Variant report

Variant	nsv1066277
Chromosome Location	chr19:53261575-53364138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1343)
CpG islands
(count:1958)
Chromatin interactive
region (count:21)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:53289778-53290273	K562	blood:	n/a	n/a
2	ATF2	chr19:53281984-53282357	GM12878	blood:	n/a	n/a
3	BACH1	chr19:53360719-53361014	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:53324738-53324945	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:53289805-53290074	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr19:53281917-53282463	GM12878	blood:	n/a	chr19:53282197-53282207 chr19:53282192-53282203 chr19:53282193-53282203
7	BATF	chr19:53281931-53282380	GM12878	blood:	n/a	chr19:53282197-53282207 chr19:53282192-53282203 chr19:53282193-53282203
8	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
9	BATF	chr19:53294643-53295039	GM12878	blood:	n/a	chr19:53294862-53294873 chr19:53294863-53294873 chr19:53294867-53294877
10	BATF	chr19:53294543-53294932	GM12878	blood:	n/a	chr19:53294862-53294873 chr19:53294863-53294873 chr19:53294867-53294877
11	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
12	BCL11A	chr19:53282060-53282342	GM12878	blood:	n/a	chr19:53282195-53282204
13	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
14	BCL11A	chr19:53282016-53282371	GM12878	blood:	n/a	chr19:53282195-53282204
15	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
16	BCLAF1	chr19:53289804-53290138	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:53289858-53290162	K562	blood:	n/a	chr19:53290133-53290149
18	BHLHE40	chr19:53324867-53324898	K562	blood:	n/a	n/a
19	BHLHE40	chr19:53289647-53290152	GM12878	blood:	n/a	chr19:53290133-53290149
20	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
21	BHLHE40	chr19:53282085-53282438	GM12878	blood:	n/a	n/a
22	CBX3	chr19:53324640-53325255	K562	blood:	n/a	n/a
23	CBX3	chr19:53303081-53303524	K562	blood:	n/a	n/a
24	CBX3	chr19:53269115-53269526	K562	blood:	n/a	n/a
25	CBX3	chr19:53303091-53303540	K562	blood:	n/a	n/a
26	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
27	CBX3	chr19:53269789-53270224	K562	blood:	n/a	n/a
28	CBX3	chr19:53289830-53290471	K562	blood:	n/a	n/a
29	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
30	CCNT2	chr19:53289971-53290185	K562	blood:	n/a	n/a
31	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
32	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
33	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
34	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
35	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
36	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
37	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
39	CEBPB	chr19:53273806-53273907	A549	lung:	n/a	n/a
40	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr19:53300965-53301050	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
43	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:53274681-53274816	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:53319087-53319167	HepG2	liver:	n/a	chr19:53319119-53319130
46	CEBPD	chr19:53289841-53290077	HepG2	liver:	n/a	n/a
47	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
48	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
49	CHD1	chr19:53289738-53290083	GM12878	blood:	n/a	n/a
50	CHD2	chr19:53289809-53290170	GM12878	blood:	n/a	n/a

