Variant report

Variant	esv3523522
Chromosome Location	chr16:34488718-34776362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1259)
CpG islands
(count:2015)
Chromatin interactive
region (count:5)
LncRNA
region (count:58)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
2	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
3	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
4	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
5	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
6	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
7	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
8	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
9	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
10	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
11	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
12	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
13	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
14	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
15	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
16	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
20	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
22	BHLHE40	chr16:34732021-34732023	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	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
26	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
28	CEBPB	chr16:34621247-34621265	A549	lung:	n/a	n/a
29	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417
30	CEBPB	chr16:34537186-34537555	IMR90	lung:	n/a	n/a
31	CEBPB	chr16:34683500-34683711	A549	lung:	n/a	chr16:34683618-34683629
32	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34759185-34759725	HepG2	liver:	n/a	chr16:34759593-34759604 chr16:34759630-34759641 chr16:34759565-34759576
34	CEBPB	chr16:34729321-34729674	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:34532887-34533747	HepG2	liver:	n/a	chr16:34533406-34533417
36	CEBPB	chr16:34759219-34759383	MCF-7	breast:	n/a	n/a
37	CEBPB	chr16:34603883-34604326	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34611204-34611408	HepG2	liver:	n/a	chr16:34611274-34611285
39	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
40	CEBPB	chr16:34715416-34715653	IMR90	lung:	n/a	n/a
41	CEBPB	chr16:34539085-34539474	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34597947-34598296	A549	lung:	n/a	n/a
43	CEBPB	chr16:34730731-34731119	A549	lung:	n/a	n/a
44	CEBPB	chr16:34768107-34768405	K562	blood:	n/a	n/a
45	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
46	CEBPB	chr16:34599864-34600530	HepG2	liver:	n/a	chr16:34600335-34600346
47	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285
49	CEBPB	chr16:34600114-34600449	MCF-7	breast:	n/a	chr16:34600335-34600346
50	CEBPB	chr16:34683490-34683958	HepG2	liver:	n/a	chr16:34683618-34683629

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34760531-34760581	HCT-116	colon:	n/a
2	chr16:34741493-34741543	HEK293	kidney:	embryo
3	chr16:34760531-34760581	HCT-116	colon:	n/a
4	chr16:34741493-34741543	HEK293	kidney:	embryo
5	chr16:34726856-34726906	AG04449	skin:	fetal
6	chr16:34648955-34649005	H1-hESC	embryonic stem cell:	embryo
7	chr16:34740585-34740635	LNCaP	prostate:	n/a
8	chr16:34596941-34596991	HAEpiC	amniotic membrane:	n/a
9	chr16:34741304-34741354	MCF-7	breast:	n/a
10	chr16:34663929-34663979	Jurkat	blood:	n/a
11	chr16:34598029-34598079	NB4	blood:	n/a
12	chr16:34741251-34741301	HEEpiC	esophagus:	n/a
13	chr16:34726734-34726784	AG10803	skin:	n/a
14	chr16:34740585-34740635	H1-hESC	embryonic stem cell:	embryo
15	chr16:34587307-34587357	PANC-1	pancreas:	n/a
16	chr16:34587120-34587170	IMR90	lung:	fetal
17	chr16:34648842-34648892	RPTEC	kidney:	n/a
18	chr16:34716002-34716052	SK-N-SH_RA	brain:	n/a
19	chr16:34741304-34741354	NHDF-neo	bronchial:	n/a
20	chr16:34579002-34579052	AG09309	skin:	n/a
21	chr16:34741493-34741543	K562	blood:	n/a
22	chr16:34598029-34598079	AG09319	gingival:	n/a
23	chr16:34741304-34741354	Hela-S3	cervix:	n/a
24	chr16:34740520-34740570	SAEC	small airway:	n/a
25	chr16:34741251-34741301	Hepatocyte	liver:	n/a
26	chr16:34586837-34586887	MCF-7	breast:	n/a
27	chr16:34741304-34741354	HIPEpiC	eye:	n/a
28	chr16:34648842-34648892	SKMC	muscle:	n/a
29	chr16:34490033-34490083	Caco-2	colon:	n/a
30	chr16:34659771-34659821	HNPCEpiC	eye:	n/a
31	chr16:34648842-34648892	CMK	blood:	n/a
32	chr16:34659771-34659821	HCT-116	colon:	n/a
33	chr16:34490033-34490083	ovcar-3	ovarian:	n/a
34	chr16:34579002-34579052	GM06990	blood:	n/a
35	chr16:34659664-34659714	MCF10A-Er-Src	breast:	n/a
36	chr16:34740520-34740570	SKMC	muscle:	n/a
37	chr16:34726734-34726784	ovcar-3	ovarian:	n/a
38	chr16:34659664-34659714	K562	blood:	n/a
39	chr16:34740934-34740984	PrEC	prostate:	n/a
40	chr16:34587307-34587357	SK-N-SH_RA	brain:	n/a
41	chr16:34741493-34741543	HMEC	breast:	n/a
42	chr16:34598029-34598079	SK-N-SH	brain:	n/a
43	chr16:34579002-34579052	NHDF-neo	bronchial:	n/a
44	chr16:34598029-34598079	PrEC	prostate:	n/a
45	chr16:34737523-34737573	HIPEpiC	eye:	n/a
46	chr16:34598029-34598079	HRE	kidney:	n/a
47	chr16:34490033-34490083	PrEC	prostate:	n/a
48	chr16:34740585-34740635	HCT-116	colon:	n/a
49	chr16:34649152-34649202	HRCEpiC	kidney:	n/a
50	chr16:34659664-34659714	MCF-7	breast:	n/a

