Variant report

Variant	esv33642
Chromosome Location	chr5:120380525-120848760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1245)
CpG islands
(count:123)
Chromatin interactive
region (count:50)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr5:120609660-120610180	A549	lung:	n/a	n/a
6	ATF3	chr5:120587704-120588047	A549	lung:	n/a	n/a
7	ATF3	chr5:120609671-120610135	A549	lung:	n/a	n/a
8	BACH1	chr5:120609897-120610216	K562	blood:	n/a	n/a
9	BATF	chr5:120735502-120735964	GM12878	blood:	n/a	n/a
10	BATF	chr5:120737102-120737339	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	chr5:120587530-120588099	A549	lung:	n/a	n/a
14	BCL3	chr5:120609611-120610175	A549	lung:	n/a	n/a
15	BCL3	chr5:120737037-120737376	GM12878	blood:	n/a	n/a
16	BCL3	chr5:120609574-120610233	A549	lung:	n/a	n/a
17	BCL3	chr5:120735445-120735944	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	chr5:120694893-120694952	GM12878	blood:	n/a	n/a
22	BRCA1	chr5:120576292-120576344	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr5:120823846-120823847	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr5:120609626-120610276	HCT-116	colon:	n/a	n/a
25	CBX3	chr5:120587730-120588017	HCT-116	colon:	n/a	n/a
26	CBX3	chr5:120563378-120563655	K562	blood:	n/a	n/a
27	CEBPB	chr5:120518614-120519156	HepG2	liver:	n/a	chr5:120518723-120518734
28	CEBPB	chr5:120518774-120519213	Hela-S3	cervix:	n/a	n/a
29	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
30	CEBPB	chr5:120650738-120651081	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:120587647-120588158	A549	lung:	n/a	n/a
32	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
33	CEBPB	chr5:120712104-120712359	HepG2	liver:	n/a	chr5:120712234-120712245
34	CEBPB	chr5:120609534-120610174	Hela-S3	cervix:	n/a	chr5:120609623-120609636
35	CEBPB	chr5:120650741-120651097	A549	lung:	n/a	n/a
36	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
37	CEBPB	chr5:120518577-120518857	K562	blood:	n/a	chr5:120518723-120518734
38	CEBPB	chr5:120665093-120665414	IMR90	lung:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262
39	CEBPB	chr5:120796956-120797209	HepG2	liver:	n/a	chr5:120797071-120797082 chr5:120797071-120797084 chr5:120797068-120797085
40	CEBPB	chr5:120702142-120702659	A549	lung:	n/a	n/a
41	CEBPB	chr5:120497794-120498111	K562	blood:	n/a	chr5:120497966-120497977
42	CEBPB	chr5:120650781-120651061	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:120615541-120615802	K562	blood:	n/a	n/a
44	CEBPB	chr5:120817859-120817911	K562	blood:	n/a	n/a
45	CEBPB	chr5:120796913-120797225	IMR90	lung:	n/a	chr5:120797071-120797082 chr5:120797071-120797084 chr5:120797068-120797085
46	CEBPB	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
47	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
48	CEBPB	chr5:120702168-120702578	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
50	CEBPB	chr5:120665178-120665393	Hela-S3	cervix:	n/a	chr5:120665251-120665262 chr5:120665252-120665263 chr5:120665253-120665262

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120444080-120444130	HepG2	liver:	n/a
2	chr5:120444080-120444130	HepG2	liver:	n/a
3	chr5:120400115-120400165	SKMC	muscle:	n/a
4	chr5:120400115-120400165	HCM	heart:	n/a
5	chr5:120400115-120400165	ProgFib	skin:	n/a
6	chr5:120400115-120400165	T-47D	breast:	n/a
7	chr5:120444080-120444130	AG09309	skin:	n/a
8	chr5:120400115-120400165	MCF10A-Er-Src	breast:	n/a
9	chr5:120444080-120444130	LNCaP	prostate:	n/a
10	chr5:120400115-120400165	HCT-116	colon:	n/a
11	chr5:120444080-120444130	HCPEpiC	choroid plexus:	n/a
12	chr5:120400115-120400165	SK-N-MC	brain:	n/a
13	chr5:120444080-120444130	SKMC	muscle:	n/a
14	chr5:120444080-120444130	HCF	heart:	n/a
15	chr5:120444080-120444130	Hepatocyte	liver:	n/a
16	chr5:120444080-120444130	NH-A	brain:	n/a
17	chr5:120444080-120444130	ovcar-3	ovarian:	n/a
18	chr5:120400115-120400165	PFSK-1	brain:	n/a
19	chr5:120444080-120444130	A549	lung:	n/a
20	chr5:120400115-120400165	HepG2	liver:	n/a
21	chr5:120444080-120444130	AG04450	lung:	fetal
22	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
23	chr5:120444080-120444130	HUVEC	blood vessel:	n/a
24	chr5:120444080-120444130	CMK	blood:	n/a
25	chr5:120444080-120444130	Jurkat	blood:	n/a
26	chr5:120444080-120444130	T-47D	breast:	n/a
27	chr5:120400115-120400165	Caco-2	colon:	n/a
28	chr5:120400115-120400165	H1-hESC	embryonic stem cell:	embryo
29	chr5:120400115-120400165	Hela-S3	cervix:	n/a
30	chr5:120444080-120444130	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:120400115-120400165	ECC-1	luminal epithelium:	n/a
32	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
