Variant report

Variant	nsv881540
Chromosome Location	chr4:189331266-189654390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1355)
CpG islands
(count:2322)
Chromatin interactive
region (count:7)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1355 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189376606-189376828	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189456095-189456482	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189527693-189528168	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:189359441-189359980	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:189455499-189455789	HepG2	liver:	n/a	n/a
7	BACH1	chr4:189365427-189366156	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:189580313-189580512	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:189353505-189353712	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:189372985-189373571	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:189366501-189366863	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:189370074-189371014	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:189649632-189649850	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr4:189373274-189373489	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr4:189370110-189370622	A549	lung:	n/a	n/a
16	BCL3	chr4:189344161-189344742	A549	lung:	n/a	n/a
17	BHLHE40	chr4:189539576-189539609	K562	blood:	n/a	n/a
18	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:189527879-189528027	HepG2	liver:	n/a	n/a
20	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:189549105-189549301	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:189365565-189366090	A549	lung:	n/a	chr4:189365858-189365869
23	CEBPB	chr4:189365679-189366052	IMR90	lung:	n/a	chr4:189365858-189365869
24	CEBPB	chr4:189351132-189351486	IMR90	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
25	CEBPB	chr4:189351143-189351497	H1-hESC	embryonic stem cell:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
26	CEBPB	chr4:189351226-189351392	K562	blood:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
27	CEBPB	chr4:189371727-189371894	A549	lung:	n/a	n/a
28	CEBPB	chr4:189514320-189514661	IMR90	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
29	CEBPB	chr4:189424052-189424344	IMR90	lung:	n/a	chr4:189424170-189424181
30	CEBPB	chr4:189618245-189618777	HCT-116	colon:	n/a	chr4:189618559-189618570
31	CEBPB	chr4:189584536-189584848	A549	lung:	n/a	n/a
32	CEBPB	chr4:189348245-189348520	HepG2	liver:	n/a	chr4:189348399-189348410 chr4:189348381-189348392
33	CEBPB	chr4:189514348-189514658	HepG2	liver:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
34	CEBPB	chr4:189370895-189371048	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:189636117-189636455	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:189424045-189424347	HepG2	liver:	n/a	chr4:189424047-189424059 chr4:189424170-189424181
37	CEBPB	chr4:189365683-189366034	A549	lung:	n/a	chr4:189365858-189365869
38	CEBPB	chr4:189618409-189618665	H1-hESC	embryonic stem cell:	n/a	chr4:189618559-189618570
39	CEBPB	chr4:189533974-189534058	A549	lung:	n/a	n/a
40	CEBPB	chr4:189493638-189493884	IMR90	lung:	n/a	chr4:189493776-189493787
41	CEBPB	chr4:189365674-189365990	A549	lung:	n/a	chr4:189365858-189365869
42	CEBPB	chr4:189618403-189618710	Hela-S3	cervix:	n/a	chr4:189618559-189618570
43	CEBPB	chr4:189517237-189517434	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:189456046-189456370	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:189380428-189380719	HepG2	liver:	n/a	chr4:189380547-189380558
46	CEBPB	chr4:189516061-189516240	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:189581873-189582175	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:189628220-189628566	IMR90	lung:	n/a	chr4:189628489-189628497
49	CEBPB	chr4:189560714-189560941	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr4:189591136-189591163	HepG2	liver:	n/a	chr4:189591147-189591158