(count:1958 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53324198-53324248	HCM	heart:	n/a
2	chr19:53290445-53290495	AoSMC	blood vessel:	n/a
3	chr19:53290126-53290176	AoSMC	blood vessel:	n/a
4	chr19:53302456-53302506	BE2_C	brain:	n/a
5	chr19:53357134-53357184	SK-N-SH_RA	brain:	n/a
6	chr19:53290126-53290176	HRPEpiC	eye:	n/a
7	chr19:53324198-53324248	HCM	heart:	n/a
8	chr19:53290445-53290495	AoSMC	blood vessel:	n/a
9	chr19:53290126-53290176	AoSMC	blood vessel:	n/a
10	chr19:53302456-53302506	BE2_C	brain:	n/a
11	chr19:53357134-53357184	SK-N-SH_RA	brain:	n/a
12	chr19:53290126-53290176	HRPEpiC	eye:	n/a
13	chr19:53290205-53290255	HCF	heart:	n/a
14	chr19:53290205-53290255	SKMC	muscle:	n/a
15	chr19:53325913-53325963	AG09309	skin:	n/a
16	chr19:53344366-53344416	HIPEpiC	eye:	n/a
17	chr19:53290445-53290495	ovcar-3	ovarian:	n/a
18	chr19:53325913-53325963	PFSK-1	brain:	n/a
19	chr19:53325913-53325963	AoSMC	blood vessel:	n/a
20	chr19:53324278-53324328	Hepatocyte	liver:	n/a
21	chr19:53361448-53361498	GM12891	blood:	n/a
22	chr19:53325104-53325154	HAEpiC	amniotic membrane:	n/a
23	chr19:53324732-53324782	SAEC	small airway:	n/a
24	chr19:53324198-53324248	AG09319	gingival:	n/a
25	chr19:53360728-53360778	GM12892	blood:	n/a
26	chr19:53344366-53344416	K562	blood:	n/a
27	chr19:53359733-53359783	SK-N-SH_RA	brain:	n/a
28	chr19:53293012-53293062	GM12892	blood:	n/a
29	chr19:53360728-53360778	HNPCEpiC	eye:	n/a
30	chr19:53324732-53324782	A549	lung:	n/a
31	chr19:53325913-53325963	AG09319	gingival:	n/a
32	chr19:53290102-53290152	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:53363482-53363532	Caco-2	colon:	n/a
34	chr19:53357134-53357184	HCM	heart:	n/a
35	chr19:53325913-53325963	Caco-2	colon:	n/a
36	chr19:53360728-53360778	AoSMC	blood vessel:	n/a
37	chr19:53289933-53289983	SAEC	small airway:	n/a
38	chr19:53290147-53290197	HCT-116	colon:	n/a
39	chr19:53290102-53290152	AG10803	skin:	n/a
40	chr19:53357134-53357184	AG04449	skin:	fetal
41	chr19:53290445-53290495	HL-60	blood:	n/a
42	chr19:53360213-53360263	HRPEpiC	eye:	n/a
43	chr19:53360213-53360263	SAEC	small airway:	n/a
44	chr19:53290126-53290176	NHBE	bronchial:	n/a
45	chr19:53290079-53290129	SK-N-SH_RA	brain:	n/a
46	chr19:53290147-53290197	HUVEC	blood vessel:	n/a
47	chr19:53363482-53363532	GM12891	blood:	n/a
48	chr19:53290079-53290129	HCM	heart:	n/a
49	chr19:53290312-53290362	AoSMC	blood vessel:	n/a
50	chr19:53290445-53290495	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr19:53296635..53299410-chr19:53311177..53313587,2	K562	blood:
2	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
3	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
4	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
5	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
6	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
7	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
8	chr19:53288948..53291766-chr19:53301308..53304079,2	K562	blood:
9	chr19:53280779..53283746-chr19:53287922..53290818,5	K562	blood:
10	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
11	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
12	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
13	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
14	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
15	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
16	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
17	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
18	chr19:53284850..53287271-chr19:53288897..53290598,2	MCF-7	breast:
19	chr19:53324392..53324894-chr19:53934932..53935516,2	MCF-7	breast:
20	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
21	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF600-1	chr19:53284245-53284717	NONHSAT067584
2	lnc-ZNF600-1	chr19:53283906-53284308	NONHSAT067582
3	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
4	lnc-ZNF468-3	chr19:53321197-53321284	NONHSAT067588
5	lnc-ZNF600-1	chr19:53284570-53284717	NONHSAT067583
6	lnc-ZNF468-3	chr19:53321197-53321281	NONHSAT067589
7	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
8	lnc-ZNF600-1	chr19:53284081-53284308	NONHSAT067583
9	lnc-ZNF600-1	chr19:53289848-53290044	NONHSAT067582
10	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
11	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
12	lnc-ZNF468-3	chr19:53317537-53317679	NONHSAT067589
13	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
14	lnc-ZNF701-2	chr19:53300917-53301869	NONHSAT067585
15	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
16	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
17	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
18	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
19	lnc-ZNF600-1	chr19:53289848-53290024	NONHSAT067584
20	lnc-ZNF468-3	chr19:53311129-53311386	NONHSAT067588
21	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
22	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
23	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
24	lnc-ZNF600-1	chr19:53289848-53289977	NONHSAT067583
25	lnc-ZNF701-2	chr19:53301030-53301858	NONHSAT067586
26	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
27	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
28	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
29	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
30	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
31	lnc-ZNF468-3	chr19:53324839-53324886	NONHSAT067588
32	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF28	hsa-miR-155-5p	chr19:53301585-53301611
2	ZNF28	hsa-miR-155-5p	chr19:53301652-53301677

