Variant report

Variant	nsv580069
Chromosome Location	chr19:53599618-53626513
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:489)
Chromatin interactive
region (count:21)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr19:53606550-53607222	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:53607015-53607178	K562	blood:	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	chr19:53604884-53605062	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	chr19:53606365-53606565	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr19:53605155-53607496	IMR90	lung:	n/a	chr19:53606338-53606348
17	CHD1	chr19:53605620-53607121	GM12878	blood:	n/a	chr19:53606338-53606348
18	CHD2	chr19:53606569-53606802	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr19:53606410-53607157	GM12878	blood:	n/a	n/a
20	CHD2	chr19:53606469-53606501	K562	blood:	n/a	n/a
21	CHD2	chr19:53606419-53607232	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr19:53606624-53606810	HepG2	liver:	n/a	n/a
23	CHD2	chr19:53606942-53607168	K562	blood:	n/a	n/a
24	CREB1	chr19:53606450-53606985	A549	lung:	n/a	n/a
25	CREB1	chr19:53606391-53607205	K562	blood:	n/a	n/a
26	CREB1	chr19:53606433-53607089	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr19:53606393-53607249	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr19:53606521-53607254	GM12878	blood:	n/a	n/a
29	CREB1	chr19:53606415-53607268	HepG2	liver:	n/a	n/a
30	CREB1	chr19:53606581-53606800	A549	lung:	n/a	n/a
31	CTBP2	chr19:53606571-53607142	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:53606260-53606410	WI-38	lung:	n/a	n/a
33	CTCF	chr19:53606200-53606350	AG04449	skin:	n/a	chr19:53606223-53606236
34	CTCF	chr19:53623018-53623081	GM10266	blood:	n/a	n/a
35	CTCF	chr19:53616720-53616870	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr19:53606610-53606654	NHEK	skin:	n/a	n/a
37	CTCF	chr19:53606533-53607030	GM12878	blood:	n/a	n/a
38	CTCF	chr19:53606140-53606290	HCPEpiC	choroid plexus:	n/a	chr19:53606223-53606236
39	CTCF	chr19:53611781-53611861	GM13976	blood:	n/a	n/a
40	CTCF	chr19:53606591-53606671	GM19239	blood:	n/a	n/a
41	CTCF	chr19:53606666-53606696	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr19:53606411-53606595	K562	blood:	n/a	n/a
43	CTCF	chr19:53614791-53614891	GM20000	blood:	n/a	n/a
44	CTCF	chr19:53606220-53606370	AG09319	gingival:	n/a	chr19:53606223-53606236
45	CTCF	chr19:53606060-53606210	BJ	skin:	n/a	n/a
46	CTCF	chr19:53606239-53606292	GM12878	blood:	n/a	n/a
47	CTCF	chr19:53606180-53606330	AG04449	skin:	n/a	chr19:53606223-53606236
48	CTCF	chr19:53606975-53607285	K562	blood:	n/a	n/a
49	CTCF	chr19:53606232-53606287	MCF-7	breast:	n/a	n/a
50	CTCF	chr19:53606120-53606270	HRE	kidney:	n/a	chr19:53606223-53606236

