Variant report

Variant	nsv1061635
Chromosome Location	chr16:32208734-32950241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4082)
CpG islands
(count:4399)
Chromatin interactive
region (count:2)
LncRNA
region (count:59)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4082 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32345726-32345816	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
6	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
7	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:32295698-32295892	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
11	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
12	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
13	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
14	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
15	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
16	ATF1	chr16:32363593-32363793	K562	blood:	n/a	n/a
17	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
18	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
19	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
20	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
21	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
22	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
23	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
24	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
25	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
26	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
27	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
28	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
29	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr16:32805422-32805612	GM12878	blood:	n/a	n/a
31	BATF	chr16:32727057-32727270	GM12878	blood:	n/a	n/a
32	BATF	chr16:32451259-32451478	GM12878	blood:	n/a	n/a
33	BATF	chr16:32333643-32333817	GM12878	blood:	n/a	n/a
34	BATF	chr16:32799795-32800035	GM12878	blood:	n/a	n/a
35	BATF	chr16:32361068-32361342	GM12878	blood:	n/a	n/a
36	BATF	chr16:32366962-32367454	GM12878	blood:	n/a	chr16:32367243-32367254
37	BATF	chr16:32801669-32801940	GM12878	blood:	n/a	n/a
38	BATF	chr16:32368458-32368823	GM12878	blood:	n/a	n/a
39	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
40	BATF	chr16:32335047-32335307	GM12878	blood:	n/a	n/a
41	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
42	BATF	chr16:32815984-32816173	GM12878	blood:	n/a	n/a
43	BATF	chr16:32652782-32652951	GM12878	blood:	n/a	n/a
44	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
45	BATF	chr16:32652784-32652999	GM12878	blood:	n/a	n/a
46	BATF	chr16:32373029-32373235	GM12878	blood:	n/a	n/a
47	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
48	BATF	chr16:32368414-32368848	GM12878	blood:	n/a	n/a
49	BATF	chr16:32805420-32805638	GM12878	blood:	n/a	n/a
50	BATF	chr16:32435147-32435451	GM12878	blood:	n/a	n/a

(count:4399 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32489820-32489870	AoSMC	blood vessel:	n/a
2	chr16:32485636-32485686	ovcar-3	ovarian:	n/a
3	chr16:32936895-32936945	HEEpiC	esophagus:	n/a
4	chr16:32486117-32486167	HMEC	breast:	n/a
5	chr16:32937040-32937090	AG04449	skin:	fetal
6	chr16:32936895-32936945	NHBE	bronchial:	n/a
7	chr16:32937057-32937107	MCF10A-Er-Src	breast:	n/a
8	chr16:32489820-32489870	AoSMC	blood vessel:	n/a
9	chr16:32485636-32485686	ovcar-3	ovarian:	n/a
10	chr16:32936895-32936945	HEEpiC	esophagus:	n/a
11	chr16:32486117-32486167	HMEC	breast:	n/a
12	chr16:32937040-32937090	AG04449	skin:	fetal
13	chr16:32936895-32936945	NHBE	bronchial:	n/a
14	chr16:32937057-32937107	MCF10A-Er-Src	breast:	n/a
15	chr16:32289757-32289807	Hepatocyte	liver:	n/a
16	chr16:32452725-32452775	HIPEpiC	eye:	n/a
17	chr16:32355981-32356031	SK-N-SH_RA	brain:	n/a
18	chr16:32265041-32265091	AG04450	lung:	fetal
19	chr16:32214185-32214235	HPAEpiC	pulmonary alveolar:	n/a
20	chr16:32822612-32822662	SK-N-MC	brain:	n/a
21	chr16:32252365-32252415	HEK293	kidney:	embryo
22	chr16:32288799-32288849	NH-A	brain:	n/a
23	chr16:32486334-32486384	AG10803	skin:	n/a
24	chr16:32359536-32359586	MCF10A-Er-Src	breast:	n/a
25	chr16:32857551-32857601	HMEC	breast:	n/a
26	chr16:32360428-32360478	SKMC	muscle:	n/a
27	chr16:32858846-32858896	GM12878	blood:	n/a
28	chr16:32857872-32857922	HCF	heart:	n/a
29	chr16:32934020-32934070	PFSK-1	brain:	n/a
30	chr16:32599433-32599483	NB4	blood:	n/a
31	chr16:32289757-32289807	GM19239	blood:	n/a
32	chr16:32360419-32360469	HEEpiC	esophagus:	n/a
33	chr16:32822612-32822662	ovcar-3	ovarian:	n/a
34	chr16:32252365-32252415	SK-N-SH_RA	brain:	n/a
35	chr16:32934020-32934070	AG09319	gingival:	n/a
36	chr16:32659887-32659937	NT2-D1	testis:	n/a
37	chr16:32940983-32941033	AG10803	skin:	n/a
38	chr16:32822392-32822442	HAEpiC	amniotic membrane:	n/a
39	chr16:32213913-32213963	NH-A	brain:	n/a
40	chr16:32276952-32277002	NHBE	bronchial:	n/a
41	chr16:32822612-32822662	AG10803	skin:	n/a
42	chr16:32359756-32359806	HepG2	liver:	n/a
43	chr16:32857923-32857973	NB4	blood:	n/a
44	chr16:32940983-32941033	NHBE	bronchial:	n/a
45	chr16:32486117-32486167	GM12891	blood:	n/a
46	chr16:32360428-32360478	HCM	heart:	n/a
47	chr16:32822392-32822442	SK-N-SH	brain:	n/a
48	chr16:32255825-32255875	HepG2	liver:	n/a
49	chr16:32290281-32290331	AG09309	skin:	n/a
50	chr16:32857347-32857397	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
2	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:

(count:59 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53TG3-4	chr16:32275068-32275108	ENSG00000260402.1
2	lnc-TP53TG3-7	chr16:32261941-32262132	ENSG00000260575.1
3	lnc-AC133485.1.1-8	chr16:32403379-32403556	NONHSAT142015
4	lnc-TP53TG3-2	chr16:32465933-32470079	ENSG00000261541.1
5	lnc-AC133485.1.1-2	chr16:32613844-32613953	NONHSAT142021
6	lnc-TP53TG3-16	chr16:32450390-32451887	NONHSAT142016
7	lnc-TP53TG3-3	chr16:32334099-32334218	XLOC_011921
8	lnc-RP11-1277H1.1.1-11	chr16:32926395-32926440	NONHSAT142052
9	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
10	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
11	lnc-AC133485.1.1-3	chr16:32677470-32677854	ENSG00000260311.1
12	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
13	lnc-RP11-1277H1.1.1-4	chr16:32897796-32898008	ENSG00000214614.2
14	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
15	lnc-TP53TG3-1	chr16:32747230-32748010	ENSG00000260845.1
16	lnc-AC133485.1.1-2	chr16:32626287-32626324	NONHSAT142022
17	lnc-TP53TG3-7	chr16:32265674-32265743	ENSG00000260575.1
18	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
19	lnc-RP11-1277H1.1.1-4	chr16:32897547-32898093	ENSG00000214614.2
20	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
21	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
22	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
23	lnc-AC133485.1.1-8	chr16:32416298-32416473	NONHSAT142015
24	lnc-TP53TG3-11	chr16:32751296-32751487	NONHSAT142041
25	lnc-AC133485.1.1-4	chr16:32686358-32686427	ENSG00000260974.1
26	lnc-AC133485.1.1-8	chr16:32443002-32443139	NONHSAT142015
27	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
28	lnc-AC133485.1.1-2	chr16:32619006-32619076	NONHSAT142022
29	lnc-AC133485.1.1-8	chr16:32442004-32442108	NONHSAT142015
30	lnc-AC133485.1.1-3	chr16:32660514-32660649	ENSG00000261569.1
31	lnc-TP53TG3-3	chr16:32335100-32335382	XLOC_011921
32	lnc-TP53TG3-1	chr16:32752331-32752415	ENSG00000260845.1
33	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022
34	lnc-TP53TG3-16	chr16:32452294-32452480	NONHSAT142016
35	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
36	lnc-TP53TG3-17	chr16:32943089-32943890	NONHSAT142053
37	lnc-AC133485.1.1-3	chr16:32674902-32675277	ENSG00000261569.1
38	lnc-AC133485.1.1-8	chr16:32447309-32447521	NONHSAT142015
39	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
40	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
41	lnc-AC133485.1.1-4	chr16:32689961-32690152	ENSG00000260974.1
42	lnc-AC133485.1.1-8	chr16:32402131-32402273	NONHSAT142015
43	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
44	lnc-AC133485.1.1-2	chr16:32611620-32611754	NONHSAT142021
45	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
46	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
47	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
48	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142022
49	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
50	lnc-AC133485.1.1-3	chr16:32661463-32661540	ENSG00000261569.1

