Variant report

Variant	nsv457411
Chromosome Location	chr16:12363304-12520199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1853)
CpG islands
(count:489)
Chromatin interactive
region (count:65)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1853 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12518903-12519615	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12435377-12435548	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:12392318-12392503	K562	blood:	n/a	n/a
4	ARID3A	chr16:12413001-12413168	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:12382840-12384000	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:12514612-12515012	K562	blood:	n/a	n/a
7	ARID3A	chr16:12387221-12387517	K562	blood:	n/a	n/a
8	ARID3A	chr16:12379093-12379410	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:12500950-12501680	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:12409154-12409881	HepG2	liver:	n/a	n/a
11	ATF1	chr16:12520091-12520401	K562	blood:	n/a	n/a
12	ATF1	chr16:12387043-12387492	K562	blood:	n/a	n/a
13	ATF1	chr16:12514506-12515078	K562	blood:	n/a	n/a
14	ATF1	chr16:12460301-12460303	K562	blood:	n/a	n/a
15	ATF1	chr16:12510044-12510374	K562	blood:	n/a	n/a
16	ATF1	chr16:12397588-12397814	K562	blood:	n/a	n/a
17	ATF1	chr16:12471415-12471623	K562	blood:	n/a	n/a
18	ATF2	chr16:12416881-12417410	GM12878	blood:	n/a	n/a
19	ATF2	chr16:12498593-12499380	GM12878	blood:	n/a	n/a
20	ATF2	chr16:12385759-12386367	GM12878	blood:	n/a	n/a
21	ATF2	chr16:12498893-12499336	GM12878	blood:	n/a	n/a
22	ATF2	chr16:12416866-12417337	GM12878	blood:	n/a	n/a
23	ATF3	chr16:12514505-12514851	K562	blood:	n/a	n/a
24	BACH1	chr16:12403201-12403219	K562	blood:	n/a	n/a
25	BACH1	chr16:12387279-12387399	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr16:12500647-12500932	GM12878	blood:	n/a	n/a
27	BATF	chr16:12499005-12499319	GM12878	blood:	n/a	n/a
28	BATF	chr16:12385809-12386550	GM12878	blood:	n/a	chr16:12386360-12386369
29	BATF	chr16:12416598-12417218	GM12878	blood:	n/a	chr16:12417152-12417162
30	BATF	chr16:12489866-12490225	GM12878	blood:	n/a	chr16:12490064-12490075
31	BATF	chr16:12498959-12499361	GM12878	blood:	n/a	n/a
32	BATF	chr16:12416598-12417287	GM12878	blood:	n/a	chr16:12417152-12417162
33	BCL11A	chr16:12416596-12417208	GM12878	blood:	n/a	n/a
34	BCL11A	chr16:12416522-12417258	GM12878	blood:	n/a	n/a
35	BCL11A	chr16:12499012-12499281	GM12878	blood:	n/a	n/a
36	BCL3	chr16:12498913-12499348	GM12878	blood:	n/a	n/a
37	BCL3	chr16:12450872-12451135	GM12878	blood:	n/a	n/a
38	BCL3	chr16:12403831-12404057	GM12878	blood:	n/a	n/a
39	BCL3	chr16:12416893-12417263	GM12878	blood:	n/a	n/a
40	BCL3	chr16:12470020-12470262	GM12878	blood:	n/a	n/a
41	BCLAF1	chr16:12498874-12499394	GM12878	blood:	n/a	n/a
42	BCLAF1	chr16:12416895-12417228	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:12481300-12481504	K562	blood:	n/a	n/a
44	BHLHE40	chr16:12481857-12482095	K562	blood:	n/a	n/a
45	BHLHE40	chr16:12443836-12444154	K562	blood:	n/a	n/a
46	BHLHE40	chr16:12514564-12515070	K562	blood:	n/a	n/a
47	BHLHE40	chr16:12416963-12417204	GM12878	blood:	n/a	n/a
48	BHLHE40	chr16:12409285-12409752	HepG2	liver:	n/a	n/a
49	BHLHE40	chr16:12364999-12365243	K562	blood:	n/a	n/a
50	BHLHE40	chr16:12462564-12462808	K562	blood:	n/a	chr16:12462692-12462701 chr16:12462691-12462700 chr16:12462691-12462700 chr16:12462685-12462706 chr16:12462689-12462702

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12414821-12414871	BE2_C	brain:	n/a
2	chr16:12414821-12414871	BE2_C	brain:	n/a
3	chr16:12484175-12484225	HRPEpiC	eye:	n/a
4	chr16:12501787-12501837	BJ	skin:	n/a
5	chr16:12484175-12484225	HCT-116	colon:	n/a
6	chr16:12411139-12411189	U87	brain:	n/a
7	chr16:12434580-12434630	PFSK-1	brain:	n/a
8	chr16:12414821-12414871	PrEC	prostate:	n/a
9	chr16:12411139-12411189	AG10803	skin:	n/a
10	chr16:12405425-12405475	HCM	heart:	n/a
11	chr16:12501787-12501837	NHDF-neo	bronchial:	n/a
12	chr16:12442738-12442788	A549	lung:	n/a
13	chr16:12411139-12411189	HNPCEpiC	eye:	n/a
14	chr16:12434580-12434630	NHBE	bronchial:	n/a
15	chr16:12484175-12484225	AG10803	skin:	n/a
16	chr16:12405425-12405475	MCF10A-Er-Src	breast:	n/a
17	chr16:12373566-12373616	HMEC	breast:	n/a
18	chr16:12414821-12414871	MCF-7	breast:	n/a
19	chr16:12405425-12405475	HL-60	blood:	n/a
20	chr16:12414821-12414871	AG09309	skin:	n/a
21	chr16:12442738-12442788	RPTEC	kidney:	n/a
22	chr16:12434580-12434630	AG10803	skin:	n/a
23	chr16:12373566-12373616	Hepatocyte	liver:	n/a
24	chr16:12405425-12405475	ECC-1	luminal epithelium:	n/a
25	chr16:12405425-12405475	NB4	blood:	n/a
26	chr16:12484175-12484225	GM06990	blood:	n/a
