Variant report

Variant	nsv1065660
Chromosome Location	chr16:33526608-33837886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2200)
CpG islands
(count:1527)
Chromatin interactive
region (count:18)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

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	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
3	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
4	ATF3	chr16:33569464-33569595	GM12878	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	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
9	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
10	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
11	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
12	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
13	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
14	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
15	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
16	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
17	BCL11A	chr16:33722347-33722700	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
19	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:33582517-33582748	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:33563810-33564006	GM12878	blood:	n/a	n/a
26	BHLHE40	chr16:33618946-33619398	K562	blood:	n/a	n/a
27	BHLHE40	chr16:33569455-33569658	K562	blood:	n/a	n/a
28	BHLHE40	chr16:33771097-33771304	HepG2	liver:	n/a	n/a
29	CBX3	chr16:33763911-33764377	K562	blood:	n/a	n/a
30	CBX3	chr16:33733357-33733705	K562	blood:	n/a	n/a
31	CBX3	chr16:33618771-33619525	K562	blood:	n/a	n/a
32	CBX3	chr16:33711192-33711411	K562	blood:	n/a	n/a
33	CBX3	chr16:33618795-33619465	K562	blood:	n/a	n/a
34	CBX3	chr16:33763935-33764312	K562	blood:	n/a	n/a
35	CBX3	chr16:33673445-33673662	K562	blood:	n/a	n/a
36	CBX3	chr16:33715789-33716311	K562	blood:	n/a	n/a
37	CEBPB	chr16:33820719-33821164	HepG2	liver:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
38	CEBPB	chr16:33576972-33577416	K562	blood:	n/a	n/a
39	CEBPB	chr16:33576460-33577636	A549	lung:	n/a	n/a
40	CEBPB	chr16:33820812-33821002	Hela-S3	cervix:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
41	CEBPB	chr16:33820888-33821000	K562	blood:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
42	CEBPB	chr16:33537224-33537385	MCF-7	breast:	n/a	n/a
43	CEBPB	chr16:33577167-33577374	K562	blood:	n/a	n/a
44	CEBPB	chr16:33820733-33821084	K562	blood:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
45	CEBPB	chr16:33576499-33577640	HepG2	liver:	n/a	n/a
46	CEBPB	chr16:33577137-33577377	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr16:33619032-33619432	K562	blood:	n/a	n/a
48	CEBPB	chr16:33820735-33821142	IMR90	lung:	n/a	chr16:33820891-33820902 chr16:33820904-33820915
49	CEBPB	chr16:33584245-33584272	IMR90	lung:	n/a	chr16:33584247-33584256 chr16:33584247-33584256 chr16:33584245-33584258 chr16:33584247-33584256 chr16:33584245-33584258 chr16:33584247-33584258 chr16:33584247-33584258 chr16:33584245-33584256 chr16:33584247-33584256 chr16:33584245-33584258
50	CEBPB	chr16:33731398-33731812	K562	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33570021-33570071	NT2-D1	testis:	n/a
2	chr16:33817992-33818042	HEEpiC	esophagus:	n/a
3	chr16:33570021-33570071	NT2-D1	testis:	n/a
4	chr16:33817992-33818042	HEEpiC	esophagus:	n/a
5	chr16:33783802-33783852	AG09309	skin:	n/a
6	chr16:33604228-33604278	HepG2	liver:	n/a
7	chr16:33605185-33605235	T-47D	breast:	n/a
8	chr16:33605185-33605235	HPAEpiC	pulmonary alveolar:	n/a
9	chr16:33574151-33574201	Caco-2	colon:	n/a
10	chr16:33570115-33570165	GM12892	blood:	n/a
11	chr16:33783802-33783852	HCT-116	colon:	n/a
12	chr16:33783802-33783852	NHDF-neo	bronchial:	n/a
13	chr16:33570021-33570071	MCF-7	breast:	n/a
14	chr16:33817992-33818042	PANC-1	pancreas:	n/a
15	chr16:33776910-33776960	SAEC	small airway:	n/a
16	chr16:33732255-33732305	PFSK-1	brain:	n/a
17	chr16:33604228-33604278	HCPEpiC	choroid plexus:	n/a
18	chr16:33573857-33573907	NHBE	bronchial:	n/a
19	chr16:33730539-33730589	HMEC	breast:	n/a
20	chr16:33732255-33732305	K562	blood:	n/a
21	chr16:33817992-33818042	HRCEpiC	kidney:	n/a
22	chr16:33730558-33730608	AG09309	skin:	n/a
23	chr16:33570021-33570071	GM12878	blood:	n/a
24	chr16:33604228-33604278	ECC-1	luminal epithelium:	n/a
25	chr16:33730720-33730770	ovcar-3	ovarian:	n/a
26	chr16:33570021-33570071	HEEpiC	esophagus:	n/a
27	chr16:33817992-33818042	NT2-D1	testis:	n/a
28	chr16:33627215-33627265	HepG2	liver:	n/a
29	chr16:33817129-33817179	U87	brain:	n/a
30	chr16:33573857-33573907	ovcar-3	ovarian:	n/a
31	chr16:33821339-33821389	HRPEpiC	eye:	n/a
32	chr16:33570115-33570165	AG04449	skin:	fetal
33	chr16:33627536-33627586	HAEpiC	amniotic membrane:	n/a
34	chr16:33573857-33573907	HIPEpiC	eye:	n/a
35	chr16:33730558-33730608	HRE	kidney:	n/a
36	chr16:33573272-33573322	HIPEpiC	eye:	n/a
37	chr16:33730720-33730770	SK-N-SH	brain:	n/a
38	chr16:33605185-33605235	PrEC	prostate:	n/a
39	chr16:33570115-33570165	Caco-2	colon:	n/a
40	chr16:33776910-33776960	ProgFib	skin:	n/a
41	chr16:33776910-33776960	Jurkat	blood:	n/a
42	chr16:33573857-33573907	A549	lung:	n/a
43	chr16:33817992-33818042	IMR90	lung:	fetal
44	chr16:33817129-33817179	HIPEpiC	eye:	n/a
45	chr16:33779917-33779967	HEK293	kidney:	embryo
46	chr16:33781365-33781415	BJ	skin:	n/a
47	chr16:33573857-33573907	ProgFib	skin:	n/a
48	chr16:33627215-33627265	GM12892	blood:	n/a
49	chr16:33730720-33730770	BJ	skin:	n/a
50	chr16:33817129-33817179	HEK293	kidney:	embryo

