Variant report

Variant	nsv1058588
Chromosome Location	chr16:32954713-33604030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4760)
CpG islands
(count:2627)
Chromatin interactive
region (count:11)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4760 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

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	chr16:33577202-33577382	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
4	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
5	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
6	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
7	ATF3	chr16:33240952-33241267	HepG2	liver:	n/a	n/a
8	ATF3	chr16:33569376-33569681	K562	blood:	n/a	n/a
9	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
10	ATF3	chr16:33293710-33294426	HepG2	liver:	n/a	n/a
11	ATF3	chr16:33569464-33569595	GM12878	blood:	n/a	n/a
12	BACH1	chr16:33293845-33294023	K562	blood:	n/a	n/a
13	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
14	BATF	chr16:33092972-33093212	GM12878	blood:	n/a	n/a
15	BATF	chr16:33051640-33051829	GM12878	blood:	n/a	n/a
16	BATF	chr16:33328184-33328483	GM12878	blood:	n/a	chr16:33328300-33328311
17	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
18	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
19	BATF	chr16:33046042-33046353	GM12878	blood:	n/a	n/a
20	BATF	chr16:33365688-33366003	GM12878	blood:	n/a	n/a
21	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
22	BATF	chr16:33358267-33358522	GM12878	blood:	n/a	n/a
23	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
24	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a
25	BATF	chr16:33369625-33369914	GM12878	blood:	n/a	n/a
26	BATF	chr16:33087692-33087910	GM12878	blood:	n/a	n/a
27	BATF	chr16:33043855-33044053	GM12878	blood:	n/a	n/a
28	BATF	chr16:33087718-33087908	GM12878	blood:	n/a	n/a
29	BATF	chr16:33051517-33051717	GM12878	blood:	n/a	n/a
30	BATF	chr16:33048704-33048907	GM12878	blood:	n/a	n/a
31	BATF	chr16:33042313-33042791	GM12878	blood:	n/a	n/a
32	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
33	BATF	chr16:33082292-33082557	GM12878	blood:	n/a	n/a
34	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
35	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
36	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
37	BATF	chr16:33002452-33002671	GM12878	blood:	n/a	n/a
38	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
39	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
40	BATF	chr16:33042934-33043504	GM12878	blood:	n/a	n/a
41	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
42	BATF	chr16:33370078-33370545	GM12878	blood:	n/a	n/a
43	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
44	BATF	chr16:33331077-33331251	GM12878	blood:	n/a	n/a
45	BATF	chr16:32993933-32994319	GM12878	blood:	n/a	n/a
46	BATF	chr16:33044181-33044885	GM12878	blood:	n/a	chr16:33044727-33044738
47	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
48	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
49	BATF	chr16:33091390-33091661	GM12878	blood:	n/a	n/a
50	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a

(count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33070551-33070601	MCF10A-Er-Src	breast:	n/a
2	chr16:33510089-33510139	H1-hESC	embryonic stem cell:	embryo
3	chr16:33374161-33374211	U87	brain:	n/a
4	chr16:33574151-33574201	NHDF-neo	bronchial:	n/a
5	chr16:33070551-33070601	MCF10A-Er-Src	breast:	n/a
6	chr16:33510089-33510139	H1-hESC	embryonic stem cell:	embryo
7	chr16:33374161-33374211	U87	brain:	n/a
8	chr16:33574151-33574201	NHDF-neo	bronchial:	n/a
9	chr16:33483462-33483512	SK-N-MC	brain:	n/a
10	chr16:33297688-33297738	A549	lung:	n/a
11	chr16:33071657-33071707	ProgFib	skin:	n/a
12	chr16:33374161-33374211	K562	blood:	n/a
13	chr16:33357426-33357476	HCM	heart:	n/a
14	chr16:33573272-33573322	HRPEpiC	eye:	n/a
15	chr16:33510089-33510139	Caco-2	colon:	n/a
16	chr16:33374131-33374181	HRCEpiC	kidney:	n/a
17	chr16:33355024-33355074	NHDF-neo	bronchial:	n/a
18	chr16:33570115-33570165	NH-A	brain:	n/a
19	chr16:33070551-33070601	HPAEpiC	pulmonary alveolar:	n/a
20	chr16:33358227-33358277	HEK293	kidney:	embryo
21	chr16:33038922-33038972	SK-N-SH	brain:	n/a
22	chr16:33259538-33259588	AG04449	skin:	fetal
23	chr16:33302523-33302573	ECC-1	luminal epithelium:	n/a
24	chr16:33038657-33038707	SK-N-SH	brain:	n/a
25	chr16:33298952-33299002	SK-N-MC	brain:	n/a
26	chr16:33481620-33481670	HRCEpiC	kidney:	n/a
