Variant report

Variant	nsv1065259
Chromosome Location	chr16:33380754-33811489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3265)
CpG islands
(count:1773)
Chromatin interactive
region (count:22)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3265 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

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	chr16:33446622-33446661	K562	blood:	n/a	n/a
4	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
5	ATF1	chr16:33535249-33535260	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	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
11	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
12	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
13	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
14	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
15	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
16	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
17	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
18	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
19	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
20	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
21	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
22	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
23	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
24	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
25	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
26	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
27	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
28	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
29	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
30	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
31	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
32	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:33446218-33446393	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:33458814-33459180	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:33518137-33518397	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
41	BCL11A	chr16:33517674-33517848	GM12878	blood:	n/a	n/a
42	BCL11A	chr16:33722347-33722700	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:33460213-33460485	GM12878	blood:	n/a	chr16:33460375-33460384
44	BCL11A	chr16:33431460-33431699	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:33521194-33521489	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:33431491-33431778	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:33524561-33524846	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:33647047-33647229	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:33448833-33449216	GM12878	blood:	n/a	chr16:33449056-33449065 chr16:33449055-33449064

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33730539-33730589	SAEC	small airway:	n/a
2	chr16:33483462-33483512	NHDF-neo	bronchial:	n/a
3	chr16:33570115-33570165	SK-N-SH	brain:	n/a
4	chr16:33779917-33779967	NHBE	bronchial:	n/a
5	chr16:33730539-33730589	SAEC	small airway:	n/a
6	chr16:33483462-33483512	NHDF-neo	bronchial:	n/a
7	chr16:33570115-33570165	SK-N-SH	brain:	n/a
8	chr16:33779917-33779967	NHBE	bronchial:	n/a
9	chr16:33574151-33574201	BE2_C	brain:	n/a
10	chr16:33730539-33730589	NT2-D1	testis:	n/a
11	chr16:33627536-33627586	HMEC	breast:	n/a
12	chr16:33627215-33627265	RPTEC	kidney:	n/a
13	chr16:33783802-33783852	Jurkat	blood:	n/a
14	chr16:33570021-33570071	ProgFib	skin:	n/a
15	chr16:33779917-33779967	GM12878	blood:	n/a
16	chr16:33730539-33730589	Hela-S3	cervix:	n/a
17	chr16:33573272-33573322	ovcar-3	ovarian:	n/a
18	chr16:33783802-33783852	HEEpiC	esophagus:	n/a
19	chr16:33483299-33483349	HPAEpiC	pulmonary alveolar:	n/a
20	chr16:33483297-33483347	HCT-116	colon:	n/a
21	chr16:33627215-33627265	IMR90	lung:	fetal
22	chr16:33509433-33509483	HRE	kidney:	n/a
23	chr16:33604228-33604278	NHBE	bronchial:	n/a
24	chr16:33509523-33509573	SAEC	small airway:	n/a
25	chr16:33483462-33483512	HRCEpiC	kidney:	n/a
26	chr16:33481620-33481670	HIPEpiC	eye:	n/a
27	chr16:33605185-33605235	ECC-1	luminal epithelium:	n/a
28	chr16:33730558-33730608	HEEpiC	esophagus:	n/a
29	chr16:33783802-33783852	HAEpiC	amniotic membrane:	n/a
30	chr16:33604228-33604278	HCF	heart:	n/a
31	chr16:33487438-33487488	HCPEpiC	choroid plexus:	n/a
32	chr16:33730558-33730608	HNPCEpiC	eye:	n/a
33	chr16:33570021-33570071	HRCEpiC	kidney:	n/a
34	chr16:33483591-33483641	NB4	blood:	n/a
35	chr16:33574151-33574201	AG09309	skin:	n/a
36	chr16:33734837-33734887	H1-hESC	embryonic stem cell:	embryo
37	chr16:33509433-33509483	NHDF-neo	bronchial:	n/a
38	chr16:33574151-33574201	AG04450	lung:	fetal
39	chr16:33574151-33574201	NB4	blood:	n/a
40	chr16:33574151-33574201	HRE	kidney:	n/a
41	chr16:33627536-33627586	GM06990	blood:	n/a
42	chr16:33509433-33509483	ProgFib	skin:	n/a
43	chr16:33730539-33730589	NHDF-neo	bronchial:	n/a
44	chr16:33605185-33605235	BE2_C	brain:	n/a
45	chr16:33483244-33483294	Hela-S3	cervix:	n/a
46	chr16:33570021-33570071	AG10803	skin:	n/a
47	chr16:33627536-33627586	Hepatocyte	liver:	n/a
48	chr16:33571945-33571995	HRE	kidney:	n/a
49	chr16:33776910-33776960	AG04450	lung:	fetal
50	chr16:33783802-33783852	A549	lung:	n/a

(count:22 , 50 per page) page: 1

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

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

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

No data

Variant related genes	Relation type
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
IGHV3OR16-13	TF binding region
ENPP7P13	TF binding region
ENSG00000198555	TF binding region
ENSG00000261607	TF binding region
IGHV3OR16-12	TF binding region
ENSG00000259882	TF binding region
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
ENSG00000261217	TF binding region
IGHV3OR16-11	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ARHGAP23P1	TF binding region
BMS1P8	TF binding region
ENSG00000205452	CpG island
ENSG00000260525	CpG island
IGHV3OR16-16	CpG island
ENSG00000261153	CpG island
ENSG00000259680	CpG island
ENSG00000260312	CpG island
IGHV3OR16-13	CpG island
ENPP7P13	CpG island
ENSG00000198555	CpG island
ENSG00000261607	CpG island
IGHV3OR16-12	CpG island
ENSG00000259882	CpG island
ENSG00000270401	CpG island
ENSG00000260308	CpG island
ENSG00000261217	CpG island
IGHV3OR16-11	CpG island
IGHV3OR16-7	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000259680	chromatin interactions

