Variant report

Variant	esv3373403
Chromosome Location	chr19:56913940-56918638
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	ARID3A	chr19:56915260-56915738	HepG2	liver:	n/a	n/a
2	ATF3	chr19:56915162-56915692	A549	lung:	n/a	chr19:56915650-56915659
3	ATF3	chr19:56915310-56915485	GM12878	blood:	n/a	n/a
4	ATF3	chr19:56915514-56915819	K562	blood:	n/a	chr19:56915650-56915659
5	ATF3	chr19:56915297-56915505	K562	blood:	n/a	n/a
6	BACH1	chr19:56915472-56915593	K562	blood:	n/a	n/a
7	BACH1	chr19:56915357-56915904	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr19:56914712-56915009	GM12878	blood:	n/a	n/a
9	BCL3	chr19:56915760-56916356	A549	lung:	n/a	n/a
10	BCL3	chr19:56915682-56916866	GM12878	blood:	n/a	chr19:56915723-56915736 chr19:56915722-56915735
11	BCL3	chr19:56915688-56916871	GM12878	blood:	n/a	chr19:56915723-56915736 chr19:56915722-56915735
12	BHLHE40	chr19:56915310-56916331	K562	blood:	n/a	chr19:56915676-56915692 chr19:56915606-56915622
13	BRCA1	chr19:56915774-56915919	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr19:56915272-56915548	GM12878	blood:	n/a	n/a
15	CBX3	chr19:56915466-56916519	K562	blood:	n/a	n/a
16	CCNT2	chr19:56915246-56915917	K562	blood:	n/a	n/a
17	CEBPB	chr19:56915189-56915412	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr19:56915539-56915567	GM12878	blood:	n/a	n/a
19	CHD2	chr19:56915389-56915902	H1-hESC	embryonic stem cell:	n/a	chr19:56915710-56915717
20	CHD2	chr19:56915391-56915727	K562	blood:	n/a	chr19:56915710-56915717
21	CHD2	chr19:56915107-56916284	GM12878	blood:	n/a	chr19:56915710-56915717
22	CHD2	chr19:56915198-56915760	HepG2	liver:	n/a	chr19:56915710-56915717
23	CREB1	chr19:56915151-56915970	A549	lung:	n/a	n/a
24	CREB1	chr19:56915162-56915938	K562	blood:	n/a	n/a
25	CREB1	chr19:56915206-56915942	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr19:56915097-56915953	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr19:56915320-56915470	NHEK	skin:	n/a	n/a
28	CTCF	chr19:56915720-56915726	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr19:56915697-56915719	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr19:56915300-56915450	HepG2	liver:	n/a	n/a
31	CTCF	chr19:56915640-56915790	HUVEC	blood vessel:	n/a	chr19:56915680-56915693
32	CTCF	chr19:56915680-56915830	AG04449	skin:	n/a	chr19:56915803-56915816 chr19:56915680-56915693
33	CTCF	chr19:56915240-56915390	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr19:56915040-56915190	GM12873	blood:	n/a	n/a
35	CTCF	chr19:56915427-56915555	K562	blood:	n/a	n/a
36	CTCF	chr19:56915640-56915790	WI-38	lung:	n/a	chr19:56915680-56915693
37	CTCF	chr19:56915681-56915684	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr19:56915080-56915230	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr19:56915420-56915570	SK-N-SH_RA	brain:	n/a	n/a
40	E2F4	chr19:56915144-56915734	MCF10A-Er-Src	breast:	n/a	chr19:56915386-56915395 chr19:56915479-56915488 chr19:56915710-56915717 chr19:56915447-56915456 chr19:56915652-56915661
41	E2F6	chr19:56915203-56916474	K562	blood:	n/a	chr19:56915386-56915395 chr19:56915479-56915488 chr19:56915710-56915717 chr19:56915447-56915456 chr19:56915806-56915817 chr19:56915652-56915661
42	E2F6	chr19:56915562-56915936	K562	blood:	n/a	chr19:56915710-56915717 chr19:56915806-56915817 chr19:56915652-56915661
43	E2F6	chr19:56915273-56915408	K562	blood:	n/a	chr19:56915386-56915395
44	E2F6	chr19:56915580-56915832	K562	blood:	n/a	chr19:56915710-56915717 chr19:56915806-56915817 chr19:56915652-56915661
45	EBF1	chr19:56914976-56915843	GM12878	blood:	n/a	n/a
46	EBF1	chr19:56914993-56915516	GM12878	blood:	n/a	n/a
47	EBF1	chr19:56915148-56915682	GM12878	blood:	n/a	n/a
48	ELF1	chr19:56915015-56915847	GM12878	blood:	n/a	n/a
49	ELF1	chr19:56915186-56915882	K562	blood:	n/a	n/a
50	ELF1	chr19:56915044-56915971	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56915403-56915453	HMEC	breast:	n/a
2	chr19:56915658-56915708	HCM	heart:	n/a
3	chr19:56915148-56915198	SK-N-MC	brain:	n/a
4	chr19:56915403-56915453	HMEC	breast:	n/a
5	chr19:56915658-56915708	HCM	heart:	n/a
6	chr19:56915148-56915198	SK-N-MC	brain:	n/a
7	chr19:56914764-56914814	HEK293	kidney:	embryo
8	chr19:56915148-56915198	AG10803	skin:	n/a
9	chr19:56915879-56915929	LNCaP	prostate:	n/a
10	chr19:56915522-56915572	PrEC	prostate:	n/a
11	chr19:56915732-56915782	NH-A	brain:	n/a
12	chr19:56915522-56915572	GM12878	blood:	n/a
13	chr19:56915855-56915905	ECC-1	luminal epithelium:	n/a
14	chr19:56915403-56915453	K562	blood:	n/a
15	chr19:56915855-56915905	MCF10A-Er-Src	breast:	n/a
16	chr19:56915658-56915708	HIPEpiC	eye:	n/a
17	chr19:56915522-56915572	HMEC	breast:	n/a
18	chr19:56915732-56915782	NT2-D1	testis:	n/a
19	chr19:56915148-56915198	HL-60	blood:	n/a
20	chr19:56915658-56915708	T-47D	breast:	n/a
21	chr19:56915658-56915708	ovcar-3	ovarian:	n/a
22	chr19:56915403-56915453	GM12878	blood:	n/a
23	chr19:56914764-56914814	PFSK-1	brain:	n/a
24	chr19:56915658-56915708	PANC-1	pancreas:	n/a
25	chr19:56915184-56915234	HRPEpiC	eye:	n/a
26	chr19:56916205-56916255	HAEpiC	amniotic membrane:	n/a
27	chr19:56915650-56915700	PrEC	prostate:	n/a
28	chr19:56915403-56915453	LNCaP	prostate:	n/a
