Variant report

Variant	nsv912351
Chromosome Location	chr19:53655493-53702508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1123)
CpG islands
(count:2014)
Chromatin interactive
region (count:13)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53664406-53664819	K562	blood:	n/a	n/a
2	ATF1	chr19:53676238-53676490	K562	blood:	n/a	n/a
3	ATF1	chr19:53664403-53664837	K562	blood:	n/a	n/a
4	ATF2	chr19:53696341-53696692	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr19:53664416-53664788	K562	blood:	n/a	n/a
6	BACH1	chr19:53696179-53696305	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:53664790-53664860	K562	blood:	n/a	n/a
8	BACH1	chr19:53700005-53700557	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr19:53661692-53661744	K562	blood:	n/a	n/a
10	BHLHE40	chr19:53664400-53664738	K562	blood:	n/a	n/a
11	BHLHE40	chr19:53698652-53698829	K562	blood:	n/a	n/a
12	BHLHE40	chr19:53662160-53662389	K562	blood:	n/a	n/a
13	BHLHE40	chr19:53698601-53698837	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:53696330-53696718	K562	blood:	n/a	n/a
15	BRCA1	chr19:53696315-53697043	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr19:53688313-53688728	K562	blood:	n/a	n/a
17	CBX3	chr19:53664292-53664796	K562	blood:	n/a	n/a
18	CBX3	chr19:53664263-53664816	K562	blood:	n/a	n/a
19	CBX3	chr19:53696473-53696709	K562	blood:	n/a	n/a
20	CCNT2	chr19:53664343-53664849	K562	blood:	n/a	n/a
21	CCNT2	chr19:53662189-53662571	K562	blood:	n/a	chr19:53662348-53662357
22	CCNT2	chr19:53696493-53696794	K562	blood:	n/a	n/a
23	CEBPB	chr19:53663742-53663949	A549	lung:	n/a	chr19:53663784-53663795 chr19:53663881-53663893 chr19:53663784-53663797 chr19:53663784-53663797 chr19:53663784-53663797
24	CEBPB	chr19:53664450-53664840	K562	blood:	n/a	n/a
25	CEBPB	chr19:53663617-53663975	K562	blood:	n/a	chr19:53663784-53663795 chr19:53663881-53663893 chr19:53663784-53663797 chr19:53663784-53663797 chr19:53663784-53663797
26	CEBPB	chr19:53663650-53663931	HepG2	liver:	n/a	chr19:53663784-53663795 chr19:53663881-53663893 chr19:53663784-53663797 chr19:53663784-53663797 chr19:53663784-53663797
27	CEBPB	chr19:53696413-53696725	K562	blood:	n/a	n/a
28	CEBPB	chr19:53664377-53664845	K562	blood:	n/a	n/a
29	CEBPB	chr19:53676206-53676375	K562	blood:	n/a	n/a
30	CEBPB	chr19:53659497-53659684	K562	blood:	n/a	chr19:53659606-53659617
31	CEBPB	chr19:53676130-53676515	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:53676237-53676414	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:53676161-53676505	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:53659586-53659607	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:53676213-53676474	MCF-7	breast:	n/a	n/a
36	CEBPB	chr19:53676182-53676483	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:53663769-53663845	H1-hESC	embryonic stem cell:	n/a	chr19:53663784-53663795 chr19:53663784-53663797 chr19:53663784-53663797 chr19:53663784-53663797
38	CEBPB	chr19:53676150-53676487	K562	blood:	n/a	n/a
39	CEBPB	chr19:53696599-53696928	K562	blood:	n/a	n/a
40	CEBPB	chr19:53676139-53676526	K562	blood:	n/a	n/a
41	CEBPB	chr19:53685649-53685941	IMR90	lung:	n/a	n/a
42	CEBPD	chr19:53662105-53662361	HepG2	liver:	n/a	n/a
43	CEBPD	chr19:53664264-53664820	K562	blood:	n/a	n/a
44	CEBPD	chr19:53664263-53664849	K562	blood:	n/a	n/a
45	CEBPD	chr19:53676214-53676520	K562	blood:	n/a	n/a
46	CHD1	chr19:53696275-53696352	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr19:53696117-53696928	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr19:53686488-53686939	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr19:53700567-53700576	K562	blood:	n/a	n/a
50	CHD2	chr19:53696473-53696936	K562	blood:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53697124-53697174	HL-60	blood:	n/a
2	chr19:53697124-53697174	HL-60	blood:	n/a
3	chr19:53697284-53697334	Caco-2	colon:	n/a
4	chr19:53665821-53665871	A549	lung:	n/a
5	chr19:53696753-53696803	HNPCEpiC	eye:	n/a
6	chr19:53693063-53693113	HRCEpiC	kidney:	n/a
7	chr19:53693063-53693113	BJ	skin:	n/a
8	chr19:53662499-53662549	MCF-7	breast:	n/a
9	chr19:53685874-53685924	GM12878	blood:	n/a
10	chr19:53696326-53696376	GM19239	blood:	n/a
