Variant report

Variant	nsv869490
Chromosome Location	chr4:92506402-93219336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2396)
CpG islands
(count:916)
Chromatin interactive
region (count:46)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2396 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:93174807-93176629	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:93176968-93178653	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:93179240-93179981	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:93192015-93192704	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:92551366-92551627	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:93173256-93173722	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:93174553-93180548	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:92679711-92680078	HCT-116	colon:	n/a	n/a
9	BACH1	chr4:92874021-92874050	K562	blood:	n/a	n/a
10	BACH1	chr4:93174926-93175130	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:93175421-93178227	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:93192112-93192392	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:93191451-93191756	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr4:92685314-92685539	GM12878	blood:	n/a	n/a
15	BATF	chr4:92812540-92812781	GM12878	blood:	n/a	chr4:92812671-92812682
16	BATF	chr4:92956979-92957141	GM12878	blood:	n/a	chr4:92957060-92957071
17	BATF	chr4:92812456-92812830	GM12878	blood:	n/a	chr4:92812671-92812682
18	BATF	chr4:92956941-92957201	GM12878	blood:	n/a	chr4:92957060-92957071
19	BATF	chr4:93139203-93139461	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:92956890-92957081	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:92572273-92572591	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:92767508-92767581	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:92831092-92831515	GM12878	blood:	n/a	n/a
24	BRCA1	chr4:93177241-93178533	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr4:93155474-93156185	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr4:92827208-92827254	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr4:92695586-92695633	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:92758741-92759534	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr4:93178843-93178896	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr4:93023011-93023329	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr4:92679542-92680072	HCT-116	colon:	n/a	chr4:92679572-92679583
32	CBX3	chr4:92679695-92680141	HCT-116	colon:	n/a	n/a
33	CBX3	chr4:93160637-93161060	HCT-116	colon:	n/a	n/a
34	CEBPB	chr4:93155533-93155975	HepG2	liver:	n/a	chr4:93155713-93155724
35	CEBPB	chr4:92935286-92935564	HepG2	liver:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
36	CEBPB	chr4:92935217-92935603	K562	blood:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
37	CEBPB	chr4:93155490-93155983	A549	lung:	n/a	chr4:93155713-93155724
38	CEBPB	chr4:93155536-93156008	HCT-116	colon:	n/a	chr4:93155713-93155724
39	CEBPB	chr4:92935220-92935612	ECC-1	luminal epithelium:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
40	CEBPB	chr4:92932501-92932580	Hela-S3	cervix:	n/a	chr4:92932505-92932516
41	CEBPB	chr4:92835366-92835674	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:92777276-92777573	Hela-S3	cervix:	n/a	chr4:92777378-92777389 chr4:92777378-92777391
43	CEBPB	chr4:92835385-92835609	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:92717074-92717365	K562	blood:	n/a	chr4:92717222-92717233
45	CEBPB	chr4:92935223-92935591	A549	lung:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
46	CEBPB	chr4:93158043-93158385	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:93209810-93209977	K562	blood:	n/a	chr4:93209877-93209888
48	CEBPB	chr4:92932347-92932681	IMR90	lung:	n/a	chr4:92932505-92932516
49	CEBPB	chr4:92935216-92935599	IMR90	lung:	n/a	chr4:92935406-92935415 chr4:92935406-92935417 chr4:92935406-92935415 chr4:92935404-92935415 chr4:92935406-92935415 chr4:92935404-92935417 chr4:92935404-92935417 chr4:92935406-92935415
50	CEBPB	chr4:93119773-93120082	IMR90	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92522792-92522842	PFSK-1	brain:	n/a
2	chr4:92522792-92522842	PFSK-1	brain:	n/a
3	chr4:92556548-92556598	U87	brain:	n/a
4	chr4:93198846-93198896	Caco-2	colon:	n/a
5	chr4:93198846-93198896	ovcar-3	ovarian:	n/a
6	chr4:93105138-93105188	GM12891	blood:	n/a
7	chr4:92879355-92879405	AoSMC	blood vessel:	n/a
8	chr4:92556548-92556598	NH-A	brain:	n/a
9	chr4:93104334-93104384	MCF10A-Er-Src	breast:	n/a
10	chr4:93103551-93103601	SKMC	muscle:	n/a
11	chr4:92522792-92522842	NHDF-neo	bronchial:	n/a
12	chr4:93126098-93126148	HEEpiC	esophagus:	n/a
13	chr4:93217985-93218035	Hepatocyte	liver:	n/a
14	chr4:92522792-92522842	GM06990	blood:	n/a
15	chr4:93103551-93103601	K562	blood:	n/a