33	chr5:120444080-120444130	GM12892	blood:	n/a
34	chr5:120400115-120400165	NB4	blood:	n/a
35	chr5:120400115-120400165	PrEC	prostate:	n/a
36	chr5:120444080-120444130	Hela-S3	cervix:	n/a
37	chr5:120444080-120444130	AG10803	skin:	n/a
38	chr5:120400115-120400165	ovcar-3	ovarian:	n/a
39	chr5:120444080-120444130	Caco-2	colon:	n/a
40	chr5:120444080-120444130	AG04449	skin:	fetal
41	chr5:120400115-120400165	AG04450	lung:	fetal
42	chr5:120400115-120400165	BJ	skin:	n/a
43	chr5:120400115-120400165	HRPEpiC	eye:	n/a
44	chr5:120444080-120444130	K562	blood:	n/a
45	chr5:120444080-120444130	NT2-D1	testis:	n/a
46	chr5:120444080-120444130	U87	brain:	n/a
47	chr5:120444080-120444130	HCM	heart:	n/a
48	chr5:120400115-120400165	HCPEpiC	choroid plexus:	n/a
49	chr5:120444080-120444130	MCF10A-Er-Src	breast:	n/a
50	chr5:120400115-120400165	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:120745325..120747316-chr5:120750608..120752395,2	K562	blood:
2	chr5:120810139..120812318-chr5:120820921..120823113,2	K562	blood:
3	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
4	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
5	chr5:120785380..120788010-chr5:120790362..120792575,2	K562	blood:
6	chr5:120816268..120817790-chr5:120825536..120828254,2	K562	blood:
7	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
8	chr5:120744891..120747171-chr5:120755277..120758269,2	K562	blood:
9	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
10	chr12:60563916..60564532-chr5:120756222..120756804,2	MCF-7	breast:
11	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
12	chr5:120753180..120754863-chr5:120756669..120758697,2	K562	blood:
13	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
14	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
15	chr5:120684041..120685887-chr5:120689318..120691883,2	K562	blood:
16	chr5:120753180..120754863-chr5:120756669..120758697,2	K562	blood:
17	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
18	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
19	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
20	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
21	chr5:120631738..120633506-chr5:120633517..120635841,2	K562	blood:
22	chr5:120628569..120631260-chr5:120631938..120634860,2	MCF-7	breast:
23	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
24	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
25	chr5:120597959..120600237-chr5:120894989..120897698,2	K562	blood:
26	chr5:120643239..120645271-chr5:120645522..120647194,2	K562	blood:
27	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
28	chr5:120785380..120788010-chr5:120790362..120792575,2	K562	blood:
29	chr5:120621053..120623969-chr5:120627723..120630035,2	MCF-7	breast:
30	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
31	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
32	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
33	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
34	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
35	chr5:120810139..120812318-chr5:120820921..120823113,2	K562	blood:
36	chr5:120744891..120747171-chr5:120755277..120758269,2	K562	blood:
37	chr5:120739808..120742284-chr5:120742802..120745420,2	K562	blood:
38	chr5:120604790..120607005-chr5:120607199..120609992,2	K562	blood:
39	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
40	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
41	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
42	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
43	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
44	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
45	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
46	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
47	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
48	chr5:120816268..120817790-chr5:120825536..120828254,2	K562	blood:
49	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
50	chr5:120745325..120747316-chr5:120750608..120752395,2	K562	blood:

(count:32 , 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	chr5:120685681-120686145	ENSG00000229855.4
3	lnc-FTMT-2	chr5:120659733-120659765	NONHSAT103454
4	lnc-LOX-8	chr5:120531675-120531905	NONHSAT103452
5	lnc-FTMT-2	chr5:120692501-120693093	ENSG00000229855.4
6	lnc-FTMT-2	chr5:120661117-120661532	XLOC_004529
7	lnc-FTMT-2	chr5:120661122-120661174	ENSG00000229855.4
8	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
9	lnc-FTMT-2	chr5:120658244-120658302	NONHSAT103454
10	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
11	lnc-FTMT-2	chr5:120661041-120661595	NONHSAT103454
12	lnc-FTMT-2	chr5:120656659-120656681	NONHSAT103454
