Variant report

Variant	nsv906657
Chromosome Location	chr16:34284743-34517789
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	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
2	BHLHE40	chr16:34429795-34429892	K562	blood:	n/a	chr16:34429875-34429891
3	CEBPB	chr16:34368818-34369342	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
4	CEBPB	chr16:34486751-34487148	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr16:34486702-34487146	IMR90	lung:	n/a	chr16:34486713-34486730
6	CEBPB	chr16:34296958-34297110	A549	lung:	n/a	n/a
7	CEBPB	chr16:34425354-34425572	A549	lung:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
8	CEBPB	chr16:34368784-34369416	ECC-1	luminal epithelium:	n/a	chr16:34369018-34369029
9	CEBPB	chr16:34425327-34425632	HepG2	liver:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
10	CEBPB	chr16:34425405-34425572	K562	blood:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
11	CEBPB	chr16:34369463-34369642	A549	lung:	n/a	chr16:34369584-34369595
12	CEBPB	chr16:34369427-34369724	ECC-1	luminal epithelium:	n/a	chr16:34369584-34369595
13	CEBPB	chr16:34411891-34412110	IMR90	lung:	n/a	n/a
14	CEBPB	chr16:34368953-34369173	HepG2	liver:	n/a	chr16:34369018-34369029
15	CEBPB	chr16:34486734-34487193	K562	blood:	n/a	n/a
16	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:34486670-34487169	HepG2	liver:	n/a	chr16:34486713-34486730
18	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
19	CEBPB	chr16:34411851-34412016	HepG2	liver:	n/a	n/a
20	CEBPB	chr16:34449706-34449977	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr16:34456087-34456203	HepG2	liver:	n/a	n/a
22	CEBPB	chr16:34449667-34450116	A549	lung:	n/a	n/a
23	CEBPB	chr16:34425315-34425607	IMR90	lung:	n/a	chr16:34425466-34425477 chr16:34425464-34425477 chr16:34425464-34425477 chr16:34425464-34425475
24	CEBPB	chr16:34449685-34450030	K562	blood:	n/a	n/a
25	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
26	CEBPB	chr16:34449647-34450070	IMR90	lung:	n/a	n/a
27	CEBPB	chr16:34357489-34357722	HepG2	liver:	n/a	chr16:34357610-34357623 chr16:34357611-34357622
28	CEBPB	chr16:34369435-34369709	HepG2	liver:	n/a	chr16:34369584-34369595
29	CEBPB	chr16:34449630-34450134	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:34483511-34483748	HepG2	liver:	n/a	n/a
31	CREB1	chr16:34449721-34450025	ECC-1	luminal epithelium:	n/a	n/a
32	CREB1	chr16:34486635-34487120	GM12878	blood:	n/a	n/a
33	CREB1	chr16:34486680-34487127	HepG2	liver:	n/a	n/a
34	CREB1	chr16:34449619-34450140	K562	blood:	n/a	n/a
35	CREB1	chr16:34449713-34450017	GM12878	blood:	n/a	n/a
36	CREB1	chr16:34486601-34487272	K562	blood:	n/a	n/a
37	CREB1	chr16:34486669-34487187	ECC-1	luminal epithelium:	n/a	n/a
38	CREB1	chr16:34486748-34487179	GM12878	blood:	n/a	n/a
39	CREB1	chr16:34486733-34487118	K562	blood:	n/a	n/a
40	CTCF	chr16:34337320-34337470	A549	lung:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
41	CTCF	chr16:34423040-34423190	MCF-7	breast:	n/a	chr16:34423112-34423128 chr16:34423114-34423127 chr16:34423113-34423134 chr16:34423111-34423129
42	CTCF	chr16:34423000-34423150	HCT-116	colon:	n/a	chr16:34423112-34423128 chr16:34423114-34423127 chr16:34423113-34423134 chr16:34423111-34423129
43	CTCF	chr16:34423060-34423210	MCF-7	breast:	n/a	chr16:34423112-34423128 chr16:34423114-34423127 chr16:34423113-34423134 chr16:34423111-34423129
44	CTCF	chr16:34337240-34337390	HPF	lung:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
45	CTCF	chr16:34337293-34337413	ProgFib	skin:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
46	CTCF	chr16:34337280-34337430	HepG2	liver:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
47	CTCF	chr16:34422979-34423262	K562	blood:	n/a	chr16:34423112-34423128 chr16:34423114-34423127 chr16:34423113-34423134 chr16:34423111-34423129
48	CTCF	chr16:34347480-34347630	GM12866	blood:	n/a	n/a
49	CTCF	chr16:34337220-34337370	GM12868	blood:	n/a	chr16:34337333-34337351 chr16:34337338-34337346 chr16:34337328-34337349 chr16:34337334-34337350
50	CTCF	chr16:34423040-34423190	Hela-S3	cervix:	n/a	chr16:34423112-34423128 chr16:34423114-34423127 chr16:34423113-34423134 chr16:34423111-34423129

