Variant report

Variant	esv2752273
Chromosome Location	chr9:1062218-1824888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3267)
CpG islands
(count:0)
Chromatin interactive
region (count:102)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3267 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1165172-1165199	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:1262535-1262860	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:1454262-1454586	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:1232418-1233152	HepG2	liver:	n/a	n/a
5	ATF2	chr9:1536424-1536957	GM12878	blood:	n/a	n/a
6	ATF2	chr9:1469886-1470491	GM12878	blood:	n/a	n/a
7	ATF2	chr9:1469879-1470564	GM12878	blood:	n/a	n/a
8	ATF2	chr9:1490307-1491149	GM12878	blood:	n/a	n/a
9	ATF2	chr9:1273849-1274227	GM12878	blood:	n/a	n/a
10	ATF2	chr9:1490362-1491115	GM12878	blood:	n/a	n/a
11	ATF2	chr9:1536421-1536930	GM12878	blood:	n/a	n/a
12	ATF2	chr9:1267004-1267465	GM12878	blood:	n/a	n/a
13	ATF2	chr9:1267069-1267434	GM12878	blood:	n/a	n/a
14	BATF	chr9:1311457-1311704	GM12878	blood:	n/a	n/a
15	BATF	chr9:1536479-1536843	GM12878	blood:	n/a	chr9:1536673-1536683
16	BATF	chr9:1535619-1535903	GM12878	blood:	n/a	n/a
17	BATF	chr9:1536433-1537132	GM12878	blood:	n/a	chr9:1536673-1536683
18	BATF	chr9:1267089-1267384	GM12878	blood:	n/a	n/a
19	BATF	chr9:1522199-1522450	GM12878	blood:	n/a	n/a
20	BATF	chr9:1232670-1232943	GM12878	blood:	n/a	n/a
21	BATF	chr9:1267065-1267439	GM12878	blood:	n/a	n/a
22	BATF	chr9:1514759-1515190	GM12878	blood:	n/a	chr9:1514963-1514974
23	BATF	chr9:1490384-1491050	GM12878	blood:	n/a	n/a
24	BATF	chr9:1505545-1505846	GM12878	blood:	n/a	n/a
25	BATF	chr9:1470009-1470366	GM12878	blood:	n/a	chr9:1470172-1470183 chr9:1470265-1470278
26	BATF	chr9:1666546-1666849	GM12878	blood:	n/a	chr9:1666712-1666723
27	BATF	chr9:1490300-1491164	GM12878	blood:	n/a	n/a
28	BATF	chr9:1273755-1274200	GM12878	blood:	n/a	chr9:1274007-1274018
29	BATF	chr9:1522204-1522433	GM12878	blood:	n/a	n/a
30	BATF	chr9:1468627-1468906	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:1267051-1267422	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:1273784-1274155	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:1554412-1554724	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:1536584-1536781	GM12878	blood:	n/a	chr9:1536675-1536684
35	BCL11A	chr9:1522572-1522804	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:1273798-1274241	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:1267058-1267389	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:1271872-1272106	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:1490371-1491127	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:1536449-1536835	GM12878	blood:	n/a	chr9:1536675-1536684
41	BCL11A	chr9:1490707-1491032	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:1522157-1522444	GM12878	blood:	n/a	n/a
43	BCL3	chr9:1458553-1458815	GM12878	blood:	n/a	chr9:1458740-1458749 chr9:1458739-1458748
44	BCL3	chr9:1536446-1536852	GM12878	blood:	n/a	chr9:1536675-1536684
45	BCL3	chr9:1458432-1458804	GM12878	blood:	n/a	chr9:1458740-1458749 chr9:1458739-1458748
46	BCL3	chr9:1469934-1470495	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:1490297-1491172	GM12878	blood:	n/a	n/a
48	BCLAF1	chr9:1490418-1491093	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:1604933-1605323	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:1267023-1267355	GM12878	blood:	n/a	n/a

