Variant report

Variant	nsv1058355
Chromosome Location	chr16:33404128-33864347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3255)
CpG islands
(count:2565)
Chromatin interactive
region (count:21)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3255 , 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	chr16:33535249-33535260	K562	blood:	n/a	n/a
5	ATF1	chr16:33544959-33544976	K562	blood:	n/a	n/a
6	ATF3	chr16:33764110-33764276	K562	blood:	n/a	n/a
7	ATF3	chr16:33569376-33569681	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	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
11	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
12	BATF	chr16:33763898-33764246	GM12878	blood:	n/a	n/a
13	BATF	chr16:33445892-33446115	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
14	BATF	chr16:33563865-33564062	GM12878	blood:	n/a	n/a
15	BATF	chr16:33585762-33586003	GM12878	blood:	n/a	n/a
16	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
17	BATF	chr16:33647061-33647311	GM12878	blood:	n/a	n/a
18	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
19	BATF	chr16:33431441-33431744	GM12878	blood:	n/a	chr16:33431606-33431617
20	BATF	chr16:33673521-33673717	GM12878	blood:	n/a	n/a
21	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
22	BATF	chr16:33589201-33589438	GM12878	blood:	n/a	n/a
23	BATF	chr16:33564248-33564454	GM12878	blood:	n/a	n/a
24	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
25	BATF	chr16:33722423-33722618	GM12878	blood:	n/a	n/a
26	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
27	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
28	BATF	chr16:33517619-33517865	GM12878	blood:	n/a	n/a
29	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
30	BATF	chr16:33716043-33716353	GM12878	blood:	n/a	n/a
31	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
32	BATF	chr16:33446462-33446750	GM12878	blood:	n/a	n/a
33	BCL11A	chr16:33664436-33664652	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:33524471-33525029	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:33763969-33764256	GM12878	blood:	n/a	n/a
36	BCL11A	chr16:33492453-33492646	GM12878	blood:	n/a	n/a
37	BCL11A	chr16:33446218-33446393	GM12878	blood:	n/a	n/a
38	BCL11A	chr16:33585333-33585647	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:33582517-33582748	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	chr16:33460174-33460528	GM12878	blood:	n/a	chr16:33460375-33460384
43	BCL11A	chr16:33589217-33589463	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:33563810-33564006	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:33722355-33722924	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:33521254-33521467	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:33722347-33722700	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:33524561-33524846	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:33458814-33459180	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:33431491-33431778	GM12878	blood:	n/a	n/a

