Variant report

Variant	nsv1058508
Chromosome Location	chr16:32158595-32879772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3835)
CpG islands
(count:4217)
Chromatin interactive
region (count:2)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3835 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32345726-32345816	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
3	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:32295698-32295892	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
9	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
11	ATF1	chr16:32194699-32194908	K562	blood:	n/a	n/a
12	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
13	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
14	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
15	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
16	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
17	ATF1	chr16:32363593-32363793	K562	blood:	n/a	n/a
18	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
19	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
20	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
21	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
22	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
23	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
24	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
25	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
26	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
27	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
28	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
29	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr16:32335083-32335294	GM12878	blood:	n/a	n/a
31	BATF	chr16:32368458-32368823	GM12878	blood:	n/a	n/a
32	BATF	chr16:32800340-32800564	GM12878	blood:	n/a	n/a
33	BATF	chr16:32333643-32333817	GM12878	blood:	n/a	n/a
34	BATF	chr16:32435147-32435451	GM12878	blood:	n/a	n/a
35	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
36	BATF	chr16:32451259-32451478	GM12878	blood:	n/a	n/a
37	BATF	chr16:32373029-32373235	GM12878	blood:	n/a	n/a
38	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
39	BATF	chr16:32361068-32361342	GM12878	blood:	n/a	n/a
40	BATF	chr16:32815984-32816173	GM12878	blood:	n/a	n/a
41	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
42	BATF	chr16:32801669-32801940	GM12878	blood:	n/a	n/a
43	BATF	chr16:32805420-32805638	GM12878	blood:	n/a	n/a
44	BATF	chr16:32727057-32727270	GM12878	blood:	n/a	n/a
45	BATF	chr16:32805422-32805612	GM12878	blood:	n/a	n/a
46	BATF	chr16:32652784-32652999	GM12878	blood:	n/a	n/a
47	BATF	chr16:32368414-32368848	GM12878	blood:	n/a	n/a
48	BATF	chr16:32652782-32652951	GM12878	blood:	n/a	n/a
49	BATF	chr16:32366962-32367454	GM12878	blood:	n/a	chr16:32367243-32367254
50	BATF	chr16:32799795-32800035	GM12878	blood:	n/a	n/a

(count:4217 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32165196-32165246	SKMC	muscle:	n/a
2	chr16:32858241-32858291	PANC-1	pancreas:	n/a
3	chr16:32290281-32290331	AG09319	gingival:	n/a
4	chr16:32858241-32858291	GM12891	blood:	n/a
5	chr16:32857923-32857973	HMEC	breast:	n/a
6	chr16:32452502-32452552	NT2-D1	testis:	n/a
7	chr16:32360338-32360388	HPAEpiC	pulmonary alveolar:	n/a
8	chr16:32178973-32179023	NHDF-neo	bronchial:	n/a
9	chr16:32165196-32165246	SKMC	muscle:	n/a
10	chr16:32858241-32858291	PANC-1	pancreas:	n/a
11	chr16:32290281-32290331	AG09319	gingival:	n/a
12	chr16:32858241-32858291	GM12891	blood:	n/a
13	chr16:32857923-32857973	HMEC	breast:	n/a
14	chr16:32452502-32452552	NT2-D1	testis:	n/a
15	chr16:32360338-32360388	HPAEpiC	pulmonary alveolar:	n/a
16	chr16:32178973-32179023	NHDF-neo	bronchial:	n/a
17	chr16:32305114-32305164	PANC-1	pancreas:	n/a
18	chr16:32486334-32486384	SK-N-MC	brain:	n/a
19	chr16:32662543-32662593	HRE	kidney:	n/a
20	chr16:32289928-32289978	HMEC	breast:	n/a
21	chr16:32289928-32289978	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:32359673-32359723	HIPEpiC	eye:	n/a
23	chr16:32820218-32820268	NHDF-neo	bronchial:	n/a
24	chr16:32326062-32326112	AG04450	lung:	fetal
25	chr16:32659887-32659937	K562	blood:	n/a
26	chr16:32212399-32212449	Hepatocyte	liver:	n/a
27	chr16:32452502-32452552	NH-A	brain:	n/a
28	chr16:32290371-32290421	A549	lung:	n/a
29	chr16:32485636-32485686	HAEpiC	amniotic membrane:	n/a
30	chr16:32359673-32359723	GM12892	blood:	n/a
31	chr16:32330265-32330315	H1-hESC	embryonic stem cell:	embryo
32	chr16:32487825-32487875	CMK	blood:	n/a
33	chr16:32452725-32452775	PrEC	prostate:	n/a
34	chr16:32276952-32277002	BE2_C	brain:	n/a