No data

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
2	chr9:1492000..1494748-chr9:1498884..1501267,2	MCF-7	breast:
3	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
4	chr9:1017784..1019327-chr9:1158625..1160475,2	MCF-7	breast:
5	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
6	chr9:1048965..1051949-chr9:1170856..1173228,2	MCF-7	breast:
7	chr9:1453549..1456481-chr9:1457480..1459717,2	K562	blood:
8	chr9:1017828..1018465-chr9:1337011..1337699,2	MCF-7	breast:
9	chr9:1459862..1460804-chr9:1527712..1529112,4	MCF-7	breast:
10	chr9:1049307..1051830-chr9:1209993..1212929,2	MCF-7	breast:
11	chr9:1156562..1162179-chr9:1163960..1167701,5	MCF-7	breast:
12	chr9:1155504..1158028-chr9:1171284..1172916,2	MCF-7	breast:
13	chr9:1453549..1456481-chr9:1457480..1459717,2	K562	blood:
14	chr9:1100633..1101579-chr9:1428962..1429946,8	MCF-7	breast:
15	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
16	chr9:1167206..1169983-chr9:1171593..1173584,2	MCF-7	breast:
17	chr9:1315772..1318545-chr9:1320375..1322632,2	K562	blood:
18	chr9:1197110..1199229-chr9:1201325..1204281,3	MCF-7	breast:
19	chr9:1058546..1060876-chr9:1062329..1064196,2	MCF-7	breast:
20	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
21	chr9:1196174..1202144-chr9:1204882..1208508,8	MCF-7	breast:
22	chr9:1100954..1101519-chr9:1619985..1620571,2	MCF-7	breast:
23	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
24	chr9:1376504..1378788-chr9:1379688..1382512,2	MCF-7	breast:
25	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:
26	chr9:1821753..1823506-chr9:1830601..1832415,2	K562	blood:
27	chr9:1050662..1052458-chr9:1210912..1212810,2	MCF-7	breast:
28	chr9:1207734..1210015-chr9:1211203..1213257,2	MCF-7	breast:
29	chr9:1199075..1201039-chr9:1246978..1249972,2	K562	blood:
30	chr9:1050169..1051008-chr9:1198034..1198952,5	MCF-7	breast:
31	chr9:1049962..1051601-chr9:1206448..1208602,2	MCF-7	breast:
32	chr9:1048644..1051362-chr9:1182528..1184402,2	MCF-7	breast:
33	chr9:1433839..1434724-chr9:1619824..1620539,2	MCF-7	breast:
34	chr9:1100638..1101499-chr9:1337048..1337780,3	MCF-7	breast:
35	chr9:1050560..1053222-chr9:1082736..1084655,2	MCF-7	breast:
36	chr17:35897413..35898334-chr9:1234312..1235126,2	MCF-7	breast:
37	chr9:1459729..1460626-chr9:1605062..1605562,2	MCF-7	breast:
38	chr9:1444036..1446024-chr9:1452969..1455867,2	MCF-7	breast:
39	chr9:1474110..1476318-chr9:1485269..1488138,2	MCF-7	breast:
40	chr9:1463195..1465097-chr9:1468058..1470697,2	MCF-7	breast:
41	chr9:1100620..1101481-chr9:1337009..1337893,4	MCF-7	breast:
42	chr9:1100633..1101579-chr9:1428962..1429946,8	MCF-7	breast:
43	chr9:1172064..1174566-chr9:1177825..1179718,2	MCF-7	breast:
44	chr9:1459777..1461278-chr9:1604683..1605512,7	MCF-7	breast:
45	chr9:1414222..1417184-chr9:1419869..1422079,2	K562	blood:
46	chr9:1049884..1050964-chr9:1336243..1337456,4	MCF-7	breast:
47	chr9:1721060..1723569-chr9:1724371..1726152,2	MCF-7	breast:
48	chr9:1017795..1018400-chr9:1429068..1429992,2	MCF-7	breast:
49	chr9:1474110..1476318-chr9:1485269..1488138,2	MCF-7	breast:
50	chr4:183090047..183090870-chr9:1152117..1153038,2	MCF-7	breast:

(count:43 , 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	chr9:1298277-1298431	XLOC_007263
3	lnc-DMRT2-5	chr9:1328664-1328987	NONHSAT129974
4	lnc-DMRT2-2	chr9:1328425-1328435	XLOC_007263
5	lnc-DMRT2-6	chr9:1368147-1368400	NONHSAT129976
6	lnc-DMRT2-2	chr9:1328425-1328584	XLOC_007263
7	lnc-DMRT2-2	chr9:1321457-1321494	XLOC_007263
8	lnc-DMRT2-4	chr9:1302841-1302899	l_3725_chr9:1288276-1302899_breast
9	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
10	lnc-C9orf66-13	chr9:1164414-1164867	NONHSAT129966
11	lnc-DMRT2-2	chr9:1312841-1312897	XLOC_007263
12	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
13	lnc-DMRT2-2	chr9:1328424-1328584	NONHSAT129967
14	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
15	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
16	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
17	lnc-DMRT2-2	chr9:1312841-1312899	XLOC_007263
18	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
19	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
20	lnc-DMRT2-2	chr9:1299314-1299412	XLOC_007263
21	lnc-DMRT2-2	chr9:1327073-1327173	NONHSAT129967
22	lnc-DMRT2-4	chr9:1300940-1301032	l_3725_chr9:1288276-1302899_breast
23	lnc-DMRT2-2	chr9:1298286-1298431	XLOC_007263
24	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
25	lnc-SMARCA2-2	chr9:1718867-1718912	XLOC_007264
26	lnc-DMRT2-2	chr9:1310939-1311032	NONHSAT129967
27	lnc-DMRT2-2	chr9:1327074-1327173	XLOC_007263
28	lnc-DMRT2-2	chr9:1299313-1299412	NONHSAT129967
29	lnc-DMRT2-2	chr9:1312840-1312899	NONHSAT129967
30	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
31	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
32	lnc-C9orf66-12	chr9:1151807-1152140	NONHSAT129965
33	lnc-DMRT2-2	chr9:1298276-1298431	NONHSAT129967
34	lnc-SMARCA2-2	chr9:1633518-1633545	XLOC_007264
35	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263
36	lnc-DMRT2-4	chr9:1288277-1288431	l_3725_chr9:1288276-1302899_breast
37	lnc-DMRT2-2	chr9:1321456-1321494	NONHSAT129967
38	lnc-DMRT2-4	chr9:1318425-1318584	l_3725_chr9:1288276-1302899_breast
39	lnc-DMRT2-6	chr9:1354235-1354272	NONHSAT129976
40	lnc-DMRT2-2	chr9:1310940-1311032	XLOC_007263
41	lnc-DMRT2-4	chr9:1317074-1317173	l_3725_chr9:1288276-1302899_breast
42	lnc-DMRT2-4	chr9:1289314-1289412	l_3725_chr9:1288276-1302899_breast
43	lnc-DMRT2-2	chr9:1298277-1298431	XLOC_007263

No data

Variant related genes	Relation type
ENSG00000233575	TF binding region
ENSG00000224836	TF binding region
RPS27AP14	TF binding region
RNA5SP279	TF binding region
ENSG00000006114	chromatin interactions
ENSG00000236594	chromatin interactions
ENSG00000221227	chromatin interactions
ENSG00000173253	chromatin interactions
AP3D1	miRNA target sites
AP2M1	miRNA target sites

Extended variants
information (count: 26064 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:26064 , 50 per page) page: 1 2 3 4 5 6 7 ... 522

