Variant report

Variant	nsv530442
Chromosome Location	chr4:92528849-93184304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2160)
CpG islands
(count:611)
Chromatin interactive
region (count:41)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2160 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:93179240-93179981	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:93173256-93173722	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	ATF3	chr4:92679711-92680078	HCT-116	colon:	n/a	n/a
8	BACH1	chr4:92874021-92874050	K562	blood:	n/a	n/a
9	BACH1	chr4:93175421-93178227	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:93174926-93175130	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:92956979-92957141	GM12878	blood:	n/a	chr4:92957060-92957071
12	BATF	chr4:92812456-92812830	GM12878	blood:	n/a	chr4:92812671-92812682
13	BATF	chr4:92956941-92957201	GM12878	blood:	n/a	chr4:92957060-92957071
14	BATF	chr4:92812540-92812781	GM12878	blood:	n/a	chr4:92812671-92812682
15	BATF	chr4:93139203-93139461	GM12878	blood:	n/a	n/a
16	BATF	chr4:92685314-92685539	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:92956890-92957081	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:92831092-92831515	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:92572273-92572591	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:92767508-92767581	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:92827208-92827254	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr4:93023011-93023329	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr4:92758741-92759534	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr4:93155474-93156185	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr4:92695586-92695633	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:93177241-93178533	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr4:93178843-93178896	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr4:93160637-93161060	HCT-116	colon:	n/a	n/a
29	CBX3	chr4:92679542-92680072	HCT-116	colon:	n/a	chr4:92679572-92679583
30	CBX3	chr4:92679695-92680141	HCT-116	colon:	n/a	n/a
31	CEBPB	chr4:93155490-93155983	A549	lung:	n/a	chr4:93155713-93155724
32	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
33	CEBPB	chr4:92833707-92833907	A549	lung:	n/a	chr4:92833836-92833847 chr4:92833838-92833849
34	CEBPB	chr4:93155536-93156008	HCT-116	colon:	n/a	chr4:93155713-93155724
35	CEBPB	chr4:93022867-93023188	A549	lung:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
36	CEBPB	chr4:92539277-92539600	HepG2	liver:	n/a	chr4:92539440-92539451
37	CEBPB	chr4:92717046-92717407	HepG2	liver:	n/a	chr4:92717222-92717233
38	CEBPB	chr4:92835385-92835609	MCF-7	breast:	n/a	n/a
39	CEBPB	chr4:92660005-92660254	HepG2	liver:	n/a	chr4:92660174-92660185
40	CEBPB	chr4:92750683-92751085	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:93022790-93023139	HepG2	liver:	n/a	chr4:93023015-93023028 chr4:93022982-93022993 chr4:93023015-93023026 chr4:93023016-93023027 chr4:93022983-93022994
42	CEBPB	chr4:92554586-92554881	A549	lung:	n/a	chr4:92554731-92554744 chr4:92554731-92554742
43	CEBPB	chr4:93155415-93156185	Hela-S3	cervix:	n/a	chr4:93155713-93155724
44	CEBPB	chr4:92758691-92759082	MCF-7	breast:	n/a	n/a
45	CEBPB	chr4:92635356-92635564	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:92565122-92565385	MCF-7	breast:	n/a	n/a
47	CEBPB	chr4:92539303-92539596	IMR90	lung:	n/a	chr4:92539440-92539451
48	CEBPB	chr4:92839736-92840064	HepG2	liver:	n/a	chr4:92839903-92839914
49	CEBPB	chr4:92758628-92759069	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:92839741-92840062	H1-hESC	embryonic stem cell:	n/a	chr4:92839903-92839914

