Variant report

Variant	nsv1066780
Chromosome Location	chr16:33463426-33837886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2716)
CpG islands
(count:2137)
Chromatin interactive
region (count:20)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2716 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33577202-33577382	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
3	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
4	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
5	ATF3	chr16:33569376-33569681	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	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
10	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
11	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
12	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
13	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
14	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
15	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
16	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
17	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
18	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
19	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
20	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
21	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
22	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
23	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:33722347-33722700	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:33493442-33493790	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:33518137-33518397	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:33582517-33582748	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:33524561-33524846	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:33563810-33564006	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:33521194-33521489	GM12878	blood:	n/a	n/a
41	BHLHE40	chr16:33618946-33619398	K562	blood:	n/a	n/a
42	BHLHE40	chr16:33524786-33525031	HepG2	liver:	n/a	n/a
43	BHLHE40	chr16:33569455-33569658	K562	blood:	n/a	n/a
44	BHLHE40	chr16:33507671-33507877	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:33771097-33771304	HepG2	liver:	n/a	n/a
46	CBX3	chr16:33715789-33716311	K562	blood:	n/a	n/a
47	CBX3	chr16:33711192-33711411	K562	blood:	n/a	n/a
48	CBX3	chr16:33673445-33673662	K562	blood:	n/a	n/a
49	CBX3	chr16:33618771-33619525	K562	blood:	n/a	n/a
50	CBX3	chr16:33763935-33764312	K562	blood:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33570021-33570071	SK-N-SH	brain:	n/a
2	chr16:33573272-33573322	HCT-116	colon:	n/a
3	chr16:33570021-33570071	SK-N-SH	brain:	n/a
4	chr16:33573272-33573322	HCT-116	colon:	n/a
5	chr16:33509523-33509573	HEK293	kidney:	embryo
6	chr16:33730720-33730770	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:33730720-33730770	H1-hESC	embryonic stem cell:	embryo
8	chr16:33487438-33487488	HUVEC	blood vessel:	n/a
9	chr16:33817457-33817507	LNCaP	prostate:	n/a
10	chr16:33573272-33573322	NB4	blood:	n/a
11	chr16:33783802-33783852	NHDF-neo	bronchial:	n/a
12	chr16:33815990-33816040	NH-A	brain:	n/a
13	chr16:33776910-33776960	ovcar-3	ovarian:	n/a
14	chr16:33483462-33483512	PFSK-1	brain:	n/a
15	chr16:33487438-33487488	Hepatocyte	liver:	n/a
16	chr16:33821339-33821389	Hepatocyte	liver:	n/a
17	chr16:33627215-33627265	SKMC	muscle:	n/a
18	chr16:33574151-33574201	PANC-1	pancreas:	n/a
19	chr16:33732255-33732305	HEK293	kidney:	embryo
20	chr16:33571945-33571995	PFSK-1	brain:	n/a
21	chr16:33815990-33816040	A549	lung:	n/a
22	chr16:33781365-33781415	AG10803	skin:	n/a
23	chr16:33779917-33779967	GM06990	blood:	n/a
24	chr16:33730558-33730608	NH-A	brain:	n/a
25	chr16:33573272-33573322	U87	brain:	n/a
26	chr16:33779917-33779967	HEEpiC	esophagus:	n/a
27	chr16:33573857-33573907	MCF10A-Er-Src	breast:	n/a
28	chr16:33573857-33573907	CMK	blood:	n/a
29	chr16:33509523-33509573	IMR90	lung:	fetal
30	chr16:33570021-33570071	HCF	heart:	n/a
31	chr16:33483462-33483512	HRCEpiC	kidney:	n/a
32	chr16:33605185-33605235	CMK	blood:	n/a
33	chr16:33732255-33732305	MCF-7	breast:	n/a
34	chr16:33509523-33509573	HL-60	blood:	n/a
35	chr16:33783802-33783852	BJ	skin:	n/a
36	chr16:33483462-33483512	HCF	heart:	n/a
37	chr16:33573857-33573907	HCF	heart:	n/a
38	chr16:33509523-33509573	PrEC	prostate:	n/a
39	chr16:33817992-33818042	HMEC	breast:	n/a
40	chr16:33571945-33571995	PrEC	prostate:	n/a
41	chr16:33781365-33781415	PANC-1	pancreas:	n/a
42	chr16:33483591-33483641	HCF	heart:	n/a
43	chr16:33483462-33483512	HCM	heart:	n/a
44	chr16:33783802-33783852	AG09319	gingival:	n/a
45	chr16:33730539-33730589	HRCEpiC	kidney:	n/a
46	chr16:33574151-33574201	HEK293	kidney:	embryo
47	chr16:33509433-33509483	BJ	skin:	n/a
48	chr16:33730720-33730770	HNPCEpiC	eye:	n/a
49	chr16:33734837-33734887	Hela-S3	cervix:	n/a
50	chr16:33574151-33574201	A549	lung:	n/a

(count:20 , 50 per page) page: 1

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

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
2	lnc-AC136428.1.1-1	chr16:33661001-33661077	ENSG00000260312.1
3	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
4	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
5	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
6	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
7	lnc-AC136428.1.1-10	chr16:33677506-33677808	NONHSAT142113
8	lnc-AC136428.1.1-1	chr16:33661251-33661331	ENSG00000260312.1
9	lnc-AC136428.1.1-10	chr16:33677891-33677935	NONHSAT142113
10	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
11	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
12	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
13	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
14	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
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	chr16:33776448-33776670	ENSG00000205452.4

