Variant report

Variant	nsv144
Chromosome Location	chr16:34390796-34715796
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1393)
CpG islands
(count:3487)
Chromatin interactive
region (count:3)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1393 , 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	chr16:34643912-34644196	K562	blood:	n/a	n/a
3	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
4	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
5	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
6	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
7	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
8	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
9	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
10	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
11	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
12	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
13	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
14	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
16	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
18	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
19	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
20	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
21	CEBPB	chr16:34637648-34637812	K562	blood:	n/a	chr16:34637709-34637720
22	CEBPB	chr16:34573756-34574077	A549	lung:	n/a	chr16:34573875-34573886
23	CEBPB	chr16:34532926-34533600	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
24	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a
25	CEBPB	chr16:34602083-34602267	A549	lung:	n/a	n/a
26	CEBPB	chr16:34715416-34715653	IMR90	lung:	n/a	n/a
27	CEBPB	chr16:34715384-34715712	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:34573711-34574084	HepG2	liver:	n/a	chr16:34573875-34573886
29	CEBPB	chr16:34611204-34611408	HepG2	liver:	n/a	chr16:34611274-34611285
30	CEBPB	chr16:34540417-34540828	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:34486734-34487193	K562	blood:	n/a	n/a
32	CEBPB	chr16:34621172-34621181	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34449667-34450116	A549	lung:	n/a	n/a
34	CEBPB	chr16:34600051-34600514	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
35	CEBPB	chr16:34643898-34644263	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:34449630-34450134	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34637662-34637759	A549	lung:	n/a	chr16:34637709-34637720
39	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285
40	CEBPB	chr16:34603901-34604333	A549	lung:	n/a	n/a
41	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
42	CEBPB	chr16:34643905-34644193	A549	lung:	n/a	n/a
43	CEBPB	chr16:34483511-34483748	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:34486751-34487148	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr16:34540421-34540653	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr16:34632715-34632941	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:34573755-34574035	K562	blood:	n/a	chr16:34573875-34573886
48	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
49	CEBPB	chr16:34542362-34542582	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:34600044-34600501	Hela-S3	cervix:	n/a	chr16:34600335-34600346

(count:3487 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34404054-34404104	Jurkat	blood:	n/a
2	chr16:34403971-34404021	ECC-1	luminal epithelium:	n/a
3	chr16:34583045-34583095	Hela-S3	cervix:	n/a
4	chr16:34596941-34596991	HAEpiC	amniotic membrane:	n/a
5	chr16:34578819-34578869	HMEC	breast:	n/a
6	chr16:34579002-34579052	NB4	blood:	n/a
7	chr16:34430837-34430887	HL-60	blood:	n/a
8	chr16:34432979-34433029	HUVEC	blood vessel:	n/a
9	chr16:34404774-34404824	HAEpiC	amniotic membrane:	n/a
10	chr16:34404619-34404669	LNCaP	prostate:	n/a
11	chr16:34404054-34404104	Jurkat	blood:	n/a
12	chr16:34403971-34404021	ECC-1	luminal epithelium:	n/a
13	chr16:34583045-34583095	Hela-S3	cervix:	n/a
14	chr16:34596941-34596991	HAEpiC	amniotic membrane:	n/a
15	chr16:34578819-34578869	HMEC	breast:	n/a
16	chr16:34579002-34579052	NB4	blood:	n/a
17	chr16:34430837-34430887	HL-60	blood:	n/a
18	chr16:34432979-34433029	HUVEC	blood vessel:	n/a
19	chr16:34404774-34404824	HAEpiC	amniotic membrane:	n/a
20	chr16:34404619-34404669	LNCaP	prostate:	n/a
21	chr16:34489904-34489954	NHDF-neo	bronchial:	n/a
22	chr16:34404774-34404824	Hepatocyte	liver:	n/a
23	chr16:34404673-34404723	HL-60	blood:	n/a
24	chr16:34430382-34430432	NT2-D1	testis:	n/a
25	chr16:34430837-34430887	PrEC	prostate:	n/a
26	chr16:34404772-34404822	HCF	heart:	n/a
27	chr16:34407918-34407968	AG09319	gingival:	n/a
28	chr16:34430837-34430887	NHDF-neo	bronchial:	n/a
29	chr16:34659664-34659714	Hela-S3	cervix:	n/a
30	chr16:34596583-34596633	AG04450	lung:	fetal
31	chr16:34403971-34404021	RPTEC	kidney:	n/a
32	chr16:34411816-34411866	ProgFib	skin:	n/a
33	chr16:34405690-34405740	HCM	heart:	n/a
34	chr16:34404524-34404574	Hepatocyte	liver:	n/a
35	chr16:34432979-34433029	HMEC	breast:	n/a
36	chr16:34598029-34598079	NH-A	brain:	n/a
37	chr16:34587120-34587170	HMEC	breast:	n/a
38	chr16:34429609-34429659	HUVEC	blood vessel:	n/a
39	chr16:34596583-34596633	H1-hESC	embryonic stem cell:	embryo
40	chr16:34443120-34443170	SK-N-SH_RA	brain:	n/a
41	chr16:34712713-34712763	ECC-1	luminal epithelium:	n/a
42	chr16:34578819-34578869	A549	lung:	n/a
43	chr16:34660044-34660094	HCF	heart:	n/a
44	chr16:34659771-34659821	HL-60	blood:	n/a
45	chr16:34430905-34430955	AG09309	skin:	n/a
46	chr16:34663929-34663979	AG04449	skin:	fetal
47	chr16:34429609-34429659	U87	brain:	n/a
48	chr16:34428985-34429035	AoSMC	blood vessel:	n/a
49	chr16:34663929-34663979	HRPEpiC	eye:	n/a
50	chr16:34408014-34408064	CMK	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
2	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:
3	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:

(count:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
2	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
3	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
4	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
5	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
6	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
7	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
8	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
9	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
10	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
11	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
12	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142191
13	lnc-CTD-2144E22.5.1-5	chr16:34442308-34442392	ENSG00000260958.2
14	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
15	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
16	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
17	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
18	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
19	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
20	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
21	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
22	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
23	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
24	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
25	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
26	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
27	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
28	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
29	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
30	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
31	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
32	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
33	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
34	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
35	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
36	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
37	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
38	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
39	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
40	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
41	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
42	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
43	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
44	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
45	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
46	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
47	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
48	lnc-CTD-2144E22.5.1-6	chr16:34625678-34626084	NONHSAT142183
49	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
50	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2

No data

Variant related genes	Relation type
UBE2MP1	TF binding region
ENSG00000260073	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	TF binding region
ENSG00000261398	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
AGGF1P4	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000260590	TF binding region
ENSG00000261274	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
SLC25A1P4	TF binding region
RARRES2P9	TF binding region
ENSG00000264479	TF binding region
ENSG00000260427	TF binding region
ENSG00000260598	TF binding region
ENSG00000260958	TF binding region
ENSG00000259841	TF binding region
ENSG00000261711	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
UBE2MP1	CpG island
ENSG00000260073	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000261398	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
AGGF1P4	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000260590	CpG island
ENSG00000261274	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
SLC25A1P4	CpG island
RARRES2P9	CpG island
ENSG00000264479	CpG island
ENSG00000260427	CpG island
ENSG00000260598	CpG island
ENSG00000260958	CpG island
ENSG00000259841	CpG island
ENSG00000261711	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000261398	chromatin interactions
ENSG00000260073	chromatin interactions

Extended variants
information (count: 5510 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:5510 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs207475857	chr16:34403918-34403919	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs376447700	chr16:34403962-34403963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs550027453	chr16:34403965-34403966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568048991	chr16:34403966-34403967	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553599270	chr16:34403971-34403972	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs571914493	chr16:34403975-34403976	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs534260968	chr16:34403976-34403977	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs111444300	chr16:34403979-34403980	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs558801378	chr16:34403980-34403981	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs2170422	chr16:34403989-34403990	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544310123	chr16:34403995-34403996	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs549879501	chr16:34404006-34404007	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs545855022	chr16:34404080-34404081	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs564054509	chr16:34404092-34404093	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs530442470	chr16:34404328-34404329	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564199246	chr16:34404346-34404347	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs531352975	chr16:34404445-34404446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs543117936	chr16:34404464-34404465	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs561308734	chr16:34404512-34404513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528876619	chr16:34404539-34404540	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs7206496	chr16:34404560-34404561	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565866078	chr16:34404561-34404562	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs533136672	chr16:34404608-34404609	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs551331136	chr16:34404619-34404620	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
25	rs569833031	chr16:34404629-34404630	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
26	rs538299730	chr16:34404714-34404715	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
27	rs556707968	chr16:34404722-34404723	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
28	rs568435788	chr16:34404784-34404785	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
29	rs367614885	chr16:34404802-34404803	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
30	rs535878460	chr16:34404839-34404840	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs576901376	chr16:34405039-34405040	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs558022275	chr16:34405080-34405081	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs576589011	chr16:34405149-34405150	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs370596190	chr16:34405151-34405152	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs72810758	chr16:34405187-34405188	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs543529249	chr16:34405199-34405200	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs114297266	chr16:34405216-34405217	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs573464246	chr16:34405256-34405257	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs144138303	chr16:34405259-34405260	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs148280072	chr16:34405269-34405270	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs559055357	chr16:34405276-34405277	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs371098976	chr16:34405280-34405281	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs191366192	chr16:34405307-34405308	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs533028357	chr16:34405332-34405333	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs76282148	chr16:34405643-34405644	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs370169201	chr16:34405710-34405711	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs183724556	chr16:34405728-34405729	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs577580162	chr16:34405733-34405734	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs531565408	chr16:34405760-34405761	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs544944361	chr16:34405784-34405785	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
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
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	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
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	18414403	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34407600-34409200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:34408200-34409000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:34408400-34409000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:34409000-34410800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr16:34409200-34410600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr16:34410600-34411600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr16:34410800-34411600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr16:34411200-34411400	Enhancers	Right Atrium	heart
9	chr16:34415000-34419400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr16:34416200-34416400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr16:34416200-34417400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
12	chr16:34418800-34419400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
13	chr16:34419600-34422800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:34420000-34422200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr16:34420400-34420800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
16	chr16:34421000-34421200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr16:34423000-34423200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:34429200-34433000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr16:34429400-34429600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr16:34429400-34430400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:34432200-34433400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
26	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:34442200-34443000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr16:34442200-34443000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr16:34442600-34442800	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr16:34456000-34456800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:34456200-34456400	ZNF genes & repeats	Gastric	stomach
32	chr16:34456200-34456600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
41	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
43	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
44	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
45	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr16:34531200-34534000	Enhancers	HMEC	breast

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