Variant report

Variant	nsv881362
Chromosome Location	chr4:189247773-189536211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1523)
CpG islands
(count:1466)
Chromatin interactive
region (count:10)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189455499-189455789	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	chr4:189376606-189376828	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:189324598-189324718	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:189359441-189359980	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
8	ATF2	chr4:189320870-189321336	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:189320962-189321575	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:189353505-189353712	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:189308557-189308573	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:189366501-189366863	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:189365427-189366156	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:189324595-189324738	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:189370074-189371014	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:189372985-189373571	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:189321022-189321611	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr4:189312088-189312284	GM12878	blood:	n/a	chr4:189312224-189312235
19	BCL11A	chr4:189320997-189321292	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr4:189373274-189373489	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr4:189344161-189344742	A549	lung:	n/a	n/a
22	BCL3	chr4:189370110-189370622	A549	lung:	n/a	n/a
23	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:189291962-189292207	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:189324559-189324730	HepG2	liver:	n/a	n/a
26	BHLHE40	chr4:189527879-189528027	HepG2	liver:	n/a	n/a
27	BRCA1	chr4:189324508-189324656	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr4:189304915-189305326	HCT-116	colon:	n/a	n/a
30	CEBPB	chr4:189262860-189263130	K562	blood:	n/a	chr4:189263022-189263033
31	CEBPB	chr4:189321942-189322198	HepG2	liver:	n/a	chr4:189322034-189322045
32	CEBPB	chr4:189288202-189288489	IMR90	lung:	n/a	chr4:189288365-189288376
33	CEBPB	chr4:189351226-189351392	K562	blood:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
34	CEBPB	chr4:189355920-189356134	HepG2	liver:	n/a	chr4:189356098-189356109
35	CEBPB	chr4:189437762-189437878	HepG2	liver:	n/a	chr4:189437793-189437804
36	CEBPB	chr4:189493605-189493919	HepG2	liver:	n/a	chr4:189493776-189493787
37	CEBPB	chr4:189351138-189351492	A549	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
38	CEBPB	chr4:189262873-189263190	IMR90	lung:	n/a	chr4:189263022-189263033
39	CEBPB	chr4:189365674-189365990	A549	lung:	n/a	chr4:189365858-189365869
40	CEBPB	chr4:189533974-189534058	A549	lung:	n/a	n/a
41	CEBPB	chr4:189514350-189514601	A549	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
42	CEBPB	chr4:189288199-189288526	HepG2	liver:	n/a	chr4:189288365-189288376
43	CEBPB	chr4:189355972-189356262	IMR90	lung:	n/a	chr4:189356098-189356109
44	CEBPB	chr4:189371727-189371894	A549	lung:	n/a	n/a
45	CEBPB	chr4:189347694-189347925	A549	lung:	n/a	n/a
46	CEBPB	chr4:189516061-189516240	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:189262859-189263200	HepG2	liver:	n/a	chr4:189263022-189263033
48	CEBPB	chr4:189254888-189255129	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:189262870-189263143	A549	lung:	n/a	chr4:189263022-189263033
50	CEBPB	chr4:189365695-189366033	Hela-S3	cervix:	n/a	chr4:189365858-189365869