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93103772-93103822	SKMC	muscle:	n/a
2	chr4:93103772-93103822	SKMC	muscle:	n/a
3	chr4:93126098-93126148	GM06990	blood:	n/a
4	chr4:93105176-93105226	HepG2	liver:	n/a
5	chr4:92556548-92556598	HIPEpiC	eye:	n/a
6	chr4:93104012-93104062	SAEC	small airway:	n/a
7	chr4:92879355-92879405	ECC-1	luminal epithelium:	n/a
8	chr4:93105176-93105226	K562	blood:	n/a
9	chr4:93103914-93103964	AoSMC	blood vessel:	n/a
10	chr4:93104334-93104384	NT2-D1	testis:	n/a
11	chr4:93105138-93105188	AG09309	skin:	n/a
12	chr4:93104334-93104384	MCF10A-Er-Src	breast:	n/a
13	chr4:93104012-93104062	NT2-D1	testis:	n/a
14	chr4:93105138-93105188	ECC-1	luminal epithelium:	n/a
15	chr4:93103914-93103964	T-47D	breast:	n/a
16	chr4:93105138-93105188	HRE	kidney:	n/a
17	chr4:93126098-93126148	SK-N-SH_RA	brain:	n/a
18	chr4:92556548-92556598	NHDF-neo	bronchial:	n/a
19	chr4:93103772-93103822	AG09319	gingival:	n/a
20	chr4:93105138-93105188	PrEC	prostate:	n/a
21	chr4:93103772-93103822	AG10803	skin:	n/a
22	chr4:93104334-93104384	GM06990	blood:	n/a
23	chr4:93103772-93103822	HNPCEpiC	eye:	n/a
24	chr4:93104012-93104062	T-47D	breast:	n/a
25	chr4:93104012-93104062	AG04449	skin:	fetal
26	chr4:92556548-92556598	Hela-S3	cervix:	n/a
27	chr4:93104012-93104062	HCM	heart:	n/a
28	chr4:93104012-93104062	CMK	blood:	n/a
29	chr4:93103551-93103601	IMR90	lung:	fetal
30	chr4:93103914-93103964	AG09319	gingival:	n/a
31	chr4:92879355-92879405	Hepatocyte	liver:	n/a
32	chr4:93105176-93105226	HEEpiC	esophagus:	n/a
33	chr4:93103914-93103964	ovcar-3	ovarian:	n/a
34	chr4:93105176-93105226	BJ	skin:	n/a
35	chr4:92879355-92879405	ProgFib	skin:	n/a
36	chr4:93103914-93103964	HRCEpiC	kidney:	n/a
37	chr4:93103772-93103822	HRPEpiC	eye:	n/a
38	chr4:93104334-93104384	HRCEpiC	kidney:	n/a
39	chr4:93104334-93104384	HCT-116	colon:	n/a
40	chr4:93103551-93103601	AG04449	skin:	fetal
41	chr4:93103772-93103822	HEK293	kidney:	embryo
42	chr4:93105138-93105188	GM06990	blood:	n/a
43	chr4:92556548-92556598	H1-hESC	embryonic stem cell:	embryo
44	chr4:93105138-93105188	Caco-2	colon:	n/a
45	chr4:93126098-93126148	AG09319	gingival:	n/a
46	chr4:92879355-92879405	AG09309	skin:	n/a
47	chr4:93126098-93126148	GM12892	blood:	n/a
48	chr4:93105138-93105188	HAEpiC	amniotic membrane:	n/a
49	chr4:93126098-93126148	NH-A	brain:	n/a
50	chr4:93103914-93103964	PrEC	prostate:	n/a

(count:41 , 50 per page) page: 1

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

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-9B6.1.1-3	chr4:93181519-93181902	NONHSAT097429
2	lnc-RP11-9B6.1.1-1	chr4:93176335-93177884	NONHSAT097428
3	lnc-RP11-9B6.1.1-5	chr4:92806197-92806405	NONHSAT097422
4	lnc-FAM190A-3	chr4:92580174-92580494	NONHSAT097421
5	lnc-FAM190A-1	chr4:92825397-92825486	XLOC_003610
6	lnc-RP11-9B6.1.1-1	chr4:93183998-93184506	NONHSAT097428
7	lnc-GRID2-2	chr4:92947431-92947539	NONHSAT097424
8	lnc-RP11-9B6.1.1-1	chr4:93179004-93179171	NONHSAT097428
9	lnc-FAM190A-1	chr4:92816603-92816760	XLOC_003610
10	lnc-FAM190A-3	chr4:92580579-92581267	NONHSAT097421
11	lnc-FAM190A-1	chr4:92809037-92809255	XLOC_003610
12	lnc-FAM190A-1	chr4:92810110-92810219	XLOC_003610
13	lnc-GRID2-2	chr4:92951738-92951863	NONHSAT097424

