Variant report

Variant	nsv949612
Chromosome Location	chr14:36996206-37121633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1391)
CpG islands
(count:2870)
Chromatin interactive
region (count:78)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1391 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37073991-37074490	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37022867-37023210	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37025997-37026389	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:37022926-37023126	K562	blood:	n/a	n/a
5	ARID3A	chr14:37074700-37075018	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:37026059-37026346	K562	blood:	n/a	n/a
7	ARID3A	chr14:37117226-37117385	HepG2	liver:	n/a	n/a
8	BACH1	chr14:37050966-37050999	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:37050310-37050435	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:37116389-37117625	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr14:37096102-37096228	K562	blood:	n/a	n/a
12	BRCA1	chr14:37117148-37117269	HepG2	liver:	n/a	n/a
13	BRCA1	chr14:37117750-37117752	HepG2	liver:	n/a	n/a
14	BRCA1	chr14:37117109-37117596	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr14:37117061-37117384	K562	blood:	n/a	n/a
16	CEBPB	chr14:37016481-37016766	HepG2	liver:	n/a	chr14:37016615-37016626 chr14:37016614-37016627 chr14:37016614-37016625
17	CEBPB	chr14:37120702-37120954	HepG2	liver:	n/a	chr14:37120842-37120853
18	CEBPB	chr14:37016537-37016771	A549	lung:	n/a	chr14:37016615-37016626 chr14:37016614-37016627 chr14:37016614-37016625
19	CEBPB	chr14:37076569-37076751	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:37097075-37097430	MCF-7	breast:	n/a	chr14:37097150-37097161
21	CEBPB	chr14:37120726-37120902	A549	lung:	n/a	chr14:37120842-37120853
22	CEBPB	chr14:37097151-37097468	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr14:37082949-37083070	HepG2	liver:	n/a	chr14:37083013-37083024
24	CEBPB	chr14:37073926-37074388	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:37039258-37039659	Hela-S3	cervix:	n/a	chr14:37039488-37039505
26	CEBPB	chr14:37102595-37102918	HepG2	liver:	n/a	chr14:37102749-37102760 chr14:37102747-37102758
27	CEBPB	chr14:37102626-37102891	A549	lung:	n/a	chr14:37102749-37102760 chr14:37102747-37102758
28	CHD2	chr14:37063020-37063027	HepG2	liver:	n/a	n/a
29	CHD2	chr14:37117049-37117211	K562	blood:	n/a	n/a
30	CHD2	chr14:37116955-37117339	HepG2	liver:	n/a	n/a
31	CHD2	chr14:37116951-37117780	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr14:37117093-37117442	A549	lung:	n/a	n/a
33	CREB1	chr14:37049964-37050491	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr14:37115840-37117918	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTBP2	chr14:37058851-37059340	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr14:37048727-37050904	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr14:37051980-37054092	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:37116820-37116970	HPF	lung:	n/a	n/a
39	CTCF	chr14:37022948-37023190	Kidney_OC	kidney:	n/a	chr14:37023048-37023057 chr14:37023045-37023063 chr14:37023047-37023068
40	CTCF	chr14:37026140-37026290	Caco-2	colon:	n/a	chr14:37026201-37026219 chr14:37026196-37026217
41	CTCF	chr14:37074582-37074682	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr14:37022918-37023181	MCF-7	breast:	n/a	chr14:37023048-37023057 chr14:37023045-37023063 chr14:37023047-37023068
43	CTCF	chr14:37074220-37074370	HEEpiC	esophagus:	n/a	chr14:37074306-37074324 chr14:37074301-37074322 chr14:37074307-37074323
44	CTCF	chr14:37026028-37026374	ECC-1	luminal epithelium:	n/a	chr14:37026201-37026219 chr14:37026196-37026217
45	CTCF	chr14:37116838-37116897	Fibrobl	skin:	n/a	n/a
46	CTCF	chr14:37116400-37116550	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr14:37074780-37074930	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr14:37026120-37026270	HCFaa	heart:	n/a	chr14:37026201-37026219 chr14:37026196-37026217
49	CTCF	chr14:37074720-37074870	AG09319	gingival:	n/a	n/a
50	CTCF	chr14:37116320-37116470	HBMEC	blood vessel:	n/a	n/a

(count:2870 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37117758-37117808	K562	blood:	n/a
2	chr14:37116408-37116458	HCPEpiC	choroid plexus:	n/a
3	chr14:37069791-37069841	GM19239	blood:	n/a
4	chr14:37117758-37117808	K562	blood:	n/a
5	chr14:37116408-37116458	HCPEpiC	choroid plexus:	n/a
6	chr14:37069791-37069841	GM19239	blood:	n/a
7	chr14:36997867-36997917	HCPEpiC	choroid plexus:	n/a
8	chr14:37116121-37116171	CMK	blood:	n/a
9	chr14:37053664-37053714	HL-60	blood:	n/a
10	chr14:37053689-37053739	NH-A	brain:	n/a
11	chr14:37117947-37117997	MCF-7	breast:	n/a
12	chr14:37116408-37116458	SK-N-SH_RA	brain:	n/a
13	chr14:37075527-37075577	A549	lung:	n/a
