Variant report

Variant	nsv1055578
Chromosome Location	chr16:33338112-33773053
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3408)
CpG islands
(count:2018)
Chromatin interactive
region (count:25)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3408 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

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	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
3	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
4	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
5	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
6	ATF3	chr16:33569464-33569595	GM12878	blood:	n/a	n/a
7	ATF3	chr16:33569376-33569681	K562	blood:	n/a	n/a
8	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
9	ATF3	chr16:33619018-33619453	K562	blood:	n/a	n/a
10	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
11	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
12	BATF	chr16:33369625-33369914	GM12878	blood:	n/a	n/a
13	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
14	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
15	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
16	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
17	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
18	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
19	BATF	chr16:33370078-33370545	GM12878	blood:	n/a	n/a
20	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
21	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
22	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
23	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
24	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
25	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
26	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
27	BATF	chr16:33365688-33366003	GM12878	blood:	n/a	n/a
28	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
29	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
30	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
31	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
32	BATF	chr16:33358267-33358522	GM12878	blood:	n/a	n/a
33	BATF	chr16:33365611-33366045	GM12878	blood:	n/a	n/a
34	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
35	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
36	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
37	BATF	chr16:33364185-33364651	GM12878	blood:	n/a	chr16:33364440-33364451
38	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33365658-33366042	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:33521194-33521489	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:33582517-33582748	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:33366862-33367059	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:33518137-33518397	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:33359781-33360055	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33487438-33487488	RPTEC	kidney:	n/a
2	chr16:33483591-33483641	SAEC	small airway:	n/a
3	chr16:33481620-33481670	AG09319	gingival:	n/a
4	chr16:33510089-33510139	SKMC	muscle:	n/a
5	chr16:33605185-33605235	ovcar-3	ovarian:	n/a
6	chr16:33487438-33487488	RPTEC	kidney:	n/a
7	chr16:33483591-33483641	SAEC	small airway:	n/a
8	chr16:33481620-33481670	AG09319	gingival:	n/a
9	chr16:33510089-33510139	SKMC	muscle:	n/a
10	chr16:33605185-33605235	ovcar-3	ovarian:	n/a
11	chr16:33374028-33374078	AG04450	lung:	fetal
12	chr16:33481620-33481670	HCPEpiC	choroid plexus:	n/a
13	chr16:33483299-33483349	HAEpiC	amniotic membrane:	n/a
14	chr16:33730539-33730589	HMEC	breast:	n/a
15	chr16:33355024-33355074	HRPEpiC	eye:	n/a
16	chr16:33730539-33730589	A549	lung:	n/a
17	chr16:33574151-33574201	SKMC	muscle:	n/a
18	chr16:33374131-33374181	HEEpiC	esophagus:	n/a
19	chr16:33374161-33374211	AG04449	skin:	fetal
20	chr16:33570115-33570165	AG10803	skin:	n/a
21	chr16:33483244-33483294	HUVEC	blood vessel:	n/a
22	chr16:33730720-33730770	HL-60	blood:	n/a
23	chr16:33481620-33481670	HPAEpiC	pulmonary alveolar:	n/a
24	chr16:33730539-33730589	H1-hESC	embryonic stem cell:	embryo
25	chr16:33571945-33571995	ECC-1	luminal epithelium:	n/a
26	chr16:33355024-33355074	NT2-D1	testis:	n/a
27	chr16:33510089-33510139	Jurkat	blood:	n/a
28	chr16:33374028-33374078	HepG2	liver:	n/a
29	chr16:33574151-33574201	HCF	heart:	n/a
30	chr16:33374028-33374078	HCT-116	colon:	n/a
31	chr16:33627536-33627586	HRE	kidney:	n/a
32	chr16:33358227-33358277	GM12878	blood:	n/a
33	chr16:33730720-33730770	NT2-D1	testis:	n/a
34	chr16:33734837-33734887	HUVEC	blood vessel:	n/a
35	chr16:33355024-33355074	BE2_C	brain:	n/a
36	chr16:33574151-33574201	HEEpiC	esophagus:	n/a
37	chr16:33481620-33481670	NHDF-neo	bronchial:	n/a
38	chr16:33355024-33355074	RPTEC	kidney:	n/a
39	chr16:33605185-33605235	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:33574151-33574201	HMEC	breast:	n/a
41	chr16:33357151-33357201	BJ	skin:	n/a
42	chr16:33483462-33483512	GM12878	blood:	n/a
43	chr16:33730558-33730608	BJ	skin:	n/a
44	chr16:33573857-33573907	HCF	heart:	n/a
45	chr16:33734837-33734887	MCF10A-Er-Src	breast:	n/a
46	chr16:33571945-33571995	HMEC	breast:	n/a
47	chr16:33483297-33483347	GM12892	blood:	n/a
48	chr16:33571945-33571995	SAEC	small airway:	n/a
49	chr16:33487438-33487488	K562	blood:	n/a
50	chr16:33487438-33487488	SAEC	small airway:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33618975..33619481-chr6:120699536..120700074,2	MCF-7	breast:
2	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
3	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
4	chr12:123886567..123888097-chr16:33420189..33423186,2	K562	blood:
5	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:
6	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
7	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
8	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
9	chr16:33618687..33619546-chr21:22589708..22590404,2	MCF-7	breast:
10	chr16:33618887..33619679-chr16:33739842..33740784,2	MCF-7	breast:
11	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
12	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
13	chr16:33618869..33619686-chr16:33955996..33956882,3	MCF-7	breast:
14	chr16:33618559..33619759-chr16:33646461..33647717,8	MCF-7	breast:
15	chr13:30046484..30047067-chr16:33618956..33619795,2	MCF-7	breast:
16	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
17	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
18	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
19	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
20	chr14:107287133..107287781-chr16:33618600..33619120,3	MCF-7	breast:
21	chr16:33618632..33619607-chr16:33646788..33647301,2	MCF-7	breast:
22	chr16:33535568..33538409-chr16:33539107..33541473,2	K562	blood:
23	chr16:33357445..33357965-chrX:123093937..123094556,2	MCF-7	breast:
24	chr16:33599590..33601128-chr16:33607194..33610110,2	K562	blood:
25	chr1:121484857..121485377-chr16:33618718..33619247,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
2	lnc-AC136428.1.1-10	chr16:33677891-33677935	NONHSAT142113
3	lnc-AC136428.1.1-1	chr16:33661251-33661331	ENSG00000260312.1
4	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
5	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
6	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
7	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
8	lnc-AC136428.1.1-1	chr16:33661001-33661077	ENSG00000260312.1
9	lnc-AC136428.1.1-1	chr16:33660402-33660589	ENSG00000260312.1
10	lnc-AC136428.1.1-10	chr16:33677506-33677808	NONHSAT142113

