Variant report

Variant	nsv1065241
Chromosome Location	chr16:32843688-33485603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4861)
CpG islands
(count:2993)
Chromatin interactive
region (count:10)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4861 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33293788-33294209	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
3	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
4	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
5	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
6	ATF3	chr16:33293710-33294426	HepG2	liver:	n/a	n/a
7	ATF3	chr16:33240952-33241267	HepG2	liver:	n/a	n/a
8	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
9	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
10	BACH1	chr16:33293845-33294023	K562	blood:	n/a	n/a
11	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
12	BATF	chr16:33002452-33002671	GM12878	blood:	n/a	n/a
13	BATF	chr16:33044491-33044914	GM12878	blood:	n/a	chr16:33044727-33044738
14	BATF	chr16:33051517-33051717	GM12878	blood:	n/a	n/a
15	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
16	BATF	chr16:33046034-33046402	GM12878	blood:	n/a	n/a
17	BATF	chr16:33052311-33052561	GM12878	blood:	n/a	n/a
18	BATF	chr16:33370078-33370545	GM12878	blood:	n/a	n/a
19	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a
20	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
21	BATF	chr16:33042313-33042791	GM12878	blood:	n/a	n/a
22	BATF	chr16:33046042-33046353	GM12878	blood:	n/a	n/a
23	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
24	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
25	BATF	chr16:33082292-33082557	GM12878	blood:	n/a	n/a
26	BATF	chr16:33087692-33087910	GM12878	blood:	n/a	n/a
27	BATF	chr16:33328184-33328483	GM12878	blood:	n/a	chr16:33328300-33328311
28	BATF	chr16:33365688-33366003	GM12878	blood:	n/a	n/a
29	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
30	BATF	chr16:33091390-33091661	GM12878	blood:	n/a	n/a
31	BATF	chr16:32951300-32951515	GM12878	blood:	n/a	chr16:32951446-32951457
32	BATF	chr16:33042432-33043800	GM12878	blood:	n/a	n/a
33	BATF	chr16:33043855-33044053	GM12878	blood:	n/a	n/a
34	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
35	BATF	chr16:33041862-33042137	GM12878	blood:	n/a	n/a
36	BATF	chr16:33364185-33364651	GM12878	blood:	n/a	chr16:33364440-33364451
37	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
38	BATF	chr16:33051640-33051829	GM12878	blood:	n/a	n/a
39	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
40	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
41	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
42	BATF	chr16:33165745-33165958	GM12878	blood:	n/a	n/a
43	BATF	chr16:33365611-33366045	GM12878	blood:	n/a	n/a
44	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
45	BATF	chr16:33331077-33331251	GM12878	blood:	n/a	n/a
46	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
47	BATF	chr16:33092972-33093212	GM12878	blood:	n/a	n/a
48	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
49	BATF	chr16:33042934-33043504	GM12878	blood:	n/a	n/a
50	BATF	chr16:32993933-32994319	GM12878	blood:	n/a	n/a

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33297688-33297738	BE2_C	brain:	n/a
2	chr16:32857872-32857922	RPTEC	kidney:	n/a
3	chr16:33044270-33044320	AoSMC	blood vessel:	n/a
4	chr16:33318910-33318960	HCF	heart:	n/a
5	chr16:33297688-33297738	BE2_C	brain:	n/a
6	chr16:32857872-32857922	RPTEC	kidney:	n/a
7	chr16:33044270-33044320	AoSMC	blood vessel:	n/a
8	chr16:33318910-33318960	HCF	heart:	n/a
9	chr16:32895392-32895442	HCT-116	colon:	n/a
10	chr16:33040275-33040325	GM12878	blood:	n/a
11	chr16:33357151-33357201	BE2_C	brain:	n/a
12	chr16:33038657-33038707	GM12891	blood:	n/a
13	chr16:33070551-33070601	GM12878	blood:	n/a
14	chr16:33039897-33039947	HRPEpiC	eye:	n/a
15	chr16:33317852-33317902	ovcar-3	ovarian:	n/a
16	chr16:33038922-33038972	GM12891	blood:	n/a
17	chr16:32895392-32895442	U87	brain:	n/a
18	chr16:32936895-32936945	NH-A	brain:	n/a
19	chr16:32898433-32898483	PFSK-1	brain:	n/a
20	chr16:33318910-33318960	ProgFib	skin:	n/a
21	chr16:33483462-33483512	HepG2	liver:	n/a
22	chr16:33038657-33038707	HepG2	liver:	n/a
23	chr16:33356843-33356893	PrEC	prostate:	n/a
24	chr16:33319362-33319412	HCPEpiC	choroid plexus:	n/a
25	chr16:33302523-33302573	ECC-1	luminal epithelium:	n/a
26	chr16:33319353-33319403	K562	blood:	n/a
27	chr16:33298952-33299002	T-47D	breast:	n/a
28	chr16:33317852-33317902	HRCEpiC	kidney:	n/a
29	chr16:33070632-33070682	GM12892	blood:	n/a
30	chr16:33483591-33483641	SK-N-MC	brain:	n/a
31	chr16:32937040-32937090	GM06990	blood:	n/a
