Variant report

Variant	esv3389334
Chromosome Location	chr19:56914840-56917838
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	chr19:56915310-56915485	GM12878	blood:	n/a	n/a
3	ATF3	chr19:56915297-56915505	K562	blood:	n/a	n/a
4	ATF3	chr19:56915514-56915819	K562	blood:	n/a	chr19:56915650-56915659
5	ATF3	chr19:56915162-56915692	A549	lung:	n/a	chr19:56915650-56915659
6	BACH1	chr19:56915357-56915904	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:56915472-56915593	K562	blood:	n/a	n/a
8	BATF	chr19:56914712-56915009	GM12878	blood:	n/a	n/a
9	BCL3	chr19:56915688-56916871	GM12878	blood:	n/a	chr19:56915723-56915736 chr19:56915722-56915735
10	BCL3	chr19:56915760-56916356	A549	lung:	n/a	n/a
11	BCL3	chr19:56915682-56916866	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	chr19:56915272-56915548	GM12878	blood:	n/a	n/a
14	BRCA1	chr19:56915774-56915919	H1-hESC	embryonic stem cell:	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	chr19:56915198-56915760	HepG2	liver:	n/a	chr19:56915710-56915717
21	CHD2	chr19:56915107-56916284	GM12878	blood:	n/a	chr19:56915710-56915717
22	CHD2	chr19:56915391-56915727	K562	blood:	n/a	chr19:56915710-56915717
23	CREB1	chr19:56915162-56915938	K562	blood:	n/a	n/a
24	CREB1	chr19:56915151-56915970	A549	lung:	n/a	n/a
25	CREB1	chr19:56915097-56915953	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr19:56915206-56915942	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr19:56915640-56915790	HUVEC	blood vessel:	n/a	chr19:56915680-56915693
28	CTCF	chr19:56915040-56915190	GM12873	blood:	n/a	n/a
29	CTCF	chr19:56915681-56915684	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr19:56915420-56915570	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr19:56915680-56915830	AG04449	skin:	n/a	chr19:56915803-56915816 chr19:56915680-56915693
32	CTCF	chr19:56915240-56915390	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr19:56915720-56915726	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr19:56915427-56915555	K562	blood:	n/a	n/a
35	CTCF	chr19:56915080-56915230	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr19:56915640-56915790	WI-38	lung:	n/a	chr19:56915680-56915693
37	CTCF	chr19:56915300-56915450	HepG2	liver:	n/a	n/a
38	CTCF	chr19:56915697-56915719	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr19:56915320-56915470	NHEK	skin:	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	chr19:56915273-56915408	K562	blood:	n/a	chr19:56915386-56915395
42	E2F6	chr19:56915580-56915832	K562	blood:	n/a	chr19:56915710-56915717 chr19:56915806-56915817 chr19:56915652-56915661
43	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
44	E2F6	chr19:56915562-56915936	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	chr19:56915044-56915971	GM12878	blood:	n/a	n/a
50	ELF1	chr19:56915186-56915882	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56915658-56915708	BJ	skin:	n/a
2	chr19:56915184-56915234	ECC-1	luminal epithelium:	n/a
3	chr19:56915653-56915703	HCPEpiC	choroid plexus:	n/a
4	chr19:56916205-56916255	ovcar-3	ovarian:	n/a
5	chr19:56915650-56915700	PFSK-1	brain:	n/a
6	chr19:56915658-56915708	A549	lung:	n/a
7	chr19:56915079-56915129	HCF	heart:	n/a
8	chr19:56915184-56915234	K562	blood:	n/a
9	chr19:56915658-56915708	AG09309	skin:	n/a
10	chr19:56915879-56915929	SAEC	small airway:	n/a
11	chr19:56916205-56916255	K562	blood:	n/a
12	chr19:56915655-56915705	NB4	blood:	n/a
13	chr19:56915148-56915198	PANC-1	pancreas:	n/a
14	chr19:56915403-56915453	HEK293	kidney:	embryo
15	chr19:56915658-56915708	PANC-1	pancreas:	n/a
16	chr19:56915522-56915572	RPTEC	kidney:	n/a
17	chr19:56915079-56915129	GM06990	blood:	n/a
18	chr19:56915403-56915453	ProgFib	skin:	n/a
19	chr19:56915653-56915703	MCF-7	breast:	n/a
20	chr19:56915855-56915905	BE2_C	brain:	n/a
21	chr19:56915184-56915234	GM06990	blood:	n/a
22	chr19:56915650-56915700	BE2_C	brain:	n/a
23	chr19:56916205-56916255	GM12892	blood:	n/a
24	chr19:56915732-56915782	HNPCEpiC	eye:	n/a
25	chr19:56915079-56915129	HRPEpiC	eye:	n/a
26	chr19:56915653-56915703	AG04450	lung:	fetal
27	chr19:56915079-56915129	AG04449	skin:	fetal
28	chr19:56915658-56915708	HEEpiC	esophagus:	n/a
29	chr19:56915879-56915929	K562	blood:	n/a
30	chr19:56915732-56915782	NH-A	brain:	n/a
31	chr19:56915855-56915905	HEEpiC	esophagus:	n/a
32	chr19:56915148-56915198	HUVEC	blood vessel:	n/a
33	chr19:56915403-56915453	GM12892	blood:	n/a
34	chr19:56915879-56915929	GM19239	blood:	n/a
35	chr19:56915403-56915453	HMEC	breast:	n/a
36	chr19:56915879-56915929	MCF10A-Er-Src	breast:	n/a
37	chr19:56915079-56915129	ProgFib	skin:	n/a
38	chr19:56915650-56915700	RPTEC	kidney:	n/a
39	chr19:56915079-56915129	HL-60	blood:	n/a
40	chr19:56915403-56915453	HepG2	liver:	n/a
41	chr19:56915403-56915453	HCT-116	colon:	n/a
42	chr19:56915403-56915453	SKMC	muscle:	n/a
43	chr19:56915879-56915929	HRE	kidney:	n/a
44	chr19:56915522-56915572	HCT-116	colon:	n/a
45	chr19:56915522-56915572	AG10803	skin:	n/a
46	chr19:56915855-56915905	PANC-1	pancreas:	n/a
47	chr19:56915653-56915703	PANC-1	pancreas:	n/a
48	chr19:56915658-56915708	MCF10A-Er-Src	breast:	n/a
49	chr19:56915403-56915453	GM19239	blood:	n/a
50	chr19:56915879-56915929	SKMC	muscle:	n/a

