Variant report

Variant	nsv912340
Chromosome Location	chr19:53370345-53430362
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:984)
CpG islands
(count:1040)
Chromatin interactive
region (count:35)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53427687-53427726	K562	blood:	n/a	n/a
2	ATF1	chr19:53427511-53427796	K562	blood:	n/a	n/a
3	ATF1	chr19:53426298-53426976	K562	blood:	n/a	n/a
4	ATF2	chr19:53426188-53426746	GM12878	blood:	n/a	n/a
5	ATF3	chr19:53427509-53427761	K562	blood:	n/a	n/a
6	BACH1	chr19:53426291-53426669	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:53400547-53401042	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr19:53426374-53426640	K562	blood:	n/a	n/a
9	BATF	chr19:53407016-53407286	GM12878	blood:	n/a	n/a
10	BCL11A	chr19:53428812-53428959	GM12878	blood:	n/a	n/a
11	BCL3	chr19:53426498-53426869	GM12878	blood:	n/a	chr19:53426812-53426821 chr19:53426810-53426823
12	BCLAF1	chr19:53426282-53426729	GM12878	blood:	n/a	chr19:53426424-53426433
13	BHLHE40	chr19:53401560-53401600	K562	blood:	n/a	n/a
14	BHLHE40	chr19:53400452-53401079	K562	blood:	n/a	n/a
15	BHLHE40	chr19:53427608-53427722	K562	blood:	n/a	n/a
16	BHLHE40	chr19:53426214-53426710	K562	blood:	n/a	n/a
17	BHLHE40	chr19:53426291-53426835	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:53376302-53376339	K562	blood:	n/a	n/a
19	BHLHE40	chr19:53400368-53401093	GM12878	blood:	n/a	n/a
20	BRCA1	chr19:53426297-53426678	HepG2	liver:	n/a	n/a
21	BRCA1	chr19:53400246-53400961	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr19:53426170-53426696	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:53400551-53400898	GM12878	blood:	n/a	n/a
24	BRCA1	chr19:53400249-53401056	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr19:53426334-53426571	GM12878	blood:	n/a	n/a
26	CBX3	chr19:53426096-53426809	K562	blood:	n/a	n/a
27	CBX3	chr19:53376216-53376620	K562	blood:	n/a	n/a
28	CBX3	chr19:53383913-53384365	K562	blood:	n/a	n/a
29	CBX3	chr19:53400349-53401271	K562	blood:	n/a	n/a
30	CBX3	chr19:53399712-53400079	K562	blood:	n/a	n/a
31	CBX3	chr19:53427433-53427925	K562	blood:	n/a	n/a
32	CCNT2	chr19:53426217-53426965	K562	blood:	n/a	n/a
33	CCNT2	chr19:53427516-53427800	K562	blood:	n/a	n/a
34	CCNT2	chr19:53400798-53401141	K562	blood:	n/a	n/a
35	CEBPB	chr19:53427096-53427246	HepG2	liver:	n/a	chr19:53427191-53427202
36	CEBPB	chr19:53400920-53401034	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr19:53427010-53427373	H1-hESC	embryonic stem cell:	n/a	chr19:53427191-53427202
38	CEBPB	chr19:53400754-53401233	K562	blood:	n/a	n/a
39	CEBPB	chr19:53426991-53427679	K562	blood:	n/a	chr19:53427191-53427202
40	CEBPB	chr19:53427057-53427283	HepG2	liver:	n/a	chr19:53427191-53427202
41	CEBPB	chr19:53427031-53427282	K562	blood:	n/a	chr19:53427191-53427202
42	CEBPB	chr19:53426868-53427409	K562	blood:	n/a	chr19:53427191-53427202
43	CEBPB	chr19:53426302-53427395	Hela-S3	cervix:	n/a	chr19:53427191-53427202
44	CEBPB	chr19:53427108-53427414	ECC-1	luminal epithelium:	n/a	chr19:53427191-53427202
45	CEBPB	chr19:53426972-53427395	ECC-1	luminal epithelium:	n/a	chr19:53427191-53427202
46	CEBPB	chr19:53399436-53399442	K562	blood:	n/a	n/a
47	CEBPB	chr19:53427022-53427356	IMR90	lung:	n/a	chr19:53427191-53427202
48	CEBPB	chr19:53427009-53427387	HepG2	liver:	n/a	chr19:53427191-53427202
49	CEBPB	chr19:53407854-53408032	HepG2	liver:	n/a	n/a
50	CEBPD	chr19:53376161-53376655	K562	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53383549-53383599	Caco-2	colon:	n/a
2	chr19:53424670-53424720	MCF10A-Er-Src	breast:	n/a
3	chr19:53424670-53424720	HRPEpiC	eye:	n/a
4	chr19:53383549-53383599	Caco-2	colon:	n/a
5	chr19:53424670-53424720	MCF10A-Er-Src	breast:	n/a
6	chr19:53424670-53424720	HRPEpiC	eye:	n/a
7	chr19:53393512-53393562	HCF	heart:	n/a
8	chr19:53429005-53429055	BE2_C	brain:	n/a
9	chr19:53400981-53401031	HEK293	kidney:	embryo
10	chr19:53426802-53426852	GM19239	blood:	n/a
11	chr19:53400933-53400983	K562	blood:	n/a
12	chr19:53395635-53395685	NH-A	brain:	n/a
13	chr19:53400933-53400983	HNPCEpiC	eye:	n/a
14	chr19:53426802-53426852	HUVEC	blood vessel:	n/a
15	chr19:53426233-53426283	AG09309	skin:	n/a
16	chr19:53429005-53429055	Hepatocyte	liver:	n/a
17	chr19:53400933-53400983	AoSMC	blood vessel:	n/a
18	chr19:53401204-53401254	SK-N-SH	brain:	n/a
19	chr19:53383549-53383599	ProgFib	skin:	n/a
20	chr19:53400545-53400595	NT2-D1	testis:	n/a
21	chr19:53426388-53426438	SKMC	muscle:	n/a
22	chr19:53394977-53395027	PrEC	prostate:	n/a
