Variant report

Variant	nsv1020391
Chromosome Location	chr4:188322240-188833871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1441)
CpG islands
(count:2016)
Chromatin interactive
region (count:23)
LncRNA
region (count:87)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:188527707-188527965	HepG2	liver:	n/a	n/a
2	ATF1	chr4:188538300-188538599	K562	blood:	n/a	n/a
3	ATF1	chr4:188735920-188736251	K562	blood:	n/a	n/a
4	ATF3	chr4:188527774-188527903	K562	blood:	n/a	n/a
5	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
6	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
8	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
9	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
11	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
12	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
13	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:188574591-188574791	HepG2	liver:	n/a	chr4:188574678-188574689 chr4:188574677-188574690
18	CEBPB	chr4:188600607-188601013	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
20	CEBPB	chr4:188578046-188578537	IMR90	lung:	n/a	chr4:188578218-188578229
21	CEBPB	chr4:188517628-188517892	HepG2	liver:	n/a	chr4:188517748-188517759
22	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
23	CEBPB	chr4:188632761-188633106	HepG2	liver:	n/a	chr4:188632937-188632948
24	CEBPB	chr4:188735832-188736143	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:188690637-188690931	HepG2	liver:	n/a	chr4:188690750-188690761
26	CEBPB	chr4:188529058-188529739	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
28	CEBPB	chr4:188570202-188570305	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:188632768-188633111	IMR90	lung:	n/a	chr4:188632937-188632948
30	CEBPB	chr4:188608959-188609177	K562	blood:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
31	CEBPB	chr4:188538148-188538851	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
32	CEBPB	chr4:188591052-188591273	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:188570695-188571039	A549	lung:	n/a	chr4:188570868-188570879
34	CEBPB	chr4:188632833-188633099	H1-hESC	embryonic stem cell:	n/a	chr4:188632937-188632948
35	CEBPB	chr4:188538301-188538611	HepG2	liver:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
36	CEBPB	chr4:188690662-188690861	H1-hESC	embryonic stem cell:	n/a	chr4:188690750-188690761
37	CEBPB	chr4:188608828-188609265	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
38	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
40	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
41	CEBPB	chr4:188538314-188538633	A549	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
42	CEBPB	chr4:188608901-188609233	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
43	CEBPB	chr4:188539916-188540476	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:188728733-188729010	IMR90	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
45	CEBPB	chr4:188570725-188570925	K562	blood:	n/a	chr4:188570868-188570879
46	CEBPB	chr4:188735760-188736147	K562	blood:	n/a	n/a
47	CEBPB	chr4:188538086-188538843	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
48	CEBPB	chr4:188578082-188578310	HepG2	liver:	n/a	chr4:188578218-188578229
49	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
50	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188686726-188686776	HL-60	blood:	n/a
2	chr4:188426506-188426556	Hepatocyte	liver:	n/a
3	chr4:188528319-188528369	A549	lung:	n/a
4	chr4:188686726-188686776	HL-60	blood:	n/a
5	chr4:188426506-188426556	Hepatocyte	liver:	n/a
6	chr4:188528319-188528369	A549	lung:	n/a
7	chr4:188534509-188534559	NHDF-neo	bronchial:	n/a
8	chr4:188686664-188686714	HEEpiC	esophagus:	n/a
9	chr4:188530842-188530892	HIPEpiC	eye:	n/a
10	chr4:188534873-188534923	SK-N-SH_RA	brain:	n/a
11	chr4:188539183-188539233	NB4	blood:	n/a
12	chr4:188426278-188426328	HNPCEpiC	eye:	n/a
13	chr4:188686763-188686813	HEK293	kidney:	embryo
14	chr4:188423066-188423116	HRCEpiC	kidney:	n/a
15	chr4:188554583-188554633	SAEC	small airway:	n/a
16	chr4:188686763-188686813	HNPCEpiC	eye:	n/a
17	chr4:188426278-188426328	AoSMC	blood vessel:	n/a
18	chr4:188686763-188686813	SK-N-SH_RA	brain:	n/a
19	chr4:188686726-188686776	MCF-7	breast:	n/a
20	chr4:188736112-188736162	NHBE	bronchial:	n/a
21	chr4:188426437-188426487	GM06990	blood:	n/a
22	chr4:188530842-188530892	AG09319	gingival:	n/a
23	chr4:188686726-188686776	LNCaP	prostate:	n/a
24	chr4:188736112-188736162	AoSMC	blood vessel:	n/a
25	chr4:188534448-188534498	MCF-7	breast:	n/a
26	chr4:188534509-188534559	HCPEpiC	choroid plexus:	n/a
27	chr4:188428637-188428687	A549	lung:	n/a
28	chr4:188534912-188534962	HNPCEpiC	eye:	n/a
29	chr4:188534912-188534962	LNCaP	prostate:	n/a
30	chr4:188462685-188462735	PANC-1	pancreas:	n/a
31	chr4:188824073-188824123	SAEC	small airway:	n/a
32	chr4:188534509-188534559	Jurkat	blood:	n/a
33	chr4:188427966-188428016	HEK293	kidney:	embryo
34	chr4:188534776-188534826	HRE	kidney:	n/a
35	chr4:188426437-188426487	AG04449	skin:	fetal
36	chr4:188398437-188398487	PFSK-1	brain:	n/a
37	chr4:188686763-188686813	IMR90	lung:	fetal
38	chr4:188528319-188528369	AG10803	skin:	n/a
39	chr4:188426437-188426487	HEEpiC	esophagus:	n/a
40	chr4:188736112-188736162	Hela-S3	cervix:	n/a
41	chr4:188539183-188539233	PANC-1	pancreas:	n/a
42	chr4:188686726-188686776	SK-N-SH	brain:	n/a
43	chr4:188534693-188534743	GM12878	blood:	n/a
44	chr4:188539183-188539233	HMEC	breast:	n/a
45	chr4:188530842-188530892	HL-60	blood:	n/a
46	chr4:188736112-188736162	LNCaP	prostate:	n/a
47	chr4:188686726-188686776	AG10803	skin:	n/a
48	chr4:188401038-188401088	NHDF-neo	bronchial:	n/a
49	chr4:188534448-188534498	MCF10A-Er-Src	breast:	n/a
50	chr4:188426278-188426328	GM19239	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
2	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
3	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
4	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
5	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
6	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
7	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
8	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:
9	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
10	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
11	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
12	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
13	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
14	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
15	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
16	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
17	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
18	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
19	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
20	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
21	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
22	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
23	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:

(count:87 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
2	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
3	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
4	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
5	lnc-ZFP42-2	chr4:188647752-188647874	NONHSAT099717
6	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
7	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
8	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
9	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
10	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
11	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
12	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099706
13	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
14	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
15	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829
16	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
17	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
18	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
19	lnc-ZFP42-2	chr4:188534086-188535153	XLOC_003829
20	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
21	lnc-ZFP42-2	chr4:188632897-188633241	NONHSAT099717
22	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
23	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
24	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
25	lnc-ZFP42-2	chr4:188553805-188553988	XLOC_003829
26	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829
27	lnc-ZFP42-9	chr4:188779825-188780051	l_2821_chr4:188771633-188780051_testes
28	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
29	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
30	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
31	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
32	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
33	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
34	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
35	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
36	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
37	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
38	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
39	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
40	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
41	lnc-ZFP42-10	chr4:188501769-188501890	NONHSAT099705
42	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
43	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
44	lnc-TRIML2-4	chr4:188586916-188586992	NR_110436
45	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
46	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
47	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
48	lnc-ZFP42-2	chr4:188542831-188543333	XLOC_003829
49	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
50	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717

No data

Variant related genes	Relation type
ADAM20P3	TF binding region
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000249642	TF binding region
ENSG00000250590	TF binding region
ADAM20P3	CpG island
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000251643	chromatin interactions
ENSG00000029993	chromatin interactions
ENSG00000206737	chromatin interactions
PHF6	miRNA target sites
CDC42	miRNA target sites
TAGLN2	miRNA target sites
KLF12	miRNA target sites
TIMP3	miRNA target sites
NDP	miRNA target sites
ANP32E	miRNA target sites
KIF13B	miRNA target sites
FSCN1	miRNA target sites
MED20	miRNA target sites
ANTXR1	miRNA target sites
MCL1	miRNA target sites

Extended variants
information (count: 9017 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:9017 , 50 per page) page: 1 2 3 4 5 6 7 ... 181

