Variant report

Variant	nsv882797
Chromosome Location	chr5:120359319-120757262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1177)
CpG islands
(count:122)
Chromatin interactive
region (count:44)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr5:120735521-120735958	GM12878	blood:	n/a	n/a
4	ATF2	chr5:120735400-120736165	GM12878	blood:	n/a	n/a
5	ATF3	chr5:120609660-120610180	A549	lung:	n/a	n/a
6	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
7	ATF3	chr5:120587704-120588047	A549	lung:	n/a	n/a
8	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
9	BATF	chr5:120735476-120736026	GM12878	blood:	n/a	n/a
10	BATF	chr5:120737102-120737339	GM12878	blood:	n/a	n/a
11	BATF	chr5:120735502-120735964	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:120735493-120735946	GM12878	blood:	n/a	n/a
13	BCL3	chr5:120735445-120735944	GM12878	blood:	n/a	n/a
14	BCL3	chr5:120587530-120588099	A549	lung:	n/a	n/a
15	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
16	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
17	BCL3	chr5:120737037-120737376	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:120735422-120735896	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:120582702-120582968	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:120735520-120735942	GM12878	blood:	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	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
27	CEBPB	chr5:120712104-120712359	HepG2	liver:	n/a	chr5:120712234-120712245
28	CEBPB	chr5:120362854-120363100	A549	lung:	n/a	chr5:120362980-120362991
29	CEBPB	chr5:120587649-120588101	HCT-116	colon:	n/a	n/a
30	CEBPB	chr5:120602603-120602824	HepG2	liver:	n/a	chr5:120602751-120602762
31	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
32	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
33	CEBPB	chr5:120672127-120672318	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:120497839-120498066	HepG2	liver:	n/a	chr5:120497966-120497977
35	CEBPB	chr5:120650741-120651097	A549	lung:	n/a	n/a
36	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
37	CEBPB	chr5:120694614-120695283	A549	lung:	n/a	n/a
38	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
39	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
40	CEBPB	chr5:120640554-120640918	ECC-1	luminal epithelium:	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
41	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
42	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
43	CEBPB	chr5:120640491-120640969	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
44	CEBPB	chr5:120609455-120610277	A549	lung:	n/a	chr5:120609623-120609636
45	CEBPB	chr5:120500288-120500607	K562	blood:	n/a	n/a
46	CEBPB	chr5:120587556-120588192	A549	lung:	n/a	n/a
47	CEBPB	chr5:120665080-120665327	A549	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
48	CEBPB	chr5:120665137-120665399	H1-hESC	embryonic stem cell:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
49	CEBPB	chr5:120602594-120602886	K562	blood:	n/a	chr5:120602751-120602762
50	CEBPB	chr5:120489382-120489687	HepG2	liver:	n/a	chr5:120489508-120489519

