Variant report

Variant	esv3445164
Chromosome Location	chr8:63997798-63999646
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:855)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63997253-63997844	HepG2	liver:	n/a	n/a
2	BACH1	chr8:63998473-63998876	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr8:63998038-63998204	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr8:63997945-63998026	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:63998697-63998819	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr8:63998425-63998807	H1-hESC	embryonic stem cell:	n/a	chr8:63998633-63998643
7	CHD2	chr8:63998374-63998504	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr8:63998443-63999051	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:63998240-63998390	Caco-2	colon:	n/a	n/a
10	CTCF	chr8:63998421-63998559	MCF-7	breast:	n/a	n/a
11	CTCF	chr8:63998443-63998535	A549	lung:	n/a	n/a
12	CTCF	chr8:63998534-63998538	Fibrobl	skin:	n/a	n/a
13	CTCF	chr8:63998557-63998596	Fibrobl	skin:	n/a	n/a
14	CTCF	chr8:63998516-63998595	MCF-7	breast:	n/a	n/a
15	E2F4	chr8:63998553-63998704	MCF10A-Er-Src	breast:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
16	E2F4	chr8:63997851-63998051	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F6	chr8:63998426-63998850	A549	lung:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
18	E2F6	chr8:63998399-63998986	A549	lung:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
19	E2F6	chr8:63998219-63998842	H1-hESC	embryonic stem cell:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
20	EBF1	chr8:63998480-63998759	GM12878	blood:	n/a	n/a
21	EP300	chr8:63998124-63998188	HepG2	liver:	n/a	n/a
22	FOS	chr8:63998988-63999198	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr8:63997859-63997898	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr8:63998928-63999124	MCF10A-Er-Src	breast:	n/a	n/a
25	FOXA1	chr8:63998511-63998759	T-47D	breast:	n/a	n/a
26	FOXP2	chr8:63998241-63998774	PFSK-1	brain:	n/a	n/a
27	GABPA	chr8:63998304-63998809	H1-hESC	embryonic stem cell:	n/a	n/a
28	HA-E2F1	chr8:63997886-63999102	MCF-7	breast:	n/a	chr8:63998582-63998592 chr8:63998624-63998638 chr8:63998581-63998590
29	HDAC2	chr8:63998321-63998641	HepG2	liver:	n/a	n/a
30	MAX	chr8:63998513-63998694	HepG2	liver:	n/a	n/a
31	MAX	chr8:63998200-63998872	H1-hESC	embryonic stem cell:	n/a	chr8:63998228-63998237
32	MAX	chr8:63998100-63998875	MCF-7	breast:	n/a	chr8:63998228-63998237
33	MAX	chr8:63998349-63999050	HCT-116	colon:	n/a	n/a
34	MAX	chr8:63998429-63998997	HCT-116	colon:	n/a	n/a
35	MAX	chr8:63997887-63998084	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr8:63998431-63998897	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAX	chr8:63998448-63999256	ECC-1	luminal epithelium:	n/a	n/a
38	MAX	chr8:63998463-63998832	SK-N-SH	brain:	n/a	n/a
39	MAX	chr8:63998900-63999216	H1-hESC	embryonic stem cell:	n/a	n/a
40	MAX	chr8:63998121-63999294	ECC-1	luminal epithelium:	n/a	chr8:63998228-63998237
41	MAX	chr8:63998315-63999259	A549	lung:	n/a	n/a
42	MAX	chr8:63998358-63999259	A549	lung:	n/a	n/a
