Variant report

Variant	nsv1064229
Chromosome Location	chr16:33476430-33827050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2680)
CpG islands
(count:2141)
Chromatin interactive
region (count:20)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2680 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

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	chr16:33535249-33535260	K562	blood:	n/a	n/a
4	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
5	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
6	ATF3	chr16:33569464-33569595	GM12878	blood:	n/a	n/a
7	ATF3	chr16:33619018-33619453	K562	blood:	n/a	n/a
8	ATF3	chr16:33569376-33569681	K562	blood:	n/a	n/a
9	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
10	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
11	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
12	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
13	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
14	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
15	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
16	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
17	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
18	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
19	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
20	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
21	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
22	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
23	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:33582517-33582748	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:33493442-33493790	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:33518137-33518397	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:33563810-33564006	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:33521194-33521489	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:33722347-33722700	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:33524561-33524846	GM12878	blood:	n/a	n/a
41	BHLHE40	chr16:33507671-33507877	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:33618946-33619398	K562	blood:	n/a	n/a
43	BHLHE40	chr16:33569455-33569658	K562	blood:	n/a	n/a
44	BHLHE40	chr16:33524786-33525031	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:33771097-33771304	HepG2	liver:	n/a	n/a
46	CBX3	chr16:33673445-33673662	K562	blood:	n/a	n/a
47	CBX3	chr16:33618771-33619525	K562	blood:	n/a	n/a
48	CBX3	chr16:33711192-33711411	K562	blood:	n/a	n/a
49	CBX3	chr16:33763911-33764377	K562	blood:	n/a	n/a
50	CBX3	chr16:33618795-33619465	K562	blood:	n/a	n/a

(count:2141 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33509433-33509483	HCM	heart:	n/a
2	chr16:33605185-33605235	SK-N-SH	brain:	n/a
3	chr16:33817992-33818042	HRPEpiC	eye:	n/a
4	chr16:33483591-33483641	U87	brain:	n/a
5	chr16:33574151-33574201	HCPEpiC	choroid plexus:	n/a
6	chr16:33483299-33483349	AoSMC	blood vessel:	n/a
7	chr16:33509433-33509483	HCM	heart:	n/a
8	chr16:33605185-33605235	SK-N-SH	brain:	n/a
9	chr16:33817992-33818042	HRPEpiC	eye:	n/a
10	chr16:33483591-33483641	U87	brain:	n/a
11	chr16:33574151-33574201	HCPEpiC	choroid plexus:	n/a
12	chr16:33483299-33483349	AoSMC	blood vessel:	n/a
13	chr16:33509523-33509573	NHBE	bronchial:	n/a
14	chr16:33730558-33730608	PFSK-1	brain:	n/a
15	chr16:33817457-33817507	ovcar-3	ovarian:	n/a
16	chr16:33783802-33783852	BJ	skin:	n/a
17	chr16:33730558-33730608	IMR90	lung:	fetal
18	chr16:33627215-33627265	LNCaP	prostate:	n/a
19	chr16:33510089-33510139	HepG2	liver:	n/a
20	chr16:33510089-33510139	HNPCEpiC	eye:	n/a
21	chr16:33574151-33574201	HRE	kidney:	n/a
22	chr16:33509433-33509483	NT2-D1	testis:	n/a
23	chr16:33573857-33573907	Hela-S3	cervix:	n/a
24	chr16:33781365-33781415	HL-60	blood:	n/a
25	chr16:33571945-33571995	HEK293	kidney:	embryo
26	chr16:33627536-33627586	H1-hESC	embryonic stem cell:	embryo
27	chr16:33483462-33483512	BJ	skin:	n/a
28	chr16:33627215-33627265	IMR90	lung:	fetal
29	chr16:33783802-33783852	A549	lung:	n/a
30	chr16:33627536-33627586	IMR90	lung:	fetal
31	chr16:33730558-33730608	Caco-2	colon:	n/a
32	chr16:33730720-33730770	GM12878	blood:	n/a
33	chr16:33817457-33817507	GM12891	blood:	n/a
34	chr16:33815990-33816040	LNCaP	prostate:	n/a
35	chr16:33730720-33730770	H1-hESC	embryonic stem cell:	embryo
36	chr16:33481620-33481670	GM19239	blood:	n/a
37	chr16:33483299-33483349	ECC-1	luminal epithelium:	n/a
38	chr16:33487438-33487488	ovcar-3	ovarian:	n/a
39	chr16:33483299-33483349	RPTEC	kidney:	n/a
40	chr16:33571945-33571995	HRCEpiC	kidney:	n/a
41	chr16:33570021-33570071	AG04449	skin:	fetal
42	chr16:33509523-33509573	BE2_C	brain:	n/a
43	chr16:33730539-33730589	SKMC	muscle:	n/a
44	chr16:33570021-33570071	HCPEpiC	choroid plexus:	n/a
45	chr16:33483297-33483347	HL-60	blood:	n/a
46	chr16:33481620-33481670	HNPCEpiC	eye:	n/a
47	chr16:33573272-33573322	GM06990	blood:	n/a
48	chr16:33510089-33510139	HMEC	breast:	n/a
49	chr16:33730558-33730608	LNCaP	prostate:	n/a
50	chr16:33574151-33574201	GM12891	blood:	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	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