27	chr16:12414821-12414871	Caco-2	colon:	n/a
28	chr16:12405425-12405475	NH-A	brain:	n/a
29	chr16:12414821-12414871	ProgFib	skin:	n/a
30	chr16:12434580-12434630	PANC-1	pancreas:	n/a
31	chr16:12411139-12411189	AoSMC	blood vessel:	n/a
32	chr16:12414821-12414871	HAEpiC	amniotic membrane:	n/a
33	chr16:12414821-12414871	HNPCEpiC	eye:	n/a
34	chr16:12442738-12442788	HCT-116	colon:	n/a
35	chr16:12501787-12501837	HIPEpiC	eye:	n/a
36	chr16:12442738-12442788	NHBE	bronchial:	n/a
37	chr16:12405425-12405475	AoSMC	blood vessel:	n/a
38	chr16:12411139-12411189	AG09309	skin:	n/a
39	chr16:12501787-12501837	NHBE	bronchial:	n/a
40	chr16:12405425-12405475	PrEC	prostate:	n/a
41	chr16:12484175-12484225	SK-N-SH_RA	brain:	n/a
42	chr16:12434580-12434630	A549	lung:	n/a
43	chr16:12405425-12405475	HRCEpiC	kidney:	n/a
44	chr16:12484175-12484225	T-47D	breast:	n/a
45	chr16:12414821-12414871	ECC-1	luminal epithelium:	n/a
46	chr16:12414821-12414871	AoSMC	blood vessel:	n/a
47	chr16:12411139-12411189	NT2-D1	testis:	n/a
48	chr16:12414821-12414871	AG04450	lung:	fetal
49	chr16:12414821-12414871	HepG2	liver:	n/a
50	chr16:12405425-12405475	ProgFib	skin:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:12407586..12410005-chr16:12412153..12414940,2	K562	blood:
2	chr16:12470715..12473444-chr16:12481044..12482837,2	K562	blood:
3	chr16:12412998..12415794-chr16:12417822..12420522,2	MCF-7	breast:
4	chr16:12466341..12467907-chr16:12469867..12472609,2	K562	blood:
5	chr16:12493474..12495978-chr16:12497042..12499822,2	K562	blood:
6	chr16:12448404..12450435-chr16:12463465..12466291,2	K562	blood:
7	chr16:12407586..12410005-chr16:12412153..12414940,2	K562	blood:
8	chr16:12188787..12189461-chr16:12364695..12365675,3	MCF-7	breast:
9	chr16:12371620..12373730-chr16:12377552..12379421,2	K562	blood:
10	chr16:12479812..12482629-chr16:12484351..12486474,2	K562	blood:
11	chr16:12434031..12434617-chr16:12912936..12913439,2	K562	blood:
12	chr16:12398011..12399512-chr16:12401673..12404265,2	K562	blood:
13	chr16:12388084..12390009-chr16:12417985..12420361,2	MCF-7	breast:
14	chr16:12453383..12455322-chr16:12457065..12459582,2	MCF-7	breast:
15	chr16:12426103..12428836-chr16:12432217..12434096,4	K562	blood:
16	chr16:12485456..12487109-chr16:12487672..12489526,2	MCF-7	breast:
17	chr16:12322254..12322886-chr16:12364731..12365264,2	MCF-7	breast:
18	chr16:12434035..12434594-chr16:12912889..12913804,2	MCF-7	breast:
19	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
20	chr16:12388084..12390009-chr16:12417985..12420361,2	MCF-7	breast:
21	chr16:12496114..12497637-chr16:12507756..12510093,2	K562	blood:
22	chr16:12494822..12496351-chr16:12505081..12507751,2	K562	blood:
23	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:
24	chr16:12415388..12417131-chr16:12421455..12424382,2	MCF-7	breast:
25	chr16:12415388..12417131-chr16:12421455..12424382,2	MCF-7	breast:
26	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
27	chr16:12352461..12354731-chr16:12381586..12384125,2	MCF-7	breast:
28	chr16:12412998..12415794-chr16:12417822..12420522,2	MCF-7	breast:
29	chr16:12384757..12387424-chr16:12410690..12412315,2	MCF-7	breast:
30	chr16:12289297..12291901-chr16:12382629..12384781,2	MCF-7	breast:
31	chr16:12404079..12406298-chr16:12408481..12410395,2	K562	blood:
32	chr16:12485157..12486773-chr16:12498470..12500396,2	K562	blood:
33	chr16:12485456..12487109-chr16:12487672..12489526,2	MCF-7	breast:
34	chr16:12493474..12495978-chr16:12497042..12499822,2	K562	blood:
35	chr16:12507545..12509858-chr16:12539210..12540734,2	K562	blood:
36	chr16:12322566..12323224-chr16:12365049..12365589,2	MCF-7	breast:
37	chr16:12322281..12324102-chr16:12364596..12366480,2	MCF-7	breast:
38	chr16:12389501..12392073-chr16:12392861..12394450,2	K562	blood:
39	chr16:12496114..12497637-chr16:12507756..12510093,2	K562	blood:
40	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:
41	chr16:12494822..12496351-chr16:12505081..12507751,2	K562	blood:
42	chr16:12385748..12388371-chr16:12390061..12392651,3	K562	blood:
43	chr16:12518273..12521008-chr16:12521973..12524305,2	MCF-7	breast:
44	chr16:12381810..12383489-chr16:12387831..12390561,2	MCF-7	breast:
45	chr16:12480350..12482159-chr16:12485408..12486962,2	MCF-7	breast:
46	chr16:12366529..12368519-chr16:12369108..12371101,2	MCF-7	breast:
47	chr16:12479812..12482629-chr16:12484351..12486474,2	K562	blood:
48	chr16:12470715..12473444-chr16:12481044..12482837,2	K562	blood:
49	chr16:12453383..12455322-chr16:12457065..12459582,2	MCF-7	breast:
50	chr16:12480350..12482159-chr16:12485408..12486962,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-276H1.3.1-2	chr16:12466389-12466455	NONHSAT140620
