Variant report

Variant	nsv1058152
Chromosome Location	chr19:56703368-56805035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:1588)
Chromatin interactive
region (count:40)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1112 , 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	chr19:56765176-56765431	K562	blood:	n/a	n/a
2	ARID3A	chr19:56760286-56760731	K562	blood:	n/a	n/a
3	ATF1	chr19:56769608-56769749	K562	blood:	n/a	n/a
4	ATF1	chr19:56760362-56760671	K562	blood:	n/a	n/a
5	ATF1	chr19:56732773-56733067	K562	blood:	n/a	n/a
6	BACH1	chr19:56782798-56782836	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:56764319-56764415	K562	blood:	n/a	n/a
8	BATF	chr19:56745875-56746197	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:56769582-56769849	K562	blood:	n/a	n/a
10	BHLHE40	chr19:56764145-56764486	K562	blood:	n/a	chr19:56764224-56764240
11	BHLHE40	chr19:56760454-56760539	K562	blood:	n/a	n/a
12	BRCA1	chr19:56720561-56720808	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr19:56745473-56745601	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr19:56764077-56764484	K562	blood:	n/a	n/a
15	CBX3	chr19:56764011-56764558	K562	blood:	n/a	n/a
16	CCNT2	chr19:56774769-56775046	K562	blood:	n/a	n/a
17	CCNT2	chr19:56760428-56760663	K562	blood:	n/a	n/a
18	CEBPB	chr19:56705414-56705462	HepG2	liver:	n/a	chr19:56705438-56705449
19	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
20	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
21	CEBPB	chr19:56720517-56720847	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:56736709-56737013	Hela-S3	cervix:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
23	CEBPB	chr19:56716430-56716674	HepG2	liver:	n/a	chr19:56716533-56716544
24	CEBPB	chr19:56716455-56716760	IMR90	lung:	n/a	chr19:56716533-56716544
25	CEBPB	chr19:56705349-56705533	A549	lung:	n/a	chr19:56705438-56705449
26	CEBPB	chr19:56707830-56708066	K562	blood:	n/a	n/a
27	CEBPB	chr19:56711153-56711485	Hela-S3	cervix:	n/a	chr19:56711325-56711336
28	CEBPB	chr19:56736715-56737020	A549	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
29	CEBPB	chr19:56760233-56760622	K562	blood:	n/a	chr19:56760446-56760457
30	CEBPB	chr19:56741646-56741970	HepG2	liver:	n/a	chr19:56741810-56741821
31	CEBPB	chr19:56711145-56711495	H1-hESC	embryonic stem cell:	n/a	chr19:56711325-56711336
32	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
33	CEBPB	chr19:56711122-56711514	HepG2	liver:	n/a	chr19:56711325-56711336
34	CEBPB	chr19:56716510-56716908	K562	blood:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
35	CEBPB	chr19:56764258-56764496	K562	blood:	n/a	n/a
36	CEBPB	chr19:56736713-56736976	K562	blood:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
37	CEBPB	chr19:56741673-56741957	K562	blood:	n/a	chr19:56741810-56741821
38	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
39	CEBPB	chr19:56716429-56716798	A549	lung:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
40	CEBPB	chr19:56736697-56737012	IMR90	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
41	CEBPB	chr19:56711159-56711500	A549	lung:	n/a	chr19:56711325-56711336
42	CEBPB	chr19:56760261-56760657	K562	blood:	n/a	chr19:56760446-56760457
43	CEBPB	chr19:56775946-56776215	K562	blood:	n/a	n/a
44	CEBPB	chr19:56782158-56782338	K562	blood:	n/a	n/a
45	CEBPB	chr19:56799963-56800165	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
47	CEBPB	chr19:56744051-56744221	K562	blood:	n/a	n/a
48	CEBPB	chr19:56705321-56705483	K562	blood:	n/a	chr19:56705438-56705449
49	CEBPB	chr19:56736739-56736963	HepG2	liver:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
50	CEBPB	chr19:56741741-56741909	H1-hESC	embryonic stem cell:	n/a	chr19:56741810-56741821

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56739741-56739791	HepG2	liver:	n/a
2	chr19:56742355-56742405	NT2-D1	testis:	n/a
3	chr19:56739741-56739791	HepG2	liver:	n/a
4	chr19:56742355-56742405	NT2-D1	testis:	n/a
5	chr19:56738933-56738983	HL-60	blood:	n/a
6	chr19:56732932-56732982	HepG2	liver:	n/a
7	chr19:56733045-56733095	GM12891	blood:	n/a
8	chr19:56738933-56738983	SK-N-MC	brain:	n/a
9	chr19:56726303-56726353	NT2-D1	testis:	n/a
10	chr19:56739749-56739799	AG09309	skin:	n/a
11	chr19:56705433-56705483	PrEC	prostate:	n/a
12	chr19:56728589-56728639	SKMC	muscle:	n/a
13	chr19:56705386-56705436	HEEpiC	esophagus:	n/a
14	chr19:56739749-56739799	HEEpiC	esophagus:	n/a
15	chr19:56705497-56705547	HCM	heart:	n/a
16	chr19:56704341-56704391	AG09309	skin:	n/a
