	chr9:1368147-1368400	NONHSAT129976
5	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
6	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
7	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
8	lnc-DMRT2-2	chr9:1328425-1328435	XLOC_007263
9	lnc-DMRT2-2	chr9:1327073-1327173	NONHSAT129967
10	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
11	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
12	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
13	lnc-DMRT2-2	chr9:1298276-1298431	NONHSAT129967
14	lnc-DMRT2-2	chr9:1310939-1311032	NONHSAT129967
15	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
16	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
17	lnc-DMRT2-5	chr9:1328664-1328987	NONHSAT129974
18	lnc-DMRT2-6	chr9:1354235-1354272	NONHSAT129976
19	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
20	lnc-DMRT2-4	chr9:1302841-1302899	l_3725_chr9:1288276-1302899_breast
21	lnc-DMRT2-4	chr9:1317074-1317173	l_3725_chr9:1288276-1302899_breast
22	lnc-DMRT2-2	chr9:1312840-1312899	NONHSAT129967
23	lnc-DMRT2-2	chr9:1312841-1312899	XLOC_007263
24	lnc-DMRT2-2	chr9:1298286-1298431	XLOC_007263
25	lnc-DMRT2-2	chr9:1328424-1328584	NONHSAT129967
26	lnc-DMRT2-4	chr9:1318425-1318584	l_3725_chr9:1288276-1302899_breast
27	lnc-DMRT2-2	chr9:1312841-1312897	XLOC_007263
28	lnc-DMRT2-4	chr9:1289314-1289412	l_3725_chr9:1288276-1302899_breast
29	lnc-DMRT2-2	chr9:1328425-1328584	XLOC_007263
30	lnc-DMRT2-2	chr9:1321456-1321494	NONHSAT129967
31	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
32	lnc-DMRT2-2	chr9:1321457-1321494	XLOC_007263
33	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
34	lnc-DMRT2-2	chr9:1321457-1321494	XLOC_007263
35	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
36	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
37	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
38	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
39	lnc-DMRT2-4	chr9:1300940-1301032	l_3725_chr9:1288276-1302899_breast

No data

Variant related genes	Relation type
ENSG00000233575	TF binding region
RNA5SP279	TF binding region
ENSG00000173253	chromatin interactions
AP2M1	miRNA target sites
AP3D1	miRNA target sites

Extended variants
information (count: 3865 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3865 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546215808	chr9:1288307-1288308	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs79798711	chr9:1288318-1288319	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs1538157	chr9:1288320-1288321	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs542161949	chr9:1288321-1288322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs567433669	chr9:1288360-1288361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs190913974	chr9:1288363-1288364	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs556391494	chr9:1288365-1288366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs550759219	chr9:1288398-1288399	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs142973171	chr9:1288405-1288406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs181682762	chr9:1288427-1288428	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs189174584	chr9:1289314-1289315	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs547453169	chr9:1289344-1289345	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs200346964	chr9:1289365-1289366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs570716048	chr9:1289394-1289395	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs557135087	chr9:1297809-1297810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190003028	chr9:1297850-1297851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34834120	chr9:1297852-1297853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539446541	chr9:1297856-1297857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140410362	chr9:1297876-1297877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34485636	chr9:1297881-1297882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546557227	chr9:1297887-1297888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573186248	chr9:1297922-1297923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542789430	chr9:1297924-1297925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542126335	chr9:1297929-1297930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372962085	chr9:1297935-1297936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559625585	chr9:1297945-1297946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555947815	chr9:1297946-1297947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10809852	chr9:1297949-1297950	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181641383	chr9:1297964-1297965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185544932	chr9:1297980-1297981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188442679	chr9:1297988-1297989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545793224	chr9:1298007-1298008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144257046	chr9:1298053-1298054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528418005	chr9:1298066-1298067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548139030	chr9:1298104-1298105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568254684	chr9:1298116-1298117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530609587	chr9:1298134-1298135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78960426	chr9:1298143-1298144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs58359592	chr9:1298149-1298150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573642947	chr9:1298177-1298178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180953597	chr9:1298180-1298181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552967672	chr9:1298190-1298191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566497870	chr9:1298196-1298197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11998942	chr9:1298223-1298224	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555739784	chr9:1298227-1298228	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs200627430	chr9:1298255-1298256	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544475934	chr9:1298261-1298262	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs1340012	chr9:1298291-1298292	Enhancers Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs576995325	chr9:1298345-1298346	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs565397760	chr9:1298358-1298359	Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	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
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
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
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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1297800-1298200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr9:1297800-1298200	Enhancers	Adipose Nuclei	Adipose
3	chr9:1297800-1298400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:1298000-1298800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:1298200-1300000	Active TSS	Adipose Nuclei	Adipose
6	chr9:1298400-1298800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:1298800-1299800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:1298800-1303600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:1300000-1300800	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr9:1300800-1302200	Enhancers	Adipose Nuclei	Adipose
11	chr9:1302200-1302400	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr9:1302400-1302600	Enhancers	Adipose Nuclei	Adipose
13	chr9:1302600-1302800	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr9:1302800-1318400	Weak transcription	Adipose Nuclei	Adipose
15	chr9:1303600-1304400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:1309800-1310200	Enhancers	Fetal Muscle Leg	muscle
17	chr9:1318200-1321600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:1318400-1321600	Enhancers	Adipose Nuclei	Adipose
19	chr9:1318600-1321200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:1318600-1321400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr9:1318800-1321400	Enhancers	Fetal Stomach	stomach
22	chr9:1318800-1321600	Enhancers	Fetal Muscle Leg	muscle
23	chr9:1320000-1321600	Enhancers	Fetal Lung	lung
24	chr9:1320600-1320800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
25	chr9:1321000-1321400	Enhancers	Colon Smooth Muscle	Colon
26	chr9:1321000-1321400	Enhancers	Fetal Muscle Trunk	muscle
27	chr9:1321200-1321800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr9:1321600-1332200	Weak transcription	Adipose Nuclei	Adipose
29	chr9:1323400-1323600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:1325600-1326000	Enhancers	Fetal Brain Male	brain
31	chr9:1326000-1331600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:1327200-1328800	Enhancers	Fetal Lung	lung
33	chr9:1327400-1327600	Enhancers	Fetal Stomach	stomach
34	chr9:1328400-1328800	Enhancers	Gastric	stomach
35	chr9:1328800-1340400	Weak transcription	Fetal Lung	lung
36	chr9:1331000-1331800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr9:1331400-1332800	Enhancers	Fetal Stomach	stomach
38	chr9:1331600-1332400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr9:1332000-1332600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr9:1332200-1332600	Enhancers	Adipose Nuclei	Adipose
41	chr9:1332400-1332800	Enhancers	Colon Smooth Muscle	Colon
42	chr9:1332600-1340200	Weak transcription	Adipose Nuclei	Adipose
43	chr9:1337200-1337600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:1337400-1337800	Enhancers	Liver	Liver
45	chr9:1339000-1339400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr9:1340000-1341000	Enhancers	Fetal Stomach	stomach
47	chr9:1340200-1340800	Enhancers	Adipose Nuclei	Adipose
48	chr9:1340400-1340600	Enhancers	Fetal Lung	lung
49	chr9:1349200-1349800	Enhancers	Adipose Nuclei	Adipose
50	chr9:1349800-1354600	Weak transcription	Adipose Nuclei	Adipose

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