Variant report

Variant	esv3361728
Chromosome Location	chr16:77467476-77470324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:77468365-77468638	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr16:77469290-77469530	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr16:77468868-77469068	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr16:77469125-77469403	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr16:77469189-77469264	HepG2	liver:	n/a	n/a
6	CTBP2	chr16:77468212-77469044	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr16:77468386-77468517	A549	lung:	n/a	n/a
8	CTCF	chr16:77468257-77468638	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr16:77468420-77468570	RPTEC	kidney:	n/a	n/a
10	CTCF	chr16:77468304-77468629	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr16:77468960-77469110	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr16:77468440-77468590	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr16:77468404-77468501	LNCaP	prostate:	n/a	n/a
14	CTCF	chr16:77468380-77468530	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr16:77468320-77468470	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr16:77468381-77468580	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr16:77468360-77468510	GM12874	blood:	n/a	n/a
18	CTCF	chr16:77468900-77469050	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr16:77468400-77468550	AG09319	gingival:	n/a	n/a
20	CTCF	chr16:77468348-77468538	HepG2	liver:	n/a	n/a
21	E2F6	chr16:77468270-77468765	H1-hESC	embryonic stem cell:	n/a	chr16:77468607-77468617 chr16:77468649-77468658 chr16:77468734-77468743
22	EP300	chr16:77468420-77469063	ECC-1	luminal epithelium:	n/a	chr16:77468711-77468720 chr16:77468966-77468982 chr16:77468729-77468745 chr16:77468698-77468714
23	FOXA2	chr16:77469629-77469801	HepG2	liver:	n/a	n/a
24	GATA3	chr16:77469291-77469973	MCF-7	breast:	n/a	chr16:77469849-77469859
25	HDAC2	chr16:77469346-77469860	MCF-7	breast:	n/a	chr16:77469846-77469860
26	HDAC2	chr16:77468719-77468980	H1-hESC	embryonic stem cell:	n/a	n/a
27	HDAC2	chr16:77468416-77468772	HepG2	liver:	n/a	n/a
28	MAFF	chr16:77469448-77469555	HepG2	liver:	n/a	chr16:77469456-77469474
29	MAFK	chr16:77469376-77469535	HepG2	liver:	n/a	n/a
30	MAFK	chr16:77469335-77469485	HepG2	liver:	n/a	n/a
31	MAFK	chr16:77469273-77469566	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr16:77468209-77468799	H1-hESC	embryonic stem cell:	n/a	chr16:77468460-77468470
33	MAX	chr16:77468299-77468818	H1-hESC	embryonic stem cell:	n/a	chr16:77468460-77468470
34	MAX	chr16:77468282-77468843	ECC-1	luminal epithelium:	n/a	chr16:77468460-77468470
35	MXI1	chr16:77468236-77468630	H1-hESC	embryonic stem cell:	n/a	n/a
36	MXI1	chr16:77469389-77469652	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYC	chr16:77468361-77468568	H1-hESC	embryonic stem cell:	n/a	chr16:77468460-77468470
38	NANOG	chr16:77468279-77468889	H1-hESC	embryonic stem cell:	n/a	n/a
39	NR2F2	chr16:77469356-77469930	MCF-7	breast:	n/a	n/a
40	POLR2A	chr16:77468188-77469026	H1-neurons	neurons:	n/a	n/a
41	POLR2A	chr16:77468805-77469051	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr16:77468482-77468965	ECC-1	luminal epithelium:	n/a	n/a
43	RAD21	chr16:77468113-77469203	H1-hESC	embryonic stem cell:	n/a	chr16:77468610-77468624 chr16:77468623-77468637 chr16:77468457-77468467
44	RAD21	chr16:77468197-77468725	ECC-1	luminal epithelium:	n/a	chr16:77468610-77468624 chr16:77468623-77468637 chr16:77468457-77468467
45	RAD21	chr16:77468212-77468672	H1-hESC	embryonic stem cell:	n/a	chr16:77468610-77468624 chr16:77468623-77468637 chr16:77468457-77468467
46	RAD21	chr16:77468301-77468548	HepG2	liver:	n/a	chr16:77468457-77468467
47	RAD21	chr16:77468259-77468644	H1-hESC	embryonic stem cell:	n/a	chr16:77468610-77468624 chr16:77468623-77468637 chr16:77468457-77468467
48	SIN3A	chr16:77468177-77469628	H1-hESC	embryonic stem cell:	n/a	chr16:77468948-77468957
49	TCF12	chr16:77468488-77468779	H1-hESC	embryonic stem cell:	n/a	chr16:77468691-77468698 chr16:77468597-77468604
50	TCF12	chr16:77468354-77468950	ECC-1	luminal epithelium:	n/a	chr16:77468691-77468698 chr16:77468597-77468604

