Variant report

Variant	esv3312534
Chromosome Location	chr16:75599276-75601824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:504)
CpG islands
(count:552)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75600244-75600324	HepG2	liver:	n/a	n/a
2	ATF1	chr16:75598881-75599280	K562	blood:	n/a	n/a
3	ATF2	chr16:75598743-75599371	GM12878	blood:	n/a	n/a
4	ATF2	chr16:75598804-75599302	GM12878	blood:	n/a	n/a
5	BACH1	chr16:75600813-75600842	K562	blood:	n/a	n/a
6	BCLAF1	chr16:75599838-75600501	GM12878	blood:	n/a	chr16:75600374-75600383 chr16:75600455-75600464 chr16:75600368-75600381 chr16:75600222-75600235
7	BHLHE40	chr16:75599813-75600346	GM12878	blood:	n/a	n/a
8	BHLHE40	chr16:75598924-75599283	HepG2	liver:	n/a	n/a
9	BHLHE40	chr16:75599726-75600300	K562	blood:	n/a	n/a
10	BHLHE40	chr16:75598802-75599317	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:75598873-75599309	K562	blood:	n/a	n/a
12	BRCA1	chr16:75599896-75600186	GM12878	blood:	n/a	n/a
13	BRCA1	chr16:75600043-75600362	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr16:75599638-75600199	K562	blood:	n/a	n/a
15	CCNT2	chr16:75600013-75601099	K562	blood:	n/a	chr16:75600449-75600458 chr16:75600471-75600480 chr16:75600222-75600231
16	CEBPB	chr16:75598925-75599330	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:75598896-75599338	HepG2	liver:	n/a	n/a
18	CEBPB	chr16:75598909-75599326	K562	blood:	n/a	n/a
19	CEBPB	chr16:75598820-75599317	MCF-7	breast:	n/a	n/a
20	CEBPB	chr16:75598959-75599308	A549	lung:	n/a	n/a
21	CEBPB	chr16:75600095-75600352	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr16:75598942-75599317	K562	blood:	n/a	n/a
23	CEBPB	chr16:75598749-75599379	HCT-116	colon:	n/a	n/a
24	CEBPB	chr16:75598877-75599328	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr16:75598852-75599323	MCF-7	breast:	n/a	n/a
26	CEBPB	chr16:75598751-75599373	HCT-116	colon:	n/a	n/a
27	CEBPB	chr16:75598913-75599316	IMR90	lung:	n/a	n/a
28	CEBPB	chr16:75598922-75599325	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:75598835-75599351	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPD	chr16:75600126-75600465	HepG2	liver:	n/a	n/a
31	CHD1	chr16:75599702-75600227	GM12878	blood:	n/a	n/a
32	CHD1	chr16:75600422-75600475	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr16:75600503-75600718	GM12878	blood:	n/a	n/a
34	CHD1	chr16:75600928-75600941	GM12878	blood:	n/a	n/a
35	CHD2	chr16:75600146-75600597	HepG2	liver:	n/a	n/a
36	CHD2	chr16:75599937-75600666	K562	blood:	n/a	n/a
37	CHD2	chr16:75599861-75600992	GM12878	blood:	n/a	n/a
38	CHD2	chr16:75599809-75599829	HepG2	liver:	n/a	n/a
39	CHD2	chr16:75600012-75600669	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr16:75599897-75600336	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr16:75599725-75600649	GM12878	blood:	n/a	n/a
42	CREB1	chr16:75599987-75600591	A549	lung:	n/a	n/a
43	CREB1	chr16:75599762-75600833	HepG2	liver:	n/a	n/a
44	CTCF	chr16:75599959-75600115	K562	blood:	n/a	n/a
45	CTCF	chr16:75599760-75599910	GM12866	blood:	n/a	n/a
46	CTCF	chr16:75600460-75600610	GM12871	blood:	n/a	n/a
47	CTCF	chr16:75600000-75600150	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr16:75600043-75600183	GM12878	blood:	n/a	n/a
49	CUX1	chr16:75599973-75600078	GM12878	blood:	n/a	n/a
50	CUX1	chr16:75601123-75601126	GM12878	blood:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75600014-75600064	AG10803	skin:	n/a
