Variant report

Variant	nsv1015355
Chromosome Location	chr8:112558586-113154605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1765)
CpG islands
(count:610)
Chromatin interactive
region (count:59)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1765 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112576305-112577602	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:112976470-112976714	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:112809453-112809783	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:113038752-113039444	HepG2	liver:	n/a	n/a
5	ATF1	chr8:113041124-113041245	K562	blood:	n/a	n/a
6	BACH1	chr8:113114422-113114764	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr8:112692464-112692870	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:112929242-112929439	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:112691006-112691050	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:112565168-112565174	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr8:112929118-112929489	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr8:112929219-112929426	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr8:112809530-112809825	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:112576576-112576903	HepG2	liver:	n/a	n/a
15	BHLHE40	chr8:112716680-112716782	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:112980773-112980798	GM12878	blood:	n/a	n/a
17	BRCA1	chr8:112691833-112692033	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr8:112678378-112678702	K562	blood:	n/a	n/a
19	CCNT2	chr8:112730529-112730729	K562	blood:	n/a	n/a
20	CEBPB	chr8:112929312-112929597	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:112889694-112890040	A549	lung:	n/a	chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889855-112889868 chr8:112889855-112889866 chr8:112889855-112889868 chr8:112889857-112889866 chr8:112889857-112889868
22	CEBPB	chr8:112722331-112722655	ECC-1	luminal epithelium:	n/a	chr8:112722472-112722483
23	CEBPB	chr8:112949249-112949366	A549	lung:	n/a	chr8:112949283-112949294
24	CEBPB	chr8:112979515-112979804	K562	blood:	n/a	chr8:112979671-112979682
25	CEBPB	chr8:113130509-113130814	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:113148569-113148923	MCF-7	breast:	n/a	chr8:113148765-113148776
27	CEBPB	chr8:112977586-112978064	MCF-7	breast:	n/a	n/a
28	CEBPB	chr8:112576445-112576921	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:112912650-112912908	HepG2	liver:	n/a	chr8:112912824-112912835
30	CEBPB	chr8:112979555-112979799	H1-hESC	embryonic stem cell:	n/a	chr8:112979671-112979682
31	CEBPB	chr8:112968915-112969112	HepG2	liver:	n/a	chr8:112968968-112968979
32	CEBPB	chr8:113022244-113022537	IMR90	lung:	n/a	chr8:113022392-113022403
33	CEBPB	chr8:112656669-112656973	A549	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
34	CEBPB	chr8:113124365-113124706	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:112860528-112860630	A549	lung:	n/a	n/a
36	CEBPB	chr8:113038800-113039355	MCF-7	breast:	n/a	chr8:113039120-113039133
37	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
38	CEBPB	chr8:112809471-112809708	A549	lung:	n/a	n/a
39	CEBPB	chr8:112818835-112819234	MCF-7	breast:	n/a	n/a
40	CEBPB	chr8:112656695-112656966	IMR90	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
41	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
42	CEBPB	chr8:113016873-113017172	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
44	CEBPB	chr8:112979542-112979859	IMR90	lung:	n/a	chr8:112979671-112979682
45	CEBPB	chr8:113124360-113124710	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:112889693-112890005	HepG2	liver:	n/a	chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889855-112889868 chr8:112889855-112889866 chr8:112889855-112889868 chr8:112889857-112889866 chr8:112889857-112889868
47	CEBPB	chr8:113124367-113124716	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:113047658-113047865	HepG2	liver:	n/a	n/a
49	CEBPB	chr8:113130585-113130791	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:113016889-113017172	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112612368-112612418	AoSMC	blood vessel:	n/a
2	chr8:112612368-112612418	HEK293	kidney:	embryo
3	chr8:112835665-112835715	BE2_C	brain:	n/a
4	chr8:113113972-113114022	HRCEpiC	kidney:	n/a
5	chr8:113145005-113145055	GM12878	blood:	n/a
6	chr8:112636613-112636663	HepG2	liver:	n/a
7	chr8:113113972-113114022	ovcar-3	ovarian:	n/a
8	chr8:112691450-112691500	GM12891	blood:	n/a
9	chr8:112906823-112906873	HIPEpiC	eye:	n/a
10	chr8:112636613-112636663	A549	lung:	n/a
11	chr8:112655155-112655205	PANC-1	pancreas:	n/a
12	chr8:112906823-112906873	BE2_C	brain:	n/a
13	chr8:112835665-112835715	PANC-1	pancreas:	n/a
14	chr8:113049519-113049569	IMR90	lung:	fetal
15	chr8:112906823-112906873	Caco-2	colon:	n/a
16	chr8:112655155-112655205	HRCEpiC	kidney:	n/a
17	chr8:113113972-113114022	GM12878	blood:	n/a
18	chr8:113145005-113145055	HEEpiC	esophagus:	n/a
19	chr8:113049519-113049569	SK-N-MC	brain:	n/a
