Variant report

Variant	esv1007058
Chromosome Location	chr17:46188741-46200367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:239)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:46188924-46189546	GM12878	blood:	n/a	n/a
2	ATF2	chr17:46190376-46190913	GM12878	blood:	n/a	n/a
3	ATF2	chr17:46188938-46189793	GM12878	blood:	n/a	n/a
4	BCL3	chr17:46189027-46189532	GM12878	blood:	n/a	chr17:46189319-46189328 chr17:46189285-46189294
5	BCLAF1	chr17:46190256-46190931	GM12878	blood:	n/a	n/a
6	BCLAF1	chr17:46188980-46189597	GM12878	blood:	n/a	chr17:46189319-46189328 chr17:46189285-46189294
7	BCLAF1	chr17:46188938-46189400	GM12878	blood:	n/a	chr17:46189319-46189328 chr17:46189285-46189294
8	BHLHE40	chr17:46188160-46189547	GM12878	blood:	n/a	n/a
9	CEBPB	chr17:46188917-46189850	GM12878	blood:	n/a	n/a
10	CEBPB	chr17:46190785-46190963	HepG2	liver:	n/a	chr17:46190872-46190885 chr17:46190873-46190884
11	CHD1	chr17:46190471-46190866	GM12878	blood:	n/a	n/a
12	CHD1	chr17:46189055-46189234	GM12878	blood:	n/a	n/a
13	CHD1	chr17:46188307-46188751	GM12878	blood:	n/a	n/a
14	CHD2	chr17:46189090-46189225	GM12878	blood:	n/a	n/a
15	CTCF	chr17:46190560-46190710	GM12864	blood:	n/a	n/a
16	CTCF	chr17:46188587-46188781	GM13977	blood:	n/a	chr17:46188682-46188700
17	CTCF	chr17:46188600-46188750	GM12864	blood:	n/a	chr17:46188682-46188700
18	CTCF	chr17:46188620-46188770	GM12869	blood:	n/a	chr17:46188682-46188700
19	CTCF	chr17:46192236-46192296	LNCaP	prostate:	n/a	n/a
20	CTCF	chr17:46188600-46188750	GM12866	blood:	n/a	chr17:46188682-46188700
21	CTCF	chr17:46190659-46190769	GM12892	blood:	n/a	n/a
22	CTCF	chr17:46188599-46188770	GM10266	blood:	n/a	chr17:46188682-46188700
23	CTCF	chr17:46189020-46189170	GM06990	blood:	n/a	n/a
24	CTCF	chr17:46188600-46188750	GM12872	blood:	n/a	chr17:46188682-46188700
25	CTCF	chr17:46188548-46188806	GM12878	blood:	n/a	chr17:46188682-46188700
26	CTCF	chr17:46188580-46188788	GM19239	blood:	n/a	chr17:46188682-46188700
27	CTCF	chr17:46188620-46188770	GM12867	blood:	n/a	chr17:46188682-46188700
28	CTCF	chr17:46190597-46190753	GM12878	blood:	n/a	n/a
29	CTCF	chr17:46188574-46188802	GM12891	blood:	n/a	chr17:46188682-46188700
30	CTCF	chr17:46188600-46188750	GM12868	blood:	n/a	chr17:46188682-46188700
31	CTCF	chr17:46188600-46188750	GM12873	blood:	n/a	chr17:46188682-46188700
32	CTCF	chr17:46188609-46188765	GM20000	blood:	n/a	chr17:46188682-46188700
33	CTCF	chr17:46188600-46188750	GM12878	blood:	n/a	chr17:46188682-46188700
34	CTCF	chr17:46188604-46188768	GM13976	blood:	n/a	chr17:46188682-46188700
35	CTCF	chr17:46188555-46188812	GM19238	blood:	n/a	chr17:46188682-46188700
36	CTCF	chr17:46188477-46188871	GM12878	blood:	n/a	chr17:46188682-46188700
37	CTCF	chr17:46190640-46190790	GM12872	blood:	n/a	n/a
38	CTCF	chr17:46190671-46190762	GM19239	blood:	n/a	n/a
39	CTCF	chr17:46188547-46188804	GM12892	blood:	n/a	chr17:46188682-46188700
40	CTCF	chr17:46188593-46188761	GM10248	blood:	n/a	chr17:46188682-46188700
41	CTCF	chr17:46188600-46188750	GM12870	blood:	n/a	chr17:46188682-46188700
42	CTCF	chr17:46190620-46190770	GM12865	blood:	n/a	n/a
43	CTCF	chr17:46188600-46188750	GM12865	blood:	n/a	chr17:46188682-46188700
44	CTCF	chr17:46190687-46190741	GM19238	blood:	n/a	n/a
45	CTCF	chr17:46188600-46188750	GM12871	blood:	n/a	chr17:46188682-46188700
46	CTCF	chr17:46188529-46188797	GM19240	blood:	n/a	chr17:46188682-46188700
47	CUX1	chr17:46190454-46190915	GM12878	blood:	n/a	n/a
48	CUX1	chr17:46189062-46189794	GM12878	blood:	n/a	n/a
49	EBF1	chr17:46188921-46189406	GM12878	blood:	n/a	chr17:46189195-46189206
50	EBF1	chr17:46187646-46189774	GM12878	blood:	n/a	chr17:46189195-46189206

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46190702-46190752	A549	lung:	n/a
2	chr17:46189113-46189163	BJ	skin:	n/a
3	chr17:46199907-46199957	HIPEpiC	eye:	n/a
4	chr17:46190702-46190752	GM06990	blood:	n/a
5	chr17:46190702-46190752	AG10803	skin:	n/a
6	chr17:46189113-46189163	NT2-D1	testis:	n/a
7	chr17:46199907-46199957	GM19239	blood:	n/a
