Variant report

Variant	nsv818672
Chromosome Location	chr9:1200036-1404430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1232418-1233152	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:1262535-1262860	HepG2	liver:	n/a	n/a
3	ATF2	chr9:1273849-1274227	GM12878	blood:	n/a	n/a
4	ATF2	chr9:1267004-1267465	GM12878	blood:	n/a	n/a
5	ATF2	chr9:1267069-1267434	GM12878	blood:	n/a	n/a
6	BATF	chr9:1267089-1267384	GM12878	blood:	n/a	n/a
7	BATF	chr9:1273755-1274200	GM12878	blood:	n/a	chr9:1274007-1274018
8	BATF	chr9:1232670-1232943	GM12878	blood:	n/a	n/a
9	BATF	chr9:1267065-1267439	GM12878	blood:	n/a	n/a
10	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:1273784-1274155	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:1267058-1267389	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:1271872-1272106	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:1273798-1274241	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:1267051-1267422	GM12878	blood:	n/a	n/a
16	BCLAF1	chr9:1267023-1267355	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:1329191-1329209	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:1267079-1267545	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:1273916-1274170	GM12878	blood:	n/a	n/a
20	BHLHE40	chr9:1269746-1270488	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:1271859-1272122	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:1270807-1271031	GM12878	blood:	n/a	n/a
23	CEBPB	chr9:1383819-1384236	HepG2	liver:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
24	CEBPB	chr9:1402843-1403043	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:1320828-1321012	A549	lung:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
26	CEBPB	chr9:1337163-1337564	MCF-7	breast:	n/a	n/a
27	CEBPB	chr9:1232528-1233024	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
28	CEBPB	chr9:1387697-1387780	H1-hESC	embryonic stem cell:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
29	CEBPB	chr9:1232307-1233098	MCF-7	breast:	n/a	chr9:1233061-1233072 chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
30	CEBPB	chr9:1233454-1233961	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:1387624-1387884	IMR90	lung:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
32	CEBPB	chr9:1320743-1320979	HepG2	liver:	n/a	chr9:1320878-1320889 chr9:1320878-1320891 chr9:1320879-1320890
33	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
34	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
35	CEBPB	chr9:1383860-1384144	A549	lung:	n/a	chr9:1384079-1384090 chr9:1383940-1383953
36	CEBPB	chr9:1232593-1232789	HepG2	liver:	n/a	chr9:1232708-1232721 chr9:1232709-1232720
37	CEBPB	chr9:1233604-1233963	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:1232402-1232946	MCF-7	breast:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
39	CEBPB	chr9:1233638-1233904	A549	lung:	n/a	n/a
40	CEBPB	chr9:1232585-1232851	A549	lung:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
41	CEBPB	chr9:1387693-1387860	K562	blood:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
42	CEBPB	chr9:1263039-1263079	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:1200905-1201341	HepG2	liver:	n/a	n/a
44	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
45	CEBPB	chr9:1208265-1208585	IMR90	lung:	n/a	n/a
46	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
47	CEBPB	chr9:1232072-1232973	IMR90	lung:	n/a	chr9:1232708-1232721 chr9:1232709-1232720 chr9:1232805-1232816
48	CEBPB	chr9:1387573-1387887	HepG2	liver:	n/a	chr9:1387729-1387738 chr9:1387727-1387738 chr9:1387728-1387739
49	CHD1	chr9:1267073-1267378	GM12878	blood:	n/a	n/a
50	CHD2	chr9:1271987-1272089	GM12878	blood:	n/a	n/a