(count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189583617-189583667	ECC-1	luminal epithelium:	n/a
2	chr4:189359992-189360042	Jurkat	blood:	n/a
3	chr4:189333449-189333499	AoSMC	blood vessel:	n/a
4	chr4:189485260-189485310	T-47D	breast:	n/a
5	chr4:189583617-189583667	ECC-1	luminal epithelium:	n/a
6	chr4:189359992-189360042	Jurkat	blood:	n/a
7	chr4:189333449-189333499	AoSMC	blood vessel:	n/a
8	chr4:189485260-189485310	T-47D	breast:	n/a
9	chr4:189553390-189553440	NB4	blood:	n/a
10	chr4:189577711-189577761	PrEC	prostate:	n/a
11	chr4:189376704-189376754	HAEpiC	amniotic membrane:	n/a
12	chr4:189376704-189376754	ovcar-3	ovarian:	n/a
13	chr4:189612833-189612883	NH-A	brain:	n/a
14	chr4:189333138-189333188	HEEpiC	esophagus:	n/a
15	chr4:189476613-189476663	ovcar-3	ovarian:	n/a
16	chr4:189580633-189580683	AoSMC	blood vessel:	n/a
17	chr4:189602185-189602235	BJ	skin:	n/a
18	chr4:189612833-189612883	GM06990	blood:	n/a
19	chr4:189376729-189376779	SK-N-MC	brain:	n/a
20	chr4:189376670-189376720	AG04449	skin:	fetal
21	chr4:189580507-189580557	HNPCEpiC	eye:	n/a
22	chr4:189548707-189548757	U87	brain:	n/a
23	chr4:189485260-189485310	BJ	skin:	n/a
24	chr4:189376704-189376754	GM06990	blood:	n/a
25	chr4:189376670-189376720	T-47D	breast:	n/a
26	chr4:189553390-189553440	SK-N-SH_RA	brain:	n/a
27	chr4:189602161-189602211	HNPCEpiC	eye:	n/a
28	chr4:189552339-189552389	HUVEC	blood vessel:	n/a
29	chr4:189577711-189577761	HAEpiC	amniotic membrane:	n/a
30	chr4:189572647-189572697	HRCEpiC	kidney:	n/a
31	chr4:189602236-189602286	MCF10A-Er-Src	breast:	n/a
32	chr4:189375995-189376045	SK-N-SH	brain:	n/a
33	chr4:189577711-189577761	PFSK-1	brain:	n/a
34	chr4:189395410-189395460	Hepatocyte	liver:	n/a
35	chr4:189476745-189476795	HEK293	kidney:	embryo
36	chr4:189612833-189612883	NHBE	bronchial:	n/a
37	chr4:189602236-189602286	SK-N-SH_RA	brain:	n/a
38	chr4:189376670-189376720	HepG2	liver:	n/a
39	chr4:189554990-189555040	HUVEC	blood vessel:	n/a
40	chr4:189376729-189376779	HL-60	blood:	n/a
41	chr4:189578842-189578892	BJ	skin:	n/a
42	chr4:189376670-189376720	GM12878	blood:	n/a
43	chr4:189580798-189580848	AG10803	skin:	n/a
44	chr4:189572647-189572697	NHBE	bronchial:	n/a
45	chr4:189333449-189333499	SAEC	small airway:	n/a
46	chr4:189553390-189553440	GM12891	blood:	n/a
47	chr4:189476613-189476663	HNPCEpiC	eye:	n/a
48	chr4:189333449-189333499	AG04449	skin:	fetal
49	chr4:189476745-189476795	SK-N-SH	brain:	n/a
50	chr4:189375874-189375924	SK-N-SH	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
2	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
3	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
4	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
5	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
6	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
7	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
2	lnc-TRIML1-10	chr4:189634846-189634904	ucscGeneNc_uc003izp_1
3	lnc-TRIML1-3	chr4:189332748-189333925	XLOC_003834
4	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
5	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
6	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
7	lnc-TRIML1-10	chr4:189635786-189636060	ucscGeneNc_uc003izp_1
8	lnc-TRIML1-3	chr4:189377818-189377916	ENSG00000249378
9	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
10	lnc-TRIML1-3	chr4:189522922-189523060	XLOC_003834
11	lnc-TRIML1-10	chr4:189643927-189644013	ucscGeneNc_uc003izp_1
12	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
13	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
14	lnc-TRIML1-3	chr4:189522922-189523062	NONHSAT099745
15	lnc-TRIML1-10	chr4:189613729-189613822	ucscGeneNc_uc003izp_1
16	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
17	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834
18	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
19	lnc-TRIML1-10	chr4:189614812-189614910	ucscGeneNc_uc003izp_1
20	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
21	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
22	lnc-TRIML1-3	chr4:189376735-189376828	XLOC_003834
23	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
24	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
25	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
26	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
27	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
28	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
29	lnc-TRIML1-3	chr4:189601875-189602205	ENSG00000249378
30	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
31	lnc-TRIML1-3	chr4:189376732-189376828	NONHSAT099745
32	lnc-TRIML1-3	chr4:189376733-189376830	NONHSAT099746
33	lnc-TRIML1-3	chr4:189376768-189376828	XLOC_003834
34	lnc-TRIML1-3	chr4:189522922-189523062	ENSG00000249378
35	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099746
36	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099745
37	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
38	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
39	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
40	lnc-TRIML1-3	chr4:189376732-189376828	XLOC_003834
41	lnc-TRIML1-3	chr4:189377846-189377916	XLOC_003834
42	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
43	lnc-TRIML1-3	chr4:189398792-189399066	ENSG00000249378
44	lnc-TRIML1-3	chr4:189357858-189358015	XLOC_003834
45	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
46	lnc-TRIML1-3	chr4:189522922-189523025	NONHSAT099749
47	lnc-TRIML1-3	chr4:189376747-189376828	ENSG00000249378
48	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
49	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
50	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099746

