Variant report

Variant	nsv1064842
Chromosome Location	chr16:34197339-34472275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
2	BHLHE40	chr16:34234710-34234716	K562	blood:	n/a	n/a
3	CEBPB	chr16:34223668-34223978	A549	lung:	n/a	chr16:34223701-34223712
4	CEBPB	chr16:34238344-34238603	IMR90	lung:	n/a	chr16:34238476-34238487
5	CEBPB	chr16:34247089-34247299	K562	blood:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
6	CEBPB	chr16:34223604-34224037	IMR90	lung:	n/a	chr16:34223701-34223712
7	CEBPB	chr16:34425354-34425572	A549	lung:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
8	CEBPB	chr16:34238414-34238615	A549	lung:	n/a	chr16:34238476-34238487
9	CEBPB	chr16:34411851-34412016	HepG2	liver:	n/a	n/a
10	CEBPB	chr16:34215286-34215454	H1-hESC	embryonic stem cell:	n/a	chr16:34215341-34215352
11	CEBPB	chr16:34425315-34425607	IMR90	lung:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
12	CEBPB	chr16:34215223-34215501	K562	blood:	n/a	chr16:34215341-34215352
13	CEBPB	chr16:34223559-34224035	HepG2	liver:	n/a	chr16:34223701-34223712
14	CEBPB	chr16:34369435-34369709	HepG2	liver:	n/a	chr16:34369584-34369595
15	CEBPB	chr16:34238359-34238633	HepG2	liver:	n/a	chr16:34238476-34238487
16	CEBPB	chr16:34425327-34425632	HepG2	liver:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
17	CEBPB	chr16:34411891-34412110	IMR90	lung:	n/a	n/a
18	CEBPB	chr16:34215176-34215517	A549	lung:	n/a	chr16:34215341-34215352
19	CEBPB	chr16:34247011-34247304	IMR90	lung:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
20	CEBPB	chr16:34449667-34450116	A549	lung:	n/a	n/a
21	CEBPB	chr16:34201201-34201297	A549	lung:	n/a	n/a
22	CEBPB	chr16:34238371-34238530	K562	blood:	n/a	chr16:34238476-34238487
23	CEBPB	chr16:34357489-34357722	HepG2	liver:	n/a	chr16:34357610-34357623 chr16:34357611-34357622
24	CEBPB	chr16:34368784-34369416	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
25	CEBPB	chr16:34369427-34369724	ECC-1	luminal epithelium:	n/a	chr16:34369584-34369595
26	CEBPB	chr16:34247010-34247306	A549	lung:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
27	CEBPB	chr16:34368953-34369173	HepG2	liver:	n/a	chr16:34369018-34369029
28	CEBPB	chr16:34449706-34449977	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr16:34248339-34248461	IMR90	lung:	n/a	chr16:34248391-34248402
30	CEBPB	chr16:34425405-34425572	K562	blood:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
31	CEBPB	chr16:34449685-34450030	K562	blood:	n/a	n/a
32	CEBPB	chr16:34449630-34450134	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34247069-34247351	HepG2	liver:	n/a	chr16:34247209-34247220 chr16:34247169-34247180
34	CEBPB	chr16:34449647-34450070	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:34215170-34215503	HepG2	liver:	n/a	chr16:34215341-34215352
36	CEBPB	chr16:34368818-34369342	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
37	CEBPB	chr16:34248352-34248464	HepG2	liver:	n/a	chr16:34248391-34248402
38	CEBPB	chr16:34296958-34297110	A549	lung:	n/a	n/a
39	CEBPB	chr16:34215175-34215510	IMR90	lung:	n/a	chr16:34215341-34215352
40	CEBPB	chr16:34456087-34456203	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:34369463-34369642	A549	lung:	n/a	chr16:34369584-34369595
42	CEBPZ	chr16:34280323-34280363	HepG2	liver:	n/a	n/a
43	CHD1	chr16:34210526-34210548	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr16:34449721-34450025	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr16:34449619-34450140	K562	blood:	n/a	n/a
46	CREB1	chr16:34449713-34450017	GM12878	blood:	n/a	n/a
47	CTCF	chr16:34337152-34337490	SK-N-SH_RA	brain:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
48	CTCF	chr16:34337260-34337410	HEK293	kidney:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
49	CTCF	chr16:34281891-34281926	LNCaP	prostate:	n/a	n/a
50	CTCF	chr16:34337220-34337370	Caco-2	colon:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34208209-34208259	HAEpiC	amniotic membrane:	n/a
2	chr16:34208792-34208842	HepG2	liver:	n/a
3	chr16:34213955-34214005	NHDF-neo	bronchial:	n/a
4	chr16:34443120-34443170	Hela-S3	cervix:	n/a
5	chr16:34208209-34208259	CMK	blood:	n/a
6	chr16:34431003-34431053	MCF-7	breast:	n/a
7	chr16:34378497-34378547	PrEC	prostate:	n/a
