Variant report

Variant	nsv572212
Chromosome Location	chr16:33298121-33786141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3772)
CpG islands
(count:2687)
Chromatin interactive
region (count:25)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3772 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33577202-33577382	HepG2	liver:	n/a	n/a
3	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
4	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
5	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
6	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
7	ATF3	chr16:33619018-33619453	K562	blood:	n/a	n/a
8	ATF3	chr16:33569464-33569595	GM12878	blood:	n/a	n/a
9	ATF3	chr16:33569376-33569681	K562	blood:	n/a	n/a
10	BATF	chr16:33369625-33369914	GM12878	blood:	n/a	n/a
11	BATF	chr16:33365688-33366003	GM12878	blood:	n/a	n/a
12	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
13	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
14	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
15	BATF	chr16:33331077-33331251	GM12878	blood:	n/a	n/a
16	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
17	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
18	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
19	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
20	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
21	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
22	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
23	BATF	chr16:33365611-33366045	GM12878	blood:	n/a	n/a
24	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
25	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
26	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
27	BATF	chr16:33364185-33364651	GM12878	blood:	n/a	chr16:33364440-33364451
28	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
29	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
30	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
31	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
32	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
33	BATF	chr16:33328184-33328483	GM12878	blood:	n/a	chr16:33328300-33328311
34	BATF	chr16:33370078-33370545	GM12878	blood:	n/a	n/a
35	BATF	chr16:33358267-33358522	GM12878	blood:	n/a	n/a
36	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
37	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
38	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
39	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
40	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:33331161-33331332	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:33359781-33360055	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:33329783-33329955	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:33460213-33460485	GM12878	blood:	n/a	chr16:33460375-33460384
47	BCL11A	chr16:33365658-33366042	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:33306015-33306243	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:33493442-33493790	GM12878	blood:	n/a	n/a

(count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33318910-33318960	HRCEpiC	kidney:	n/a
2	chr16:33319610-33319660	HAEpiC	amniotic membrane:	n/a
3	chr16:33487438-33487488	HCT-116	colon:	n/a
4	chr16:33318910-33318960	HRCEpiC	kidney:	n/a
5	chr16:33319610-33319660	HAEpiC	amniotic membrane:	n/a
6	chr16:33487438-33487488	HCT-116	colon:	n/a
7	chr16:33605185-33605235	H1-hESC	embryonic stem cell:	embryo
8	chr16:33776910-33776960	GM12891	blood:	n/a
9	chr16:33510089-33510139	HRE	kidney:	n/a
10	chr16:33319610-33319660	HEEpiC	esophagus:	n/a
11	chr16:33730558-33730608	HRCEpiC	kidney:	n/a
12	chr16:33355024-33355074	HUVEC	blood vessel:	n/a
13	chr16:33509433-33509483	HRE	kidney:	n/a
14	chr16:33730558-33730608	BE2_C	brain:	n/a
15	chr16:33317852-33317902	Hepatocyte	liver:	n/a
16	chr16:33734837-33734887	AoSMC	blood vessel:	n/a
17	chr16:33481620-33481670	NH-A	brain:	n/a
18	chr16:33483462-33483512	SK-N-MC	brain:	n/a
19	chr16:33357151-33357201	BE2_C	brain:	n/a
20	chr16:33483462-33483512	HAEpiC	amniotic membrane:	n/a