11	chr19:53662439-53662489	CMK	blood:	n/a
12	chr19:53697284-53697334	K562	blood:	n/a
13	chr19:53685874-53685924	HEEpiC	esophagus:	n/a
14	chr19:53697284-53697334	GM12878	blood:	n/a
15	chr19:53685874-53685924	NB4	blood:	n/a
16	chr19:53662467-53662517	LNCaP	prostate:	n/a
17	chr19:53700527-53700577	PrEC	prostate:	n/a
18	chr19:53662261-53662311	Jurkat	blood:	n/a
19	chr19:53662620-53662670	BJ	skin:	n/a
20	chr19:53662680-53662730	AoSMC	blood vessel:	n/a
21	chr19:53662353-53662403	HepG2	liver:	n/a
22	chr19:53662467-53662517	HMEC	breast:	n/a
23	chr19:53685874-53685924	GM12892	blood:	n/a
24	chr19:53662353-53662403	BE2_C	brain:	n/a
25	chr19:53660062-53660112	GM06990	blood:	n/a
26	chr19:53696217-53696267	HCT-116	colon:	n/a
27	chr19:53693063-53693113	HEK293	kidney:	embryo
28	chr19:53696649-53696699	GM12878	blood:	n/a
29	chr19:53697534-53697584	HNPCEpiC	eye:	n/a
30	chr19:53696326-53696376	SK-N-SH_RA	brain:	n/a
31	chr19:53662467-53662517	Hepatocyte	liver:	n/a
32	chr19:53696753-53696803	GM19239	blood:	n/a
33	chr19:53700527-53700577	HIPEpiC	eye:	n/a
34	chr19:53662723-53662773	HEK293	kidney:	embryo
35	chr19:53662261-53662311	AG09319	gingival:	n/a
36	chr19:53662467-53662517	AG10803	skin:	n/a
37	chr19:53662499-53662549	GM06990	blood:	n/a
38	chr19:53662594-53662644	SK-N-SH_RA	brain:	n/a
39	chr19:53696326-53696376	HRPEpiC	eye:	n/a
40	chr19:53662353-53662403	GM12891	blood:	n/a
41	chr19:53695062-53695112	U87	brain:	n/a
42	chr19:53661755-53661805	HAEpiC	amniotic membrane:	n/a
43	chr19:53693063-53693113	AG09319	gingival:	n/a
44	chr19:53662499-53662549	T-47D	breast:	n/a
45	chr19:53696623-53696673	T-47D	breast:	n/a
46	chr19:53662353-53662403	LNCaP	prostate:	n/a
47	chr19:53700527-53700577	Hepatocyte	liver:	n/a
48	chr19:53662467-53662517	BE2_C	brain:	n/a
49	chr19:53665821-53665871	NH-A	brain:	n/a
50	chr19:53661662-53661712	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53695457..53697741-chr19:53699175..53701996,2	K562	blood:
2	chr19:53655411..53659080-chr19:53660737..53664030,3	K562	blood:
3	chr19:53698678..53699363-chr19:54014997..54015830,3	MCF-7	breast:
4	chr19:53692021..53693951-chr19:53695076..53697230,2	K562	blood:
5	chr19:53462207..53464223-chr19:53697419..53699092,2	MCF-7	breast:
6	chr19:53695457..53697741-chr19:53699175..53701996,2	K562	blood:
7	chr19:53652379..53654527-chr19:53655618..53657758,2	K562	blood:
8	chr19:53685672..53687787-chr19:53698865..53701833,2	MCF-7	breast:
9	chr19:53700585..53702772-chr19:53706802..53709941,3	MCF-7	breast:
10	chr19:53698251..53699428-chr19:54295942..54296559,3	MCF-7	breast:
11	chr19:53652920..53654746-chr19:53660355..53662254,2	K562	blood:
12	chr19:53685574..53688103-chr19:53699507..53701678,2	K562	blood:
13	chr19:53686910..53689224-chr19:53694726..53696698,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF665-2	chr19:53667103-53667152	NONHSAT067641
2	lnc-VN1R2-6	chr19:53700364-53700515	ENSG00000269051.1
3	lnc-ZNF665-1	chr19:53682950-53683237	NONHSAT067644
4	lnc-ZNF665-2	chr19:53664711-53664804	NONHSAT067641
5	lnc-ZNF665-1	chr19:53696565-53696619	NONHSAT067645
6	lnc-ZNF665-1	chr19:53686137-53686196	NONHSAT067643
7	lnc-ZNF347-1	chr19:53662262-53662328	NONHSAT067640
8	lnc-VN1R2-7	chr19:53666614-53666816	ENSG00000268842.1
9	lnc-ZNF347-1	chr19:53656986-53657046	NONHSAT067640
10	lnc-ZNF665-1	chr19:53682821-53683237	NONHSAT067643
11	lnc-ZNF665-1	chr19:53696565-53696639	NONHSAT067643
12	lnc-VN1R2-8	chr19:53669046-53669074	NONHSAT067638
13	lnc-ZNF665-1	chr19:53686137-53686196	NONHSAT067644
14	lnc-ZNF665-1	chr19:53694972-53695088	NONHSAT067644
15	lnc-VN1R2-7	chr19:53665681-53665836	ENSG00000268842.1
16	lnc-ZNF665-1	chr19:53693439-53693573	NONHSAT067644
17	lnc-ZNF665-2	chr19:53662466-53662751	NONHSAT067641
18	lnc-ZNF665-1	chr19:53683900-53686196	NONHSAT067645
19	lnc-ZNF665-1	chr19:53696565-53696580	NONHSAT067644

No data

Variant related genes	Relation type
ENSG00000268842	TF binding region
ENSG00000269051	TF binding region
ZNF665	TF binding region
ZNF347	TF binding region
ENSG00000268842	CpG island
ENSG00000269051	CpG island
ZNF665	CpG island
ZNF347	CpG island
ENSG00000197497	chromatin interactions
