Variant report

Variant	nsv1067251
Chromosome Location	chr16:32554227-33097410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3986)
CpG islands
(count:2259)
Chromatin interactive
region (count:5)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3986 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
3	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
6	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
8	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
9	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
10	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
11	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
12	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
13	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
14	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
15	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
16	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
17	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
18	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
19	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
21	BATF	chr16:33041862-33042137	GM12878	blood:	n/a	n/a
22	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
23	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
24	BATF	chr16:33043855-33044053	GM12878	blood:	n/a	n/a
25	BATF	chr16:32993933-32994319	GM12878	blood:	n/a	n/a
26	BATF	chr16:33082292-33082557	GM12878	blood:	n/a	n/a
27	BATF	chr16:33051517-33051717	GM12878	blood:	n/a	n/a
28	BATF	chr16:33092972-33093212	GM12878	blood:	n/a	n/a
29	BATF	chr16:33042432-33043800	GM12878	blood:	n/a	n/a
30	BATF	chr16:32805422-32805612	GM12878	blood:	n/a	n/a
31	BATF	chr16:33087718-33087908	GM12878	blood:	n/a	n/a
32	BATF	chr16:32801669-32801940	GM12878	blood:	n/a	n/a
33	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
34	BATF	chr16:33002463-33002715	GM12878	blood:	n/a	n/a
35	BATF	chr16:33044491-33044914	GM12878	blood:	n/a	chr16:33044727-33044738
36	BATF	chr16:33052317-33052590	GM12878	blood:	n/a	n/a
37	BATF	chr16:32727057-32727270	GM12878	blood:	n/a	n/a
38	BATF	chr16:33051640-33051829	GM12878	blood:	n/a	n/a
39	BATF	chr16:32805420-32805638	GM12878	blood:	n/a	n/a
40	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
41	BATF	chr16:32652782-32652951	GM12878	blood:	n/a	n/a
42	BATF	chr16:33048704-33048907	GM12878	blood:	n/a	n/a
43	BATF	chr16:33046034-33046402	GM12878	blood:	n/a	n/a
44	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
45	BATF	chr16:33052311-33052561	GM12878	blood:	n/a	n/a
46	BATF	chr16:33044181-33044885	GM12878	blood:	n/a	chr16:33044727-33044738
47	BATF	chr16:33091390-33091661	GM12878	blood:	n/a	n/a
48	BATF	chr16:33042934-33043504	GM12878	blood:	n/a	n/a
49	BATF	chr16:32800340-32800564	GM12878	blood:	n/a	n/a
50	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32934020-32934070	RPTEC	kidney:	n/a
2	chr16:32823000-32823050	GM12878	blood:	n/a
3	chr16:32934020-32934070	RPTEC	kidney:	n/a
4	chr16:32823000-32823050	GM12878	blood:	n/a
5	chr16:32936895-32936945	SK-N-SH	brain:	n/a
6	chr16:32937040-32937090	MCF-7	breast:	n/a
7	chr16:32823584-32823634	PFSK-1	brain:	n/a
8	chr16:33038922-33038972	HepG2	liver:	n/a
9	chr16:33040206-33040256	HAEpiC	amniotic membrane:	n/a
10	chr16:32936664-32936714	HL-60	blood:	n/a
11	chr16:32898433-32898483	HAEpiC	amniotic membrane:	n/a
12	chr16:33071657-33071707	GM12891	blood:	n/a
13	chr16:32822612-32822662	AG10803	skin:	n/a
14	chr16:33038922-33038972	H1-hESC	embryonic stem cell:	embryo
15	chr16:33071657-33071707	HEK293	kidney:	embryo
16	chr16:32857551-32857601	K562	blood:	n/a
17	chr16:33070632-33070682	ECC-1	luminal epithelium:	n/a
18	chr16:33038922-33038972	AoSMC	blood vessel:	n/a
19	chr16:32822392-32822442	HL-60	blood:	n/a
20	chr16:32599417-32599467	AG09309	skin:	n/a
21	chr16:32940983-32941033	HRCEpiC	kidney:	n/a
22	chr16:32822480-32822530	HIPEpiC	eye:	n/a
23	chr16:33039897-33039947	HL-60	blood:	n/a
24	chr16:32823000-32823050	PFSK-1	brain:	n/a
25	chr16:32823000-32823050	GM19239	blood:	n/a
26	chr16:33070632-33070682	NH-A	brain:	n/a
27	chr16:32823000-32823050	LNCaP	prostate:	n/a
28	chr16:33071657-33071707	HMEC	breast:	n/a
29	chr16:32858846-32858896	PFSK-1	brain:	n/a
30	chr16:32895392-32895442	HCT-116	colon:	n/a
31	chr16:33039897-33039947	HRCEpiC	kidney:	n/a
32	chr16:32858241-32858291	T-47D	breast:	n/a
33	chr16:32822480-32822530	AG09319	gingival:	n/a
34	chr16:32822392-32822442	IMR90	lung:	fetal
35	chr16:32898433-32898483	PrEC	prostate:	n/a
36	chr16:32662543-32662593	IMR90	lung:	fetal
37	chr16:32823584-32823634	NHDF-neo	bronchial:	n/a
38	chr16:33071657-33071707	SK-N-MC	brain:	n/a
39	chr16:32936664-32936714	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:32934020-32934070	HAEpiC	amniotic membrane:	n/a
41	chr16:32858241-32858291	A549	lung:	n/a
42	chr16:32823584-32823634	BE2_C	brain:	n/a
43	chr16:33038657-33038707	AG09309	skin:	n/a
44	chr16:33070632-33070682	HL-60	blood:	n/a
45	chr16:32857007-32857057	MCF10A-Er-Src	breast:	n/a
46	chr16:33039897-33039947	HAEpiC	amniotic membrane:	n/a
47	chr16:32822392-32822442	HIPEpiC	eye:	n/a
48	chr16:32895392-32895442	LNCaP	prostate:	n/a
49	chr16:32898433-32898483	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:33044270-33044320	GM12891	blood:	n/a