(count:18 , 50 per page) page: 1

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

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

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

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

Extended variants
information (count: 4433 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:4433 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555093579	chr16:33529607-33529608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs573336408	chr16:33529609-33529610	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs138108149	chr16:33529610-33529611	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs559071700	chr16:33529626-33529627	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs368515190	chr16:33529640-33529641	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs577386012	chr16:33529642-33529643	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs372106061	chr16:33529643-33529644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs544479785	chr16:33529656-33529657	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs193020091	chr16:33529658-33529659	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs28493989	chr16:33529691-33529692	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs376400416	chr16:33529699-33529700	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs368289190	chr16:33529707-33529708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs558300927	chr16:33529717-33529718	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs529631146	chr16:33529719-33529720	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs4887672	chr16:33529743-33529744	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs375751162	chr16:33529785-33529786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs140509666	chr16:33529812-33529813	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs4887673	chr16:33529830-33529831	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs149019313	chr16:33529835-33529836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs541469919	chr16:33529840-33529841	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs4887674	chr16:33529841-33529842	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs527339973	chr16:33529842-33529843	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs144443374	chr16:33529844-33529845	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs4102788	chr16:33529866-33529867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs4102787	chr16:33529889-33529890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs552003401	chr16:33529890-33529891	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs570597966	chr16:33529899-33529900	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs4102786	chr16:33529911-33529912	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs143586780	chr16:33529932-33529933	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs79139620	chr16:33529939-33529940	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs4102785	chr16:33529958-33529959	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs531435772	chr16:33529978-33529979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs550085747	chr16:33529993-33529994	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs62037694	chr16:33530016-33530017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs201697245	chr16:33530019-33530020	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs536645757	chr16:33530094-33530095	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs76393588	chr16:33530113-33530114	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs76023129	chr16:33530133-33530134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs561981815	chr16:33530136-33530137	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs80021073	chr16:33530149-33530150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs78940392	chr16:33530158-33530159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs74422981	chr16:33530166-33530167	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs372131181	chr16:33530191-33530192	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs374846007	chr16:33530197-33530198	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs140709080	chr16:33530233-33530234	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369069182	chr16:33530240-33530241	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201034533	chr16:33530248-33530249	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534267527	chr16:33530270-33530271	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113201135	chr16:33530271-33530272	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375525819	chr16:33530274-33530275	ZNF genes & repeats Weak transcription	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:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33529600-33542200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr16:33529800-33530200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:33530000-33530200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
4	chr16:33530200-33532000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr16:33533800-33541000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:33534200-33539200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr16:33535600-33539600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr16:33541200-33542200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr16:33543000-33543400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
10	chr16:33547200-33549000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr16:33547400-33548000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr16:33547400-33548000	ZNF genes & repeats	Fetal Brain Male	brain
13	chr16:33547400-33549200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr16:33547600-33548000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr16:33547600-33548000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:33551000-33551800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr16:33560200-33563600	Weak transcription	HepG2	liver
18	chr16:33563600-33564000	Enhancers	HepG2	liver
19	chr16:33568200-33572600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr16:33568400-33574000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr16:33568600-33573400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr16:33569000-33574200	ZNF genes & repeats	Fetal Stomach	stomach
23	chr16:33569200-33573400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
24	chr16:33569400-33569800	Enhancers	K562	blood
25	chr16:33569400-33571200	ZNF genes & repeats	Spleen	Spleen
26	chr16:33569400-33572400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
27	chr16:33569600-33569800	Bivalent Enhancer	Placenta	Placenta
28	chr16:33570000-33570200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr16:33570400-33571800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr16:33570800-33572800	Weak transcription	Right Atrium	heart
31	chr16:33571600-33571800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
32	chr16:33571800-33572000	Flanking Active TSS	HepG2	liver
33	chr16:33571800-33572400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr16:33572000-33572200	Enhancers	HepG2	liver
35	chr16:33572400-33572600	Bivalent Enhancer	Placenta	Placenta
36	chr16:33572600-33572800	Flanking Bivalent TSS/Enh	Placenta	Placenta
37	chr16:33572800-33573200	Bivalent Enhancer	Placenta	Placenta
38	chr16:33573000-33573200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr16:33573000-33573400	Bivalent/Poised TSS	Right Ventricle	heart
40	chr16:33573200-33573400	Flanking Bivalent TSS/Enh	Placenta	Placenta
41	chr16:33573200-33573600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
42	chr16:33573200-33573800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr16:33573400-33573800	Active TSS	Right Ventricle	heart
44	chr16:33573400-33574200	Bivalent Enhancer	Placenta	Placenta
45	chr16:33573800-33574000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr16:33573800-33574200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr16:33587400-33595600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr16:33592600-33595400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr16:33592800-33593000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr16:33593600-33594200	ZNF genes & repeats	Fetal Brain Male	brain

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