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53607021-53607071	HCM	heart:	n/a
2	chr19:53607021-53607071	HCM	heart:	n/a
3	chr19:53606538-53606588	NHDF-neo	bronchial:	n/a
4	chr19:53605221-53605271	HMEC	breast:	n/a
5	chr19:53606538-53606588	GM12878	blood:	n/a
6	chr19:53605221-53605271	HEEpiC	esophagus:	n/a
7	chr19:53607021-53607071	PrEC	prostate:	n/a
8	chr19:53619086-53619136	HCT-116	colon:	n/a
9	chr19:53607009-53607059	HCM	heart:	n/a
10	chr19:53602096-53602146	HCPEpiC	choroid plexus:	n/a
11	chr19:53602096-53602146	T-47D	breast:	n/a
12	chr19:53605221-53605271	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:53606538-53606588	AG10803	skin:	n/a
14	chr19:53606538-53606588	GM19239	blood:	n/a
15	chr19:53606340-53606390	HUVEC	blood vessel:	n/a
16	chr19:53607009-53607059	AoSMC	blood vessel:	n/a
17	chr19:53602096-53602146	MCF-7	breast:	n/a
18	chr19:53606340-53606390	HCPEpiC	choroid plexus:	n/a
19	chr19:53619086-53619136	HAEpiC	amniotic membrane:	n/a
20	chr19:53619086-53619136	T-47D	breast:	n/a
21	chr19:53606340-53606390	AG09319	gingival:	n/a
22	chr19:53606654-53606704	PANC-1	pancreas:	n/a
23	chr19:53607009-53607059	Caco-2	colon:	n/a
24	chr19:53606538-53606588	HNPCEpiC	eye:	n/a
25	chr19:53606538-53606588	Hepatocyte	liver:	n/a
26	chr19:53606538-53606588	T-47D	breast:	n/a
27	chr19:53605221-53605271	PrEC	prostate:	n/a
28	chr19:53619086-53619136	MCF10A-Er-Src	breast:	n/a
29	chr19:53606538-53606588	RPTEC	kidney:	n/a
30	chr19:53606340-53606390	NB4	blood:	n/a
31	chr19:53606538-53606588	SAEC	small airway:	n/a
32	chr19:53602096-53602146	MCF10A-Er-Src	breast:	n/a
33	chr19:53602096-53602146	NHBE	bronchial:	n/a
34	chr19:53607021-53607071	Hela-S3	cervix:	n/a
35	chr19:53606654-53606704	NB4	blood:	n/a
36	chr19:53605221-53605271	NH-A	brain:	n/a
37	chr19:53606654-53606704	HCT-116	colon:	n/a
38	chr19:53619086-53619136	SAEC	small airway:	n/a
39	chr19:53606654-53606704	AG09309	skin:	n/a
40	chr19:53606340-53606390	AG09309	skin:	n/a
41	chr19:53607021-53607071	HepG2	liver:	n/a
42	chr19:53607021-53607071	GM19239	blood:	n/a
43	chr19:53606654-53606704	GM12891	blood:	n/a
44	chr19:53607009-53607059	A549	lung:	n/a
45	chr19:53607021-53607071	AoSMC	blood vessel:	n/a
46	chr19:53606538-53606588	HepG2	liver:	n/a
47	chr19:53606654-53606704	AG04450	lung:	fetal
48	chr19:53606538-53606588	HMEC	breast:	n/a
49	chr19:53607009-53607059	Hela-S3	cervix:	n/a
50	chr19:53607021-53607071	GM12892	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53140133..53142689-chr19:53604558..53606639,2	MCF-7	breast:
2	chr19:53603113..53604676-chr19:53605160..53608027,2	MCF-7	breast:
3	chr19:53586275..53589046-chr19:53598456..53600578,2	K562	blood:
4	chr19:53618140..53620226-chr19:53631544..53634250,2	MCF-7	breast:
5	chr19:53605668..53607608-chr19:53634404..53636647,2	MCF-7	breast:
6	chr19:53445011..53447703-chr19:53608056..53610253,2	MCF-7	breast:
7	chr19:53598253..53601018-chr19:53604672..53606722,3	MCF-7	breast:
8	chr19:53601358..53604101-chr19:53630122..53631842,2	MCF-7	breast:
9	chr19:53580105..53582342-chr19:53607361..53608967,2	MCF-7	breast:
10	chr19:53604512..53608513-chr19:53609307..53612794,4	MCF-7	breast:
11	chr19:53596128..53598162-chr19:53599456..53601173,2	MCF-7	breast:
12	chr19:53610363..53612627-chr19:53660815..53663368,2	K562	blood:
13	chr1:161171615..161172146-chr19:53606421..53607387,2	Hela-S3	cervix:
14	chr19:53605891..53607584-chr19:58896314..58898154,2	MCF-7	breast:
15	chr19:53601090..53603099-chr19:53630653..53632192,2	MCF-7	breast:
16	chr19:53617497..53619438-chr19:53623367..53626154,3	K562	blood:
17	chr19:53606146..53606673-chr6:34759631..34760361,2	Hela-S3	cervix:
18	chr19:52691998..52694919-chr19:53605403..53608321,3	K562	blood:
19	chr19:53617497..53619438-chr19:53623367..53626154,3	K562	blood:
20	chr19:53461518..53463448-chr19:53612422..53614320,2	K562	blood:
21	chr19:53600011..53602788-chr19:53603096..53607332,6	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1238 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1238 , 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	rs4411612	chr19:53599618-53599619	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550202458	chr19:53599643-53599644	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562444447	chr19:53599681-53599682	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191729633	chr19:53599682-53599683	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540857180	chr19:53599683-53599684	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566097752	chr19:53599710-53599711	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367594621	chr19:53599727-53599728	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34973263	chr19:53599731-53599732	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs539905533	chr19:53599738-53599739	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551941717	chr19:53599747-53599748	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs62115438	chr19:53599748-53599749	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200917502	chr19:53599770-53599771	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569847303	chr19:53599785-53599786	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201841985	chr19:53599806-53599807	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200163523	chr19:53599831-53599832	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537299847	chr19:53599858-53599859	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12981958	chr19:53599877-53599878	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs573839796	chr19:53599882-53599883	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534617873	chr19:53599883-53599884	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11669168	chr19:53599902-53599903	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs34434320	chr19:53599973-53599974	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs59038863	chr19:53599974-53599975	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs56823013	chr19:53599998-53599999	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs59592867	chr19:53600003-53600004	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs544681934	chr19:53600006-53600007	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375081222	chr19:53600008-53600009	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs59972442	chr19:53600015-53600016	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12983079	chr19:53600035-53600036	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34125120	chr19:53600038-53600039	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs2013185	chr19:53600039-53600040	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35536190	chr19:53600074-53600075	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576549601	chr19:53600088-53600089	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2013241	chr19:53600191-53600192	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369306058	chr19:53600224-53600225	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543955173	chr19:53600332-53600333	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs329721	chr19:53600422-53600423	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529561497	chr19:53600436-53600437	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1867050	chr19:53600478-53600479	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs3826699	chr19:53600482-53600483	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533396033	chr19:53600486-53600487	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369062098	chr19:53600489-53600490	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs570206755	chr19:53600528-53600529	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530918833	chr19:53600538-53600539	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1867051	chr19:53600586-53600587	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs147169476	chr19:53600596-53600597	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537602798	chr19:53600617-53600618	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34142384	chr19:53600639-53600640	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1867053	chr19:53600640-53600641	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
49	rs147517854	chr19:53600645-53600646	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148373758	chr19:53600651-53600652	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS	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
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	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