21	chr16:33319610-33319660	NHDF-neo	bronchial:	n/a
22	chr16:33730539-33730589	HEEpiC	esophagus:	n/a
23	chr16:33734837-33734887	HRCEpiC	kidney:	n/a
24	chr16:33298952-33299002	LNCaP	prostate:	n/a
25	chr16:33374028-33374078	SK-N-MC	brain:	n/a
26	chr16:33374161-33374211	HUVEC	blood vessel:	n/a
27	chr16:33374028-33374078	BE2_C	brain:	n/a
28	chr16:33298952-33299002	NHBE	bronchial:	n/a
29	chr16:33571945-33571995	BJ	skin:	n/a
30	chr16:33483244-33483294	PFSK-1	brain:	n/a
31	chr16:33355024-33355074	AG10803	skin:	n/a
32	chr16:33374131-33374181	HL-60	blood:	n/a
33	chr16:33357426-33357476	BJ	skin:	n/a
34	chr16:33783802-33783852	T-47D	breast:	n/a
35	chr16:33571945-33571995	HRPEpiC	eye:	n/a
36	chr16:33570115-33570165	HNPCEpiC	eye:	n/a
37	chr16:33483591-33483641	A549	lung:	n/a
38	chr16:33318910-33318960	SKMC	muscle:	n/a
39	chr16:33510089-33510139	HCT-116	colon:	n/a
40	chr16:33605185-33605235	HMEC	breast:	n/a
41	chr16:33483591-33483641	HCT-116	colon:	n/a
42	chr16:33487438-33487488	HRPEpiC	eye:	n/a
43	chr16:33483591-33483641	NB4	blood:	n/a
44	chr16:33573272-33573322	HEEpiC	esophagus:	n/a
45	chr16:33570115-33570165	PFSK-1	brain:	n/a
46	chr16:33783802-33783852	SAEC	small airway:	n/a
47	chr16:33627536-33627586	SKMC	muscle:	n/a
48	chr16:33732255-33732305	HepG2	liver:	n/a
49	chr16:33302523-33302573	HEK293	kidney:	embryo
50	chr16:33483244-33483294	GM12891	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
2	chr16:33357445..33357965-chrX:123093937..123094556,2	MCF-7	breast:
3	chr16:33618559..33619759-chr16:33646461..33647717,8	MCF-7	breast:
4	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
5	chr1:121484857..121485377-chr16:33618718..33619247,2	MCF-7	breast:
6	chr16:33618869..33619686-chr16:33955996..33956882,3	MCF-7	breast:
7	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
8	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
9	chr16:33618975..33619481-chr6:120699536..120700074,2	MCF-7	breast:
10	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
11	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
12	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
13	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
14	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
15	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
16	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
17	chr12:123886567..123888097-chr16:33420189..33423186,2	K562	blood:
18	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
19	chr14:107287133..107287781-chr16:33618600..33619120,3	MCF-7	breast:
20	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
21	chr13:30046484..30047067-chr16:33618956..33619795,2	MCF-7	breast:
22	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
23	chr16:33618687..33619546-chr21:22589708..22590404,2	MCF-7	breast:
24	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
25	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
2	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
3	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
4	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
5	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
6	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
7	lnc-AC136428.1.1-4	chr16:33336283-33336630	ENSG00000260626.1
8	lnc-AC136428.1.1-10	chr16:33677506-33677808	NONHSAT142113
9	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
10	lnc-AC136428.1.1-4	chr16:33337232-33337443	ENSG00000260626.1
11	lnc-AC136428.1.1-10	chr16:33677891-33677935	NONHSAT142113
12	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
13	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
14	lnc-AC136428.1.1-1	chr16:33661001-33661077	ENSG00000260312.1
15	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
16	lnc-AC136428.1.1-1	chr16:33660402-33660589	ENSG00000260312.1
17	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
18	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
19	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
20	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
21	lnc-AC136428.1.1-1	chr16:33661251-33661331	ENSG00000260312.1