No data

Variant related genes	Relation type
ENSG00000260525	TF binding region
IGHV3OR16-16	TF binding region
ENSG00000261153	TF binding region
ENSG00000259680	TF binding region
ENSG00000260312	TF binding region
ENSG00000263277	TF binding region
ENSG00000261466	TF binding region
ENSG00000261405	TF binding region
IGHV3OR16-13	TF binding region
ENPP7P13	TF binding region
ENSG00000261607	TF binding region
IGHV3OR16-12	TF binding region
ENSG00000259882	TF binding region
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
IGHV3OR16-11	TF binding region
ENSG00000260626	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261200	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ARHGAP23P1	TF binding region
BMS1P8	TF binding region
ENSG00000260525	CpG island
IGHV3OR16-16	CpG island
ENSG00000261153	CpG island
ENSG00000259680	CpG island
ENSG00000260312	CpG island
ENSG00000263277	CpG island
ENSG00000261466	CpG island
ENSG00000261405	CpG island
IGHV3OR16-13	CpG island
ENPP7P13	CpG island
ENSG00000261607	CpG island
IGHV3OR16-12	CpG island
ENSG00000259882	CpG island
ENSG00000270401	CpG island
ENSG00000260308	CpG island
IGHV3OR16-11	CpG island
ENSG00000260626	CpG island
IGHV3OR16-7	CpG island
ENSG00000261200	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000101972	chromatin interactions
ENSG00000259680	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 10694 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:10694 , 50 per page) page: 1 2 3 4 5 6 7 ... 214