Chromatin state (count:1476 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53573600-53604800	Weak transcription	Hela-S3	cervix
2	chr19:53575600-53601000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr19:53576800-53605200	Weak transcription	Stomach Mucosa	stomach
4	chr19:53584600-53599800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr19:53585400-53604800	Weak transcription	Psoas Muscle	Psoas
6	chr19:53586400-53599800	Strong transcription	Duodenum Mucosa	Duodenum
7	chr19:53586400-53603400	Strong transcription	Primary T cells from cord blood	blood
8	chr19:53586600-53600000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr19:53588200-53601200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr19:53588400-53603400	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr19:53588600-53599800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:53589200-53604800	Weak transcription	Fetal Brain Male	brain
13	chr19:53589600-53604800	Weak transcription	Small Intestine	intestine
14	chr19:53590400-53605000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr19:53592800-53604800	Weak transcription	HUVEC	blood vessel
16	chr19:53594400-53600600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr19:53594400-53601000	Weak transcription	Primary B cells from cord blood	blood
18	chr19:53594400-53603400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr19:53594400-53605200	Weak transcription	Fetal Lung	lung
20	chr19:53594600-53600800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr19:53594600-53604800	Weak transcription	Fetal Kidney	kidney
22	chr19:53594600-53604800	Weak transcription	NHEK	skin
23	chr19:53595000-53600000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr19:53595000-53600800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:53595000-53600800	Weak transcription	Colon Smooth Muscle	Colon
26	chr19:53595000-53600800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr19:53595000-53601000	Weak transcription	Aorta	Aorta
28	chr19:53595000-53601000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr19:53595000-53601000	Weak transcription	HMEC	breast
30	chr19:53595200-53600600	Weak transcription	Adipose Nuclei	Adipose
31	chr19:53595200-53600800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr19:53595200-53600800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr19:53595200-53600800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr19:53595200-53600800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr19:53595200-53600800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr19:53595200-53600800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr19:53595200-53600800	Weak transcription	NHDF-Ad	bronchial
38	chr19:53595200-53601000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr19:53595200-53601000	Weak transcription	Gastric	stomach
40	chr19:53595200-53601000	Weak transcription	NHLF	lung
41	chr19:53595200-53601000	Weak transcription	Osteobl	bone
42	chr19:53595200-53601200	Weak transcription	Brain Angular Gyrus	brain
43	chr19:53595200-53601200	Weak transcription	Esophagus	oesophagus
44	chr19:53595200-53602600	Weak transcription	Brain Substantia Nigra	brain
45	chr19:53595200-53603000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr19:53595200-53604000	Weak transcription	Pancreas	Pancrea
47	chr19:53595600-53600800	Weak transcription	Colonic Mucosa	Colon
48	chr19:53596000-53600800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr19:53596600-53603200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr19:53597000-53600600	Weak transcription	Primary B cells from peripheral blood	blood

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Variant report

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