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77469167-77469217	HRPEpiC	eye:	n/a
2	chr16:77469710-77469760	NH-A	brain:	n/a
3	chr16:77468373-77468423	ProgFib	skin:	n/a
4	chr16:77469167-77469217	NHDF-neo	bronchial:	n/a
5	chr16:77469583-77469633	Hela-S3	cervix:	n/a
6	chr16:77468458-77468508	AoSMC	blood vessel:	n/a
7	chr16:77468458-77468508	GM12892	blood:	n/a
8	chr16:77469710-77469760	HRE	kidney:	n/a
9	chr16:77469998-77470048	HNPCEpiC	eye:	n/a
10	chr16:77468277-77468327	AG04449	skin:	fetal
11	chr16:77469710-77469760	HEK293	kidney:	embryo
12	chr16:77469998-77470048	LNCaP	prostate:	n/a
13	chr16:77469710-77469760	NHDF-neo	bronchial:	n/a
14	chr16:77469583-77469633	HRCEpiC	kidney:	n/a
15	chr16:77469538-77469588	HepG2	liver:	n/a
16	chr16:77469538-77469588	HAEpiC	amniotic membrane:	n/a
17	chr16:77468373-77468423	GM12891	blood:	n/a
18	chr16:77469167-77469217	PFSK-1	brain:	n/a
19	chr16:77468277-77468327	ovcar-3	ovarian:	n/a
20	chr16:77468458-77468508	HIPEpiC	eye:	n/a
21	chr16:77469667-77469717	K562	blood:	n/a
22	chr16:77468277-77468327	GM12878	blood:	n/a
23	chr16:77469540-77469590	U87	brain:	n/a
24	chr16:77469667-77469717	NB4	blood:	n/a
25	chr16:77469540-77469590	LNCaP	prostate:	n/a
26	chr16:77468373-77468423	MCF-7	breast:	n/a
27	chr16:77468486-77468536	PrEC	prostate:	n/a
28	chr16:77468893-77468943	U87	brain:	n/a
29	chr16:77468458-77468508	SK-N-MC	brain:	n/a
30	chr16:77469540-77469590	AG10803	skin:	n/a
31	chr16:77469583-77469633	CMK	blood:	n/a
32	chr16:77468277-77468327	HUVEC	blood vessel:	n/a
33	chr16:77469667-77469717	BJ	skin:	n/a
34	chr16:77468277-77468327	ProgFib	skin:	n/a
35	chr16:77468850-77468900	HRE	kidney:	n/a
36	chr16:77469538-77469588	RPTEC	kidney:	n/a
37	chr16:77468458-77468508	LNCaP	prostate:	n/a
38	chr16:77469540-77469590	PFSK-1	brain:	n/a
39	chr16:77469538-77469588	HCM	heart:	n/a
40	chr16:77468850-77468900	AG09319	gingival:	n/a
41	chr16:77469540-77469590	HCPEpiC	choroid plexus:	n/a
42	chr16:77468458-77468508	HAEpiC	amniotic membrane:	n/a
43	chr16:77468850-77468900	GM12891	blood:	n/a
44	chr16:77468893-77468943	HIPEpiC	eye:	n/a
45	chr16:77469167-77469217	PANC-1	pancreas:	n/a
46	chr16:77469167-77469217	HL-60	blood:	n/a
47	chr16:77468458-77468508	PrEC	prostate:	n/a
48	chr16:77469710-77469760	HL-60	blood:	n/a
49	chr16:77468277-77468327	NT2-D1	testis:	n/a
50	chr16:77469710-77469760	HUVEC	blood vessel:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYCE1L-2	chr16:77469122-77469237	NONHSAT143803

Variant related genes	Relation type
ENSG00000216131	TF binding region
ADAMTS18	TF binding region
ENSG00000216131	CpG island
ADAMTS18	CpG island

