Variant report

Variant	nsv1055703
Chromosome Location	chr16:32458388-33097410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4407)
CpG islands
(count:2747)
Chromatin interactive
region (count:5)
LncRNA
region (count:48)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4407 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
2	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
5	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
6	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
9	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
10	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
11	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
12	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
13	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
14	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
15	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
16	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
17	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
18	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
19	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
20	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
21	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
22	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
23	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
24	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
25	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
26	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
27	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr16:32652784-32652999	GM12878	blood:	n/a	n/a
29	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a
30	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
31	BATF	chr16:33042313-33042791	GM12878	blood:	n/a	n/a
32	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
33	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
34	BATF	chr16:33002452-33002671	GM12878	blood:	n/a	n/a
35	BATF	chr16:33052317-33052590	GM12878	blood:	n/a	n/a
36	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
37	BATF	chr16:33091390-33091661	GM12878	blood:	n/a	n/a
38	BATF	chr16:32727057-32727270	GM12878	blood:	n/a	n/a
39	BATF	chr16:32815984-32816173	GM12878	blood:	n/a	n/a
40	BATF	chr16:33046042-33046353	GM12878	blood:	n/a	n/a
41	BATF	chr16:33048704-33048907	GM12878	blood:	n/a	n/a
42	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
43	BATF	chr16:32799795-32800035	GM12878	blood:	n/a	n/a
44	BATF	chr16:33046034-33046402	GM12878	blood:	n/a	n/a
45	BATF	chr16:33044181-33044885	GM12878	blood:	n/a	chr16:33044727-33044738
46	BATF	chr16:33042432-33043800	GM12878	blood:	n/a	n/a
47	BATF	chr16:32801669-32801940	GM12878	blood:	n/a	n/a
48	BATF	chr16:33052311-33052561	GM12878	blood:	n/a	n/a
49	BATF	chr16:33051517-33051717	GM12878	blood:	n/a	n/a
50	BATF	chr16:33087718-33087908	GM12878	blood:	n/a	n/a

(count:2747 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32940983-32941033	AG04450	lung:	fetal
2	chr16:32857872-32857922	RPTEC	kidney:	n/a
3	chr16:32940983-32941033	AG04450	lung:	fetal
4	chr16:32857872-32857922	RPTEC	kidney:	n/a
5	chr16:32823000-32823050	HCF	heart:	n/a
6	chr16:32857872-32857922	A549	lung:	n/a
7	chr16:32822480-32822530	CMK	blood:	n/a
8	chr16:32823000-32823050	HRE	kidney:	n/a
9	chr16:32822480-32822530	NHBE	bronchial:	n/a
10	chr16:32820218-32820268	NT2-D1	testis:	n/a
11	chr16:32857007-32857057	NH-A	brain:	n/a
12	chr16:32937057-32937107	SK-N-MC	brain:	n/a
13	chr16:33044270-33044320	LNCaP	prostate:	n/a
14	chr16:33044270-33044320	HCM	heart:	n/a
15	chr16:33038657-33038707	HAEpiC	amniotic membrane:	n/a
16	chr16:32853952-32854002	AG04450	lung:	fetal
17	chr16:32857923-32857973	HCPEpiC	choroid plexus:	n/a
18	chr16:33038922-33038972	SAEC	small airway:	n/a
19	chr16:32822480-32822530	SK-N-SH_RA	brain:	n/a
20	chr16:32662543-32662593	U87	brain:	n/a
21	chr16:32822392-32822442	IMR90	lung:	fetal
22	chr16:32473096-32473146	Hepatocyte	liver:	n/a
23	chr16:33038922-33038972	HPAEpiC	pulmonary alveolar:	n/a
24	chr16:32937040-32937090	K562	blood:	n/a
25	chr16:32485636-32485686	GM12892	blood:	n/a
26	chr16:32937040-32937090	NH-A	brain:	n/a
27	chr16:32487825-32487875	Hepatocyte	liver:	n/a
28	chr16:32937040-32937090	HRCEpiC	kidney:	n/a
29	chr16:32853952-32854002	ECC-1	luminal epithelium:	n/a
30	chr16:32823289-32823339	K562	blood:	n/a
31	chr16:32493059-32493109	PFSK-1	brain:	n/a
32	chr16:32937057-32937107	HPAEpiC	pulmonary alveolar:	n/a
33	chr16:32822612-32822662	GM12891	blood:	n/a
34	chr16:32823000-32823050	AG10803	skin:	n/a
35	chr16:32486117-32486167	HMEC	breast:	n/a
36	chr16:32486334-32486384	HEEpiC	esophagus:	n/a
37	chr16:32485636-32485686	HEK293	kidney:	embryo
38	chr16:32895392-32895442	K562	blood:	n/a
39	chr16:32895392-32895442	MCF-7	breast:	n/a
40	chr16:32473096-32473146	AG09319	gingival:	n/a
41	chr16:32599417-32599467	RPTEC	kidney:	n/a
42	chr16:33006163-33006213	Hela-S3	cervix:	n/a
43	chr16:32822612-32822662	PANC-1	pancreas:	n/a
44	chr16:33044270-33044320	H1-hESC	embryonic stem cell:	embryo
45	chr16:32853952-32854002	HepG2	liver:	n/a
46	chr16:32485636-32485686	AoSMC	blood vessel:	n/a
47	chr16:32823584-32823634	Jurkat	blood:	n/a
48	chr16:32857347-32857397	HNPCEpiC	eye:	n/a
49	chr16:32857923-32857973	Jurkat	blood:	n/a
50	chr16:32823584-32823634	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
2	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
3	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
4	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
5	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:

(count:48 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC133485.1.1-3	chr16:32674902-32675277	ENSG00000261569.1
2	lnc-RP11-1277H1.1.1-9	chr16:32989910-32990212	NONHSAT142058
3	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
4	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
5	lnc-RP11-1277H1.1.1-3	chr16:33007600-33008091	ENSG00000260921.1
6	lnc-RP11-1277H1.1.1-3	chr16:33006858-33006938	ENSG00000260921.1
7	lnc-TP53TG3-11	chr16:32750948-32750981	NONHSAT142041
8	lnc-TP53TG3-17	chr16:32943089-32943890	NONHSAT142053
9	lnc-AC133485.1.1-2	chr16:32626287-32626324	NONHSAT142022
10	lnc-TP53TG3-11	chr16:32751296-32751487	NONHSAT142041
11	lnc-RP11-1277H1.1.1-3	chr16:33007112-33007188	ENSG00000260921.1
12	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
13	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
14	lnc-AC133485.1.1-4	chr16:32686358-32686427	ENSG00000260974.1
15	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898880	ENSG00000214614.2
16	lnc-AC133485.1.1-3	chr16:32676974-32677014	ENSG00000260311.1
17	lnc-AC133485.1.1-3	chr16:32661076-32661211	ENSG00000261569.1
18	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
19	lnc-TP53TG3-1	chr16:32752331-32752415	ENSG00000260845.1
20	lnc-TP53TG3-1	chr16:32747230-32748010	ENSG00000260845.1
21	lnc-AC133485.1.1-2	chr16:32611620-32611754	NONHSAT142021
22	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
23	lnc-AC133485.1.1-2	chr16:32613844-32613953	NONHSAT142021
24	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
25	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
26	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
27	lnc-AC133485.1.1-2	chr16:32619006-32619076	NONHSAT142022
28	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
29	lnc-AC133485.1.1-3	chr16:32677470-32677854	ENSG00000260311.1
30	lnc-TP53TG3-5	chr16:33054930-33055459	ENSG00000260141.1
31	lnc-AC133485.1.1-2	chr16:32618849-32619005	NONHSAT142021
32	lnc-AC133485.1.1-4	chr16:32689961-32690152	ENSG00000260974.1
33	lnc-RP11-1277H1.1.1-4	chr16:32897796-32898008	ENSG00000214614.2
34	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
35	lnc-AC133485.1.1-3	chr16:32661463-32661540	ENSG00000261569.1
36	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
37	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
38	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142022
39	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022
40	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
41	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
42	lnc-RP11-1277H1.1.1-4	chr16:32897547-32898093	ENSG00000214614.2
43	lnc-RP11-1277H1.1.1-11	chr16:32926395-32926440	NONHSAT142052
44	lnc-RP11-1277H1.1.1-9	chr16:32989782-32989827	NONHSAT142058
45	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
46	lnc-AC133485.1.1-3	chr16:32660514-32660649	ENSG00000261569.1
47	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
48	lnc-TP53TG3-2	chr16:32465933-32470079	ENSG00000261541.1