20	chr8:113145005-113145055	NH-A	brain:	n/a
21	chr8:112636625-112636675	HEEpiC	esophagus:	n/a
22	chr8:112691450-112691500	NB4	blood:	n/a
23	chr8:112906823-112906873	HCM	heart:	n/a
24	chr8:112691450-112691500	CMK	blood:	n/a
25	chr8:112636613-112636663	GM06990	blood:	n/a
26	chr8:113113972-113114022	Caco-2	colon:	n/a
27	chr8:112655155-112655205	GM12878	blood:	n/a
28	chr8:112612368-112612418	GM12892	blood:	n/a
29	chr8:112636625-112636675	HIPEpiC	eye:	n/a
30	chr8:113145005-113145055	IMR90	lung:	fetal
31	chr8:112655155-112655205	GM19239	blood:	n/a
32	chr8:112636613-112636663	IMR90	lung:	fetal
33	chr8:112835665-112835715	AG04449	skin:	fetal
34	chr8:112612368-112612418	SK-N-SH_RA	brain:	n/a
35	chr8:112835665-112835715	HRPEpiC	eye:	n/a
36	chr8:112835665-112835715	GM06990	blood:	n/a
37	chr8:113145005-113145055	MCF-7	breast:	n/a
38	chr8:112612368-112612418	AG09309	skin:	n/a
39	chr8:112655155-112655205	MCF-7	breast:	n/a
40	chr8:112636613-112636663	HIPEpiC	eye:	n/a
41	chr8:112636625-112636675	HL-60	blood:	n/a
42	chr8:112906823-112906873	ECC-1	luminal epithelium:	n/a
43	chr8:112612368-112612418	RPTEC	kidney:	n/a
44	chr8:112636625-112636675	HEK293	kidney:	embryo
45	chr8:112636625-112636675	MCF10A-Er-Src	breast:	n/a
46	chr8:112612368-112612418	NT2-D1	testis:	n/a
47	chr8:112906823-112906873	SK-N-MC	brain:	n/a
48	chr8:112612368-112612418	A549	lung:	n/a
49	chr8:112636613-112636663	HEK293	kidney:	embryo
50	chr8:113113972-113114022	LNCaP	prostate:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:59972667..59973359-chr8:112973092..112973952,2	MCF-7	breast:
2	chr8:112919794..112922834-chr8:112924781..112927217,3	K562	blood:
3	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
4	chr8:112980405..112982694-chr8:112982938..112985443,2	MCF-7	breast:
5	chr8:112456153..112457084-chr8:112809101..112810085,7	MCF-7	breast:
6	chr8:112870353..112871084-chr8:112943233..112944215,2	MCF-7	breast:
7	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
8	chr8:112976579..112977386-chr8:113471922..113472710,2	MCF-7	breast:
9	chr8:112946373..112947269-chr8:113476964..113477520,2	MCF-7	breast:
10	chr8:112952038..112954490-chr8:112955048..112956799,2	K562	blood:
11	chr8:112946524..112947507-chr8:113386902..113387446,2	MCF-7	breast:
12	chr8:112753150..112755193-chr8:112756669..112758806,2	MCF-7	breast:
13	chr8:112947101..112947938-chr8:113477362..113477935,2	MCF-7	breast:
14	chr8:113123396..113125846-chr8:113130246..113132854,2	MCF-7	breast:
15	chr8:112841029..112843004-chr8:112843259..112845025,2	MCF-7	breast:
16	chr8:112570236..112571107-chr8:139584283..139585016,2	MCF-7	breast:
17	chr8:112765107..112767231-chr8:112771782..112773764,2	K562	blood:
18	chr8:112980405..112982694-chr8:112982938..112985443,2	MCF-7	breast:
19	chr8:112561052..112562682-chr8:112563214..112564772,2	MCF-7	breast:
20	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:
21	chr8:113057607..113060468-chr8:113062471..113064373,2	MCF-7	breast:
22	chr11:61100776..61103699-chr8:112876194..112878368,2	MCF-7	breast:
23	chr8:112765107..112767231-chr8:112771782..112773764,2	K562	blood:
24	chr8:113123396..113125846-chr8:113130246..113132854,2	MCF-7	breast:
25	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
26	chr8:112946353..112947027-chr8:112976279..112976810,2	MCF-7	breast:
27	chr6:26214142..26215773-chr8:112896843..112899051,2	MCF-7	breast:
28	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
29	chr8:112877538..112880401-chr8:112881600..112883445,2	K562	blood:
30	chr8:112976625..112977471-chr8:114449676..114450374,2	MCF-7	breast:
31	chr17:56736027..56736822-chr8:112887594..112888361,2	MCF-7	breast:
32	chr8:112248265..112249043-chr8:112809213..112809738,2	MCF-7	breast:
33	chr8:112456214..112456969-chr8:112758072..112758694,3	MCF-7	breast:
34	chr8:112870353..112871084-chr8:112943233..112944215,2	MCF-7	breast:
35	chr8:112946347..112947268-chr8:113386770..113387527,2	MCF-7	breast:
36	chr8:112721723..112722542-chr9:119005808..119006308,2	MCF-7	breast:
37	chr8:112946353..112947027-chr8:112976279..112976810,2	MCF-7	breast:
38	chr8:112976151..112977081-chr8:113386595..113387462,4	MCF-7	breast:
39	chr8:112976187..112977006-chr8:113476921..113477813,7	MCF-7	breast:
40	chr8:112455862..112457106-chr8:112809020..112809893,6	MCF-7	breast:
41	chr8:112438643..112439991-chr8:112809151..112809703,4	MCF-7	breast:
42	chr8:112919794..112922834-chr8:112924781..112927217,3	K562	blood:
43	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:
44	chr8:112753150..112755193-chr8:112756669..112758806,2	MCF-7	breast:
45	chr8:112976314..112977253-chr8:113408305..113409151,3	MCF-7	breast:
46	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
47	chr8:112877538..112880401-chr8:112881600..112883445,2	K562	blood:
48	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
49	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
50	chr8:113121132..113122642-chr8:113123330..113125697,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-7	chr8:112837915-112838389	l_3669_chr8:112823382-112827015_testes
