Variant report

Variant	esv2752730
Chromosome Location	chr16:34449700-34790371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1441)
CpG islands
(count:2689)
Chromatin interactive
region (count:6)
LncRNA
region (count:69)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
2	ATF1	chr16:34787094-34787358	K562	blood:	n/a	n/a
3	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
4	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
5	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
6	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
7	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
8	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
9	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
10	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
11	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
12	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
13	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
14	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
15	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
16	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
17	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
18	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
19	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
20	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
24	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
25	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
26	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
27	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
28	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
30	CEBPB	chr16:34573711-34574084	HepG2	liver:	n/a	chr16:34573875-34573886
31	CEBPB	chr16:34603901-34604333	A549	lung:	n/a	n/a
32	CEBPB	chr16:34768061-34768461	IMR90	lung:	n/a	n/a
33	CEBPB	chr16:34632715-34632941	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:34643966-34644271	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:34486702-34487146	IMR90	lung:	n/a	chr16:34486713-34486730
36	CEBPB	chr16:34637648-34637812	K562	blood:	n/a	chr16:34637709-34637720
37	CEBPB	chr16:34449685-34450030	K562	blood:	n/a	n/a
38	CEBPB	chr16:34597882-34598141	IMR90	lung:	n/a	n/a
39	CEBPB	chr16:34539085-34539474	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:34611204-34611408	HepG2	liver:	n/a	chr16:34611274-34611285
41	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
42	CEBPB	chr16:34531259-34531620	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr16:34597947-34598296	A549	lung:	n/a	n/a
44	CEBPB	chr16:34768026-34768406	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr16:34790349-34790522	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:34600114-34600449	MCF-7	breast:	n/a	chr16:34600335-34600346
47	CEBPB	chr16:34597883-34598280	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:34600160-34600470	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
49	CEBPB	chr16:34540421-34540653	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a

(count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34663929-34663979	NHBE	bronchial:	n/a
2	chr16:34659771-34659821	SK-N-SH	brain:	n/a
3	chr16:34787199-34787249	A549	lung:	n/a
4	chr16:34737523-34737573	IMR90	lung:	fetal
5	chr16:34740520-34740570	HL-60	blood:	n/a
6	chr16:34663929-34663979	NHBE	bronchial:	n/a
7	chr16:34659771-34659821	SK-N-SH	brain:	n/a
8	chr16:34787199-34787249	A549	lung:	n/a
9	chr16:34737523-34737573	IMR90	lung:	fetal
10	chr16:34740520-34740570	HL-60	blood:	n/a
11	chr16:34726734-34726784	GM12878	blood:	n/a
12	chr16:34740520-34740570	PrEC	prostate:	n/a
13	chr16:34741304-34741354	Hela-S3	cervix:	n/a
14	chr16:34648955-34649005	SAEC	small airway:	n/a
15	chr16:34586894-34586944	ECC-1	luminal epithelium:	n/a
16	chr16:34586894-34586944	NT2-D1	testis:	n/a
17	chr16:34587120-34587170	AG09309	skin:	n/a
18	chr16:34648842-34648892	Hela-S3	cervix:	n/a
19	chr16:34787597-34787647	A549	lung:	n/a
20	chr16:34663929-34663979	SAEC	small airway:	n/a
21	chr16:34456429-34456479	H1-hESC	embryonic stem cell:	embryo
22	chr16:34777682-34777732	HEEpiC	esophagus:	n/a
23	chr16:34716002-34716052	A549	lung:	n/a
24	chr16:34741493-34741543	NB4	blood:	n/a
25	chr16:34787392-34787442	BJ	skin:	n/a
26	chr16:34456429-34456479	NH-A	brain:	n/a
27	chr16:34587307-34587357	HL-60	blood:	n/a
28	chr16:34787597-34787647	MCF10A-Er-Src	breast:	n/a
29	chr16:34587120-34587170	HCT-116	colon:	n/a
30	chr16:34490033-34490083	K562	blood:	n/a
31	chr16:34741493-34741543	Jurkat	blood:	n/a
32	chr16:34648842-34648892	ovcar-3	ovarian:	n/a
33	chr16:34740520-34740570	HCM	heart:	n/a
34	chr16:34490033-34490083	NH-A	brain:	n/a
35	chr16:34777881-34777931	HCM	heart:	n/a
36	chr16:34726856-34726906	U87	brain:	n/a
37	chr16:34456429-34456479	HNPCEpiC	eye:	n/a
38	chr16:34787597-34787647	Caco-2	colon:	n/a
39	chr16:34787392-34787442	U87	brain:	n/a
40	chr16:34787597-34787647	K562	blood:	n/a
41	chr16:34712713-34712763	HRPEpiC	eye:	n/a
42	chr16:34716002-34716052	SK-N-SH	brain:	n/a
43	chr16:34456429-34456479	A549	lung:	n/a
44	chr16:34787392-34787442	HCT-116	colon:	n/a
45	chr16:34760531-34760581	GM12891	blood:	n/a
46	chr16:34741304-34741354	SK-N-MC	brain:	n/a
47	chr16:34712713-34712763	HAEpiC	amniotic membrane:	n/a
48	chr16:34490033-34490083	MCF10A-Er-Src	breast:	n/a
49	chr16:34741304-34741354	ovcar-3	ovarian:	n/a
50	chr16:34586894-34586944	HCT-116	colon:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
2	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
3	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:
4	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
5	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
6	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:

(count:69 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
2	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
3	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
4	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
5	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
6	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
7	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
8	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
9	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
10	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
11	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
12	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
13	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
14	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
15	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
16	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
17	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
18	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
19	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
20	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
21	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
22	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
23	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
24	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
25	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
26	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
27	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
28	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
29	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
30	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
31	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
32	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
33	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
34	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
35	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
36	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
37	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
38	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
39	lnc-CTD-2144E22.5.1-32	chr16:34782288-34783200	NONHSAT142214
40	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
41	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
42	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
43	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
44	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
45	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
46	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
47	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
48	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
49	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
50	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179

No data

Variant related genes	Relation type
RARRES2P9	TF binding region
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000261046	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000260153	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000259841	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
RARRES2P9	CpG island
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000261046	CpG island
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000260153	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000259841	CpG island
RARRES2P8	CpG island
ENSG00000261711	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000261398	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000260073	chromatin interactions
ZNF407	miRNA target sites
ZNF451	miRNA target sites

Extended variants
information (count: 6094 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6094 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556373338	chr16:34455978-34455979	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs372599805	chr16:34456009-34456010	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
3	rs556057190	chr16:34456011-34456012	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
4	rs536712454	chr16:34456024-34456025	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
5	rs562026083	chr16:34456033-34456034	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
6	rs529008521	chr16:34456040-34456041	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
7	rs116325916	chr16:34456041-34456042	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
8	rs558267207	chr16:34456081-34456082	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs370579430	chr16:34456095-34456096	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs189245361	chr16:34456130-34456131	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs117991594	chr16:34456157-34456158	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs115010400	chr16:34456162-34456163	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs562708852	chr16:34456174-34456175	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs568580168	chr16:34456192-34456193	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs529748275	chr16:34456205-34456206	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs541478091	chr16:34456210-34456211	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs559990303	chr16:34456235-34456236	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs527324274	chr16:34456248-34456249	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs72812741	chr16:34456274-34456275	Active TSS ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570753720	chr16:34456286-34456287	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs199619803	chr16:34456297-34456298	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs531611524	chr16:34456319-34456320	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs140853961	chr16:34456346-34456347	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs376950523	chr16:34456394-34456395	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs535639692	chr16:34456404-34456405	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs11648428	chr16:34456411-34456412	Active TSS ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs566835166	chr16:34456453-34456454	Active TSS ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs566343819	chr16:34456466-34456467	Active TSS ZNF genes & repeats	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs534225859	chr16:34456483-34456484	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs36022857	chr16:34456484-34456485	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs558650276	chr16:34456493-34456494	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs11642319	chr16:34456535-34456536	Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544461512	chr16:34456546-34456547	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs569232118	chr16:34456595-34456596	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs192112773	chr16:34456636-34456637	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs574737745	chr16:34456650-34456651	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs542010643	chr16:34456693-34456694	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs62059552	chr16:34456746-34456747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573992079	chr16:34458801-34458802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs374502574	chr16:34458809-34458810	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs560068297	chr16:34465651-34465652	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs190137788	chr16:34465656-34465657	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs531285888	chr16:34465694-34465695	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs551970633	chr16:34465720-34465721	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs569790563	chr16:34465721-34465722	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs548713624	chr16:34465726-34465727	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs369631067	chr16:34465727-34465728	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs567294655	chr16:34465732-34465733	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs147284601	chr16:34465764-34465765	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs140691043	chr16:34465769-34465770	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Rett syndrome	21593744	CNVD
Myelofibrosis	22110671	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	18414403	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34456000-34456800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:34456200-34456400	ZNF genes & repeats	Gastric	stomach
3	chr16:34456200-34456600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
12	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
15	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr16:34531200-34534000	Enhancers	HMEC	breast
22	chr16:34531400-34534200	Enhancers	NHEK	skin
23	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
24	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
25	chr16:34534200-34538800	Weak transcription	NHEK	skin
26	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
27	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
28	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
29	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
30	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
31	chr16:34538600-34544000	Enhancers	HMEC	breast
32	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
33	chr16:34538800-34543800	Enhancers	NHEK	skin
34	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
39	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
46	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
49	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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