Variant report

Variant	nsv572376
Chromosome Location	chr16:34221454-34535583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:876)
CpG islands
(count:4031)
Chromatin interactive
region (count:3)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
2	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
3	BHLHE40	chr16:34234710-34234716	K562	blood:	n/a	n/a
4	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417
5	CEBPB	chr16:34223604-34224037	IMR90	lung:	n/a	chr16:34223701-34223712
6	CEBPB	chr16:34532926-34533600	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
7	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
8	CEBPB	chr16:34247069-34247351	HepG2	liver:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
9	CEBPB	chr16:34449685-34450030	K562	blood:	n/a	n/a
10	CEBPB	chr16:34532887-34533747	HepG2	liver:	n/a	chr16:34533406-34533417
11	CEBPB	chr16:34368953-34369173	HepG2	liver:	n/a	chr16:34369018-34369029
12	CEBPB	chr16:34486702-34487146	IMR90	lung:	n/a	chr16:34486713-34486730
13	CEBPB	chr16:34296958-34297110	A549	lung:	n/a	n/a
14	CEBPB	chr16:34411891-34412110	IMR90	lung:	n/a	n/a
15	CEBPB	chr16:34531259-34531620	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr16:34449647-34450070	IMR90	lung:	n/a	n/a
17	CEBPB	chr16:34486751-34487148	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr16:34247089-34247299	K562	blood:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
19	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
20	CEBPB	chr16:34247010-34247306	A549	lung:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
21	CEBPB	chr16:34449630-34450134	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:34248339-34248461	IMR90	lung:	n/a	chr16:34248391-34248402
23	CEBPB	chr16:34223668-34223978	A549	lung:	n/a	chr16:34223701-34223712
24	CEBPB	chr16:34369427-34369724	ECC-1	luminal epithelium:	n/a	chr16:34369584-34369595
25	CEBPB	chr16:34411851-34412016	HepG2	liver:	n/a	n/a
26	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:34238359-34238633	HepG2	liver:	n/a	chr16:34238476-34238487
28	CEBPB	chr16:34238371-34238530	K562	blood:	n/a	chr16:34238476-34238487
29	CEBPB	chr16:34247011-34247304	IMR90	lung:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
30	CEBPB	chr16:34456087-34456203	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:34369463-34369642	A549	lung:	n/a	chr16:34369584-34369595
32	CEBPB	chr16:34368784-34369416	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
33	CEBPB	chr16:34238414-34238615	A549	lung:	n/a	chr16:34238476-34238487
34	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
35	CEBPB	chr16:34483511-34483748	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34368818-34369342	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
37	CEBPB	chr16:34532878-34533767	A549	lung:	n/a	chr16:34533406-34533417
38	CEBPB	chr16:34238344-34238603	IMR90	lung:	n/a	chr16:34238476-34238487
39	CEBPB	chr16:34449706-34449977	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr16:34248352-34248464	HepG2	liver:	n/a	chr16:34248391-34248402
41	CEBPB	chr16:34425405-34425572	K562	blood:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
42	CEBPB	chr16:34486670-34487169	HepG2	liver:	n/a	chr16:34486713-34486730
43	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:34223559-34224035	HepG2	liver:	n/a	chr16:34223701-34223712
45	CEBPB	chr16:34425354-34425572	A549	lung:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
46	CEBPB	chr16:34530956-34532127	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:34532914-34533612	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
48	CEBPB	chr16:34357489-34357722	HepG2	liver:	n/a	chr16:34357610-34357623 chr16:34357611-34357622
49	CEBPB	chr16:34425327-34425632	HepG2	liver:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
50	CEBPB	chr16:34369435-34369709	HepG2	liver:	n/a	chr16:34369584-34369595