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147183168	chr4:188323213-188323214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs148669683	chr4:188323240-188323241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528760360	chr4:188323246-188323247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577564507	chr4:188323259-188323260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142087965	chr4:188323282-188323283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188379767	chr4:188323305-188323306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556961765	chr4:188323343-188323344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573846190	chr4:188323347-188323348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192032392	chr4:188323356-188323357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183419673	chr4:188323378-188323379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528310182	chr4:188323379-188323380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541122449	chr4:188323471-188323472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549020184	chr4:188323510-188323511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188020534	chr4:188323557-188323558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559315554	chr4:188323567-188323568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200749322	chr4:188323605-188323606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2376244	chr4:188323649-188323650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12510956	chr4:188323665-188323666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12503162	chr4:188323670-188323671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2376245	chr4:188323688-188323689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs140700081	chr4:188323692-188323693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12499680	chr4:188323706-188323707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs370680713	chr4:188323827-188323828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557865406	chr4:188323828-188323829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570714628	chr4:188323857-188323858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192515802	chr4:188323892-188323893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145298577	chr4:188323904-188323905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184519830	chr4:188323911-188323912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573565560	chr4:188323963-188323964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189308052	chr4:188324022-188324023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552894471	chr4:188324026-188324027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572679165	chr4:188324038-188324039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544835422	chr4:188324068-188324069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149194165	chr4:188324117-188324118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578023014	chr4:188324154-188324155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543553503	chr4:188324155-188324156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536357243	chr4:188324175-188324176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563661736	chr4:188324193-188324194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192714217	chr4:188324289-188324290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549697037	chr4:188324336-188324337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560119733	chr4:188324389-188324390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528681788	chr4:188324408-188324409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201133508	chr4:188324434-188324435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571770900	chr4:188324490-188324491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537103107	chr4:188324552-188324553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550443147	chr4:188324662-188324663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567250036	chr4:188324672-188324673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2217485	chr4:188324722-188324723	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184779508	chr4:188324759-188324760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572765019	chr4:188324783-188324784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188323200-188338800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:188329000-188329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:188329400-188330000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:188335600-188337800	Enhancers	Fetal Brain Male	brain
5	chr4:188335800-188336000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:188335800-188336200	Enhancers	Fetal Muscle Leg	muscle
7	chr4:188335800-188339400	Enhancers	Fetal Lung	lung
8	chr4:188336000-188336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr4:188336000-188337800	Enhancers	Fetal Heart	heart
10	chr4:188336200-188336800	Enhancers	Adipose Nuclei	Adipose
11	chr4:188336200-188336800	Enhancers	HSMM	muscle
12	chr4:188336800-188338800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr4:188336800-188339000	Weak transcription	Adipose Nuclei	Adipose
14	chr4:188337800-188338800	Weak transcription	Fetal Brain Male	brain
15	chr4:188337800-188343800	Weak transcription	Fetal Heart	heart
16	chr4:188338800-188339000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:188338800-188339800	Enhancers	Fetal Brain Male	brain
18	chr4:188338800-188340600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr4:188339000-188339200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:188339000-188339200	Enhancers	Adipose Nuclei	Adipose
21	chr4:188339200-188339600	Weak transcription	Adipose Nuclei	Adipose
22	chr4:188339400-188339600	Flanking Active TSS	Fetal Lung	lung
23	chr4:188339400-188342200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:188339600-188340000	Enhancers	Fetal Lung	lung
25	chr4:188339600-188340400	Enhancers	Adipose Nuclei	Adipose
26	chr4:188340000-188340400	Flanking Active TSS	Fetal Lung	lung
27	chr4:188342200-188342400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:188342400-188342600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:188342400-188342800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:188342600-188342800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:188342800-188346000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:188343800-188344400	Enhancers	Fetal Heart	heart
33	chr4:188345400-188346000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:188345600-188346200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:188346000-188346400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:188351800-188352000	Enhancers	Aorta	Aorta
37	chr4:188352000-188357000	Weak transcription	Aorta	Aorta
38	chr4:188353400-188353800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:188353400-188355400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr4:188353600-188355200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:188353800-188354800	Enhancers	HMEC	breast
42	chr4:188354400-188355400	Enhancers	Fetal Heart	heart
43	chr4:188354800-188355000	Flanking Active TSS	HMEC	breast
44	chr4:188355000-188355200	Active TSS	HMEC	breast
45	chr4:188355400-188357200	Weak transcription	Fetal Heart	heart
46	chr4:188357200-188357600	Enhancers	Fetal Heart	heart
47	chr4:188357200-188357600	Enhancers	Stomach Smooth Muscle	stomach
48	chr4:188357200-188357800	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:188357200-188357800	Enhancers	Colon Smooth Muscle	Colon
50	chr4:188357200-188358400	Enhancers	Rectal Smooth Muscle	rectum

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