No data

Variant related genes	Relation type
ENSG00000261607	TF binding region
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
IGHV3OR16-12	TF binding region
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
ENSG00000261217	TF binding region
IGHV3OR16-11	TF binding region
IGHV3OR16-13	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261197	TF binding region
ENPP7P13	TF binding region
ENSG00000198555	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ENSG00000259990	TF binding region
ARHGAP23P1	TF binding region
BMS1P8	TF binding region
ENSG00000261607	CpG island
ENSG00000205452	CpG island
ENSG00000260525	CpG island
IGHV3OR16-16	CpG island
ENSG00000261153	CpG island
ENSG00000259680	CpG island
ENSG00000260312	CpG island
IGHV3OR16-12	CpG island
ENSG00000270401	CpG island
ENSG00000260308	CpG island
ENSG00000261217	CpG island
IGHV3OR16-11	CpG island
IGHV3OR16-13	CpG island
IGHV3OR16-7	CpG island
ENSG00000261197	CpG island
ENPP7P13	CpG island
ENSG00000198555	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ENSG00000259990	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000259680	chromatin interactions

Extended variants
information (count: 6711 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:6711 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563807540	chr16:33463804-33463805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs370677752	chr16:33463843-33463844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs77401096	chr16:33463844-33463845	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs531113339	chr16:33463849-33463850	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs2941037	chr16:33463858-33463859	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs549359640	chr16:33463867-33463868	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs561615243	chr16:33463872-33463873	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs528739121	chr16:33463887-33463888	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs546892430	chr16:33463890-33463891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs2930015	chr16:33463990-33463991	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs570882082	chr16:33463993-33463994	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs538259469	chr16:33463998-33463999	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550243631	chr16:33464002-33464003	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs568885864	chr16:33464003-33464004	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs2967968	chr16:33464021-33464022	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs536441317	chr16:33464031-33464032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs554428879	chr16:33464047-33464048	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs566664327	chr16:33464048-33464049	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs373559994	chr16:33464070-33464071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs533820650	chr16:33464089-33464090	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs558910226	chr16:33464103-33464104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs578059147	chr16:33464104-33464105	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs201234957	chr16:33464107-33464108	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs557487925	chr16:33464116-33464117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs2931651	chr16:33464124-33464125	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs377214047	chr16:33464125-33464126	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs575690709	chr16:33464148-33464149	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs543116073	chr16:33464159-33464160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs144964411	chr16:33464178-33464179	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs191809324	chr16:33467206-33467207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140373650	chr16:33467213-33467214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559957035	chr16:33467218-33467219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183929330	chr16:33467227-33467228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533580895	chr16:33467249-33467250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188874508	chr16:33467250-33467251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552030655	chr16:33467251-33467252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570300602	chr16:33467261-33467262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146410456	chr16:33467282-33467283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560295602	chr16:33467283-33467284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548662051	chr16:33467292-33467293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373988764	chr16:33467297-33467298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190870700	chr16:33467309-33467310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552667440	chr16:33467323-33467324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577398626	chr16:33467349-33467350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538471945	chr16:33467365-33467366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28418400	chr16:33467368-33467369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550317704	chr16:33470429-33470430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562228101	chr16:33470432-33470433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529543724	chr16:33470438-33470439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548086852	chr16:33470451-33470452	Enhancers	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
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33463800-33464200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr16:33467200-33467400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr16:33470400-33470800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr16:33470400-33471800	Enhancers	Primary B cells from peripheral blood	blood
5	chr16:33476600-33477400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr16:33476600-33477400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:33477200-33477400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:33477200-33477400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:33477200-33477400	ZNF genes & repeats	Pancreas	Pancrea
10	chr16:33483000-33483800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr16:33483200-33483400	Bivalent Enhancer	Placenta	Placenta
12	chr16:33483400-33488200	Weak transcription	Placenta	Placenta
13	chr16:33488200-33488400	Enhancers	Pancreas	Pancrea
14	chr16:33488200-33488400	ZNF genes & repeats	Right Atrium	heart
15	chr16:33488200-33490600	Strong transcription	Placenta	Placenta
16	chr16:33490600-33508400	Weak transcription	Placenta	Placenta
17	chr16:33492600-33493200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
18	chr16:33492600-33493400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr16:33494400-33494800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr16:33503000-33503600	Enhancers	HepG2	liver
21	chr16:33508400-33509000	Enhancers	Placenta	Placenta
22	chr16:33508400-33510400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:33509000-33509400	Flanking Active TSS	Placenta	Placenta
24	chr16:33509000-33510400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
25	chr16:33509000-33510400	Active TSS	Right Ventricle	heart
26	chr16:33509000-33510600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr16:33509000-33510600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr16:33509000-33510600	Active TSS	K562	blood
29	chr16:33509200-33509800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr16:33509200-33510400	Active TSS	Psoas Muscle	Psoas
31	chr16:33509200-33510600	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr16:33509200-33510600	Active TSS	Thymus	Thymus
33	chr16:33509400-33509800	Active TSS	Placenta	Placenta
34	chr16:33509400-33510000	Active TSS	Left Ventricle	heart
35	chr16:33509400-33510400	Active TSS	HSMM	muscle
36	chr16:33509400-33510600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr16:33509800-33510000	Flanking Bivalent TSS/Enh	Placenta	Placenta
38	chr16:33509800-33510200	Active TSS	Small Intestine	intestine
39	chr16:33509800-33510400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr16:33509800-33510600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr16:33510000-33510400	Flanking Active TSS	Placenta	Placenta
42	chr16:33510000-33510400	Active TSS	Osteobl	bone
43	chr16:33510400-33510600	Active TSS	Placenta	Placenta
44	chr16:33510400-33512000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr16:33510400-33515000	Weak transcription	Right Ventricle	heart
46	chr16:33510800-33512000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr16:33511800-33512400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:33512000-33512200	Enhancers	Pancreas	Pancrea
49	chr16:33512000-33516400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr16:33512000-33516600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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