Variant report

Variant	nsv1055273
Chromosome Location	chr17:46735217-46784388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:749)
CpG islands
(count:489)
Chromatin interactive
region (count:35)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:46749100-46749225	HepG2	liver:	n/a	n/a
2	ATF2	chr17:46749092-46749366	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:46755667-46756098	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr17:46749085-46749377	GM12878	blood:	n/a	chr17:46749158-46749167
5	BHLHE40	chr17:46755814-46756094	K562	blood:	n/a	chr17:46755955-46755971
6	BRCA1	chr17:46755860-46756069	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr17:46756009-46756032	HepG2	liver:	n/a	n/a
8	CBX3	chr17:46736509-46736861	K562	blood:	n/a	n/a
9	CCNT2	chr17:46755799-46756128	K562	blood:	n/a	chr17:46756112-46756121
10	CEBPB	chr17:46754523-46754901	A549	lung:	n/a	n/a
11	CEBPB	chr17:46754550-46754874	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr17:46754540-46754875	IMR90	lung:	n/a	n/a
13	CEBPB	chr17:46754583-46754848	HepG2	liver:	n/a	n/a
14	CEBPB	chr17:46754615-46754895	K562	blood:	n/a	n/a
15	CEBPB	chr17:46755847-46756217	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr17:46754582-46754855	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr17:46754477-46754981	A549	lung:	n/a	chr17:46754919-46754932
18	CEBPB	chr17:46754495-46754902	MCF-7	breast:	n/a	n/a
19	CHD2	chr17:46755909-46756145	HepG2	liver:	n/a	n/a
20	CREB1	chr17:46749093-46749281	A549	lung:	n/a	n/a
21	CREB1	chr17:46755800-46756175	A549	lung:	n/a	n/a
22	CTCF	chr17:46749120-46749270	WI-38	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
23	CTCF	chr17:46755900-46756050	WERI-Rb-1	eye:	n/a	chr17:46755959-46755977
24	CTCF	chr17:46755655-46756220	HepG2	liver:	n/a	chr17:46755959-46755977
25	CTCF	chr17:46740600-46740750	HepG2	liver:	n/a	n/a
26	CTCF	chr17:46754300-46754450	Caco-2	colon:	n/a	n/a
27	CTCF	chr17:46749120-46749270	GM12874	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
28	CTCF	chr17:46755805-46756100	GM10248	blood:	n/a	chr17:46755959-46755977
29	CTCF	chr17:46749100-46749250	GM12875	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
30	CTCF	chr17:46755613-46755667	GM13977	blood:	n/a	n/a
31	CTCF	chr17:46741040-46741190	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr17:46755733-46756138	A549	lung:	n/a	chr17:46755959-46755977
33	CTCF	chr17:46755605-46755609	GM19238	blood:	n/a	n/a
34	CTCF	chr17:46755900-46756050	SK-N-SH_RA	brain:	n/a	chr17:46755959-46755977
35	CTCF	chr17:46748977-46749392	GM12878	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
36	CTCF	chr17:46754374-46754423	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr17:46740560-46740710	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr17:46748986-46749442	T-47D	breast:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
39	CTCF	chr17:46755900-46756050	Hela-S3	cervix:	n/a	chr17:46755959-46755977
40	CTCF	chr17:46749080-46749230	MCF-7	breast:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
41	CTCF	chr17:46740612-46740761	NHEK	skin:	n/a	n/a
42	CTCF	chr17:46741049-46741134	GM12878	blood:	n/a	n/a
43	CTCF	chr17:46749029-46749398	H1-hESC	embryonic stem cell:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
44	CTCF	chr17:46755860-46756010	HAc	cerebellar:	n/a	chr17:46755959-46755977
45	CTCF	chr17:46749120-46749270	GM12801	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
46	CTCF	chr17:46755736-46755742	GM12892	blood:	n/a	n/a
47	CTCF	chr17:46741066-46741145	GM19238	blood:	n/a	n/a
48	CTCF	chr17:46755400-46755550	GM12873	blood:	n/a	chr17:46755421-46755434
49	CTCF	chr17:46755920-46756070	HPF	lung:	n/a	chr17:46755959-46755977
50	CTCF	chr17:46749080-46749230	A549	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46758520-46758570	IMR90	lung:	fetal
2	chr17:46758520-46758570	IMR90	lung:	fetal
3	chr17:46755786-46755836	HL-60	blood:	n/a
4	chr17:46753282-46753332	HCPEpiC	choroid plexus:	n/a
5	chr17:46755422-46755472	ovcar-3	ovarian:	n/a
6	chr17:46758520-46758570	AG09309	skin:	n/a
7	chr17:46755422-46755472	HCF	heart:	n/a
8	chr17:46756094-46756144	HUVEC	blood vessel:	n/a
9	chr17:46753282-46753332	MCF-7	breast:	n/a
10	chr17:46756001-46756051	HUVEC	blood vessel:	n/a
11	chr17:46755719-46755769	HEK293	kidney:	embryo
12	chr17:46756094-46756144	HCT-116	colon:	n/a
13	chr17:46756001-46756051	CMK	blood:	n/a
14	chr17:46756094-46756144	HPAEpiC	pulmonary alveolar:	n/a
15	chr17:46755566-46755616	HEEpiC	esophagus:	n/a