No data

Variant related genes	Relation type
ENSG00000260864	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000261263	TF binding region
TP53TG3	TF binding region
ENSG00000259966	TF binding region
ENSG00000260540	TF binding region
ENSG00000261108	TF binding region
ENSG00000261541	TF binding region
ENSG00000260402	TF binding region
ENSG00000260610	TF binding region
ENSG00000260158	TF binding region
ENSG00000260662	TF binding region
ENSG00000260575	TF binding region
IGHV3OR16-15	TF binding region
ENSG00000259822	TF binding region
ENSG00000261719	TF binding region
ENSG00000261391	TF binding region
ENSG00000260974	TF binding region
ENSG00000261111	TF binding region
ENSG00000214614	TF binding region
ENSG00000260047	TF binding region
ENSG00000260344	TF binding region
TP53TG3D	TF binding region
SLC6A10P	TF binding region
ENSG00000261127	TF binding region
HERC2P5	TF binding region
ACTR3BP3	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261569	TF binding region
ENSG00000262187	TF binding region
ENSG00000260845	TF binding region
ENSG00000260866	TF binding region
ENSG00000259934	TF binding region
ABCD1P3	TF binding region
PABPC1P13	TF binding region
ENSG00000260516	TF binding region
ENSG00000260311	TF binding region
ENSG00000260864	CpG island
IGHV2OR16-5	CpG island
ENSG00000261263	CpG island
TP53TG3	CpG island
ENSG00000259966	CpG island
ENSG00000260540	CpG island
ENSG00000261108	CpG island
ENSG00000261541	CpG island
ENSG00000260402	CpG island
ENSG00000260610	CpG island
ENSG00000260158	CpG island
ENSG00000260662	CpG island
ENSG00000260575	CpG island
IGHV3OR16-15	CpG island
ENSG00000259822	CpG island
ENSG00000261719	CpG island
ENSG00000261391	CpG island
ENSG00000260974	CpG island
ENSG00000261111	CpG island
ENSG00000214614	CpG island
ENSG00000260047	CpG island
ENSG00000260344	CpG island
TP53TG3D	CpG island
SLC6A10P	CpG island
ENSG00000261127	CpG island
HERC2P5	CpG island
ACTR3BP3	CpG island
IGHV3OR16-6	CpG island
ENSG00000261569	CpG island
ENSG00000262187	CpG island
ENSG00000260845	CpG island
ENSG00000260866	CpG island
ENSG00000259934	CpG island
ABCD1P3	CpG island
PABPC1P13	CpG island
ENSG00000260516	CpG island
ENSG00000260311	CpG island
LBR	miRNA target sites

Extended variants
information (count: 17423 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:17423 , 50 per page) page: 1 2 3 4 5 6 7 ... 349