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

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

(count:58 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
2	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
3	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
4	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
5	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
6	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
7	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
8	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
9	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
10	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
11	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
12	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
13	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
14	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
15	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
16	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
17	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
18	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
19	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
20	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
21	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
22	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
23	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
24	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
25	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
26	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
27	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
28	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
29	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
30	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
31	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
32	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
33	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
34	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
35	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
36	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
37	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
38	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
39	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
40	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
41	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
42	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
43	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
44	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
45	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
46	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
47	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
48	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
49	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
50	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2

No data

Variant related genes	Relation type
RARRES2P9	TF binding region
ENSG00000259836	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
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
RARRES2P9	CpG island
ENSG00000259836	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
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000137871	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 5250 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5250 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566398753	chr16:34489487-34489488	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142899233	chr16:34489565-34489566	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs558575119	chr16:34489639-34489640	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs35896479	chr16:34489668-34489669	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs570457096	chr16:34489672-34489673	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs17784951	chr16:34489692-34489693	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs556479511	chr16:34489815-34489816	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542659300	chr16:34489850-34489851	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs145052770	chr16:34489924-34489925	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs368157443	chr16:34489930-34489931	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs562914456	chr16:34489974-34489975	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs118066359	chr16:34490003-34490004	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs555050437	chr16:34490006-34490007	Active TSS ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs573217489	chr16:34490011-34490012	Active TSS ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs540322479	chr16:34490023-34490024	Active TSS ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs564986910	chr16:34490045-34490046	Active TSS ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
17	rs560900963	chr16:34490067-34490068	Active TSS ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs80196887	chr16:34490107-34490108	Active TSS ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs192396176	chr16:34490183-34490184	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs563006047	chr16:34490200-34490201	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs530319236	chr16:34490227-34490228	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs548452317	chr16:34490256-34490257	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs533341668	chr16:34490261-34490262	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs567043980	chr16:34490300-34490301	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs527428216	chr16:34490318-34490319	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs552278906	chr16:34490332-34490333	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs1684569	chr16:34490454-34490455	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552531118	chr16:34490482-34490483	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs553028142	chr16:34490486-34490487	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369527513	chr16:34490545-34490546	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570493802	chr16:34490640-34490641	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs537805255	chr16:34490652-34490653	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs140967447	chr16:34490661-34490662	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs150332647	chr16:34490662-34490663	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs138467973	chr16:34490664-34490665	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs55837969	chr16:34490665-34490666	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs138692775	chr16:34490672-34490673	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs397703035	chr16:34490692-34490693	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs151092370	chr16:34490703-34490704	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182255474	chr16:34490705-34490706	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116860281	chr16:34490722-34490723	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs571803213	chr16:34490786-34490787	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs111978099	chr16:34490795-34490796	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs554505968	chr16:34492812-34492813	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs572734441	chr16:34492852-34492853	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs185983332	chr16:34492873-34492874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs189262866	chr16:34492874-34492875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs147162802	chr16:34492875-34492876	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs576690547	chr16:34492884-34492885	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs6563867	chr16:34492886-34492887	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
2	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr16:34531200-34534000	Enhancers	HMEC	breast
8	chr16:34531400-34534200	Enhancers	NHEK	skin
9	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
10	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
11	chr16:34534200-34538800	Weak transcription	NHEK	skin
12	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
13	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
14	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
15	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
16	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
17	chr16:34538600-34544000	Enhancers	HMEC	breast
18	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr16:34538800-34543800	Enhancers	NHEK	skin
20	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
25	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
32	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
33	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
36	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
38	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
39	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain
40	chr16:34554200-34554600	Enhancers	Brain Cingulate Gyrus	brain
41	chr16:34554200-34554600	Enhancers	Brain Substantia Nigra	brain
42	chr16:34562400-34562800	Active TSS	Fetal Heart	heart
43	chr16:34571600-34577800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr16:34578400-34579200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr16:34578600-34579000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr16:34578800-34579000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr16:34578800-34579200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:34586600-34587000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr16:34586600-34587000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr16:34586600-34587200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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