2	chr16:75599896-75599946	NH-A	brain:	n/a
3	chr16:75600069-75600119	GM06990	blood:	n/a
4	chr16:75600014-75600064	AG10803	skin:	n/a
5	chr16:75599896-75599946	NH-A	brain:	n/a
6	chr16:75600069-75600119	GM06990	blood:	n/a
7	chr16:75600378-75600428	AG09319	gingival:	n/a
8	chr16:75600057-75600107	MCF10A-Er-Src	breast:	n/a
9	chr16:75600014-75600064	AG09309	skin:	n/a
10	chr16:75601025-75601075	Caco-2	colon:	n/a
11	chr16:75600378-75600428	K562	blood:	n/a
12	chr16:75600564-75600614	NB4	blood:	n/a
13	chr16:75600717-75600767	ovcar-3	ovarian:	n/a
14	chr16:75600381-75600431	HMEC	breast:	n/a
15	chr16:75600057-75600107	PFSK-1	brain:	n/a
16	chr16:75600717-75600767	HepG2	liver:	n/a
17	chr16:75600717-75600767	NHBE	bronchial:	n/a
18	chr16:75600014-75600064	PANC-1	pancreas:	n/a
19	chr16:75600381-75600431	LNCaP	prostate:	n/a
20	chr16:75600717-75600767	MCF10A-Er-Src	breast:	n/a
21	chr16:75600057-75600107	NHDF-neo	bronchial:	n/a
22	chr16:75600717-75600767	HPAEpiC	pulmonary alveolar:	n/a
23	chr16:75600564-75600614	PANC-1	pancreas:	n/a
24	chr16:75600069-75600119	NHDF-neo	bronchial:	n/a
25	chr16:75599896-75599946	HCT-116	colon:	n/a
26	chr16:75600381-75600431	MCF-7	breast:	n/a
27	chr16:75600381-75600431	HCF	heart:	n/a
28	chr16:75600717-75600767	SK-N-SH	brain:	n/a
29	chr16:75600564-75600614	AG09309	skin:	n/a
30	chr16:75600014-75600064	LNCaP	prostate:	n/a
31	chr16:75600564-75600614	Caco-2	colon:	n/a
32	chr16:75599896-75599946	Caco-2	colon:	n/a
33	chr16:75600014-75600064	GM12891	blood:	n/a
34	chr16:75600381-75600431	NHDF-neo	bronchial:	n/a
35	chr16:75600381-75600431	MCF10A-Er-Src	breast:	n/a
36	chr16:75600069-75600119	BJ	skin:	n/a
37	chr16:75599896-75599946	SAEC	small airway:	n/a
38	chr16:75599896-75599946	HMEC	breast:	n/a
39	chr16:75601025-75601075	PrEC	prostate:	n/a
40	chr16:75600381-75600431	HCT-116	colon:	n/a
41	chr16:75600564-75600614	BE2_C	brain:	n/a
42	chr16:75600564-75600614	A549	lung:	n/a
43	chr16:75600014-75600064	HRPEpiC	eye:	n/a
44	chr16:75600014-75600064	ProgFib	skin:	n/a
45	chr16:75600014-75600064	SK-N-SH_RA	brain:	n/a
46	chr16:75600069-75600119	K562	blood:	n/a
47	chr16:75600381-75600431	GM12878	blood:	n/a
48	chr16:75600057-75600107	HL-60	blood:	n/a
49	chr16:75600069-75600119	NT2-D1	testis:	n/a
50	chr16:75600014-75600064	HAEpiC	amniotic membrane:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:75601777..75604413-chr16:75611390..75613643,2	K562	blood:
2	chr16:75587491..75591972-chr16:75596703..75602966,17	MCF-7	breast:
3	chr16:75596664..75600013-chr16:75654010..75656769,3	K562	blood:
4	chr16:75586208..75590870-chr16:75596068..75600585,8	K562	blood:
5	chr16:75598745..75600890-chr16:75655383..75657208,2	MCF-7	breast:
6	chr16:75496436..75498553-chr16:75596400..75601675,4	MCF-7	breast:
7	chr16:75550007..75552554-chr16:75597669..75600323,2	MCF-7	breast:
8	chr16:75600704..75602997-chr16:75682775..75685144,2	K562	blood:
9	chr16:75497166..75499836-chr16:75598619..75601609,5	MCF-7	breast:
10	chr16:75598443..75600121-chr16:75680114..75683081,2	MCF-7	breast:
11	chr16:75588622..75597419-chr16:75598326..75606239,14	K562	blood:
12	chr16:75593028..75596412-chr16:75596623..75599848,3	MCF-7	breast:
13	chr16:75587953..75591056-chr16:75597056..75601894,6	MCF-7	breast:
14	chr16:75466841..75469026-chr16:75598696..75600730,2	MCF-7	breast:
15	chr1:149858339..149860614-chr16:75599065..75602027,3	MCF-7	breast:

No data

Variant related genes	Relation type
GABARAPL2	TF binding region
GABARAPL2	CpG island
ENSG00000065427	chromatin interactions
ENSG00000153774	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000065457	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000262583	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000166848	chromatin interactions

Extended variants
information (count: 135 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:135 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78968668	chr16:75599287-75599288	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs74345059	chr16:75599288-75599289	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs11862650	chr16:75599319-75599320	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs190504476	chr16:75599321-75599322	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs556973006	chr16:75599340-75599341	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs372842401	chr16:75599358-75599359	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs552900767	chr16:75599375-75599376	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs573046392	chr16:75599377-75599378	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs545021277	chr16:75599392-75599393	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs564882737	chr16:75599467-75599468	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs144057004	chr16:75599470-75599471	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs113246551	chr16:75599479-75599480	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs544248342	chr16:75599496-75599497	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs560932408	chr16:75599526-75599527	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs369123152	chr16:75599533-75599534	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs146413422	chr16:75599537-75599538	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs375590809	chr16:75599545-75599546	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs182479970	chr16:75599618-75599619	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs532834873	chr16:75599629-75599630	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs552626866	chr16:75599673-75599674	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs185821120	chr16:75599691-75599692	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs60919196	chr16:75599748-75599749	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs55754264	chr16:75599765-75599766	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs531574083	chr16:75599773-75599774	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs568175070	chr16:75599776-75599777	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs375719522	chr16:75599783-75599784	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs534036481	chr16:75599800-75599801	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs553128873	chr16:75599826-75599827	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs79207574	chr16:75599864-75599865	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs140813043	chr16:75599895-75599896	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs373340476	chr16:75599903-75599904	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
32	rs558865071	chr16:75599915-75599916	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
33	rs144837181	chr16:75599973-75599974	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
34	rs575626654	chr16:75600075-75600076	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs544188465	chr16:75600115-75600116	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs148285279	chr16:75600116-75600117	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs574473545	chr16:75600122-75600123	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs376912130	chr16:75600142-75600143	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs539996341	chr16:75600155-75600156	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs560718621	chr16:75600168-75600169	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs532621059	chr16:75600173-75600174	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs546397817	chr16:75600191-75600192	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs562806469	chr16:75600192-75600193	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs575443820	chr16:75600201-75600202	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs548130342	chr16:75600226-75600227	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs112633452	chr16:75600232-75600233	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs568162825	chr16:75600249-75600250	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs527775679	chr16:75600274-75600275	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs547604261	chr16:75600286-75600287	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs570946508	chr16:75600289-75600290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Breast cancer	21364760	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
Bipolar disorder	19114987	CNVD

Chromatin state (count:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75591200-75599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:75594200-75599600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr16:75597800-75599600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr16:75597800-75599600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr16:75598000-75599600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr16:75598200-75599600	Enhancers	Fetal Heart	heart
7	chr16:75598200-75599800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr16:75598600-75599400	Enhancers	Fetal Intestine Small	intestine
9	chr16:75598600-75599600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr16:75598800-75599400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr16:75598800-75599400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr16:75598800-75599400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:75598800-75599600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr16:75598800-75599600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr16:75598800-75599600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr16:75598800-75599600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr16:75598800-75599600	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr16:75598800-75599600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr16:75598800-75599600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr16:75598800-75599600	Enhancers	Fetal Thymus	thymus
21	chr16:75598800-75599600	Enhancers	Stomach Mucosa	stomach
22	chr16:75598800-75599600	Flanking Active TSS	HepG2	liver
23	chr16:75598800-75599600	Enhancers	HSMM	muscle
24	chr16:75598800-75599600	Enhancers	HSMMtube	muscle
25	chr16:75598800-75599600	Enhancers	NHDF-Ad	bronchial
26	chr16:75598800-75599600	Enhancers	NHLF	lung
27	chr16:75598800-75600000	Flanking Active TSS	GM12878-XiMat	blood
28	chr16:75599000-75599400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr16:75599000-75599400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr16:75599000-75599400	Enhancers	Primary T cells from cord blood	blood
31	chr16:75599000-75599400	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr16:75599000-75599400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
33	chr16:75599000-75599400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr16:75599000-75599400	Enhancers	Adipose Nuclei	Adipose
35	chr16:75599000-75599400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr16:75599000-75599400	Flanking Active TSS	K562	blood
37	chr16:75599000-75599600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr16:75599000-75599600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr16:75599000-75599600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr16:75599000-75599600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr16:75599000-75599600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr16:75599000-75599600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr16:75599000-75599600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr16:75599000-75599600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr16:75599000-75599600	Enhancers	Brain Hippocampus Middle	brain
46	chr16:75599000-75599600	Enhancers	Esophagus	oesophagus
47	chr16:75599000-75599600	Enhancers	Fetal Muscle Leg	muscle
48	chr16:75599000-75599600	Enhancers	Placenta Amnion	Placenta Amnion
49	chr16:75599000-75599600	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr16:75599000-75599800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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