23	chr19:53400981-53401031	NB4	blood:	n/a
24	chr19:53424670-53424720	NHDF-neo	bronchial:	n/a
25	chr19:53383549-53383599	HMEC	breast:	n/a
26	chr19:53395635-53395685	SAEC	small airway:	n/a
27	chr19:53424670-53424720	HCT-116	colon:	n/a
28	chr19:53394977-53395027	AG04450	lung:	fetal
29	chr19:53394977-53395027	SK-N-SH_RA	brain:	n/a
30	chr19:53400933-53400983	NHDF-neo	bronchial:	n/a
31	chr19:53383549-53383599	HNPCEpiC	eye:	n/a
32	chr19:53395225-53395275	PANC-1	pancreas:	n/a
33	chr19:53400933-53400983	PrEC	prostate:	n/a
34	chr19:53426233-53426283	HMEC	breast:	n/a
35	chr19:53400981-53401031	A549	lung:	n/a
36	chr19:53424670-53424720	HCPEpiC	choroid plexus:	n/a
37	chr19:53400981-53401031	HPAEpiC	pulmonary alveolar:	n/a
38	chr19:53400545-53400595	SK-N-SH	brain:	n/a
39	chr19:53400778-53400828	HIPEpiC	eye:	n/a
40	chr19:53400545-53400595	RPTEC	kidney:	n/a
41	chr19:53403009-53403059	RPTEC	kidney:	n/a
42	chr19:53400933-53400983	AG09309	skin:	n/a
43	chr19:53429005-53429055	HCPEpiC	choroid plexus:	n/a
44	chr19:53394626-53394676	GM19239	blood:	n/a
45	chr19:53395225-53395275	Caco-2	colon:	n/a
46	chr19:53393512-53393562	GM12878	blood:	n/a
47	chr19:53400981-53401031	HCPEpiC	choroid plexus:	n/a
48	chr19:53426802-53426852	NHDF-neo	bronchial:	n/a
49	chr19:53400545-53400595	NB4	blood:	n/a
50	chr19:53401204-53401254	GM12892	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53424975..53429001-chr19:53430174..53432512,3	K562	blood:
2	chr19:53393138..53396276-chr19:53398172..53401096,6	MCF-7	breast:
3	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
4	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:
5	chr19:53393138..53396276-chr19:53398172..53401096,6	MCF-7	breast:
6	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
7	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
8	chr19:53400554..53402197-chr19:53402529..53405491,2	MCF-7	breast:
9	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
10	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
11	chr11:62608903..62609637-chr19:53426135..53426686,2	Hela-S3	cervix:
12	chr19:53397070..53398594-chr19:53398820..53400571,2	MCF-7	breast:
13	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
14	chr19:53424714..53426568-chr19:53443432..53446550,3	MCF-7	breast:
15	chr19:53424791..53427731-chr19:53464365..53467863,4	K562	blood:
16	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
17	chr18:61637223..61637841-chr19:53397208..53398194,2	Hela-S3	cervix:
18	chr19:53398490..53401733-chr19:53415760..53419901,4	K562	blood:
19	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:
20	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
21	chr19:53419869..53422803-chr19:53423217..53426977,4	K562	blood:
22	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
23	chr19:53426133..53428640-chr19:53444456..53447019,4	K562	blood:
24	chr19:53418400..53422745-chr19:53423096..53427800,7	K562	blood:
25	chr19:53418400..53422745-chr19:53423096..53427800,7	K562	blood:
26	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
27	chr19:53377771..53379611-chr19:53399736..53401870,2	K562	blood:
28	chr19:53398857..53399725-chr3:31226625..31227200,2	MCF-7	breast:
29	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
30	chr19:53399381..53402083-chr19:53412934..53414945,2	K562	blood:
31	chr19:53419869..53422803-chr19:53423217..53426977,4	K562	blood:
32	chr19:53425636..53428538-chr19:53430721..53433929,3	K562	blood:
33	chr19:53412333..53414642-chr19:53425536..53427807,2	K562	blood:
34	chr19:53400711..53402486-chr19:53463191..53466156,2	K562	blood:
35	chr19:53426133..53428140-chr19:53445241..53446971,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF320-2	chr19:53393514-53393581	NONHSAT067594
2	lnc-ZNF320-2	chr19:53394482-53394599	NONHSAT067594
3	lnc-ZNF320-2	chr19:53394482-53394599	NONHSAT067595
4	lnc-ZNF320-1	chr19:53379431-53379838	NONHSAT067593
5	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067592
6	lnc-ZNF320-2	chr19:53396637-53396872	NONHSAT067594
7	lnc-ZNF320-2	chr19:53400773-53400908	NONHSAT067594
8	lnc-ZNF320-2	chr19:53397032-53397174	NONHSAT067596
9	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067591
10	lnc-ZNF320-2	chr19:53394513-53394599	NONHSAT067596
11	lnc-ZNF320-2	chr19:53397032-53397109	NONHSAT067595
12	lnc-ZNF320-3	chr19:53377411-53377490	NONHSAT067591
13	lnc-ZNF320-1	chr19:53398098-53398409	NONHSAT067593
14	lnc-ZNF320-2	chr19:53398644-53399035	NONHSAT067597
15	lnc-VN1R2-12	chr19:53426926-53427328	ENSG00000269646.1