14	chr14:37117706-37117756	GM19239	blood:	n/a
15	chr14:37116296-37116346	MCF-7	breast:	n/a
16	chr14:37051949-37051999	Hela-S3	cervix:	n/a
17	chr14:37117758-37117808	HEK293	kidney:	embryo
18	chr14:37050691-37050741	SK-N-SH_RA	brain:	n/a
19	chr14:37051863-37051913	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:37049299-37049349	BE2_C	brain:	n/a
21	chr14:37117409-37117459	HUVEC	blood vessel:	n/a
22	chr14:37052668-37052718	GM19239	blood:	n/a
23	chr14:37058256-37058306	PrEC	prostate:	n/a
24	chr14:37050691-37050741	MCF-7	breast:	n/a
25	chr14:37117947-37117997	AG09309	skin:	n/a
26	chr14:37013717-37013767	HEK293	kidney:	embryo
27	chr14:37049893-37049943	K562	blood:	n/a
28	chr14:37116296-37116346	IMR90	lung:	fetal
29	chr14:37075527-37075577	AG04450	lung:	fetal
30	chr14:37050403-37050453	PFSK-1	brain:	n/a
31	chr14:37053689-37053739	HEEpiC	esophagus:	n/a
32	chr14:37053169-37053219	LNCaP	prostate:	n/a
33	chr14:37049565-37049615	HCPEpiC	choroid plexus:	n/a
34	chr14:37117706-37117756	H1-hESC	embryonic stem cell:	embryo
35	chr14:37045642-37045692	IMR90	lung:	fetal
36	chr14:37052470-37052520	HCM	heart:	n/a
37	chr14:37113177-37113227	MCF-7	breast:	n/a
38	chr14:37051703-37051753	HepG2	liver:	n/a
39	chr14:37051703-37051753	HIPEpiC	eye:	n/a
40	chr14:37069791-37069841	AG04450	lung:	fetal
41	chr14:37051949-37051999	ProgFib	skin:	n/a
42	chr14:37050455-37050505	NHBE	bronchial:	n/a
43	chr14:37116296-37116346	HAEpiC	amniotic membrane:	n/a
44	chr14:37053169-37053219	HMEC	breast:	n/a
45	chr14:37075527-37075577	NT2-D1	testis:	n/a
46	chr14:37053689-37053739	HRPEpiC	eye:	n/a
47	chr14:37116367-37116417	Caco-2	colon:	n/a
48	chr14:37053601-37053651	Jurkat	blood:	n/a
49	chr14:36997867-36997917	BJ	skin:	n/a
50	chr14:37051703-37051753	SK-N-MC	brain:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:37055658..37057192-chr14:37058194..37060437,2	MCF-7	breast:
2	chr14:37043733..37045700-chr14:37047521..37049850,2	K562	blood:
3	chr14:37115106..37119062-chr14:37125097..37130192,4	K562	blood:
4	chr14:37086596..37089360-chr14:37097437..37099326,2	MCF-7	breast:
5	chr14:37054360..37056420-chr14:37058461..37060514,2	K562	blood:
6	chr14:36989403..36989976-chr14:37074226..37074888,2	MCF-7	breast:
7	chr14:36918997..36920049-chr14:37073904..37074754,4	MCF-7	breast:
8	chr14:37029550..37032147-chr14:37039327..37042291,2	MCF-7	breast:
9	chr14:37073041..37076852-chr14:37619126..37621412,3	MCF-7	breast:
10	chr14:37043733..37046735-chr14:37047521..37050393,3	K562	blood:
11	chr14:37022207..37025712-chr14:37026672..37030530,3	MCF-7	breast:
12	chr14:37097674..37100247-chr14:37119173..37122093,2	K562	blood:
13	chr14:37053930..37056415-chr14:37057863..37059369,2	MCF-7	breast:
14	chr14:37113935..37116645-chr14:37128692..37132935,3	K562	blood:
15	chr14:37082134..37084571-chr14:37093334..37096202,2	MCF-7	breast:
16	chr14:37115811..37118059-chr14:37119729..37122052,2	K562	blood:
17	chr14:36989644..36990490-chr14:37073802..37074625,2	MCF-7	breast:
18	chr14:37111085..37113026-chr14:37114318..37117125,2	MCF-7	breast:
19	chr14:37022479..37023901-chr14:37073772..37074776,5	MCF-7	breast:
20	chr14:36540531..36541119-chr14:37073832..37074410,2	K562	blood:
21	chr14:37043777..37046012-chr14:37049120..37051344,2	MCF-7	breast:
22	chr14:37107177..37110095-chr14:37113473..37116981,4	MCF-7	breast:
23	chr14:37117455..37118380-chr14:37411140..37411900,2	MCF-7	breast:
24	chr14:37117007..37117865-chr14:37224585..37225500,2	MCF-7	breast:
25	chr14:36539391..36539941-chr14:37025739..37026663,2	MCF-7	breast:
26	chr14:36996663..36997201-chr3:11887911..11888523,2	MCF-7	breast:
27	chr14:37043777..37046012-chr14:37049120..37051344,2	MCF-7	breast:
28	chr14:37049506..37051705-chr14:37066092..37068033,2	MCF-7	breast:
29	chr14:37117154..37117736-chr14:37125062..37125846,2	MCF-7	breast:
30	chr14:37115310..37117842-chr14:37618181..37620146,4	MCF-7	breast:
31	chr14:37026010..37026647-chr14:37073760..37074750,4	MCF-7	breast:
32	chr14:37055658..37057192-chr14:37058194..37060437,2	MCF-7	breast:
33	chr14:37117246..37117989-chr14:37411042..37411700,6	MCF-7	breast:
34	chr14:37111085..37113026-chr14:37114318..37117125,2	MCF-7	breast:
35	chr14:37022639..37023491-chr14:37074030..37074795,3	K562	blood:
36	chr14:37043733..37045700-chr14:37047521..37049850,2	K562	blood:
37	chr14:37116999..37117734-chr14:37444738..37445386,2	MCF-7	breast:
38	chr14:37113050..37116916-chr14:37130582..37134618,6	MCF-7	breast:
39	chr14:37116820..37118183-chr14:37618958..37620155,6	MCF-7	breast:
40	chr14:37022207..37025712-chr14:37026672..37030530,3	MCF-7	breast:
41	chr14:36432098..36432997-chr14:37073898..37074637,2	MCF-7	breast:
42	chr14:37022063..37024293-chr14:37073305..37075306,11	MCF-7	breast:
43	chr14:37029550..37032147-chr14:37039327..37042291,2	MCF-7	breast:
44	chr14:37049506..37051705-chr14:37066092..37068033,2	MCF-7	breast:
45	chr14:36538901..36540820-chr14:37025623..37026681,8	MCF-7	breast:
46	chr14:37047105..37049296-chr14:37063391..37064918,2	MCF-7	breast:
47	chr14:36853354..36854949-chr14:37081827..37084806,2	K562	blood:
48	chr14:37051690..37053277-chr14:37640298..37642030,2	K562	blood:
49	chr14:37026010..37026647-chr14:37073760..37074750,4	MCF-7	breast:
50	chr14:37082134..37084571-chr14:37093334..37096202,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAX9-7	chr14:37117801-37117879	l_966_chr14:37103178-37117879_prostate
2	lnc-PAX9-7	chr14:37103179-37103318	l_966_chr14:37103178-37117879_prostate
3	lnc-NKX2-8-2	chr14:37063044-37063352	NONHSAT036442
4	lnc-PAX9-7	chr14:37117660-37117798	l_966_chr14:37103178-37117879_prostate
5	lnc-SLC25A21-1	chr14:37116288-37118642	ENSG00000258661.1

No data

Variant related genes	Relation type
NKX2-8	TF binding region
PHKBP2	TF binding region
RN7SKP257	TF binding region
RPL29P3	TF binding region
NKX2-8	CpG island
PHKBP2	CpG island
RN7SKP257	CpG island
RPL29P3	CpG island
ENSG00000258467	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000243730	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000198807	chromatin interactions
ENSG00000144559	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000258661	chromatin interactions
ENSG00000136352	chromatin interactions
ENSG00000136327	chromatin interactions

Extended variants
information (count: 2859 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2859 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182270216	chr14:36996670-36996671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs184990255	chr14:36996788-36996789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147312119	chr14:36996796-36996797	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192434651	chr14:36996807-36996808	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112380356	chr14:36996833-36996834	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563417706	chr14:36996842-36996843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs544822441	chr14:36996844-36996845	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575145340	chr14:36996907-36996908	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114262277	chr14:36996920-36996921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527323125	chr14:36996923-36996924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548033533	chr14:36996941-36996942	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140901783	chr14:36996958-36996959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530185224	chr14:36996993-36996994	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188847998	chr14:36996996-36996997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569964664	chr14:36997023-36997024	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145145890	chr14:36997029-36997030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558821474	chr14:36997030-36997031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34694218	chr14:36997035-36997036	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566033576	chr14:36997057-36997058	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545586308	chr14:36997093-36997094	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564051589	chr14:36997135-36997136	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114817568	chr14:36998847-36998848	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs60717855	chr14:36998898-36998899	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569526239	chr14:36998947-36998948	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs12895406	chr14:36998950-36998951	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550069446	chr14:36999020-36999021	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537651542	chr14:36999033-36999034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146497162	chr14:36999054-36999055	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs140973603	chr14:36999063-36999064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75292942	chr14:36999101-36999102	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185558321	chr14:36999114-36999115	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs190459942	chr14:36999181-36999182	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534406269	chr14:36999206-36999207	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554261887	chr14:36999207-36999208	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10130913	chr14:36999283-36999284	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543017701	chr14:36999307-36999308	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557191539	chr14:36999325-36999326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145066118	