Variant report

Variant	nsv580075
Chromosome Location	chr19:53603590-53626112
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:428)
Chromatin interactive
region (count:16)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 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	chr19:53606828-53607327	GM12878	blood:	n/a	n/a
7	BCLAF1	chr19:53606356-53607144	GM12878	blood:	n/a	chr19:53606663-53606672
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	chr19:53604884-53605062	K562	blood:	n/a	chr19:53604994-53605011
13	CEBPB	chr19:53612975-53613054	K562	blood:	n/a	n/a
14	CEBPD	chr19:53606339-53607235	K562	blood:	n/a	n/a
15	CHD1	chr19:53605155-53607496	IMR90	lung:	n/a	chr19:53606338-53606348
16	CHD1	chr19:53605620-53607121	GM12878	blood:	n/a	chr19:53606338-53606348
17	CHD1	chr19:53606365-53606565	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr19:53606410-53607157	GM12878	blood:	n/a	n/a
19	CHD2	chr19:53606624-53606810	HepG2	liver:	n/a	n/a
20	CHD2	chr19:53606469-53606501	K562	blood:	n/a	n/a
21	CHD2	chr19:53606942-53607168	K562	blood:	n/a	n/a
22	CHD2	chr19:53606419-53607232	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr19:53606569-53606802	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr19:53606581-53606800	A549	lung:	n/a	n/a
25	CREB1	chr19:53606415-53607268	HepG2	liver:	n/a	n/a
26	CREB1	chr19:53606393-53607249	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr19:53606450-53606985	A549	lung:	n/a	n/a
28	CREB1	chr19:53606521-53607254	GM12878	blood:	n/a	n/a
29	CREB1	chr19:53606391-53607205	K562	blood:	n/a	n/a
30	CREB1	chr19:53606433-53607089	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr19:53606571-53607142	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:53606533-53607030	GM12878	blood:	n/a	n/a
33	CTCF	chr19:53614791-53614891	GM20000	blood:	n/a	n/a
34	CTCF	chr19:53606239-53606292	GM12878	blood:	n/a	n/a
35	CTCF	chr19:53606232-53606287	MCF-7	breast:	n/a	n/a
36	CTCF	chr19:53606120-53606270	HRE	kidney:	n/a	chr19:53606223-53606236
37	CTCF	chr19:53606200-53606350	AG04449	skin:	n/a	chr19:53606223-53606236
38	CTCF	chr19:53606411-53606595	K562	blood:	n/a	n/a
39	CTCF	chr19:53616720-53616870	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr19:53606975-53607285	K562	blood:	n/a	n/a
41	CTCF	chr19:53606060-53606210	BJ	skin:	n/a	n/a
42	CTCF	chr19:53623018-53623081	GM10266	blood:	n/a	n/a
43	CTCF	chr19:53606666-53606696	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr19:53606220-53606370	AG09319	gingival:	n/a	chr19:53606223-53606236
45	CTCF	chr19:53606591-53606671	GM19239	blood:	n/a	n/a
46	CTCF	chr19:53606260-53606410	WI-38	lung:	n/a	n/a
47	CTCF	chr19:53606610-53606654	NHEK	skin:	n/a	n/a
48	CTCF	chr19:53606080-53606230	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr19:53606140-53606290	HCPEpiC	choroid plexus:	n/a	chr19:53606223-53606236
50	CTCF	chr19:53606180-53606330	AG04449	skin:	n/a	chr19:53606223-53606236