17	chr19:56742355-56742405	AG09309	skin:	n/a
18	chr19:56742355-56742405	ECC-1	luminal epithelium:	n/a
19	chr19:56739741-56739791	LNCaP	prostate:	n/a
20	chr19:56704341-56704391	RPTEC	kidney:	n/a
21	chr19:56739741-56739791	AG09319	gingival:	n/a
22	chr19:56711667-56711717	HPAEpiC	pulmonary alveolar:	n/a
23	chr19:56739731-56739781	HepG2	liver:	n/a
24	chr19:56711667-56711717	K562	blood:	n/a
25	chr19:56739788-56739838	Hela-S3	cervix:	n/a
26	chr19:56732932-56732982	MCF-7	breast:	n/a
27	chr19:56739573-56739623	HCF	heart:	n/a
28	chr19:56740672-56740722	SK-N-SH_RA	brain:	n/a
29	chr19:56739741-56739791	SK-N-SH	brain:	n/a
30	chr19:56728422-56728472	ovcar-3	ovarian:	n/a
31	chr19:56733045-56733095	PANC-1	pancreas:	n/a
32	chr19:56709228-56709278	GM12878	blood:	n/a
33	chr19:56733045-56733095	HRCEpiC	kidney:	n/a
34	chr19:56726303-56726353	MCF-7	breast:	n/a
35	chr19:56739749-56739799	ovcar-3	ovarian:	n/a
36	chr19:56704341-56704391	LNCaP	prostate:	n/a
37	chr19:56704341-56704391	MCF10A-Er-Src	breast:	n/a
38	chr19:56709056-56709106	A549	lung:	n/a
39	chr19:56730494-56730544	SK-N-SH_RA	brain:	n/a
40	chr19:56742355-56742405	GM12892	blood:	n/a
41	chr19:56739788-56739838	HCM	heart:	n/a
42	chr19:56733045-56733095	HIPEpiC	eye:	n/a
43	chr19:56732932-56732982	LNCaP	prostate:	n/a
44	chr19:56705386-56705436	NH-A	brain:	n/a
45	chr19:56739788-56739838	HIPEpiC	eye:	n/a
46	chr19:56705433-56705483	AG09309	skin:	n/a
47	chr19:56728422-56728472	PrEC	prostate:	n/a
48	chr19:56741019-56741069	AG04450	lung:	fetal
49	chr19:56705386-56705436	H1-hESC	embryonic stem cell:	embryo
50	chr19:56742355-56742405	RPTEC	kidney:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:56766124..56767037-chr19:56820605..56821442,2	MCF-7	breast:
2	chr19:56760039..56762057-chr19:56831322..56833020,2	K562	blood:
3	chr19:56777403..56778975-chr19:56779512..56781342,2	MCF-7	breast:
4	chr19:56797989..56800517-chr19:56824554..56828282,3	K562	blood:
5	chr19:56793005..56795545-chr19:56798620..56800184,2	K562	blood:
6	chr19:56764089..56764882-chr2:69533751..69534360,2	K562	blood:
7	chr19:56798402..56800517-chr19:56824554..56827552,3	K562	blood:
8	chr19:56750344..56752392-chr19:56783866..56786080,2	K562	blood:
9	chr19:56763438..56764980-chr19:56767122..56769734,2	K562	blood:
10	chr19:56591684..56592579-chr19:56763878..56764497,2	K562	blood:
11	chr19:56800949..56803657-chr19:56804852..56806650,2	K562	blood:
12	chr19:56631229..56633438-chr19:56759454..56761104,2	K562	blood:
13	chr19:56592228..56593017-chr19:56764764..56765328,2	K562	blood:
14	chr19:56577493..56578448-chr19:56763612..56764760,5	MCF-7	breast:
15	chr19:56773048..56775014-chr19:56779504..56781484,2	K562	blood:
16	chr19:56764396..56765751-chr19:56820601..56821654,11	MCF-7	breast:
17	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
18	chr19:56764440..56765781-chr19:56844595..56845562,7	MCF-7	breast:
19	chr19:56764606..56765477-chr19:56844677..56845421,4	MCF-7	breast:
20	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:
21	chr19:56763438..56764980-chr19:56767122..56769734,2	K562	blood:
22	chr19:56800928..56803425-chr19:56806728..56809539,2	MCF-7	breast:
23	chr19:56772426..56773119-chr19:56820978..56821526,2	MCF-7	breast:
24	chr19:56768465..56770206-chr19:56776029..56778555,2	K562	blood:
25	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
26	chr19:56577493..56578453-chr19:56763955..56765293,5	K562	blood:
27	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:
28	chr19:56587441..56588336-chr19:56763861..56764794,5	MCF-7	breast:
29	chr19:56763855..56765502-chr19:56825187..56827361,2	K562	blood:
30	chr19:56167793..56169420-chr19:56762867..56764897,2	K562	blood:
31	chr19:56764814..56765752-chr19:56820274..56821276,4	K562	blood:
32	chr19:56764916..56765950-chr19:56820818..56821640,4	MCF-7	breast:
33	chr19:56782005..56784747-chr19:56789683..56792405,2	K562	blood:
34	chr19:56764795..56766031-chr19:56844616..56845643,6	K562	blood:
35	chr19:56706835..56708923-chr19:56717136..56719247,2	K562	blood:
36	chr19:56750344..56752392-chr19:56783866..56786080,2	K562	blood:
37	chr19:56153237..56155682-chr19:56762217..56764183,2	K562	blood:
38	chr19:56616218..56617192-chr19:56763915..56764470,3	MCF-7	breast:
39	chr19:56773048..56775014-chr19:56779504..56781484,2	K562	blood:
40	chr19:56666246..56666790-chr19:56764150..56764947,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF582-5	chr19:56791971-56792069	NONHSAT068091
2	lnc-ZSCAN5C-1	chr19:56802559-56802734	NONHSAT068093
