Variant report

Variant	esv11117
Chromosome Location	chr16:71756826-71758273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:71757994-71758139	HepG2	liver:	n/a	n/a
2	ATF2	chr16:71756735-71757220	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr16:71756728-71758174	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr16:71756646-71757162	A549	lung:	n/a	n/a
5	BCL3	chr16:71756796-71757323	A549	lung:	n/a	chr16:71757198-71757211 chr16:71757178-71757187 chr16:71757271-71757284
6	BHLHE40	chr16:71757499-71758169	GM12878	blood:	n/a	chr16:71757976-71757992 chr16:71757932-71757948 chr16:71757574-71757590
7	BHLHE40	chr16:71757606-71758105	K562	blood:	n/a	chr16:71757976-71757992 chr16:71757932-71757948
8	BHLHE40	chr16:71757511-71758328	HepG2	liver:	n/a	chr16:71757976-71757992 chr16:71757932-71757948 chr16:71757574-71757590
9	BRCA1	chr16:71756908-71757108	HepG2	liver:	n/a	n/a
10	BRCA1	chr16:71757646-71757697	GM12878	blood:	n/a	n/a
11	BRCA1	chr16:71757075-71757380	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr16:71757885-71758239	K562	blood:	n/a	n/a
13	CCNT2	chr16:71756984-71758163	K562	blood:	n/a	n/a
14	CEBPB	chr16:71756783-71757117	K562	blood:	n/a	chr16:71756939-71756950
15	CEBPB	chr16:71756718-71757155	ECC-1	luminal epithelium:	n/a	chr16:71756939-71756950
16	CEBPB	chr16:71756647-71757234	MCF-7	breast:	n/a	chr16:71756939-71756950
17	CEBPB	chr16:71756873-71757079	HepG2	liver:	n/a	chr16:71756939-71756950
18	CEBPB	chr16:71756770-71757144	H1-hESC	embryonic stem cell:	n/a	chr16:71756939-71756950
19	CEBPB	chr16:71756773-71757226	HepG2	liver:	n/a	chr16:71756939-71756950
20	CEBPB	chr16:71756797-71757212	HepG2	liver:	n/a	chr16:71756939-71756950
21	CEBPB	chr16:71757699-71758233	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr16:71756695-71757122	A549	lung:	n/a	chr16:71756939-71756950
23	CEBPB	chr16:71756673-71757269	ECC-1	luminal epithelium:	n/a	chr16:71756939-71756950
24	CEBPB	chr16:71756556-71757354	Hela-S3	cervix:	n/a	chr16:71756939-71756950
25	CEBPB	chr16:71756715-71757178	A549	lung:	n/a	chr16:71756939-71756950
26	CEBPB	chr16:71756647-71757308	A549	lung:	n/a	chr16:71756939-71756950
27	CEBPB	chr16:71756758-71757138	IMR90	lung:	n/a	chr16:71756939-71756950
28	CEBPD	chr16:71757608-71758094	HepG2	liver:	n/a	n/a
29	CEBPD	chr16:71756687-71757306	HepG2	liver:	n/a	n/a
30	CHD1	chr16:71757530-71757765	GM12878	blood:	n/a	n/a
31	CHD1	chr16:71756585-71757251	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr16:71757581-71757600	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr16:71757608-71758234	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr16:71758096-71758289	HepG2	liver:	n/a	n/a
35	CHD2	chr16:71757570-71758218	GM12878	blood:	n/a	n/a
36	CHD2	chr16:71756878-71757340	HepG2	liver:	n/a	n/a
37	CHD2	chr16:71756558-71757214	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr16:71756603-71757329	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr16:71757938-71758158	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr16:71757531-71758302	K562	blood:	n/a	n/a
41	CREB1	chr16:71756556-71758432	HepG2	liver:	n/a	n/a
42	CREB1	chr16:71756835-71757565	A549	lung:	n/a	n/a
43	CREB1	chr16:71757574-71758058	A549	lung:	n/a	n/a
44	CTBP2	chr16:71756759-71757345	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr16:71757654-71758377	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr16:71757960-71758110	AG04449	skin:	n/a	n/a
47	CTCF	chr16:71758020-71758170	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr16:71757997-71758165	K562	blood:	n/a	n/a
49	CTCF	chr16:71758080-71758230	HMEC	breast:	n/a	n/a
50	CTCF	chr16:71757840-71757990	GM12873	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71757240-71757290	K562	blood:	n/a
2	chr16:71758038-71758088	H1-hESC	embryonic stem cell:	embryo
3	chr16:71757240-71757290	AG09309	skin:	n/a
4	chr16:71758038-71758088	MCF-7	breast:	n/a
5	chr16:71758038-71758088	NT2-D1	testis:	n/a
6	chr16:71757240-71757290	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:71757240-71757290	AG04450	lung:	fetal
8	chr16:71757240-71757290	AG09319	gingival:	n/a
9	chr16:71758038-71758088	A549	lung:	n/a
10	chr16:71757240-71757290	PANC-1	pancreas:	n/a
11	chr16:71757240-71757290	GM19239	blood:	n/a
12	chr16:71757240-71757290	LNCaP	prostate:	n/a
13	chr16:71758038-71758088	IMR90	lung:	fetal
14	chr16:71757240-71757290	Hepatocyte	liver:	n/a
15	chr16:71757240-71757290	Hela-S3	cervix:	n/a
16	chr16:71757240-71757290	ECC-1	luminal epithelium:	n/a
17	chr16:71758038-71758088	SK-N-SH	brain:	n/a
18	chr16:71758038-71758088	K562	blood:	n/a
19	chr16:71757240-71757290	NT2-D1	testis:	n/a
20	chr16:71757240-71757290	HRE	kidney:	n/a
21	chr16:71758038-71758088	HRCEpiC	kidney:	n/a
22	chr16:71758038-71758088	GM12878	blood:	n/a
23	chr16:71757240-71757290	CMK	blood:	n/a
24	chr16:71758038-71758088	HRPEpiC	eye:	n/a
25	chr16:71758038-71758088	ovcar-3	ovarian:	n/a
26	chr16:71758038-71758088	U87	brain:	n/a
27	chr16:71758038-71758088	BJ	skin:	n/a
28	chr16:71758038-71758088	HCM	heart:	n/a
29	chr16:71757240-71757290	GM06990	blood:	n/a
30	chr16:71758038-71758088	HepG2	liver:	n/a
31	chr16:71758038-71758088	GM19239	blood:	n/a
32	chr16:71757240-71757290	H1-hESC	embryonic stem cell:	embryo
