Variant report

Variant	nsv580074
Chromosome Location	chr19:53601649-53627777
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:564)
CpG islands
(count:488)
Chromatin interactive
region (count:18)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53624883-53625151	HepG2	liver:	n/a	n/a
2	ATF2	chr19:53606497-53607018	GM12878	blood:	n/a	n/a
3	ATF3	chr19:53606544-53606749	K562	blood:	n/a	chr19:53606712-53606721
4	BACH1	chr19:53607015-53607178	K562	blood:	n/a	n/a
5	BACH1	chr19:53606550-53607222	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr19:53606356-53607144	GM12878	blood:	n/a	chr19:53606663-53606672
7	BCLAF1	chr19:53606828-53607327	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:53606021-53607112	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:53606496-53607106	K562	blood:	n/a	n/a
10	CBX3	chr19:53606495-53607294	K562	blood:	n/a	n/a
11	CCNT2	chr19:53606567-53607217	K562	blood:	n/a	n/a
12	CEBPB	chr19:53612975-53613054	K562	blood:	n/a	n/a
13	CEBPB	chr19:53604884-53605062	K562	blood:	n/a	chr19:53604994-53605011
14	CEBPD	chr19:53606339-53607235	K562	blood:	n/a	n/a
15	CHD1	chr19:53605620-53607121	GM12878	blood:	n/a	chr19:53606338-53606348
16	CHD1	chr19:53605155-53607496	IMR90	lung:	n/a	chr19:53606338-53606348
17	CHD1	chr19:53606365-53606565	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr19:53606624-53606810	HepG2	liver:	n/a	n/a
19	CHD2	chr19:53606942-53607168	K562	blood:	n/a	n/a
20	CHD2	chr19:53606469-53606501	K562	blood:	n/a	n/a
21	CHD2	chr19:53606569-53606802	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr19:53606410-53607157	GM12878	blood:	n/a	n/a
23	CHD2	chr19:53606419-53607232	Hela-S3	cervix:	n/a	n/a
24	CREB1	chr19:53606433-53607089	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr19:53606521-53607254	GM12878	blood:	n/a	n/a
26	CREB1	chr19:53606391-53607205	K562	blood:	n/a	n/a
27	CREB1	chr19:53606581-53606800	A549	lung:	n/a	n/a
28	CREB1	chr19:53606450-53606985	A549	lung:	n/a	n/a
29	CREB1	chr19:53606393-53607249	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr19:53606415-53607268	HepG2	liver:	n/a	n/a
31	CTBP2	chr19:53606571-53607142	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:53611781-53611861	GM13976	blood:	n/a	n/a
33	CTCF	chr19:53606533-53607030	GM12878	blood:	n/a	n/a
34	CTCF	chr19:53606060-53606210	BJ	skin:	n/a	n/a
35	CTCF	chr19:53606232-53606287	MCF-7	breast:	n/a	n/a
36	CTCF	chr19:53614791-53614891	GM20000	blood:	n/a	n/a
37	CTCF	chr19:53606411-53606595	K562	blood:	n/a	n/a
38	CTCF	chr19:53623018-53623081	GM10266	blood:	n/a	n/a
39	CTCF	chr19:53606591-53606671	GM19239	blood:	n/a	n/a
40	CTCF	chr19:53606200-53606350	AG04449	skin:	n/a	chr19:53606223-53606236
41	CTCF	chr19:53606120-53606270	HRE	kidney:	n/a	chr19:53606223-53606236
42	CTCF	chr19:53606140-53606290	HCPEpiC	choroid plexus:	n/a	chr19:53606223-53606236
43	CTCF	chr19:53606220-53606370	AG09319	gingival:	n/a	chr19:53606223-53606236
44	CTCF	chr19:53606180-53606330	AG04449	skin:	n/a	chr19:53606223-53606236
45	CTCF	chr19:53606239-53606292	GM12878	blood:	n/a	n/a
46	CTCF	chr19:53606975-53607285	K562	blood:	n/a	n/a
47	CTCF	chr19:53606260-53606410	WI-38	lung:	n/a	n/a
48	CTCF	chr19:53606080-53606230	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr19:53606666-53606696	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr19:53616720-53616870	HCPEpiC	choroid plexus:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53606538-53606588	PANC-1	pancreas:	n/a
2	chr19:53605221-53605271	HRCEpiC	kidney:	n/a
3	chr19:53606654-53606704	SK-N-SH	brain:	n/a
4	chr19:53606654-53606704	PFSK-1	brain:	n/a
5	chr19:53606538-53606588	GM06990	blood:	n/a
6	chr19:53605221-53605271	U87	brain:	n/a
7	chr19:53605221-53605271	AG09319	gingival:	n/a
8	chr19:53605221-53605271	LNCaP	prostate:	n/a
9	chr19:53605221-53605271	HEK293	kidney:	embryo
10	chr19:53605221-53605271	PrEC	prostate:	n/a
11	chr19:53606340-53606390	Hepatocyte	liver:	n/a
12	chr19:53619086-53619136	T-47D	breast:	n/a
13	chr19:53606340-53606390	H1-hESC	embryonic stem cell:	embryo
14	chr19:53606340-53606390	BE2_C	brain:	n/a
15	chr19:53607021-53607071	U87	brain:	n/a
16	chr19:53619086-53619136	NB4	blood:	n/a
17	chr19:53605221-53605271	Hela-S3	cervix:	n/a
18	chr19:53606654-53606704	T-47D	breast:	n/a
19	chr19:53605221-53605271	HRPEpiC	eye:	n/a