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120444080-120444130	Hela-S3	cervix:	n/a
2	chr5:120444080-120444130	SAEC	small airway:	n/a
3	chr5:120400115-120400165	NT2-D1	testis:	n/a
4	chr5:120400115-120400165	BE2_C	brain:	n/a
5	chr5:120444080-120444130	SK-N-MC	brain:	n/a
6	chr5:120444080-120444130	GM12892	blood:	n/a
7	chr5:120400115-120400165	Caco-2	colon:	n/a
8	chr5:120400115-120400165	AoSMC	blood vessel:	n/a
9	chr5:120444080-120444130	HEEpiC	esophagus:	n/a
10	chr5:120400115-120400165	SAEC	small airway:	n/a
11	chr5:120400115-120400165	HCF	heart:	n/a
12	chr5:120400115-120400165	AG04449	skin:	fetal
13	chr5:120444080-120444130	GM06990	blood:	n/a
14	chr5:120400115-120400165	ECC-1	luminal epithelium:	n/a
15	chr5:120444080-120444130	NHBE	bronchial:	n/a
16	chr5:120400115-120400165	Jurkat	blood:	n/a
17	chr5:120444080-120444130	HEK293	kidney:	embryo
18	chr5:120444080-120444130	HCF	heart:	n/a
19	chr5:120400115-120400165	ovcar-3	ovarian:	n/a
20	chr5:120444080-120444130	HCPEpiC	choroid plexus:	n/a
21	chr5:120444080-120444130	ProgFib	skin:	n/a
22	chr5:120400115-120400165	HCT-116	colon:	n/a
23	chr5:120444080-120444130	Hepatocyte	liver:	n/a
24	chr5:120444080-120444130	HNPCEpiC	eye:	n/a
25	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
26	chr5:120444080-120444130	BJ	skin:	n/a
27	chr5:120400115-120400165	K562	blood:	n/a
28	chr5:120444080-120444130	NB4	blood:	n/a
29	chr5:120444080-120444130	MCF-7	breast:	n/a
30	chr5:120444080-120444130	GM19239	blood:	n/a
31	chr5:120400115-120400165	LNCaP	prostate:	n/a
32	chr5:120400115-120400165	CMK	blood:	n/a
33	chr5:120444080-120444130	HIPEpiC	eye:	n/a
34	chr5:120400115-120400165	SK-N-SH_RA	brain:	n/a
35	chr5:120400115-120400165	GM12878	blood:	n/a
36	chr5:120400115-120400165	SK-N-SH	brain:	n/a
37	chr5:120444080-120444130	RPTEC	kidney:	n/a
38	chr5:120444080-120444130	SK-N-SH_RA	brain:	n/a
39	chr5:120444080-120444130	SK-N-SH	brain:	n/a
40	chr5:120400115-120400165	NHBE	bronchial:	n/a
41	chr5:120444080-120444130	ECC-1	luminal epithelium:	n/a
42	chr5:120400115-120400165	HRPEpiC	eye:	n/a
43	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
44	chr5:120400115-120400165	AG09319	gingival:	n/a
45	chr5:120444080-120444130	NH-A	brain:	n/a
46	chr5:120400115-120400165	HL-60	blood:	n/a
47	chr5:120444080-120444130	AG09319	gingival:	n/a
48	chr5:120444080-120444130	PFSK-1	brain:	n/a
49	chr5:120400115-120400165	HCPEpiC	choroid plexus:	n/a
50	chr5:120444080-120444130	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
2	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
3	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
4	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
5	chr5:120745325..120747316-chr5:120750608..120752395,2	K562	blood:
6	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
7	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
8	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
9	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
10	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
11	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
12	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
13	chr5:120744891..120747171-chr5:120755277..120758269,2	K562	blood:
14	chr12:60563916..60564532-chr5:120756222..120756804,2	MCF-7	breast:
15	chr5:120753180..120754863-chr5:120756669..120758697,2	K562	blood:
16	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
17	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
18	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
19	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
20	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
21	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
22	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
23	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
24	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
25	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
26	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
27	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
28	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
29	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
30	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
31	chr5:120753180..120754863-chr5:120756669..120758697,2	K562	blood:
32	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
33	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
34	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
35	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
36	chr5:120744891..120747171-chr5:120755277..120758269,2	K562	blood:
37	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
38	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
39	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
40	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
41	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
42	chr5:120745325..120747316-chr5:120750608..120752395,2	K562	blood:
43	chr5:120597959..120600237-chr5:120894989..120897698,2	K562	blood:
44	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FTMT-2	chr5:120661117-120661793	ENSG00000229855.4
2	lnc-FTMT-2	chr5:120658245-120658302	XLOC_004529
3	lnc-FTMT-2	chr5:120659736-120659765	XLOC_004529
4	lnc-FTMT-2	chr5:120661122-120661174	ENSG00000229855.4
5	lnc-FTMT-2	chr5:120658244-120658302	NONHSAT103454
6	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
7	lnc-FTMT-2	chr5:120656659-120656681	NONHSAT103454
8	lnc-FTMT-2	chr5:120661117-120661532	XLOC_004529
9	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
10	lnc-FTMT-2	chr5:120621476-120621568	ENSG00000229855.4
11	lnc-FTMT-2	chr5:120661117-120661651	ENSG00000229855.4
12	lnc-FTMT-2	chr5:120661041-120661595	NONHSAT103454
13	lnc-FTMT-2	chr5:120659733-120659765	NONHSAT103454
14	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
15	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
16	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
17	lnc-FTMT-2	chr5:120661117-120661175	ENSG00000229855.4
18	lnc-FTMT-2	chr5:120649672-120649899	ENSG00000229855.4
19	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450
20	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
21	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
22	lnc-LOX-8	chr5:120531675-120531905	NONHSAT103452
23	lnc-FTMT-2	chr5:120649656-120649899	ENSG00000229855.4
24	lnc-FTMT-2	chr5:120540703-120540825	ENSG00000229855.4
25	lnc-FTMT-2	chr5:120658245-120658302	ENSG00000229855.4
26	lnc-FTMT-2	chr5:120685681-120686145	ENSG00000229855.4
27	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
28	lnc-FTMT-2	chr5:120692501-120693093	ENSG00000229855.4
29	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
30	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
31	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
32	lnc-FTMT-3	chr5:120698697-120701009	NONHSAT103459
33	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
34	lnc-FTMT-2	chr5:120535399-120535503	ENSG00000229855.4
35	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4

No data

Variant related genes	Relation type
ENSG00000229855	TF binding region
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000250847	TF binding region
ENSG00000229855	CpG island
ENSG00000251135	CpG island
ENSG00000248853	CpG island
ENSG00000250847	CpG island