32	chr16:32857872-32857922	SK-N-SH	brain:	n/a
33	chr16:32857551-32857601	ECC-1	luminal epithelium:	n/a
34	chr16:32858846-32858896	GM12878	blood:	n/a
35	chr16:33038922-33038972	LNCaP	prostate:	n/a
36	chr16:33374131-33374181	HNPCEpiC	eye:	n/a
37	chr16:33355024-33355074	SK-N-SH	brain:	n/a
38	chr16:32857923-32857973	PANC-1	pancreas:	n/a
39	chr16:32936664-32936714	CMK	blood:	n/a
40	chr16:33319353-33319403	NHBE	bronchial:	n/a
41	chr16:33317852-33317902	AG09319	gingival:	n/a
42	chr16:33298952-33299002	ProgFib	skin:	n/a
43	chr16:33038922-33038972	HUVEC	blood vessel:	n/a
44	chr16:33040275-33040325	HRCEpiC	kidney:	n/a
45	chr16:33040206-33040256	SK-N-SH_RA	brain:	n/a
46	chr16:33357426-33357476	HAEpiC	amniotic membrane:	n/a
47	chr16:33006163-33006213	HIPEpiC	eye:	n/a
48	chr16:33319362-33319412	ovcar-3	ovarian:	n/a
49	chr16:32934020-32934070	IMR90	lung:	fetal
50	chr16:33039897-33039947	Jurkat	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33357445..33357965-chrX:123093937..123094556,2	MCF-7	breast:
2	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:
3	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
4	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
5	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
6	chr12:123886567..123888097-chr16:33420189..33423186,2	K562	blood:
7	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
8	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
9	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
10	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53TG3-17	chr16:32943089-32943890	NONHSAT142053
2	lnc-TP53TG3-5	chr16:33054930-33055459	ENSG00000260141.1
3	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
4	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
5	lnc-RP11-1277H1.1.1-1	chr16:33145040-33145820	ENSG00000261682.1
6	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
7	lnc-AC136428.1.1-6	chr16:33217752-33218127	ENSG00000261507.1
8	lnc-CTD-2144E22.5.1-37	chr16:33263182-33263470	NONHSAT142077
9	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
10	lnc-AC136428.1.1-4	chr16:33337232-33337443	ENSG00000260626.1
11	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
12	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
13	lnc-RP11-1277H1.1.1-3	chr16:33007112-33007188	ENSG00000260921.1
14	lnc-RP11-1277H1.1.1-9	chr16:32989782-32989827	NONHSAT142058
15	lnc-RP11-1277H1.1.1-4	chr16:32897796-32898008	ENSG00000214614.2
16	lnc-AC136428.1.1-6	chr16:33215175-33215559	ENSG00000260827.1
17	lnc-RP11-1277H1.1.1-3	chr16:33007600-33008091	ENSG00000260921.1
18	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
19	lnc-RP11-1277H1.1.1-11	chr16:32926395-32926440	NONHSAT142052
20	lnc-RP11-1277H1.1.1-4	chr16:32897547-32898093	ENSG00000214614.2
21	lnc-AC136428.1.1-6	chr16:33216015-33216055	ENSG00000260827.1
22	lnc-CTD-2144E22.5.1-37	chr16:33262848-33262894	NONHSAT142077
23	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
24	lnc-AC136428.1.1-6	chr16:33231506-33231583	ENSG00000261507.1
25	lnc-RP11-1277H1.1.1-9	chr16:32989910-32990212	NONHSAT142058
26	lnc-RP11-1277H1.1.1-7	chr16:33141556-33141763	NONHSAT142067
27	lnc-AC136428.1.1-7	chr16:33206606-33206675	ENSG00000260419.1
28	lnc-RP11-1277H1.1.1-3	chr16:33006858-33006938	ENSG00000260921.1
29	lnc-AC136428.1.1-6	chr16:33231324-33231409	ENSG00000261507.1
30	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898880	ENSG00000214614.2
31	lnc-AC136428.1.1-7	chr16:33202882-33203073	ENSG00000260419.1
32	lnc-AC136428.1.1-5	chr16:33271714-33272098	ENSG00000261009.1
33	lnc-CTD-2144E22.5.1-37	chr16:33263683-33264006	NONHSAT142077
34	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
35	lnc-AC136428.1.1-5	chr16:33272554-33272594	ENSG00000261009.1
36	lnc-RP11-1277H1.1.1-1	chr16:33140637-33140721	ENSG00000261682.1
37	lnc-TP53TG3-5	chr16:33102620-33102910	ENSG00000260141.1
38	lnc-AC136428.1.1-4	chr16:33336283-33336630	ENSG00000260626.1

No data

Variant related genes	Relation type
IGHV3OR16-8	TF binding region
ENSG00000263337	TF binding region
ENSG00000260419	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000262090	TF binding region
ENSG00000214614	TF binding region
IGHV3OR16-10	TF binding region
ENSG00000260047	TF binding region
ENSG00000260414	TF binding region
ENSG00000259882	TF binding region
ENSG00000263277	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
IGHV1OR16-2	TF binding region
TP53TG3B	TF binding region
ENSG00000263204	TF binding region
ENSG00000260610	TF binding region
ENSG00000261536	TF binding region
IGHV3OR16-15	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261200	TF binding region
ENSG00000260141	TF binding region