(count:4031 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34445785-34445835	HRE	kidney:	n/a
2	chr16:34256290-34256340	MCF10A-Er-Src	breast:	n/a
3	chr16:34375288-34375338	HepG2	liver:	n/a
4	chr16:34295778-34295828	PFSK-1	brain:	n/a
5	chr16:34407868-34407918	IMR90	lung:	fetal
6	chr16:34445785-34445835	HRE	kidney:	n/a
7	chr16:34256290-34256340	MCF10A-Er-Src	breast:	n/a
8	chr16:34375288-34375338	HepG2	liver:	n/a
9	chr16:34295778-34295828	PFSK-1	brain:	n/a
10	chr16:34407868-34407918	IMR90	lung:	fetal
11	chr16:34403971-34404021	GM12892	blood:	n/a
12	chr16:34258406-34258456	HCT-116	colon:	n/a
13	chr16:34252958-34253008	Hepatocyte	liver:	n/a
14	chr16:34256776-34256826	ovcar-3	ovarian:	n/a
15	chr16:34403971-34404021	HMEC	breast:	n/a
16	chr16:34408014-34408064	GM12891	blood:	n/a
17	chr16:34265361-34265411	HRE	kidney:	n/a
18	chr16:34257749-34257799	HMEC	breast:	n/a
19	chr16:34404774-34404824	ovcar-3	ovarian:	n/a
20	chr16:34430078-34430128	NHDF-neo	bronchial:	n/a
21	chr16:34429930-34429980	PrEC	prostate:	n/a
22	chr16:34293278-34293328	T-47D	breast:	n/a
23	chr16:34252958-34253008	HNPCEpiC	eye:	n/a
24	chr16:34405690-34405740	ovcar-3	ovarian:	n/a
25	chr16:34405690-34405740	HCT-116	colon:	n/a
26	chr16:34378069-34378119	Hepatocyte	liver:	n/a
27	chr16:34441787-34441837	ovcar-3	ovarian:	n/a
28	chr16:34256290-34256340	HRE	kidney:	n/a
29	chr16:34490033-34490083	BJ	skin:	n/a
30	chr16:34429930-34429980	BE2_C	brain:	n/a
31	chr16:34295916-34295966	NHBE	bronchial:	n/a
32	chr16:34489904-34489954	HRE	kidney:	n/a
33	chr16:34293670-34293720	IMR90	lung:	fetal
34	chr16:34429930-34429980	GM12878	blood:	n/a
35	chr16:34430078-34430128	T-47D	breast:	n/a
36	chr16:34296108-34296158	BJ	skin:	n/a
37	chr16:34257170-34257220	GM12892	blood:	n/a
38	chr16:34403971-34404021	CMK	blood:	n/a
39	chr16:34405690-34405740	GM19239	blood:	n/a
40	chr16:34442373-34442423	NHDF-neo	bronchial:	n/a
41	chr16:34428061-34428111	MCF10A-Er-Src	breast:	n/a
42	chr16:34299638-34299688	AoSMC	blood vessel:	n/a
43	chr16:34375288-34375338	BE2_C	brain:	n/a
44	chr16:34431003-34431053	RPTEC	kidney:	n/a
45	chr16:34445785-34445835	MCF-7	breast:	n/a
46	chr16:34378804-34378854	MCF10A-Er-Src	breast:	n/a
47	chr16:34403971-34404021	HUVEC	blood vessel:	n/a
48	chr16:34403971-34404021	MCF10A-Er-Src	breast:	n/a
49	chr16:34295778-34295828	RPTEC	kidney:	n/a
50	chr16:34378497-34378547	HUVEC	blood vessel:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34256831..34259830-chr17:41380416..41383304,2	K562	blood:
2	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
3	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
2	lnc-CTD-2144E22.5.1-10	chr16:34232106-34232469	NONHSAT142142
3	lnc-LINC00273-4	chr16:34261392-34261835	NONHSAT142147
4	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
5	lnc-CTD-2144E22.5.1-14	chr16:34368885-34369446	NONHSAT142152
6	lnc-CTD-2144E22.5.1-12	chr16:34320267-34320490	NONHSAT142151
7	lnc-LINC00273-4	chr16:34259780-34260039	XLOC_011926
8	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170
9	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
10	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
11	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
12	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
13	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
14	lnc-LINC00273-4	chr16:34263773-34263963	NONHSAT142147
15	lnc-LINC00273-15	chr16:34383828-34384161	NONHSAT142158
16	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
17	lnc-LINC00273-4	chr16:34263773-34263920	XLOC_011926
18	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
19	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
20	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
21	lnc-CTD-2144E22.5.1-4	chr16:34477709-34479085	NONHSAT142171
22	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
23	lnc-CTD-2144E22.5.1-5	chr16:34442308-34442392	ENSG00000260958.2

No data

Variant related genes	Relation type
ENSG00000261510	TF binding region
UBE2MP1	TF binding region
ENSG00000260073	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000260449	TF binding region
ENSG00000261752	TF binding region
ENSG00000261398	TF binding region
ENSG00000261053	TF binding region
RARRES2P5	TF binding region
ENSG00000260590	TF binding region
ENSG00000261274	TF binding region
ENSG00000179755	TF binding region
RARRES2P6	TF binding region
ENSG00000262885	TF binding region
FGFR3P5	TF binding region
ENSG00000261836	TF binding region
SLC25A1P4	TF binding region
ENSG00000264479	TF binding region
CCNYL3	TF binding region
ENSG00000260809	TF binding region
ENSG00000260958	TF binding region
ENSG00000256579	TF binding region
VN1R69P	TF binding region
VN1R68P	TF binding region
ENSG00000261566	TF binding region
ENSG00000261800	TF binding region
ENSG00000261510	CpG island
UBE2MP1	CpG island
ENSG00000260073	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000260449	CpG island
ENSG00000261752	CpG island
ENSG00000261398	CpG island
ENSG00000261053	CpG island
RARRES2P5	CpG island
ENSG00000260590	CpG island
ENSG00000261274	CpG island
ENSG00000179755	CpG island
RARRES2P6	CpG island
ENSG00000262885	CpG island
FGFR3P5	CpG island
ENSG00000261836	CpG island
SLC25A1P4	CpG island
ENSG00000264479	CpG island
CCNYL3	CpG island
ENSG00000260809	CpG island
ENSG00000260958	CpG island
ENSG00000256579	CpG island
VN1R69P	CpG island
VN1R68P	CpG island
ENSG00000261566	CpG island
ENSG00000261800	CpG island
ENSG00000236383	chromatin interactions
ENSG00000260073	chromatin interactions
ENSG00000261398	chromatin interactions