3	lnc-ZNF582-5	chr19:56774587-56775051	NONHSAT068087
4	lnc-ZNF582-5	chr19:56794714-56795256	NONHSAT068092
5	lnc-ZSCAN5C-1	chr19:56799122-56799446	NONHSAT068093
6	lnc-ZSCAN5C-1	chr19:56794716-56795256	NONHSAT068093
7	lnc-ZNF582-5	chr19:56785908-56786277	NONHSAT068090
8	lnc-ZSCAN5B-1	chr19:56777587-56778130	NONHSAT068088
9	lnc-ZSCAN5C-1	chr19:56802840-56803281	NONHSAT068093
10	lnc-ZNF582-5	chr19:56785873-56786277	NONHSAT068089
11	lnc-ZSCAN5C-1	chr19:56795924-56796439	NONHSAT068093

No data

Variant related genes	Relation type
ZSCAN5B	TF binding region
ENSG00000267710	TF binding region
ZSCAN5C	TF binding region
ENSG00000242411	TF binding region
ZSCAN5D	TF binding region
ZSCAN5A	TF binding region
ZSCAN5B	CpG island
ENSG00000267710	CpG island
ZSCAN5C	CpG island
ENSG00000242411	CpG island
ZSCAN5D	CpG island
ZSCAN5A	CpG island
ENSG00000267549	chromatin interactions
ENSG00000131848	chromatin interactions
ENSG00000267908	chromatin interactions
ENSG00000267710	chromatin interactions
ENSG00000200646	chromatin interactions
ENSG00000204532	chromatin interactions
ENSG00000223060	chromatin interactions
ENSG00000171425	chromatin interactions
ENSG00000142409	chromatin interactions
ENSG00000267522	chromatin interactions
ENSG00000213015	chromatin interactions

Extended variants
information (count: 4192 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4192 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34181873	chr19:56705325-56705326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs569501010	chr19:56705326-56705327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569320789	chr19:56705342-56705343	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs60591854	chr19:56705343-56705344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs71184332	chr19:56705344-56705345	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs191925232	chr19:56705360-56705361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572768183	chr19:56705363-56705364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373534845	chr19:56705387-56705388	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs544692879	chr19:56705442-56705443	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs78444867	chr19:56705469-56705470	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs564907861	chr19:56705480-56705481	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs575986267	chr19:56705554-56705555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544968208	chr19:56705617-56705618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376547538	chr19:56705690-56705691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184110508	chr19:56705742-56705743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs560405648	chr19:56705769-56705770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375994236	chr19:56705785-56705786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190360681	chr19:56705787-56705788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375180794	chr19:56705788-56705789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369772972	chr19:56705790-56705791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568993880	chr19:56706753-56706754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537965813	chr19:56706807-56706808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554587563	chr19:56706811-56706812	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568086155	chr19:56706869-56706870	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7251435	chr19:56706894-56706895	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58916478	chr19:56706917-56706918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554460320	chr19:56706920-56706921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs28645842	chr19:56706925-56706926	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544728831	chr19:56706958-56706959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62120853	chr19:56706978-56706979	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs185227034	chr19:56706980-56706981	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4801684	chr19:56706994-56706995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576114433	chr19:56707006-56707007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7250670	chr19:56707018-56707019	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9973244	chr19:56707038-56707039	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs61469428	