Variant report

Variant	nsv881102
Chromosome Location	chr4:189388597-189931630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1909)
CpG islands
(count:2748)
Chromatin interactive
region (count:15)
LncRNA
region (count:66)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1909 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189659351-189659620	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189527693-189528168	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189455499-189455789	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:189456095-189456482	HepG2	liver:	n/a	n/a
6	ATF1	chr4:189739516-189739798	K562	blood:	n/a	n/a
7	ATF2	chr4:189897697-189898163	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:189743843-189744148	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:189649632-189649850	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:189897579-189898573	H1-hESC	embryonic stem cell:	n/a	chr4:189897879-189897893
11	BACH1	chr4:189580313-189580512	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:189855675-189855824	GM12878	blood:	n/a	n/a
13	BATF	chr4:189855678-189855822	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:189897805-189898172	H1-hESC	embryonic stem cell:	n/a	chr4:189897882-189897891
15	BCL11A	chr4:189897882-189898134	H1-hESC	embryonic stem cell:	n/a	chr4:189897882-189897891
16	BCL3	chr4:189717818-189718056	GM12878	blood:	n/a	n/a
17	BCL3	chr4:189862683-189863381	A549	lung:	n/a	n/a
18	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:189539576-189539609	K562	blood:	n/a	n/a
20	BHLHE40	chr4:189527879-189528027	HepG2	liver:	n/a	n/a
21	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr4:189732419-189732499	HepG2	liver:	n/a	n/a
23	CBX3	chr4:189852029-189852275	K562	blood:	n/a	n/a
24	CBX3	chr4:189851902-189852434	HCT-116	colon:	n/a	n/a
25	CBX3	chr4:189855440-189855898	HCT-116	colon:	n/a	n/a
26	CBX3	chr4:189862742-189863478	HCT-116	colon:	n/a	n/a
27	CBX3	chr4:189862644-189863423	HCT-116	colon:	n/a	n/a
28	CEBPB	chr4:189823307-189823526	H1-hESC	embryonic stem cell:	n/a	chr4:189823418-189823429 chr4:189823395-189823406
29	CEBPB	chr4:189809080-189809552	IMR90	lung:	n/a	chr4:189809265-189809274 chr4:189809263-189809276 chr4:189809264-189809275 chr4:189809265-189809274 chr4:189809263-189809276 chr4:189809263-189809274 chr4:189809265-189809274 chr4:189809265-189809274
30	CEBPB	chr4:189897632-189897935	ECC-1	luminal epithelium:	n/a	chr4:189897782-189897795
31	CEBPB	chr4:189549147-189549347	A549	lung:	n/a	n/a
32	CEBPB	chr4:189690675-189690948	IMR90	lung:	n/a	chr4:189690814-189690827 chr4:189690816-189690827
33	CEBPB	chr4:189877723-189878027	IMR90	lung:	n/a	chr4:189877861-189877872
34	CEBPB	chr4:189584573-189585174	A549	lung:	n/a	n/a
35	CEBPB	chr4:189456046-189456370	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:189897705-189898254	ECC-1	luminal epithelium:	n/a	chr4:189897782-189897795
37	CEBPB	chr4:189808534-189808641	H1-hESC	embryonic stem cell:	n/a	chr4:189808580-189808591 chr4:189808581-189808590
38	CEBPB	chr4:189628311-189628484	A549	lung:	n/a	n/a
39	CEBPB	chr4:189618382-189618748	IMR90	lung:	n/a	chr4:189618559-189618570
40	CEBPB	chr4:189618387-189618747	HepG2	liver:	n/a	chr4:189618559-189618570
41	CEBPB	chr4:189560699-189560954	A549	lung:	n/a	n/a
42	CEBPB	chr4:189618399-189618727	A549	lung:	n/a	chr4:189618559-189618570
43	CEBPB	chr4:189907207-189907893	A549	lung:	n/a	chr4:189907394-189907405
44	CEBPB	chr4:189789096-189789198	IMR90	lung:	n/a	chr4:189789127-189789138
45	CEBPB	chr4:189618280-189618777	HCT-116	colon:	n/a	chr4:189618559-189618570
46	CEBPB	chr4:189493631-189493895	A549	lung:	n/a	chr4:189493776-189493787
47	CEBPB	chr4:189663658-189663821	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:189618403-189618710	Hela-S3	cervix:	n/a	chr4:189618559-189618570
49	CEBPB	chr4:189808507-189808669	HepG2	liver:	n/a	chr4:189808580-189808591 chr4:189808581-189808590
50	CEBPB	chr4:189862562-189863383	A549	lung:	n/a	chr4:189862837-189862848