Extended variants
information (count: 4166 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:4166 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371189237	chr16:34225264-34225265	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs191575391	chr16:34225307-34225308	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555189792	chr16:34225320-34225321	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573508590	chr16:34225334-34225335	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs28758584	chr16:34225345-34225346	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs112624467	chr16:34225406-34225407	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs184449941	chr16:34225424-34225425	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs535831551	chr16:34225426-34225427	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs532119315	chr16:34225466-34225467	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs78247884	chr16:34225472-34225473	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77262275	chr16:34225495-34225496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144267108	chr16:34225523-34225524	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs56066726	chr16:34225526-34225527	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189581764	chr16:34225540-34225541	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147799301	chr16:34225555-34225556	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs112491704	chr16:34227397-34227398	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs555587649	chr16:34227415-34227416	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs28608925	chr16:34227480-34227481	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541249807	chr16:34227487-34227488	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs560538664	chr16:34227549-34227550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs144408182	chr16:34227551-34227552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs370733117	chr16:34227626-34227627	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545833140	chr16:34227662-34227663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373726092	chr16:34227664-34227665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs147832602	chr16:34227680-34227681	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs550482959	chr16:34227710-34227711	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568292536	chr16:34227728-34227729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529417044	chr16:34227741-34227742	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs547598180	chr16:34227742-34227743	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs62059469	chr16:34227746-34227747	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs202044711	chr16:34229591-34229592	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200024816	chr16:34229593-34229594	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs532425608	chr16:34229603-34229604	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs112721735	chr16:34229608-34229609	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562466276	chr16:34229618-34229619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529808265	chr16:34229645-34229646	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200813993	chr16:34229659-34229660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201668862	chr16:34229703-34229704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200123598	chr16:34229705-34229706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201043451	chr16:34229709-34229710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376858496	chr16:34229726-34229727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189576772	chr16:34229728-34229729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567376020	chr16:34229769-34229770	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs534852906	chr16:34229785-34229786	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs58165907	chr16:34229830-34229831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs180798942	chr16:34229896-34229897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs539296187	chr16:34229923-34229924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs371538126	chr16:34229961-34229962	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557341929	chr16:34229972-34229973	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111426982	chr16:34229975-34229976	Inactive region	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
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
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
Rett syndrome	21593744	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34225200-34225600	Active TSS	Fetal Heart	heart
2	chr16:34234400-34237600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr16:34240600-34241000	Active TSS	Fetal Heart	heart
4	chr16:34248600-34251400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:34257000-34257600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:34257400-34258200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr16:34261800-34262200	Active TSS	Fetal Heart	heart
8	chr16:34264400-34265200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr16:34267400-34267600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
10	chr16:34268200-34268400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
11	chr16:34268600-34268800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr16:34285000-34285600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr16:34285600-34286400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr16:34286200-34287200	Enhancers	Colon Smooth Muscle	Colon
15	chr16:34286400-34286800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:34287200-34288000	Weak transcription	Colon Smooth Muscle	Colon
17	chr16:34288200-34288400	Enhancers	Colon Smooth Muscle	Colon
18	chr16:34299000-34299600	ZNF genes & repeats	Spleen	Spleen
19	chr16:34299000-34303000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
20	chr16:34299000-34303200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr16:34300000-34304400	ZNF genes & repeats	Adipose Nuclei	Adipose
22	chr16:34301000-34301200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr16:34301200-34301600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr16:34301800-34302800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr16:34302000-34305400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
26	chr16:34302200-34302800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
27	chr16:34309600-34310000	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr16:34315800-34316000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:34315800-34316600	ZNF genes & repeats	Adipose Nuclei	Adipose
30	chr16:34315800-34320600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:34353000-34353200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr16:34368800-34369200	Enhancers	NHEK	skin
33	chr16:34369200-34369400	Enhancers	HMEC	breast
34	chr16:34369200-34369400	Flanking Active TSS	NHEK	skin
35	chr16:34369200-34370600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr16:34369400-34369600	Enhancers	NHEK	skin
37	chr16:34369400-34369800	Flanking Active TSS	HMEC	breast
38	chr16:34369600-34369800	Flanking Active TSS	NHEK	skin
39	chr16:34369800-34370600	Enhancers	HMEC	breast
40	chr16:34369800-34370600	Enhancers	NHEK	skin
41	chr16:34370600-34371600	Weak transcription	NHEK	skin
42	chr16:34370600-34371800	Weak transcription	HMEC	breast
43	chr16:34371600-34372400	Enhancers	NHEK	skin
44	chr16:34371800-34372200	Enhancers	HMEC	breast
45	chr16:34374000-34387000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr16:34374200-34376800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr16:34374600-34374800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:34379000-34384200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr16:34380400-34385200	ZNF genes & repeats	Fetal Brain Female	brain
50	chr16:34380800-34383200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell

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