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189376704-189376754	MCF-7	breast:	n/a
2	chr4:189485260-189485310	T-47D	breast:	n/a
3	chr4:189376704-189376754	MCF-7	breast:	n/a
4	chr4:189485260-189485310	T-47D	breast:	n/a
5	chr4:189485260-189485310	HEEpiC	esophagus:	n/a
6	chr4:189258068-189258118	MCF-7	breast:	n/a
7	chr4:189350268-189350318	NH-A	brain:	n/a
8	chr4:189350268-189350318	T-47D	breast:	n/a
9	chr4:189321244-189321294	HepG2	liver:	n/a
10	chr4:189333449-189333499	MCF10A-Er-Src	breast:	n/a
11	chr4:189376704-189376754	HIPEpiC	eye:	n/a
12	chr4:189321244-189321294	HCT-116	colon:	n/a
13	chr4:189321136-189321186	IMR90	lung:	fetal
14	chr4:189333138-189333188	NHBE	bronchial:	n/a
15	chr4:189433040-189433090	Jurkat	blood:	n/a
16	chr4:189375995-189376045	GM19239	blood:	n/a
17	chr4:189476613-189476663	HRCEpiC	kidney:	n/a
18	chr4:189485260-189485310	Caco-2	colon:	n/a
19	chr4:189476613-189476663	H1-hESC	embryonic stem cell:	embryo
20	chr4:189376670-189376720	A549	lung:	n/a
21	chr4:189258348-189258398	HCT-116	colon:	n/a
22	chr4:189333449-189333499	Caco-2	colon:	n/a
23	chr4:189321244-189321294	GM12892	blood:	n/a
24	chr4:189258195-189258245	MCF10A-Er-Src	breast:	n/a
25	chr4:189359992-189360042	NHDF-neo	bronchial:	n/a
26	chr4:189333296-189333346	ECC-1	luminal epithelium:	n/a
27	chr4:189358149-189358199	AG09319	gingival:	n/a
28	chr4:189359992-189360042	RPTEC	kidney:	n/a
29	chr4:189476613-189476663	SK-N-SH	brain:	n/a
30	chr4:189476745-189476795	RPTEC	kidney:	n/a
31	chr4:189485260-189485310	HCT-116	colon:	n/a
32	chr4:189321136-189321186	HIPEpiC	eye:	n/a
33	chr4:189395410-189395460	HMEC	breast:	n/a
34	chr4:189333296-189333346	HNPCEpiC	eye:	n/a
35	chr4:189258348-189258398	GM12891	blood:	n/a
36	chr4:189258068-189258118	LNCaP	prostate:	n/a
37	chr4:189376729-189376779	BJ	skin:	n/a
38	chr4:189258195-189258245	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:189258195-189258245	HNPCEpiC	eye:	n/a
40	chr4:189395410-189395460	HRE	kidney:	n/a
41	chr4:189350268-189350318	RPTEC	kidney:	n/a
42	chr4:189350268-189350318	HL-60	blood:	n/a
43	chr4:189395410-189395460	GM06990	blood:	n/a
44	chr4:189350268-189350318	IMR90	lung:	fetal
45	chr4:189350268-189350318	PFSK-1	brain:	n/a
46	chr4:189330030-189330080	HUVEC	blood vessel:	n/a
47	chr4:189375874-189375924	PrEC	prostate:	n/a
48	chr4:189333296-189333346	HRPEpiC	eye:	n/a
49	chr4:189321244-189321294	BE2_C	brain:	n/a
50	chr4:189485260-189485310	GM19239	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:
2	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
3	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
4	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
5	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
6	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
7	chr20:30047555..30048272-chr4:189297803..189298552,2	MCF-7	breast:
8	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
9	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
10	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099746
2	lnc-TRIML1-3	chr4:189376768-189376828	XLOC_003834
3	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378
4	lnc-TRIML1-3	chr4:189376733-189376830	NONHSAT099746
5	lnc-TRIML1-3	chr4:189522922-189523062	ENSG00000249378
6	lnc-TRIML1-3	chr4:189376732-189376828	NONHSAT099745
7	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
8	lnc-TRIML1-3	chr4:189398792-189399066	ENSG00000249378
9	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099745
10	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
11	lnc-TRIML1-3	chr4:189522922-189523062	NONHSAT099745
12	lnc-TRIML1-3	chr4:189377818-189377916	ENSG00000249378
13	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
14	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
15	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
16	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
17	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
18	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
19	lnc-TRIML1-3	chr4:189377846-189377916	XLOC_003834
20	lnc-TRIML1-3	chr4:189522922-189523025	NONHSAT099749
21	lnc-TRIML1-3	chr4:189332748-189333925	XLOC_003834
22	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
23	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
24	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834
25	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
26	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
27	lnc-TRIML1-3	chr4:189376732-189376828	XLOC_003834
28	lnc-TRIML1-3	chr4:189522922-189523060	XLOC_003834
29	lnc-TRIML1-3	chr4:189357858-189358015	XLOC_003834
30	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
31	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
32	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
33	lnc-TRIML1-3	chr4:189376735-189376828	XLOC_003834
34	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
35	lnc-TRIML1-3	chr4:189376747-189376828	ENSG00000249378
36	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378
37	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
38	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
39	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
40	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
41	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
42	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099746
43	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
44	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
45	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
46	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834