16	chr4:93103914-93103964	HCPEpiC	choroid plexus:	n/a
17	chr4:93104012-93104062	GM12891	blood:	n/a
18	chr4:93103551-93103601	ProgFib	skin:	n/a
19	chr4:93105138-93105188	ovcar-3	ovarian:	n/a
20	chr4:93105138-93105188	AG04449	skin:	fetal
21	chr4:93104012-93104062	CMK	blood:	n/a
22	chr4:93103772-93103822	HRCEpiC	kidney:	n/a
23	chr4:93104012-93104062	NB4	blood:	n/a
24	chr4:93217985-93218035	MCF-7	breast:	n/a
25	chr4:92516304-92516354	AG04450	lung:	fetal
26	chr4:92522792-92522842	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:93104334-93104384	LNCaP	prostate:	n/a
28	chr4:93103914-93103964	GM12892	blood:	n/a
29	chr4:92879355-92879405	HUVEC	blood vessel:	n/a
30	chr4:92879355-92879405	HPAEpiC	pulmonary alveolar:	n/a
31	chr4:92556548-92556598	HCF	heart:	n/a
32	chr4:93103551-93103601	NH-A	brain:	n/a
33	chr4:93105176-93105226	T-47D	breast:	n/a
34	chr4:92879355-92879405	LNCaP	prostate:	n/a
35	chr4:93103772-93103822	SK-N-SH	brain:	n/a
36	chr4:93104012-93104062	MCF-7	breast:	n/a
37	chr4:93104012-93104062	HEK293	kidney:	embryo
38	chr4:93105176-93105226	GM06990	blood:	n/a
39	chr4:93105176-93105226	SK-N-SH_RA	brain:	n/a
40	chr4:92516304-92516354	NH-A	brain:	n/a
41	chr4:93198846-93198896	T-47D	breast:	n/a
42	chr4:93105138-93105188	Caco-2	colon:	n/a
43	chr4:93126098-93126148	MCF10A-Er-Src	breast:	n/a
44	chr4:92516304-92516354	CMK	blood:	n/a
45	chr4:92516304-92516354	A549	lung:	n/a
46	chr4:92556548-92556598	HCPEpiC	choroid plexus:	n/a
47	chr4:93105176-93105226	RPTEC	kidney:	n/a
48	chr4:92879355-92879405	HEK293	kidney:	embryo
49	chr4:92516304-92516354	PANC-1	pancreas:	n/a
50	chr4:93217985-93218035	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:62608619..62609552-chr4:93076936..93077935,6	HCT-116	colon:
2	chr4:92852985..92854522-chr4:92856972..92859223,2	K562	blood:
3	chr4:93202258..93204813-chr4:93248472..93250667,2	K562	blood:
4	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
5	chr4:93041952..93042462-chr4:93063543..93064136,2	MCF-7	breast:
6	chr4:92862741..92865102-chr4:92873846..92875562,2	MCF-7	breast:
7	chr4:93156131..93157837-chr4:93174936..93177548,2	MCF-7	breast:
8	chr4:93161950..93163771-chr4:93165936..93168179,2	MCF-7	breast:
9	chr4:92733503..92735821-chr4:92736564..92739014,2	K562	blood:
10	chr20:43379044..43379544-chr4:92594658..92595640,2	K562	blood:
11	chr17:56736322..56736880-chr4:92908655..92909344,2	MCF-7	breast:
12	chr4:93041952..93042761-chr4:93063494..93064136,3	MCF-7	breast:
13	chr4:93102928..93105874-chr4:93109166..93111796,3	K562	blood:
14	chr4:92649464..92651523-chr4:92652088..92654167,2	MCF-7	breast:
15	chr4:92539576..92542400-chr4:92543063..92544579,2	MCF-7	breast:
16	chr4:92522210..92524943-chr4:92527057..92528806,2	K562	blood:
17	chr4:93161950..93163771-chr4:93165936..93168179,2	MCF-7	breast:
18	chr4:92649464..92651523-chr4:92652088..92654167,2	MCF-7	breast:
19	chr14:89306981..89307680-chr4:92635846..92636574,2	MCF-7	breast:
20	chr4:93096975..93099301-chr4:93100034..93102705,3	K562	blood:
21	chr4:93041952..93042761-chr4:93063494..93064136,3	MCF-7	breast:
22	chr4:92522210..92524943-chr4:92527057..92528806,2	K562	blood:
23	chr4:92862741..92865102-chr4:92873846..92875562,2	MCF-7	breast:
24	chr19:18390428..18392471-chr4:92786104..92787624,2	K562	blood:
25	chr4:93096975..93099301-chr4:93100034..93102705,3	K562	blood:
26	chr4:92763071..92764755-chr4:92766152..92768101,2	MCF-7	breast:
27	chr4:93190438..93192624-chr4:93198856..93200491,2	K562	blood:
28	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
29	chr1:150602085..150602904-chr4:92944319..92945074,2	NB4	blood:
30	chr2:39076189..39078927-chr4:92754563..92756152,2	MCF-7	breast:
31	chr4:93190438..93192624-chr4:93198856..93200491,2	K562	blood:
32	chr4:92702026..92702759-chr6:57445422..57446224,2	MCF-7	breast:
33	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:
34	chr4:92539576..92542400-chr4:92543063..92544579,2	MCF-7	breast:
35	chr4:92852985..92854522-chr4:92856972..92859223,2	K562	blood:
36	chr4:93102928..93104754-chr4:93108794..93111056,2	K562	blood:
37	chr4:92733503..92735821-chr4:92736564..92739014,2	K562	blood:
38	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
39	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
40	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
41	chr4:93102928..93104754-chr4:93108794..93111056,2	K562	blood:
42	chr4:93156131..93157837-chr4:93174936..93177548,2	MCF-7	breast:
43	chr4:92763071..92764755-chr4:92766152..92768101,2	MCF-7	breast:
44	chr4:93041952..93042462-chr4:93063543..93064136,2	MCF-7	breast:
45	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
46	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-9B6.1.1-1	chr4:93185631-93186322	NONHSAT097428
2	lnc-FAM190A-2	chr4:92524426-92526443	NONHSAT097419
3	lnc-FAM190A-3	chr4:92580174-92580494	NONHSAT097421
4	lnc-RP11-9B6.1.1-1	chr4:93183998-93184506	NONHSAT097428