27	chr16:33070551-33070601	GM12891	blood:	n/a
28	chr16:33509523-33509573	K562	blood:	n/a
29	chr16:33483591-33483641	HMEC	breast:	n/a
30	chr16:33357426-33357476	ProgFib	skin:	n/a
31	chr16:33038657-33038707	ovcar-3	ovarian:	n/a
32	chr16:33038922-33038972	HepG2	liver:	n/a
33	chr16:33038657-33038707	HEEpiC	esophagus:	n/a
34	chr16:33571945-33571995	LNCaP	prostate:	n/a
35	chr16:33355024-33355074	K562	blood:	n/a
36	chr16:33483244-33483294	PANC-1	pancreas:	n/a
37	chr16:33509523-33509573	HIPEpiC	eye:	n/a
38	chr16:33318910-33318960	MCF-7	breast:	n/a
39	chr16:33374131-33374181	MCF-7	breast:	n/a
40	chr16:33571945-33571995	NH-A	brain:	n/a
41	chr16:33318910-33318960	PANC-1	pancreas:	n/a
42	chr16:33483297-33483347	RPTEC	kidney:	n/a
43	chr16:33006163-33006213	HCM	heart:	n/a
44	chr16:33573272-33573322	BJ	skin:	n/a
45	chr16:33570115-33570165	NHBE	bronchial:	n/a
46	chr16:33319353-33319403	GM12878	blood:	n/a
47	chr16:33487438-33487488	MCF10A-Er-Src	breast:	n/a
48	chr16:33044270-33044320	AG04449	skin:	fetal
49	chr16:33483591-33483641	HRCEpiC	kidney:	n/a
50	chr16:33297688-33297738	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:
2	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
3	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
4	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
5	chr16:33357445..33357965-chrX:123093937..123094556,2	MCF-7	breast:
6	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
7	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
8	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
9	chr12:123886567..123888097-chr16:33420189..33423186,2	K562	blood:
10	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
11	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC136428.1.1-6	chr16:33231506-33231583	ENSG00000261507.1
2	lnc-AC136428.1.1-6	chr16:33216015-33216055	ENSG00000260827.1
3	lnc-CTD-2144E22.5.1-37	chr16:33263683-33264006	NONHSAT142077
4	lnc-AC136428.1.1-5	chr16:33271714-33272098	ENSG00000261009.1
5	lnc-RP11-1277H1.1.1-9	chr16:32989782-32989827	NONHSAT142058
6	lnc-AC136428.1.1-6	chr16:33217752-33218127	ENSG00000261507.1
7	lnc-AC136428.1.1-6	chr16:33231324-33231409	ENSG00000261507.1
8	lnc-AC136428.1.1-6	chr16:33215175-33215559	ENSG00000260827.1
9	lnc-AC136428.1.1-5	chr16:33272554-33272594	ENSG00000261009.1
10	lnc-CTD-2144E22.5.1-37	chr16:33262848-33262894	NONHSAT142077
11	lnc-RP11-1277H1.1.1-3	chr16:33006858-33006938	ENSG00000260921.1
12	lnc-RP11-1277H1.1.1-7	chr16:33141556-33141763	NONHSAT142067
13	lnc-TP53TG3-5	chr16:33054930-33055459	ENSG00000260141.1
14	lnc-AC136428.1.1-7	chr16:33206606-33206675	ENSG00000260419.1
15	lnc-RP11-1277H1.1.1-9	chr16:32989910-32990212	NONHSAT142058
16	lnc-AC136428.1.1-4	chr16:33336283-33336630	ENSG00000260626.1
17	lnc-RP11-1277H1.1.1-1	chr16:33140637-33140721	ENSG00000261682.1
18	lnc-TP53TG3-5	chr16:33102620-33102910	ENSG00000260141.1
19	lnc-RP11-1277H1.1.1-3	chr16:33007112-33007188	ENSG00000260921.1
20	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
21	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
22	lnc-RP11-1277H1.1.1-3	chr16:33007600-33008091	ENSG00000260921.1
23	lnc-AC136428.1.1-7	chr16:33202882-33203073	ENSG00000260419.1
24	lnc-CTD-2144E22.5.1-37	chr16:33263182-33263470	NONHSAT142077
25	lnc-RP11-1277H1.1.1-1	chr16:33145040-33145820	ENSG00000261682.1
26	lnc-AC136428.1.1-4	chr16:33337232-33337443	ENSG00000260626.1

No data

Variant related genes	Relation type
IGHV3OR16-8	TF binding region
ENSG00000263337	TF binding region
ENSG00000260419	TF binding region
ENSG00000262090	TF binding region
IGHV3OR16-10	TF binding region
ENSG00000260414	TF binding region
IGHV3OR16-12	TF binding region
ENSG00000259882	TF binding region
ENSG00000263277	TF binding region
ENSG00000260308	TF binding region
ENSG00000261682	TF binding region
ENSG00000260827	TF binding region
ENSG00000261466	TF binding region
ENSG00000261405	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
ENSG00000261536	TF binding region
ENPP7P13	TF binding region
ENSG00000261200	TF binding region
ENSG00000260141	TF binding region
ENSG00000261009	TF binding region
ENSG00000260921	TF binding region
ENSG00000260900	TF binding region
ENSG00000259800	TF binding region
TP53TG3C	TF binding region
IGHV1OR16-4	TF binding region
BMS1P8	TF binding region
HERC2P8	TF binding region
IGHV3OR16-8	CpG island
ENSG00000263337	CpG island
ENSG00000260419	CpG island
ENSG00000262090	CpG island
IGHV3OR16-10	CpG island