2	lnc-RP11-67H2.1.1-3	chr8:112711744-112711881	XLOC_006902
3	lnc-RP11-67H2.1.1-2	chr8:112768535-112768629	ENSG00000254262
4	lnc-RP11-67H2.1.1-3	chr8:112712240-112712497	XLOC_006902
5	lnc-RP11-67H2.1.1-7	chr8:112823383-112823488	l_3669_chr8:112823382-112827015_testes
6	lnc-CSMD3-4	chr8:112633687-112634026	NONHSAT128329
7	lnc-RP11-67H2.1.1-7	chr8:112837712-112837805	l_3669_chr8:112823382-112827015_testes
8	lnc-RP11-67H2.1.1-2	chr8:112757671-112757836	ENSG00000254262
9	lnc-RP11-67H2.1.1-3	chr8:112712239-112712497	NONHSAT128330
10	lnc-RP11-67H2.1.1-2	chr8:112768739-112769213	XLOC_006903
11	lnc-RP11-67H2.1.1-2	chr8:112754207-112754312	XLOC_006903
12	lnc-RP11-67H2.1.1-2	chr8:112754225-112754312	XLOC_006903
13	lnc-RP11-67H2.1.1-3	chr8:112711743-112711881	NONHSAT128330
14	lnc-RP11-67H2.1.1-2	chr8:112757671-112757916	XLOC_006903
15	lnc-RP11-67H2.1.1-2	chr8:112768739-112770625	XLOC_006903
16	lnc-RP11-67H2.1.1-2	chr8:112757671-112757836	XLOC_006903
17	lnc-RP11-67H2.1.1-2	chr8:112768536-112768629	XLOC_006903
18	lnc-RP11-67H2.1.1-2	chr8:112768738-112770625	NONHSAT128333
19	lnc-RP11-67H2.1.1-7	chr8:112826847-112827015	l_3669_chr8:112823382-112827015_testes
20	lnc-RP11-67H2.1.1-2	chr8:112768739-112768861	ENSG00000254262
21	lnc-RP11-67H2.1.1-2	chr8:112757670-112757836	NONHSAT128333
22	lnc-RP11-67H2.1.1-2	chr8:112754224-112754312	NONHSAT128333
23	lnc-RP11-67H2.1.1-2	chr8:112754241-112754312	ENSG00000254262

No data

Variant related genes	Relation type
ENSG00000253156	TF binding region
ENSG00000254262	TF binding region
ENSG00000253156	CpG island
ENSG00000254262	CpG island
ENSG00000167986	chromatin interactions
ENSG00000254262	chromatin interactions
ENSG00000253103	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000149476	chromatin interactions
ACSL1	miRNA target sites
RPRD1A	miRNA target sites
ACPL2	miRNA target sites

Extended variants
information (count: 7027 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:7027 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150009280	chr8:112558626-112558627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs544868005	chr8:112558632-112558633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146556790	chr8:112558650-112558651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574536372	chr8:112558654-112558655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577591018	chr8:112558738-112558739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543554912	chr8:112558766-112558767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563791735	chr8:112558770-112558771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529326402	chr8:112558803-112558804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543211427	chr8:112558806-112558807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559666938	chr8:112558809-112558810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551127079	chr8:112558814-112558815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140017401	chr8:112558835-112558836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552089148	chr8:112558889-112558890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543463336	chr8:112558964-112558965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571292730	chr8:112558986-112558987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10102136	chr8:112558999-112559000	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187663690	chr8:112559020-112559021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567364859	chr8:112559058-112559059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192580825	chr8:112559079-112559080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143552571	chr8:112559095-112559096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184801339	chr8:112559145-112559146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566532053	chr8:112559150-112559151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538573895	chr8:112559190-112559191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558423445	chr8:112559207-112559208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576889328	chr8:112559264-112559265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577655084	chr8:112559270-112559271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567473376	chr8:112559280-112559281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545804628	chr8:112559281-112559282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557029299	chr8:112559300-112559301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116169252	chr8:112559372-112559373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559592991	chr8:112559425-112559426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528313736	chr8:112559488-112559489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114021043	chr8:112559537-112559538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189663341	chr8:112559583-112559584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192995024	