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189602161-189602211	RPTEC	kidney:	n/a
2	chr4:189612833-189612883	SAEC	small airway:	n/a
3	chr4:189612833-189612883	GM06990	blood:	n/a
4	chr4:189602161-189602211	RPTEC	kidney:	n/a
5	chr4:189612833-189612883	SAEC	small airway:	n/a
6	chr4:189612833-189612883	GM06990	blood:	n/a
7	chr4:189602236-189602286	IMR90	lung:	fetal
8	chr4:189895469-189895519	K562	blood:	n/a
9	chr4:189871012-189871062	BJ	skin:	n/a
10	chr4:189433040-189433090	AG09319	gingival:	n/a
11	chr4:189602161-189602211	HUVEC	blood vessel:	n/a
12	chr4:189659523-189659573	HRCEpiC	kidney:	n/a
13	chr4:189476745-189476795	MCF-7	breast:	n/a
14	chr4:189433040-189433090	NH-A	brain:	n/a
15	chr4:189433040-189433090	SK-N-SH	brain:	n/a
16	chr4:189476745-189476795	Hepatocyte	liver:	n/a
17	chr4:189700628-189700678	HCT-116	colon:	n/a
18	chr4:189602161-189602211	U87	brain:	n/a
19	chr4:189895469-189895519	HRPEpiC	eye:	n/a
20	chr4:189577711-189577761	Hepatocyte	liver:	n/a
21	chr4:189541174-189541224	T-47D	breast:	n/a
22	chr4:189433040-189433090	T-47D	breast:	n/a
23	chr4:189659523-189659573	NB4	blood:	n/a
24	chr4:189860869-189860919	BJ	skin:	n/a
25	chr4:189552339-189552389	NH-A	brain:	n/a
26	chr4:189580633-189580683	HRE	kidney:	n/a
27	chr4:189552677-189552727	PrEC	prostate:	n/a
28	chr4:189895923-189895973	GM12892	blood:	n/a
29	chr4:189541174-189541224	HIPEpiC	eye:	n/a
30	chr4:189572647-189572697	AG10803	skin:	n/a
31	chr4:189928662-189928712	IMR90	lung:	fetal
32	chr4:189578842-189578892	NB4	blood:	n/a
33	chr4:189551752-189551802	AG09309	skin:	n/a
34	chr4:189659523-189659573	AG04449	skin:	fetal
35	chr4:189395410-189395460	SK-N-MC	brain:	n/a
36	chr4:189433040-189433090	AG10803	skin:	n/a
37	chr4:189895469-189895519	HEEpiC	esophagus:	n/a
38	chr4:189548707-189548757	PrEC	prostate:	n/a
39	chr4:189580331-189580381	SKMC	muscle:	n/a
40	chr4:189485260-189485310	HRPEpiC	eye:	n/a
41	chr4:189552386-189552436	AG04449	skin:	fetal
42	chr4:189700628-189700678	MCF-7	breast:	n/a
43	chr4:189743072-189743122	HMEC	breast:	n/a
44	chr4:189476613-189476663	BJ	skin:	n/a
45	chr4:189871012-189871062	HCPEpiC	choroid plexus:	n/a
46	chr4:189860820-189860870	MCF-7	breast:	n/a
47	chr4:189655175-189655225	AG04449	skin:	fetal
48	chr4:189552622-189552672	GM12891	blood:	n/a
49	chr4:189580633-189580683	NH-A	brain:	n/a
50	chr4:189580633-189580683	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:189659615..189661129-chr6:153313575..153315096,2	K562	blood:
2	chr4:189658248..189662329-chr6:153321108..153324955,4	K562	blood:
3	chr4:189704602..189705331-chr9:126840912..126841898,2	MCF-7	breast:
4	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
5	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
6	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:
7	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
8	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
9	chr4:189855824..189858176-chr4:189947358..189950070,2	K562	blood:
10	chr4:189659109..189659751-chr6:153323423..153323945,2	NB4	blood:
11	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
12	chr4:189702571..189703442-chr4:190123148..190123787,2	MCF-7	breast:
13	chr4:189658110..189659728-chr6:153322361..153324298,2	MCF-7	breast:
14	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
15	chr4:189659633..189661135-chr6:153323368..153324975,2	MCF-7	breast:

(count:66 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-4	chr4:189699838-189700133	ENSG00000249269
2	lnc-TRIML1-10	chr4:189613729-189613822	ucscGeneNc_uc003izp_1
3	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
4	lnc-TRIML2-6	chr4:189716390-189716718	NONHSAT099763
5	lnc-TRIML2-6	chr4:189698770-189699205	XLOC_004227
6	lnc-TRIML2-6	chr4:189712226-189712445	XLOC_004227
7	lnc-TRIML2-6	chr4:189712226-189712445	NONHSAT099763
8	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
9	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834
10	lnc-TRIML2-6	chr4:189698833-189699205	ENSG00000250626
11	lnc-TRIML1-4	chr4:189689945-189690019	ENSG00000249269
12	lnc-TRIML1-5	chr4:189697811-189697921	XLOC_003836
13	lnc-TRIML2-6	chr4:189712226-189712445	XLOC_004227
14	lnc-TRIML2-6	chr4:189712226-189712445	XLOC_004227
15	lnc-TRIML1-10	chr4:189694883-189696700	ucscGeneNc_uc003izp_1
16	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
17	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
18	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
19	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
20	lnc-TRIML2-6	chr4:189716390-189716930	XLOC_004227
21	lnc-TRIML2-6	chr4:189738798-189738928	XLOC_004227
22	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
23	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
24	lnc-TRIML2-6	chr4:189738716-189738928	XLOC_004227
25	lnc-TRIML1-3	chr4:189522922-189523062	ENSG00000249378
26	lnc-TRIML2-6	chr4:189739480-189739775	XLOC_004227
27	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
28	lnc-TRIML1-5	chr4:189706916-189707064	XLOC_003836
29	lnc-TRIML2-6	chr4:189716390-189717788	XLOC_004227
30	lnc-TRIML2-6	chr4:189712226-189712445	XLOC_004227
31	lnc-TRIML2-6	chr4:189716390-189717787	ENSG00000250626
32	lnc-TRIML2-6	chr4:189698833-189699205	XLOC_004227
33	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
34	lnc-TRIML1-5	chr4:189706450-189706665	XLOC_003836
35	lnc-TRIML1-10	chr4:189634846-189634904	ucscGeneNc_uc003izp_1
36	lnc-TRIML1-5	chr4:189706415-189706559	XLOC_003836
37	lnc-TRIML1-3	chr4:189522922-189523062	NONHSAT099745
38	lnc-TRIML1-5	chr4:189705067-189705165	XLOC_003836
39	lnc-TRIML1-10	chr4:189635786-189636060	ucscGeneNc_uc003izp_1
40	lnc-TRIML2-6	chr4:189712226-189712445	ENSG00000250626
41	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
42	lnc-TRIML2-6	chr4:189739480-189739606	XLOC_004227
43	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
44	lnc-TRIML2-7	chr4:189911869-189912208	XLOC_004228
45	lnc-TRIML2-7	chr4:189922924-189923229	XLOC_004228
46	lnc-TRIML2-6	chr4:189717890-189717959	XLOC_004227
47	lnc-TRIML1-3	chr4:189601875-189602205	ENSG00000249378
48	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
49	lnc-TRIML1-3	chr4:189522922-189523025	NONHSAT099749
50	lnc-TRIML1-9	chr4:189661661-189662435	NONHSAT099754

