Variant report

Variant	esv2751573
Chromosome Location	chr16:34437589-34790371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1482)
CpG islands
(count:3236)
Chromatin interactive
region (count:6)
LncRNA
region (count:71)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
2	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
3	ATF1	chr16:34573796-34574082	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	chr16:34787094-34787358	K562	blood:	n/a	n/a
7	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
10	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
11	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
12	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
13	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
14	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
15	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
16	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
21	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
22	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
23	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
24	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
25	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
26	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
27	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
29	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
30	CEBPB	chr16:34597947-34598296	A549	lung:	n/a	n/a
31	CEBPB	chr16:34767984-34768445	A549	lung:	n/a	n/a
32	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34637648-34637812	K562	blood:	n/a	chr16:34637709-34637720
34	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
35	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a
36	CEBPB	chr16:34730735-34731108	IMR90	lung:	n/a	n/a
37	CEBPB	chr16:34532887-34533747	HepG2	liver:	n/a	chr16:34533406-34533417
38	CEBPB	chr16:34685018-34685433	A549	lung:	n/a	n/a
39	CEBPB	chr16:34449647-34450070	IMR90	lung:	n/a	n/a
40	CEBPB	chr16:34768107-34768405	K562	blood:	n/a	n/a
41	CEBPB	chr16:34540547-34540747	K562	blood:	n/a	n/a
42	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
43	CEBPB	chr16:34683490-34683958	HepG2	liver:	n/a	chr16:34683618-34683629
44	CEBPB	chr16:34603883-34604326	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:34597883-34598280	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:34598745-34598792	K562	blood:	n/a	n/a
47	CEBPB	chr16:34540533-34540804	A549	lung:	n/a	n/a
48	CEBPB	chr16:34598584-34598949	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
50	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417

(count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34587120-34587170	AG10803	skin:	n/a
2	chr16:34712713-34712763	HPAEpiC	pulmonary alveolar:	n/a
3	chr16:34760531-34760581	BJ	skin:	n/a
4	chr16:34587120-34587170	AG10803	skin:	n/a
5	chr16:34712713-34712763	HPAEpiC	pulmonary alveolar:	n/a
6	chr16:34760531-34760581	BJ	skin:	n/a
7	chr16:34489904-34489954	AG10803	skin:	n/a
8	chr16:34777881-34777931	SK-N-SH_RA	brain:	n/a
9	chr16:34578819-34578869	NT2-D1	testis:	n/a
10	chr16:34777881-34777931	HepG2	liver:	n/a
11	chr16:34740585-34740635	A549	lung:	n/a
12	chr16:34741966-34742016	NH-A	brain:	n/a
13	chr16:34439811-34439861	BE2_C	brain:	n/a
14	chr16:34787199-34787249	GM12892	blood:	n/a
15	chr16:34781451-34781501	NHDF-neo	bronchial:	n/a
16	chr16:34781451-34781501	SK-N-SH	brain:	n/a
17	chr16:34778087-34778137	NH-A	brain:	n/a
18	chr16:34663929-34663979	PrEC	prostate:	n/a
19	chr16:34781451-34781501	HCM	heart:	n/a
20	chr16:34716002-34716052	T-47D	breast:	n/a
21	chr16:34596941-34596991	PrEC	prostate:	n/a
22	chr16:34777963-34778013	AoSMC	blood vessel:	n/a
23	chr16:34456419-34456469	HEEpiC	esophagus:	n/a
24	chr16:34741493-34741543	U87	brain:	n/a
25	chr16:34456419-34456469	Jurkat	blood:	n/a
26	chr16:34439811-34439861	GM12878	blood:	n/a
27	chr16:34578819-34578869	SAEC	small airway:	n/a
28	chr16:34625446-34625496	Hepatocyte	liver:	n/a
29	chr16:34598029-34598079	HNPCEpiC	eye:	n/a
30	chr16:34741966-34742016	AG09319	gingival:	n/a
31	chr16:34787392-34787442	HPAEpiC	pulmonary alveolar:	n/a
32	chr16:34586837-34586887	HPAEpiC	pulmonary alveolar:	n/a
33	chr16:34737523-34737573	HCPEpiC	choroid plexus:	n/a
34	chr16:34741966-34742016	H1-hESC	embryonic stem cell:	embryo
35	chr16:34726856-34726906	NH-A	brain:	n/a
36	chr16:34787392-34787442	MCF10A-Er-Src	breast:	n/a
37	chr16:34587120-34587170	U87	brain:	n/a
38	chr16:34741966-34742016	Jurkat	blood:	n/a
39	chr16:34489904-34489954	GM19239	blood:	n/a
40	chr16:34442602-34442652	HepG2	liver:	n/a
41	chr16:34443612-34443662	MCF10A-Er-Src	breast:	n/a
42	chr16:34596583-34596633	GM12891	blood:	n/a
43	chr16:34445785-34445835	HAEpiC	amniotic membrane:	n/a
44	chr16:34442602-34442652	HMEC	breast:	n/a
45	chr16:34741966-34742016	PrEC	prostate:	n/a
46	chr16:34740934-34740984	RPTEC	kidney:	n/a
47	chr16:34587307-34587357	A549	lung:	n/a
48	chr16:34586837-34586887	MCF-7	breast:	n/a
49	chr16:34741966-34742016	HL-60	blood:	n/a
50	chr16:34596941-34596991	BE2_C	brain:	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	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:
3	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
4	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
5	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
6	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:

(count:71 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
2	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
3	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
4	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
5	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
6	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
7	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
8	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
9	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
10	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
11	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
12	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
13	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
14	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
15	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
16	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
17	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
18	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
19	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
20	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
21	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
22	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
23	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
24	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
25	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
26	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
27	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
28	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
29	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
30	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
31	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
32	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
33	lnc-CTD-2144E22.5.1-32	chr16:34782288-34783200	NONHSAT142214
34	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
35	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
36	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
37	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
38	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
39	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
40	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
41	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
42	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
43	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
44	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
45	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
46	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
47	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
48	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
49	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
50	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2

No data

Variant related genes	Relation type
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000261274	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
RARRES2P9	TF binding region
ENSG00000261046	TF binding region
ENSG00000264479	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
ENSG00000260958	TF binding region
ENSG00000260153	TF binding region
ENSG00000259841	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000261274	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
RARRES2P9	CpG island
ENSG00000261046	CpG island
ENSG00000264479	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
ENSG00000260958	CpG island
ENSG00000260153	CpG island
ENSG00000259841	CpG island
RARRES2P8	CpG island
ENSG00000261711	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: 6314 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6314 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs748250	chr16:34437589-34437590	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564485522	chr16:34437617-34437618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs576318846	chr16:34437618-34437619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs541025275	chr16:34437631-34437632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs559769634	chr16:34437684-34437685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs543641894	chr16:34437707-34437708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs562284931	chr16:34437738-34437739	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs60580821	chr16:34437768-34437769	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369373796	chr16:34437772-34437773	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559097979	chr16:34437775-34437776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs532912346	chr16:34437811-34437812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs189843444	chr16:34437854-34437855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs60943089	chr16:34437855-34437856	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs530402743	chr16:34437856-34437857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs537328205	chr16:34437896-34437897	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs7404459	chr16:34437898-34437899	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372544081	chr16:34437910-34437911	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs193260909	chr16:34437987-34437988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs7404474	chr16:34438015-34438016	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554190775	chr16:34438070-34438071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs572204025	chr16:34438079-34438080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs369084964	chr16:34438119-34438120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs539487242	chr16:34438155-34438156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs185366996	chr16:34438164-34438165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs576353955	chr16:34438217-34438218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs543678849	chr16:34438221-34438222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs562156967	chr16:34438223-34438224	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs574134900	chr16:34438225-34438226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs540774554	chr16:34438267-34438268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs189632997	chr16:34438297-34438298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs1843651	chr16:34438299-34438300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs545057999	chr16:34438332-34438333	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs563253434	chr16:34438333-34438334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs572390974	chr16:34438404-34438405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546600266	chr16:34438437-34438438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552210341	chr16:34438607-34438608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530848787	chr16:34438662-34438663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549227118	chr16:34438720-34438721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7186710	chr16:34438740-34438741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528335139	chr16:34438758-34438759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373340818	chr16:34438782-34438783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565869283	chr16:34438798-34438799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180790252	chr16:34438809-34438810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539523802	chr16:34438816-34438817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557749471	chr16:34438836-34438837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151129286	chr16:34438863-34438864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185594557	chr16:34438910-34438911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555982589	chr16:34438956-34438957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574250203	chr16:34438989-34438990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568398520	chr16:34439017-34439018	Weak transcription	TF binding 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:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr16:34442200-34443000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr16:34442200-34443000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr16:34442600-34442800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr16:34456000-34456800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:34456200-34456400	ZNF genes & repeats	Gastric	stomach
11	chr16:34456200-34456600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
20	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
23	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr16:34531200-34534000	Enhancers	HMEC	breast
30	chr16:34531400-34534200	Enhancers	NHEK	skin
31	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
32	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
33	chr16:34534200-34538800	Weak transcription	NHEK	skin
34	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
35	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
36	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
37	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
38	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
39	chr16:34538600-34544000	Enhancers	HMEC	breast
40	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr16:34538800-34543800	Enhancers	NHEK	skin
42	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
47	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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