16	lnc-VN1R2-12	chr19:53426635-53426717	ENSG00000269646.1
17	lnc-ZNF320-2	chr19:53396637-53396872	NONHSAT067595
18	lnc-ZNF320-3	chr19:53382704-53382886	NONHSAT067592
19	lnc-ZNF320-2	chr19:53400773-53400888	NONHSAT067597
20	lnc-ZNF320-2	chr19:53400773-53400902	NONHSAT067595
21	lnc-ZNF320-2	chr19:53393562-53393581	NONHSAT067595

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF320	hsa-miR-192-5p	chr19:53381440-53381461

Variant related genes	Relation type
ENSG00000268225	TF binding region
ZNF320	TF binding region
ENSG00000269646	TF binding region
ZNF888	TF binding region
ENSG00000268225	CpG island
ZNF320	CpG island
ENSG00000269646	CpG island
ZNF888	CpG island
ENSG00000166401	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000213801	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000180257	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 2917 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2917 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13345475	chr19:53370345-53370346	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186619077	chr19:53370348-53370349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs59852828	chr19:53370352-53370353	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559276148	chr19:53370358-53370359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113883376	chr19:53370390-53370391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376840458	chr19:53370409-53370410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140702799	chr19:53370420-53370421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544585640	chr19:53370430-53370431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201096840	chr19:53370434-53370435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1469450	chr19:53370438-53370439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1469451	chr19:53370442-53370443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375112749	chr19:53370443-53370444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574944982	chr19:53370446-53370447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200858656	chr19:53370448-53370449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542298346	chr19:53370450-53370451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191057832	chr19:53370452-53370453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527466600	chr19:53370457-53370458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545696326	chr19:53370459-53370460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147693032	chr19:53370520-53370521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376362635	chr19:53370592-53370593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180899291	chr19:53370597-53370598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577348713	chr19:53370608-53370609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185783437	chr19:53370612-53370613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528931329	chr19:53370624-53370625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554555401	chr19:53370632-53370633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192462119	chr19:53370657-53370658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572839127	chr19:53370661-53370662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183364787	chr19:53370665-53370666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534366103	chr19:53370715-53370716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187616997	chr19:53370717-53370718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571107097	chr19:53370819-53370820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539844949	chr19:53370839-53370840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190585030	chr19:53370888-53370889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182923212	chr19:53370939-53370940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375109169	chr19:53370979-53370980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564995788	chr19:53371000-53371001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7250666	chr19:53371018-53371019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs71183845	chr19:53371036-53371037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369347029	chr19:53371048-53371049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370705874	chr19:53371072-53371073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372948215	chr19:53371088-53371089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35196412	