Variant report

Variant	esv3346626
Chromosome Location	chr19:53602317-53629991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:578)
CpG islands
(count:428)
Chromatin interactive
region (count:18)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:578 , 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	chr19:53606550-53607222	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	chr19:53612975-53613054	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	chr19:53606365-53606565	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr19:53605620-53607121	GM12878	blood:	n/a	chr19:53606338-53606348
17	CHD1	chr19:53605155-53607496	IMR90	lung:	n/a	chr19:53606338-53606348
18	CHD2	chr19:53606469-53606501	K562	blood:	n/a	n/a
19	CHD2	chr19:53606624-53606810	HepG2	liver:	n/a	n/a
20	CHD2	chr19:53606942-53607168	K562	blood:	n/a	n/a
21	CHD2	chr19:53606410-53607157	GM12878	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	chr19:53606433-53607089	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr19:53606450-53606985	A549	lung:	n/a	n/a
27	CREB1	chr19:53606391-53607205	K562	blood:	n/a	n/a
28	CREB1	chr19:53606393-53607249	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr19:53606415-53607268	HepG2	liver:	n/a	n/a
30	CREB1	chr19:53606521-53607254	GM12878	blood:	n/a	n/a
31	CTBP2	chr19:53606571-53607142	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr19:53606975-53607285	K562	blood:	n/a	n/a
33	CTCF	chr19:53606533-53607030	GM12878	blood:	n/a	n/a
34	CTCF	chr19:53606232-53606287	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:53616720-53616870	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr19:53623018-53623081	GM10266	blood:	n/a	n/a
37	CTCF	chr19:53606591-53606671	GM19239	blood:	n/a	n/a
38	CTCF	chr19:53606220-53606370	AG09319	gingival:	n/a	chr19:53606223-53606236
39	CTCF	chr19:53606120-53606270	HRE	kidney:	n/a	chr19:53606223-53606236
40	CTCF	chr19:53606140-53606290	HCPEpiC	choroid plexus:	n/a	chr19:53606223-53606236
41	CTCF	chr19:53606080-53606230	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr19:53606610-53606654	NHEK	skin:	n/a	n/a
43	CTCF	chr19:53629497-53629571	GM10266	blood:	n/a	n/a
44	CTCF	chr19:53606239-53606292	GM12878	blood:	n/a	n/a
45	CTCF	chr19:53606200-53606350	AG04449	skin:	n/a	chr19:53606223-53606236
46	CTCF	chr19:53606260-53606410	WI-38	lung:	n/a	n/a
47	CTCF	chr19:53606411-53606595	K562	blood:	n/a	n/a
48	CTCF	chr19:53614791-53614891	GM20000	blood:	n/a	n/a
49	CTCF	chr19:53606666-53606696	Spleen_OC	spleen:	n/a	n/a
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	chr19:53619086-53619136	HIPEpiC	eye:	n/a
2	chr19:53619086-53619136	HIPEpiC	eye:	n/a
3	chr19:53606538-53606588	PFSK-1	brain:	n/a
4	chr19:53619086-53619136	Hepatocyte	liver:	n/a
5	chr19:53605221-53605271	RPTEC	kidney:	n/a
6	chr19:53605221-53605271	NT2-D1	testis:	n/a
7	chr19:53619086-53619136	T-47D	breast:	n/a
8	chr19:53606654-53606704	ProgFib	skin:	n/a
9	chr19:53605221-53605271	HMEC	breast:	n/a
10	chr19:53607021-53607071	AG10803	skin:	n/a
11	chr19:53606654-53606704	HRCEpiC	kidney:	n/a
12	chr19:53607021-53607071	HepG2	liver:	n/a
13	chr19:53605221-53605271	AG10803	skin:	n/a
14	chr19:53606340-53606390	ECC-1	luminal epithelium:	n/a
15	chr19:53605221-53605271	PFSK-1	brain:	n/a
16	chr19:53619086-53619136	AG09309	skin:	n/a
17	chr19:53619086-53619136	GM12891	blood:	n/a
18	chr19:53605221-53605271	AG04449	skin:	fetal
19	chr19:53606538-53606588	HRCEpiC	kidney:	n/a
20	chr19:53606538-53606588	ovcar-3	ovarian:	n/a
21	chr19:53607021-53607071	MCF10A-Er-Src	breast:	n/a
22	chr19:53605221-53605271	GM12878	blood:	n/a
23	chr19:53607009-53607059	BE2_C	brain:	n/a
24	chr19:53606538-53606588	HCF	heart:	n/a
25	chr19:53606654-53606704	AG04449	skin:	fetal
26	chr19:53607021-53607071	HRE	kidney:	n/a
27	chr19:53619086-53619136	HCM	heart:	n/a
28	chr19:53607021-53607071	HIPEpiC	eye:	n/a
29	chr19:53607021-53607071	HEEpiC	esophagus:	n/a
30	chr19:53619086-53619136	Jurkat	blood:	n/a
31	chr19:53619086-53619136	AG09319	gingival:	n/a
32	chr19:53606340-53606390	LNCaP	prostate:	n/a
33	chr19:53606538-53606588	ECC-1	luminal epithelium:	n/a
34	chr19:53607021-53607071	AoSMC	blood vessel:	n/a
35	chr19:53619086-53619136	U87	brain:	n/a
36	chr19:53605221-53605271	IMR90	lung:	fetal
37	chr19:53606538-53606588	Jurkat	blood:	n/a
38	chr19:53607009-53607059	PFSK-1	brain:	n/a
39	chr19:53606538-53606588	SAEC	small airway:	n/a
40	chr19:53619086-53619136	HRCEpiC	kidney:	n/a
41	chr19:53619086-53619136	LNCaP	prostate:	n/a
42	chr19:53619086-53619136	HRPEpiC	eye:	n/a
43	chr19:53606340-53606390	HCM	heart:	n/a
44	chr19:53606654-53606704	HEEpiC	esophagus:	n/a
45	chr19:53619086-53619136	Hela-S3	cervix:	n/a
46	chr19:53606654-53606704	MCF-7	breast:	n/a
47	chr19:53606340-53606390	HMEC	breast:	n/a
48	chr19:53607021-53607071	AG04449	skin:	fetal
49	chr19:53607021-53607071	HAEpiC	amniotic membrane:	n/a