16	chr17:46756094-46756144	AG10803	skin:	n/a
17	chr17:46753282-46753332	CMK	blood:	n/a
18	chr17:46753282-46753332	AG04449	skin:	fetal
19	chr17:46755422-46755472	HPAEpiC	pulmonary alveolar:	n/a
20	chr17:46755719-46755769	HIPEpiC	eye:	n/a
21	chr17:46755566-46755616	NT2-D1	testis:	n/a
22	chr17:46755786-46755836	NH-A	brain:	n/a
23	chr17:46755566-46755616	NHBE	bronchial:	n/a
24	chr17:46755719-46755769	PrEC	prostate:	n/a
25	chr17:46753282-46753332	GM12891	blood:	n/a
26	chr17:46753282-46753332	LNCaP	prostate:	n/a
27	chr17:46755719-46755769	H1-hESC	embryonic stem cell:	embryo
28	chr17:46753282-46753332	IMR90	lung:	fetal
29	chr17:46755719-46755769	CMK	blood:	n/a
30	chr17:46755566-46755616	GM19239	blood:	n/a
31	chr17:46755422-46755472	HMEC	breast:	n/a
32	chr17:46755719-46755769	LNCaP	prostate:	n/a
33	chr17:46755786-46755836	AG09319	gingival:	n/a
34	chr17:46755422-46755472	SK-N-MC	brain:	n/a
35	chr17:46755566-46755616	SK-N-SH_RA	brain:	n/a
36	chr17:46758520-46758570	NHDF-neo	bronchial:	n/a
37	chr17:46753282-46753332	AG09309	skin:	n/a
38	chr17:46756001-46756051	U87	brain:	n/a
39	chr17:46755422-46755472	AG09309	skin:	n/a
40	chr17:46758520-46758570	ProgFib	skin:	n/a
41	chr17:46755719-46755769	T-47D	breast:	n/a
42	chr17:46755566-46755616	SKMC	muscle:	n/a
43	chr17:46756001-46756051	ProgFib	skin:	n/a
44	chr17:46756001-46756051	SAEC	small airway:	n/a
45	chr17:46755786-46755836	HIPEpiC	eye:	n/a
46	chr17:46755566-46755616	GM12878	blood:	n/a
47	chr17:46755422-46755472	RPTEC	kidney:	n/a
48	chr17:46755566-46755616	HEK293	kidney:	embryo
49	chr17:46756094-46756144	Hela-S3	cervix:	n/a
50	chr17:46755786-46755836	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:46782767..46785297-chr17:46786816..46788651,2	K562	blood:
2	chr17:46748726..46749588-chr17:46801756..46802493,2	K562	blood:
3	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
4	chr17:46709730..46712661-chr17:46739293..46740902,2	K562	blood:
5	chr17:46748711..46749583-chr17:46956106..46956875,4	MCF-7	breast:
6	chr17:46749857..46752584-chr17:46924851..46927771,2	K562	blood:
7	chr17:46702462..46704437-chr17:46745558..46748045,2	K562	blood:
8	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
9	chr17:46748727..46749627-chr17:46867991..46868777,6	MCF-7	breast:
10	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
11	chr17:46748703..46749676-chr17:46867980..46869288,6	K562	blood:
12	chr17:46706915..46708436-chr17:46753619..46755678,2	K562	blood:
13	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
14	chr17:46680120..46680636-chr17:46740659..46741505,2	K562	blood:
15	chr17:46755465..46756849-chr17:46867926..46869081,19	MCF-7	breast:
16	chr17:46755465..46756352-chr17:46801247..46802560,4	MCF-7	breast:
17	chr17:46755434..46756698-chr17:46954846..46957173,15	K562	blood:
18	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
19	chr17:46755482..46756508-chr17:46867920..46869021,7	K562	blood:
20	chr17:46713679..46714197-chr17:46749118..46749636,2	MCF-7	breast:
21	chr17:46749070..46750038-chr17:46868565..46869067,2	MCF-7	breast:
22	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
23	chr17:46679617..46680600-chr17:46748738..46749566,2	K562	blood:
24	chr17:46779621..46782109-chr17:46788288..46789802,2	K562	blood:
25	chr17:46693389..46695056-chr17:46744998..46747380,2	K562	blood:
26	chr17:46720335..46721842-chr17:46734718..46736545,2	K562	blood:
27	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
28	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
29	chr17:46755541..46756386-chr17:46881997..46882806,2	MCF-7	breast:
30	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
31	chr17:46755112..46756375-chr17:46868085..46869415,8	MCF-7	breast:
32	chr17:46754810..46756534-chr17:46956012..46957174,7	MCF-7	breast:
33	chr17:46783854..46786293-chr17:46833476..46835255,2	K562	blood:
34	chr17:46753552..46755878-chr17:46875165..46876959,2	K562	blood:
35	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALCOCO2-3	chr17:46782360-46783045	ENSG00000244649.2
2	lnc-CALCOCO2-3	chr17:46783421-46783692	ENSG00000244649.2
3	lnc-CALCOCO2-3	chr17:46782565-46782712	XLOC_012227
4	lnc-CALCOCO2-3	chr17:46783421-46783692	XLOC_012227
5	lnc-CALCOCO2-4	chr17:46781363-46781655	XLOC_012226
6	lnc-CALCOCO2-12	chr17:46769075-46770280	ucscGeneNc_uc002itt_1
7	lnc-CALCOCO2-12	chr17:46771967-46772084	ucscGeneNc_uc002itt_1
8	lnc-CALCOCO2-4	chr17:46781363-46781844	ENSG00000262745.1
9	lnc-CALCOCO2-4	chr17:46777974-46778058	ENSG00000262745.1
10	lnc-CALCOCO2-12	chr17:46773611-46774931	ucscGeneNc_uc002itt_1
