Variant report

Variant	nsv1061787
Chromosome Location	chr16:34466559-34775301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1359)
CpG islands
(count:2015)
Chromatin interactive
region (count:6)
LncRNA
region (count:67)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1359 , 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	chr16:34715569-34715609	K562	blood:	n/a	n/a
2	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
3	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
4	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
5	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
6	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
7	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
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	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
14	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
15	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
16	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
18	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
21	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
22	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
24	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
25	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
26	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
27	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
29	CEBPB	chr16:34715391-34715623	K562	blood:	n/a	n/a
30	CEBPB	chr16:34600114-34600449	MCF-7	breast:	n/a	chr16:34600335-34600346
31	CEBPB	chr16:34685080-34685431	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34730731-34731119	A549	lung:	n/a	n/a
34	CEBPB	chr16:34715416-34715653	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
36	CEBPB	chr16:34685018-34685433	A549	lung:	n/a	n/a
37	CEBPB	chr16:34603883-34604326	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34598745-34598792	K562	blood:	n/a	n/a
39	CEBPB	chr16:34573756-34574077	A549	lung:	n/a	chr16:34573875-34573886
40	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
41	CEBPB	chr16:34573755-34574035	K562	blood:	n/a	chr16:34573875-34573886
42	CEBPB	chr16:34730704-34731069	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr16:34532914-34533612	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
44	CEBPB	chr16:34611204-34611408	HepG2	liver:	n/a	chr16:34611274-34611285
45	CEBPB	chr16:34683490-34683958	HepG2	liver:	n/a	chr16:34683618-34683629
46	CEBPB	chr16:34632715-34632941	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
48	CEBPB	chr16:34602083-34602267	A549	lung:	n/a	n/a
49	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
50	CEBPB	chr16:34486702-34487146	IMR90	lung:	n/a	chr16:34486713-34486730

