Variant report

Variant	esv13317
Chromosome Location	chr17:46732109-46783718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:488)
Chromatin interactive
region (count:36)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 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	chr17:46754582-46754855	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr17:46755847-46756217	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr17:46754550-46754874	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr17:46754615-46754895	K562	blood:	n/a	n/a
14	CEBPB	chr17:46754477-46754981	A549	lung:	n/a	chr17:46754919-46754932
15	CEBPB	chr17:46754583-46754848	HepG2	liver:	n/a	n/a
16	CEBPB	chr17:46754495-46754902	MCF-7	breast:	n/a	n/a
17	CEBPB	chr17:46754540-46754875	IMR90	lung:	n/a	n/a
18	CEBPB	chr17:46754523-46754901	A549	lung:	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	chr17:46749080-46749230	RPTEC	kidney:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
23	CTCF	chr17:46748975-46749374	A549	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
24	CTCF	chr17:46755754-46756122	MCF-7	breast:	n/a	chr17:46755959-46755977
25	CTCF	chr17:46756247-46756265	GM12892	blood:	n/a	n/a
26	CTCF	chr17:46740620-46740770	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr17:46755714-46756197	A549	lung:	n/a	chr17:46755959-46755977
28	CTCF	chr17:46749100-46749250	AG04450	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
29	CTCF	chr17:46755736-46755742	GM12892	blood:	n/a	n/a
30	CTCF	chr17:46740621-46740748	Fibrobl	skin:	n/a	n/a
31	CTCF	chr17:46752885-46752974	GM20000	blood:	n/a	n/a
32	CTCF	chr17:46755900-46756050	GM12865	blood:	n/a	chr17:46755959-46755977
33	CTCF	chr17:46755812-46756105	Pancreas_OC	pancreas:	n/a	chr17:46755959-46755977
34	CTCF	chr17:46740582-46740819	K562	blood:	n/a	n/a
35	CTCF	chr17:46754300-46754450	Caco-2	colon:	n/a	n/a
36	CTCF	chr17:46740640-46740790	K562	blood:	n/a	n/a
37	CTCF	chr17:46755900-46756050	GM12866	blood:	n/a	chr17:46755959-46755977
38	CTCF	chr17:46748972-46749783	HCT-116	colon:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
39	CTCF	chr17:46755769-46756068	ECC-1	luminal epithelium:	n/a	chr17:46755959-46755977
40	CTCF	chr17:46749030-46749282	LNCaP	prostate:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
41	CTCF	chr17:46749100-46749250	GM12868	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
42	CTCF	chr17:46740600-46740750	HMEC	breast:	n/a	n/a
43	CTCF	chr17:46749060-46749210	HRE	kidney:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
44	CTCF	chr17:46740620-46740770	HCM	heart:	n/a	n/a
45	CTCF	chr17:46755585-46756271	K562	blood:	n/a	chr17:46755959-46755977
46	CTCF	chr17:46749100-46749250	GM12869	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
47	CTCF	chr17:46748988-46749374	A549	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
48	CTCF	chr17:46755980-46756130	GM12872	blood:	n/a	n/a
49	CTCF	chr17:46740671-46740712	Medullo	brain:	n/a	n/a
50	CTCF	chr17:46740889-46741282	H1-hESC	embryonic stem cell:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46756001-46756051	HMEC	breast:	n/a
2	chr17:46758520-46758570	HCT-116	colon:	n/a
3	chr17:46756001-46756051	HRCEpiC	kidney:	n/a
4	chr17:46755719-46755769	BJ	skin:	n/a
5	chr17:46756001-46756051	HUVEC	blood vessel:	n/a
6	chr17:46758520-46758570	SK-N-MC	brain:	n/a
7	chr17:46755422-46755472	AG09319	gingival:	n/a
8	chr17:46753282-46753332	HCF	heart:	n/a
9	chr17:46755786-46755836	AG09309	skin:	n/a
10	chr17:46758520-46758570	Hepatocyte	liver:	n/a
11	chr17:46758520-46758570	Caco-2	colon:	n/a
12	chr17:46758520-46758570	ECC-1	luminal epithelium:	n/a
13	chr17:46755786-46755836	K562	blood:	n/a
14	chr17:46755422-46755472	NH-A	brain:	n/a
15	chr17:46758520-46758570	GM12892	blood:	n/a
16	chr17:46756094-46756144	Caco-2	colon:	n/a
17	chr17:46755566-46755616	HNPCEpiC	eye:	n/a
18	chr17:46756001-46756051	BE2_C	brain:	n/a