2	lnc-TNFRSF17-3	chr16:12467526-12467756	ENSG00000260723.1
3	lnc-RP11-276H1.3.1-2	chr16:12466389-12466439	ENSG00000261394.1
4	lnc-TNFRSF17-3	chr16:12466669-12466766	ENSG00000260723.1
5	lnc-TNFRSF17-3	chr16:12467526-12467754	ENSG00000260723.1
6	lnc-RP11-276H1.3.1-2	chr16:12460839-12461326	ENSG00000261394.1
7	lnc-TNFRSF17-3	chr16:12466680-12466885	ENSG00000260723.1
8	lnc-RP11-276H1.3.1-2	chr16:12460012-12461326	NONHSAT140620

No data

Variant related genes	Relation type
ENSG00000260723	TF binding region
ENSG00000261394	TF binding region
ENSG00000238685	TF binding region
SNX29	TF binding region
ENSG00000260723	CpG island
ENSG00000261394	CpG island
ENSG00000238685	CpG island
SNX29	CpG island
ENSG00000238685	chromatin interactions
ENSG00000261394	chromatin interactions
ENSG00000261293	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000260723	chromatin interactions

Extended variants
information (count: 8571 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:8571 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10500379	chr16:12363304-12363305	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567372751	chr16:12363334-12363335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4781200	chr16:12363340-12363341	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs4780417	chr16:12363400-12363401	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572993959	chr16:12363427-12363428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538443266	chr16:12363462-12363463	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558451819	chr16:12363465-12363466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575176778	chr16:12363497-12363498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs558482392	chr16:12363499-12363500	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564383829	chr16:12363532-12363533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4780418	chr16:12363540-12363541	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188048517	chr16:12363567-12363568	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34664022	chr16:12363585-12363586	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542712178	chr16:12363599-12363600	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117078167	chr16:12363602-12363603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528744845	chr16:12363616-12363617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79093870	chr16:12363620-12363621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146108647	chr16:12363661-12363662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549570556	chr16:12363691-12363692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569868597	chr16:12363694-12363695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567105526	chr16:12363697-12363698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140129133	chr16:12363700-12363701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546424118	chr16:12363716-12363717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72147365	chr16:12363717-12363718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201886063	chr16:12363718-12363719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5025577	chr16:12363719-12363720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143843672	chr16:12363734-12363735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144830445	chr16:12363736-12363737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191347145	chr16:12363742-12363743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575185911	chr16:12363757-12363758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537697675	chr16:12363762-12363763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548716634	chr16:12363843-12363844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184651282	chr16:12363844-12363845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111459273	chr16:12363878-12363879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367675274	chr16:12363926-12363927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543007931	chr16:12363932-12363933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553221700	chr16:12363943-12363944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9889154	chr16:12363951-12363952	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111576081	chr16:12363971-12363972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs8056108	chr16:12364004-12364005	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs531234959	chr16:12364013-12364014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544539279	