Variant report

Variant	esv1843648
Chromosome Location	chr16:32433632-33387574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6312)
CpG islands
(count:3910)
Chromatin interactive
region (count:8)
LncRNA
region (count:75)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6312 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
2	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
4	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
7	ARID3A	chr16:33293788-33294209	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
10	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
11	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
12	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
13	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
14	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
15	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
16	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
17	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
18	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
19	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
20	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
21	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
22	ATF3	chr16:33293710-33294426	HepG2	liver:	n/a	n/a
23	ATF3	chr16:33240952-33241267	HepG2	liver:	n/a	n/a
24	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
25	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
26	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
27	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
28	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
29	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
30	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr16:33293845-33294023	K562	blood:	n/a	n/a
32	BATF	chr16:33364185-33364651	GM12878	blood:	n/a	chr16:33364440-33364451
33	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
34	BATF	chr16:33002452-33002671	GM12878	blood:	n/a	n/a
35	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a
36	BATF	chr16:33002463-33002715	GM12878	blood:	n/a	n/a
37	BATF	chr16:33046034-33046402	GM12878	blood:	n/a	n/a
38	BATF	chr16:33042313-33042791	GM12878	blood:	n/a	n/a
39	BATF	chr16:32805422-32805612	GM12878	blood:	n/a	n/a
40	BATF	chr16:32805420-32805638	GM12878	blood:	n/a	n/a
41	BATF	chr16:32652782-32652951	GM12878	blood:	n/a	n/a
42	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
43	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
44	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
45	BATF	chr16:33041862-33042137	GM12878	blood:	n/a	n/a
46	BATF	chr16:33358267-33358522	GM12878	blood:	n/a	n/a
47	BATF	chr16:33331077-33331251	GM12878	blood:	n/a	n/a
48	BATF	chr16:33370078-33370545	GM12878	blood:	n/a	n/a
49	BATF	chr16:33042432-33043800	GM12878	blood:	n/a	n/a
50	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a

(count:3910 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33317852-33317902	AG04450	lung:	fetal
2	chr16:33374131-33374181	ECC-1	luminal epithelium:	n/a
3	chr16:32823584-32823634	A549	lung:	n/a
4	chr16:32857872-32857922	HPAEpiC	pulmonary alveolar:	n/a
5	chr16:32662543-32662593	NHBE	bronchial:	n/a
6	chr16:32857923-32857973	IMR90	lung:	fetal
7	chr16:33317852-33317902	AG04450	lung:	fetal
8	chr16:33374131-33374181	ECC-1	luminal epithelium:	n/a
9	chr16:32823584-32823634	A549	lung:	n/a
10	chr16:32857872-32857922	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:32662543-32662593	NHBE	bronchial:	n/a
12	chr16:32857923-32857973	IMR90	lung:	fetal
13	chr16:32452725-32452775	SK-N-MC	brain:	n/a
14	chr16:33357151-33357201	Hepatocyte	liver:	n/a
15	chr16:33317852-33317902	H1-hESC	embryonic stem cell:	embryo
16	chr16:33040206-33040256	HNPCEpiC	eye:	n/a
17	chr16:32857007-32857057	HRPEpiC	eye:	n/a
18	chr16:32473096-32473146	NHDF-neo	bronchial:	n/a
19	chr16:33071657-33071707	GM12892	blood:	n/a
20	chr16:33259538-33259588	MCF10A-Er-Src	breast:	n/a
21	chr16:33318910-33318960	SK-N-SH	brain:	n/a
22	chr16:32487825-32487875	GM12891	blood:	n/a
23	chr16:32823289-32823339	HRCEpiC	kidney:	n/a
24	chr16:33071657-33071707	MCF10A-Er-Src	breast:	n/a
25	chr16:32485636-32485686	SAEC	small airway:	n/a
26	chr16:33038657-33038707	HepG2	liver:	n/a
27	chr16:33038657-33038707	NH-A	brain:	n/a
28	chr16:32489820-32489870	AG04450	lung:	fetal
29	chr16:33297688-33297738	HUVEC	blood vessel:	n/a
30	chr16:33038657-33038707	HRPEpiC	eye:	n/a
31	chr16:32452502-32452552	PrEC	prostate:	n/a
32	chr16:32599417-32599467	NHDF-neo	bronchial:	n/a
33	chr16:32599433-32599483	HL-60	blood:	n/a
34	chr16:33319610-33319660	HUVEC	blood vessel:	n/a
35	chr16:32857007-32857057	Jurkat	blood:	n/a
36	chr16:32487825-32487875	BJ	skin:	n/a
37	chr16:32857551-32857601	PANC-1	pancreas:	n/a
38	chr16:32452502-32452552	ProgFib	skin:	n/a
39	chr16:33318910-33318960	NHBE	bronchial:	n/a
40	chr16:32823289-32823339	IMR90	lung:	fetal
41	chr16:32659887-32659937	HCT-116	colon:	n/a
42	chr16:33040206-33040256	HepG2	liver:	n/a
43	chr16:32858241-32858291	HRPEpiC	eye:	n/a
44	chr16:32937057-32937107	AG10803	skin:	n/a
45	chr16:33071657-33071707	AG09319	gingival:	n/a
46	chr16:33357426-33357476	HepG2	liver:	n/a
47	chr16:32822392-32822442	HRCEpiC	kidney:	n/a
48	chr16:33038922-33038972	Hela-S3	cervix:	n/a
49	chr16:32936664-32936714	BJ	skin:	n/a
50	chr16:33356843-33356893	ECC-1	luminal epithelium:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
2	chr16:33357445..33357965-chrX:123093937..123094556,2	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	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:
6	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
7	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
8	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:

(count:75 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
2	lnc-CTD-2144E22.5.1-37	chr16:33263182-33263470	NONHSAT142077
3	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
4	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
5	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
6	lnc-TP53TG3-2	chr16:32465933-32470079	ENSG00000261541.1
7	lnc-TP53TG3-1	chr16:32752331-32752415	ENSG00000260845.1
8	lnc-AC136428.1.1-6	chr16:33215175-33215559	ENSG00000260827.1
9	lnc-AC136428.1.1-5	chr16:33272554-33272594	ENSG00000261009.1
10	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
11	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
12	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022
13	lnc-RP11-1277H1.1.1-9	chr16:32989782-32989827	NONHSAT142058
14	lnc-AC136428.1.1-5	chr16:33271714-33272098	ENSG00000261009.1
15	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
16	lnc-TP53TG3-1	chr16:32747230-32748010	ENSG00000260845.1
17	lnc-TP53TG3-11	chr16:32750948-32750981	NONHSAT142041
18	lnc-TP53TG3-5	chr16:33102620-33102910	ENSG00000260141.1
19	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
20	lnc-AC133485.1.1-8	chr16:32442004-32442108	NONHSAT142015
21	lnc-AC133485.1.1-4	chr16:32689961-32690152	ENSG00000260974.1
22	lnc-RP11-1277H1.1.1-3	chr16:33007112-33007188	ENSG00000260921.1
23	lnc-AC133485.1.1-3	chr16:32674902-32675277	ENSG00000261569.1
24	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
25	lnc-RP11-1277H1.1.1-3	chr16:33006858-33006938	ENSG00000260921.1
26	lnc-AC133485.1.1-3	chr16:32676974-32677014	ENSG00000260311.1
27	lnc-AC133485.1.1-4	chr16:32686358-32686427	ENSG00000260974.1
28	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
29	lnc-RP11-1277H1.1.1-9	chr16:32989910-32990212	NONHSAT142058
30	lnc-CTD-2144E22.5.1-37	chr16:33263683-33264006	NONHSAT142077
31	lnc-AC133485.1.1-3	chr16:32677470-32677854	ENSG00000260311.1
32	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
33	lnc-AC133485.1.1-3	chr16:32661076-32661211	ENSG00000261569.1
34	lnc-RP11-1277H1.1.1-3	chr16:33007600-33008091	ENSG00000260921.1
35	lnc-TP53TG3-16	chr16:32452294-32452480	NONHSAT142016
36	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
37	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
38	lnc-TP53TG3-5	chr16:33054930-33055459	ENSG00000260141.1
39	lnc-RP11-1277H1.1.1-1	chr16:33140637-33140721	ENSG00000261682.1
40	lnc-RP11-1277H1.1.1-7	chr16:33141556-33141763	NONHSAT142067
41	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
42	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
43	lnc-AC136428.1.1-7	chr16:33202882-33203073	ENSG00000260419.1
44	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
45	lnc-CTD-2144E22.5.1-37	chr16:33262848-33262894	NONHSAT142077
46	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
47	lnc-AC136428.1.1-6	chr16:33231506-33231583	ENSG00000261507.1
48	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
49	lnc-TP53TG3-11	chr16:32751296-32751487	NONHSAT142041
50	lnc-AC133485.1.1-8	chr16:32447309-32447521	NONHSAT142015