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34411816-34411866	HRCEpiC	kidney:	n/a
2	chr16:34430837-34430887	HL-60	blood:	n/a
3	chr16:34295778-34295828	PrEC	prostate:	n/a
4	chr16:34443612-34443662	HCPEpiC	choroid plexus:	n/a
5	chr16:34404673-34404723	AG04450	lung:	fetal
6	chr16:34411816-34411866	HRCEpiC	kidney:	n/a
7	chr16:34430837-34430887	HL-60	blood:	n/a
8	chr16:34295778-34295828	PrEC	prostate:	n/a
9	chr16:34443612-34443662	HCPEpiC	choroid plexus:	n/a
10	chr16:34404673-34404723	AG04450	lung:	fetal
11	chr16:34407868-34407918	HMEC	breast:	n/a
12	chr16:34428061-34428111	ProgFib	skin:	n/a
13	chr16:34404772-34404822	HRPEpiC	eye:	n/a
14	chr16:34456429-34456479	SAEC	small airway:	n/a
15	chr16:34295778-34295828	HL-60	blood:	n/a
16	chr16:34429930-34429980	HIPEpiC	eye:	n/a
17	chr16:34445785-34445835	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:34432979-34433029	SK-N-MC	brain:	n/a
19	chr16:34430837-34430887	HAEpiC	amniotic membrane:	n/a
20	chr16:34456429-34456479	CMK	blood:	n/a
21	chr16:34404774-34404824	AG09309	skin:	n/a
22	chr16:34443612-34443662	HepG2	liver:	n/a
23	chr16:34456419-34456469	GM12878	blood:	n/a
24	chr16:34296306-34296356	HPAEpiC	pulmonary alveolar:	n/a
25	chr16:34404772-34404822	PrEC	prostate:	n/a
26	chr16:34489904-34489954	HEEpiC	esophagus:	n/a
27	chr16:34429609-34429659	Hepatocyte	liver:	n/a
28	chr16:34439811-34439861	HEEpiC	esophagus:	n/a
29	chr16:34442373-34442423	NH-A	brain:	n/a
30	chr16:34407715-34407765	HCT-116	colon:	n/a
31	chr16:34403971-34404021	K562	blood:	n/a
32	chr16:34442373-34442423	Hepatocyte	liver:	n/a
33	chr16:34443120-34443170	HEEpiC	esophagus:	n/a
34	chr16:34295778-34295828	SK-N-MC	brain:	n/a
35	chr16:34293278-34293328	NHDF-neo	bronchial:	n/a
36	chr16:34428985-34429035	MCF10A-Er-Src	breast:	n/a
37	chr16:34296306-34296356	ProgFib	skin:	n/a
38	chr16:34407918-34407968	HRCEpiC	kidney:	n/a
39	chr16:34430837-34430887	ovcar-3	ovarian:	n/a
40	chr16:34404774-34404824	T-47D	breast:	n/a
41	chr16:34456419-34456469	BJ	skin:	n/a
42	chr16:34408014-34408064	HCF	heart:	n/a
43	chr16:34296108-34296158	HCT-116	colon:	n/a
44	chr16:34296108-34296158	MCF-7	breast:	n/a
45	chr16:34428985-34429035	HNPCEpiC	eye:	n/a
46	chr16:34428985-34429035	GM12892	blood:	n/a
47	chr16:34441787-34441837	BJ	skin:	n/a
48	chr16:34432979-34433029	Caco-2	colon:	n/a
49	chr16:34293278-34293328	H1-hESC	embryonic stem cell:	embryo
50	chr16:34296108-34296158	AG09309	skin:	n/a