19	chr17:46756001-46756051	ProgFib	skin:	n/a
20	chr17:46755422-46755472	LNCaP	prostate:	n/a
21	chr17:46755786-46755836	HCT-116	colon:	n/a
22	chr17:46756094-46756144	NT2-D1	testis:	n/a
23	chr17:46756001-46756051	U87	brain:	n/a
24	chr17:46753282-46753332	PFSK-1	brain:	n/a
25	chr17:46753282-46753332	AG09319	gingival:	n/a
26	chr17:46755566-46755616	A549	lung:	n/a
27	chr17:46755422-46755472	GM06990	blood:	n/a
28	chr17:46756094-46756144	AoSMC	blood vessel:	n/a
29	chr17:46756001-46756051	SK-N-MC	brain:	n/a
30	chr17:46753282-46753332	Hela-S3	cervix:	n/a
31	chr17:46756001-46756051	HEEpiC	esophagus:	n/a
32	chr17:46758520-46758570	SK-N-SH	brain:	n/a
33	chr17:46753282-46753332	Hepatocyte	liver:	n/a
34	chr17:46753282-46753332	PANC-1	pancreas:	n/a
35	chr17:46758520-46758570	H1-hESC	embryonic stem cell:	embryo
36	chr17:46753282-46753332	IMR90	lung:	fetal
37	chr17:46753282-46753332	SKMC	muscle:	n/a
38	chr17:46755566-46755616	HIPEpiC	eye:	n/a
39	chr17:46755422-46755472	HMEC	breast:	n/a
40	chr17:46753282-46753332	AG10803	skin:	n/a
41	chr17:46755786-46755836	SK-N-SH_RA	brain:	n/a
42	chr17:46756094-46756144	AG04449	skin:	fetal
43	chr17:46756001-46756051	HL-60	blood:	n/a
44	chr17:46758520-46758570	GM12891	blood:	n/a
45	chr17:46755566-46755616	AG04450	lung:	fetal
46	chr17:46755719-46755769	U87	brain:	n/a
47	chr17:46755566-46755616	NHBE	bronchial:	n/a
48	chr17:46756094-46756144	PANC-1	pancreas:	n/a
49	chr17:46755422-46755472	BJ	skin:	n/a
50	chr17:46755786-46755836	HIPEpiC	eye:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46749857..46752584-chr17:46924851..46927771,2	K562	blood:
2	chr17:46748711..46749583-chr17:46956106..46956875,4	MCF-7	breast:
3	chr17:46749070..46750038-chr17:46868565..46869067,2	MCF-7	breast:
4	chr17:46755541..46756386-chr17:46881997..46882806,2	MCF-7	breast:
5	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
6	chr17:46782767..46785297-chr17:46786816..46788651,2	K562	blood:
7	chr17:46748703..46749676-chr17:46867980..46869288,6	K562	blood:
8	chr17:46679617..46680600-chr17:46748738..46749566,2	K562	blood:
9	chr17:46755482..46756508-chr17:46867920..46869021,7	K562	blood:
10	chr17:46748727..46749627-chr17:46867991..46868777,6	MCF-7	breast:
11	chr17:46693389..46695056-chr17:46744998..46747380,2	K562	blood:
12	chr17:46755465..46756352-chr17:46801247..46802560,4	MCF-7	breast:
13	chr17:46779621..46782109-chr17:46788288..46789802,2	K562	blood:
14	chr17:46702462..46704437-chr17:46745558..46748045,2	K562	blood:
15	chr17:46727732..46729730-chr17:46732348..46734217,2	K562	blood:
16	chr17:46717343..46719162-chr17:46732030..46734552,2	K562	blood:
17	chr17:46755112..46756375-chr17:46868085..46869415,8	MCF-7	breast:
18	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
19	chr17:46713679..46714197-chr17:46749118..46749636,2	MCF-7	breast:
20	chr17:46748726..46749588-chr17:46801756..46802493,2	K562	blood:
21	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
22	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
23	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
24	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
25	chr17:46680120..46680636-chr17:46740659..46741505,2	K562	blood:
26	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
27	chr17:46755434..46756698-chr17:46954846..46957173,15	K562	blood:
28	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
29	chr17:46754810..46756534-chr17:46956012..46957174,7	MCF-7	breast:
30	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
31	chr17:46706915..46708436-chr17:46753619..46755678,2	K562	blood:
32	chr17:46755465..46756849-chr17:46867926..46869081,19	MCF-7	breast:
33	chr17:46720335..46721842-chr17:46734718..46736545,2	K562	blood:
34	chr17:46753552..46755878-chr17:46875165..46876959,2	K562	blood:
35	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
36	chr17:46709730..46712661-chr17:46739293..46740902,2	K562	blood:

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

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

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
ENSG00000233101	chromatin interactions
ENSG00000260027	chromatin interactions
ENSG00000210741	chromatin interactions
ENSG00000136436	chromatin interactions
ZNFX1	miRNA target sites
ZNF828	miRNA target sites

Extended variants
information (count: 1885 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200897881	chr17:46732136-46732137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138145123	chr17:46732144-46732145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28828688	chr17:46732153-46732154	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs397753696	chr17:46732160-46732161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62064610	chr17:46732161-46732162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541773362	chr17:46732181-46732182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561854437	chr17:46732185-46732186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575680909	chr17:46732209-46732210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549975035	chr17:46732251-46732252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55682497	chr17:46732393-46732394	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs185543577	chr17:46732396-46732397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552514492	chr17:46732485-46732486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190082445	chr17:46732486-46732487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115317273	chr17:46732512-46732513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548199257	chr17:46732515-46732516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568109821	chr17:46732526-46732527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4793965	chr17:46732557-46732558	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs76573860	chr17:46732580-46732581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571042454	chr17:46732583-46732584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75154003	chr17:46732598-46732599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553252213	chr17:46732631-46732632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181379781	chr17:46732636-46732637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185519656	chr17:46732735-46732736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555335843	chr17:46732739-46732740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150315728	chr17:46732740-46732741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544676956	chr17:46732763-46732764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs137908324	chr17:46732787-46732788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190277296	chr17:46732815-46732816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142309345	chr17:46732871-46732872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181190409	chr17:46732910-46732911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145937027	chr17:46732926-46732927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528392812	chr17:46732959-46732960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138502262	chr17:46733004-46733005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143038824	chr17:46733086-46733087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565780783	chr17:46733136-46733137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186068146	chr17:46733137-46733138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550674723	chr17:46733166-46733167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190972497	chr17:46733217-46733218	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539653215	chr17:46733239-46733240	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183950978	chr17:46733257-46733258	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs55786154	chr17:46733272-46733273	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188863586	chr17:46733273-46733274	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144356211	chr17:46733323-46733324	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563733217	chr17:46733338-46733339	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575609666	chr17:46733402-46733403	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537822154	chr17:46733415-46733416	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558243237	chr17:46733468-46733469	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs578027049	chr17:46733470-46733471	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546066546	chr17:46733475-46733476	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148761806	chr17:46733497-46733498	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:343 , 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	chr17:46730000-46733200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr17:46732000-46732600	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr17:46732600-46748800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr17:46733200-46734600	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr17:46733600-46733800	Bivalent/Poised TSS	Dnd41	blood
8	chr17:46734600-46736400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr17:46736400-46737200	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr17:46737200-46740600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr17:46740600-46740800	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr17:46740800-46741000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr17:46743800-46744600	Bivalent Enhancer	HepG2	liver
14	chr17:46744200-46744400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
15	chr17:46744200-46744400	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr17:46746400-46746600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
17	chr17:46748000-46748200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr17:46748200-46749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr17:46748800-46749000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr17:46748800-46749200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
21	chr17:46748800-46749200	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr17:46748800-46749200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
23	chr17:46748800-46749600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr17:46749000-46749200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr17:46749000-46749200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr17:46749000-46749200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr17:46749000-46749200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
28	chr17:46749000-46749200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr17:46749000-46749200	Enhancers	Liver	Liver
30	chr17:46749000-46749200	Enhancers	Brain Germinal Matrix	brain
31	chr17:46749000-46749200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr17:46749000-46749200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
33	chr17:46749000-46749200	Active TSS	HSMM	muscle
34	chr17:46749000-46749400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
35	chr17:46749000-46749400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr17:46749000-46749400	Active TSS	Rectal Mucosa Donor 31	rectum
37	chr17:46749000-46749400	Active TSS	A549	lung
38	chr17:46749000-46749400	Active TSS	HSMMtube	muscle
39	chr17:46749000-46749600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
40	chr17:46749000-46749600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr17:46749000-46749600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr17:46749000-46749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr17:46749000-46749600	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr17:46749000-46749800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr17:46749000-46749800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr17:46749200-46749400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
47	chr17:46749200-46749400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr17:46749200-46749400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr17:46749200-46749400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr17:46749200-46749400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell

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