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33570021-33570071	AG04449	skin:	fetal
2	chr16:33781365-33781415	HIPEpiC	eye:	n/a
3	chr16:33627215-33627265	AG09309	skin:	n/a
4	chr16:33570021-33570071	AG04449	skin:	fetal
5	chr16:33781365-33781415	HIPEpiC	eye:	n/a
6	chr16:33627215-33627265	AG09309	skin:	n/a
7	chr16:33483299-33483349	A549	lung:	n/a
8	chr16:33481620-33481670	SK-N-SH_RA	brain:	n/a
9	chr16:33570021-33570071	K562	blood:	n/a
10	chr16:33783802-33783852	GM12892	blood:	n/a
11	chr16:33730720-33730770	ProgFib	skin:	n/a
12	chr16:33604228-33604278	NB4	blood:	n/a
13	chr16:33781365-33781415	PANC-1	pancreas:	n/a
14	chr16:33852801-33852851	GM12892	blood:	n/a
15	chr16:33627215-33627265	SAEC	small airway:	n/a
16	chr16:33604228-33604278	HCT-116	colon:	n/a
17	chr16:33483244-33483294	MCF10A-Er-Src	breast:	n/a
18	chr16:33853544-33853594	IMR90	lung:	fetal
19	chr16:33817457-33817507	GM19239	blood:	n/a
20	chr16:33627215-33627265	HAEpiC	amniotic membrane:	n/a
21	chr16:33730558-33730608	NHBE	bronchial:	n/a
22	chr16:33852823-33852873	HepG2	liver:	n/a
23	chr16:33852801-33852851	T-47D	breast:	n/a
24	chr16:33815990-33816040	HPAEpiC	pulmonary alveolar:	n/a
25	chr16:33734837-33734887	HCM	heart:	n/a
26	chr16:33779917-33779967	MCF10A-Er-Src	breast:	n/a
27	chr16:33627536-33627586	PANC-1	pancreas:	n/a
28	chr16:33604228-33604278	PANC-1	pancreas:	n/a
29	chr16:33483591-33483641	ECC-1	luminal epithelium:	n/a
30	chr16:33730720-33730770	HIPEpiC	eye:	n/a
31	chr16:33573272-33573322	ECC-1	luminal epithelium:	n/a
32	chr16:33852823-33852873	HCPEpiC	choroid plexus:	n/a
33	chr16:33815990-33816040	GM19239	blood:	n/a
34	chr16:33854086-33854136	K562	blood:	n/a
35	chr16:33852801-33852851	PANC-1	pancreas:	n/a
36	chr16:33854086-33854136	A549	lung:	n/a
37	chr16:33481620-33481670	MCF-7	breast:	n/a
38	chr16:33851284-33851334	PFSK-1	brain:	n/a
39	chr16:33817129-33817179	ProgFib	skin:	n/a
40	chr16:33605185-33605235	HRCEpiC	kidney:	n/a
41	chr16:33573272-33573322	PFSK-1	brain:	n/a
42	chr16:33481620-33481670	HRE	kidney:	n/a
43	chr16:33730558-33730608	ProgFib	skin:	n/a
44	chr16:33487438-33487488	SK-N-SH_RA	brain:	n/a
45	chr16:33734837-33734887	PrEC	prostate:	n/a
46	chr16:33851284-33851334	NT2-D1	testis:	n/a
47	chr16:33783802-33783852	NHDF-neo	bronchial:	n/a
48	chr16:33817129-33817179	HNPCEpiC	eye:	n/a
49	chr16:33509523-33509573	PANC-1	pancreas:	n/a
50	chr16:33817992-33818042	HNPCEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC140658.1-6	chr16:33776476-33776670	ENSG00000205452.4
2	lnc-AC136428.1.1-1	chr16:33661001-33661077	ENSG00000260312.1
3	lnc-AC140658.1-6	chr16:33777320-33777532	ENSG00000205452.4
4	lnc-AC140658.1-6	chr16:33776448-33776670	ENSG00000205452.4
5	lnc-AC140658.1-5	chr16:33768122-33768427	NONHSAT142119
6	lnc-AC136428.1.1-1	chr16:33660402-33660589	ENSG00000260312.1
7	lnc-AC136428.1.1-10	chr16:33677506-33677808	NONHSAT142113
8	lnc-AC140658.1-6	chr16:33778750-33778813	ENSG00000205452.4
9	lnc-AC140658.1-6	chr16:33775379-33776670	ENSG00000205452.4
10	lnc-AC136428.1.1-1	chr16:33661251-33661331	ENSG00000260312.1
11	lnc-AC140658.1-6	chr16:33777416-33777550	ENSG00000205452.4
12	lnc-AC140658.1-3	chr16:33750745-33751015	NONHSAT142117
13	lnc-AC136428.1.1-10	chr16:33677891-33677935	NONHSAT142113
14	lnc-AC140658.1-6	chr16:33777235-33777744	ENSG00000205452.4
15	lnc-AC140658.1-5	chr16:33768513-33768558	NONHSAT142119
16	lnc-AC140658.1-6	chr16:33775514-33776189	ENSG00000205452.4
17	lnc-AC140658.1-6	chr16:33776833-33776957	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
ENSG00000270401	TF binding region
ENSG00000260308	TF binding region
ENSG00000261217	TF binding region
IGHV3OR16-11	TF binding region
IGHV3OR16-7	TF binding region
ENSG00000261197	TF binding region
ENSG00000271691	TF binding region
ENSG00000270924	TF binding region
ENSG00000259990	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
ENSG00000270401	CpG island
ENSG00000260308	CpG island
ENSG00000261217	CpG island
IGHV3OR16-11	CpG island
IGHV3OR16-7	CpG island
ENSG00000261197	CpG island
ENSG00000271691	CpG island
ENSG00000270924	CpG island
ENSG00000259990	CpG island
ARHGAP23P1	CpG island
BMS1P8	CpG island
ENSG00000259680	chromatin interactions

Extended variants
information (count: 9097 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:9097 , 50 per page) page: 1 2 3 4 5 6 7 ... 182