35	chr16:32599433-32599483	A549	lung:	n/a
36	chr16:32359673-32359723	SK-N-SH	brain:	n/a
37	chr16:32214185-32214235	HAEpiC	amniotic membrane:	n/a
38	chr16:32857551-32857601	Hepatocyte	liver:	n/a
39	chr16:32165196-32165246	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:32858846-32858896	Hepatocyte	liver:	n/a
41	chr16:32165153-32165203	HepG2	liver:	n/a
42	chr16:32823584-32823634	BJ	skin:	n/a
43	chr16:32486334-32486384	GM12878	blood:	n/a
44	chr16:32255825-32255875	HCM	heart:	n/a
45	chr16:32853952-32854002	HIPEpiC	eye:	n/a
46	chr16:32288799-32288849	HEEpiC	esophagus:	n/a
47	chr16:32289757-32289807	PFSK-1	brain:	n/a
48	chr16:32822612-32822662	CMK	blood:	n/a
49	chr16:32322028-32322078	GM12878	blood:	n/a
50	chr16:32452725-32452775	AG10803	skin:	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:50 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53TG3-1	chr16:32747230-32748010	ENSG00000260845.1
2	lnc-TP53TG3-2	chr16:32465933-32470079	ENSG00000261541.1
3	lnc-AC133485.1.1-8	chr16:32402131-32402273	NONHSAT142015
4	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022
5	lnc-AC133485.1.1-8	chr16:32443002-32443139	NONHSAT142015
6	lnc-TP53TG3-7	chr16:32265674-32265743	ENSG00000260575.1
7	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
8	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
9	lnc-AC133485.1.1-3	chr16:32661463-32661540	ENSG00000261569.1
10	lnc-AC133485.1.1-8	chr16:32399456-32399634	NONHSAT142015
11	lnc-TP53TG3-11	chr16:32750948-32750981	NONHSAT142041
12	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
13	lnc-TP53TG3-16	chr16:32450390-32451887	NONHSAT142016
14	lnc-AC133485.1.1-3	chr16:32676974-32677014	ENSG00000260311.1
15	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
16	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142022
17	lnc-TP53TG3-4	chr16:32274229-32274612	ENSG00000260402.1
18	lnc-AC133485.1.1-3	chr16:32674902-32675277	ENSG00000261569.1
19	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
20	lnc-AC133485.1.1-7	chr16:32200583-32200802	NONHSAT141994
21	lnc-AC133485.1.1-8	chr16:32403379-32403556	NONHSAT142015
22	lnc-AC133485.1.1-8	chr16:32416298-32416473	NONHSAT142015
23	lnc-TP53TG3-4	chr16:32275068-32275108	ENSG00000260402.1
24	lnc-TP53TG3-16	chr16:32452294-32452480	NONHSAT142016
25	lnc-AC133485.1.1-1	chr16:32204071-32204851	ENSG00000260847.1
26	lnc-TP53TG3-3	chr16:32335100-32335382	XLOC_011921
27	lnc-TP53TG3-11	chr16:32751296-32751487	NONHSAT142041
28	lnc-AC133485.1.1-4	chr16:32686358-32686427	ENSG00000260974.1
29	lnc-AC133485.1.1-2	chr16:32619006-32619076	NONHSAT142022
30	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
31	lnc-AC133485.1.1-3	chr16:32660514-32660649	ENSG00000261569.1
32	lnc-TP53TG3-3	chr16:32334099-32334218	XLOC_011921
33	lnc-AC133485.1.1-8	chr16:32442004-32442108	NONHSAT142015
34	lnc-TP53TG3-7	chr16:32261941-32262132	ENSG00000260575.1
35	lnc-AC133485.1.1-2	chr16:32613844-32613953	NONHSAT142021
36	lnc-AC133485.1.1-2	chr16:32611620-32611754	NONHSAT142021
37	lnc-AC133485.1.1-2	chr16:32618849-32619005	NONHSAT142021
38	lnc-AC133485.1.1-4	chr16:32689961-32690152	ENSG00000260974.1
39	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
40	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
41	lnc-AC133485.1.1-2	chr16:32626287-32626324	NONHSAT142022
42	lnc-AC133485.1.1-8	chr16:32438035-32438184	NONHSAT142015
43	lnc-AC133485.1.1-8	chr16:32447309-32447521	NONHSAT142015
44	lnc-AC133485.1.1-3	chr16:32677470-32677854	ENSG00000260311.1
45	lnc-TP53TG3-1	chr16:32752331-32752415	ENSG00000260845.1
46	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
47	lnc-AC133485.1.1-1	chr16:32199654-32199738	ENSG00000260847.1
48	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
49	lnc-AC133485.1.1-3	chr16:32661076-32661211	ENSG00000261569.1
50	lnc-AC133485.1.1-8	chr16:32437097-32437203	NONHSAT142015

No data

Variant related genes	Relation type
ENSG00000260864	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000261111	TF binding region
ENSG00000261263	TF binding region
TP53TG3	TF binding region
ENSG00000260047	TF binding region
ENSG00000259966	TF binding region
ENSG00000260540	TF binding region
ENSG00000260344	TF binding region
TP53TG3D	TF binding region
ENSG00000261108	TF binding region
ENSG00000261541	TF binding region
ENSG00000260402	TF binding region
ENSG00000261127	TF binding region
ENSG00000260649	TF binding region
HERC2P5	TF binding region
ACTR3BP3	TF binding region
ENSG00000260158	TF binding region
ENSG00000260662	TF binding region