33	chr16:71757240-71757290	HIPEpiC	eye:	n/a
34	chr16:71757240-71757290	BE2_C	brain:	n/a
35	chr16:71757240-71757290	HRPEpiC	eye:	n/a
36	chr16:71757240-71757290	ovcar-3	ovarian:	n/a
37	chr16:71758038-71758088	PrEC	prostate:	n/a
38	chr16:71757240-71757290	RPTEC	kidney:	n/a
39	chr16:71757240-71757290	SK-N-SH	brain:	n/a
40	chr16:71758038-71758088	HIPEpiC	eye:	n/a
41	chr16:71757240-71757290	MCF-7	breast:	n/a
42	chr16:71757240-71757290	HepG2	liver:	n/a
43	chr16:71757240-71757290	NB4	blood:	n/a
44	chr16:71757240-71757290	U87	brain:	n/a
45	chr16:71758038-71758088	NH-A	brain:	n/a
46	chr16:71757240-71757290	PrEC	prostate:	n/a
47	chr16:71757240-71757290	SK-N-SH_RA	brain:	n/a
48	chr16:71758038-71758088	T-47D	breast:	n/a
49	chr16:71758038-71758088	AG09319	gingival:	n/a
50	chr16:71758038-71758088	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:71696881..71698945-chr16:71757287..71759170,2	MCF-7	breast:
2	chr16:71756102..71758936-chr16:71915033..71919382,3	MCF-7	breast:
3	chr16:71756649..71759449-chr16:71879809..71882216,3	MCF-7	breast:
4	chr16:71757196..71759664-chr16:71766555..71771218,5	MCF-7	breast:
5	chr16:71755537..71758357-chr16:71878950..71881033,2	K562	blood:
6	chr16:71756422..71758416-chr16:71842004..71843953,2	MCF-7	breast:
7	chr16:71756383..71758703-chr16:71759355..71761226,2	MCF-7	breast:
8	chr16:71756413..71761113-chr16:71764688..71769079,7	K562	blood:
9	chr16:71758014..71760790-chr16:71779924..71782486,2	K562	blood:
10	chr1:11967125..11969776-chr16:71755847..71757507,2	MCF-7	breast:
11	chr16:71755880..71759578-chr16:71759607..71764621,8	MCF-7	breast:
12	chr16:71697444..71699494-chr16:71756866..71759011,2	MCF-7	breast:
13	chr16:71755635..71758602-chr16:71927230..71929480,2	MCF-7	breast:
14	chr16:71756009..71758513-chr16:71878989..71881221,2	K562	blood:
15	chr16:71748955..71755873-chr16:71756069..71760101,14	MCF-7	breast:
16	chr1:6844657..6845258-chr16:71757161..71757923,2	Hela-S3	cervix:
17	chr16:71756273..71758753-chr16:71927656..71930818,3	MCF-7	breast:
18	chr16:71756712..71759795-chr16:71768156..71771579,4	MCF-7	breast:
19	chr16:71756251..71759040-chr16:71918074..71919809,2	K562	blood:
20	chr16:71658952..71666464-chr16:71755738..71760832,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARVELD3-2	chr16:71757619-71758133	ENSG00000261513.1
2	lnc-MARVELD3-2	chr16:71757083-71757344	ENSG00000261513.1

No data

Variant related genes	Relation type
ENSG00000261513	TF binding region
PHLPP2	TF binding region
ENSG00000260612	TF binding region
ENSG00000261513	CpG island
PHLPP2	CpG island
ENSG00000260612	CpG island
ENSG00000237436	chromatin interactions
ENSG00000040199	chromatin interactions
ENSG00000102984	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000224470	chromatin interactions
ENSG00000182149	chromatin interactions
ENSG00000260612	chromatin interactions
ENSG00000261765	chromatin interactions
ENSG00000260593	chromatin interactions
ENSG00000166747	chromatin interactions
ENSG00000140832	chromatin interactions

Extended variants
information (count: 41 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9934301	chr16:71756845-71756846	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186913063	chr16:71756909-71756910	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs368022470	chr16:71756924-71756925	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs78304444	chr16:71756941-71756942	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs575454116	chr16:71756943-71756944	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs554807719	chr16:71756947-71756948	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs560897694	chr16:71756959-71756960	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs11860518	chr16:71756961-71756962	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540547817	chr16:71756992-71756993	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs565048377	chr16:71756994-71756995	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs116338900	chr16:71757015-71757016	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
12	rs568177575	chr16:71757020-71757021	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs550796410	chr16:71757124-71757125	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
14	rs563620779	chr16:71757145-71757146	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
15	rs147174874	chr16:71757230-71757231	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
16	rs557036498	chr16:71757237-71757238	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
17	rs548942450	chr16:71757245-71757246	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
18	rs567343289	chr16:71757248-71757249	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
19	rs534947355	chr16:71757261-71757262	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
20	rs115620559	chr16:71757283-71757284	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