3	chr16:33618869..33619686-chr16:33955996..33956882,3	MCF-7	breast:
4	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
5	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
6	chr16:33618687..33619546-chr21:22589708..22590404,2	MCF-7	breast:
7	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
8	chr14:107287133..107287781-chr16:33618600..33619120,3	MCF-7	breast:
9	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
10	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
11	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
12	chr13:30046484..30047067-chr16:33618956..33619795,2	MCF-7	breast:
13	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
14	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
15	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
16	chr1:121484857..121485377-chr16:33618718..33619247,2	MCF-7	breast:
17	chr16:33618975..33619481-chr6:120699536..120700074,2	MCF-7	breast:
18	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
19	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
20	chr16:33618559..33619759-chr16:33646461..33647717,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
2	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
3	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
4	lnc-AC136428.1.1-1	chr16:33661251-33661331	ENSG00000260312.1
5	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
6	lnc-AC140658.1-6	chr16:33776833-33776957	ENSG00000205452.4
7	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
8	lnc-AC136428.1.1-10	chr16:33677891-33677935	NONHSAT142113
9	lnc-AC136428.1.1-1	chr16:33661001-33661077	ENSG00000260312.1
10	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
11	lnc-AC136428.1.1-10	chr16:33677506-33677808	NONHSAT142113
12	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
13	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
14	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
15	lnc-AC136428.1.1-1	chr16:33660402-33660589	ENSG00000260312.1
16	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
17	lnc-AC140658.1-6	chr16:33777416-33777550	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: 6536 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:6536 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542173321	chr16:33476636-33476637	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs535950158	chr16:33476672-33476673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs555185098	chr16:33476710-33476711	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs528164758	chr16:33476717-33476718	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs539970712	chr16:33476718-33476719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs565077022	chr16:33476729-33476730	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs532378967	chr16:33476746-33476747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs368659274	chr16:33476753-33476754	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140568454	chr16:33476754-33476755	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559304219	chr16:33476760-33476761	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs189948500	chr16:33476770-33476771	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs577579794	chr16:33476773-33476774	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs117653666	chr16:33476796-33476797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs181947315	chr16:33476851-33476852	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs138544537	chr16:33476854-33476855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs3925825	chr16:33476883-33476884	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs553217990	chr16:33476889-33476890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs553072602	chr16:33476897-33476898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs574913757	chr16:33476908-33476909	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs186288753	chr16:33476960-33476961	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs557140005	chr16:33476966-33476967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs74015370	chr16:33476972-33476973	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs377099315	chr16:33477003-33477004	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs3927998	chr16:33477043-33477044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs189927096	chr16:33477053-33477054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs554517875	chr16:33477072-33477073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs182136774	chr16:33477073-33477074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs111471999	chr16:33477080-33477081	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs572786166	chr16:33477081-33477082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs540303765	chr16:33477082-33477083	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs185880110	chr16:33477085-33477086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs28416763	chr16:33477112-33477113	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs532338467	