ENSG00000260575	TF binding region
ENSG00000259822	TF binding region
HERC2P4	TF binding region
ENSG00000261569	TF binding region
ENSG00000261719	TF binding region
ENSG00000261391	TF binding region
ENSG00000260847	TF binding region
ENSG00000260974	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
ENSG00000261111	CpG island
ENSG00000261263	CpG island
TP53TG3	CpG island
ENSG00000260047	CpG island
ENSG00000259966	CpG island
ENSG00000260540	CpG island
ENSG00000260344	CpG island
TP53TG3D	CpG island
ENSG00000261108	CpG island
ENSG00000261541	CpG island
ENSG00000260402	CpG island
ENSG00000261127	CpG island
ENSG00000260649	CpG island
HERC2P5	CpG island
ACTR3BP3	CpG island
ENSG00000260158	CpG island
ENSG00000260662	CpG island
ENSG00000260575	CpG island
ENSG00000259822	CpG island
HERC2P4	CpG island
ENSG00000261569	CpG island
ENSG00000261719	CpG island
ENSG00000261391	CpG island
ENSG00000260847	CpG island
ENSG00000260974	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: 17518 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:17518 , 50 per page) page: 1 2 3 4 5 6 7 ... 351

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553539019	chr16:32163842-32163843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs572149705	chr16:32163935-32163936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs468566	chr16:32163940-32163941	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs545470032	chr16:32163944-32163945	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs564140145	chr16:32163948-32163949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs372396120	chr16:32163949-32163950	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180980462	chr16:32163956-32163957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs543676765	chr16:32164009-32164010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs58456141	chr16:32164030-32164031	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562055298	chr16:32164040-32164041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs529402350	chr16:32164061-32164062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs548017174	chr16:32164062-32164063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs62042678	chr16:32164063-32164064	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs533500961	chr16:32164097-32164098	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs551463630	chr16:32164124-32164125	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570036485	chr16:32164125-32164126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs537457838	chr16:32164144-32164145	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556454883	chr16:32164145-32164146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs62042679	chr16:32164153-32164154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535286517	chr16:32164165-32164166	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572741048	chr16:32164180-32164181	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs202090773	chr16:32164181-32164182	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs630187	chr16:32164197-32164198	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553971503	chr16:32164204-32164205	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs572027954	chr16:32164206-32164207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs539494501	chr16:32164238-32164239	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs557586122	chr16:32164253-32164254	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575593150	chr16:32164270-32164271	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs543017858	chr16:32164278-32164279	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562043051	chr16:32164279-32164280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs574035056	chr16:32164291-32164292	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs150031	chr16:32164313-32164314	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185253451	chr16:32164323-32164324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs371066	chr16:32164327-32164328	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs460199	chr16:32164335-32164336	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559924576	chr16:32164357-32164358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs148666090	chr16:32164363-32164364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs190309381	chr16:32164365-32164366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs467815	