Variant report

Variant	nsv1031506
Chromosome Location	chr9:1216007-1472056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1187)
CpG islands
(count:0)
Chromatin interactive
region (count:34)
LncRNA
region (count:39)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1187 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1454262-1454586	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:1262535-1262860	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:1232418-1233152	HepG2	liver:	n/a	n/a
4	ATF2	chr9:1267069-1267434	GM12878	blood:	n/a	n/a
5	ATF2	chr9:1469886-1470491	GM12878	blood:	n/a	n/a
6	ATF2	chr9:1267004-1267465	GM12878	blood:	n/a	n/a
7	ATF2	chr9:1273849-1274227	GM12878	blood:	n/a	n/a
8	ATF2	chr9:1469879-1470564	GM12878	blood:	n/a	n/a
9	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
10	BATF	chr9:1267065-1267439	GM12878	blood:	n/a	n/a
11	BATF	chr9:1273755-1274200	GM12878	blood:	n/a	chr9:1274007-1274018
12	BATF	chr9:1470009-1470366	GM12878	blood:	n/a	chr9:1470172-1470183 chr9:1470265-1470278
13	BATF	chr9:1468627-1468906	GM12878	blood:	n/a	n/a
14	BATF	chr9:1232670-1232943	GM12878	blood:	n/a	n/a
15	BATF	chr9:1267089-1267384	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:1271872-1272106	GM12878	blood:	n/a	n/a
17	BCL11A	chr9:1267058-1267389	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:1273784-1274155	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:1267051-1267422	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:1273798-1274241	GM12878	blood:	n/a	n/a
21	BCL3	chr9:1469934-1470495	GM12878	blood:	n/a	n/a
22	BCL3	chr9:1458553-1458815	GM12878	blood:	n/a	chr9:1458740-1458749 chr9:1458739-1458748
23	BCL3	chr9:1458432-1458804	GM12878	blood:	n/a	chr9:1458740-1458749 chr9:1458739-1458748
24	BCLAF1	chr9:1267023-1267355	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:1267079-1267545	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:1469908-1470375	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:1425741-1425826	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:1273916-1274170	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:1270807-1271031	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:1329191-1329209	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:1271859-1272122	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:1269746-1270488	GM12878	blood:	n/a	n/a
33	BHLHE40	chr9:1460181-1460500	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:1232528-1233024	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
35	CEBPB	chr9:1387573-1387887	HepG2	liver:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
36	CEBPB	chr9:1402843-1403043	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:1458352-1458894	Hela-S3	cervix:	n/a	chr9:1458491-1458503
38	CEBPB	chr9:1454712-1454764	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:1383819-1384236	HepG2	liver:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
40	CEBPB	chr9:1320828-1321012	A549	lung:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
41	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
42	CEBPB	chr9:1233638-1233904	A549	lung:	n/a	n/a
43	CEBPB	chr9:1232593-1232789	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720
44	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
45	CEBPB	chr9:1458518-1458888	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr9:1458404-1458900	MCF-7	breast:	n/a	chr9:1458491-1458503
47	CEBPB	chr9:1233604-1233963	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:1387693-1387860	K562	blood:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
49	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
50	CEBPB	chr9:1434128-1434396	MCF-7	breast:	n/a	n/a