20	chr19:53606340-53606390	AG04449	skin:	fetal
21	chr19:53602096-53602146	AG09319	gingival:	n/a
22	chr19:53607009-53607059	GM12878	blood:	n/a
23	chr19:53606654-53606704	Hepatocyte	liver:	n/a
24	chr19:53607009-53607059	SK-N-SH_RA	brain:	n/a
25	chr19:53605221-53605271	ProgFib	skin:	n/a
26	chr19:53607021-53607071	HCT-116	colon:	n/a
27	chr19:53606340-53606390	AG09309	skin:	n/a
28	chr19:53607009-53607059	A549	lung:	n/a
29	chr19:53607021-53607071	GM19239	blood:	n/a
30	chr19:53619086-53619136	H1-hESC	embryonic stem cell:	embryo
31	chr19:53606538-53606588	U87	brain:	n/a
32	chr19:53606340-53606390	A549	lung:	n/a
33	chr19:53606654-53606704	ovcar-3	ovarian:	n/a
34	chr19:53606340-53606390	AG04450	lung:	fetal
35	chr19:53606654-53606704	HepG2	liver:	n/a
36	chr19:53607009-53607059	HEEpiC	esophagus:	n/a
37	chr19:53606654-53606704	AG10803	skin:	n/a
38	chr19:53607021-53607071	AG04450	lung:	fetal
39	chr19:53607021-53607071	AG04449	skin:	fetal
40	chr19:53606538-53606588	RPTEC	kidney:	n/a
41	chr19:53619086-53619136	HEK293	kidney:	embryo
42	chr19:53605221-53605271	PANC-1	pancreas:	n/a
43	chr19:53605221-53605271	AG09309	skin:	n/a
44	chr19:53606654-53606704	U87	brain:	n/a
45	chr19:53602096-53602146	NH-A	brain:	n/a
46	chr19:53606538-53606588	AG09309	skin:	n/a
47	chr19:53602096-53602146	Hela-S3	cervix:	n/a
48	chr19:53607009-53607059	AG04450	lung:	fetal
49	chr19:53606340-53606390	NH-A	brain:	n/a
50	chr19:53606654-53606704	PrEC	prostate:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53580105..53582342-chr19:53607361..53608967,2	MCF-7	breast:
2	chr19:53601358..53604101-chr19:53630122..53631842,2	MCF-7	breast:
3	chr19:53618140..53620226-chr19:53631544..53634250,2	MCF-7	breast:
4	chr19:53604512..53608513-chr19:53609307..53612794,4	MCF-7	breast:
5	chr19:53606146..53606673-chr6:34759631..34760361,2	Hela-S3	cervix:
6	chr19:53617497..53619438-chr19:53623367..53626154,3	K562	blood:
7	chr19:53617497..53619438-chr19:53623367..53626154,3	K562	blood:
8	chr19:53603113..53604676-chr19:53605160..53608027,2	MCF-7	breast:
9	chr19:52691998..52694919-chr19:53605403..53608321,3	K562	blood:
10	chr19:53600011..53602788-chr19:53603096..53607332,6	MCF-7	breast:
11	chr19:53605891..53607584-chr19:58896314..58898154,2	MCF-7	breast:
12	chr19:53610363..53612627-chr19:53660815..53663368,2	K562	blood:
13	chr19:53461518..53463448-chr19:53612422..53614320,2	K562	blood:
14	chr19:53445011..53447703-chr19:53608056..53610253,2	MCF-7	breast:
15	chr19:53601090..53603099-chr19:53630653..53632192,2	MCF-7	breast:
16	chr1:161171615..161172146-chr19:53606421..53607387,2	Hela-S3	cervix:
17	chr19:53605668..53607608-chr19:53634404..53636647,2	MCF-7	breast:
18	chr19:53140133..53142689-chr19:53604558..53606639,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF347-2	chr19:53619566-53619686	NONHSAT067635
2	lnc-ZNF347-2	chr19:53618511-53618585	NONHSAT067632
3	lnc-ZNF347-2	chr19:53625657-53625869	NONHSAT067636
4	lnc-ZNF347-2	chr19:53619566-53619686	NONHSAT067632
5	lnc-ZNF347-2	chr19:53618957-53619064	NONHSAT067632
6	lnc-ZNF347-2	chr19:53625657-53625865	NONHSAT067630
7	lnc-ZNF347-2	chr19:53612860-53613161	NONHSAT067630
8	lnc-ZNF347-2	chr19:53619010-53619064	NONHSAT067634
9	lnc-ZNF347-2	chr19:53618987-53619177	NONHSAT067633
10	lnc-ZNF347-2	chr19:53619037-53619177	NONHSAT067635
11	lnc-ZNF415-2	chr19:53606518-53606580	NONHSAT067628
12	lnc-ZNF347-2	chr19:53625915-53625996	NONHSAT067631
13	lnc-ZNF347-2	chr19:53612991-53613161	NONHSAT067631
14	lnc-ZNF347-2	chr19:53625657-53625869	NONHSAT067634
15	lnc-ZNF347-2	chr19:53619566-53619686	NONHSAT067633
16	lnc-ZNF347-2	chr19:53627046-53627159	NONHSAT067632
17	lnc-ZNF415-2	chr19:53606518-53606631	NONHSAT067624
18	lnc-ZNF347-2	chr19:53626754-53626908	NONHSAT067633
19	lnc-ZNF347-2	chr19:53619513-53619686	NONHSAT067636
20	lnc-ZNF347-2	chr19:53619566-53619686	NONHSAT067634
21	lnc-ZNF347-2	chr19:53625915-53625996	NONHSAT067632
22	lnc-ZNF347-2	chr19:53625915-53625996	NONHSAT067633
23	lnc-ZNF347-2	chr19:53625657-53625869	NONHSAT067635
24	lnc-VN1R2-9	chr19:53611890-53613152	NONHSAT067620

No data

Variant related genes	Relation type
ZNF160	TF binding region
ZNF415	TF binding region
ZNF160	CpG island
ZNF415	CpG island
ENSG00000167766	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000170954	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000105568	chromatin interactions