ENSG00000261009	TF binding region
ENSG00000260921	TF binding region
ENSG00000259934	TF binding region
ENSG00000260900	TF binding region
ENSG00000259800	TF binding region
TP53TG3C	TF binding region
IGHV1OR16-4	TF binding region
HERC2P8	TF binding region
IGHV3OR16-8	CpG island
ENSG00000263337	CpG island
ENSG00000260419	CpG island
IGHV2OR16-5	CpG island
ENSG00000262090	CpG island
ENSG00000214614	CpG island
IGHV3OR16-10	CpG island
ENSG00000260047	CpG island
ENSG00000260414	CpG island
ENSG00000259882	CpG island
ENSG00000263277	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
IGHV1OR16-2	CpG island
TP53TG3B	CpG island
ENSG00000263204	CpG island
ENSG00000260610	CpG island
ENSG00000261536	CpG island
IGHV3OR16-15	CpG island
IGHV3OR16-6	CpG island
ENSG00000261200	CpG island
ENSG00000260141	CpG island
ENSG00000261009	CpG island
ENSG00000260921	CpG island
ENSG00000259934	CpG island
ENSG00000260900	CpG island
ENSG00000259800	CpG island
TP53TG3C	CpG island
IGHV1OR16-4	CpG island
HERC2P8	CpG island
ENSG00000101972	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 7462 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:7462 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78064787	chr16:32843688-32843689	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs58059974	chr16:32843693-32843694	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs79315953	chr16:32843704-32843705	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs559281842	chr16:32843723-32843724	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs572023202	chr16:32843734-32843735	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545662243	chr16:32843755-32843756	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs80156515	chr16:32843765-32843766	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs374111559	chr16:32843767-32843768	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs78490785	chr16:32843768-32843769	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs150665274	chr16:32843770-32843771	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs145188849	chr16:32843772-32843773	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs74453360	chr16:32843787-32843788	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs563965703	chr16:32843788-32843789	Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs1833393	chr16:32847418-32847419	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs540560992	chr16:32847424-32847425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs558814967	chr16:32847426-32847427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs76369163	chr16:32847436-32847437	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs77368375	chr16:32847455-32847456	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs544484162	chr16:32847459-32847460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs78426536	chr16:32847464-32847465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs112990349	chr16:32847465-32847466	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs1811276	chr16:32847476-32847477	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs201618973	chr16:32847482-32847483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs563058335	chr16:32847506-32847507	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs4309405	chr16:32847513-32847514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs530156537	chr16:32847524-32847525	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs200717074	chr16:32847528-32847529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs202147365	chr16:32847536-32847537	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs200327747	chr16:32847547-32847548	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs1833394	chr16:32847549-32847550	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs542285958	chr16:32847572-32847573	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs76322503	chr16:32847574-32847575	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs12102862	chr16:32847586-32847587	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4280252	chr16:32847588-32847589	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs200790748	chr16:32849209-32849210	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs10153088	chr16:32849211-32849212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs576371689	chr16:32849219-32849220	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs10153198	chr16:32849225-32849226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs544223542	chr16:32849242-32849243	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373205041	