ENSG00000269051	chromatin interactions
ENSG00000197937	chromatin interactions

Extended variants
information (count: 2060 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2060 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4575636	chr19:53655493-53655494	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528661630	chr19:53655566-53655567	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547210989	chr19:53655581-53655582	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538160958	chr19:53655597-53655598	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs568550812	chr19:53655611-53655612	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs8101245	chr19:53655612-53655613	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs569241952	chr19:53655633-53655634	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530141160	chr19:53655641-53655642	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548683058	chr19:53655666-53655667	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146740854	chr19:53655694-53655695	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533740983	chr19:53655761-53655762	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558670047	chr19:53655773-53655774	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570562441	chr19:53655784-53655785	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12975093	chr19:53655785-53655786	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs562631424	chr19:53655808-53655809	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144876359	chr19:53655814-53655815	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570532300	chr19:53655905-53655906	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs541459399	chr19:53655906-53655907	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557793297	chr19:53655921-53655922	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191226854	chr19:53655935-53655936	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548343268	chr19:53655939-53655940	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373414733	chr19:53655950-53655951	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545584081	chr19:53655979-53655980	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10409942	chr19:53656015-53656016	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566514542	chr19:53656056-53656057	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542340977	chr19:53656068-53656069	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185809537	chr19:53656125-53656126	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190382028	chr19:53656139-53656140	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527605583	chr19:53656177-53656178	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376102026	chr19:53656208-53656209	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544892679	chr19:53656262-53656263	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115724872	chr19:53656269-53656270	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113923899	chr19:53656315-53656316	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182146653	chr19:53656320-53656321	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566851625	chr19:53656417-53656418	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552142381	chr19:53656476-53656477	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10411402	chr19:53656526-53656527	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs570595732	chr19:53656541-53656542	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566465227	chr19:53656563-53656564	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs76106988	chr19:53656592-53656593	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs148217353	chr19:53656608-53656609	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs374878569	chr19:53656617-53656618	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568053099	chr19:53656640-53656641	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs535078009	chr19:53656682-53656683	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs553682446	chr19:53656688-53656689	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537833032	chr19:53656697-53656698	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368016536	chr19:53656726-53656727	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs377572225	chr19:53656736-53656737	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs142776161	chr19:53656792-53656793	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577350011	chr19:53656800-53656801	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53640000-53660600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
