Variant report

Variant	esv3334779
Chromosome Location	chr19:37050161-37076919
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:672)
CpG islands
(count:978)
Chromatin interactive
region (count:41)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:37065043-37065282	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:37063435-37064342	K562	blood:	n/a	n/a
3	ARID3A	chr19:37063849-37064361	HepG2	liver:	n/a	n/a
4	ATF1	chr19:37063723-37064412	K562	blood:	n/a	n/a
5	ATF2	chr19:37063700-37064216	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr19:37063666-37064252	GM12878	blood:	n/a	n/a
7	ATF2	chr19:37063647-37064427	GM12878	blood:	n/a	n/a
8	ATF2	chr19:37063693-37064500	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr19:37055351-37055567	GM12878	blood:	n/a	n/a
10	BATF	chr19:37063960-37064323	GM12878	blood:	n/a	n/a
11	BCL3	chr19:37063605-37064602	A549	lung:	n/a	n/a
12	BCL3	chr19:37063665-37064508	A549	lung:	n/a	n/a
13	BCLAF1	chr19:37063708-37064555	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:37063478-37063481	K562	blood:	n/a	n/a
15	BHLHE40	chr19:37063830-37065151	K562	blood:	n/a	chr19:37064596-37064612
16	BHLHE40	chr19:37063774-37064788	GM12878	blood:	n/a	chr19:37064596-37064612
17	BRCA1	chr19:37063835-37064518	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr19:37063964-37064294	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:37063805-37064300	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr19:37063920-37064234	K562	blood:	n/a	n/a
21	CBX3	chr19:37063812-37064352	K562	blood:	n/a	n/a
22	CCNT2	chr19:37063850-37064472	K562	blood:	n/a	chr19:37063929-37063938
23	CEBPB	chr19:37058610-37058720	A549	lung:	n/a	n/a
24	CEBPB	chr19:37063930-37064262	K562	blood:	n/a	n/a
25	CEBPB	chr19:37065711-37066009	K562	blood:	n/a	n/a
26	CEBPB	chr19:37070196-37070483	Hela-S3	cervix:	n/a	chr19:37070349-37070360
27	CEBPB	chr19:37063836-37064399	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:37057834-37058253	A549	lung:	n/a	n/a
29	CEBPB	chr19:37064072-37064268	K562	blood:	n/a	n/a
30	CEBPB	chr19:37070191-37070500	K562	blood:	n/a	chr19:37070349-37070360
31	CEBPB	chr19:37070193-37070517	A549	lung:	n/a	chr19:37070349-37070360
32	CEBPB	chr19:37063783-37064438	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr19:37064047-37064393	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:37070190-37070511	HepG2	liver:	n/a	chr19:37070349-37070360
35	CEBPB	chr19:37063967-37064147	GM12878	blood:	n/a	n/a
36	CEBPB	chr19:37070191-37070525	IMR90	lung:	n/a	chr19:37070349-37070360
37	CEBPD	chr19:37063957-37064531	HepG2	liver:	n/a	n/a
38	CEBPD	chr19:37063357-37064396	K562	blood:	n/a	n/a
39	CEBPD	chr19:37063379-37064272	K562	blood:	n/a	n/a
40	CHD1	chr19:37063563-37063846	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr19:37063754-37065008	GM12878	blood:	n/a	n/a
42	CHD2	chr19:37063884-37064433	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr19:37063778-37064431	K562	blood:	n/a	n/a
44	CHD2	chr19:37063849-37064522	HepG2	liver:	n/a	n/a
45	CHD2	chr19:37063877-37064450	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr19:37062806-37062833	K562	blood:	n/a	n/a
47	CHD2	chr19:37063914-37064432	GM12878	blood:	n/a	n/a
48	CREB1	chr19:37063608-37064688	HepG2	liver:	n/a	chr19:37063893-37063906
49	CREB1	chr19:37063552-37064501	K562	blood:	n/a	chr19:37063893-37063906
50	CREB1	chr19:37063750-37064387	ECC-1	luminal epithelium:	n/a	chr19:37063893-37063906