chr16:32849247-32849248	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs372645030	chr16:32849248-32849249	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs9708791	chr16:32849257-32849258	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs9708418	chr16:32849277-32849278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs376122457	chr16:32849291-32849292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs562801478	chr16:32849308-32849309	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs74554498	chr16:32849314-32849315	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs370179760	chr16:32849317-32849318	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs201485480	chr16:32849323-32849324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs182278466	chr16:32849336-32849337	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs201082063	chr16:32849362-32849363	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Autism	21865298	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32843600-32843800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
2	chr16:32847400-32847600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:32849200-32849800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr16:32853800-32854200	Enhancers	HepG2	liver
5	chr16:32855800-32856000	Bivalent/Poised TSS	Brain Substantia Nigra	brain
6	chr16:32856600-32858000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:32857000-32858200	ZNF genes & repeats	Fetal Stomach	stomach
8	chr16:32857200-32858000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
9	chr16:32857400-32858000	Flanking Bivalent TSS/Enh	Placenta	Placenta
10	chr16:32858000-32858200	Bivalent/Poised TSS	Right Ventricle	heart
11	chr16:32858000-32858400	Bivalent Enhancer	Placenta	Placenta
12	chr16:32858600-32859000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr16:32858800-32859200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr16:32859000-32859400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:32870000-32870800	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr16:32876600-32876800	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr16:32876800-32877000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:32876800-32877000	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr16:32876800-32877200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
20	chr16:32876800-32881000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr16:32877000-32877400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr16:32877200-32877400	Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr16:32877400-32877600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr16:32877400-32877800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr16:32877600-32877800	Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr16:32877800-32878000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr16:32877800-32878200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr16:32878000-32878200	Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr16:32878200-32878600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr16:32878200-32880000	Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr16:32878600-32879400	Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr16:32879400-32879800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr16:32879800-32880200	Enhancers	Left Ventricle	heart
34	chr16:32879800-32881000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr16:32880000-32880800	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr16:32880800-32883800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr16:32881000-32881800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr16:32881000-32886000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr16:32883800-32884200	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr16:32884200-32885400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr16:32885400-32887600	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr16:32886000-32887400	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr16:32890600-32891000	Active TSS	HSMM	muscle
44	chr16:32957400-32957800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr16:33006000-33007200	Enhancers	Dnd41	blood
46	chr16:33039600-33040000	Bivalent Enhancer	Placenta	Placenta
47	chr16:33039600-33040800	Active TSS	K562	blood
48	chr16:33040000-33040400	Flanking Bivalent TSS/Enh	Placenta	Placenta
49	chr16:33040400-33040800	Bivalent Enhancer	Placenta	Placenta
50	chr16:33070400-33071000	Bivalent Enhancer	Placenta	Placenta

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