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53606654-53606704	AG10803	skin:	n/a
2	chr19:53606654-53606704	AG10803	skin:	n/a
3	chr19:53606538-53606588	MCF10A-Er-Src	breast:	n/a
4	chr19:53607021-53607071	U87	brain:	n/a
5	chr19:53606340-53606390	HNPCEpiC	eye:	n/a
6	chr19:53606340-53606390	HRCEpiC	kidney:	n/a
7	chr19:53607021-53607071	ovcar-3	ovarian:	n/a
8	chr19:53607021-53607071	A549	lung:	n/a
9	chr19:53606538-53606588	MCF-7	breast:	n/a
10	chr19:53607009-53607059	Hela-S3	cervix:	n/a
11	chr19:53619086-53619136	HCF	heart:	n/a
12	chr19:53619086-53619136	HRCEpiC	kidney:	n/a
13	chr19:53605221-53605271	A549	lung:	n/a
14	chr19:53606538-53606588	HepG2	liver:	n/a
15	chr19:53606654-53606704	RPTEC	kidney:	n/a
16	chr19:53606538-53606588	HRE	kidney:	n/a
17	chr19:53606654-53606704	A549	lung:	n/a
18	chr19:53607009-53607059	AG09309	skin:	n/a
19	chr19:53606654-53606704	HepG2	liver:	n/a
20	chr19:53606538-53606588	AG04449	skin:	fetal
21	chr19:53606538-53606588	PANC-1	pancreas:	n/a
22	chr19:53607021-53607071	GM12878	blood:	n/a
23	chr19:53607021-53607071	Jurkat	blood:	n/a
24	chr19:53619086-53619136	BE2_C	brain:	n/a
25	chr19:53606538-53606588	AG09309	skin:	n/a
26	chr19:53619086-53619136	HCM	heart:	n/a
27	chr19:53605221-53605271	AG09319	gingival:	n/a
28	chr19:53619086-53619136	GM12891	blood:	n/a
29	chr19:53606654-53606704	IMR90	lung:	fetal
30	chr19:53607009-53607059	T-47D	breast:	n/a
31	chr19:53607021-53607071	HNPCEpiC	eye:	n/a
32	chr19:53606538-53606588	CMK	blood:	n/a
33	chr19:53605221-53605271	RPTEC	kidney:	n/a
34	chr19:53606340-53606390	RPTEC	kidney:	n/a
35	chr19:53619086-53619136	SK-N-SH_RA	brain:	n/a
36	chr19:53606538-53606588	ProgFib	skin:	n/a
37	chr19:53606654-53606704	H1-hESC	embryonic stem cell:	embryo
38	chr19:53605221-53605271	HEEpiC	esophagus:	n/a
39	chr19:53606340-53606390	HEK293	kidney:	embryo
40	chr19:53619086-53619136	SK-N-MC	brain:	n/a
41	chr19:53607009-53607059	PrEC	prostate:	n/a
42	chr19:53606538-53606588	RPTEC	kidney:	n/a
43	chr19:53607021-53607071	Caco-2	colon:	n/a
44	chr19:53605221-53605271	SK-N-SH_RA	brain:	n/a
45	chr19:53606340-53606390	AG04449	skin:	fetal
46	chr19:53606538-53606588	HPAEpiC	pulmonary alveolar:	n/a
47	chr19:53607009-53607059	HCPEpiC	choroid plexus:	n/a
48	chr19:53607009-53607059	SK-N-SH_RA	brain:	n/a
49	chr19:53607021-53607071	HAEpiC	amniotic membrane:	n/a
50	chr19:53606538-53606588	AG10803	skin:	n/a