No data

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:1414222..1417184-chr9:1419869..1422079,2	K562	blood:
2	chr9:1459862..1460804-chr9:1527712..1529112,4	MCF-7	breast:
3	chr9:1049884..1051008-chr9:1336243..1337579,9	MCF-7	breast:
4	chr9:1444036..1446024-chr9:1452969..1455867,2	MCF-7	breast:
5	chr9:1463195..1465097-chr9:1468058..1470697,2	MCF-7	breast:
6	chr9:1101941..1102561-chr9:1429407..1430134,2	MCF-7	breast:
7	chr9:1459863..1460538-chr9:1837555..1838175,2	MCF-7	breast:
8	chr9:1463195..1465097-chr9:1468058..1470697,2	MCF-7	breast:
9	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:
10	chr9:1453549..1456481-chr9:1457480..1459717,2	K562	blood:
11	chr9:1100633..1101579-chr9:1428962..1429946,8	MCF-7	breast:
12	chr9:1414222..1417184-chr9:1419869..1422079,2	K562	blood:
13	chr9:1433839..1434724-chr9:1619824..1620539,2	MCF-7	breast:
14	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
15	chr9:1454281..1457237-chr9:1457484..1459959,2	MCF-7	breast:
16	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
17	chr9:1049884..1050964-chr9:1336243..1337456,4	MCF-7	breast:
18	chr9:1329896..1332390-chr9:1334019..1336447,2	MCF-7	breast:
19	chr17:35897413..35898334-chr9:1234312..1235126,2	MCF-7	breast:
20	chr9:1017795..1018400-chr9:1429068..1429992,2	MCF-7	breast:
21	chr9:1100620..1101481-chr9:1337009..1337893,4	MCF-7	breast:
22	chr9:1017910..1018696-chr9:1429132..1429802,2	MCF-7	breast:
23	chr9:1459777..1461278-chr9:1604683..1605512,7	MCF-7	breast:
24	chr9:1444036..1446024-chr9:1452969..1455867,2	MCF-7	breast:
25	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
26	chr9:1017828..1018465-chr9:1337011..1337699,2	MCF-7	breast:
27	chr9:1459729..1460626-chr9:1605062..1605562,2	MCF-7	breast:
28	chr9:1453549..1456481-chr9:1457480..1459717,2	K562	blood:
29	chr9:1100638..1101499-chr9:1337048..1337780,3	MCF-7	breast:
30	chr9:1459863..1460905-chr9:1619604..1620748,6	MCF-7	breast:
31	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
32	chr9:1454281..1457237-chr9:1457484..1459959,2	MCF-7	breast:
33	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
34	chr9:1196784..1199122-chr9:1220785..1223370,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRT2-2	chr9:1312841-1312899	XLOC_007263
2	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
3	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
4	lnc-DMRT2-4	chr9:1289314-1289412	l_3725_chr9:1288276-1302899_breast
5	lnc-DMRT2-4	chr9:1300940-1301032	l_3725_chr9:1288276-1302899_breast
6	lnc-DMRT2-2	chr9:1298286-1298431	XLOC_007263
7	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
8	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
9	lnc-DMRT2-2	chr9:1328425-1328435	XLOC_007263
10	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
11	lnc-DMRT2-2	chr9:1321457-1321494	XLOC_007263
12	lnc-DMRT2-2	chr9:1321456-1321494	NONHSAT129967
13	lnc-DMRT2-4	chr9:1302841-1302899	l_3725_chr9:1288276-1302899_breast
14	lnc-DMRT2-2	chr9:1321457-1321494	XLOC_007263
15	lnc-DMRT2-6	chr9:1368147-1368400	NONHSAT129976
16	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
17	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
18	lnc-DMRT2-2	chr9:1328424-1328584	NONHSAT129967
19	lnc-DMRT2-6	chr9:1354235-1354272	NONHSAT129976
20	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
21	lnc-DMRT2-2	chr9:1299313-1299412	NONHSAT129967
22	lnc-DMRT2-4	chr9:1318425-1318584	l_3725_chr9:1288276-1302899_breast
23	lnc-DMRT2-2	chr9:1298276-1298431	NONHSAT129967
24	lnc-DMRT2-4	chr9:1288277-1288431	l_3725_chr9:1288276-1302899_breast
25	lnc-DMRT2-2	chr9:1312840-1312899	NONHSAT129967
26	lnc-DMRT2-2	chr9:1327073-1327173	NONHSAT129967
27	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
28	lnc-DMRT2-2	chr9:1312841-1312897	XLOC_007263
29	lnc-DMRT2-5	chr9:1328664-1328987	NONHSAT129974
30	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
31	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
32	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
33	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
34	lnc-DMRT2-2	chr9:1328425-1328584	XLOC_007263
35	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
36	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
37	lnc-DMRT2-4	chr9:1317074-1317173	l_3725_chr9:1288276-1302899_breast
38	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
39	lnc-DMRT2-2	chr9:1310939-1311032	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: 9997 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:9997 , 50 per page) page: 1 2 3 4 5 6 7 ... 200