ENSG00000083845	chromatin interactions
ENSG00000213801	chromatin interactions
ENSG00000197937	chromatin interactions
ENSG00000158864	chromatin interactions
ENSG00000170949	chromatin interactions

Extended variants
information (count: 1205 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1205 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10407043	chr19:53601649-53601650	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564757574	chr19:53601704-53601705	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532237061	chr19:53601723-53601724	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs77096174	chr19:53601736-53601737	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537690855	chr19:53601739-53601740	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550493777	chr19:53601740-53601741	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs57142738	chr19:53601757-53601758	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs115954730	chr19:53601773-53601774	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs60317521	chr19:53601774-53601775	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs190540098	chr19:53601781-53601782	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112563812	chr19:53601784-53601785	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533879828	chr19:53601786-53601787	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553577283	chr19:53601787-53601788	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs578227282	chr19:53601790-53601791	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146737570	chr19:53601793-53601794	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2913988	chr19:53601798-53601799	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557398722	chr19:53601799-53601800	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7259791	chr19:53601823-53601824	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575585066	chr19:53601837-53601838	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542613936	chr19:53601886-53601887	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73935236	chr19:53601893-53601894	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs561337266	chr19:53601896-53601897	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181745025	chr19:53601897-53601898	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs386810640	chr19:53601927-53601928	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1650971	chr19:53601928-53601929	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs532201397	chr19:53601949-53601950	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112950227	chr19:53601984-53601985	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550846336	chr19:53601995-53601996	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs562683011	chr19:53602007-53602008	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs74176199	chr19:53602032-53602033	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117964478	chr19:53602040-53602041	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs74176200	chr19:53602041-53602042	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547831194	chr19:53602055-53602056	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs58630062	chr19:53602056-53602057	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566496179	chr19:53602063-53602064	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533837715	chr19:53602065-53602066	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11673565	chr19:53602066-53602067	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552337581	chr19:53602079-53602080	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200457129	chr19:53602083-53602084	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs111994470	chr19:53602096-53602097	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539275324	chr19:53602115-53602116	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557540072	chr19:53602177-53602178	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4803048	chr19:53602202-53602203	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540070470	chr19:53602203-53602204	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372147427	chr19:53602204-53602205	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184492965	chr19:53602213-53602214	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs79471578	chr19:53602242-53602243	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