Extended variants
information (count: 154 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565119789	chr16:77467490-77467491	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs527485348	chr16:77467499-77467500	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs527906715	chr16:77467517-77467518	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs189339073	chr16:77467554-77467555	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs180889983	chr16:77467572-77467573	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs538058666	chr16:77467590-77467591	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547870722	chr16:77467593-77467594	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs34958839	chr16:77467621-77467622	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs573614560	chr16:77467657-77467658	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs536363760	chr16:77467663-77467664	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs367734092	chr16:77467699-77467700	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs145014153	chr16:77467725-77467726	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572484666	chr16:77467737-77467738	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs544641332	chr16:77467748-77467749	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs12925025	chr16:77467749-77467750	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs528858375	chr16:77467830-77467831	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs78622374	chr16:77467842-77467843	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs75622931	chr16:77467852-77467853	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs200038212	chr16:77467853-77467854	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs529338836	chr16:77467887-77467888	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186361035	chr16:77467928-77467929	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs559919925	chr16:77467965-77467966	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs549510659	chr16:77467974-77467975	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs570234685	chr16:77467982-77467983	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs551845439	chr16:77467984-77467985	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs373723733	chr16:77468047-77468048	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs398078768	chr16:77468058-77468059	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs397856007	chr16:77468059-77468060	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs201234273	chr16:77468060-77468061	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs3750156	chr16:77468141-77468142	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs142353053	chr16:77468143-77468144	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs190092625	chr16:77468144-77468145	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550861255	chr16:77468180-77468181	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs115284586	chr16:77468184-77468185	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs377316778	chr16:77468203-77468204	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552636773	chr16:77468204-77468205	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs566274148	chr16:77468221-77468222	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs569674076	chr16:77468225-77468226	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs538247031	chr16:77468276-77468277	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183096578	chr16:77468283-77468284	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs372213738	chr16:77468285-77468286	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs544515269	chr16:77468298-77468299	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs376531513	chr16:77468324-77468325	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs201304352	chr16:77468327-77468328	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs185990292	chr16:77468358-77468359	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs199523966	chr16:77468360-77468361	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540472609	chr16:77468380-77468381	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs373891774	chr16:77468382-77468383	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs559883231	chr16:77468389-77468390	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs397515469	chr16:77468396-77468397	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77465200-77469200	Bivalent/Poised TSS	Adipose Nuclei	Adipose
2	chr16:77467000-77467600	Enhancers	Brain Cingulate Gyrus	brain
3	chr16:77467200-77468000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
4	chr16:77467200-77468000	Bivalent Enhancer	Brain Substantia Nigra	brain
5	chr16:77467400-77467800	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr16:77467400-77468000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr16:77467400-77468000	Weak transcription	Ovary	ovary
8	chr16:77467400-77468600	Flanking Active TSS	HUVEC	blood vessel
9	chr16:77467400-77469200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr16:77467600-77467800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
11	chr16:77467600-77467800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr16:77467600-77467800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
13	chr16:77467600-77467800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
14	chr16:77467600-77468000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr16:77467600-77468200	Bivalent Enhancer	Fetal Lung	lung
16	chr16:77467600-77469200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr16:77467600-77469400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
18	chr16:77467600-77469400	Bivalent/Poised TSS	Fetal Kidney	kidney
19	chr16:77467800-77468000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
20	chr16:77467800-77468000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
21	chr16:77467800-77468200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:77467800-77468200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
23	chr16:77467800-77468200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr16:77467800-77468200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr16:77467800-77468200	Bivalent Enhancer	A549	lung
26	chr16:77467800-77469800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr16:77467800-77469800	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr16:77468000-77468200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
29	chr16:77468000-77468200	Bivalent/Poised TSS	Brain Angular Gyrus	brain
30	chr16:77468000-77468200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
31	chr16:77468000-77468200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
32	chr16:77468000-77468200	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
33	chr16:77468000-77468400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr16:77468000-77468400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
35	chr16:77468000-77468400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr16:77468000-77468400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
37	chr16:77468000-77468400	Flanking Active TSS	Brain Cingulate Gyrus	brain
38	chr16:77468000-77468800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr16:77468000-77469200	Active TSS	Ovary	ovary
40	chr16:77468000-77469400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr16:77468000-77469400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr16:77468000-77469600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
43	chr16:77468000-77469600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr16:77468000-77469600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
45	chr16:77468000-77469800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr16:77468000-77470000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr16:77468200-77468400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr16:77468200-77468400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
49	chr16:77468200-77468400	Bivalent Enhancer	Duodenum Mucosa	Duodenum
50	chr16:77468200-77468400	Bivalent Enhancer	Fetal Intestine Small	intestine

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