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1417085	chr9:1062218-1062219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544251867	chr9:1062221-1062222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188180053	chr9:1062225-1062226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375657503	chr9:1062231-1062232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143980495	chr9:1062237-1062238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190973388	chr9:1062239-1062240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113787938	chr9:1062257-1062258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182262720	chr9:1062269-1062270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71507938	chr9:1062280-1062281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs5895888	chr9:1062284-1062285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397816776	chr9:1062288-1062289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200527833	chr9:1062289-1062290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114827425	chr9:1062292-1062293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531948261	chr9:1062299-1062300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186635607	chr9:1062312-1062313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575353339	chr9:1062313-1062314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192536040	chr9:1062409-1062410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539396016	chr9:1062442-1062443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546323821	chr9:1062465-1062466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566746189	chr9:1062512-1062513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537499013	chr9:1062535-1062536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560014688	chr9:1062564-1062565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555638197	chr9:1062573-1062574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184811735	chr9:1062574-1062575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537664404	chr9:1062660-1062661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557814473	chr9:1062661-1062662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10959157	chr9:1062676-1062677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs187578003	chr9:1062677-1062678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2375075	chr9:1062695-1062696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573989015	chr9:1062696-1062697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140898438	chr9:1062710-1062711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563199786	chr9:1062735-1062736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs193082427	chr9:1062790-1062791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184880908	chr9:1062806-1062807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112974239	chr9:1062811-1062812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537794055	chr9:1062812-1062813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs959480	chr9:1062815-1062816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs189825566	chr9:1062824-1062825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557439234	chr9:1062839-1062840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181027132	chr9:1062851-1062852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10122013	chr9:1062925-1062926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs546146552	chr9:1062929-1062930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145109588	chr9:1062940-1062941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548829349	chr9:1062969-1062970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568846063	chr9:1062970-1062971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs959481	chr9:1062999-1063000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs77828697	chr9:1063065-1063066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12353118	chr9:1063085-1063086	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs578042704	chr9:1063101-1063102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75992211	chr9:1063142-1063143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Esophageal cancer	21851588	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	21215367	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:1058400-1063400	Weak transcription	Fetal Muscle Leg	muscle
2	chr9:1058400-1065600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr9:1063400-1063800	Enhancers	Fetal Muscle Leg	muscle
4	chr9:1063800-1064800	Weak transcription	Fetal Muscle Leg	muscle
5	chr9:1065000-1065200	Enhancers	Fetal Muscle Leg	muscle
6	chr9:1065600-1065800	Enhancers	Fetal Muscle Trunk	muscle
7	chr9:1071000-1072000	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr9:1072000-1072400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
9	chr9:1072400-1072600	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr9:1072400-1072600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr9:1082600-1082800	Enhancers	NHDF-Ad	bronchial
12	chr9:1082800-1083000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:1082800-1084000	Active TSS	NHDF-Ad	bronchial
14	chr9:1083000-1083200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr9:1083000-1083200	Enhancers	Brain Hippocampus Middle	brain
16	chr9:1083000-1083400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:1083000-1083400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr9:1083000-1083800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:1083000-1084000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:1083000-1084200	Active TSS	Brain Cingulate Gyrus	brain
21	chr9:1083200-1083400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr9:1083200-1083600	Active TSS	Fetal Muscle Trunk	muscle
23	chr9:1083200-1083800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr9:1083200-1083800	Active TSS	Cortex derived primary cultured neurospheres	brain
25	chr9:1083200-1083800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr9:1083200-1083800	Active TSS	Adipose Nuclei	Adipose
27	chr9:1083200-1083800	Active TSS	Brain Hippocampus Middle	brain
28	chr9:1083200-1083800	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr9:1083200-1083800	Active TSS	HSMM	muscle
30	chr9:1083200-1084000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
31	chr9:1083200-1084000	Active TSS	Brain Anterior Caudate	brain
32	chr9:1083200-1084000	Active TSS	Psoas Muscle	Psoas
33	chr9:1083400-1083600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr9:1083400-1083600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:1083400-1083600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
36	chr9:1083400-1083800	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr9:1083400-1083800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr9:1083400-1083800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr9:1083400-1083800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr9:1083400-1083800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:1083400-1083800	Active TSS	Muscle Satellite Cultured Cells	--
42	chr9:1083400-1083800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr9:1083400-1083800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr9:1083400-1083800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr9:1083400-1083800	Active TSS	Brain Substantia Nigra	brain
46	chr9:1083400-1083800	Active TSS	Colon Smooth Muscle	Colon
47	chr9:1083400-1083800	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr9:1083400-1083800	Active TSS	Fetal Brain Female	brain
49	chr9:1083400-1083800	Bivalent/Poised TSS	Fetal Lung	lung
50	chr9:1083400-1083800	Active TSS	Fetal Muscle Leg	muscle

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