Variant report

Variant	esv34351
Chromosome Location	chr9:1184213-1413700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:590)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1262535-1262860	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:1232418-1233152	HepG2	liver:	n/a	n/a
3	ATF2	chr9:1267069-1267434	GM12878	blood:	n/a	n/a
4	ATF2	chr9:1273849-1274227	GM12878	blood:	n/a	n/a
5	ATF2	chr9:1267004-1267465	GM12878	blood:	n/a	n/a
6	BATF	chr9:1273755-1274200	GM12878	blood:	n/a	chr9:1274007-1274018
7	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
8	BATF	chr9:1267065-1267439	GM12878	blood:	n/a	n/a
9	BATF	chr9:1267089-1267384	GM12878	blood:	n/a	n/a
10	BATF	chr9:1232670-1232943	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:1267051-1267422	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:1273798-1274241	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:1273784-1274155	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:1267058-1267389	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:1271872-1272106	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:1267023-1267355	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:1271859-1272122	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:1270807-1271031	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:1184742-1184955	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:1269746-1270488	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:1267079-1267545	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:1273916-1274170	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:1329191-1329209	GM12878	blood:	n/a	n/a
24	CEBPB	chr9:1232585-1232851	A549	lung:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
25	CEBPB	chr9:1233604-1233963	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:1200905-1201341	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:1198214-1198422	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr9:1337163-1337564	MCF-7	breast:	n/a	n/a
29	CEBPB	chr9:1387693-1387860	K562	blood:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
30	CEBPB	chr9:1232528-1233024	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
31	CEBPB	chr9:1232402-1232946	MCF-7	breast:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
32	CEBPB	chr9:1208265-1208585	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:1198034-1198533	MCF-7	breast:	n/a	n/a
34	CEBPB	chr9:1233454-1233961	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:1387697-1387780	H1-hESC	embryonic stem cell:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
36	CEBPB	chr9:1320743-1320979	HepG2	liver:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
37	CEBPB	chr9:1233638-1233904	A549	lung:	n/a	n/a
38	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
39	CEBPB	chr9:1383860-1384144	A549	lung:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
40	CEBPB	chr9:1198121-1198664	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:1387624-1387884	IMR90	lung:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
42	CEBPB	chr9:1232593-1232789	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720
43	CEBPB	chr9:1320828-1321012	A549	lung:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
44	CEBPB	chr9:1263039-1263079	HepG2	liver:	n/a	n/a
45	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
46	CEBPB	chr9:1198107-1198494	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr9:1232307-1233098	MCF-7	breast:	n/a	chr9:1233061-1233072 chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
48	CEBPB	chr9:1402843-1403043	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:1383819-1384236	HepG2	liver:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
50	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

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:
2	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
3	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
4	chr9:1017828..1018465-chr9:1337011..1337699,2	MCF-7	breast:
5	chr17:35897413..35898334-chr9:1234312..1235126,2	MCF-7	breast:
6	chr9:1196784..1199122-chr9:1220785..1223370,2	MCF-7	breast:
7	chr9:1050736..1051474-chr9:1211377..1212172,7	MCF-7	breast:
8	chr9:1049307..1051830-chr9:1209993..1212929,2	MCF-7	breast:
9	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
10	chr9:1100638..1101499-chr9:1337048..1337780,3	MCF-7	breast:
11	chr9:1049884..1051008-chr9:1336243..1337579,9	MCF-7	breast:
12	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
13	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
14	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
15	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
16	chr9:1050302..1051381-chr9:1211162..1212085,6	MCF-7	breast:
17	chr9:1100620..1101481-chr9:1337009..1337893,4	MCF-7	breast:
18	chr9:1048644..1051362-chr9:1182528..1184402,2	MCF-7	breast:
19	chr9:1050050..1050882-chr9:1198084..1198894,4	MCF-7	breast:
20	chr9:1050169..1051008-chr9:1198034..1198952,5	MCF-7	breast:
21	chr9:1048582..1050101-chr9:1206689..1209470,2	MCF-7	breast:
22	chr9:1048591..1051547-chr9:1195558..1198367,2	MCF-7	breast:
23	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:
24	chr9:1050662..1052458-chr9:1210912..1212810,2	MCF-7	breast:
25	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
26	chr9:1049962..1051601-chr9:1206448..1208602,2	MCF-7	breast:
27	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
28	chr9:1196784..1199122-chr9:1220785..1223370,2	MCF-7	breast:
29	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
30	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:
31	chr9:1050299..1051218-chr9:1211358..1212168,3	MCF-7	breast:
32	chr9:1049884..1050964-chr9:1336243..1337456,4	MCF-7	breast:
33	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000233575	TF binding region
RNA5SP279	TF binding region
ENSG00000173253	chromatin interactions
ENSG00000006114	chromatin interactions
AP3D1	miRNA target sites
AP2M1	miRNA target sites