No data

Variant related genes	Relation type
LINC01060	TF binding region
NARG2P1	TF binding region
ENSG00000242169	TF binding region
LINC01060	CpG island
NARG2P1	CpG island
ENSG00000242169	CpG island
ENSG00000178409	chromatin interactions
C1orf144	miRNA target sites
DCAF7	miRNA target sites
SHCBP1	miRNA target sites
BMPR2	miRNA target sites
PFN2	miRNA target sites
PRNP	miRNA target sites
TAPBP	miRNA target sites
NCOA3	miRNA target sites
ARRDC3	miRNA target sites
CREBL2	miRNA target sites
RASSF2	miRNA target sites
KCNK1	miRNA target sites
PDZD11	miRNA target sites
FAM104A	miRNA target sites

Extended variants
information (count: 12605 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:12605 , 50 per page) page: 1 2 3 4 5 6 7 ... 253

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11930915	chr4:189247773-189247774	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574218655	chr4:189247832-189247833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7687203	chr4:189247938-189247939	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553123599	chr4:189247959-189247960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573273643	chr4:189247972-189247973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114161331	chr4:189247987-189247988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565338668	chr4:189247988-189247989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7687876	chr4:189247993-189247994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs544049115	chr4:189248001-189248002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10551641	chr4:189248003-189248004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374508552	chr4:189248005-189248006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561249876	chr4:189248029-189248030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529977086	chr4:189248063-189248064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546850658	chr4:189248074-189248075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375383824	chr4:189248075-189248076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551559515	chr4:189248091-189248092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566908856	chr4:189248110-189248111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551862232	chr4:189248132-189248133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7687790	chr4:189248152-189248153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs7687963	chr4:189248207-189248208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs79688474	chr4:189248239-189248240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7687995	chr4:189248263-189248264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs567828261	chr4:189248276-189248277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536592880	chr4:189248281-189248282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553623524	chr4:189248304-189248305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73031046	chr4:189248358-189248359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs62354010	chr4:189248399-189248400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371217896	chr4:189248409-189248410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72711424	chr4:189248483-189248484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs72711426	chr4:189248484-189248485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114288863	chr4:189248528-189248529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs66935224	chr4:189248540-189248541	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139300095	chr4:189248541-189248542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540199083	chr4:189248545-189248546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141909747	chr4:189248557-189248558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531981694	chr4:189248578-189248579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551725302	chr4:189248583-189248584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369050197	chr4:189248599-189248600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372293021	chr4:189248605-189248606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs67210379	chr4:189248606-189248607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201332313	chr4:189248631-189248632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568498388	chr4:189248663-189248664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531335941	chr4:189248668-189248669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4863028	chr4:189248673-189248674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs567806408	chr4:189248677-189248678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199968380	chr4:189248689-189248690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77385310	chr4:189248693-189248694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62354011	chr4:189248711-189248712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188653659	chr4:189248712-189248713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12498515	chr4:189248732-189248733	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

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
Autism	20808228	CNVD
Epilepsy	21635232	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	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

Chromatin state (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189246600-189247800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:189247800-189249600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:189249600-189250600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:189250000-189250800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:189250200-189250800	Enhancers	Fetal Intestine Small	intestine
6	chr4:189250200-189251200	Bivalent Enhancer	HepG2	liver
7	chr4:189250800-189251800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:189251800-189252000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:189253200-189254400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:189253200-189255400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:189253400-189254200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:189253400-189254800	Enhancers	Osteobl	bone
13	chr4:189254800-189255200	Enhancers	NHDF-Ad	bronchial
14	chr4:189256000-189256400	Enhancers	Fetal Brain Male	brain
15	chr4:189256200-189256600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr4:189257600-189258400	Enhancers	Placenta	Placenta
17	chr4:189258200-189258400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:189258200-189259000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:189262000-189262800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:189267400-189267800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:189270800-189271200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:189274200-189274400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr4:189274200-189282400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:189274400-189274800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr4:189278200-189278600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:189278600-189278800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:189278600-189279200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:189278800-189279200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr4:189279600-189279800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:189280000-189283600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:189282400-189282600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:189282400-189282600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:189282400-189283000	Enhancers	Placenta Amnion	Placenta Amnion
34	chr4:189282600-189283800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:189282600-189283800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:189283600-189284000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:189283600-189284200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:189283800-189284000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:189283800-189284200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:189283800-189284400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:189284000-189284400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:189286000-189286200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:189286800-189287200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:189287200-189288800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:189288200-189289000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:189288800-189289400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr4:189289400-189290600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr4:189292000-189292200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:189292000-189292200	Enhancers	A549	lung
50	chr4:189292000-189292400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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