No data

Variant related genes	Relation type
IGHV3OR16-8	TF binding region
ENSG00000260864	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000261263	TF binding region
TP53TG3	TF binding region
ENSG00000259966	TF binding region
ENSG00000261108	TF binding region
ENSG00000261541	TF binding region
ENSG00000260610	TF binding region
ENSG00000260158	TF binding region
ENSG00000260662	TF binding region
IGHV3OR16-15	TF binding region
ENSG00000261719	TF binding region
ENSG00000261391	TF binding region
ENSG00000260974	TF binding region
ENSG00000261111	TF binding region
ENSG00000214614	TF binding region
IGHV3OR16-10	TF binding region
ENSG00000260047	TF binding region
SLC6A10P	TF binding region
ENSG00000261259	TF binding region
HERC2P5	TF binding region
IGHV1OR16-2	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261569	TF binding region
ENSG00000262187	TF binding region
ENSG00000260845	TF binding region
ENSG00000260921	TF binding region
ENSG00000259934	TF binding region
ABCD1P3	TF binding region
ENSG00000260900	TF binding region
IGHV1OR16-4	TF binding region
ENSG00000260311	TF binding region
IGHV3OR16-8	CpG island
ENSG00000260864	CpG island
IGHV2OR16-5	CpG island
ENSG00000261263	CpG island
TP53TG3	CpG island
ENSG00000259966	CpG island
ENSG00000261108	CpG island
ENSG00000261541	CpG island
ENSG00000260610	CpG island
ENSG00000260158	CpG island
ENSG00000260662	CpG island
IGHV3OR16-15	CpG island
ENSG00000261719	CpG island
ENSG00000261391	CpG island
ENSG00000260974	CpG island
ENSG00000261111	CpG island
ENSG00000214614	CpG island
IGHV3OR16-10	CpG island
ENSG00000260047	CpG island
SLC6A10P	CpG island
ENSG00000261259	CpG island
HERC2P5	CpG island
IGHV1OR16-2	CpG island
IGHV3OR16-6	CpG island
ENSG00000261569	CpG island
ENSG00000262187	CpG island
ENSG00000260845	CpG island
ENSG00000260921	CpG island
ENSG00000259934	CpG island
ABCD1P3	CpG island
ENSG00000260900	CpG island
IGHV1OR16-4	CpG island
ENSG00000260311	CpG island

Extended variants
information (count: 15792 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:15792 , 50 per page) page: 1 2 3 4 5 6 7 ... 316