2	chr19:53640600-53655800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:53642800-53655600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr19:53643400-53660400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr19:53645400-53655800	Strong transcription	Muscle Satellite Cultured Cells	--
6	chr19:53645800-53660800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr19:53647400-53656400	ZNF genes & repeats	Fetal Intestine Large	intestine
8	chr19:53647600-53658000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
9	chr19:53647800-53655600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr19:53647800-53659200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:53649000-53660800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:53651400-53656400	Weak transcription	K562	blood
13	chr19:53651400-53657400	Strong transcription	Brain Angular Gyrus	brain
14	chr19:53651800-53655800	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr19:53651800-53660800	Weak transcription	Fetal Heart	heart
16	chr19:53652000-53657400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr19:53652000-53658000	Strong transcription	Dnd41	blood
18	chr19:53652000-53660400	Weak transcription	Brain Substantia Nigra	brain
19	chr19:53652200-53661000	Weak transcription	HSMMtube	muscle
20	chr19:53652600-53659200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:53652600-53660600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr19:53652800-53656600	Weak transcription	Brain Hippocampus Middle	brain
23	chr19:53653000-53655600	Strong transcription	Fetal Kidney	kidney
24	chr19:53653000-53657200	Strong transcription	Osteobl	bone
25	chr19:53653000-53660400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr19:53653000-53660600	Weak transcription	Colon Smooth Muscle	Colon
27	chr19:53653200-53660200	Strong transcription	Fetal Stomach	stomach
28	chr19:53653400-53656400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
29	chr19:53653600-53656000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr19:53653600-53656400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr19:53653600-53656600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr19:53653600-53656600	Weak transcription	Aorta	Aorta
33	chr19:53653600-53656600	Weak transcription	Gastric	stomach
34	chr19:53653600-53656800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr19:53653600-53656800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr19:53653600-53657000	Weak transcription	Esophagus	oesophagus
37	chr19:53653600-53657000	Weak transcription	Spleen	Spleen
38	chr19:53653600-53657200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr19:53653600-53657200	Weak transcription	Pancreas	Pancrea
40	chr19:53653600-53658200	Strong transcription	Ovary	ovary
41	chr19:53653600-53658600	Weak transcription	Left Ventricle	heart
42	chr19:53653600-53659200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr19:53653600-53659600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr19:53653600-53660000	Weak transcription	Brain Anterior Caudate	brain
45	chr19:53653600-53660000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr19:53653600-53660000	Weak transcription	Fetal Brain Male	brain
47	chr19:53653600-53660400	Weak transcription	Right Ventricle	heart
48	chr19:53653600-53660600	Weak transcription	Psoas Muscle	Psoas
49	chr19:53653600-53660800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr19:53653600-53661000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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