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

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

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

Extended variants
information (count: 3326 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:3326 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578150048	chr16:34285000-34285001	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs189955991	chr16:34285004-34285005	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs575919788	chr16:34285043-34285044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs78858036	chr16:34285044-34285045	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs546075051	chr16:34285055-34285056	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs530670730	chr16:34285111-34285112	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs549014953	chr16:34285121-34285122	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs561125621	chr16:34285132-34285133	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs115779898	chr16:34285138-34285139	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs545639923	chr16:34285170-34285171	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs367810444	chr16:34285173-34285174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs566144614	chr16:34285180-34285181	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs564714848	chr16:34285198-34285199	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs77603810	chr16:34285213-34285214	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs183503503	chr16:34285251-34285252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs146714457	chr16:34285275-34285276	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs557654512	chr16:34285286-34285287	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs140345228	chr16:34285291-34285292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs555831627	chr16:34285314-34285315	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs145494861	chr16:34285364-34285365	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs534938581	chr16:34285443-34285444	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs137933363	chr16:34285495-34285496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs576019350	chr16:34285518-34285519	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs577291247	chr16:34285552-34285553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs544706530	chr16:34285598-34285599	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs149490497	chr16:34285606-34285607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574934088	chr16:34285612-34285613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542887386	chr16:34285648-34285649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188555149	chr16:34285666-34285667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528402683	chr16:34285696-34285697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540024919	chr16:34285701-34285702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565081436	chr16:34285731-34285732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533427672	chr16:34285785-34285786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192861598	chr16:34285793-34285794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542998724	chr16:34285822-34285823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561383395	chr16:34285826-34285827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371375867	chr16:34285827-34285828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62059480	chr16:34285832-34285833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143010709	chr16:34285863-34285864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528571049	chr16:34285864-34285865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530836702	chr16:34285948-34285949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549634236	chr16:34285954-34285955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34963504	chr16:34286046-34286047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546713313	chr16:34286075-34286076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567826627	chr16:34286150-34286151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535346375	chr16:34286151-34286152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184187858	chr16:34286165-34286166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187858553	chr16:34286184-34286185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1481826	chr16:34286191-34286192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556684193	chr16:34286201-34286202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	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
Breast cancer	22522925	CNVD
Rett syndrome	21593744	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34285000-34285600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:34285600-34286400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr16:34286200-34287200	Enhancers	Colon Smooth Muscle	Colon
4	chr16:34286400-34286800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr16:34287200-34288000	Weak transcription	Colon Smooth Muscle	Colon
6	chr16:34288200-34288400	Enhancers	Colon Smooth Muscle	Colon
7	chr16:34299000-34299600	ZNF genes & repeats	Spleen	Spleen
8	chr16:34299000-34303000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
9	chr16:34299000-34303200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr16:34300000-34304400	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr16:34301000-34301200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr16:34301200-34301600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr16:34301800-34302800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr16:34302000-34305400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
15	chr16:34302200-34302800	ZNF genes & repeats	Rectal Smooth Muscle	rectum
16	chr16:34309600-34310000	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr16:34315800-34316000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:34315800-34316600	ZNF genes & repeats	Adipose Nuclei	Adipose
19	chr16:34315800-34320600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:34353000-34353200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr16:34368800-34369200	Enhancers	NHEK	skin
22	chr16:34369200-34369400	Enhancers	HMEC	breast
23	chr16:34369200-34369400	Flanking Active TSS	NHEK	skin
24	chr16:34369200-34370600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:34369400-34369600	Enhancers	NHEK	skin
26	chr16:34369400-34369800	Flanking Active TSS	HMEC	breast
27	chr16:34369600-34369800	Flanking Active TSS	NHEK	skin
28	chr16:34369800-34370600	Enhancers	HMEC	breast
29	chr16:34369800-34370600	Enhancers	NHEK	skin
30	chr16:34370600-34371600	Weak transcription	NHEK	skin
31	chr16:34370600-34371800	Weak transcription	HMEC	breast
32	chr16:34371600-34372400	Enhancers	NHEK	skin
33	chr16:34371800-34372200	Enhancers	HMEC	breast
34	chr16:34374000-34387000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr16:34374200-34376800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:34374600-34374800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr16:34379000-34384200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:34380400-34385200	ZNF genes & repeats	Fetal Brain Female	brain
39	chr16:34380800-34383200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
40	chr16:34381000-34382400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr16:34382600-34382800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr16:34385200-34385800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr16:34386000-34386200	ZNF genes & repeats	Fetal Stomach	stomach
44	chr16:34407600-34409200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr16:34408200-34409000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:34408400-34409000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr16:34409000-34410800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:34409200-34410600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:34410600-34411600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr16:34410800-34411600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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