chr8:112559599-112559600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs16882151	chr8:112559603-112559604	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs565568684	chr8:112559657-112559658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561052517	chr8:112559668-112559669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184300381	chr8:112559716-112559717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189435646	chr8:112559782-112559783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549778468	chr8:112559783-112559784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116666052	chr8:112559784-112559785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs16882157	chr8:112559785-112559786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546354739	chr8:112559789-112559790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112528752	chr8:112559801-112559802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538435116	chr8:112559842-112559843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551910379	chr8:112559846-112559847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375964972	chr8:112559856-112559857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149099868	chr8:112559899-112559900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537722227	chr8:112559909-112559910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112557200-112558800	Enhancers	Fetal Lung	lung
2	chr8:112557800-112558600	Strong transcription	Adipose Nuclei	Adipose
3	chr8:112558600-112560200	Weak transcription	Adipose Nuclei	Adipose
4	chr8:112575200-112577600	Enhancers	Liver	Liver
5	chr8:112575800-112578400	Enhancers	HepG2	liver
6	chr8:112578200-112578400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:112593600-112593800	Enhancers	Pancreas	Pancrea
8	chr8:112597000-112598400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:112611000-112611800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr8:112611400-112612000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr8:112611600-112611800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr8:112611600-112612200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:112611800-112612000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr8:112611800-112612800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
15	chr8:112615400-112615800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:112623600-112624000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:112623800-112624200	ZNF genes & repeats	Spleen	Spleen
18	chr8:112624000-112624200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:112624000-112624200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
20	chr8:112624000-112627600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:112624200-112633800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:112627200-112628000	Enhancers	Brain Germinal Matrix	brain
23	chr8:112627600-112628200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:112633800-112634000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:112633800-112634000	Bivalent Enhancer	Aorta	Aorta
26	chr8:112655000-112655200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:112655200-112655400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:112665400-112666000	Enhancers	Fetal Muscle Leg	muscle
29	chr8:112688200-112689400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:112688200-112690400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr8:112689400-112689800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:112689600-112690400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:112689600-112690400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:112689800-112690200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:112690000-112690400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr8:112690000-112690600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr8:112690000-112690600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr8:112690000-112690800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr8:112690200-112691400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:112690200-112692200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:112690200-112692400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr8:112690200-112694000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr8:112690400-112690600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr8:112690400-112691000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr8:112690400-112691200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr8:112690400-112691200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr8:112690400-112691400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr8:112690400-112693400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr8:112690400-112693400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:112690600-112691000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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