8	chr16:34265361-34265411	CMK	blood:	n/a
9	chr16:34208209-34208259	HAEpiC	amniotic membrane:	n/a
10	chr16:34208792-34208842	HepG2	liver:	n/a
11	chr16:34213955-34214005	NHDF-neo	bronchial:	n/a
12	chr16:34443120-34443170	Hela-S3	cervix:	n/a
13	chr16:34208209-34208259	CMK	blood:	n/a
14	chr16:34431003-34431053	MCF-7	breast:	n/a
15	chr16:34378497-34378547	PrEC	prostate:	n/a
16	chr16:34265361-34265411	CMK	blood:	n/a
17	chr16:34441787-34441837	PFSK-1	brain:	n/a
18	chr16:34378497-34378547	HCM	heart:	n/a
19	chr16:34431003-34431053	HCF	heart:	n/a
20	chr16:34430837-34430887	HL-60	blood:	n/a
21	chr16:34445785-34445835	AG04450	lung:	fetal
22	chr16:34445785-34445835	HUVEC	blood vessel:	n/a
23	chr16:34428985-34429035	NH-A	brain:	n/a
24	chr16:34204266-34204316	HUVEC	blood vessel:	n/a
25	chr16:34456429-34456479	AoSMC	blood vessel:	n/a
26	chr16:34378497-34378547	HIPEpiC	eye:	n/a
27	chr16:34430078-34430128	HCM	heart:	n/a
28	chr16:34404054-34404104	HUVEC	blood vessel:	n/a
29	chr16:34430382-34430432	AG09309	skin:	n/a
30	chr16:34408014-34408064	HRPEpiC	eye:	n/a
31	chr16:34213955-34214005	PANC-1	pancreas:	n/a
32	chr16:34206688-34206738	NHBE	bronchial:	n/a
33	chr16:34206688-34206738	NHDF-neo	bronchial:	n/a
34	chr16:34256428-34256478	BJ	skin:	n/a
35	chr16:34206688-34206738	HRCEpiC	kidney:	n/a
36	chr16:34407760-34407810	HRE	kidney:	n/a
37	chr16:34255535-34255585	SK-N-SH	brain:	n/a
38	chr16:34407918-34407968	HepG2	liver:	n/a
39	chr16:34430837-34430887	GM12892	blood:	n/a
40	chr16:34439811-34439861	NT2-D1	testis:	n/a
41	chr16:34442090-34442140	CMK	blood:	n/a
42	chr16:34428985-34429035	Jurkat	blood:	n/a
43	chr16:34213955-34214005	K562	blood:	n/a
44	chr16:34404673-34404723	HCT-116	colon:	n/a
45	chr16:34442283-34442333	PANC-1	pancreas:	n/a
46	chr16:34292178-34292228	AG04450	lung:	fetal
47	chr16:34456429-34456479	NH-A	brain:	n/a
48	chr16:34257170-34257220	Hepatocyte	liver:	n/a
49	chr16:34456419-34456469	SK-N-MC	brain:	n/a
50	chr16:34293278-34293328	ECC-1	luminal epithelium:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-2	chr16:34214112-34214215	ENSG00000260854.1
2	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
3	lnc-LINC00273-4	chr16:34263773-34263920	XLOC_011926
4	lnc-CTD-2144E22.5.1-12	chr16:34320267-34320490	NONHSAT142151
5	lnc-LINC00273-2	chr16:34213115-34213562	ENSG00000260854.1
6	lnc-LINC00273-4	chr16:34261392-34261835	NONHSAT142147
7	lnc-LINC00273-15	chr16:34383828-34384161	NONHSAT142158
8	lnc-CTD-2144E22.5.1-11	chr16:34213746-34213986	NONHSAT142141
9	lnc-LINC00273-4	chr16:34259780-34260039	XLOC_011926
10	lnc-CTD-2144E22.5.1-5	chr16:34442308-34442392	ENSG00000260958.2
11	lnc-LINC00273-4	chr16:34263773-34263963	NONHSAT142147
12	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
13	lnc-CTD-2144E22.5.1-10	chr16:34232106-34232469	NONHSAT142142
14	lnc-CTD-2144E22.5.1-17	chr16:34427706-34428105	NONHSAT142163
15	lnc-CTD-2144E22.5.1-14	chr16:34368885-34369446	NONHSAT142152
16	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170

Variant related genes	Relation type
SLC25A1P4	TF binding region
ENSG00000261510	TF binding region
UBE2MP1	TF binding region
ENSG00000260073	TF binding region
ENSG00000260449	TF binding region
ENSG00000264479	TF binding region
ENSG00000261331	TF binding region
CCNYL3	TF binding region
ENSG00000260854	TF binding region
ENSG00000261398	TF binding region
ENSG00000260809	TF binding region
ENSG00000260958	TF binding region
ENSG00000256579	TF binding region
ENSG00000261053	TF binding region
RARRES2P5	TF binding region
ENSG00000260590	TF binding region
ENSG00000261274	TF binding region
VN1R69P	TF binding region
ENSG00000179755	TF binding region
VN1R68P	TF binding region
ENSG00000261566	TF binding region
ENSG00000261800	TF binding region
ENSG00000262885	TF binding region
FGFR3P5	TF binding region
ENSG00000261836	TF binding region
SLC25A1P4	CpG island
ENSG00000261510	CpG island
UBE2MP1	CpG island
ENSG00000260073	CpG island
ENSG00000260449	CpG island
ENSG00000264479	CpG island
ENSG00000261331	CpG island
CCNYL3	CpG island
ENSG00000260854	CpG island
ENSG00000261398	CpG island
ENSG00000260809	CpG island
ENSG00000260958	CpG island
ENSG00000256579	CpG island
ENSG00000261053	CpG island
RARRES2P5	CpG island
ENSG00000260590	CpG island
