Variant report

Variant	nsv1065413
Chromosome Location	chr16:34459025-34767999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1355)
CpG islands
(count:2015)
Chromatin interactive
region (count:6)
LncRNA
region (count:67)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1355 , 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	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
2	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
3	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
4	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
5	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
6	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
7	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
8	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
9	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
10	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
11	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
12	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
13	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
14	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
15	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
16	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
19	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
21	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
22	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
23	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
24	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
25	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
27	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
28	CEBPB	chr16:34600160-34600470	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
29	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
30	CEBPB	chr16:34486734-34487193	K562	blood:	n/a	n/a
31	CEBPB	chr16:34599887-34600514	A549	lung:	n/a	chr16:34600335-34600346
32	CEBPB	chr16:34605882-34606100	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34683490-34683958	HepG2	liver:	n/a	chr16:34683618-34683629
34	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a
35	CEBPB	chr16:34532878-34533767	A549	lung:	n/a	chr16:34533406-34533417
36	CEBPB	chr16:34685080-34685431	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:34767993-34768467	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34573755-34574035	K562	blood:	n/a	chr16:34573875-34573886
39	CEBPB	chr16:34759185-34759725	HepG2	liver:	n/a	chr16:34759593-34759604 chr16:34759630-34759641 chr16:34759565-34759576
40	CEBPB	chr16:34573756-34574077	A549	lung:	n/a	chr16:34573875-34573886
41	CEBPB	chr16:34662373-34662658	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34715391-34715623	K562	blood:	n/a	n/a
43	CEBPB	chr16:34540417-34540828	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:34730735-34731108	IMR90	lung:	n/a	n/a
45	CEBPB	chr16:34540533-34540804	A549	lung:	n/a	n/a
46	CEBPB	chr16:34759219-34759383	MCF-7	breast:	n/a	n/a
47	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34537186-34537555	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:34637589-34637802	HepG2	liver:	n/a	chr16:34637709-34637720

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34740520-34740570	NHBE	bronchial:	n/a
2	chr16:34596941-34596991	SK-N-SH_RA	brain:	n/a
3	chr16:34740520-34740570	NHBE	bronchial:	n/a
4	chr16:34596941-34596991	SK-N-SH_RA	brain:	n/a
5	chr16:34659771-34659821	H1-hESC	embryonic stem cell:	embryo
6	chr16:34489904-34489954	SK-N-SH_RA	brain:	n/a
7	chr16:34578819-34578869	HL-60	blood:	n/a
8	chr16:34648842-34648892	Jurkat	blood:	n/a
9	chr16:34741966-34742016	LNCaP	prostate:	n/a
10	chr16:34649152-34649202	BE2_C	brain:	n/a
11	chr16:34760531-34760581	HepG2	liver:	n/a
12	chr16:34586837-34586887	SK-N-SH_RA	brain:	n/a
13	chr16:34490033-34490083	GM06990	blood:	n/a
14	chr16:34740585-34740635	A549	lung:	n/a
15	chr16:34741493-34741543	Hela-S3	cervix:	n/a
16	chr16:34741493-34741543	HCM	heart:	n/a
17	chr16:34663929-34663979	PFSK-1	brain:	n/a
18	chr16:34583045-34583095	PrEC	prostate:	n/a
19	chr16:34741251-34741301	SK-N-SH	brain:	n/a
20	chr16:34726734-34726784	NH-A	brain:	n/a
21	chr16:34741251-34741301	GM06990	blood:	n/a
22	chr16:34578819-34578869	GM19239	blood:	n/a
23	chr16:34586837-34586887	HepG2	liver:	n/a
24	chr16:34741966-34742016	HCPEpiC	choroid plexus:	n/a
25	chr16:34587307-34587357	IMR90	lung:	fetal
26	chr16:34489904-34489954	MCF10A-Er-Src	breast:	n/a
27	chr16:34587307-34587357	HCPEpiC	choroid plexus:	n/a
28	chr16:34583045-34583095	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:34760531-34760581	Caco-2	colon:	n/a
30	chr16:34740520-34740570	HRCEpiC	kidney:	n/a
31	chr16:34741304-34741354	SK-N-SH_RA	brain:	n/a
32	chr16:34586894-34586944	NHDF-neo	bronchial:	n/a
33	chr16:34586837-34586887	NHDF-neo	bronchial:	n/a
34	chr16:34596583-34596633	AG09309	skin:	n/a
35	chr16:34586894-34586944	HUVEC	blood vessel:	n/a
36	chr16:34740934-34740984	K562	blood:	n/a
37	chr16:34712713-34712763	K562	blood:	n/a
38	chr16:34579002-34579052	MCF10A-Er-Src	breast:	n/a
39	chr16:34579002-34579052	NHDF-neo	bronchial:	n/a
40	chr16:34660044-34660094	IMR90	lung:	fetal
41	chr16:34716002-34716052	HRE	kidney:	n/a
42	chr16:34737523-34737573	PFSK-1	brain:	n/a
43	chr16:34663929-34663979	PrEC	prostate:	n/a
44	chr16:34741251-34741301	Caco-2	colon:	n/a
45	chr16:34598029-34598079	HUVEC	blood vessel:	n/a
46	chr16:34490033-34490083	ovcar-3	ovarian:	n/a
47	chr16:34596583-34596633	AoSMC	blood vessel:	n/a
48	chr16:34579002-34579052	ProgFib	skin:	n/a
49	chr16:34586837-34586887	Caco-2	colon:	n/a
50	chr16:34712713-34712763	SKMC	muscle:	n/a