13	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
14	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
15	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
16	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
17	lnc-FTMT-2	chr5:120661117-120661175	ENSG00000229855.4
18	lnc-FTMT-2	chr5:120658245-120658302	XLOC_004529
19	lnc-FTMT-2	chr5:120683388-120683561	ENSG00000229855.4
20	lnc-FTMT-2	chr5:120659736-120659765	ENSG00000229855.4
21	lnc-FTMT-2	chr5:120659736-120659765	XLOC_004529
22	lnc-FTMT-2	chr5:120649672-120649899	ENSG00000229855.4
23	lnc-FTMT-2	chr5:120658249-120658302	ENSG00000229855.4
24	lnc-FTMT-3	chr5:120698697-120701009	NONHSAT103459
25	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
26	lnc-FTMT-2	chr5:120661117-120661651	ENSG00000229855.4
27	lnc-FTMT-2	chr5:120658245-120658302	ENSG00000229855.4
28	lnc-FTMT-2	chr5:120649656-120649899	ENSG00000229855.4
29	lnc-FTMT-2	chr5:120621476-120621568	ENSG00000229855.4
30	lnc-FTMT-2	chr5:120540703-120540825	ENSG00000229855.4
31	lnc-FTMT-2	chr5:120656575-120656681	ENSG00000229855.4
32	lnc-FTMT-2	chr5:120535399-120535503	ENSG00000229855.4

No data

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

Extended variants
information (count: 8846 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:8846 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142808896	chr5:120380539-120380540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147393148	chr5:120380558-120380559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561147162	chr5:120380562-120380563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556253781	chr5:120380566-120380567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116737495	chr5:120380568-120380569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78956786	chr5:120380591-120380592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78972298	chr5:120380618-120380619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532647079	chr5:120380622-120380623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369804152	chr5:120380650-120380651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527241476	chr5:120380666-120380667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139663756	chr5:120380721-120380722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371806940	chr5:120380729-120380730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143774974	chr5:120380730-120380731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182696130	chr5:120380746-120380747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75409008	chr5:120380779-120380780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567162485	chr5:120380793-120380794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534358870	chr5:120380795-120380796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs744047	chr5:120380796-120380797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577348608	chr5:120380840-120380841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538332661	chr5:120380848-120380849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556753919	chr5:120380849-120380850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186928529	chr5:120380932-120380933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529941870	chr5:120380959-120380960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191422981	chr5:120380964-120380965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182633322	chr5:120380971-120380972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201755248	chr5:120381004-120381005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573043275	chr5:120381029-120381030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564398952	chr5:120381061-120381062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1363383	chr5:120381112-120381113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs565256331	chr5:120381149-120381150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116737634	chr5:120381209-120381210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1363382	chr5:120381226-120381227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570380930	chr5:120381234-120381235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72787783	chr5:120381249-120381250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530277687	chr5:120381283-120381284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1806826	chr5:120381341-120381342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs567202789	chr5:120381349-120381350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527958635	