ENSG00000260414	CpG island
IGHV3OR16-12	CpG island
ENSG00000259882	CpG island
ENSG00000263277	CpG island
ENSG00000260308	CpG island
ENSG00000261682	CpG island
ENSG00000260827	CpG island
ENSG00000261466	CpG island
ENSG00000261405	CpG island
ENSG00000261259	CpG island
ENSG00000261507	CpG island
ENSG00000260626	CpG island
IGHV1OR16-2	CpG island
TP53TG3B	CpG island
ENSG00000263204	CpG island
ENSG00000261536	CpG island
ENPP7P13	CpG island
ENSG00000261200	CpG island
ENSG00000260141	CpG island
ENSG00000261009	CpG island
ENSG00000260921	CpG island
ENSG00000260900	CpG island
ENSG00000259800	CpG island
TP53TG3C	CpG island
IGHV1OR16-4	CpG island
BMS1P8	CpG island
HERC2P8	CpG island
ENSG00000101972	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 10593 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:10593 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190887602	chr16:32957463-32957464	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs543962336	chr16:32957470-32957471	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs372385218	chr16:32957489-32957490	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs529876225	chr16:32957508-32957509	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs183309717	chr16:32957511-32957512	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs186891100	chr16:32957530-32957531	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs116910183	chr16:32957531-32957532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs547022160	chr16:32957533-32957534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs571730903	chr16:32957550-32957551	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs374847339	chr16:32957559-32957560	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs532644927	chr16:32957566-32957567	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs551144294	chr16:32957598-32957599	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs569408433	chr16:32957601-32957602	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs536478681	chr16:32957613-32957614	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs1713728	chr16:32957630-32957631	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs191014729	chr16:32957633-32957634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs567071632	chr16:32957643-32957644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs533496472	chr16:32957661-32957662	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs558138232	chr16:32957696-32957697	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs576471101	chr16:32957705-32957706	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs498893	chr16:32957749-32957750	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs498849	chr16:32957769-32957770	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs574540912	chr16:32957780-32957781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs541680958	chr16:32957791-32957792	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs370556305	chr16:32987018-32987019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560724499	chr16:32989804-32989805	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs528302078	chr16:32989815-32989816	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs570172452	chr16:33002440-33002441	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs537934035	chr16:33002466-33002467	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs556256859	chr16:33002522-33002523	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs574666450	chr16:33002624-33002625	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs542024640	chr16:33002664-33002665	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs560584812	chr16:33002681-33002682	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs572694417	chr16:33002694-33002695	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs546205788	chr16:33002695-33002696	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs370811427	chr16:33002708-33002709	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs531345977	chr16:33002765-33002766	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs556193540	chr16:33003570-33003571	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs570229443	chr16:33006022-33006023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537664075	chr16:33006127-33006128	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs549654073	chr16:33006138-33006139	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs567876789	chr16:33006155-33006156	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs146317219	chr16:33006163-33006164	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