29	chr19:56915650-56915700	T-47D	breast:	n/a
30	chr19:56915148-56915198	MCF10A-Er-Src	breast:	n/a
31	chr19:56915148-56915198	HAEpiC	amniotic membrane:	n/a
32	chr19:56915879-56915929	HRPEpiC	eye:	n/a
33	chr19:56916205-56916255	GM19239	blood:	n/a
34	chr19:56914764-56914814	HIPEpiC	eye:	n/a
35	chr19:56915522-56915572	AG09309	skin:	n/a
36	chr19:56915658-56915708	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:56915653-56915703	HCM	heart:	n/a
38	chr19:56915655-56915705	SK-N-SH	brain:	n/a
39	chr19:56915732-56915782	U87	brain:	n/a
40	chr19:56915079-56915129	U87	brain:	n/a
41	chr19:56915079-56915129	SK-N-SH_RA	brain:	n/a
42	chr19:56915650-56915700	AG10803	skin:	n/a
43	chr19:56915658-56915708	GM12892	blood:	n/a
44	chr19:56915653-56915703	Jurkat	blood:	n/a
45	chr19:56915653-56915703	HRPEpiC	eye:	n/a
46	chr19:56915653-56915703	Hepatocyte	liver:	n/a
47	chr19:56915655-56915705	GM12878	blood:	n/a
48	chr19:56915184-56915234	NHBE	bronchial:	n/a
49	chr19:56915658-56915708	HEEpiC	esophagus:	n/a
50	chr19:56915403-56915453	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56902006..56908060-chr19:56909612..56917978,15	K562	blood:
2	chr19:56914950..56917627-chr19:56917967..56921707,4	K562	blood:
3	chr19:56824960..56826803-chr19:56913604..56915630,2	K562	blood:
4	chr19:56902257..56906485-chr19:56913118..56917978,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF582-1	chr19:56915271-56915351	NONHSAT068148
2	lnc-ZNF582-1	chr19:56915271-56915279	XLOC_013415
3	lnc-ZNF582-1	chr19:56914145-56915302	NONHSAT068149
4	lnc-ZNF583-1	chr19:56918395-56918429	NONHSAT068147

Variant related genes	Relation type
ZNF583	TF binding region
ZNF583	CpG island
ENSG00000266631	chromatin interactions
ENSG00000267454	chromatin interactions
ENSG00000131848	chromatin interactions
ENSG00000018869	chromatin interactions
ENSG00000198440	chromatin interactions
ENSG00000267549	chromatin interactions
TES	miRNA target sites

Extended variants
information (count: 199 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:199 , 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	rs183153236	chr19:56913969-56913970	Weak transcription ZNF genes & repeats	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs569942079	chr19:56914006-56914007	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs560606793	chr19:56914013-56914014	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs545832035	chr19:56914038-56914039	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs186671364	chr19:56914049-56914050	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs558446133	chr19:56914141-56914142	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs563024321	chr19:56914142-56914143	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs373302018	chr19:56914161-56914162	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs530669179	chr19:56914203-56914204	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs578207706	chr19:56914227-56914228	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs145337856	chr19:56914254-56914255	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs560884768	chr19:56914475-56914476	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs190627359	chr19:56914494-56914495	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs10418970	chr19:56914500-56914501	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs538201830	chr19:56914519-56914520	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs566612920	chr19:56914530-56914531	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
17	rs147679598	chr19:56914546-56914547	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
18	rs551838794	chr19:56914591-56914592	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
19	rs568842730	chr19:56914593-56914594	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
20	rs538119452	chr19:56914615-56914616	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
21	rs555262942	chr19:56914618-56914619	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
22	rs568290563	chr19:56914624-56914625	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
23	rs534160888	chr19:56914669-56914670	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs545767225	chr19:56914686-56914687	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs149958391	chr19:56914738-56914739	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs539928003	chr19:56914766-56914767	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs144986277	chr19:56914804-56914805	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs149090144	chr19:56914805-56914806	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