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

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

(count:47 , 50 per page) page: 1

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

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
ENSG00000260610	TF binding region
ENSG00000260158	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
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
ENSG00000260610	CpG island
ENSG00000260158	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
ENSG00000260900	CpG island
IGHV1OR16-4	CpG island
ENSG00000260311	CpG island

Extended variants
information (count: 10273 )
Associated
traits (count: 133 )

Variant overlapped rSNPs/rCNVs (count:10273 , 50 per page) page: 1 2 3 4 5 6 7 ... 206

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548609307	chr16:32554238-32554239	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs560479617	chr16:32554253-32554254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs528407907	chr16:32554267-32554268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs546886769	chr16:32554271-32554272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs142875489	chr16:32554319-32554320	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs113290099	chr16:32554320-32554321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs571542679	chr16:32554330-32554331	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs77852414	chr16:32554331-32554332	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs34756831	chr16:32554356-32554357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs4106210	chr16:32554364-32554365	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs113739466	chr16:32554389-32554390	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs550492028	chr16:32554409-32554410	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs568980427	chr16:32554416-32554417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs535920064	chr16:32554444-32554445	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs4045332	chr16:32554452-32554453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs3969554	chr16:32554486-32554487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs554159514	chr16:32554499-32554500	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs572478714	chr16:32554507-32554508	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs533524640	chr16:32554510-32554511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs558858259	chr16:32554512-32554513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs4045330	chr16:32554545-32554546	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs577461050	chr16:32554558-32554559	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs544839906	chr16:32554570-32554571	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs55711349	chr16:32554578-32554579	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs574883079	chr16:32554588-32554589	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs542307187	chr16:32554624-32554625	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs560495363	chr16:32554652-32554653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs76672705	chr16:32554653-32554654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs377616940	chr16:32554658-32554659	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs2520044	chr16:32554672-32554673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs552587846	chr16:32554679-32554680	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs565224085	chr16:32554688-32554689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs532301184	chr16:32554689-32554690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs375147107	chr16:32554714-32554715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs568924497	chr16:32554729-32554730	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs2335648	chr16:32554730-32554731	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs2878476	chr16:32554733-32554734	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs2335647	chr16:32554753-32554754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs2878475	chr16:32554764-32554765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs535964710	chr16:32554769-32554770	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs78738000	chr16:32554790-32554791	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs2335646	chr16:32554823-32554824	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs2335645	chr16:32554843-32554844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs2335644	chr16:32554859-32554860	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs72483491	chr16:32554873-32554874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs149298562	chr16:32554888-32554889	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs74577121	chr16:32554889-32554890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs75005954	chr16:32554902-32554903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs58088096	chr16:32554903-32554904	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs77937429	chr16:32554966-32554967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:133)