44	rs535370975	chr16:33006164-33006165	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
45	rs56390628	chr16:33006191-33006192	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs552692673	chr16:33006194-33006195	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs577598725	chr16:33006206-33006207	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs538310467	chr16:33006352-33006353	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs556657580	chr16:33006372-33006373	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575046169	chr16:33006441-33006442	Enhancers	TF binding region	1 gene(s)	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32957400-32957800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr16:33006000-33007200	Enhancers	Dnd41	blood
3	chr16:33039600-33040000	Bivalent Enhancer	Placenta	Placenta
4	chr16:33039600-33040800	Active TSS	K562	blood
5	chr16:33040000-33040400	Flanking Bivalent TSS/Enh	Placenta	Placenta
6	chr16:33040400-33040800	Bivalent Enhancer	Placenta	Placenta
7	chr16:33070400-33071000	Bivalent Enhancer	Placenta	Placenta
8	chr16:33070600-33071000	Active TSS	Psoas Muscle	Psoas
9	chr16:33070800-33071000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr16:33071400-33071600	Enhancers	Right Ventricle	heart
11	chr16:33140000-33140400	Active TSS	HSMM	muscle
12	chr16:33140200-33140400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr16:33140200-33140400	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr16:33236400-33241000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr16:33236600-33241600	Weak transcription	Fetal Lung	lung
16	chr16:33237400-33237600	Bivalent Enhancer	Placenta	Placenta
17	chr16:33237400-33237600	Enhancers	Right Ventricle	heart
18	chr16:33237400-33238000	Active TSS	Primary T helper naive cells from peripheral blood	blood
19	chr16:33237400-33238000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr16:33237400-33238200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr16:33237400-33238200	Active TSS	Primary T cells from cord blood	blood
22	chr16:33237400-33238200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
23	chr16:33237400-33238200	ZNF genes & repeats	Right Atrium	heart
24	chr16:33237400-33238400	ZNF genes & repeats	Colonic Mucosa	Colon
25	chr16:33237400-33238600	ZNF genes & repeats	Esophagus	oesophagus
26	chr16:33237400-33239200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr16:33237400-33239200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr16:33237400-33239400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr16:33237400-33239600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr16:33237400-33239600	ZNF genes & repeats	Gastric	stomach
31	chr16:33237400-33240000	ZNF genes & repeats	Pancreas	Pancrea
32	chr16:33237400-33241400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr16:33237400-33241400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr16:33237400-33241400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
35	chr16:33237400-33241400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
36	chr16:33237400-33241400	ZNF genes & repeats	Lung	lung
37	chr16:33237400-33241400	ZNF genes & repeats	Spleen	Spleen
38	chr16:33237600-33237800	Weak transcription	Right Ventricle	heart
39	chr16:33237800-33238200	ZNF genes & repeats	Right Ventricle	heart
40	chr16:33237800-33238200	Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr16:33237800-33238200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
42	chr16:33237800-33239600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
43	chr16:33238000-33238200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
44	chr16:33238000-33238200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
45	chr16:33238200-33238600	Weak transcription	Right Atrium	heart
46	chr16:33238200-33240800	Weak transcription	Right Ventricle	heart
47	chr16:33238200-33240800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr16:33238200-33241000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr16:33238200-33241000	Weak transcription	Primary T cells from cord blood	blood
50	chr16:33238600-33241000	Strong transcription	Right Atrium	heart

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