11	lnc-CALCOCO2-4	chr17:46760729-46760779	ENSG00000262745.1
12	lnc-CALCOCO2-4	chr17:46777978-46778062	XLOC_012226
13	lnc-PRAC-1	chr17:46768478-46769056	NONHSAT054466
14	lnc-CALCOCO2-3	chr17:46783421-46784708	XLOC_012227
15	lnc-CALCOCO2-3	chr17:46782623-46783045	XLOC_012227

No data

Variant related genes	Relation type
RPL9P28	TF binding region
ENSG00000244649	TF binding region
ENSG00000244559	TF binding region
ENSG00000262745	TF binding region
RPL9P28	CpG island
ENSG00000244649	CpG island
ENSG00000244559	CpG island
ENSG00000262745	CpG island
ENSG00000263602	chromatin interactions
ENSG00000170689	chromatin interactions
ENSG00000136436	chromatin interactions
ENSG00000210741	chromatin interactions
ENSG00000260027	chromatin interactions
ENSG00000233101	chromatin interactions
ZNF828	miRNA target sites
ZNFX1	miRNA target sites

Extended variants
information (count: 1799 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1799 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562925541	chr17:46735263-46735264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140643972	chr17:46735298-46735299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551811950	chr17:46735356-46735357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565534047	chr17:46735380-46735381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149736116	chr17:46735514-46735515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11079833	chr17:46735520-46735521	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567804853	chr17:46735596-46735597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184096163	chr17:46735605-46735606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187642528	chr17:46735617-46735618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568970764	chr17:46735631-46735632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145576144	chr17:46735740-46735741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368543723	chr17:46735789-46735790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553069616	chr17:46735818-46735819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373455798	chr17:46735819-46735820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557632632	chr17:46735822-46735823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199732940	chr17:46735823-46735824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200613762	chr17:46735824-46735825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542576989	chr17:46735825-46735826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs58045519	chr17:46735827-46735828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148864241	chr17:46735878-46735879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112278739	chr17:46735886-46735887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146466236	chr17:46735946-46735947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576566525	chr17:46735956-46735957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545544600	chr17:46735969-46735970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573020818	chr17:46735970-46735971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565620266	chr17:46735978-46735979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561223140	chr17:46736039-46736040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571005225	chr17:46736040-46736041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527984810	chr17:46736071-46736072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547838018	chr17:46736096-46736097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561248447	chr17:46736098-46736099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192626723	chr17:46736107-46736108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371812170	chr17:46736109-46736110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185576861	chr17:46736172-46736173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540214116	chr17:46736209-46736210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79494568	chr17:46736221-46736222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537652732	chr17:46736236-46736237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551151609	chr17:46736245-46736246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571236740	chr17:46736279-46736280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533822557	chr17:46736316-46736317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553615925	