Variant report

Variant	nsv537178
Chromosome Location	chr4:92396538-93213898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2593)
CpG islands
(count:854)
Chromatin interactive
region (count:47)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2593 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:93192015-93192704	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:93179240-93179981	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:93174807-93176629	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:93176968-93178653	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	chr4:93174553-93180548	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:93173256-93173722	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:92679711-92680078	HCT-116	colon:	n/a	n/a
9	BACH1	chr4:93174926-93175130	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:92874021-92874050	K562	blood:	n/a	n/a
11	BACH1	chr4:93192112-93192392	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:93191451-93191756	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:93175421-93178227	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr4:92812456-92812830	GM12878	blood:	n/a	chr4:92812671-92812682
15	BATF	chr4:92956979-92957141	GM12878	blood:	n/a	chr4:92957060-92957071
16	BATF	chr4:93139203-93139461	GM12878	blood:	n/a	n/a
17	BATF	chr4:92685314-92685539	GM12878	blood:	n/a	n/a
18	BATF	chr4:92956941-92957201	GM12878	blood:	n/a	chr4:92957060-92957071
19	BATF	chr4:92812540-92812781	GM12878	blood:	n/a	chr4:92812671-92812682
20	BHLHE40	chr4:92767508-92767581	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:92831092-92831515	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:92572273-92572591	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:92956890-92957081	GM12878	blood:	n/a	n/a
24	BRCA1	chr4:93155474-93156185	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr4:92758741-92759534	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr4:92695586-92695633	GM12878	blood:	n/a	n/a
27	BRCA1	chr4:93177241-93178533	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr4:93178843-93178896	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr4:93023011-93023329	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr4:92827208-92827254	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr4:93160637-93161060	HCT-116	colon:	n/a	n/a
32	CBX3	chr4:92679542-92680072	HCT-116	colon:	n/a	chr4:92679572-92679583
33	CBX3	chr4:92679695-92680141	HCT-116	colon:	n/a	n/a
34	CEBPB	chr4:93155405-93156024	ECC-1	luminal epithelium:	n/a	chr4:93155713-93155724
35	CEBPB	chr4:92747311-92748011	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:92935277-92935519	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
37	CEBPB	chr4:92639714-92640000	IMR90	lung:	n/a	chr4:92639838-92639849 chr4:92639838-92639851 chr4:92639840-92639851 chr4:92639835-92639852 chr4:92639838-92639851
38	CEBPB	chr4:92498684-92498998	H1-hESC	embryonic stem cell:	n/a	chr4:92498950-92498963
39	CEBPB	chr4:92839741-92840062	H1-hESC	embryonic stem cell:	n/a	chr4:92839903-92839914
40	CEBPB	chr4:92635356-92635564	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:92758635-92759377	Hela-S3	cervix:	n/a	chr4:92759191-92759203
42	CEBPB	chr4:92539277-92539526	A549	lung:	n/a	chr4:92539440-92539451
43	CEBPB	chr4:92470801-92471006	HepG2	liver:	n/a	chr4:92470936-92470947
44	CEBPB	chr4:93153796-93154098	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:93209720-93210061	IMR90	lung:	n/a	chr4:93209877-93209888
46	CEBPB	chr4:93022867-93023188	A549	lung:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
47	CEBPB	chr4:92498418-92498468	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:92835356-92835641	MCF-7	breast:	n/a	n/a
49	CEBPB	chr4:92470891-92471002	H1-hESC	embryonic stem cell:	n/a	chr4:92470936-92470947
50	CEBPB	chr4:93077726-93077806	H1-hESC	embryonic stem cell:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:92879355-92879405	HIPEpiC	eye:	n/a
2	chr4:93105176-93105226	GM12892	blood:	n/a
3	chr4:93105138-93105188	AG09309	skin:	n/a
4	chr4:93104012-93104062	H1-hESC	embryonic stem cell:	embryo
5	chr4:93103551-93103601	NT2-D1	testis:	n/a
6	chr4:92556548-92556598	HUVEC	blood vessel:	n/a
7	chr4:92879355-92879405	GM19239	blood:	n/a
8	chr4:93198846-93198896	GM12892	blood:	n/a
9	chr4:93105138-93105188	ProgFib	skin:	n/a
10	chr4:93198846-93198896	HCF	heart:	n/a
11	chr4:93104012-93104062	GM19239	blood:	n/a
12	chr4:92516304-92516354	HRCEpiC	kidney:	n/a
13	chr4:92879355-92879405	PANC-1	pancreas:	n/a
14	chr4:92879355-92879405	Jurkat	blood:	n/a
15	chr4:92516304-92516354	LNCaP	prostate:	n/a
16	chr4:93103772-93103822	HCPEpiC	choroid plexus:	n/a
17	chr4:93103914-93103964	MCF10A-Er-Src	breast:	n/a