chr16:33477117-33477118	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs544381613	chr16:33477118-33477119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs562677136	chr16:33477130-33477131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs191523211	chr16:33477144-33477145	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs182997639	chr16:33477177-33477178	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs567628365	chr16:33477179-33477180	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs573172643	chr16:33477230-33477231	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs59718261	chr16:33477253-33477254	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs528521871	chr16:33477267-33477268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs374831787	chr16:33477270-33477271	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs28676596	chr16:33477280-33477281	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs547060058	chr16:33477283-33477284	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs28370557	chr16:33477325-33477326	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs28410893	chr16:33477339-33477340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs28706923	chr16:33477387-33477388	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs139826372	chr16:33477392-33477393	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs74380030	chr16:33477400-33477401	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs28546534	chr16:33483005-33483006	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
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:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33476600-33477400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:33476600-33477400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:33477200-33477400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr16:33477200-33477400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr16:33477200-33477400	ZNF genes & repeats	Pancreas	Pancrea
6	chr16:33483000-33483800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr16:33483200-33483400	Bivalent Enhancer	Placenta	Placenta
8	chr16:33483400-33488200	Weak transcription	Placenta	Placenta
9	chr16:33488200-33488400	Enhancers	Pancreas	Pancrea
10	chr16:33488200-33488400	ZNF genes & repeats	Right Atrium	heart
11	chr16:33488200-33490600	Strong transcription	Placenta	Placenta
12	chr16:33490600-33508400	Weak transcription	Placenta	Placenta
13	chr16:33492600-33493200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
14	chr16:33492600-33493400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr16:33494400-33494800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:33503000-33503600	Enhancers	HepG2	liver
17	chr16:33508400-33509000	Enhancers	Placenta	Placenta
18	chr16:33508400-33510400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:33509000-33509400	Flanking Active TSS	Placenta	Placenta
20	chr16:33509000-33510400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr16:33509000-33510400	Active TSS	Right Ventricle	heart
22	chr16:33509000-33510600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr16:33509000-33510600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr16:33509000-33510600	Active TSS	K562	blood
25	chr16:33509200-33509800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr16:33509200-33510400	Active TSS	Psoas Muscle	Psoas
27	chr16:33509200-33510600	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr16:33509200-33510600	Active TSS	Thymus	Thymus
29	chr16:33509400-33509800	Active TSS	Placenta	Placenta
30	chr16:33509400-33510000	Active TSS	Left Ventricle	heart
31	chr16:33509400-33510400	Active TSS	HSMM	muscle
32	chr16:33509400-33510600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:33509800-33510000	Flanking Bivalent TSS/Enh	Placenta	Placenta
34	chr16:33509800-33510200	Active TSS	Small Intestine	intestine
35	chr16:33509800-33510400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr16:33509800-33510600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr16:33510000-33510400	Flanking Active TSS	Placenta	Placenta
38	chr16:33510000-33510400	Active TSS	Osteobl	bone
39	chr16:33510400-33510600	Active TSS	Placenta	Placenta
40	chr16:33510400-33512000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr16:33510400-33515000	Weak transcription	Right Ventricle	heart
42	chr16:33510800-33512000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr16:33511800-33512400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr16:33512000-33512200	Enhancers	Pancreas	Pancrea
45	chr16:33512000-33516400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr16:33512000-33516600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr16:33512400-33513800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr16:33513000-33516200	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr16:33513200-33513400	ZNF genes & repeats	Gastric	stomach
50	chr16:33514800-33516000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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