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

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

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

Extended variants
information (count: 7595 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:7595 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs883177	chr9:1200036-1200037	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7863819	chr9:1200045-1200046	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs115173598	chr9:1200071-1200072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10960360	chr9:1200108-1200109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs58074744	chr9:1200123-1200124	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs883178	chr9:1200130-1200131	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs115938190	chr9:1200135-1200136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549915101	chr9:1200149-1200150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571827992	chr9:1200171-1200172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534162684	chr9:1200184-1200185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146718286	chr9:1200245-1200246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566620064	chr9:1200271-1200272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556760026	chr9:1200274-1200275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535537756	chr9:1200283-1200284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs371151593	chr9:1200318-1200319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7864211	chr9:1200391-1200392	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7867335	chr9:1200400-1200401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs34404666	chr9:1200404-1200405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557799509	chr9:1200411-1200412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577844713	chr9:1200430-1200431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559466454	chr9:1200454-1200455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7867369	chr9:1200477-1200478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368391376	chr9:1200486-1200487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7864344	chr9:1200491-1200492	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs7849307	chr9:1200494-1200495	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200289515	chr9:1200502-1200503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7867480	chr9:1200508-1200509	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs185296553	chr9:1200511-1200512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531573466	chr9:1200523-1200524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72705275	chr9:1200533-1200534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs192794570	chr9:1200538-1200539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374186750	chr9:1200545-1200546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184844414	chr9:1200657-1200658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188513036	chr9:1200695-1200696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10960363	chr9:1200703-1200704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs535549880	chr9:1200737-1200738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139215840	chr9:1200764-1200765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12336853	chr9:1200771-1200772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537469144	chr9:1200775-1200776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs868085	chr9:1200784-1200785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs577899178	chr9:1200821-1200822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114844183	chr9:1200839-1200840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545891016	chr9:1200871-1200872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180891379	chr9:1200897-1200898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542729413	chr9:1200898-1200899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562877536	chr9:1200917-1200918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576460490	chr9:1200919-1200920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545120751	chr9:1200941-1200942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12341136	chr9:1200946-1200947	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs114085627	chr9:1201011-1201012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1198800-1200800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:1198800-1202600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr9:1199400-1200600	Weak transcription	Psoas Muscle	Psoas
4	chr9:1199800-1200600	Weak transcription	Esophagus	oesophagus
5	chr9:1200000-1203600	Enhancers	Liver	Liver
6	chr9:1200400-1201400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr9:1200600-1201600	Enhancers	Esophagus	oesophagus
8	chr9:1200600-1201600	Enhancers	Fetal Lung	lung
9	chr9:1200600-1201600	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr9:1200600-1201800	Enhancers	HepG2	liver
11	chr9:1200600-1202200	Enhancers	Fetal Muscle Leg	muscle
12	chr9:1200600-1202200	Enhancers	Pancreas	Pancrea
13	chr9:1200600-1203000	Enhancers	Psoas Muscle	Psoas
14	chr9:1200800-1201200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr9:1200800-1201400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:1201000-1201600	Enhancers	Adipose Nuclei	Adipose
17	chr9:1201000-1201600	Enhancers	Gastric	stomach
18	chr9:1201000-1202000	Enhancers	Fetal Brain Male	brain
19	chr9:1201000-1202000	Enhancers	Fetal Muscle Trunk	muscle
20	chr9:1201000-1202000	Enhancers	Lung	lung
21	chr9:1201000-1202200	Enhancers	Left Ventricle	heart
22	chr9:1201200-1201600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:1201200-1202800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:1201400-1202000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr9:1201400-1202400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:1201600-1202600	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr9:1201600-1202800	Weak transcription	Adipose Nuclei	Adipose
28	chr9:1201600-1209400	Weak transcription	Gastric	stomach
29	chr9:1202000-1202400	Weak transcription	Fetal Brain Male	brain
30	chr9:1202000-1203000	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr9:1202400-1203400	Enhancers	Fetal Brain Male	brain
32	chr9:1202400-1203800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:1202600-1202800	Weak transcription	Brain Substantia Nigra	brain
34	chr9:1202600-1203000	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:1202600-1203000	Enhancers	Brain Germinal Matrix	brain
36	chr9:1202600-1203000	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr9:1202600-1203400	Enhancers	NHDF-Ad	bronchial
38	chr9:1202600-1203600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr9:1202800-1203000	Enhancers	Adipose Nuclei	Adipose
40	chr9:1202800-1203200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr9:1202800-1203200	Enhancers	Brain Substantia Nigra	brain
42	chr9:1202800-1203400	Enhancers	Fetal Brain Female	brain
43	chr9:1203000-1204200	Weak transcription	Psoas Muscle	Psoas
44	chr9:1203200-1203800	Enhancers	Brain Hippocampus Middle	brain
45	chr9:1203200-1208200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:1203400-1207600	Weak transcription	NHDF-Ad	bronchial
47	chr9:1203600-1207400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr9:1203800-1207400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:1204200-1204400	Enhancers	Psoas Muscle	Psoas
50	chr9:1207400-1208000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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