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

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

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

Extended variants
information (count: 111 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	rs73621272	chr19:56915440-56915441	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
23	rs371321591	chr19:56915457-56915458	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs142117757	chr19:56915458-56915459	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs3059572	chr19:56915464-56915465	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs548999932	chr19:56915466-56915467	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs570703868	chr19:56915479-56915480	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs188154322	chr19:56915586-56915587	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs574738013	chr19:56915615-56915616	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs12609819	chr19:56915621-56915622	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs560353747	chr19:56915661-56915662	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs576987397	chr19:56915683-56915684	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs374784761	chr19:56915688-56915689	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs545555513	chr19:56915707-56915708	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs150488943	chr19:56915711-56915712	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs550139986	chr19:56915720-56915721	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs367599155	chr19:56915732-56915733	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs531202712	chr19:56915737-56915738	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543157409	chr19:56915745-56915746	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs370318057	chr19:56915755-56915756	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs535911518	chr19:56915768-56915769	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs548218452	chr19:56915796-56915797	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs561351571	chr19:56915850-56915851	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs12610115	chr19:56915855-56915856	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs192864685	chr19:56915858-56915859	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs114846502	chr19:56916020-56916021	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs540053732	chr19:56916039-56916040	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs117514798	chr19:56916073-56916074	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs140314575	chr19:56916074-56916075	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535580894	chr19:56916091-56916092	Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	3 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:499 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56911000-56915000	Weak transcription	Aorta	Aorta
2	chr19:56914200-56915000	Flanking Active TSS	Dnd41	blood
3	chr19:56914200-56915200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
4	chr19:56914200-56915200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:56914200-56916000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr19:56914200-56916000	Active TSS	Duodenum Smooth Muscle	Duodenum
7	chr19:56914200-56916000	Active TSS	HSMMtube	muscle
8	chr19:56914200-56916000	Active TSS	NHDF-Ad	bronchial
9	chr19:56914200-56916200	Active TSS	Muscle Satellite Cultured Cells	--
10	chr19:56914400-56915000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:56914400-56915000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
12	chr19:56914400-56915000	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr19:56914400-56915000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
14	chr19:56914400-56915000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr19:56914400-56915000	Flanking Active TSS	Liver	Liver
16	chr19:56914400-56915000	Flanking Active TSS	Colon Smooth Muscle	Colon
17	chr19:56914400-56915000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr19:56914400-56915000	Enhancers	Small Intestine	intestine
19	chr19:56914400-56915200	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr19:56914400-56915200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
21	chr19:56914400-56915200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
22	chr19:56914400-56915800	Active TSS	Stomach Smooth Muscle	stomach
23	chr19:56914400-56915800	Active TSS	HSMM	muscle
24	chr19:56914400-56915800	Active TSS	Osteobl	bone
25	chr19:56914400-56916000	Active TSS	H1 Cell Line	embryonic stem cell
26	chr19:56914400-56916000	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr19:56914400-56916000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr19:56914400-56916000	Active TSS	Brain Cingulate Gyrus	brain
29	chr19:56914400-56916000	Active TSS	Fetal Brain Female	brain
30	chr19:56914400-56916000	Active TSS	Rectal Mucosa Donor 29	rectum
31	chr19:56914400-56916000	Active TSS	NHLF	lung
32	chr19:56914400-56916200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr19:56914400-56916400	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr19:56914400-56916800	Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr19:56914600-56915000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr19:56914600-56915000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:56914600-56915000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr19:56914600-56915000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr19:56914600-56915000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr19:56914600-56915000	Flanking Active TSS	Brain Angular Gyrus	brain
41	chr19:56914600-56915000	Flanking Active TSS	Brain Substantia Nigra	brain
42	chr19:56914600-56915000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr19:56914600-56915000	Flanking Active TSS	Fetal Brain Male	brain
44	chr19:56914600-56915000	Flanking Active TSS	Fetal Heart	heart
45	chr19:56914600-56915000	Flanking Active TSS	Fetal Muscle Trunk	muscle
46	chr19:56914600-56915000	Flanking Active TSS	Fetal Muscle Leg	muscle
47	chr19:56914600-56915000	Flanking Active TSS	Fetal Stomach	stomach
48	chr19:56914600-56915000	Enhancers	Lung	lung
49	chr19:56914600-56915000	Enhancers	Pancreas	Pancrea
50	chr19:56914600-56915000	Flanking Active TSS	Rectal Smooth Muscle	rectum

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