chr14:36999416-36999417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557554952	chr14:36999576-36999577	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs546524526	chr14:36999583-36999584	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535287824	chr14:36999586-36999587	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559668978	chr14:36999587-36999588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138760139	chr14:36999621-36999622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1956965	chr14:36999637-36999638	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149353678	chr14:36999653-36999654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530877677	chr14:36999718-36999719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs77540390	chr14:36999802-36999803	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79179874	chr14:36999821-36999822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17104628	chr14:36999938-36999939	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs532300836	chr14:36999977-36999978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	21272361	CNVD

Chromatin state (count:838 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37005600-37005800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:37012000-37025400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:37019800-37020400	Enhancers	Liver	Liver
4	chr14:37019800-37020600	Enhancers	HepG2	liver
5	chr14:37022600-37023000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr14:37022800-37023000	Enhancers	Liver	Liver
7	chr14:37023200-37023400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:37023400-37024400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:37023800-37024600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr14:37024200-37026200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr14:37024400-37026000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:37024400-37026000	Enhancers	Dnd41	blood
13	chr14:37024600-37025600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr14:37025400-37025800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr14:37025400-37026000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:37025600-37026000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr14:37025600-37026000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr14:37025800-37027200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:37026000-37027200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr14:37026000-37027400	Weak transcription	Dnd41	blood
21	chr14:37027200-37027400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr14:37027200-37027400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr14:37027200-37027600	Enhancers	Fetal Lung	lung
24	chr14:37027600-37027800	Bivalent Enhancer	Fetal Lung	lung
25	chr14:37027800-37028000	Enhancers	Dnd41	blood
26	chr14:37027800-37028200	Enhancers	Fetal Lung	lung
27	chr14:37029000-37029200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr14:37029800-37030000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
29	chr14:37030200-37031000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:37043600-37043800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr14:37044800-37045000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:37045400-37045600	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:37046200-37046400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
34	chr14:37046800-37047000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr14:37047800-37048000	Bivalent Enhancer	Brain Hippocampus Middle	brain
36	chr14:37047800-37048200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:37048000-37054800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr14:37048200-37048400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:37048200-37048800	Enhancers	Brain Substantia Nigra	brain
40	chr14:37048200-37048800	Weak transcription	Spleen	Spleen
41	chr14:37048400-37048600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
42	chr14:37048400-37048800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr14:37048400-37048800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
44	chr14:37048400-37048800	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
45	chr14:37048400-37050000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr14:37048400-37050200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:37048600-37049200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:37048800-37049000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr14:37048800-37049000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
50	chr14:37048800-37049000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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