8	chr17:46199907-46199957	HepG2	liver:	n/a
9	chr17:46189113-46189163	ProgFib	skin:	n/a
10	chr17:46190702-46190752	HRE	kidney:	n/a
11	chr17:46189113-46189163	IMR90	lung:	fetal
12	chr17:46199907-46199957	T-47D	breast:	n/a
13	chr17:46199907-46199957	HCF	heart:	n/a
14	chr17:46190702-46190752	HCPEpiC	choroid plexus:	n/a
15	chr17:46190702-46190752	HCT-116	colon:	n/a
16	chr17:46189113-46189163	AG04449	skin:	fetal
17	chr17:46199907-46199957	HRPEpiC	eye:	n/a
18	chr17:46199907-46199957	HRE	kidney:	n/a
19	chr17:46189113-46189163	PFSK-1	brain:	n/a
20	chr17:46190702-46190752	PANC-1	pancreas:	n/a
21	chr17:46189113-46189163	HCM	heart:	n/a
22	chr17:46190702-46190752	H1-hESC	embryonic stem cell:	embryo
23	chr17:46199907-46199957	Hela-S3	cervix:	n/a
24	chr17:46189113-46189163	H1-hESC	embryonic stem cell:	embryo
25	chr17:46189113-46189163	Hela-S3	cervix:	n/a
26	chr17:46189113-46189163	PANC-1	pancreas:	n/a
27	chr17:46190702-46190752	MCF10A-Er-Src	breast:	n/a
28	chr17:46189113-46189163	HUVEC	blood vessel:	n/a
29	chr17:46199907-46199957	Caco-2	colon:	n/a
30	chr17:46190702-46190752	SK-N-SH	brain:	n/a
31	chr17:46199907-46199957	SK-N-SH	brain:	n/a
32	chr17:46199907-46199957	HAEpiC	amniotic membrane:	n/a
33	chr17:46190702-46190752	AoSMC	blood vessel:	n/a
34	chr17:46190702-46190752	Jurkat	blood:	n/a
35	chr17:46189113-46189163	BE2_C	brain:	n/a
36	chr17:46199907-46199957	SKMC	muscle:	n/a
37	chr17:46199907-46199957	GM12878	blood:	n/a
38	chr17:46189113-46189163	HL-60	blood:	n/a
39	chr17:46189113-46189163	RPTEC	kidney:	n/a
40	chr17:46199907-46199957	NT2-D1	testis:	n/a
41	chr17:46189113-46189163	ECC-1	luminal epithelium:	n/a
42	chr17:46199907-46199957	MCF10A-Er-Src	breast:	n/a
43	chr17:46199907-46199957	SAEC	small airway:	n/a
44	chr17:46199907-46199957	NHDF-neo	bronchial:	n/a
45	chr17:46189113-46189163	NHDF-neo	bronchial:	n/a
46	chr17:46189113-46189163	HEEpiC	esophagus:	n/a
47	chr17:46190702-46190752	RPTEC	kidney:	n/a
48	chr17:46189113-46189163	HEK293	kidney:	embryo
49	chr17:46189113-46189163	HRPEpiC	eye:	n/a
50	chr17:46189113-46189163	MCF-7	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46183753..46186040-chr17:46196094..46199275,3	MCF-7	breast:
2	chr17:46124943..46127247-chr17:46188061..46189641,2	K562	blood:
3	chr17:46184571..46186273-chr17:46193637..46195242,2	MCF-7	breast:
4	chr17:46175023..46180196-chr17:46181333..46189268,23	MCF-7	breast:
5	chr17:46188096..46189774-chr17:46193080..46195986,2	K562	blood:
6	chr17:46108859..46110468-chr17:46197931..46199848,2	MCF-7	breast:
7	chr17:46183064..46186607-chr17:46198439..46200674,3	MCF-7	breast:
8	chr17:46194453..46197293-chr17:46201950..46204423,2	MCF-7	breast:
9	chr17:46102851..46105550-chr17:46199872..46202014,2	MCF-7	breast:
10	chr17:46197608..46199562-chr17:46200754..46203056,2	MCF-7	breast:
11	chr17:46187740..46191239-chr17:46199544..46202144,3	MCF-7	breast:
12	chr17:46125014..46129511-chr17:46182877..46189561,8	K562	blood:
13	chr17:46184602..46186632-chr17:46186895..46189927,3	MCF-7	breast:
14	chr17:46198773..46201065-chr17:46205294..46206959,2	K562	blood:
15	chr17:46186937..46189774-chr17:46193080..46195996,3	K562	blood:
16	chr17:46177057..46179428-chr17:46199731..46201687,2	MCF-7	breast:
17	chr17:46185085..46187937-chr17:46198335..46200407,2	K562	blood:
18	chr17:46183569..46185892-chr17:46198700..46202089,3	K562	blood:
19	chr17:46123246..46128677-chr17:46197755..46203630,8	MCF-7	breast:
20	chr17:46197348..46200242-chr17:46209628..46212447,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX11-4	chr17:46189393-46189817	NONHSAT054382

No data

Variant related genes	Relation type
SNX11	TF binding region
SNX11	CpG island
ENSG00000082641	chromatin interactions
ENSG00000108468	chromatin interactions
ENSG00000002919	chromatin interactions
ENSG00000263412	chromatin interactions

Extended variants