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113701593	chr16:32211141-32211142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62043461	chr16:32211185-32211186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs150012	chr16:32211206-32211207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555756959	chr16:32214007-32214008	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370047186	chr16:32214010-32214011	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111332501	chr16:32214054-32214055	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541752701	chr16:32214103-32214104	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560434720	chr16:32214105-32214106	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527477441	chr16:32214123-32214124	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111681640	chr16:32214126-32214127	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191701581	chr16:32214145-32214146	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs62043482	chr16:32226443-32226444	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs371590136	chr16:32226684-32226685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs576488371	chr16:32227221-32227222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs543865428	chr16:32227235-32227236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs555499000	chr16:32227239-32227240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs574638764	chr16:32227246-32227247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs541764825	chr16:32227247-32227248	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374055429	chr16:32228906-32228907	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs150018	chr16:32228980-32228981	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs367966186	chr16:32229008-32229009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372445114	chr16:32229058-32229059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs547778784	chr16:32229084-32229085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs578152692	chr16:32256606-32256607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377118010	chr16:32256693-32256694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546557840	chr16:32257439-32257440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201195970	chr16:32257482-32257483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs28564277	chr16:32257485-32257486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551702823	chr16:32257506-32257507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76175912	chr16:32257509-32257510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569733702	chr16:32257535-32257536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537276587	chr16:32257562-32257563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375499320	chr16:32257574-32257575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542988672	chr16:32259306-32259307	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs201434040	chr16:32259307-32259308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs188378176	chr16:32259314-32259315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs546356654	chr16:32259322-32259323	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs571293362	chr16:32259327-32259328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs543206646	chr16:32259888-32259889	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs113760463	chr16:32259919-32259920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs544381891	chr16:32259944-32259945	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs556517305	chr16:32259947-32259948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369085295	chr16:32259965-32259966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs574926378	chr16:32260053-32260054	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs185351677	chr16:32260068-32260069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs371945031	chr16:32260084-32260085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542927384	chr16:32260155-32260156	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs62043557	chr16:32260209-32260210	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs573197769	chr16:32260235-32260236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs58558661	chr16:32260708-32260709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
Breast cancer	21509527	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
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	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	18451855	CNVD
Breast cancer	22522925	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32214000-32214200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr16:32214000-32214200	Enhancers	Placenta	Placenta
3	chr16:32256600-32256800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr16:32257400-32257600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr16:32264200-32266000	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr16:32264400-32265000	Active TSS	Rectal Mucosa Donor 29	rectum
7	chr16:32264400-32265800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr16:32264800-32265000	Active TSS	Primary T cells fromperipheralblood	blood
9	chr16:32264800-32265000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:32264800-32265200	Active TSS	Brain Hippocampus Middle	brain
11	chr16:32264800-32265200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
12	chr16:32264800-32265200	Active TSS	HSMMtube	muscle
13	chr16:32264800-32265200	Active TSS	Osteobl	bone
14	chr16:32264800-32265800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
15	chr16:32264800-32265800	Active TSS	Primary B cells from peripheral blood	blood
16	chr16:32264800-32265800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr16:32264800-32265800	Active TSS	Ovary	ovary
18	chr16:32264800-32265800	Active TSS	Right Atrium	heart
19	chr16:32264800-32265800	Active TSS	Dnd41	blood
20	chr16:32264800-32266000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr16:32264800-32266000	Active TSS	Adipose Nuclei	Adipose
22	chr16:32264800-32266000	Active TSS	Brain Anterior Caudate	brain
23	chr16:32264800-32266000	Active TSS	Brain Cingulate Gyrus	brain
24	chr16:32264800-32266000	Active TSS	Placenta	Placenta
25	chr16:32264800-32266000	Active TSS	HSMM	muscle
26	chr16:32264800-32266000	Active TSS	K562	blood
27	chr16:32264800-32266200	Active TSS	A549	lung
28	chr16:32265000-32265200	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
29	chr16:32265000-32266000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr16:32265200-32265600	Active TSS	Primary T cells fromperipheralblood	blood
31	chr16:32265600-32265800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:32265600-32265800	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
33	chr16:32265600-32266000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr16:32265600-32266000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr16:32265600-32266000	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr16:32265600-32266000	Active TSS	Esophagus	oesophagus
37	chr16:32265600-32266000	Active TSS	Left Ventricle	heart
38	chr16:32265600-32266000	Active TSS	Rectal Smooth Muscle	rectum
39	chr16:32265600-32266000	Active TSS	Stomach Smooth Muscle	stomach
40	chr16:32265800-32266000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr16:32265800-32266000	Flanking Active TSS	Primary B cells from peripheral blood	blood
42	chr16:32265800-32266000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
43	chr16:32265800-32266000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr16:32265800-32266000	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr16:32265800-32266000	Flanking Active TSS	Dnd41	blood
46	chr16:32266000-32266200	Enhancers	Dnd41	blood
47	chr16:32282200-32282600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr16:32289800-32290200	Enhancers	Pancreas	Pancrea
49	chr16:32289800-32290200	Active TSS	Right Atrium	heart
50	chr16:32289800-32290200	Active TSS	Osteobl	bone

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