chr16:12364014-12364015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568435887	chr16:12364020-12364021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115303369	chr16:12364028-12364029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546559245	chr16:12364065-12364066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189435710	chr16:12364126-12364127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567721134	chr16:12364146-12364147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111390013	chr16:12364157-12364158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76443107	chr16:12364174-12364175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368100982	chr16:12364221-12364222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
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	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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2461 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12308000-12371400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr16:12309800-12371200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr16:12323400-12394200	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr16:12323800-12373000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr16:12330800-12373000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr16:12334600-12371800	Weak transcription	Adipose Nuclei	Adipose
7	chr16:12338200-12396200	Weak transcription	Thymus	Thymus
8	chr16:12347800-12395200	Weak transcription	Right Ventricle	heart
9	chr16:12348200-12371400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr16:12350200-12371600	Weak transcription	GM12878-XiMat	blood
11	chr16:12351200-12373000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr16:12351200-12382800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr16:12354800-12382800	Weak transcription	Gastric	stomach
14	chr16:12355000-12366200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr16:12355200-12372000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr16:12356000-12390200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr16:12356400-12378000	Weak transcription	Spleen	Spleen
18	chr16:12356600-12371600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr16:12356600-12372800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr16:12356800-12364800	Weak transcription	Psoas Muscle	Psoas
21	chr16:12356800-12371800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:12356800-12373000	Weak transcription	Fetal Intestine Small	intestine
23	chr16:12356800-12373000	Weak transcription	Fetal Stomach	stomach
24	chr16:12357000-12365000	Weak transcription	Pancreas	Pancrea
25	chr16:12357200-12383000	Weak transcription	Esophagus	oesophagus
26	chr16:12357400-12370400	Weak transcription	Aorta	Aorta
27	chr16:12357400-12373000	Weak transcription	Liver	Liver
28	chr16:12358200-12364600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr16:12358600-12373200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr16:12359200-12377400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr16:12359400-12380800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr16:12359800-12418000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr16:12361200-12372600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr16:12361800-12365000	Strong transcription	Primary B cells from cord blood	blood
35	chr16:12361800-12383000	Weak transcription	Fetal Muscle Leg	muscle
36	chr16:12362000-12368600	Weak transcription	HepG2	liver
37	chr16:12362000-12374600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr16:12362000-12382600	Weak transcription	Placenta	Placenta
39	chr16:12362600-12363600	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr16:12362800-12365400	Weak transcription	Primary B cells from peripheral blood	blood
41	chr16:12362800-12370400	Weak transcription	Primary T cells from cord blood	blood
42	chr16:12364600-12365200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr16:12364800-12365000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr16:12364800-12365000	Weak transcription	Brain Hippocampus Middle	brain
45	chr16:12365000-12365200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr16:12365000-12365200	Enhancers	Brain Hippocampus Middle	brain
47	chr16:12365000-12365200	Enhancers	Pancreas	Pancrea
48	chr16:12365000-12365200	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr16:12365000-12365200	Enhancers	HSMM	muscle
50	chr16:12365000-12365400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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