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34625446-34625496	HEEpiC	esophagus:	n/a
2	chr16:34625446-34625496	SK-N-SH	brain:	n/a
3	chr16:34625446-34625496	HEEpiC	esophagus:	n/a
4	chr16:34625446-34625496	SK-N-SH	brain:	n/a
5	chr16:34583045-34583095	HRCEpiC	kidney:	n/a
6	chr16:34659771-34659821	NHDF-neo	bronchial:	n/a
7	chr16:34587307-34587357	HAEpiC	amniotic membrane:	n/a
8	chr16:34726856-34726906	U87	brain:	n/a
9	chr16:34587307-34587357	RPTEC	kidney:	n/a
10	chr16:34489904-34489954	IMR90	lung:	fetal
11	chr16:34740934-34740984	T-47D	breast:	n/a
12	chr16:34490033-34490083	NB4	blood:	n/a
13	chr16:34740934-34740984	HIPEpiC	eye:	n/a
14	chr16:34741304-34741354	HNPCEpiC	eye:	n/a
15	chr16:34490033-34490083	HepG2	liver:	n/a
16	chr16:34760531-34760581	HRCEpiC	kidney:	n/a
17	chr16:34741966-34742016	NHDF-neo	bronchial:	n/a
18	chr16:34489904-34489954	NT2-D1	testis:	n/a
19	chr16:34586894-34586944	PANC-1	pancreas:	n/a
20	chr16:34659771-34659821	H1-hESC	embryonic stem cell:	embryo
21	chr16:34726856-34726906	HRE	kidney:	n/a
22	chr16:34579002-34579052	GM06990	blood:	n/a
23	chr16:34596583-34596633	AG09319	gingival:	n/a
24	chr16:34625446-34625496	NB4	blood:	n/a
25	chr16:34726734-34726784	GM12892	blood:	n/a
26	chr16:34740520-34740570	T-47D	breast:	n/a
27	chr16:34741304-34741354	HRE	kidney:	n/a
28	chr16:34660044-34660094	BE2_C	brain:	n/a
29	chr16:34741493-34741543	GM06990	blood:	n/a
30	chr16:34760531-34760581	HAEpiC	amniotic membrane:	n/a
31	chr16:34716002-34716052	SAEC	small airway:	n/a
32	chr16:34598029-34598079	HUVEC	blood vessel:	n/a
33	chr16:34716002-34716052	T-47D	breast:	n/a
34	chr16:34737523-34737573	GM12891	blood:	n/a
35	chr16:34659771-34659821	SK-N-MC	brain:	n/a
36	chr16:34586837-34586887	HL-60	blood:	n/a
37	chr16:34598029-34598079	Jurkat	blood:	n/a
38	chr16:34741251-34741301	Hela-S3	cervix:	n/a
39	chr16:34648955-34649005	H1-hESC	embryonic stem cell:	embryo
40	chr16:34741304-34741354	GM12878	blood:	n/a
41	chr16:34760531-34760581	BJ	skin:	n/a
42	chr16:34587307-34587357	PFSK-1	brain:	n/a
43	chr16:34663929-34663979	ECC-1	luminal epithelium:	n/a
44	chr16:34741304-34741354	SK-N-SH	brain:	n/a
45	chr16:34598029-34598079	MCF10A-Er-Src	breast:	n/a
46	chr16:34489904-34489954	HL-60	blood:	n/a
47	chr16:34663929-34663979	SK-N-SH	brain:	n/a
48	chr16:34579002-34579052	HPAEpiC	pulmonary alveolar:	n/a
49	chr16:34587120-34587170	Hela-S3	cervix:	n/a
50	chr16:34649152-34649202	AG09309	skin:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
2	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
3	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
4	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
5	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
6	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
7	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
8	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
9	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
10	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
11	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
12	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
13	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
14	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
15	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
16	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
17	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
18	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
19	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
20	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
21	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
22	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
23	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
24	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
25	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
26	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
27	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
28	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
29	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
30	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
31	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
32	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
33	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
34	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
35	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
36	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
37	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
38	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
39	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
40	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
41	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
42	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
43	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
44	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
45	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
46	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
47	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
48	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
49	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
50	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	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
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
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
ENSG00000137871	chromatin interactions
ENSG00000260073	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 5753 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5753 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546188852	chr16:34466584-34466585	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570867717	chr16:34466590-34466591	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531969376	chr16:34466591-34466592	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550491593	chr16:34466613-34466614	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537011819	chr16:34466648-34466649	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536465539	chr16:34466652-34466653	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs145571323	chr16:34466753-34466754	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs148888301	chr16:34466859-34466860	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376414635	chr16:34466864-34466865	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs117119121	chr16:34466924-34466925	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553495733	chr16:34466931-34466932	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs578104638	chr16:34466988-34466989	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545398284	chr16:34467006-34467007	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs55859506	chr16:34467008-34467009	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189844380	chr16:34467065-34467066	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145346199	chr16:34467068-34467069	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543225563	chr16:34467227-34467228	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561275604	chr16:34467261-34467262	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs4887579	chr16:34467267-34467268	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570782434	chr16:34467273-34467274	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539978082	chr16:34467291-34467292	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564618629	chr16:34467314-34467315	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532015082	chr16:34467318-34467319	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538920119	chr16:34467334-34467335	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146463360	chr16:34467338-34467339	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562826029	chr16:34467347-34467348	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529900795	chr16:34467348-34467349	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144613997	chr16:34467374-34467375	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566592035	chr16:34467414-34467415	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs368816803	chr16:34467443-34467444	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374372525	chr16:34467450-34467451	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs182818598	chr16:34467467-34467468	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs8046955	chr16:34467504-34467505	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs7499910	chr16:34467540-34467541	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs539049908	chr16:34467583-34467584	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557043805	chr16:34467621-34467622	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148369538	chr16:34467646-34467647	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188201774	chr16:34467654-34467655	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs555232290	chr16:34467682-34467683	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs573145788	chr16:34467713-34467714	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs540413279	chr16:34467720-34467721	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs191707007	chr16:34467725-34467726	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576504222	chr16:34467741-34467742	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76455224	chr16:34467743-34467744	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562304475	chr16:34467779-34467780	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs529684260	chr16:34467797-34467798	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs576222719	chr16:34467799-34467800	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7500004	chr16:34467802-34467803	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs183761808	chr16:34467817-34467818	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527515845	chr16:34467822-34467823	ZNF genes & repeats	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	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
7	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
10	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
11	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
16	chr16:34531200-34534000	Enhancers	HMEC	breast
17	chr16:34531400-34534200	Enhancers	NHEK	skin
18	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
19	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
20	chr16:34534200-34538800	Weak transcription	NHEK	skin
21	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
22	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
23	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
24	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
25	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
26	chr16:34538600-34544000	Enhancers	HMEC	breast
27	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr16:34538800-34543800	Enhancers	NHEK	skin
29	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
34	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
41	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
42	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
44	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
45	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
46	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
47	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
48	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain
49	chr16:34554200-34554600	Enhancers	Brain Cingulate Gyrus	brain
50	chr16:34554200-34554600	Enhancers	Brain Substantia Nigra	brain

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