chr5:120381350-120381351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546224874	chr5:120381381-120381382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570877733	chr5:120381389-120381390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187760551	chr5:120381397-120381398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17506430	chr5:120381414-120381415	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs568966768	chr5:120381432-120381433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536487470	chr5:120381434-120381435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115573683	chr5:120381455-120381456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs17506458	chr5:120381460-120381461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111439329	chr5:120381501-120381502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150585477	chr5:120381505-120381506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74549648	chr5:120381538-120381539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73264497	chr5:120381545-120381546	Weak transcription	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
Breast cancer	22522925	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:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120380200-120383800	Weak transcription	Dnd41	blood
2	chr5:120383800-120384200	Enhancers	Dnd41	blood
3	chr5:120384200-120385000	Weak transcription	Dnd41	blood
4	chr5:120385000-120386400	Enhancers	Dnd41	blood
5	chr5:120385200-120385600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:120385200-120385600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr5:120385600-120386000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr5:120386400-120386800	Weak transcription	Dnd41	blood
9	chr5:120386800-120388800	Enhancers	Dnd41	blood
10	chr5:120388200-120389400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:120388400-120389400	Enhancers	Hela-S3	cervix
12	chr5:120388400-120389600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr5:120388800-120389600	Flanking Active TSS	Dnd41	blood
14	chr5:120389000-120389600	Enhancers	Fetal Kidney	kidney
15	chr5:120389600-120392200	Enhancers	Dnd41	blood
16	chr5:120399800-120400200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr5:120399800-120400400	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr5:120399800-120400400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr5:120399800-120400400	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr5:120400000-120400200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:120400000-120400400	Active TSS	H9 Cell Line	embryonic stem cell
22	chr5:120400000-120400400	Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr5:120400000-120400400	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr5:120400000-120400400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:120400000-120400400	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr5:120413000-120414200	Enhancers	Dnd41	blood
27	chr5:120423200-120424400	ZNF genes & repeats	Dnd41	blood
28	chr5:120424400-120425400	Weak transcription	Dnd41	blood
29	chr5:120425400-120427000	Enhancers	Dnd41	blood
30	chr5:120440400-120440800	Enhancers	Spleen	Spleen
31	chr5:120442200-120442800	ZNF genes & repeats	Dnd41	blood
32	chr5:120442800-120444000	Weak transcription	Dnd41	blood
33	chr5:120443000-120447600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:120443400-120445000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:120443800-120444000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:120444000-120444400	ZNF genes & repeats	Dnd41	blood
37	chr5:120444000-120444600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr5:120444000-120444600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:120444000-120444800	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr5:120444200-120444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr5:120444200-120444600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr5:120444400-120444600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr5:120444400-120444800	Enhancers	Placenta	Placenta
44	chr5:120444400-120444800	Active TSS	Hela-S3	cervix
45	chr5:120444400-120445600	Enhancers	Dnd41	blood
46	chr5:120444600-120444800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:120445000-120449000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:120447600-120447800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:120449000-120449600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:120449600-120450200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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