Extended variants
information (count: 8181 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:8181 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10125101	chr9:1184213-1184214	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560575658	chr9:1184266-1184267	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181350922	chr9:1184301-1184302	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549128343	chr9:1184322-1184323	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569093811	chr9:1184341-1184342	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540254891	chr9:1184349-1184350	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377447621	chr9:1184350-1184351	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530548113	chr9:1184382-1184383	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530954853	chr9:1184400-1184401	Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572102928	chr9:1184505-1184506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550400025	chr9:1184555-1184556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570466577	chr9:1184587-1184588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10122418	chr9:1184588-1184589	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10123090	chr9:1184613-1184614	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150862604	chr9:1184630-1184631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535731422	chr9:1184657-1184658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555630948	chr9:1184693-1184694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139603116	chr9:1184748-1184749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10123123	chr9:1184757-1184758	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562267932	chr9:1184775-1184776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112708082	chr9:1184802-1184803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540233480	chr9:1184828-1184829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186495429	chr9:1184840-1184841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115905552	chr9:1184844-1184845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10119315	chr9:1184854-1184855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562788412	chr9:1185011-1185012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563144029	chr9:1185028-1185029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531778302	chr9:1185037-1185038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79655027	chr9:1185052-1185053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530793074	chr9:1185062-1185063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563999382	chr9:1185083-1185084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532959694	chr9:1185098-1185099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546313530	chr9:1185138-1185139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566456733	chr9:1185144-1185145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10123785	chr9:1185158-1185159	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111477629	chr9:1185161-1185162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569084421	chr9:1185247-1185248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537595323	chr9:1185250-1185251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139266865	chr9:1185271-1185272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs578006758	chr9:1185289-1185290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115215691	chr9:1185298-1185299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180917896	chr9:1185322-1185323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573694172	chr9:1185330-1185331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542954125	chr9:1185341-1185342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562800504	chr9:1185364-1185365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576599543	chr9:1185389-1185390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545239363	chr9:1185403-1185404	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs35274588	chr9:1185475-1185476	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs559301531	chr9:1185481-1185482	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs149959703	chr9:1185506-1185507	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Pancreatic ductal adenocarcinoma	19077451	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
Cancer	21272361	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:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1183800-1184800	Enhancers	NHDF-Ad	bronchial
2	chr9:1184000-1185000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr9:1184200-1184400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:1184200-1184800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr9:1184400-1185400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr9:1185400-1185600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:1187200-1187800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:1187400-1187800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:1197400-1198000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr9:1197600-1197800	Enhancers	Esophagus	oesophagus
11	chr9:1197600-1198600	Enhancers	NHDF-Ad	bronchial
12	chr9:1197600-1198800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:1197600-1198800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr9:1197800-1198800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr9:1197800-1198800	Weak transcription	Esophagus	oesophagus
16	chr9:1198000-1198400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr9:1198400-1199200	Enhancers	Placenta Amnion	Placenta Amnion
18	chr9:1198800-1199000	Enhancers	Psoas Muscle	Psoas
19	chr9:1198800-1199800	Enhancers	Esophagus	oesophagus
20	chr9:1198800-1200800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:1198800-1202600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:1199400-1199600	Enhancers	Brain Substantia Nigra	brain
23	chr9:1199400-1200600	Weak transcription	Psoas Muscle	Psoas
24	chr9:1199800-1200600	Weak transcription	Esophagus	oesophagus
25	chr9:1200000-1203600	Enhancers	Liver	Liver
26	chr9:1200400-1201400	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr9:1200600-1201600	Enhancers	Esophagus	oesophagus
28	chr9:1200600-1201600	Enhancers	Fetal Lung	lung
29	chr9:1200600-1201600	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr9:1200600-1201800	Enhancers	HepG2	liver
31	chr9:1200600-1202200	Enhancers	Fetal Muscle Leg	muscle
32	chr9:1200600-1202200	Enhancers	Pancreas	Pancrea
33	chr9:1200600-1203000	Enhancers	Psoas Muscle	Psoas
34	chr9:1200800-1201200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:1200800-1201400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr9:1201000-1201600	Enhancers	Adipose Nuclei	Adipose
37	chr9:1201000-1201600	Enhancers	Gastric	stomach
38	chr9:1201000-1202000	Enhancers	Fetal Brain Male	brain
39	chr9:1201000-1202000	Enhancers	Fetal Muscle Trunk	muscle
40	chr9:1201000-1202000	Enhancers	Lung	lung
41	chr9:1201000-1202200	Enhancers	Left Ventricle	heart
42	chr9:1201200-1201600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr9:1201200-1202800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:1201400-1202000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr9:1201400-1202400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:1201600-1202600	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr9:1201600-1202800	Weak transcription	Adipose Nuclei	Adipose
48	chr9:1201600-1209400	Weak transcription	Gastric	stomach
49	chr9:1202000-1202400	Weak transcription	Fetal Brain Male	brain
50	chr9:1202000-1203000	Enhancers	Skeletal Muscle Male	skeletal muscle

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