Variant report

Variant	nsv892021
Chromosome Location	chr9:1270931-1339391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr9:1273849-1274227	GM12878	blood:	n/a	n/a
2	BATF	chr9:1273755-1274200	GM12878	blood:	n/a	chr9:1274007-1274018
3	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
4	BCL11A	chr9:1271872-1272106	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:1273784-1274155	GM12878	blood:	n/a	n/a
6	BCL11A	chr9:1273798-1274241	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:1273916-1274170	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:1271859-1272122	GM12878	blood:	n/a	n/a
9	BHLHE40	chr9:1329191-1329209	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:1270807-1271031	GM12878	blood:	n/a	n/a
11	CEBPB	chr9:1320828-1321012	A549	lung:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
12	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
13	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
14	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
15	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
16	CEBPB	chr9:1320743-1320979	HepG2	liver:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
17	CEBPB	chr9:1337163-1337564	MCF-7	breast:	n/a	n/a
18	CHD2	chr9:1271987-1272089	GM12878	blood:	n/a	n/a
19	CHD2	chr9:1273912-1274194	GM12878	blood:	n/a	n/a
20	CTCF	chr9:1337400-1337550	AG04449	skin:	n/a	n/a
21	CTCF	chr9:1337380-1337530	AG09319	gingival:	n/a	n/a
22	CTCF	chr9:1337400-1337550	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr9:1337420-1337570	HMF	breast:	n/a	n/a
24	CTCF	chr9:1337400-1337550	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr9:1337440-1337590	GM12874	blood:	n/a	n/a
26	CTCF	chr9:1337380-1337530	SAEC	small airway:	n/a	n/a
27	CTCF	chr9:1337360-1337510	AG09319	gingival:	n/a	n/a
28	CTCF	chr9:1337440-1337590	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr9:1337320-1337470	HVMF	connective:	n/a	n/a
30	CTCF	chr9:1337440-1337590	GM12878	blood:	n/a	n/a
31	CTCF	chr9:1337340-1337490	BJ	skin:	n/a	n/a
32	CTCF	chr9:1333087-1333159	GM10248	blood:	n/a	n/a
33	CTCF	chr9:1337386-1337525	HepG2	liver:	n/a	n/a
34	CTCF	chr9:1337212-1337744	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:1337260-1337410	HFF	foreskin:	n/a	n/a
36	CTCF	chr9:1312083-1312130	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr9:1319693-1319720	MCF-7	breast:	n/a	n/a
38	CTCF	chr9:1337400-1337550	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:1337434-1337546	NHEK	skin:	n/a	n/a
40	CTCF	chr9:1337318-1337634	GM12878	blood:	n/a	n/a
41	CTCF	chr9:1337400-1337550	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr9:1337368-1337612	MCF-7	breast:	n/a	n/a
43	CTCF	chr9:1337400-1337550	HEK293	kidney:	n/a	n/a
44	CTCF	chr9:1319725-1319737	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:1337420-1337570	AG04449	skin:	n/a	n/a
46	CTCF	chr9:1337433-1337576	HepG2	liver:	n/a	n/a
47	CTCF	chr9:1337360-1337510	GM06990	blood:	n/a	n/a
48	CTCF	chr9:1287720-1287870	HPF	lung:	n/a	n/a
49	CTCF	chr9:1337440-1337590	HFF	foreskin:	n/a	n/a
50	CTCF	chr9:1337480-1337630	AG10803	skin:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