chr19:56707048-56707049	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs56864483	chr19:56707050-56707051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs560411982	chr19:56707086-56707087	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561231197	chr19:56707098-56707099	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532317238	chr19:56707163-56707164	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368676605	chr19:56707220-56707221	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs10410743	chr19:56707221-56707222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs397760015	chr19:56707222-56707223	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs9973245	chr19:56707343-56707344	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542055087	chr19:56707370-56707371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577564170	chr19:56707374-56707375	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139789363	chr19:56707419-56707420	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs58805847	chr19:56707468-56707469	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547747490	chr19:56707473-56707474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181283933	chr19:56707484-56707485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56705400-56705800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:56710800-56712400	Enhancers	Liver	Liver
3	chr19:56711000-56711200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr19:56711000-56711800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr19:56711600-56711800	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr19:56716600-56717200	Bivalent Enhancer	Hela-S3	cervix
7	chr19:56723600-56727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr19:56724400-56728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr19:56725000-56725200	Active TSS	A549	lung
10	chr19:56725200-56727400	Weak transcription	A549	lung
11	chr19:56727400-56727600	ZNF genes & repeats	A549	lung
12	chr19:56727400-56727800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:56727400-56728200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:56727600-56735800	Weak transcription	A549	lung
15	chr19:56727800-56728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr19:56727800-56729000	Enhancers	Dnd41	blood
17	chr19:56728000-56728400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr19:56728000-56728400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr19:56728000-56728400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr19:56728000-56728400	Enhancers	Esophagus	oesophagus
23	chr19:56728000-56728800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:56728000-56729400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:56728200-56728400	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr19:56728200-56728400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:56728200-56728400	Enhancers	Primary hematopoietic stem cells	blood
28	chr19:56728200-56728400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr19:56728200-56728400	Enhancers	HMEC	breast
32	chr19:56728200-56728400	Enhancers	HUVEC	blood vessel
33	chr19:56728200-56728600	Bivalent Enhancer	Thymus	Thymus
34	chr19:56728200-56728800	Bivalent Enhancer	Placenta	Placenta
35	chr19:56728200-56728800	Bivalent Enhancer	Fetal Thymus	thymus
36	chr19:56728200-56729200	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr19:56728200-56729400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr19:56728200-56729400	Enhancers	Fetal Heart	heart
39	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
40	chr19:56728400-56728600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr19:56728400-56728600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr19:56728400-56728600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr19:56728400-56728600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr19:56728400-56728600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:56728400-56728600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:56728400-56728600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr19:56728400-56728600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
48	chr19:56728400-56728600	Bivalent Enhancer	Brain Germinal Matrix	brain
49	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
50	chr19:56728400-56728600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain

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