chr19:53371095-53371096	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs188349220	chr19:53371112-53371113	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs137915919	chr19:53371120-53371121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545547482	chr19:53371121-53371122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563948879	chr19:53371128-53371129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531444727	chr19:53371154-53371155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192538033	chr19:53371161-53371162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561677909	chr19:53371172-53371173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531109867	chr19:53371208-53371209	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2421 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53361400-53381800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:53361400-53381800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:53361400-53381800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr19:53361400-53381800	Weak transcription	Brain Angular Gyrus	brain
5	chr19:53361400-53382000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr19:53361400-53382000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:53361600-53371200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr19:53361600-53380400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr19:53361600-53381800	Weak transcription	Psoas Muscle	Psoas
10	chr19:53361800-53381800	Weak transcription	Brain Anterior Caudate	brain
11	chr19:53361800-53381800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr19:53361800-53381800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr19:53361800-53383800	Weak transcription	Brain Cingulate Gyrus	brain
14	chr19:53362000-53382000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr19:53369000-53380400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:53369800-53372000	Enhancers	Placenta	Placenta
17	chr19:53370200-53371200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:53370600-53382000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr19:53371200-53371400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr19:53371200-53371600	Strong transcription	Stomach Smooth Muscle	stomach
21	chr19:53371600-53372600	Enhancers	HepG2	liver
22	chr19:53371600-53382000	Weak transcription	Stomach Smooth Muscle	stomach
23	chr19:53372000-53381800	Weak transcription	Placenta	Placenta
24	chr19:53374600-53381800	Weak transcription	Fetal Stomach	stomach
25	chr19:53374800-53381800	Weak transcription	Left Ventricle	heart
26	chr19:53374800-53382000	Weak transcription	Brain Hippocampus Middle	brain
27	chr19:53375000-53381200	Weak transcription	Primary T cells from cord blood	blood
28	chr19:53375200-53379000	Enhancers	K562	blood
29	chr19:53375400-53381800	Weak transcription	Colon Smooth Muscle	Colon
30	chr19:53375400-53381800	Weak transcription	Fetal Muscle Leg	muscle
31	chr19:53376000-53383200	Weak transcription	Brain Substantia Nigra	brain
32	chr19:53376400-53377200	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr19:53376800-53377000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr19:53377000-53377400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr19:53377000-53377800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr19:53377200-53383400	Weak transcription	Brain Germinal Matrix	brain
37	chr19:53377400-53379000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr19:53377400-53380400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr19:53377600-53382000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr19:53377800-53383600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr19:53378200-53378400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr19:53378400-53381200	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr19:53378800-53380600	Weak transcription	Fetal Brain Female	brain
44	chr19:53378800-53382000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr19:53379000-53380600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr19:53379000-53381800	Weak transcription	K562	blood
47	chr19:53379000-53383400	Weak transcription	Fetal Kidney	kidney
48	chr19:53379000-53383800	Weak transcription	Fetal Brain Male	brain
49	chr19:53379200-53381800	Weak transcription	HSMM	muscle
50	chr19:53379200-53382000	Weak transcription	Fetal Lung	lung

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