No data

Variant related genes	Relation type
IGHV3OR16-8	TF binding region
ENSG00000260864	TF binding region
ENSG00000263337	TF binding region
ENSG00000260419	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000262090	TF binding region
ENSG00000261111	TF binding region
ENSG00000261263	TF binding region
ENSG00000214614	TF binding region
TP53TG3	TF binding region
IGHV3OR16-10	TF binding region
ENSG00000260047	TF binding region
ENSG00000259966	TF binding region
ENSG00000260414	TF binding region
ENSG00000261108	TF binding region
ENSG00000259882	TF binding region
ENSG00000263277	TF binding region
ENSG00000261541	TF binding region
ENSG00000261682	TF binding region
ENSG00000260827	TF binding region
ENSG00000261466	TF binding region
ENSG00000261405	TF binding region
SLC6A10P	TF binding region
ENSG00000261259	TF binding region
ENSG00000261507	TF binding region
ENSG00000260626	TF binding region
HERC2P5	TF binding region
IGHV1OR16-2	TF binding region
TP53TG3B	TF binding region
ENSG00000263204	TF binding region
ENSG00000260610	TF binding region
ENSG00000260158	TF binding region
ENSG00000261536	TF binding region
ENSG00000260662	TF binding region
IGHV3OR16-15	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261569	TF binding region
ENSG00000261719	TF binding region
ENSG00000261200	TF binding region
ENSG00000261391	TF binding region
ENSG00000260141	TF binding region
ENSG00000260974	TF binding region
ENSG00000261009	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
ENSG00000259800	TF binding region
PABPC1P13	TF binding region
TP53TG3C	TF binding region
IGHV1OR16-4	TF binding region
ENSG00000260311	TF binding region
HERC2P8	TF binding region
IGHV3OR16-8	CpG island
ENSG00000260864	CpG island
ENSG00000263337	CpG island
ENSG00000260419	CpG island
IGHV2OR16-5	CpG island
ENSG00000262090	CpG island
ENSG00000261111	CpG island
ENSG00000261263	CpG island
ENSG00000214614	CpG island
TP53TG3	CpG island
IGHV3OR16-10	CpG island
ENSG00000260047	CpG island
ENSG00000259966	CpG island
ENSG00000260414	CpG island
ENSG00000261108	CpG island
ENSG00000259882	CpG island
ENSG00000263277	CpG island
ENSG00000261541	CpG island
ENSG00000261682	CpG island
ENSG00000260827	CpG island
ENSG00000261466	CpG island
ENSG00000261405	CpG island
SLC6A10P	CpG island
ENSG00000261259	CpG island
ENSG00000261507	CpG island
ENSG00000260626	CpG island
HERC2P5	CpG island
IGHV1OR16-2	CpG island
TP53TG3B	CpG island
ENSG00000263204	CpG island
ENSG00000260610	CpG island
ENSG00000260158	CpG island
ENSG00000261536	CpG island
ENSG00000260662	CpG island
IGHV3OR16-15	CpG island
IGHV3OR16-6	CpG island
ENSG00000261569	CpG island
ENSG00000261719	CpG island
ENSG00000261200	CpG island
ENSG00000261391	CpG island
ENSG00000260141	CpG island
ENSG00000260974	CpG island
ENSG00000261009	CpG island
ENSG00000262187	CpG island
ENSG00000260845	CpG island
ENSG00000260921	CpG island
ENSG00000259934	CpG island
ABCD1P3	CpG island
ENSG00000260900	CpG island
ENSG00000259800	CpG island
PABPC1P13	CpG island
TP53TG3C	CpG island
IGHV1OR16-4	CpG island
ENSG00000260311	CpG island
HERC2P8	CpG island
ENSG00000101972	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 18769 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:18769 , 50 per page) page: 1 2 3 4 5 6 7 ... 376

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537129182	chr16:32437097-32437098	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs549380850	chr16:32437100-32437101	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs567631169	chr16:32437125-32437126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs535757196	chr16:32437134-32437135	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs369766060	chr16:32437138-32437139	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs78055635	chr16:32437141-32437142	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs181692603	chr16:32437171-32437172	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs201887063	chr16:32437180-32437181	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs539660292	chr16:32437181-32437182	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs181646784	chr16:32437184-32437185	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs576113075	chr16:32437192-32437193	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs199876884	chr16:32437194-32437195	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs3913834	chr16:32437203-32437204	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs201822222	chr16:32438046-32438047	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs547042654	chr16:32438048-32438049	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs571521536	chr16:32438075-32438076	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs533271252	chr16:32438110-32438111	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs551343631	chr16:32438146-32438147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs4080263	chr16:32438164-32438165	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs569931899	chr16:32438171-32438172	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs536889138	chr16:32438173-32438174	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs545810259	chr16:32442007-32442008	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs563895757	chr16:32442012-32442013	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs531896595	chr16:32442030-32442031	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs550018657	chr16:32442049-32442050	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs368235216	chr16:32442053-32442054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs561947840	chr16:32442089-32442090	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs371432079	chr16:32442093-32442094	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs139974249	chr16:32442105-32442106	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs398119348	chr16:32442107-32442108	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs539520530	chr16:32443003-32443004	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs62040898	chr16:32443006-32443007	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs62040899	chr16:32443009-32443010	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs201652667	chr16:32443014-32443015	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs370570878	chr16:32443020-32443021	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs77300494	chr16:32443041-32443042	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs78561941	chr16:32443053-32443054	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs557614775	chr16:32443058-32443059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs575722304	chr16:32443082-32443083	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs200607933	chr16:32443125-32443126	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs62040906	chr16:32447350-32447351	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs558794425	chr16:32447351-32447352	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs192430006	chr16:32447363-32447364	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs544410867	chr16:32447390-32447391	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs111945715	chr16:32447397-32447398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs562606230	chr16:32447408-32447409	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs371815687	chr16:32447413-32447414	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs541833013	chr16:32447451-32447452	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs559862566	chr16:32447487-32447488	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs527998610	chr16:32447504-32447505	Inactive region	lncRNA	n/a	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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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