information (count: 450 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60455972	chr17:46188747-46188748	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs144436116	chr17:46188772-46188773	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs372804892	chr17:46188776-46188777	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs557552141	chr17:46188785-46188786	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs113351240	chr17:46188878-46188879	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs112784015	chr17:46188879-46188880	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs376294614	chr17:46188901-46188902	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs367843047	chr17:46188919-46188920	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs372230539	chr17:46188934-46188935	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs3785737	chr17:46188949-46188950	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs546485636	chr17:46188961-46188962	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs559441545	chr17:46188969-46188970	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs373047022	chr17:46188993-46188994	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs370062856	chr17:46189009-46189010	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs36043565	chr17:46189025-46189026	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs528510281	chr17:46189084-46189085	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs541908438	chr17:46189089-46189090	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs561879120	chr17:46189098-46189099	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs140087642	chr17:46189099-46189100	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs185163876	chr17:46189114-46189115	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs569851079	chr17:46189133-46189134	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs113151423	chr17:46189202-46189203	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs552450950	chr17:46189203-46189204	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs565536532	chr17:46189204-46189205	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs35292745	chr17:46189205-46189206	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs140936606	chr17:46189235-46189236	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs79073047	chr17:46189245-46189246	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs534646377	chr17:46189261-46189262	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs552813901	chr17:46189267-46189268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs554690433	chr17:46189287-46189288	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs34221004	chr17:46189294-46189295	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs568190604	chr17:46189296-46189297	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189578068	chr17:46189297-46189298	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs574521307	chr17:46189338-46189339	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs555391017	chr17:46189382-46189383	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368910906	chr17:46189400-46189401	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs537158881	chr17:46189403-46189404	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs557232985	chr17:46189428-46189429	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs183247852	chr17:46189433-46189434	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs370238181	chr17:46189491-46189492	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs187942539	chr17:46189539-46189540	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs111834120	chr17:46189542-46189543	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs193086095	chr17:46189596-46189597	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs541847225	chr17:46189657-46189658	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs183804905	chr17:46189690-46189691	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs151251392	chr17:46189707-46189708	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs188297760	chr17:46189751-46189752	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs192959924	chr17:46189879-46189880	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs199560203	chr17:46189900-46189901	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200064194	chr17:46189902-46189903	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Urothelial carcinoma	21177765	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
