Variant report

Variant	nsv1064228
Chromosome Location	chr16:33432148-33828054
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3093)
CpG islands
(count:2140)
Chromatin interactive
region (count:20)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3093 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33577202-33577382	HepG2	liver:	n/a	n/a
3	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
4	ATF1	chr16:33535249-33535260	K562	blood:	n/a	n/a
5	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
6	ATF3	chr16:33569376-33569681	K562	blood:	n/a	n/a
7	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
8	ATF3	chr16:33619018-33619453	K562	blood:	n/a	n/a
9	ATF3	chr16:33569464-33569595	GM12878	blood:	n/a	n/a
10	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
11	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
12	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
13	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
14	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
15	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
16	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
17	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
18	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
19	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
20	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
21	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
22	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
23	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
24	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
25	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
26	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
27	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
28	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
29	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
30	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:33518137-33518397	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:33563810-33564006	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:33460213-33460485	GM12878	blood:	n/a	chr16:33460375-33460384
37	BCL11A	chr16:33458814-33459180	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:33493442-33493790	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:33582517-33582748	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:33446218-33446393	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:33524561-33524846	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:33460174-33460528	GM12878	blood:	n/a	chr16:33460375-33460384
49	BCL11A	chr16:33521194-33521489	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a

(count:2140 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33573272-33573322	GM12878	blood:	n/a
2	chr16:33570115-33570165	NT2-D1	testis:	n/a
3	chr16:33817129-33817179	Hepatocyte	liver:	n/a
4	chr16:33732255-33732305	HCPEpiC	choroid plexus:	n/a
5	chr16:33817129-33817179	HIPEpiC	eye:	n/a
6	chr16:33573272-33573322	GM12878	blood:	n/a
7	chr16:33570115-33570165	NT2-D1	testis:	n/a
8	chr16:33817129-33817179	Hepatocyte	liver:	n/a
9	chr16:33732255-33732305	HCPEpiC	choroid plexus:	n/a
10	chr16:33817129-33817179	HIPEpiC	eye:	n/a
11	chr16:33818253-33818303	Hepatocyte	liver:	n/a
12	chr16:33776910-33776960	HCPEpiC	choroid plexus:	n/a
13	chr16:33510089-33510139	AoSMC	blood vessel:	n/a
14	chr16:33574151-33574201	HNPCEpiC	eye:	n/a
15	chr16:33483462-33483512	NHDF-neo	bronchial:	n/a
16	chr16:33604228-33604278	BJ	skin:	n/a
17	chr16:33570115-33570165	BJ	skin:	n/a
18	chr16:33483244-33483294	AoSMC	blood vessel:	n/a
19	chr16:33821339-33821389	HCM	heart:	n/a
20	chr16:33815990-33816040	AG04450	lung:	fetal
21	chr16:33818253-33818303	AG09309	skin:	n/a
22	chr16:33627215-33627265	Jurkat	blood:	n/a
23	chr16:33730558-33730608	HCM	heart:	n/a
24	chr16:33818253-33818303	AG04449	skin:	fetal
25	chr16:33481620-33481670	HEK293	kidney:	embryo
26	chr16:33481620-33481670	A549	lung:	n/a
27	chr16:33573857-33573907	ovcar-3	ovarian:	n/a
28	chr16:33821339-33821389	HEK293	kidney:	embryo
29	chr16:33779917-33779967	HCM	heart:	n/a
30	chr16:33483244-33483294	HepG2	liver:	n/a
31	chr16:33573857-33573907	HMEC	breast:	n/a
32	chr16:33487438-33487488	SAEC	small airway:	n/a
33	chr16:33730539-33730589	MCF-7	breast:	n/a
34	chr16:33573272-33573322	HRCEpiC	kidney:	n/a
35	chr16:33817992-33818042	RPTEC	kidney:	n/a
36	chr16:33730558-33730608	GM12891	blood:	n/a
37	chr16:33483462-33483512	RPTEC	kidney:	n/a
38	chr16:33730558-33730608	AG09319	gingival:	n/a
39	chr16:33483297-33483347	NT2-D1	testis:	n/a
40	chr16:33821339-33821389	NT2-D1	testis:	n/a
41	chr16:33483591-33483641	SK-N-SH_RA	brain:	n/a
42	chr16:33510089-33510139	GM12878	blood:	n/a
43	chr16:33815990-33816040	PrEC	prostate:	n/a
44	chr16:33571945-33571995	HEEpiC	esophagus:	n/a
45	chr16:33730539-33730589	HRCEpiC	kidney:	n/a
46	chr16:33510089-33510139	GM19239	blood:	n/a
47	chr16:33573857-33573907	HCM	heart:	n/a
48	chr16:33509523-33509573	NB4	blood:	n/a
49	chr16:33627536-33627586	AG09309	skin:	n/a
50	chr16:33481620-33481670	HRE	kidney:	n/a