No data

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

Extended variants
information (count: 9318 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:9318 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548857533	chr4:92532672-92532673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192293894	chr4:92532689-92532690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531444089	chr4:92532760-92532761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529387590	chr4:92532761-92532762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73836301	chr4:92532768-92532769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565963039	chr4:92532769-92532770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184248726	chr4:92532781-92532782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147907488	chr4:92532819-92532820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375062455	chr4:92532838-92532839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375444851	chr4:92532841-92532842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551438264	chr4:92532844-92532845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547439568	chr4:92532864-92532865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539418696	chr4:92532930-92532931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189656610	chr4:92532951-92532952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536358035	chr4:92532969-92532970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368530483	chr4:92532984-92532985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181170977	chr4:92532993-92532994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148943749	chr4:92532998-92532999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1114625	chr4:92533008-92533009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538876389	chr4:92533021-92533022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs989119	chr4:92533035-92533036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs151035182	chr4:92533039-92533040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540997825	chr4:92533108-92533109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375999383	chr4:92533201-92533202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141118608	chr4:92533207-92533208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574798048	chr4:92533218-92533219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543887228	chr4:92533219-92533220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35531607	chr4:92533225-92533226	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs531510767	chr4:92533230-92533231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186210623	chr4:92533262-92533263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77443826	chr4:92533270-92533271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527589469	chr4:92533275-92533276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547039504	chr4:92533317-92533318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567243911	chr4:92533385-92533386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557328072	chr4:92533390-92533391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141709960	chr4:92533397-92533398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377263196	chr4:92533399-92533400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535915680	chr4:92533441-92533442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549826467	chr4:92533453-92533454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569685933	chr4:92533456-92533457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189016450	chr4:92533479-92533480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145155013	chr4:92533502-92533503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6821624	chr4:92533513-92533514	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs369758388	chr4:92533551-92533552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572357097	chr4:92533576-92533577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374951590	chr4:92533580-92533581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534994659	chr4:92533605-92533606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531362268	chr4:92533611-92533612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538543661	chr4:92533613-92533614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182057455	chr4:92533635-92533636	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:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92532600-92533400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:92532600-92533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:92532600-92533400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:92532600-92533600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:92532600-92533800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:92532800-92533200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:92532800-92533200	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:92532800-92533400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:92532800-92533600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:92533000-92533200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:92533000-92533400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr4:92533200-92533400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:92533200-92534200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:92533400-92543600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:92533600-92545600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:92534200-92534600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:92534600-92534800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:92534800-92536000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:92538400-92538600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr4:92538800-92544000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr4:92541800-92542600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:92542000-92542600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:92543600-92544000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:92543600-92544000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr4:92543600-92544200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:92543600-92544200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:92543600-92544400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:92543600-92544600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:92543800-92544000	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr4:92544000-92544200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr4:92544000-92544200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:92544000-92544400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:92544000-92544600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr4:92544000-92544600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr4:92544000-92544800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr4:92544000-92544800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr4:92544200-92544400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
38	chr4:92544200-92544400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:92544200-92544400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
40	chr4:92544200-92544400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr4:92544200-92544400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:92544200-92544600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr4:92544400-92544600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr4:92544400-92544600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr4:92544400-92544800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:92544400-92544800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr4:92544400-92548600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:92544600-92544800	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr4:92544600-92545000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:92544600-92546200	Active TSS	H9 Cell Line	embryonic stem cell

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