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

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

(count:67 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
2	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
3	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
4	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
5	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
6	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
7	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
8	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
9	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
10	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
11	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
12	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
13	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
14	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
15	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
16	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
17	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
18	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
19	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
20	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
21	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
22	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
23	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
24	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
25	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
26	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
27	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
28	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
29	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
30	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
31	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
32	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
33	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
34	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
35	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
36	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
37	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
38	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
39	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
40	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
41	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
42	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
43	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
44	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
45	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
46	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
47	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
48	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
49	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
50	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2

No data

Variant related genes	Relation type
RARRES2P9	TF binding region
ENSG00000259836	TF binding region
ENSG00000259897	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
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
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
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260291	CpG island
ENSG00000261299	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
ENSG00000261711	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000261398	chromatin interactions
ENSG00000260073	chromatin interactions
ENSG00000137871	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 5660 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5660 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560068297	chr16:34465651-34465652	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs190137788	chr16:34465656-34465657	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs531285888	chr16:34465694-34465695	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs551970633	chr16:34465720-34465721	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs569790563	chr16:34465721-34465722	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs548713624	chr16:34465726-34465727	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs369631067	chr16:34465727-34465728	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs567294655	chr16:34465732-34465733	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs147284601	chr16:34465764-34465765	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs140691043	chr16:34465769-34465770	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs181761716	chr16:34465775-34465776	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs144650564	chr16:34465776-34465777	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs374588759	chr16:34465783-34465784	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs7404809	chr16:34465818-34465819	Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565404741	chr16:34465822-34465823	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs576460052	chr16:34465838-34465839	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs543854927	chr16:34465846-34465847	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs562042490	chr16:34465855-34465856	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs574009477	chr16:34465872-34465873	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs9923818	chr16:34465885-34465886	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs111585711	chr16:34465914-34465915	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs192367605	chr16:34465915-34465916	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs545621568	chr16:34465934-34465935	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs181804774	chr16:34465935-34465936	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs34943023	chr16:34465938-34465939	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs531001980	chr16:34465941-34465942	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs549108655	chr16:34465943-34465944	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs373815334	chr16:34465975-34465976	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs12444315	chr16:34465979-34465980	Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370909432	chr16:34465984-34465985	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs528121657	chr16:34465985-34465986	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs547805300	chr16:34466003-34466004	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs566263401	chr16:34466024-34466025	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs571228350	chr16:34466060-34466061	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs538495894	chr16:34466067-34466068	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs149706207	chr16:34466081-34466082	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs530272893	chr16:34466113-34466114	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs569082840	chr16:34466119-34466120	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs374542455	chr16:34466120-34466121	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs368264906	chr16:34466135-34466136	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs555866174	chr16:34466157-34466158	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs574018805	chr16:34466159-34466160	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs372098317	chr16:34466177-34466178	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs548238924	chr16:34466182-34466183	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs553358556	chr16:34466208-34466209	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185337096	chr16:34466217-34466218	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545756877	chr16:34466236-34466237	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs12926901	chr16:34466252-34466253	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368208333	chr16:34466312-34466313	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531161793	chr16:34466357-34466358	Inactive region	Chromatin interactive region	2 gene(s)	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:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
9	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
12	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
16	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr16:34531200-34534000	Enhancers	HMEC	breast
19	chr16:34531400-34534200	Enhancers	NHEK	skin
20	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
21	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
22	chr16:34534200-34538800	Weak transcription	NHEK	skin
23	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
24	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
25	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
26	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
27	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
28	chr16:34538600-34544000	Enhancers	HMEC	breast
29	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr16:34538800-34543800	Enhancers	NHEK	skin
31	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
36	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
43	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
46	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
47	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
49	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
50	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain

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