ENSG00000261274	CpG island
VN1R69P	CpG island
ENSG00000179755	CpG island
VN1R68P	CpG island
ENSG00000261566	CpG island
ENSG00000261800	CpG island
ENSG00000262885	CpG island
FGFR3P5	CpG island
ENSG00000261836	CpG island
ENSG00000261398	chromatin interactions
ENSG00000260073	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 3798 )
Associated
traits (count: 129 )

Variant overlapped rSNPs/rCNVs (count:3798 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569201293	chr16:34197341-34197342	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547782276	chr16:34197344-34197345	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78158582	chr16:34197345-34197346	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536419936	chr16:34197353-34197354	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555125912	chr16:34197364-34197365	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566989913	chr16:34197366-34197367	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569663628	chr16:34197395-34197396	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558730262	chr16:34197414-34197415	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149388151	chr16:34197453-34197454	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537331263	chr16:34197471-34197472	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544234275	chr16:34197482-34197483	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9936279	chr16:34197492-34197493	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574696629	chr16:34197528-34197529	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117270001	chr16:34197534-34197535	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560277915	chr16:34197551-34197552	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527540481	chr16:34197554-34197555	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201831034	chr16:34197555-34197556	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs57418863	chr16:34197557-34197558	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565049005	chr16:34197598-34197599	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192265256	chr16:34197600-34197601	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199981061	chr16:34197610-34197611	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535234306	chr16:34197652-34197653	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372933198	chr16:34197653-34197654	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550585592	chr16:34197665-34197666	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184327495	chr16:34197667-34197668	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530408527	chr16:34197712-34197713	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148515700	chr16:34197717-34197718	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375493742	chr16:34197728-34197729	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548645178	chr16:34197760-34197761	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369889070	chr16:34197767-34197768	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567049774	chr16:34197771-34197772	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112714336	chr16:34197791-34197792	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs8048213	chr16:34197818-34197819	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570575394	chr16:34197824-34197825	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537811777	chr16:34197833-34197834	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556102006	chr16:34197857-34197858	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538407017	chr16:34197887-34197888	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535737074	chr16:34197894-34197895	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539797971	chr16:34197926-34197927	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572166219	chr16:34197939-34197940	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190391146	chr16:34197955-34197956	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565012285	chr16:34197972-34197973	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12921999	chr16:34197985-34197986	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs544336273	chr16:34198058-34198059	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562893683	chr16:34198068-34198069	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530083755	chr16:34198083-34198084	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548813942	chr16:34198090-34198091	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560629390	chr16:34198111-34198112	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527850808	chr16:34198130-34198131	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182224691	chr16:34198137-34198138	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:129)