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
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
Breast cancer	21364760	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	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:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32511200-32562600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr16:32513800-32564000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr16:32513800-32572000	ZNF genes & repeats	Liver	Liver
4	chr16:32514600-32561200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr16:32515200-32562800	ZNF genes & repeats	Adipose Nuclei	Adipose
6	chr16:32529400-32570400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
7	chr16:32536800-32565200	ZNF genes & repeats	Psoas Muscle	Psoas
8	chr16:32544800-32555200	ZNF genes & repeats	Fetal Brain Male	brain
9	chr16:32545800-32554600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr16:32551200-32559000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
11	chr16:32551800-32555000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
12	chr16:32552200-32555200	ZNF genes & repeats	Brain Anterior Caudate	brain
13	chr16:32552600-32556200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:32552800-32558400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
15	chr16:32554000-32558400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr16:32554200-32561400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
17	chr16:32555800-32556200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr16:32556200-32560200	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
19	chr16:32557200-32562200	ZNF genes & repeats	Fetal Brain Male	brain
20	chr16:32557600-32558600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr16:32557600-32560800	Active TSS	Right Atrium	heart
22	chr16:32557800-32558200	Active TSS	Aorta	Aorta
23	chr16:32557800-32558600	ZNF genes & repeats	Primary T cells from cord blood	blood
24	chr16:32558200-32566800	Weak transcription	Aorta	Aorta
25	chr16:32559200-32562600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
26	chr16:32559600-32561000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
27	chr16:32559600-32562800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr16:32559800-32560800	ZNF genes & repeats	Brain Angular Gyrus	brain
29	chr16:32559800-32561400	ZNF genes & repeats	Brain Substantia Nigra	brain
30	chr16:32560000-32560200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr16:32560000-32560200	ZNF genes & repeats	HMEC	breast
32	chr16:32560000-32560200	ZNF genes & repeats	HSMM	muscle
33	chr16:32560000-32560200	ZNF genes & repeats	HSMMtube	muscle
34	chr16:32560000-32560200	ZNF genes & repeats	HUVEC	blood vessel
35	chr16:32560000-32560200	ZNF genes & repeats	NHLF	lung
36	chr16:32561000-32562200	ZNF genes & repeats	Colon Smooth Muscle	Colon
37	chr16:32561800-32562000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
38	chr16:32566400-32567400	ZNF genes & repeats	Psoas Muscle	Psoas
39	chr16:32566800-32567600	Active TSS	Aorta	Aorta
40	chr16:32567200-32569800	ZNF genes & repeats	Brain Substantia Nigra	brain
41	chr16:32568000-32570400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr16:32569200-32572200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr16:32569800-32571400	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr16:32569800-32572200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr16:32570200-32572200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr16:32570800-32572200	ZNF genes & repeats	Fetal Brain Male	brain
47	chr16:32574400-32574600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr16:32575200-32578000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:32576000-32581200	ZNF genes & repeats	Liver	Liver
50	chr16:32576200-32577000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell

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