5	lnc-RP11-9B6.1.1-1	chr4:93198201-93198226	XLOC_004018
6	lnc-FAM190A-1	chr4:92809037-92809255	XLOC_003610
7	lnc-RP11-9B6.1.1-1	chr4:93189918-93190643	NONHSAT097428
8	lnc-RP11-9B6.1.1-1	chr4:93176335-93177884	NONHSAT097428
9	lnc-FAM190A-3	chr4:92580579-92581267	NONHSAT097421
10	lnc-FAM190A-1	chr4:92825397-92825486	XLOC_003610
11	lnc-GRID2-2	chr4:92947431-92947539	NONHSAT097424
12	lnc-RP11-9B6.1.1-1	chr4:93189918-93190507	XLOC_004018
13	lnc-RP11-9B6.1.1-1	chr4:93198201-93198528	NONHSAT097428
14	lnc-RP11-9B6.1.1-1	chr4:93179004-93179171	NONHSAT097428
15	lnc-RP11-9B6.1.1-5	chr4:92806197-92806405	NONHSAT097422
16	lnc-GRID2-1	chr4:93196110-93196329	NONHSAT097432
17	lnc-FAM190A-1	chr4:92816603-92816760	XLOC_003610
18	lnc-GRID2-1	chr4:93194582-93194836	NONHSAT097432
19	lnc-RP11-9B6.1.1-3	chr4:93181519-93181902	NONHSAT097429
20	lnc-GRID2-2	chr4:92951738-92951863	NONHSAT097424
21	lnc-FAM190A-1	chr4:92810110-92810219	XLOC_003610
22	lnc-GRID2-1	chr4:93195832-93195994	NONHSAT097432

No data

Variant related genes	Relation type
ENSG00000249052	TF binding region
KRT19P6	TF binding region
ENSG00000248817	TF binding region
ENSG00000249152	TF binding region
ENSG00000256889	TF binding region
ENSG00000249052	CpG island
KRT19P6	CpG island
ENSG00000248817	CpG island
ENSG00000249152	CpG island
ENSG00000256889	CpG island
ENSG00000133316	chromatin interactions
ENSG00000165533	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000248817	chromatin interactions
IL6ST	miRNA target sites
SERTAD4	miRNA target sites
UBXN2A	miRNA target sites

Extended variants
information (count: 11266 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:11266 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541591200	chr4:92511017-92511018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374922740	chr4:92511031-92511032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71924725	chr4:92511049-92511050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111818314	chr4:92511050-92511051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531908899	chr4:92511052-92511053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561345669	chr4:92511177-92511178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561430702	chr4:92511180-92511181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571729027	chr4:92511198-92511199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530388108	chr4:92511274-92511275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550074102	chr4:92511295-92511296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372023219	chr4:92511311-92511312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144890746	chr4:92511351-92511352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377135218	chr4:92511402-92511403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557387276	chr4:92511447-92511448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532370910	chr4:92511452-92511453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34475103	chr4:92511454-92511455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73836286	chr4:92511480-92511481	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565813196	chr4:92511493-92511494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112378074	chr4:92511535-92511536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547532401	chr4:92511587-92511588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567358070	chr4:92511597-92511598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113211907	chr4:92511623-92511624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567390098	chr4:92511624-92511625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531854923	chr4:92511641-92511642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545357718	chr4:92511685-92511686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187724068	chr4:92511691-92511692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549860632	chr4:92511742-92511743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538624388	chr4:92511762-92511763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191006256	chr4:92511766-92511767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76260251	chr4:92511773-92511774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151057815	chr4:92511793-92511794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144866478	chr4:92511819-92511820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11733934	chr4:92511820-92511821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574939551	chr4:92511830-92511831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs78981264	chr4:92511850-92511851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563632481	chr4:92511871-92511872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532692111	