Variant report

Variant	esv2754268
Chromosome Location	chr5:120398198-120745053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1032)
CpG islands
(count:122)
Chromatin interactive
region (count:38)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120480659-120480718	K562	blood:	n/a	n/a
2	ATF1	chr5:120609797-120610099	K562	blood:	n/a	n/a
3	ATF2	chr5:120735400-120736165	GM12878	blood:	n/a	n/a
4	ATF2	chr5:120735521-120735958	GM12878	blood:	n/a	n/a
5	ATF3	chr5:120587704-120588047	A549	lung:	n/a	n/a
6	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
7	ATF3	chr5:120609660-120610180	A549	lung:	n/a	n/a
8	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
9	BATF	chr5:120737102-120737339	GM12878	blood:	n/a	n/a
10	BATF	chr5:120735502-120735964	GM12878	blood:	n/a	n/a
11	BATF	chr5:120735476-120736026	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:120735493-120735946	GM12878	blood:	n/a	n/a
13	BCL3	chr5:120737037-120737376	GM12878	blood:	n/a	n/a
14	BCL3	chr5:120587530-120588099	A549	lung:	n/a	n/a
15	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
16	BCL3	chr5:120735445-120735944	GM12878	blood:	n/a	n/a
17	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
18	BCLAF1	chr5:120735422-120735896	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:120735520-120735942	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:120582702-120582968	HepG2	liver:	n/a	n/a
21	BRCA1	chr5:120576292-120576344	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr5:120694893-120694952	GM12878	blood:	n/a	n/a
23	CBX3	chr5:120587730-120588017	HCT-116	colon:	n/a	n/a
24	CBX3	chr5:120563378-120563655	K562	blood:	n/a	n/a
25	CBX3	chr5:120609626-120610276	HCT-116	colon:	n/a	n/a
26	CEBPB	chr5:120665178-120665393	Hela-S3	cervix:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
27	CEBPB	chr5:120465336-120465526	K562	blood:	n/a	chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447 chr5:120465434-120465445 chr5:120465434-120465447 chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447
28	CEBPB	chr5:120518577-120518857	K562	blood:	n/a	chr5:120518723-120518734
29	CEBPB	chr5:120650749-120651103	K562	blood:	n/a	n/a
30	CEBPB	chr5:120615503-120615753	K562	blood:	n/a	n/a
31	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
32	CEBPB	chr5:120640550-120640906	HepG2	liver:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
33	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
34	CEBPB	chr5:120602581-120602901	IMR90	lung:	n/a	chr5:120602751-120602762
35	CEBPB	chr5:120702142-120702659	A549	lung:	n/a	n/a
36	CEBPB	chr5:120535010-120535378	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:120587635-120588242	HCT-116	colon:	n/a	n/a
38	CEBPB	chr5:120602603-120602824	HepG2	liver:	n/a	chr5:120602751-120602762
39	CEBPB	chr5:120587647-120588158	A549	lung:	n/a	n/a
40	CEBPB	chr5:120702194-120702588	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:120650883-120651016	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr5:120489382-120489687	HepG2	liver:	n/a	chr5:120489508-120489519
43	CEBPB	chr5:120650738-120651104	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:120602594-120602886	K562	blood:	n/a	chr5:120602751-120602762
45	CEBPB	chr5:120609534-120610174	Hela-S3	cervix:	n/a	chr5:120609623-120609636
46	CEBPB	chr5:120665120-120665392	HepG2	liver:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
47	CEBPB	chr5:120587556-120588192	A549	lung:	n/a	n/a
48	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
49	CEBPB	chr5:120640581-120640927	A549	lung:	n/a	chr5:120640725-120640734 chr5:120640725-120640734 chr5:120640723-120640736 chr5:120640723-120640736 chr5:120640720-120640737 chr5:120640723-120640734 chr5:120640793-120640806 chr5:120640725-120640734
50	CEBPB	chr5:120609529-120610117	A549	lung:	n/a	chr5:120609623-120609636