48	rs370966941	chr19:53602248-53602249	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs58340873	chr19:53602271-53602272	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs60799483	chr19:53602274-53602275	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	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
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD

Chromatin state (count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53573600-53604800	Weak transcription	Hela-S3	cervix
2	chr19:53576800-53605200	Weak transcription	Stomach Mucosa	stomach
3	chr19:53585400-53604800	Weak transcription	Psoas Muscle	Psoas
4	chr19:53586400-53603400	Strong transcription	Primary T cells from cord blood	blood
5	chr19:53588400-53603400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr19:53589200-53604800	Weak transcription	Fetal Brain Male	brain
7	chr19:53589600-53604800	Weak transcription	Small Intestine	intestine
8	chr19:53590400-53605000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr19:53592800-53604800	Weak transcription	HUVEC	blood vessel
10	chr19:53594400-53603400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr19:53594400-53605200	Weak transcription	Fetal Lung	lung
12	chr19:53594600-53604800	Weak transcription	Fetal Kidney	kidney
13	chr19:53594600-53604800	Weak transcription	NHEK	skin
14	chr19:53595200-53602600	Weak transcription	Brain Substantia Nigra	brain
15	chr19:53595200-53603000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr19:53595200-53604000	Weak transcription	Pancreas	Pancrea
17	chr19:53596600-53603200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr19:53597600-53604800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr19:53597800-53604800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:53597800-53604800	Weak transcription	NH-A	brain
21	chr19:53598800-53604800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:53599000-53604800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr19:53599000-53604800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr19:53599000-53604800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:53599000-53604800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:53599000-53604800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr19:53599000-53604800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr19:53599000-53604800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr19:53599000-53604800	Weak transcription	HSMM	muscle
30	chr19:53599000-53605000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr19:53599000-53605400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr19:53599200-53604800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr19:53599200-53604800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr19:53600000-53603200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr19:53600400-53603400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr19:53600600-53601800	Strong transcription	Fetal Brain Female	brain
37	chr19:53600600-53603400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr19:53600600-53603400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
39	chr19:53600600-53603400	Strong transcription	Primary B cells from peripheral blood	blood
40	chr19:53600600-53603400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr19:53600600-53603600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:53600600-53603800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:53600800-53602200	Strong transcription	Placenta Amnion	Placenta Amnion
44	chr19:53600800-53602400	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr19:53600800-53602800	Strong transcription	Brain Germinal Matrix	brain
46	chr19:53600800-53602800	Genic enhancers	Spleen	Spleen
47	chr19:53600800-53603000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:53600800-53603000	Strong transcription	Dnd41	blood
49	chr19:53600800-53603200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr19:53600800-53603200	Strong transcription	Liver	Liver

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