No data

Variant related genes	Relation type
ENSG00000205452	TF binding region
ENSG00000260525	TF binding region
IGHV3OR16-16	TF binding region
ENSG00000261153	TF binding region
ENSG00000259680	TF binding region
ENSG00000260312	TF binding region
ENSG00000263277	TF binding region
ENSG00000261466	TF binding region
ENSG00000261405	TF binding region
IGHV3OR16-13	TF binding region
ENPP7P13	TF binding region
ENSG00000198555	TF binding region
ENSG00000262090	TF binding region
ENSG00000261607	TF binding region
IGHV3OR16-12	TF binding region
ENSG00000259882	TF binding region
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
IGHV3OR16-11	TF binding region
ENSG00000260626	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261200	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ARHGAP23P1	TF binding region
BMS1P8	TF binding region
ENSG00000205452	CpG island
ENSG00000260525	CpG island
IGHV3OR16-16	CpG island
ENSG00000261153	CpG island
ENSG00000259680	CpG island
ENSG00000260312	CpG island
ENSG00000263277	CpG island
ENSG00000261466	CpG island
ENSG00000261405	CpG island
IGHV3OR16-13	CpG island
ENPP7P13	CpG island
ENSG00000198555	CpG island
ENSG00000262090	CpG island
ENSG00000261607	CpG island
IGHV3OR16-12	CpG island
ENSG00000259882	CpG island
ENSG00000270401	CpG island
ENSG00000260308	CpG island
IGHV3OR16-11	CpG island
ENSG00000260626	CpG island
IGHV3OR16-7	CpG island
ENSG00000261200	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000101972	chromatin interactions
ENSG00000259680	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 11007 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:11007 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62029157	chr16:33298829-33298830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs561955200	chr16:33298900-33298901	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs141269386	chr16:33298931-33298932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs201046913	chr16:33298953-33298954	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs529324471	chr16:33298960-33298961	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs541146611	chr16:33298962-33298963	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs159513	chr16:33299052-33299053	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs62029158	chr16:33299064-33299065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs202192702	chr16:33299147-33299148	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200464878	chr16:33299306-33299307	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563486937	chr16:33302523-33302524	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs575739642	chr16:33302524-33302525	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs139673738	chr16:33302533-33302534	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs376321124	chr16:33302534-33302535	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs200300813	chr16:33302536-33302537	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs543213630	chr16:33302552-33302553	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs181304409	chr16:33318811-33318812	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs550713941	chr16:33318815-33318816	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs569306340	chr16:33318822-33318823	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs370294817	chr16:33318829-33318830	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs140660444	chr16:33318842-33318843	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs141332578	chr16:33318863-33318864	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs185662275	chr16:33318866-33318867	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs189249620	chr16:33318873-33318874	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs200800764	chr16:33318896-33318897	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs370818067	chr16:33318920-33318921	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs375691941	chr16:33318937-33318938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536325327	chr16:33318980-33318981	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77352595	chr16:33318983-33318984	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs548733126	chr16:33318990-33318991	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7499822	chr16:33318997-33318998	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534439422	chr16:33318998-33318999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs368377184	chr16:33319025-33319026	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs76016901	chr16:33319040-33319041	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577485768	chr16:33319075-33319076	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs376516630	chr16:33319084-33319085	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537822652	chr16:33319088-33319089	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs79602727	chr16:33319116-33319117	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76646801	chr16:33319118-33319119	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs555865908	chr16:33319121-33319122	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574409606	chr16:33319125-33319126	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541516728	chr16:33319126-33319127	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs559863632	chr16:33319146-33319147	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs571863107	chr16:33319157-33319158	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs79508078	chr16:33319174-33319175	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs78742290	chr16:33319181-33319182	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs79197453	chr16:33319224-33319225	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs371453766	chr16:33319247-33319248	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs560779397	chr16:33319251-33319252	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs527876470	chr16:33319257-33319258	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

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
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33318800-33319400	Active TSS	Placenta	Placenta
2	chr16:33318800-33319600	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr16:33319000-33319400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:33319000-33319600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr16:33319400-33319600	Flanking Active TSS	Placenta	Placenta
6	chr16:33331200-33332400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr16:33332400-33332800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr16:33347200-33348200	Enhancers	Left Ventricle	heart
9	chr16:33347200-33348800	Enhancers	Right Ventricle	heart
10	chr16:33347200-33349200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr16:33347200-33350600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr16:33347800-33348000	ZNF genes & repeats	Pancreas	Pancrea
13	chr16:33347800-33348200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:33348000-33348200	ZNF genes & repeats	Gastric	stomach
15	chr16:33348200-33349400	Weak transcription	Left Ventricle	heart
16	chr16:33348800-33350000	Weak transcription	Right Ventricle	heart
17	chr16:33349400-33350200	Enhancers	Left Ventricle	heart
18	chr16:33349400-33351600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr16:33350000-33350200	Enhancers	Right Ventricle	heart
20	chr16:33350000-33350600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr16:33351200-33352000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr16:33351600-33352000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:33351800-33352000	ZNF genes & repeats	Right Atrium	heart
24	chr16:33352000-33356200	Weak transcription	Right Atrium	heart
25	chr16:33356800-33357600	Enhancers	Placenta	Placenta
26	chr16:33357200-33357800	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr16:33357600-33357800	Flanking Bivalent TSS/Enh	Placenta	Placenta
28	chr16:33365600-33369800	Weak transcription	Right Atrium	heart
29	chr16:33369600-33370400	Enhancers	Primary B cells from peripheral blood	blood
30	chr16:33370000-33371200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr16:33371200-33372400	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr16:33371200-33372800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
33	chr16:33371600-33372600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr16:33373600-33373800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr16:33373800-33374000	Enhancers	Placenta	Placenta
36	chr16:33373800-33374400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr16:33373800-33377000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr16:33374000-33374400	Bivalent Enhancer	Placenta	Placenta
39	chr16:33374600-33376600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:33375200-33375400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr16:33375200-33375800	ZNF genes & repeats	Right Ventricle	heart
42	chr16:33375400-33375800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:33375400-33376000	Bivalent Enhancer	Placenta	Placenta
44	chr16:33375400-33377200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr16:33376000-33376800	Enhancers	Placenta	Placenta
46	chr16:33377600-33382200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr16:33378200-33382600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr16:33379400-33380400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:33379600-33380200	ZNF genes & repeats	Gastric	stomach
50	chr16:33379600-33380600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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