29	rs544151133	chr19:56914825-56914826	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs8112683	chr19:56914862-56914863	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs565403489	chr19:56914879-56914880	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs5828681	chr19:56914909-56914910	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs397700504	chr19:56914916-56914917	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs113248740	chr19:56914919-56914920	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs143150622	chr19:56914969-56914970	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs6509996	chr19:56914994-56914995	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112817716	chr19:56915073-56915074	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs560390857	chr19:56915109-56915110	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs73621270	chr19:56915121-56915122	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561508170	chr19:56915191-56915192	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs552263989	chr19:56915198-56915199	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs182787612	chr19:56915216-56915217	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
43	rs531361927	chr19:56915217-56915218	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
44	rs10424112	chr19:56915219-56915220	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs148214952	chr19:56915283-56915284	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
46	rs2058320	chr19:56915324-56915325	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs547541374	chr19:56915353-56915354	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs570721701	chr19:56915366-56915367	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs73937276	chr19:56915422-56915423	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs556641781	chr19:56915432-56915433	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56905600-56914600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:56905800-56914400	Weak transcription	Fetal Heart	heart
3	chr19:56908000-56914800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:56908200-56914600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:56910000-56914200	ZNF genes & repeats	Dnd41	blood
6	chr19:56910200-56914000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr19:56910400-56914600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
8	chr19:56910600-56914200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr19:56910600-56914200	Weak transcription	Brain Anterior Caudate	brain
10	chr19:56910600-56914400	Weak transcription	Brain Substantia Nigra	brain
11	chr19:56910600-56914400	Weak transcription	Fetal Brain Male	brain
12	chr19:56910800-56914400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr19:56910800-56914600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr19:56911000-56914200	Weak transcription	Brain Angular Gyrus	brain
15	chr19:56911000-56914400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr19:56911000-56914400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr19:56911000-56914600	Weak transcription	Ovary	ovary
18	chr19:56911000-56914600	Weak transcription	Right Ventricle	heart
19	chr19:56911000-56914800	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr19:56911000-56915000	Weak transcription	Aorta	Aorta
21	chr19:56911200-56914400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr19:56911400-56914200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr19:56912000-56914200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr19:56912000-56914200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:56912000-56914400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr19:56912000-56914400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr19:56912000-56914400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr19:56912000-56914400	Weak transcription	Brain Germinal Matrix	brain
29	chr19:56912000-56914400	Weak transcription	Brain Hippocampus Middle	brain
30	chr19:56912000-56914400	Weak transcription	Fetal Lung	lung
31	chr19:56912200-56914400	Weak transcription	Fetal Kidney	kidney
32	chr19:56912200-56914400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr19:56912200-56914600	Weak transcription	Left Ventricle	heart
34	chr19:56912400-56914000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr19:56913000-56914200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr19:56913000-56914200	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr19:56913400-56914200	Weak transcription	Primary T cells from cord blood	blood
38	chr19:56913400-56914200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr19:56913400-56914200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:56913400-56914200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr19:56913400-56914200	Weak transcription	HSMMtube	muscle
42	chr19:56913400-56914400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr19:56913400-56914400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr19:56913400-56914400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr19:56913600-56914000	Weak transcription	Primary B cells from cord blood	blood
46	chr19:56913600-56914000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr19:56913600-56914200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr19:56913600-56914200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr19:56913600-56914200	Weak transcription	Liver	Liver
50	chr19:56913600-56914400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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