43	MAX	chr8:63998719-63999141	H1-hESC	embryonic stem cell:	n/a	n/a
44	MXI1	chr8:63998459-63998876	HepG2	liver:	n/a	n/a
45	MYC	chr8:63998628-63998726	MCF-7	breast:	n/a	n/a
46	MYC	chr8:63998561-63998581	MCF-7	breast:	n/a	n/a
47	MYC	chr8:63998376-63998750	MCF-7	breast:	n/a	n/a
48	MYC	chr8:63998583-63998596	MCF-7	breast:	n/a	n/a
49	MYC	chr8:63998753-63998760	NB4	blood:	n/a	n/a
50	MYC	chr8:63998567-63999061	MCF10A-Er-Src	breast:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63998164-63998214	NHBE	bronchial:	n/a
2	chr8:63998164-63998214	NHBE	bronchial:	n/a
3	chr8:63998327-63998377	AG04449	skin:	fetal
4	chr8:63999003-63999053	ovcar-3	ovarian:	n/a
5	chr8:63999003-63999053	Jurkat	blood:	n/a
6	chr8:63998327-63998377	SAEC	small airway:	n/a
7	chr8:63999202-63999252	HEEpiC	esophagus:	n/a
8	chr8:63998667-63998717	GM12878	blood:	n/a
9	chr8:63998778-63998828	AoSMC	blood vessel:	n/a
10	chr8:63998164-63998214	SAEC	small airway:	n/a
11	chr8:63998736-63998786	U87	brain:	n/a
12	chr8:63999003-63999053	AG09319	gingival:	n/a
13	chr8:63998228-63998278	SK-N-MC	brain:	n/a
14	chr8:63998778-63998828	HRCEpiC	kidney:	n/a
15	chr8:63999003-63999053	SKMC	muscle:	n/a
16	chr8:63998736-63998786	A549	lung:	n/a
17	chr8:63999202-63999252	SK-N-SH	brain:	n/a
18	chr8:63998649-63998699	HL-60	blood:	n/a
19	chr8:63999202-63999252	GM12892	blood:	n/a
20	chr8:63998649-63998699	NHDF-neo	bronchial:	n/a
21	chr8:63998640-63998690	Hepatocyte	liver:	n/a
22	chr8:63998327-63998377	HepG2	liver:	n/a
23	chr8:63998649-63998699	NHBE	bronchial:	n/a
24	chr8:63997977-63998027	HCM	heart:	n/a
25	chr8:63998667-63998717	BE2_C	brain:	n/a
26	chr8:63999003-63999053	HCPEpiC	choroid plexus:	n/a
27	chr8:63999202-63999252	HCM	heart:	n/a
28	chr8:63998667-63998717	HCT-116	colon:	n/a
29	chr8:63998164-63998214	HAEpiC	amniotic membrane:	n/a
30	chr8:63998327-63998377	MCF10A-Er-Src	breast:	n/a
31	chr8:63999003-63999053	T-47D	breast:	n/a
32	chr8:63998164-63998214	HMEC	breast:	n/a
33	chr8:63998667-63998717	MCF10A-Er-Src	breast:	n/a
34	chr8:63999030-63999080	K562	blood:	n/a
35	chr8:63999003-63999053	NHDF-neo	bronchial:	n/a
36	chr8:63998164-63998214	HNPCEpiC	eye:	n/a
37	chr8:63998228-63998278	HCT-116	colon:	n/a
38	chr8:63998228-63998278	AG09309	skin:	n/a
39	chr8:63998649-63998699	Caco-2	colon:	n/a
40	chr8:63998736-63998786	HMEC	breast:	n/a
41	chr8:63998736-63998786	HIPEpiC	eye:	n/a
42	chr8:63998640-63998690	HIPEpiC	eye:	n/a
43	chr8:63998640-63998690	MCF10A-Er-Src	breast:	n/a
44	chr8:63998736-63998786	BE2_C	brain:	n/a
45	chr8:63998731-63998781	MCF-7	breast:	n/a
46	chr8:63998649-63998699	MCF-7	breast:	n/a
47	chr8:63997977-63998027	NHDF-neo	bronchial:	n/a
48	chr8:63999030-63999080	HNPCEpiC	eye:	n/a
49	chr8:63998731-63998781	PrEC	prostate:	n/a
50	chr8:63998640-63998690	HMEC	breast:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:63949699..63952423-chr8:63997523..63999992,2	K562	blood:
2	chr8:63996810..63998343-chr8:64003518..64005481,2	K562	blood:
3	chr8:63983680..63986260-chr8:63995711..63998023,2	MCF-7	breast:
4	chr8:63995378..63997013-chr8:63999187..64001966,2	K562	blood:

No data

Variant related genes	Relation type
TTPA	TF binding region
TTPA	CpG island
ENSG00000137563	chromatin interactions

Extended variants
information (count: 64 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:64 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564340175	chr8:63997847-63997848	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187850618	chr8:63997863-63997864	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546853601	chr8:63997873-63997874	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561742843	chr8:63997994-63997995	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528835299	chr8:63998001-63998002	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577517704	chr8:63998032-63998033	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550658160	chr8:63998039-63998040	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375004597	chr8:63998067-63998068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149997066	chr8:63998171-63998172	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs72659829	chr8:63998231-63998232	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs551630439	chr8:63998263-63998264	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566654615	chr8:63998280-63998281	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369019692	chr8:63998310-63998311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs191599269	chr8:63998328-63998329	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555671816	chr8:63998332-63998333	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574780098	chr8:63998371-63998372	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs535442955	chr8:63998388-63998389	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557316937	chr8:63998389-63998390	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs397515523	chr8:63998390-63998391	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199636231	chr8:63998403-63998404	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs397515522	chr8:63998406-63998407	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs199805621	chr8:63998434-63998435	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557966488	chr8:63998477-63998478	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573070621	chr8:63998497-63998498	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144290434	chr8:63998524-63998525	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562202164	chr8:63998533-63998534	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140010311	chr8:63998557-63998558	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13257608	chr8:63998574-63998575	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543916738	chr8:63998629-63998630	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs562483069	chr8:63998639-63998640	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533094043	chr8:63998649-63998650	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372863215	chr8:63998663-63998664	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143565227	chr8:63998706-63998707	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183782874	chr8:63998713-63998714	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552717281	chr8:63998764-63998765	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569329535	chr8:63998854-63998855	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139028457	chr8:63998856-63998857	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs549270229	chr8:63998891-63998892	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141105652	chr8:63998898-63998899	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs5891888	chr8:63998915-63998916	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs398095840	chr8:63998925-63998926	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs114523345	chr8:63998949-63998950	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557108297	chr8:63998950-63998951	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs116502178	chr8:63998969-63998970	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142246381	chr8:63999003-63999004	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs73684515	chr8:63999020-63999021	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573109391	chr8:63999048-63999049	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs146447726	chr8:63999137-63999138	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540464502	chr8:63999205-63999206	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs555923637	chr8:63999236-63999237	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63996800-63997800	Enhancers	HepG2	liver
2	chr8:63997200-63998800	Active TSS	Liver	Liver
3	chr8:63997400-63998000	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:63997400-63998800	Active TSS	Rectal Mucosa Donor 29	rectum
5	chr8:63997400-63999200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:63997400-63999200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:63997600-63997800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
8	chr8:63997600-63997800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr8:63997600-63997800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:63997600-63997800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr8:63997600-63997800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:63997600-63997800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr8:63997600-63997800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
14	chr8:63997600-63997800	Enhancers	Brain Cingulate Gyrus	brain
15	chr8:63997600-63997800	Enhancers	Brain Germinal Matrix	brain
16	chr8:63997600-63997800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr8:63997600-63997800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr8:63997600-63997800	Enhancers	Fetal Intestine Small	intestine
19	chr8:63997600-63997800	Bivalent Enhancer	Fetal Lung	lung
20	chr8:63997600-63997800	Active TSS	Stomach Smooth Muscle	stomach
21	chr8:63997600-63997800	Enhancers	NH-A	brain
22	chr8:63997600-63998000	Enhancers	Pancreas	Pancrea
23	chr8:63997600-63998000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
24	chr8:63997600-63998200	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr8:63997600-63998200	Bivalent/Poised TSS	Brain Substantia Nigra	brain
26	chr8:63997600-63998600	Active TSS	Fetal Muscle Trunk	muscle
27	chr8:63997600-63999000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:63997600-63999000	Active TSS	A549	lung
29	chr8:63997600-63999200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr8:63997600-63999200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
31	chr8:63997600-63999200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr8:63997600-63999200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
33	chr8:63997600-63999200	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr8:63997600-63999200	Active TSS	Rectal Smooth Muscle	rectum
35	chr8:63997600-64000000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
36	chr8:63997800-63998000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:63997800-63998000	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
38	chr8:63997800-63998000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
39	chr8:63997800-63998000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr8:63997800-63998000	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
41	chr8:63997800-63998000	Active TSS	Fetal Intestine Large	intestine
42	chr8:63997800-63998000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
43	chr8:63997800-63998000	Active TSS	Fetal Stomach	stomach
44	chr8:63997800-63998000	Active TSS	Ovary	ovary
45	chr8:63997800-63998000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
46	chr8:63997800-63998000	Bivalent/Poised TSS	NHDF-Ad	bronchial
47	chr8:63997800-63998200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
48	chr8:63997800-63998200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:63997800-63998200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr8:63997800-63998200	Flanking Active TSS	Brain Cingulate Gyrus	brain

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