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:37067342-37067392	Hela-S3	cervix:	n/a
2	chr19:37064254-37064304	HAEpiC	amniotic membrane:	n/a
3	chr19:37067342-37067392	Hela-S3	cervix:	n/a
4	chr19:37064254-37064304	HAEpiC	amniotic membrane:	n/a
5	chr19:37061383-37061433	HCF	heart:	n/a
6	chr19:37064289-37064339	BE2_C	brain:	n/a
7	chr19:37064289-37064339	HEEpiC	esophagus:	n/a
8	chr19:37063800-37063850	NB4	blood:	n/a
9	chr19:37067342-37067392	PrEC	prostate:	n/a
10	chr19:37064171-37064221	U87	brain:	n/a
11	chr19:37064171-37064221	NH-A	brain:	n/a
12	chr19:37061383-37061433	ProgFib	skin:	n/a
13	chr19:37064171-37064221	SK-N-MC	brain:	n/a
14	chr19:37064719-37064769	IMR90	lung:	fetal
15	chr19:37064289-37064339	AG04449	skin:	fetal
16	chr19:37064572-37064622	AoSMC	blood vessel:	n/a
17	chr19:37064886-37064936	HIPEpiC	eye:	n/a
18	chr19:37064166-37064216	SK-N-SH_RA	brain:	n/a
19	chr19:37063800-37063850	PFSK-1	brain:	n/a
20	chr19:37064303-37064353	RPTEC	kidney:	n/a
21	chr19:37064254-37064304	GM12891	blood:	n/a
22	chr19:37064303-37064353	HRE	kidney:	n/a
23	chr19:37064375-37064425	HRPEpiC	eye:	n/a
24	chr19:37064719-37064769	NB4	blood:	n/a
25	chr19:37064303-37064353	AG04449	skin:	fetal
26	chr19:37064572-37064622	SK-N-SH_RA	brain:	n/a
27	chr19:37064719-37064769	HRPEpiC	eye:	n/a
28	chr19:37064572-37064622	PFSK-1	brain:	n/a
29	chr19:37063800-37063850	NT2-D1	testis:	n/a
30	chr19:37064254-37064304	CMK	blood:	n/a
31	chr19:37063800-37063850	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:37061383-37061433	Caco-2	colon:	n/a
33	chr19:37064219-37064269	ECC-1	luminal epithelium:	n/a
34	chr19:37064375-37064425	HepG2	liver:	n/a
35	chr19:37061383-37061433	K562	blood:	n/a
36	chr19:37064572-37064622	HCF	heart:	n/a
37	chr19:37064380-37064430	HMEC	breast:	n/a
38	chr19:37064748-37064798	NT2-D1	testis:	n/a
39	chr19:37063800-37063850	HL-60	blood:	n/a
40	chr19:37064380-37064430	AG04450	lung:	fetal
41	chr19:37064166-37064216	NT2-D1	testis:	n/a
42	chr19:37064219-37064269	CMK	blood:	n/a
43	chr19:37064171-37064221	HL-60	blood:	n/a
44	chr19:37064156-37064206	NHBE	bronchial:	n/a
45	chr19:37064375-37064425	AG09309	skin:	n/a
46	chr19:37064380-37064430	ovcar-3	ovarian:	n/a
47	chr19:37064719-37064769	MCF-7	breast:	n/a
48	chr19:37064886-37064936	NH-A	brain:	n/a
49	chr19:37067342-37067392	ProgFib	skin:	n/a
50	chr19:37064166-37064216	AG09309	skin:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:37018711..37023188-chr19:37060299..37065354,5	K562	blood:
2	chr19:36979379..36982047-chr19:37063909..37066157,2	K562	blood:
3	chr19:37047289..37050700-chr19:37061573..37063531,3	K562	blood:
4	chr19:36704361..36705921-chr19:37063810..37066277,2	K562	blood:
5	chr19:37063664..37064432-chr3:73159959..73160622,2	Hela-S3	cervix:
6	chr19:37017781..37019790-chr19:37064970..37066905,2	MCF-7	breast:
7	chr19:37062757..37066475-chr19:37067178..37075829,11	K562	blood:
8	chr19:37037541..37041127-chr19:37063019..37065545,3	K562	blood:
9	chr19:37017864..37019585-chr19:37067468..37069306,2	K562	blood:
10	chr1:144533722..144534489-chr19:37063772..37064389,2	Hela-S3	cervix:
11	chr19:37063014..37065659-chr19:37066533..37068326,2	MCF-7	breast:
12	chr19:37038594..37041681-chr19:37063019..37065867,3	K562	blood:
13	chr19:37041320..37043979-chr19:37059170..37061159,2	K562	blood:
14	chr19:37053248..37055445-chr19:37061969..37063522,2	K562	blood:
15	chr19:37018040..37020429-chr19:37065746..37067402,2	K562	blood:
16	chr19:36940091..36943076-chr19:37061156..37065481,3	K562	blood:
17	chr19:36867523..36870095-chr19:37064121..37065626,2	MCF-7	breast:
18	chr19:36703935..36706933-chr19:37068866..37070631,2	K562	blood:
19	chr19:37062757..37067111-chr19:37067178..37071986,8	K562	blood:
20	chr19:37050035..37052914-chr19:37064018..37065875,2	K562	blood:
21	chr15:65596793..65597620-chr19:37071052..37071553,2	MCF-7	breast:
22	chr19:37062757..37067111-chr19:37067178..37071986,8	K562	blood:
23	chr1:153963085..153963674-chr19:37063863..37064467,2	Hela-S3	cervix:
24	chr19:37065150..37067798-chr19:37072514..37074047,2	K562	blood:
25	chr19:37063854..37065418-chr19:37262714..37265586,2	K562	blood:
26	chr19:37017989..37021035-chr19:37064029..37066517,3	MCF-7	breast:
27	chr19:37047289..37050700-chr19:37061573..37063531,3	K562	blood:
28	chr19:37057613..37059554-chr19:37062678..37064206,2	MCF-7	breast:
29	chr19:36979193..36981748-chr19:37061672..37065426,4	K562	blood:
30	chr1:90290948..90293135-chr19:37069121..37070641,2	K562	blood:
31	chr1:249132382..249132990-chr19:37063673..37064639,2	Hela-S3	cervix:
32	chr19:36977340..36979938-chr19:37058785..37061352,2	K562	blood:
33	chr19:37057331..37060985-chr19:37062478..37065341,6	K562	blood:
34	chr19:37053248..37055445-chr19:37061969..37063522,2	K562	blood:
35	chr19:37062686..37064573-chr19:37176993..37178796,2	MCF-7	breast:
36	chr19:37063014..37065659-chr19:37066533..37068326,2	MCF-7	breast:
37	chr19:37050035..37052115-chr19:37063712..37065875,2	K562	blood:
38	chr19:37065150..37067798-chr19:37072514..37074047,2	K562	blood:
39	chr19:37062757..37066475-chr19:37067178..37075829,11	K562	blood:
40	chr19:37019103..37021335-chr19:37062459..37064743,4	K562	blood:
41	chr19:37063335..37065551-chr19:37068652..37070249,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC092295.7.1-3	chr19:37068130-37068185	ENSG00000233527.4
2	lnc-AC092295.7.1-3	chr19:37063972-37064427	ENSG00000233527.4
3	lnc-ZNF529-2	chr19:37073300-37073606	NONHSAT066018
4	lnc-ZNF461-3	chr19:37069369-37069724	l_1675_chr19:37069368-37128185_testes
5	lnc-AC092295.7.1-3	chr19:37068043-37068817	ENSG00000233527.4
6	lnc-AC092295.7.1-3	chr19:37065720-37065802	NONHSAT066015
7	lnc-AC092295.7.1-3	chr19:37064279-37064427	ENSG00000233527.4
8	lnc-AC092295.7.1-3	chr19:37065723-37065802	ENSG00000233527.4
9	lnc-AC092295.7.1-3	chr19:37065723-37065802	ENSG00000233527.4
10	lnc-AC092295.7.1-3	chr19:37064439-37064457	ENSG00000233527.4
11	lnc-ZNF461-3	chr19:37070501-37070672	l_1675_chr19:37069368-37128185_testes
12	lnc-AC092295.7.1-3	chr19:37065723-37065802	ENSG00000233527.4
13	lnc-ZNF529-2	chr19:37071155-37073606	NONHSAT066017