(count:20 , 50 per page) page: 1

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

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

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

No data

Variant related genes	Relation type
ENSG00000261607	TF binding region
ENSG00000205452	TF binding region
ENSG00000260525	TF binding region
IGHV3OR16-16	TF binding region
ENSG00000261153	TF binding region
ENSG00000259680	TF binding region
ENSG00000260312	TF binding region
IGHV3OR16-12	TF binding region
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
ENSG00000261217	TF binding region
IGHV3OR16-11	TF binding region
IGHV3OR16-13	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261197	TF binding region
ENPP7P13	TF binding region
ENSG00000198555	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ENSG00000259990	TF binding region
ARHGAP23P1	TF binding region
BMS1P8	TF binding region
ENSG00000261607	CpG island
ENSG00000205452	CpG island
ENSG00000260525	CpG island
IGHV3OR16-16	CpG island
ENSG00000261153	CpG island
ENSG00000259680	CpG island
ENSG00000260312	CpG island
IGHV3OR16-12	CpG island
ENSG00000270401	CpG island
ENSG00000260308	CpG island
ENSG00000261217	CpG island
IGHV3OR16-11	CpG island
IGHV3OR16-13	CpG island
IGHV3OR16-7	CpG island
ENSG00000261197	CpG island
ENPP7P13	CpG island
ENSG00000198555	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ENSG00000259990	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000259680	chromatin interactions

Extended variants
information (count: 7329 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:7329 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556404257	chr16:33436601-33436602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574814431	chr16:33436615-33436616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541377832	chr16:33436675-33436676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553360519	chr16:33436696-33436697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374704982	chr16:33436727-33436728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367706982	chr16:33436738-33436739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571805048	chr16:33436790-33436791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556618869	chr16:33436797-33436798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577579716	chr16:33436809-33436810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs56163015	chr16:33436818-33436819	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs2927983	chr16:33436819-33436820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2927984	chr16:33436857-33436858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2927985	chr16:33436867-33436868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56111217	chr16:33436895-33436896	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142459362	chr16:33436930-33436931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2448208	chr16:33436931-33436932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561920356	chr16:33436953-33436954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529216479	chr16:33436954-33436955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548595495	chr16:33436961-33436962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2448209	chr16:33436977-33436978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs369334014	chr16:33436989-33436990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527761314	chr16:33436990-33436991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552422692	chr16:33437019-33437020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4044913	chr16:33437023-33437024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548655656	chr16:33437024-33437025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538026082	chr16:33437063-33437064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2448210	chr16:33437066-33437067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4456513	chr16:33437078-33437079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556340614	chr16:33437110-33437111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180740412	chr16:33437123-33437124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140668487	chr16:33437132-33437133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535793088	chr16:33437190-33437191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs57864558	chr16:33437200-33437201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553329898	chr16:33437219-33437220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571981284	chr16:33437220-33437221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539436395	chr16:33437225-33437226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557541402	chr16:33437250-33437251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576092686	chr16:33437251-33437252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543603520	chr16:33437274-33437275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561908119	chr16:33437284-33437285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2448211	chr16:33437296-33437297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185536101	chr16:33437298-33437299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370665128	chr16:33437342-33437343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541362997	chr16:33437344-33437345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560485929	chr16:33437351-33437352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2219806	chr16:33437361-33437362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527649526	chr16:33437390-33437391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370032620	chr16:33437392-33437393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564376919	chr16:33437413-33437414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373618906	chr16:33437437-33437438	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33436600-33437600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr16:33445200-33446400	Enhancers	GM12878-XiMat	blood
3	chr16:33446200-33447000	Enhancers	Primary B cells from peripheral blood	blood
4	chr16:33446400-33446800	Weak transcription	GM12878-XiMat	blood
5	chr16:33446800-33447800	Enhancers	GM12878-XiMat	blood
6	chr16:33447000-33447600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr16:33447000-33447600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr16:33447600-33448800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr16:33447600-33451800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr16:33448800-33449400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr16:33451200-33452000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr16:33451800-33452000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr16:33457400-33457800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr16:33457600-33457800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:33457600-33458600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr16:33457600-33460400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr16:33457600-33461000	Enhancers	Primary B cells from peripheral blood	blood
18	chr16:33457800-33458400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr16:33457800-33458800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr16:33457800-33459000	Enhancers	Primary hematopoietic stem cells	blood
21	chr16:33457800-33459000	Enhancers	GM12878-XiMat	blood
22	chr16:33457800-33459200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr16:33458000-33458600	Enhancers	Placenta	Placenta
24	chr16:33458000-33459600	Enhancers	Primary B cells from cord blood	blood
25	chr16:33458400-33459200	Active TSS	Monocytes-CD14+_RO01746	blood
26	chr16:33458600-33459000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr16:33459000-33459400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr16:33459000-33459400	Weak transcription	GM12878-XiMat	blood
29	chr16:33459200-33459400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr16:33459200-33460600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr16:33459400-33459600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr16:33459400-33459800	Enhancers	GM12878-XiMat	blood
33	chr16:33459400-33460000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr16:33459800-33460200	Flanking Active TSS	GM12878-XiMat	blood
35	chr16:33460000-33460200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:33460000-33460600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr16:33460600-33460800	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr16:33463800-33464200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
39	chr16:33467200-33467400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr16:33470400-33470800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr16:33470400-33471800	Enhancers	Primary B cells from peripheral blood	blood
42	chr16:33476600-33477400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:33476600-33477400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr16:33477200-33477400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr16:33477200-33477400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr16:33477200-33477400	ZNF genes & repeats	Pancreas	Pancrea
47	chr16:33483000-33483800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:33483200-33483400	Bivalent Enhancer	Placenta	Placenta
49	chr16:33483400-33488200	Weak transcription	Placenta	Placenta
50	chr16:33488200-33488400	Enhancers	Pancreas	Pancrea

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