chr16:32164370-32164371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs530877958	chr16:32164390-32164391	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs139857306	chr16:32164391-32164392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs2909267	chr16:32164394-32164395	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549443734	chr16:32164407-32164408	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs57800158	chr16:32164413-32164414	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs549379828	chr16:32165114-32165115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs561240611	chr16:32165123-32165124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs528495979	chr16:32165137-32165138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547631811	chr16:32165153-32165154	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs565841147	chr16:32165163-32165164	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs544415509	chr16:32165171-32165172	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	18451855	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:457 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32178000-32179600	Weak transcription	Placenta	Placenta
2	chr16:32178200-32180000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr16:32178400-32193000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr16:32178800-32181200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr16:32179000-32181600	Weak transcription	K562	blood
6	chr16:32179200-32192400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr16:32179600-32180000	Enhancers	Dnd41	blood
8	chr16:32179600-32181000	Strong transcription	Placenta	Placenta
9	chr16:32179800-32181000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:32180000-32180200	Active TSS	Pancreas	Pancrea
11	chr16:32180000-32180800	Genic enhancers	Dnd41	blood
12	chr16:32180000-32181200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr16:32180200-32180400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr16:32180200-32180800	ZNF genes & repeats	Aorta	Aorta
15	chr16:32180200-32181000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr16:32180200-32185800	Weak transcription	Pancreas	Pancrea
17	chr16:32180200-32191200	Weak transcription	Gastric	stomach
18	chr16:32180800-32181200	Enhancers	Dnd41	blood
19	chr16:32180800-32184200	Weak transcription	Aorta	Aorta
20	chr16:32181000-32184400	Weak transcription	Placenta	Placenta
21	chr16:32181200-32183000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr16:32181200-32199000	Weak transcription	Ovary	ovary
23	chr16:32198000-32198600	Active TSS	Dnd41	blood
24	chr16:32198200-32199200	Active TSS	A549	lung
25	chr16:32198600-32199400	Weak transcription	Dnd41	blood
26	chr16:32198800-32199200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr16:32199000-32199600	Active TSS	Ovary	ovary
28	chr16:32199200-32199600	Active TSS	Esophagus	oesophagus
29	chr16:32199400-32199800	Active TSS	Primary B cells from peripheral blood	blood
30	chr16:32199400-32199800	Active TSS	Primary T cells fromperipheralblood	blood
31	chr16:32199400-32199800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr16:32199400-32199800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr16:32199400-32200200	Active TSS	Dnd41	blood
34	chr16:32200200-32200400	Flanking Active TSS	Dnd41	blood
35	chr16:32214000-32214200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr16:32214000-32214200	Enhancers	Placenta	Placenta
37	chr16:32256600-32256800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:32257400-32257600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:32264200-32266000	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr16:32264400-32265000	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr16:32264400-32265800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr16:32264800-32265000	Active TSS	Primary T cells fromperipheralblood	blood
43	chr16:32264800-32265000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr16:32264800-32265200	Active TSS	Brain Hippocampus Middle	brain
45	chr16:32264800-32265200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr16:32264800-32265200	Active TSS	HSMMtube	muscle
47	chr16:32264800-32265200	Active TSS	Osteobl	bone
48	chr16:32264800-32265800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
49	chr16:32264800-32265800	Active TSS	Primary B cells from peripheral blood	blood
50	chr16:32264800-32265800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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