18	chr4:92879355-92879405	SK-N-SH_RA	brain:	n/a
19	chr4:92879355-92879405	HRPEpiC	eye:	n/a
20	chr4:93198609-93198659	HRCEpiC	kidney:	n/a
21	chr4:93104012-93104062	SKMC	muscle:	n/a
22	chr4:92522792-92522842	BJ	skin:	n/a
23	chr4:93104334-93104384	GM12892	blood:	n/a
24	chr4:93103551-93103601	AG10803	skin:	n/a
25	chr4:93198609-93198659	Hepatocyte	liver:	n/a
26	chr4:93198846-93198896	K562	blood:	n/a
27	chr4:92879355-92879405	AG04450	lung:	fetal
28	chr4:92516304-92516354	Jurkat	blood:	n/a
29	chr4:93126098-93126148	NHBE	bronchial:	n/a
30	chr4:93105176-93105226	HNPCEpiC	eye:	n/a
31	chr4:93126098-93126148	H1-hESC	embryonic stem cell:	embryo
32	chr4:93103772-93103822	PANC-1	pancreas:	n/a
33	chr4:92879355-92879405	SAEC	small airway:	n/a
34	chr4:93198609-93198659	HepG2	liver:	n/a
35	chr4:93103772-93103822	PFSK-1	brain:	n/a
36	chr4:93103914-93103964	HUVEC	blood vessel:	n/a
37	chr4:93126098-93126148	AG10803	skin:	n/a
38	chr4:93104334-93104384	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:92556548-92556598	A549	lung:	n/a
40	chr4:93105138-93105188	AoSMC	blood vessel:	n/a
41	chr4:93198609-93198659	NHDF-neo	bronchial:	n/a
42	chr4:92516304-92516354	GM06990	blood:	n/a
43	chr4:93198846-93198896	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:93103772-93103822	LNCaP	prostate:	n/a
45	chr4:92516304-92516354	SK-N-MC	brain:	n/a
46	chr4:93103551-93103601	HRPEpiC	eye:	n/a
47	chr4:93104334-93104384	ovcar-3	ovarian:	n/a
48	chr4:93105176-93105226	SKMC	muscle:	n/a
49	chr4:93103914-93103964	NT2-D1	testis:	n/a
50	chr4:93126098-93126148	BE2_C	brain:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:92862741..92865102-chr4:92873846..92875562,2	MCF-7	breast:
2	chr11:62608619..62609552-chr4:93076936..93077935,6	HCT-116	colon:
3	chr2:39076189..39078927-chr4:92754563..92756152,2	MCF-7	breast:
4	chr4:92034306..92035417-chr4:92423226..92424074,5	MCF-7	breast:
5	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:
6	chr4:93161950..93163771-chr4:93165936..93168179,2	MCF-7	breast:
7	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
8	chr14:89306981..89307680-chr4:92635846..92636574,2	MCF-7	breast:
9	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
10	chr4:93044602..93046787-chr4:93048127..93050943,2	MCF-7	breast:
11	chr4:92733503..92735821-chr4:92736564..92739014,2	K562	blood:
12	chr17:56736322..56736880-chr4:92908655..92909344,2	MCF-7	breast:
13	chr4:92539576..92542400-chr4:92543063..92544579,2	MCF-7	breast:
14	chr4:92522210..92524943-chr4:92527057..92528806,2	K562	blood:
15	chr4:93190438..93192624-chr4:93198856..93200491,2	K562	blood:
16	chr4:93190438..93192624-chr4:93198856..93200491,2	K562	blood:
17	chr4:92733503..92735821-chr4:92736564..92739014,2	K562	blood:
18	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
19	chr4:92852985..92854522-chr4:92856972..92859223,2	K562	blood:
20	chr4:93102928..93104754-chr4:93108794..93111056,2	K562	blood:
21	chr4:92862741..92865102-chr4:92873846..92875562,2	MCF-7	breast:
22	chr4:92649464..92651523-chr4:92652088..92654167,2	MCF-7	breast:
23	chr4:92649464..92651523-chr4:92652088..92654167,2	MCF-7	breast:
24	chr4:93102928..93104754-chr4:93108794..93111056,2	K562	blood:
25	chr4:92702026..92702759-chr6:57445422..57446224,2	MCF-7	breast:
26	chr4:93022151..93024082-chr4:93025859..93028241,2	MCF-7	breast:
27	chr19:18390428..18392471-chr4:92786104..92787624,2	K562	blood:
28	chr4:92763071..92764755-chr4:92766152..92768101,2	MCF-7	breast:
29	chr4:93096975..93099301-chr4:93100034..93102705,3	K562	blood:
30	chr4:93041952..93042761-chr4:93063494..93064136,3	MCF-7	breast:
31	chr4:93202258..93204813-chr4:93248472..93250667,2	K562	blood:
32	chr4:93036522..93038692-chr4:93040395..93042762,2	MCF-7	breast:
33	chr4:93156131..93157837-chr4:93174936..93177548,2	MCF-7	breast:
34	chr4:93027385..93029729-chr4:93033798..93036678,2	K562	blood:
35	chr4:93161950..93163771-chr4:93165936..93168179,2	MCF-7	breast:
36	chr20:43379044..43379544-chr4:92594658..92595640,2	K562	blood:
37	chr1:150602085..150602904-chr4:92944319..92945074,2	NB4	blood:
38	chr4:93156131..93157837-chr4:93174936..93177548,2	MCF-7	breast:
39	chr4:93102928..93105874-chr4:93109166..93111796,3	K562	blood:
40	chr4:93041952..93042462-chr4:93063543..93064136,2	MCF-7	breast:
41	chr4:93096975..93099301-chr4:93100034..93102705,3	K562	blood:
42	chr4:93041952..93042761-chr4:93063494..93064136,3	MCF-7	breast:
43	chr4:92539576..92542400-chr4:92543063..92544579,2	MCF-7	breast:
44	chr4:92763071..92764755-chr4:92766152..92768101,2	MCF-7	breast:
45	chr4:93041952..93042462-chr4:93063543..93064136,2	MCF-7	breast:
46	chr4:92522210..92524943-chr4:92527057..92528806,2	K562	blood:
47	chr4:92852985..92854522-chr4:92856972..92859223,2	K562	blood:

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

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

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
ENSG00000202077	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000165533	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000248817	chromatin interactions
SERTAD4	miRNA target sites
IL6ST	miRNA target sites
UBXN2A	miRNA target sites

Extended variants
information (count: 12522 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:12522 , 50 per page) page: 1 2 3 4 5 6 7 ... 251

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530832482	chr4:92408029-92408030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550917956	chr4:92408030-92408031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184372754	chr4:92408039-92408040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533648119	chr4:92408085-92408086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13103495	chr4:92408133-92408134	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567062860	chr4:92408149-92408150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536005187	chr4:92408165-92408166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188761348	chr4:92408293-92408294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559981567	chr4:92408340-92408341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568110775	chr4:92408365-92408366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559011262	chr4:92408398-92408399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116346031	chr4:92408415-92408416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577119944	chr4:92408518-92408519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527319637	chr4:92408532-92408533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565147189	chr4:92408533-92408534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556893544	chr4:92408539-92408540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532159578	chr4:92408581-92408582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145810232	chr4:92408616-92408617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550555842	chr4:92408690-92408691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138247208	chr4:92408697-92408698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115642592	chr4:92408741-92408742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149496791	chr4:92408766-92408767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541403150	chr4:92408811-92408812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112381967	chr4:92408815-92408816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74767295	chr4:92408831-92408832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116830324	chr4:92408867-92408868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13138113	chr4:92408898-92408899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs74426515	chr4:92408899-92408900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12640730	chr4:92408975-92408976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs73837624	chr4:92408987-92408988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563847339	chr4:92409166-92409167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547319138	chr4:92409171-92409172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112799162	chr4:92409175-92409176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148620281	chr4:92409282-92409283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181952307	chr4:92409283-92409284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147645378	chr4:92409313-92409314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62309608	chr4:92409328-92409329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550200756	chr4:92409357-92409358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570121582	chr4:92409368-92409369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539001251	chr4:92409385-92409386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187054060	chr4:92409386-92409387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572767175	chr4:92409406-92409407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs66754254	chr4:92409421-92409422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs78330206	chr4:92409440-92409441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575698781	chr4:92409512-92409513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76457446	chr4:92409583-92409584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2178657	chr4:92409607-92409608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142684238	chr4:92409686-92409687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28741030	chr4:92409712-92409713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565370461	chr4:92409723-92409724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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	17122850	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:1022 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92408000-92408800	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:92408200-92408600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr4:92408200-92408600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr4:92408200-92408800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr4:92408400-92408600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr4:92408400-92408800	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:92408600-92409600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:92408600-92409600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr4:92408800-92410000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr4:92408800-92410000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr4:92409600-92410000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:92409800-92410000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:92410000-92410400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:92410200-92410400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:92432400-92432800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:92432800-92439600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:92439600-92440000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:92439800-92440000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:92440000-92440200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:92440200-92443600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:92446200-92446600	Enhancers	Fetal Intestine Large	intestine
22	chr4:92446200-92446600	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr4:92446600-92447000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:92446600-92447000	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr4:92446600-92447000	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr4:92446600-92447000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr4:92459600-92460200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:92480000-92487000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:92487000-92487600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:92487600-92491000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:92488200-92490600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:92488400-92489000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:92488400-92490600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr4:92488600-92489800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:92488800-92489400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:92488800-92490200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:92489000-92489400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr4:92489000-92490400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:92489200-92489600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:92489400-92489600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr4:92489400-92490400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:92489600-92490400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:92489800-92490000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr4:92490000-92490400	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:92490000-92491600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr4:92490200-92490600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:92490200-92490600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:92490200-92490600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:92490200-92491800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr4:92490400-92490600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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