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549694695	chr16:32465944-32465945	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs111733841	chr16:32465950-32465951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs76177225	chr16:32465968-32465969	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs567800399	chr16:32466006-32466007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs77424838	chr16:32466023-32466024	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187157780	chr16:32466043-32466044	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs3878595	chr16:32466064-32466065	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs546806288	chr16:32466079-32466080	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs571685531	chr16:32466080-32466081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs79977048	chr16:32466084-32466085	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs377402313	chr16:32466112-32466113	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs75514791	chr16:32466118-32466119	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs75108367	chr16:32466119-32466120	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs538662887	chr16:32466124-32466125	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs556895013	chr16:32466128-32466129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs201832039	chr16:32466129-32466130	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs200607703	chr16:32466132-32466133	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs201367577	chr16:32466137-32466138	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs202204209	chr16:32466178-32466179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs569619237	chr16:32466198-32466199	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs80059550	chr16:32466221-32466222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs373750643	chr16:32466226-32466227	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs536996760	chr16:32466244-32466245	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs80162701	chr16:32466253-32466254	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs79004787	chr16:32466260-32466261	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs2078837	chr16:32466268-32466269	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs2078838	chr16:32466271-32466272	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs28703023	chr16:32466293-32466294	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs555233227	chr16:32466298-32466299	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs573789140	chr16:32466316-32466317	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs139510677	chr16:32466345-32466346	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs74674534	chr16:32466356-32466357	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs552817006	chr16:32466423-32466424	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs577635298	chr16:32466431-32466432	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs545022405	chr16:32466443-32466444	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs200524808	chr16:32466444-32466445	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs563317318	chr16:32466467-32466468	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs530506742	chr16:32466468-32466469	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs192848585	chr16:32466476-32466477	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs561604644	chr16:32466487-32466488	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs187536276	chr16:32466508-32466509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs2135399	chr16:32466520-32466521	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs77921122	chr16:32466525-32466526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201003142	chr16:32466543-32466544	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs76575049	chr16:32466588-32466589	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs75585115	chr16:32466589-32466590	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs2335301	chr16:32466609-32466610	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs2335300	chr16:32466619-32466620	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs79036889	chr16:32466623-32466624	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs370935957	chr16:32466625-32466626	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	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
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Recurrent pregnancy loss	19789632	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Osteosarcoma	21215367	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	21509527	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32472800-32474200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr16:32473000-32473400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:32473200-32473600	Active TSS	K562	blood
4	chr16:32484200-32490000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:32484600-32485400	ZNF genes & repeats	Pancreas	Pancrea
6	chr16:32484600-32490200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr16:32486000-32488400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr16:32486400-32486600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
9	chr16:32486400-32488400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr16:32486600-32487400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr16:32487200-32488600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr16:32487400-32487600	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
13	chr16:32487600-32488200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr16:32488200-32488400	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr16:32489400-32489600	ZNF genes & repeats	Gastric	stomach
16	chr16:32494200-32494600	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr16:32494200-32499600	ZNF genes & repeats	Liver	Liver
18	chr16:32497400-32503200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr16:32500800-32501200	ZNF genes & repeats	Liver	Liver
20	chr16:32500800-32501400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr16:32500800-32501400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
22	chr16:32501400-32502200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr16:32502200-32504200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
24	chr16:32504600-32508200	ZNF genes & repeats	Liver	Liver
25	chr16:32505200-32505800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
26	chr16:32507000-32508000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:32507800-32508000	Bivalent/Poised TSS	Right Atrium	heart
28	chr16:32511200-32562600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
29	chr16:32513800-32526800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr16:32513800-32564000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr16:32513800-32572000	ZNF genes & repeats	Liver	Liver
32	chr16:32514600-32561200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr16:32515200-32518000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr16:32515200-32562800	ZNF genes & repeats	Adipose Nuclei	Adipose
35	chr16:32515400-32516000	ZNF genes & repeats	Psoas Muscle	Psoas
36	chr16:32515400-32518400	ZNF genes & repeats	Brain Substantia Nigra	brain
37	chr16:32515600-32517800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
38	chr16:32515600-32521600	ZNF genes & repeats	Brain Anterior Caudate	brain
39	chr16:32515800-32518400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr16:32516200-32521600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr16:32516200-32524200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
42	chr16:32516800-32517400	Active TSS	Aorta	Aorta
43	chr16:32517000-32517600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
44	chr16:32517400-32519000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
45	chr16:32518000-32518600	ZNF genes & repeats	Fetal Brain Male	brain
46	chr16:32518200-32519000	Active TSS	Right Atrium	heart
47	chr16:32520200-32520400	ZNF genes & repeats	Brain Substantia Nigra	brain
48	chr16:32520400-32523400	ZNF genes & repeats	Psoas Muscle	Psoas
49	chr16:32520600-32523600	ZNF genes & repeats	Fetal Brain Male	brain
50	chr16:32521000-32524200	ZNF genes & repeats	Brain Substantia Nigra	brain

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