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

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34180400-34198000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr16:34180400-34199800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr16:34197000-34198200	Weak transcription	Fetal Heart	heart
4	chr16:34208200-34211000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:34208600-34209600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr16:34208600-34210000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr16:34209400-34209600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr16:34212800-34214400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr16:34219400-34219800	Active TSS	Fetal Heart	heart
10	chr16:34219800-34220000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr16:34219800-34220000	ZNF genes & repeats	Pancreas	Pancrea
12	chr16:34225200-34225600	Active TSS	Fetal Heart	heart
13	chr16:34234400-34237600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr16:34240600-34241000	Active TSS	Fetal Heart	heart
15	chr16:34248600-34251400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr16:34257000-34257600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:34257400-34258200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr16:34261800-34262200	Active TSS	Fetal Heart	heart
19	chr16:34264400-34265200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr16:34267400-34267600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr16:34268200-34268400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr16:34268600-34268800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:34285000-34285600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr16:34285600-34286400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:34286200-34287200	Enhancers	Colon Smooth Muscle	Colon
26	chr16:34286400-34286800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr16:34287200-34288000	Weak transcription	Colon Smooth Muscle	Colon
28	chr16:34288200-34288400	Enhancers	Colon Smooth Muscle	Colon
29	chr16:34299000-34299600	ZNF genes & repeats	Spleen	Spleen
30	chr16:34299000-34303000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
31	chr16:34299000-34303200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:34300000-34304400	ZNF genes & repeats	Adipose Nuclei	Adipose
33	chr16:34301000-34301200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr16:34301200-34301600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
35	chr16:34301800-34302800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr16:34302000-34305400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
37	chr16:34302200-34302800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
38	chr16:34309600-34310000	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr16:34315800-34316000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:34315800-34316600	ZNF genes & repeats	Adipose Nuclei	Adipose
41	chr16:34315800-34320600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chr16:34353000-34353200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr16:34368800-34369200	Enhancers	NHEK	skin
44	chr16:34369200-34369400	Enhancers	HMEC	breast
45	chr16:34369200-34369400	Flanking Active TSS	NHEK	skin
46	chr16:34369200-34370600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr16:34369400-34369600	Enhancers	NHEK	skin
48	chr16:34369400-34369800	Flanking Active TSS	HMEC	breast
49	chr16:34369600-34369800	Flanking Active TSS	NHEK	skin
50	chr16:34369800-34370600	Enhancers	HMEC	breast

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