Extended variants
information (count: 8205 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:8205 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1862280	chr5:120359319-120359320	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10042502	chr5:120359321-120359322	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs563449038	chr5:120359324-120359325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575285521	chr5:120359343-120359344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543103857	chr5:120359371-120359372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189271498	chr5:120359376-120359377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9327177	chr5:120359466-120359467	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs547006478	chr5:120359485-120359486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540991413	chr5:120359494-120359495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10070487	chr5:120359542-120359543	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574420567	chr5:120359571-120359572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541707789	chr5:120359634-120359635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9327178	chr5:120359648-120359649	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs575048108	chr5:120359668-120359669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6896387	chr5:120359672-120359673	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs536788247	chr5:120359705-120359706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545502499	chr5:120359767-120359768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375617424	chr5:120359813-120359814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141267550	chr5:120359837-120359838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534785787	chr5:120359861-120359862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553005197	chr5:120359877-120359878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577472033	chr5:120359888-120359889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538648294	chr5:120359910-120359911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13166268	chr5:120359918-120359919	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528095153	chr5:120359933-120359934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181779470	chr5:120359981-120359982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575223111	chr5:120360064-120360065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542789734	chr5:120360070-120360071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545268270	chr5:120360080-120360081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185872682	chr5:120360109-120360110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561412152	chr5:120360114-120360115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573373440	chr5:120360160-120360161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540780081	chr5:120360207-120360208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191659828	chr5:120360361-120360362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76587817	chr5:120360368-120360369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544910688	chr5:120360391-120360392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150339652	chr5:120360456-120360457	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530502216	chr5:120360460-120360461	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs376448670	chr5:120360482-120360483	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs181426195	chr5:120360484-120360485	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371323664	chr5:120360486-120360487	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs1422311	chr5:120360489-120360490	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs149549332	chr5:120360507-120360508	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs77538881	chr5:120360564-120360565	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs571109203	chr5:120360583-120360584	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs538589483	chr5:120360598-120360599	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556823268	chr5:120360636-120360637	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs569186821	chr5:120360643-120360644	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs146028769	chr5:120360668-120360669	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs560887453	chr5:120360688-120360689	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120358800-120360400	Enhancers	Dnd41	blood
2	chr5:120360400-120361600	Flanking Active TSS	Dnd41	blood
3	chr5:120361600-120368400	Enhancers	Dnd41	blood
4	chr5:120364000-120364200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr5:120365200-120367000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:120365600-120367000	Enhancers	NHDF-Ad	bronchial
7	chr5:120365800-120366000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:120366000-120366800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr5:120366800-120367000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:120366800-120367200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr5:120366800-120367600	Enhancers	Fetal Heart	heart
12	chr5:120366800-120367600	Enhancers	Fetal Muscle Leg	muscle
13	chr5:120366800-120367800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:120367000-120367200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:120367000-120367200	Flanking Active TSS	NHDF-Ad	bronchial
16	chr5:120367000-120367600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:120367000-120367600	Enhancers	Adipose Nuclei	Adipose
18	chr5:120367000-120367800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr5:120367000-120367800	Bivalent Enhancer	Fetal Lung	lung
20	chr5:120367200-120367400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr5:120367200-120367400	Active TSS	NHDF-Ad	bronchial
22	chr5:120367200-120367600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr5:120367200-120369200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:120367400-120367600	Flanking Active TSS	NHDF-Ad	bronchial
25	chr5:120367600-120367800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:120367600-120367800	Bivalent Enhancer	Fetal Heart	heart
27	chr5:120368400-120368800	Weak transcription	Dnd41	blood
28	chr5:120368800-120370800	Enhancers	Dnd41	blood
29	chr5:120369200-120369400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr5:120369400-120369800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr5:120369800-120370200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:120379400-120380200	Enhancers	Dnd41	blood
33	chr5:120380200-120383800	Weak transcription	Dnd41	blood
34	chr5:120383800-120384200	Enhancers	Dnd41	blood
35	chr5:120384200-120385000	Weak transcription	Dnd41	blood
36	chr5:120385000-120386400	Enhancers	Dnd41	blood
37	chr5:120385200-120385600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr5:120385200-120385600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr5:120385600-120386000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:120386400-120386800	Weak transcription	Dnd41	blood
41	chr5:120386800-120388800	Enhancers	Dnd41	blood
42	chr5:120388200-120389400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:120388400-120389400	Enhancers	Hela-S3	cervix
44	chr5:120388400-120389600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr5:120388800-120389600	Flanking Active TSS	Dnd41	blood
46	chr5:120389000-120389600	Enhancers	Fetal Kidney	kidney
47	chr5:120389600-120392200	Enhancers	Dnd41	blood
48	chr5:120399800-120400200	Enhancers	H1 Cell Line	embryonic stem cell
49	chr5:120399800-120400400	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr5:120399800-120400400	Active TSS	ES-WA7 Cell Line	embryonic stem cell

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