(count:16 , 50 per page) page: 1

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

(count:22 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1010 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12979992	chr19:53603590-53603591	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146711384	chr19:53603601-53603602	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576013154	chr19:53603616-53603617	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374283177	chr19:53603624-53603625	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539479335	chr19:53603631-53603632	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35433418	chr19:53603634-53603635	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs370389282	chr19:53603635-53603636	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34716452	chr19:53603638-53603639	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543146425	chr19:53603643-53603644	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561859918	chr19:53603659-53603660	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528987196	chr19:53603718-53603719	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187396369	chr19:53603720-53603721	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190397351	chr19:53603731-53603732	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373364714	chr19:53603732-53603733	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs28368410	chr19:53603787-53603788	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs386810641	chr19:53603809-53603810	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570735492	chr19:53603851-53603852	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372566016	chr19:53603858-53603859	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs555414095	chr19:53603864-53603865	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142658429	chr19:53603874-53603875	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568494367	chr19:53603891-53603892	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113144791	chr19:53603901-53603902	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs16984442	chr19:53603912-53603913	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs16984443	chr19:53603917-53603918	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572304985	chr19:53603929-53603930	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542369689	chr19:53603944-53603945	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs16984444	chr19:53603952-53603953	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs558077653	chr19:53603958-53603959	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575935939	chr19:53603971-53603972	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112243698	chr19:53603985-53603986	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs28662846	chr19:53603987-53603988	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573653886	chr19:53603990-53603991	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540744486	chr19:53604014-53604015	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs28726276	chr19:53604030-53604031	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs28701520	chr19:53604034-53604035	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs113975084	chr19:53604053-53604054	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544469160	chr19:53604107-53604108	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs28528321	chr19:53604159-53604160	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564840516	chr19:53604180-53604181	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531564082	chr19:53604195-53604196	Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550027882	chr19:53604233-53604234	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144340073	chr19:53604241-53604242	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531922062	chr19:53604360-53604361	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192508062	chr19:53604365-53604366	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7253566	chr19:53604405-53604406	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs529085644	chr19:53604415-53604416	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568376706	chr19:53604424-53604425	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535937074	chr19:53604455-53604456	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182571780	chr19:53604489-53604490	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565874750	chr19:53604515-53604516	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	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:1233 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr19:53589200-53604800	Weak transcription	Fetal Brain Male	brain
5	chr19:53589600-53604800	Weak transcription	Small Intestine	intestine
6	chr19:53590400-53605000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr19:53592800-53604800	Weak transcription	HUVEC	blood vessel
8	chr19:53594400-53605200	Weak transcription	Fetal Lung	lung
9	chr19:53594600-53604800	Weak transcription	Fetal Kidney	kidney
10	chr19:53594600-53604800	Weak transcription	NHEK	skin
11	chr19:53595200-53604000	Weak transcription	Pancreas	Pancrea
12	chr19:53597600-53604800	Weak transcription	Primary hematopoietic stem cells	blood
13	chr19:53597800-53604800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:53597800-53604800	Weak transcription	NH-A	brain
15	chr19:53598800-53604800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr19:53599000-53604800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr19:53599000-53604800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr19:53599000-53604800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:53599000-53604800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr19:53599000-53604800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr19:53599000-53604800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr19:53599000-53604800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr19:53599000-53604800	Weak transcription	HSMM	muscle
24	chr19:53599000-53605000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr19:53599000-53605400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr19:53599200-53604800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr19:53599200-53604800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr19:53600600-53603600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:53600600-53603800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr19:53600800-53603600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr19:53600800-53603600	ZNF genes & repeats	A549	lung
32	chr19:53600800-53604600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr19:53600800-53605600	ZNF genes & repeats	GM12878-XiMat	blood
34	chr19:53601000-53604200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr19:53601000-53604200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:53601000-53604400	Strong transcription	Fetal Stomach	stomach
37	chr19:53601400-53604800	Weak transcription	Brain Hippocampus Middle	brain
38	chr19:53601400-53604800	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr19:53601400-53604800	Weak transcription	Rectal Smooth Muscle	rectum
40	chr19:53601400-53604800	Weak transcription	HMEC	breast
41	chr19:53601400-53605000	Weak transcription	Colon Smooth Muscle	Colon
42	chr19:53601600-53603600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr19:53601600-53604200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr19:53601600-53604800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr19:53601600-53604800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr19:53601600-53604800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr19:53601600-53604800	Weak transcription	Brain Angular Gyrus	brain
48	chr19:53601600-53604800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr19:53601600-53604800	Weak transcription	Fetal Heart	heart
50	chr19:53601600-53604800	Weak transcription	Fetal Thymus	thymus

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