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547689702	chr16:33339803-33339804	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs3861347	chr16:33339877-33339878	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569987489	chr16:33339885-33339886	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537371072	chr16:33339910-33339911	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556504956	chr16:33339954-33339955	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs369195451	chr16:33339976-33339977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113131311	chr16:33340012-33340013	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373359479	chr16:33340025-33340026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs527349572	chr16:33340030-33340031	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs574779404	chr16:33340040-33340041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs9673328	chr16:33340085-33340086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs553984872	chr16:33340088-33340089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs572565424	chr16:33340111-33340112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556316083	chr16:33340157-33340158	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546010426	chr16:33340171-33340172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs377327900	chr16:33340194-33340195	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs184687480	chr16:33340207-33340208	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs531870841	chr16:33340216-33340217	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs543749230	chr16:33340227-33340228	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs561724117	chr16:33340234-33340235	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs528882917	chr16:33340280-33340281	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs547426697	chr16:33340315-33340316	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs565650100	chr16:33340338-33340339	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs9673883	chr16:33340352-33340353	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs551580796	chr16:33340357-33340358	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs569899304	chr16:33340372-33340373	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs549187427	chr16:33340409-33340410	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs537332382	chr16:33340469-33340470	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs188302523	chr16:33340509-33340510	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs568404007	chr16:33340517-33340518	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs141933518	chr16:33340525-33340526	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs371289784	chr16:33340534-33340535	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs535497746	chr16:33340540-33340541	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs554211314	chr16:33340545-33340546	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs140613841	chr16:33340560-33340561	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs541022739	chr16:33340574-33340575	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs572187812	chr16:33340578-33340579	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs561123123	chr16:33340627-33340628	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs529053341	chr16:33340654-33340655	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs545930425	chr16:33340664-33340665	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs527728455	chr16:33340667-33340668	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs145072793	chr16:33340705-33340706	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs557923193	chr16:33340706-33340707	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs576278576	chr16:33340732-33340733	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs12919667	chr16:33340736-33340737	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs562251742	chr16:33340766-33340767	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs573544578	chr16:33340772-33340773	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs540689682	chr16:33340788-33340789	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs369121792	chr16:33340842-33340843	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs148830792	chr16:33340853-33340854	Inactive region	TF binding region lncRNA	1 gene(s)	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33347200-33348200	Enhancers	Left Ventricle	heart
2	chr16:33347200-33348800	Enhancers	Right Ventricle	heart
3	chr16:33347200-33349200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:33347200-33350600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr16:33347800-33348000	ZNF genes & repeats	Pancreas	Pancrea
6	chr16:33347800-33348200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr16:33348000-33348200	ZNF genes & repeats	Gastric	stomach
8	chr16:33348200-33349400	Weak transcription	Left Ventricle	heart
9	chr16:33348800-33350000	Weak transcription	Right Ventricle	heart
10	chr16:33349400-33350200	Enhancers	Left Ventricle	heart
11	chr16:33349400-33351600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr16:33350000-33350200	Enhancers	Right Ventricle	heart
13	chr16:33350000-33350600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr16:33351200-33352000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr16:33351600-33352000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr16:33351800-33352000	ZNF genes & repeats	Right Atrium	heart
17	chr16:33352000-33356200	Weak transcription	Right Atrium	heart
18	chr16:33356800-33357600	Enhancers	Placenta	Placenta
19	chr16:33357200-33357800	Active TSS	iPS-18 Cell Line	embryonic stem cell
20	chr16:33357600-33357800	Flanking Bivalent TSS/Enh	Placenta	Placenta
21	chr16:33365600-33369800	Weak transcription	Right Atrium	heart
22	chr16:33369600-33370400	Enhancers	Primary B cells from peripheral blood	blood
23	chr16:33370000-33371200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr16:33371200-33372400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr16:33371200-33372800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr16:33371600-33372600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr16:33373600-33373800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr16:33373800-33374000	Enhancers	Placenta	Placenta
29	chr16:33373800-33374400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
30	chr16:33373800-33377000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:33374000-33374400	Bivalent Enhancer	Placenta	Placenta
32	chr16:33374600-33376600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:33375200-33375400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr16:33375200-33375800	ZNF genes & repeats	Right Ventricle	heart
35	chr16:33375400-33375800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:33375400-33376000	Bivalent Enhancer	Placenta	Placenta
37	chr16:33375400-33377200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr16:33376000-33376800	Enhancers	Placenta	Placenta
39	chr16:33377600-33382200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr16:33378200-33382600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr16:33379400-33380400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr16:33379600-33380200	ZNF genes & repeats	Gastric	stomach
43	chr16:33379600-33380600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr16:33380000-33380400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
45	chr16:33381200-33383400	Enhancers	Placenta	Placenta
46	chr16:33382200-33382400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr16:33383200-33383600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr16:33383400-33388600	Weak transcription	Placenta	Placenta
49	chr16:33384600-33389000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr16:33385800-33387400	Enhancers	GM12878-XiMat	blood

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