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120444080-120444130	SKMC	muscle:	n/a
2	chr5:120444080-120444130	HCF	heart:	n/a
3	chr5:120444080-120444130	GM12892	blood:	n/a
4	chr5:120400115-120400165	Hepatocyte	liver:	n/a
5	chr5:120400115-120400165	AG04449	skin:	fetal
6	chr5:120400115-120400165	NHDF-neo	bronchial:	n/a
7	chr5:120400115-120400165	HAEpiC	amniotic membrane:	n/a
8	chr5:120444080-120444130	NHBE	bronchial:	n/a
9	chr5:120444080-120444130	Caco-2	colon:	n/a
10	chr5:120444080-120444130	A549	lung:	n/a
11	chr5:120400115-120400165	PrEC	prostate:	n/a
12	chr5:120444080-120444130	GM12891	blood:	n/a
13	chr5:120444080-120444130	HCT-116	colon:	n/a
14	chr5:120444080-120444130	Jurkat	blood:	n/a
15	chr5:120400115-120400165	GM12892	blood:	n/a
16	chr5:120400115-120400165	PANC-1	pancreas:	n/a
17	chr5:120400115-120400165	AG10803	skin:	n/a
18	chr5:120444080-120444130	ovcar-3	ovarian:	n/a
19	chr5:120400115-120400165	NT2-D1	testis:	n/a
20	chr5:120400115-120400165	HL-60	blood:	n/a
21	chr5:120444080-120444130	HEK293	kidney:	embryo
22	chr5:120400115-120400165	ProgFib	skin:	n/a
23	chr5:120444080-120444130	HIPEpiC	eye:	n/a
24	chr5:120444080-120444130	SK-N-MC	brain:	n/a
25	chr5:120400115-120400165	HIPEpiC	eye:	n/a
26	chr5:120444080-120444130	MCF-7	breast:	n/a
27	chr5:120400115-120400165	HRE	kidney:	n/a
28	chr5:120400115-120400165	PFSK-1	brain:	n/a
29	chr5:120400115-120400165	Hela-S3	cervix:	n/a
30	chr5:120400115-120400165	SK-N-SH	brain:	n/a
31	chr5:120444080-120444130	U87	brain:	n/a
32	chr5:120444080-120444130	IMR90	lung:	fetal
33	chr5:120400115-120400165	T-47D	breast:	n/a
34	chr5:120444080-120444130	BJ	skin:	n/a
35	chr5:120400115-120400165	HCM	heart:	n/a
36	chr5:120400115-120400165	NB4	blood:	n/a
37	chr5:120444080-120444130	HCPEpiC	choroid plexus:	n/a
38	chr5:120444080-120444130	HMEC	breast:	n/a
39	chr5:120400115-120400165	HCF	heart:	n/a
40	chr5:120444080-120444130	SK-N-SH_RA	brain:	n/a
41	chr5:120444080-120444130	HepG2	liver:	n/a
42	chr5:120400115-120400165	HEEpiC	esophagus:	n/a
43	chr5:120444080-120444130	HRPEpiC	eye:	n/a
44	chr5:120444080-120444130	HRCEpiC	kidney:	n/a
45	chr5:120444080-120444130	PFSK-1	brain:	n/a
46	chr5:120400115-120400165	A549	lung:	n/a
47	chr5:120444080-120444130	AG04449	skin:	fetal
48	chr5:120444080-120444130	CMK	blood:	n/a
49	chr5:120444080-120444130	SAEC	small airway:	n/a
50	chr5:120444080-120444130	K562	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
2	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
3	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
4	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
5	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
6	chr5:120597959..120600237-chr5:120894989..120897698,2	K562	blood:
7	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
8	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
9	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
10	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
11	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
12	chr5:120744891..120747171-chr5:120755277..120758269,2	K562	blood:
13	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
14	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
15	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
16	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
17	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
18	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
19	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
20	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
21	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
22	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
23	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
24	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
25	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
26	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
27	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
28	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
29	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
30	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
31	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
32	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
33	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
34	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
35	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
36	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
37	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
38	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTMT-2	chr5:120658245-120658302	ENSG00000229855.4
2	lnc-FTMT-2	chr5:120685681-120686145	ENSG00000229855.4
3	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
4	lnc-FTMT-2	chr5:120661117-120661175	ENSG00000229855.4
5	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
6	lnc-FTMT-2	chr5:120661122-120661174	ENSG00000229855.4
7	lnc-FTMT-2	chr5:120656659-120656681	NONHSAT103454
8	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
9	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
10	lnc-FTMT-2	chr5:120540703-120540825	ENSG00000229855.4
11	lnc-FTMT-2	chr5:120661117-120661651	ENSG00000229855.4
12	lnc-FTMT-2	chr5:120659733-120659765	NONHSAT103454
13	lnc-FTMT-2	chr5:120692501-120693093	ENSG00000229855.4
14	lnc-FTMT-2	chr5:120649672-120649899	ENSG00000229855.4
15	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
16	lnc-FTMT-2	chr5:120658244-120658302	NONHSAT103454
17	lnc-FTMT-2	chr5:120659736-120659765	XLOC_004529
18	lnc-FTMT-2	chr5:120621476-120621568	ENSG00000229855.4
19	lnc-FTMT-2	chr5:120658245-120658302	XLOC_004529
20	lnc-FTMT-2	chr5:120661041-120661595	NONHSAT103454
21	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
22	lnc-FTMT-2	chr5:120535399-120535503	ENSG00000229855.4
23	lnc-LOX-8	chr5:120531675-120531905	NONHSAT103452
24	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
25	lnc-FTMT-3	chr5:120698697-120701009	NONHSAT103459
26	lnc-FTMT-2	chr5:120661117-120661793	ENSG00000229855.4
27	lnc-FTMT-2	chr5:120649656-120649899	ENSG00000229855.4
28	lnc-FTMT-2	chr5:120661117-120661532	XLOC_004529
29	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
30	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4