Extended variants
information (count: 9375 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:9375 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530256389	chr16:33380763-33380764	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs542477898	chr16:33380764-33380765	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs560633446	chr16:33380772-33380773	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs527240613	chr16:33380776-33380777	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs552246537	chr16:33380810-33380811	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs570550947	chr16:33380831-33380832	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs531465970	chr16:33380855-33380856	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs549686156	chr16:33380897-33380898	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs370679270	chr16:33380937-33380938	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs60062762	chr16:33380948-33380949	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs535305704	chr16:33380949-33380950	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs375500067	chr16:33380956-33380957	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs565639300	chr16:33380959-33380960	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs533924010	chr16:33380960-33380961	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs558564179	chr16:33380968-33380969	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs576905121	chr16:33380988-33380989	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs200939196	chr16:33381018-33381019	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs368604296	chr16:33381101-33381102	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs376025579	chr16:33381142-33381143	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs202090438	chr16:33381147-33381148	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs79091384	chr16:33381161-33381162	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs78214109	chr16:33381162-33381163	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs79183673	chr16:33381164-33381165	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs533748861	chr16:33381165-33381166	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs59489807	chr16:33381166-33381167	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs2450581	chr16:33381173-33381174	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs182470226	chr16:33381196-33381197	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs556401046	chr16:33381220-33381221	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374302932	chr16:33381222-33381223	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9925612	chr16:33381234-33381235	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76960863	chr16:33381254-33381255	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574938011	chr16:33381300-33381301	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542062997	chr16:33381304-33381305	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369392587	chr16:33381330-33381331	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113471229	chr16:33381332-33381333	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149565211	chr16:33381336-33381337	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186883179	chr16:33381348-33381349	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9925518	chr16:33381367-33381368	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111235657	chr16:33381384-33381385	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528030465	chr16:33381387-33381388	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191824678	chr16:33381398-33381399	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564096812	chr16:33381459-33381460	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531354246	chr16:33381519-33381520	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549813871	chr16:33381533-33381534	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9925968	chr16:33381558-33381559	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs377670063	chr16:33381563-33381564	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113247761	chr16:33381581-33381582	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529036802	chr16:33381588-33381589	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370731674	chr16:33381594-33381595	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547316903	chr16:33381625-33381626	Weak transcription ZNF genes & repeats 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:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33377600-33382200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr16:33378200-33382600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr16:33381200-33383400	Enhancers	Placenta	Placenta
4	chr16:33382200-33382400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr16:33383200-33383600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr16:33383400-33388600	Weak transcription	Placenta	Placenta
7	chr16:33384600-33389000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
8	chr16:33385800-33387400	Enhancers	GM12878-XiMat	blood
9	chr16:33388600-33388800	Enhancers	Placenta	Placenta
10	chr16:33388800-33390000	Weak transcription	Placenta	Placenta
11	chr16:33390000-33392800	Enhancers	Placenta	Placenta
12	chr16:33390600-33391600	Enhancers	Left Ventricle	heart
13	chr16:33390600-33392200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr16:33391600-33392400	ZNF genes & repeats	Fetal Brain Male	brain
15	chr16:33395800-33396200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr16:33396000-33396400	Bivalent Enhancer	Placenta	Placenta
17	chr16:33397600-33398400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr16:33401200-33407200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:33401400-33402400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr16:33402200-33406200	Enhancers	Primary B cells from peripheral blood	blood
21	chr16:33403000-33403600	Enhancers	Primary B cells from cord blood	blood
22	chr16:33403400-33403800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr16:33403400-33405000	Enhancers	GM12878-XiMat	blood
24	chr16:33403400-33407000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr16:33406600-33406800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
26	chr16:33406600-33406800	Bivalent Enhancer	Placenta	Placenta
27	chr16:33406600-33406800	ZNF genes & repeats	Gastric	stomach
28	chr16:33406600-33407000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:33406600-33407000	ZNF genes & repeats	Spleen	Spleen
30	chr16:33406800-33408400	Weak transcription	Gastric	stomach
31	chr16:33407000-33408200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr16:33407000-33408400	Weak transcription	Spleen	Spleen
33	chr16:33408200-33408600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr16:33408200-33408800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr16:33408200-33409000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:33408400-33408600	ZNF genes & repeats	Gastric	stomach
37	chr16:33408400-33408600	ZNF genes & repeats	Spleen	Spleen
38	chr16:33408400-33408800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
39	chr16:33408400-33408800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:33409600-33413400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr16:33412000-33412200	Weak transcription	Right Atrium	heart
42	chr16:33412000-33413200	Enhancers	Primary B cells from peripheral blood	blood
43	chr16:33412600-33413000	Enhancers	GM12878-XiMat	blood
44	chr16:33412800-33413000	ZNF genes & repeats	Right Atrium	heart
45	chr16:33412800-33413200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr16:33412800-33417000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr16:33413000-33425600	Weak transcription	Right Atrium	heart
48	chr16:33415800-33416200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:33415800-33416200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr16:33421600-33422000	Active TSS	Breast Myoepithelial Primary Cells	Breast

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