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374456481	chr16:33404128-33404129	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs62029430	chr16:33404129-33404130	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs578018258	chr16:33404135-33404136	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11866756	chr16:33404174-33404175	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545341878	chr16:33404181-33404182	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558151812	chr16:33404192-33404193	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11863724	chr16:33404275-33404276	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576516381	chr16:33404276-33404277	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11863723	chr16:33404293-33404294	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs543854599	chr16:33404312-33404313	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147985782	chr16:33404330-33404331	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574167864	chr16:33404333-33404334	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541299405	chr16:33404375-33404376	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs60374011	chr16:33404398-33404399	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559598215	chr16:33404418-33404419	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149015223	chr16:33404433-33404434	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143804957	chr16:33404447-33404448	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533420419	chr16:33404451-33404452	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377388209	chr16:33404463-33404464	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112611163	chr16:33404471-33404472	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148145526	chr16:33404478-33404479	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112078794	chr16:33404530-33404531	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551665323	chr16:33404544-33404545	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562894786	chr16:33404580-33404581	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575341201	chr16:33404588-33404589	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530467590	chr16:33404623-33404624	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549050866	chr16:33404661-33404662	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370357617	chr16:33404683-33404684	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141024827	chr16:33404684-33404685	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202040953	chr16:33404685-33404686	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567283216	chr16:33404699-33404700	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534794558	chr16:33404724-33404725	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377258145	chr16:33404761-33404762	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7186361	chr16:33404765-33404766	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546448605	chr16:33404802-33404803	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571481368	chr16:33404805-33404806	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7186202	chr16:33404815-33404816	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367719926	chr16:33404823-33404824	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10871480	chr16:33404853-33404854	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183304256	chr16:33404866-33404867	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538895624	chr16:33404875-33404876	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4617870	chr16:33404893-33404894	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557296268	chr16:33404909-33404910	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576502541	chr16:33404911-33404912	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113475266	chr16:33404968-33404969	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555818567	chr16:33404992-33404993	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574080502	chr16:33405004-33405005	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541537542	chr16:33405024-33405025	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367940460	chr16:33405031-33405032	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559478143	chr16:33405047-33405048	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:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:33401200-33407200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr16:33402200-33406200	Enhancers	Primary B cells from peripheral blood	blood
3	chr16:33403400-33405000	Enhancers	GM12878-XiMat	blood
4	chr16:33403400-33407000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:33406600-33406800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
6	chr16:33406600-33406800	Bivalent Enhancer	Placenta	Placenta
7	chr16:33406600-33406800	ZNF genes & repeats	Gastric	stomach
8	chr16:33406600-33407000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr16:33406600-33407000	ZNF genes & repeats	Spleen	Spleen
10	chr16:33406800-33408400	Weak transcription	Gastric	stomach
11	chr16:33407000-33408200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:33407000-33408400	Weak transcription	Spleen	Spleen
13	chr16:33408200-33408600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:33408200-33408800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr16:33408200-33409000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:33408400-33408600	ZNF genes & repeats	Gastric	stomach
17	chr16:33408400-33408600	ZNF genes & repeats	Spleen	Spleen
18	chr16:33408400-33408800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr16:33408400-33408800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr16:33409600-33413400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr16:33412000-33412200	Weak transcription	Right Atrium	heart
22	chr16:33412000-33413200	Enhancers	Primary B cells from peripheral blood	blood
23	chr16:33412600-33413000	Enhancers	GM12878-XiMat	blood
24	chr16:33412800-33413000	ZNF genes & repeats	Right Atrium	heart
25	chr16:33412800-33413200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr16:33412800-33417000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:33413000-33425600	Weak transcription	Right Atrium	heart
28	chr16:33415800-33416200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr16:33415800-33416200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr16:33421600-33422000	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr16:33421600-33422400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:33426000-33426200	Bivalent Enhancer	Brain Anterior Caudate	brain
33	chr16:33428400-33429600	Enhancers	GM12878-XiMat	blood
34	chr16:33436600-33437600	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr16:33445200-33446400	Enhancers	GM12878-XiMat	blood
36	chr16:33446200-33447000	Enhancers	Primary B cells from peripheral blood	blood
37	chr16:33446400-33446800	Weak transcription	GM12878-XiMat	blood
38	chr16:33446800-33447800	Enhancers	GM12878-XiMat	blood
39	chr16:33447000-33447600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr16:33447000-33447600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr16:33447600-33448800	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr16:33447600-33451800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr16:33448800-33449400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr16:33451200-33452000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr16:33451800-33452000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr16:33457400-33457800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr16:33457600-33457800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr16:33457600-33458600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr16:33457600-33460400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr16:33457600-33461000	Enhancers	Primary B cells from peripheral blood	blood

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