No data

Variant related genes	Relation type
RNU7-192P	TF binding region
LINC01060	TF binding region
ENSG00000250523	TF binding region
RNU7-192P	CpG island
LINC01060	CpG island
ENSG00000250523	CpG island
ENSG00000178409	chromatin interactions
RASSF2	miRNA target sites
PRNP	miRNA target sites
TAPBP	miRNA target sites
KCNK1	miRNA target sites
C1orf144	miRNA target sites
BMPR2	miRNA target sites
SHCBP1	miRNA target sites
PDZD11	miRNA target sites
DCAF7	miRNA target sites
FAM104A	miRNA target sites
PFN2	miRNA target sites
NCOA3	miRNA target sites
USP1	miRNA target sites

Extended variants
information (count: 14594 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:14594 , 50 per page) page: 1 2 3 4 5 6 7 ... 292

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6837538	chr4:189331266-189331267	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35092624	chr4:189331302-189331303	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530680104	chr4:189331331-189331332	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550397972	chr4:189331343-189331344	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181501732	chr4:189331399-189331400	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535653543	chr4:189331410-189331411	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549140327	chr4:189331467-189331468	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114374246	chr4:189331474-189331475	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534411764	chr4:189331481-189331482	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555981881	chr4:189331545-189331546	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534943470	chr4:189331561-189331562	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187647831	chr4:189331567-189331568	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149405363	chr4:189331606-189331607	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17954	chr4:189331626-189331627	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs145227943	chr4:189331636-189331637	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538535412	chr4:189331642-189331643	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557159507	chr4:189331668-189331669	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573806994	chr4:189331669-189331670	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542863967	chr4:189331691-189331692	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559550080	chr4:189331716-189331717	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72713559	chr4:189331759-189331760	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs191957990	chr4:189331785-189331786	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75947585	chr4:189331806-189331807	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115436874	chr4:189331808-189331809	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182965643	chr4:189331814-189331815	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553595478	chr4:189331853-189331854	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377652	chr4:189331928-189331929	Flanking Active TSS Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572878082	chr4:189332003-189332004	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185259497	chr4:189332032-189332033	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565886857	chr4:189332084-189332085	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189721712	chr4:189332085-189332086	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561538585	chr4:189332098-189332099	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529189471	chr4:189332153-189332154	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182762251	chr4:189332166-189332167	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571462710	chr4:189332234-189332235	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114325631	chr4:189332321-189332322	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368859953	chr4:189332355-189332356	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12510370	chr4:189332390-189332391	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187000857	chr4:189332421-189332422	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149039355	chr4:189332515-189332516	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192305933	chr4:189332566-189332567	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183411810	chr4:189332612-189332613	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573066022	chr4:189332614-189332615	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143795559	chr4:189332624-189332625	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370022263	chr4:189332681-189332682	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148167243	chr4:189332735-189332736	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs449363	chr4:189332739-189332740	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11936254	chr4:189332743-189332744	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs437327	chr4:189332759-189332760	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs70940976	chr4:189332764-189332765	Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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

Chromatin state (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189328000-189331800	Enhancers	NHDF-Ad	bronchial
2	chr4:189328400-189331800	Enhancers	Fetal Intestine Small	intestine
3	chr4:189330200-189334800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr4:189330400-189333000	Weak transcription	Osteobl	bone
5	chr4:189331000-189331800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:189331000-189331800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr4:189331200-189331400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:189331400-189331600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:189331600-189332000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:189331800-189332400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:189331800-189333000	Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr4:189332000-189333200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:189332400-189333200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:189333000-189333200	Flanking Bivalent TSS/Enh	Placenta	Placenta
15	chr4:189333000-189333400	Active TSS	Osteobl	bone
16	chr4:189333000-189334600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
17	chr4:189333200-189333600	Active TSS	Ovary	ovary
18	chr4:189333200-189334000	Bivalent Enhancer	Placenta	Placenta
19	chr4:189333200-189340600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:189333200-189344400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:189333400-189344200	Weak transcription	Osteobl	bone
22	chr4:189334600-189335000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:189335000-189338400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr4:189335600-189336000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:189336200-189337600	Enhancers	HMEC	breast
26	chr4:189336600-189337200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:189336800-189337200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr4:189337600-189345200	Weak transcription	HMEC	breast
29	chr4:189338400-189338800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr4:189338800-189340800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:189340600-189341400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:189340800-189342600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:189341400-189343000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:189342600-189343400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr4:189343000-189344000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:189343400-189346400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr4:189344000-189345200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:189344200-189344600	Enhancers	A549	lung
39	chr4:189344200-189344800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:189344200-189345000	Enhancers	Osteobl	bone
41	chr4:189344400-189345200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:189344600-189345200	Flanking Active TSS	A549	lung
43	chr4:189344800-189353400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:189345000-189349400	Weak transcription	Osteobl	bone
45	chr4:189345200-189345800	Enhancers	A549	lung
46	chr4:189345200-189348400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:189345200-189348600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:189345800-189346600	Weak transcription	A549	lung
49	chr4:189346400-189346800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
50	chr4:189346600-189346800	ZNF genes & repeats	A549	lung

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