No data

Variant related genes	Relation type
ZNF529	TF binding region
ENSG00000233527	TF binding region
ZNF529	CpG island
ENSG00000233527	CpG island
ENSG00000177954	chromatin interactions
ENSG00000267309	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000228629	chromatin interactions
ENSG00000233527	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000267260	chromatin interactions
ENSG00000225975	chromatin interactions
ENSG00000171161	chromatin interactions
ENSG00000189042	chromatin interactions
ENSG00000186017	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000186020	chromatin interactions
ENSG00000267041	chromatin interactions
ENSG00000266973	chromatin interactions
ENSG00000196357	chromatin interactions
ENSG00000167635	chromatin interactions

Extended variants
information (count: 834 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:834 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569361157	chr19:37050214-37050215	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551078398	chr19:37050221-37050222	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199922985	chr19:37050255-37050256	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115181203	chr19:37050266-37050267	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559790679	chr19:37050269-37050270	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527512770	chr19:37050329-37050330	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571437137	chr19:37050345-37050346	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2967438	chr19:37050469-37050470	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567591332	chr19:37050474-37050475	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554915549	chr19:37050476-37050477	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550001264	chr19:37050477-37050478	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs113210626	chr19:37050488-37050489	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs116722504	chr19:37050497-37050498	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs538987577	chr19:37050521-37050522	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554328201	chr19:37050542-37050543	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2912402	chr19:37050560-37050561	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs536879976	chr19:37050583-37050584	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs147914215	chr19:37050631-37050632	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576717611	chr19:37050638-37050639	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543771841	chr19:37050655-37050656	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117222757	chr19:37050703-37050704	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs561291167	chr19:37050708-37050709	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192231469	chr19:37050720-37050721	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374088429	chr19:37050724-37050725	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3108548	chr19:37050782-37050783	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs559851515	chr19:37050925-37050926	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs544825804	chr19:37050929-37050930	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs139661364	chr19:37050931-37050932	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542461209	chr19:37050937-37050938	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560927912	chr19:37050958-37050959	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs531493927	chr19:37050998-37050999	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549821621	chr19:37051004-37051005	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs145193909	chr19:37051027-37051028	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs532576564	chr19:37051075-37051076	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12462921	chr19:37051081-37051082	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575262730	chr19:37051107-37051108	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs566215998	chr19:37051108-37051109	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs536738895	chr19:37051154-37051155	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs398040985	chr19:37051161-37051162	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs71171455	chr19:37051178-37051179	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs58196878	chr19:37051180-37051181	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs78486436	chr19:37051181-37051182	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113359285	chr19:37051182-37051183	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs77411020	chr19:37051186-37051187	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555009005	chr19:37051239-37051240	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188743525	chr19:37051258-37051259	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558750104	chr19:37051385-37051386	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs147619246	chr19:37051393-37051394	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs559017577	chr19:37051394-37051395	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200109728	chr19:37051488-37051489	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Wilms tumour	21544195	CNVD

Chromatin state (count:1606 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:37021400-37061600	ZNF genes & repeats	Liver	Liver
2	chr19:37022800-37061200	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:37023000-37061800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr19:37023200-37060200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
5	chr19:37023200-37061600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:37023400-37060000	ZNF genes & repeats	Fetal Lung	lung
7	chr19:37023400-37062000	ZNF genes & repeats	Fetal Brain Female	brain
8	chr19:37023400-37063000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr19:37023600-37061000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
10	chr19:37023800-37057800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:37023800-37058200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr19:37023800-37058200	ZNF genes & repeats	Dnd41	blood
13	chr19:37023800-37061600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:37025400-37052400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
15	chr19:37025600-37053000	ZNF genes & repeats	Brain Anterior Caudate	brain
16	chr19:37025600-37061000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
17	chr19:37025600-37062800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr19:37025800-37060200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
19	chr19:37027400-37054400	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr19:37028600-37050800	ZNF genes & repeats	Primary B cells from cord blood	blood
21	chr19:37028600-37055000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr19:37028600-37061800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
23	chr19:37028800-37054400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
24	chr19:37029000-37060000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
25	chr19:37031400-37056800	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
26	chr19:37031400-37057800	ZNF genes & repeats	Primary T cells from cord blood	blood
27	chr19:37033400-37051000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr19:37034000-37054000	ZNF genes & repeats	A549	lung
29	chr19:37034000-37063000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:37034200-37052800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
31	chr19:37034200-37059600	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
32	chr19:37034400-37052600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
33	chr19:37034800-37057200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
34	chr19:37036200-37059400	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:37045600-37054400	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
36	chr19:37047000-37058800	Weak transcription	K562	blood
37	chr19:37047600-37050400	Weak transcription	NH-A	brain
38	chr19:37047600-37050400	Weak transcription	Osteobl	bone
39	chr19:37047800-37050200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:37047800-37050200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:37047800-37050400	Weak transcription	Fetal Thymus	thymus
42	chr19:37048000-37051800	Weak transcription	HSMMtube	muscle
43	chr19:37048400-37050200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:37048400-37050200	Weak transcription	Esophagus	oesophagus
45	chr19:37048400-37050200	Weak transcription	Fetal Stomach	stomach
46	chr19:37048400-37050200	Weak transcription	Lung	lung
47	chr19:37048400-37051600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr19:37048400-37062800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr19:37048600-37050200	Weak transcription	Pancreas	Pancrea
50	chr19:37048600-37050200	Weak transcription	Thymus	Thymus

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