chr17:46736319-46736320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553944362	chr17:46736363-46736364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536200479	chr17:46736403-46736404	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140900768	chr17:46736501-46736502	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371571192	chr17:46736508-46736509	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144620273	chr17:46736516-46736517	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559171425	chr17:46736548-46736549	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572809456	chr17:46736587-46736588	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541758319	chr17:46736606-46736607	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367881899	chr17:46736609-46736610	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46725400-46739000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:46725600-46749000	Weak transcription	A549	lung
3	chr17:46732600-46748800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr17:46734600-46736400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr17:46736400-46737200	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr17:46737200-46740600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr17:46740600-46740800	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr17:46740800-46741000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr17:46743800-46744600	Bivalent Enhancer	HepG2	liver
10	chr17:46744200-46744400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:46744200-46744400	Bivalent Enhancer	Stomach Mucosa	stomach
12	chr17:46746400-46746600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
13	chr17:46748000-46748200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr17:46748200-46749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr17:46748800-46749000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr17:46748800-46749200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
17	chr17:46748800-46749200	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr17:46748800-46749200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
19	chr17:46748800-46749600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr17:46749000-46749200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr17:46749000-46749200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr17:46749000-46749200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr17:46749000-46749200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
24	chr17:46749000-46749200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr17:46749000-46749200	Enhancers	Liver	Liver
26	chr17:46749000-46749200	Enhancers	Brain Germinal Matrix	brain
27	chr17:46749000-46749200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr17:46749000-46749200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
29	chr17:46749000-46749200	Active TSS	HSMM	muscle
30	chr17:46749000-46749400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
31	chr17:46749000-46749400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr17:46749000-46749400	Active TSS	Rectal Mucosa Donor 31	rectum
33	chr17:46749000-46749400	Active TSS	A549	lung
34	chr17:46749000-46749400	Active TSS	HSMMtube	muscle
35	chr17:46749000-46749600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
36	chr17:46749000-46749600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
37	chr17:46749000-46749600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr17:46749000-46749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr17:46749000-46749600	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr17:46749000-46749800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr17:46749000-46749800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr17:46749200-46749400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
43	chr17:46749200-46749400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr17:46749200-46749400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr17:46749200-46749400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr17:46749200-46749400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
47	chr17:46749200-46749400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr17:46749200-46749400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr17:46749200-46749400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr17:46749200-46749400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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