No data

Variant related genes	Relation type
ENSG00000250024	TF binding region
ENSG00000249269	TF binding region
RNU7-192P	TF binding region
LINC01060	TF binding region
ENSG00000251619	TF binding region
ENSG00000250523	TF binding region
ENSG00000180015	TF binding region
ENSG00000250626	TF binding region
ENSG00000250024	CpG island
ENSG00000249269	CpG island
RNU7-192P	CpG island
LINC01060	CpG island
ENSG00000251619	CpG island
ENSG00000250523	CpG island
ENSG00000180015	CpG island
ENSG00000250626	CpG island
ENSG00000178409	chromatin interactions
ENSG00000112031	chromatin interactions
PRNP	miRNA target sites
RASSF2	miRNA target sites
KCNK1	miRNA target sites
PTGFRN	miRNA target sites
FAM104A	miRNA target sites
BMPR2	miRNA target sites
TAPBP	miRNA target sites
UBFD1	miRNA target sites
USP1	miRNA target sites
SHCBP1	miRNA target sites
MAP2K4	miRNA target sites
DIP2C	miRNA target sites
MPP5	miRNA target sites
PFN2	miRNA target sites

Extended variants
information (count: 18812 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:18812 , 50 per page) page: 1 2 3 4 5 6 7 ... 377

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs314064	chr4:189388597-189388598	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567611081	chr4:189388638-189388639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs314063	chr4:189388668-189388669	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76685042	chr4:189388690-189388691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184794728	chr4:189388749-189388750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370438461	chr4:189388769-189388770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536955336	chr4:189388836-189388837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs137997466	chr4:189388863-189388864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188349423	chr4:189388885-189388886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs56371520	chr4:189388899-189388900	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs571564674	chr4:189388908-189388909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552825083	chr4:189388946-189388947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572913249	chr4:189388955-189388956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545099866	chr4:189388994-189388995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180808075	chr4:189389004-189389005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578188631	chr4:189389047-189389048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75543037	chr4:189389073-189389074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564006179	chr4:189389125-189389126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs57393916	chr4:189389159-189389160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142096491	chr4:189389169-189389170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs314062	chr4:189389170-189389171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559460066	chr4:189389194-189389195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186691580	chr4:189389322-189389323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551420168	chr4:189389325-189389326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377326795	chr4:189389326-189389327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530614515	chr4:189389330-189389331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553999198	chr4:189389332-189389333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543129088	chr4:189389342-189389343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189552630	chr4:189389351-189389352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558002717	chr4:189389368-189389369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567532607	chr4:189389410-189389411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182140472	chr4:189389414-189389415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536124958	chr4:189389484-189389485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375113590	chr4:189389600-189389601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552957205	chr4:189389626-189389627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186791919	chr4:189389634-189389635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538749398	chr4:189389660-189389661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190314612	chr4:189389748-189389749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369614572	chr4:189389775-189389776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs398051376	chr4:189389790-189389791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536498199	chr4:189389794-189389795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62352711	chr4:189389796-189389797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544010511	chr4:189389797-189389798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557403077	chr4:189389803-189389804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369847699	chr4:189389805-189389806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574296626	chr4:189389811-189389812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369029268	chr4:189389826-189389827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542904364	chr4:189389828-189389829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368897161	chr4:189389837-189389838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528457532	chr4:189389841-189389842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Epilepsy	21635232	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	17989066	CNVD
Breast cancer	22522925	CNVD
Autism	20858243	CNVD

Chromatin state (count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189366000-189415600	Weak transcription	Osteobl	bone
2	chr4:189376800-189416200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:189385400-189415800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:189385600-189394800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr4:189387000-189394000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:189388000-189388600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:189388600-189393800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:189393800-189396000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr4:189394000-189397400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:189394200-189395400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr4:189394400-189395200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:189394400-189395400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:189394400-189396600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:189394800-189395200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:189394800-189395200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:189394800-189395200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr4:189395000-189395400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:189395000-189396000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:189395200-189395400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:189395200-189396000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:189395200-189398200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:189395400-189395600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:189395600-189395800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:189395800-189396400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:189396000-189398200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr4:189396400-189397000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:189396600-189401800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:189397400-189398200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:189397600-189407400	Weak transcription	HMEC	breast
30	chr4:189398200-189398400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:189398200-189399000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr4:189398200-189399000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr4:189398200-189401400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:189398400-189398600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:189398400-189398800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr4:189398600-189399000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr4:189398800-189401600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:189399000-189401000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:189399000-189401600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr4:189399000-189402200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr4:189401000-189402400	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr4:189401400-189402000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:189401600-189401800	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr4:189401600-189402400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr4:189401600-189402600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:189401800-189402200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr4:189401800-189402200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
48	chr4:189402000-189416200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:189402200-189403200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:189402200-189403400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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