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

(count:37 , 50 per page) page: 1

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

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: 2424 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2424 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs885043	chr9:1270931-1270932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565412938	chr9:1270935-1270936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191704765	chr9:1270963-1270964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374171316	chr9:1270982-1270983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541399588	chr9:1271009-1271010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376438164	chr9:1271016-1271017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34129912	chr9:1271018-1271019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182992185	chr9:1271030-1271031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116466546	chr9:1271058-1271059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535541929	chr9:1271069-1271070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549033468	chr9:1271073-1271074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554462636	chr9:1271092-1271093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12686237	chr9:1271102-1271103	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs151322292	chr9:1271103-1271104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577817400	chr9:1271110-1271111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375482529	chr9:1271111-1271112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533992264	chr9:1271112-1271113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553681032	chr9:1271117-1271118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7850922	chr9:1271119-1271120	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370339838	chr9:1271134-1271135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7869976	chr9:1271154-1271155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116026642	chr9:1271158-1271159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140460985	chr9:1271250-1271251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545043070	chr9:1271262-1271263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150406549	chr9:1271267-1271268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527932196	chr9:1271312-1271313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs885044	chr9:1271315-1271316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs10960724	chr9:1271349-1271350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143528414	chr9:1271365-1271366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10960725	chr9:1271369-1271370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs115437069	chr9:1271380-1271381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568938258	chr9:1271398-1271399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537856193	chr9:1271407-1271408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138178002	chr9:1271413-1271414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60519925	chr9:1271426-1271427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567793810	chr9:1271432-1271433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5895900	chr9:1271442-1271443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569052411	chr9:1271453-1271454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571561571	chr9:1271457-1271458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531470349	chr9:1271479-1271480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533834471	chr9:1271527-1271528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs946771	chr9:1271569-1271570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs74803781	chr9:1271596-1271597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536012862	chr9:1271621-1271622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376662453	chr9:1271651-1271652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185562587	chr9:1271657-1271658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs80039131	chr9:1271690-1271691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372419022	chr9:1271694-1271695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545388790	chr9:1271701-1271702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117278807	chr9:1271709-1271710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1263400-1273800	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:1273600-1274200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr9:1273600-1274200	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr9:1273600-1274200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:1273600-1274400	Enhancers	HSMM	muscle
6	chr9:1273800-1274200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr9:1273800-1274200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr9:1273800-1274200	Enhancers	HSMMtube	muscle
9	chr9:1273800-1274400	Enhancers	Fetal Muscle Leg	muscle
10	chr9:1276600-1276800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:1276600-1276800	Bivalent Enhancer	Left Ventricle	heart
12	chr9:1297800-1298200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr9:1297800-1298200	Enhancers	Adipose Nuclei	Adipose
14	chr9:1297800-1298400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:1298000-1298800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:1298200-1300000	Active TSS	Adipose Nuclei	Adipose
17	chr9:1298400-1298800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr9:1298800-1299800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:1298800-1303600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:1300000-1300800	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr9:1300800-1302200	Enhancers	Adipose Nuclei	Adipose
22	chr9:1302200-1302400	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr9:1302400-1302600	Enhancers	Adipose Nuclei	Adipose
24	chr9:1302600-1302800	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr9:1302800-1318400	Weak transcription	Adipose Nuclei	Adipose
26	chr9:1303600-1304400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:1309800-1310200	Enhancers	Fetal Muscle Leg	muscle
28	chr9:1318200-1321600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:1318400-1321600	Enhancers	Adipose Nuclei	Adipose
30	chr9:1318600-1321200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:1318600-1321400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr9:1318800-1321400	Enhancers	Fetal Stomach	stomach
33	chr9:1318800-1321600	Enhancers	Fetal Muscle Leg	muscle
34	chr9:1320000-1321600	Enhancers	Fetal Lung	lung
35	chr9:1320600-1320800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
36	chr9:1321000-1321400	Enhancers	Colon Smooth Muscle	Colon
37	chr9:1321000-1321400	Enhancers	Fetal Muscle Trunk	muscle
38	chr9:1321200-1321800	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr9:1321600-1332200	Weak transcription	Adipose Nuclei	Adipose
40	chr9:1323400-1323600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:1325600-1326000	Enhancers	Fetal Brain Male	brain
42	chr9:1326000-1331600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr9:1327200-1328800	Enhancers	Fetal Lung	lung
44	chr9:1327400-1327600	Enhancers	Fetal Stomach	stomach
45	chr9:1328400-1328800	Enhancers	Gastric	stomach
46	chr9:1328800-1340400	Weak transcription	Fetal Lung	lung
47	chr9:1331000-1331800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr9:1331400-1332800	Enhancers	Fetal Stomach	stomach
49	chr9:1331600-1332400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:1332000-1332600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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