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46185600-46191000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr17:46185800-46190000	Weak transcription	Lung	lung
3	chr17:46185800-46193000	Weak transcription	Gastric	stomach
4	chr17:46185800-46195800	Weak transcription	Ovary	ovary
5	chr17:46186000-46189200	Weak transcription	Colonic Mucosa	Colon
6	chr17:46186000-46195200	Weak transcription	Aorta	Aorta
7	chr17:46186000-46196200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr17:46186000-46198600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr17:46186200-46189000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr17:46186200-46189400	Weak transcription	Placenta	Placenta
11	chr17:46186200-46189600	Weak transcription	Fetal Muscle Leg	muscle
12	chr17:46186200-46189600	Weak transcription	Thymus	Thymus
13	chr17:46186200-46189800	Weak transcription	Fetal Stomach	stomach
14	chr17:46186200-46190000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr17:46186200-46190400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr17:46186200-46190400	Weak transcription	Esophagus	oesophagus
17	chr17:46186200-46190400	Weak transcription	Fetal Kidney	kidney
18	chr17:46186200-46190600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr17:46186200-46190600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr17:46186200-46192000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr17:46186200-46192600	Weak transcription	Colon Smooth Muscle	Colon
22	chr17:46186200-46192600	Weak transcription	A549	lung
23	chr17:46186200-46193800	Weak transcription	Fetal Lung	lung
24	chr17:46186200-46195000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr17:46186200-46195200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr17:46186200-46196200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr17:46186200-46198600	Weak transcription	Fetal Brain Male	brain
28	chr17:46186200-46203600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr17:46186400-46189200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr17:46186400-46189200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr17:46186400-46189200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr17:46186400-46189400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr17:46186400-46189600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr17:46186400-46189800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr17:46186400-46189800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr17:46186400-46190000	Weak transcription	Brain Germinal Matrix	brain
37	chr17:46186400-46190400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr17:46186400-46190400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:46186400-46190400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr17:46186400-46190400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr17:46186400-46190400	Weak transcription	NHLF	lung
42	chr17:46186400-46191800	Weak transcription	Fetal Intestine Large	intestine
43	chr17:46186400-46192200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr17:46186400-46192400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr17:46186400-46193000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr17:46186400-46193000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr17:46186400-46193400	Weak transcription	Osteobl	bone
48	chr17:46186400-46193600	Weak transcription	HSMMtube	muscle
49	chr17:46186400-46194800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr17:46186400-46195000	Weak transcription	Rectal Mucosa Donor 31	rectum

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