chr4:92511875-92511876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183161939	chr4:92511905-92511906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566409721	chr4:92511908-92511909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552887072	chr4:92511940-92511941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559501056	chr4:92511943-92511944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140351358	chr4:92511952-92511953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555222244	chr4:92511963-92511964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188292882	chr4:92511993-92511994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548396422	chr4:92512070-92512071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568586439	chr4:92512103-92512104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536439735	chr4:92512104-92512105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573606012	chr4:92512107-92512108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550036572	chr4:92512154-92512155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564899784	chr4:92512189-92512190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Esophageal cancer	21851588	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92511000-92511400	Enhancers	Fetal Heart	heart
2	chr4:92511000-92511600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:92511000-92511600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:92511000-92511600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:92511000-92511800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:92511200-92511800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr4:92511400-92511600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:92511600-92512400	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr4:92511600-92516400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:92511800-92517600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr4:92516400-92516600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr4:92516600-92517000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:92516800-92519000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:92517000-92519200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:92517200-92519000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:92517400-92518400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr4:92517400-92518600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:92517400-92520200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr4:92517600-92518000	Enhancers	H1 Cell Line	embryonic stem cell
20	chr4:92517600-92518000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:92517600-92518400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:92518000-92518200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:92518200-92519000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:92518600-92522400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:92518800-92521200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr4:92519000-92522600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr4:92519000-92522600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr4:92519000-92522600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:92519200-92522600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:92520000-92520200	Enhancers	Gastric	stomach
31	chr4:92520200-92522400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr4:92521200-92522000	Enhancers	Brain Germinal Matrix	brain
33	chr4:92521600-92522200	Enhancers	Fetal Brain Male	brain
34	chr4:92521800-92522000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:92522000-92523000	Weak transcription	Brain Germinal Matrix	brain
36	chr4:92522400-92522800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr4:92522400-92523200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:92522600-92522800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr4:92522600-92522800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:92522600-92523000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr4:92522600-92523200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:92523000-92523200	Enhancers	Brain Germinal Matrix	brain
43	chr4:92532600-92533400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:92532600-92533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:92532600-92533400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:92532600-92533600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:92532600-92533800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr4:92532800-92533200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:92532800-92533200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr4:92532800-92533400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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