21	rs571955921	chr16:71757356-71757357	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs538848878	chr16:71757362-71757363	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs9934715	chr16:71757387-71757388	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs12923990	chr16:71757395-71757396	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs536376823	chr16:71757450-71757451	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs554569250	chr16:71757482-71757483	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs572883225	chr16:71757613-71757614	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs372656363	chr16:71757620-71757621	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
29	rs540471429	chr16:71757761-71757762	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
30	rs565027517	chr16:71757788-71757789	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
31	rs191759405	chr16:71757795-71757796	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
32	rs111334255	chr16:71757837-71757838	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
33	rs577107762	chr16:71757851-71757852	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
34	rs7201649	chr16:71757939-71757940	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs182677657	chr16:71757942-71757943	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
36	rs569334111	chr16:71758010-71758011	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
37	rs76090771	chr16:71758068-71758069	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
38	rs542445459	chr16:71758131-71758132	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
39	rs528464073	chr16:71758229-71758230	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs75902215	chr16:71758260-71758261	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs571834718	chr16:71758273-71758274	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71755600-71758000	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr16:71755800-71758400	Active TSS	NHLF	lung
3	chr16:71756000-71757000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:71756000-71757000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
5	chr16:71756200-71757000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr16:71756200-71758000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr16:71756200-71758000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr16:71756200-71758000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:71756200-71758200	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr16:71756200-71758200	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr16:71756200-71758200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr16:71756200-71758200	Active TSS	Colonic Mucosa	Colon
13	chr16:71756200-71758200	Active TSS	A549	lung
14	chr16:71756200-71758200	Active TSS	HSMM	muscle
15	chr16:71756200-71758400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr16:71756200-71758400	Active TSS	Fetal Kidney	kidney
17	chr16:71756400-71757000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr16:71756400-71757000	Flanking Active TSS	Brain Anterior Caudate	brain
19	chr16:71756400-71757000	Flanking Active TSS	Brain Cingulate Gyrus	brain
20	chr16:71756400-71757000	Flanking Active TSS	Fetal Brain Female	brain
21	chr16:71756400-71757000	Flanking Active TSS	HUVEC	blood vessel
22	chr16:71756400-71757000	Flanking Active TSS	K562	blood
23	chr16:71756400-71757200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr16:71756400-71757200	Flanking Active TSS	Dnd41	blood
25	chr16:71756400-71757200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
26	chr16:71756400-71757400	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr16:71756400-71757400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr16:71756400-71757400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr16:71756400-71758000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr16:71756400-71758000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr16:71756400-71758000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr16:71756400-71758000	Active TSS	Placenta	Placenta
33	chr16:71756400-71758200	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr16:71756400-71758200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr16:71756400-71758200	Active TSS	H1 Cell Line	embryonic stem cell
36	chr16:71756400-71758200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr16:71756400-71758200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr16:71756400-71758200	Active TSS	Brain Germinal Matrix	brain
39	chr16:71756400-71758200	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr16:71756400-71758200	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr16:71756400-71758200	Active TSS	HSMMtube	muscle
42	chr16:71756400-71758200	Active TSS	NHDF-Ad	bronchial
43	chr16:71756400-71758400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr16:71756400-71758400	Active TSS	H9 Cell Line	embryonic stem cell
45	chr16:71756400-71758400	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr16:71756600-71757000	Flanking Active TSS	Primary B cells from peripheral blood	blood
47	chr16:71756600-71757000	Flanking Active TSS	Primary hematopoietic stem cells	blood
48	chr16:71756600-71757000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr16:71756600-71757000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr16:71756600-71757000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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