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12236917	chr9:1216007-1216008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12344150	chr9:1216069-1216070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540633648	chr9:1216089-1216090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540782918	chr9:1216109-1216110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185577199	chr9:1216115-1216116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555883122	chr9:1216116-1216117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576086437	chr9:1216141-1216142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190482486	chr9:1216155-1216156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577682064	chr9:1216171-1216172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74763247	chr9:1216188-1216189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572264530	chr9:1216217-1216218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372533618	chr9:1216281-1216282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561144498	chr9:1216310-1216311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574718576	chr9:1216314-1216315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111412241	chr9:1216388-1216389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563635491	chr9:1216455-1216456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532598557	chr9:1216467-1216468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs68103364	chr9:1216478-1216479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59725235	chr9:1216489-1216490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185761451	chr9:1216503-1216504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543544753	chr9:1216529-1216530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368152593	chr9:1216562-1216563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138791603	chr9:1216595-1216596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190219121	chr9:1216611-1216612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3920797	chr9:1216635-1216636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs113153703	chr9:1216647-1216648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569659019	chr9:1216657-1216658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538690124	chr9:1216667-1216668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558287747	chr9:1216773-1216774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374642862	chr9:1216811-1216812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565707967	chr9:1216836-1216837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181143238	chr9:1216850-1216851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34930932	chr9:1216860-1216861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554942819	chr9:1216893-1216894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147418377	chr9:1216916-1216917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs370820274	chr9:1216918-1216919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114760628	chr9:1217016-1217017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557086297	chr9:1217017-1217018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577290224	chr9:1217038-1217039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185229662	chr9:1217044-1217045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562405196	chr9:1217046-1217047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189698641	chr9:1217063-1217064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560405670	chr9:1217082-1217083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139501280	chr9:1217106-1217107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541820487	chr9:1217114-1217115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370943610	chr9:1217135-1217136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373773410	chr9:1217136-1217137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78327111	chr9:1217146-1217147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531422422	chr9:1217151-1217152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374185857	chr9:1217175-1217176	Weak transcription Enhancers	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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1209000-1216200	Weak transcription	HSMM	muscle
2	chr9:1210800-1217600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:1211400-1216400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:1211600-1216200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:1211600-1216200	Weak transcription	NHDF-Ad	bronchial
6	chr9:1216000-1217600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr9:1216000-1219800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:1216200-1217400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:1216200-1217400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr9:1216200-1217600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:1216200-1217600	Enhancers	HSMM	muscle
12	chr9:1216200-1217800	Enhancers	NHDF-Ad	bronchial
13	chr9:1216400-1217200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr9:1216400-1217200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr9:1216800-1217200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr9:1216800-1217200	Enhancers	HSMMtube	muscle
17	chr9:1217000-1217200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr9:1217000-1217400	Enhancers	Fetal Lung	lung
19	chr9:1217000-1217600	Enhancers	NHLF	lung
20	chr9:1217000-1217600	Enhancers	Osteobl	bone
21	chr9:1217200-1218400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:1217200-1218800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr9:1217200-1219400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:1217400-1222600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:1217600-1218600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:1217600-1218800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr9:1217600-1222000	Weak transcription	NHLF	lung
28	chr9:1217800-1218200	Weak transcription	NHDF-Ad	bronchial
29	chr9:1218200-1220000	Enhancers	NHDF-Ad	bronchial
30	chr9:1218600-1219800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr9:1218800-1219800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr9:1218800-1219800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:1219400-1219800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr9:1219800-1221800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:1219800-1222000	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr9:1219800-1222000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr9:1219800-1222200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:1220000-1221800	Weak transcription	NHDF-Ad	bronchial
39	chr9:1221400-1222800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr9:1221800-1223400	Enhancers	NHDF-Ad	bronchial
41	chr9:1221800-1223600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:1222000-1222600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr9:1222000-1223400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr9:1222000-1223400	Enhancers	NHLF	lung
45	chr9:1222200-1223200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:1222400-1223600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:1222600-1224000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:1222800-1223600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:1223600-1224000	Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr9:1223800-1224200	Active TSS	Placenta	Placenta

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