Variant related genes	Relation type
ENSG00000255875	TF binding region
ZNF600	TF binding region
ZNF28	TF binding region
ZNF468	TF binding region
ENSG00000255875	CpG island
ZNF600	CpG island
ZNF28	CpG island
ZNF468	CpG island
ENSG00000160336	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000255875	chromatin interactions
ENSG00000241015	chromatin interactions
ENSG00000189190	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000221874	chromatin interactions
HAUS6	miRNA target sites
LMNB1	miRNA target sites
PCBP2	miRNA target sites

Extended variants
information (count: 5678 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5678 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529908285	chr19:53261580-53261581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548366712	chr19:53261588-53261589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567763008	chr19:53261631-53261632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111410134	chr19:53261634-53261635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139008014	chr19:53261640-53261641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185828376	chr19:53261668-53261669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113599474	chr19:53261676-53261677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557629888	chr19:53261724-53261725	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575472334	chr19:53261748-53261749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527367570	chr19:53261782-53261783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542821373	chr19:53261789-53261790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114033961	chr19:53261792-53261793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535101452	chr19:53261793-53261794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540307834	chr19:53261794-53261795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149438845	chr19:53261807-53261808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188731170	chr19:53261818-53261819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544223618	chr19:53261863-53261864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370661490	chr19:53261892-53261893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562782542	chr19:53261917-53261918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573079921	chr19:53261951-53261952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs8113244	chr19:53262077-53262078	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533831176	chr19:53262080-53262081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181156112	chr19:53262099-53262100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368167151	chr19:53262100-53262101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547047687	chr19:53262103-53262104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185313387	chr19:53262151-53262152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371560562	chr19:53262158-53262159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190874285	chr19:53262175-53262176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550659575	chr19:53262195-53262196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144929164	chr19:53262223-53262224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11669352	chr19:53262240-53262241	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs184063330	chr19:53262258-53262259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187373425	chr19:53262265-53262266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148097788	chr19:53262295-53262296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533699496	chr19:53262308-53262309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11669394	chr19:53262327-53262328	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs8113605	chr19:53262377-53262378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs544201456	chr19:53262388-53262389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562437370	chr19:53262405-53262406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150641616	chr19:53262427-53262428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549004154	chr19:53262464-53262465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139633574	chr19:53262472-53262473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527478469	chr19:53262473-53262474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562416243	chr19:53262507-53262508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550011213	chr19:53262525-53262526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372233028	chr19:53262551-53262552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542889885	chr19:53262561-53262562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569857857	chr19:53262562-53262563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145250271	chr19:53262591-53262592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115029124	chr19:53262595-53262596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3199 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53253400-53261600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:53259000-53264600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr19:53260200-53261600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr19:53260200-53261600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr19:53260400-53261600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr19:53260400-53261600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr19:53260600-53261600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:53260600-53262000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:53261200-53262200	Enhancers	Dnd41	blood
10	chr19:53261600-53261800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr19:53261600-53261800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:53261600-53261800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr19:53261600-53262000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr19:53261600-53262000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr19:53261600-53262000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr19:53261600-53262000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr19:53261600-53262000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr19:53261600-53262200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr19:53261600-53262200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr19:53262000-53262200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:53262000-53268600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr19:53262000-53269000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr19:53262200-53262800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:53262200-53267400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:53262200-53268800	Weak transcription	Dnd41	blood
26	chr19:53263200-53267800	Enhancers	Placenta	Placenta
27	chr19:53263200-53268800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr19:53264600-53285200	ZNF genes & repeats	Liver	Liver
29	chr19:53265600-53272200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr19:53265600-53282400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
31	chr19:53266600-53267000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr19:53267000-53267400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:53267000-53269200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:53267000-53272600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr19:53267200-53271800	Weak transcription	Fetal Stomach	stomach
36	chr19:53267200-53273600	ZNF genes & repeats	Adipose Nuclei	Adipose
37	chr19:53267400-53268000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr19:53267400-53268400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr19:53267800-53268800	Weak transcription	Placenta	Placenta
40	chr19:53267800-53269400	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:53267800-53272000	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr19:53268000-53268800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr19:53268000-53278000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr19:53268000-53278000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
45	chr19:53268000-53278000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:53268200-53268400	ZNF genes & repeats	Fetal Intestine Large	intestine
47	chr19:53268200-53269000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
48	chr19:53268200-53269200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr19:53268200-53269400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:53268200-53271400	Weak transcription	Fetal Thymus	thymus

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