No data

Variant related genes	Relation type
ENSG00000229855	TF binding region
ENSG00000250847	TF binding region
ENSG00000229855	CpG island
ENSG00000250847	CpG island

Extended variants
information (count: 6640 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6640 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569730832	chr5:120399806-120399807	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530647742	chr5:120399816-120399817	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549145840	chr5:120399817-120399818	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567465058	chr5:120399832-120399833	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184159287	chr5:120399833-120399834	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553412063	chr5:120399841-120399842	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142736849	chr5:120399849-120399850	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527477212	chr5:120399858-120399859	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539031219	chr5:120399876-120399877	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188709670	chr5:120399878-120399879	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575676539	chr5:120399898-120399899	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370780906	chr5:120399899-120399900	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547844022	chr5:120399922-120399923	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547140636	chr5:120399950-120399951	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542865499	chr5:120399965-120399966	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555113701	chr5:120399981-120399982	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539675453	chr5:120399982-120399983	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112310052	chr5:120399983-120399984	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370149536	chr5:120399991-120399992	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192403991	chr5:120400001-120400002	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184617760	chr5:120400012-120400013	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376489532	chr5:120400033-120400034	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7700358	chr5:120400063-120400064	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs555484704	chr5:120400066-120400067	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187367295	chr5:120400067-120400068	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530594390	chr5:120400083-120400084	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548927136	chr5:120400095-120400096	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567413858	chr5:120400097-120400098	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528286326	chr5:120400098-120400099	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573942027	chr5:120400112-120400113	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140056832	chr5:120400125-120400126	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143379535	chr5:120400134-120400135	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2194075	chr5:120400135-120400136	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2194074	chr5:120400140-120400141	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs191817624	chr5:120400146-120400147	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569271442	chr5:120400150-120400151	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184713359	chr5:120400178-120400179	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554877812	chr5:120400218-120400219	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7700819	chr5:120400227-120400228	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189648653	chr5:120400228-120400229	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs148453304	chr5:120400229-120400230	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560386426	chr5:120400236-120400237	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558019646	chr5:120400239-120400240	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577862921	chr5:120400242-120400243	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544620855	chr5:120400250-120400251	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372146260	chr5:120400252-120400253	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527399831	chr5:120400289-120400290	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563267579	chr5:120400290-120400291	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575248542	chr5:120400297-120400298	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180791500	chr5:120400298-120400299	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120399800-120400200	Enhancers	H1 Cell Line	embryonic stem cell
2	chr5:120399800-120400400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:120399800-120400400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr5:120399800-120400400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr5:120400000-120400200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:120400000-120400400	Active TSS	H9 Cell Line	embryonic stem cell
7	chr5:120400000-120400400	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr5:120400000-120400400	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr5:120400000-120400400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:120400000-120400400	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr5:120413000-120414200	Enhancers	Dnd41	blood
12	chr5:120423200-120424400	ZNF genes & repeats	Dnd41	blood
13	chr5:120424400-120425400	Weak transcription	Dnd41	blood
14	chr5:120425400-120427000	Enhancers	Dnd41	blood
15	chr5:120440400-120440800	Enhancers	Spleen	Spleen
16	chr5:120442200-120442800	ZNF genes & repeats	Dnd41	blood
17	chr5:120442800-120444000	Weak transcription	Dnd41	blood
18	chr5:120443000-120447600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:120443400-120445000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:120443800-120444000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:120444000-120444400	ZNF genes & repeats	Dnd41	blood
22	chr5:120444000-120444600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr5:120444000-120444600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:120444000-120444800	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr5:120444200-120444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
26	chr5:120444200-120444600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr5:120444400-120444600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr5:120444400-120444800	Enhancers	Placenta	Placenta
29	chr5:120444400-120444800	Active TSS	Hela-S3	cervix
30	chr5:120444400-120445600	Enhancers	Dnd41	blood
31	chr5:120444600-120444800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:120445000-120449000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:120447600-120447800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:120449000-120449600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:120449600-120450200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:120463600-120464200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:120466400-120466800	Enhancers	Fetal Heart	heart
38	chr5:120468000-120469000	Enhancers	Dnd41	blood
39	chr5:120469000-120471000	Weak transcription	Dnd41	blood
40	chr5:120470800-120472200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:120471000-120471400	Enhancers	Dnd41	blood
42	chr5:120472200-120472600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:120472600-120474400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:120473400-120475200	Enhancers	HUVEC	blood vessel
45	chr5:120473600-120474200	Enhancers	Fetal Stomach	stomach
46	chr5:120473600-120474800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr5:120473600-120475000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:120474400-120474800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:120474800-120480200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:120475200-120480200	Weak transcription	HUVEC	blood vessel

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