50	chr19:53606340-53606390	ovcar-3	ovarian:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 1251 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1251 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs59972357	chr19:53602332-53602333	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574945767	chr19:53602343-53602344	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs57738540	chr19:53602353-53602354	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375294538	chr19:53602355-53602356	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56717860	chr19:53602356-53602357	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78442099	chr19:53602375-53602376	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs55769491	chr19:53602376-53602377	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529921290	chr19:53602383-53602384	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141976628	chr19:53602391-53602392	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367577416	chr19:53602398-53602399	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34566826	chr19:53602422-53602423	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11673697	chr19:53602426-53602427	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs74694112	chr19:53602430-53602431	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527314553	chr19:53602431-53602432	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs11673700	chr19:53602434-53602435	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552299108	chr19:53602437-53602438	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs11673644	chr19:53602441-53602442	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11673619	chr19:53602446-53602447	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139677319	chr19:53602491-53602492	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs531437137	chr19:53602543-53602544	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141933790	chr19:53602548-53602549	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542130209	chr19:53602558-53602559	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146311846	chr19:53602576-53602577	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs569449182	chr19:53602588-53602589	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs8113824	chr19:53602657-53602658	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35992545	chr19:53602659-53602660	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555268893	chr19:53602661-53602662	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190918472	chr19:53602664-53602665	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111552956	chr19:53602671-53602672	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112369425	chr19:53602676-53602677	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34624082	chr19:53602688-53602689	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113654281	chr19:53602692-53602693	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558540318	chr19:53602712-53602713	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs8100134	chr19:53602714-53602715	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs544717717	chr19:53602752-53602753	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs8099848	chr19:53602767-53602768	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34023062	chr19:53602770-53602771	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574610086	chr19:53602826-53602827	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs541738113	chr19:53602836-53602837	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs531672795	chr19:53602846-53602847	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs560477461	chr19:53602851-53602852	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs527591754	chr19:53602890-53602891	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs8102799	chr19:53602953-53602954	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs564092750	chr19:53602955-53602956	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs545989778	chr19:53602960-53602961	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs372276146	chr19:53603016-53603017	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs549879504	chr19:53603032-53603033	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs73935238	chr19:53603036-53603037	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568177409	chr19:53603089-53603090	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs530363790	chr19:53603131-53603132	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	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:1349 , 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	chr19:53600600-53603400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr19:53600600-53603400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
38	chr19:53600600-53603400	Strong transcription	Primary B cells from peripheral blood	blood
39	chr19:53600600-53603400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr19:53600600-53603600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr19:53600600-53603800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr19:53600800-53602400	Strong transcription	Skeletal Muscle Female	skeletal muscle
43	chr19:53600800-53602800	Strong transcription	Brain Germinal Matrix	brain
44	chr19:53600800-53602800	Genic enhancers	Spleen	Spleen
45	chr19:53600800-53603000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:53600800-53603000	Strong transcription	Dnd41	blood
47	chr19:53600800-53603200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:53600800-53603200	Strong transcription	Liver	Liver
49	chr19:53600800-53603200	Strong transcription	Colonic Mucosa	Colon
50	chr19:53600800-53603200	Strong transcription	Fetal Muscle Leg	muscle

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