Variant report

Variant	nsv9499
Chromosome Location	chr17:17181611-17187670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:620)
CpG islands
(count:854)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:17184579-17185040	K562	blood:	n/a	n/a
2	ARID3A	chr17:17184122-17185110	HepG2	liver:	n/a	n/a
3	ATF1	chr17:17183975-17184885	K562	blood:	n/a	n/a
4	ATF2	chr17:17184351-17184958	GM12878	blood:	n/a	chr17:17184603-17184614
5	ATF2	chr17:17184390-17184848	H1-hESC	embryonic stem cell:	n/a	chr17:17184603-17184614
6	ATF2	chr17:17184319-17184999	H1-hESC	embryonic stem cell:	n/a	chr17:17184603-17184614
7	ATF2	chr17:17184303-17184911	GM12878	blood:	n/a	chr17:17184603-17184614
8	ATF3	chr17:17184179-17184932	A549	lung:	n/a	n/a
9	BACH1	chr17:17184023-17184144	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr17:17183723-17185062	A549	lung:	n/a	chr17:17184611-17184620 chr17:17184022-17184035
11	BCLAF1	chr17:17184202-17184967	GM12878	blood:	n/a	chr17:17184611-17184620
12	BCLAF1	chr17:17184324-17184936	GM12878	blood:	n/a	chr17:17184611-17184620
13	BHLHE40	chr17:17183966-17185028	K562	blood:	n/a	chr17:17184207-17184223
14	BHLHE40	chr17:17183945-17184885	GM12878	blood:	n/a	chr17:17184207-17184223
15	BHLHE40	chr17:17183982-17184728	HepG2	liver:	n/a	chr17:17184207-17184223
16	BRCA1	chr17:17183949-17184871	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr17:17184431-17184851	GM12878	blood:	n/a	n/a
18	BRCA1	chr17:17184405-17184919	HepG2	liver:	n/a	n/a
19	BRCA1	chr17:17184422-17184901	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr17:17184366-17184789	K562	blood:	n/a	n/a
21	CCNT2	chr17:17184015-17184697	K562	blood:	n/a	chr17:17184199-17184208
22	CEBPB	chr17:17184602-17184872	HepG2	liver:	n/a	n/a
23	CEBPB	chr17:17184036-17184053	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr17:17184054-17184758	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr17:17184561-17184950	IMR90	lung:	n/a	n/a
26	CEBPB	chr17:17184568-17184924	K562	blood:	n/a	n/a
27	CEBPD	chr17:17183990-17184661	HepG2	liver:	n/a	n/a
28	CEBPD	chr17:17184319-17184623	K562	blood:	n/a	n/a
29	CHD1	chr17:17184198-17184883	GM12878	blood:	n/a	chr17:17184198-17184208
30	CHD1	chr17:17184273-17184537	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr17:17183856-17184978	GM12878	blood:	n/a	chr17:17184198-17184208
32	CHD2	chr17:17183909-17185026	H1-hESC	embryonic stem cell:	n/a	chr17:17184198-17184208
33	CHD2	chr17:17183891-17185090	Hela-S3	cervix:	n/a	chr17:17184198-17184208
34	CHD2	chr17:17183906-17185110	K562	blood:	n/a	chr17:17184198-17184208
35	CHD2	chr17:17183904-17184896	HepG2	liver:	n/a	chr17:17184198-17184208
36	CREB1	chr17:17183893-17184885	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr17:17184381-17184843	A549	lung:	n/a	n/a
38	CREB1	chr17:17183808-17184732	A549	lung:	n/a	n/a
39	CREB1	chr17:17183803-17184990	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr17:17184347-17184930	ECC-1	luminal epithelium:	n/a	n/a
41	CREB1	chr17:17183842-17185091	HepG2	liver:	n/a	n/a
42	CREB1	chr17:17183902-17184860	K562	blood:	n/a	n/a
43	CREB1	chr17:17183821-17185149	HepG2	liver:	n/a	n/a
44	CREB1	chr17:17183813-17185174	GM12878	blood:	n/a	n/a
45	CREB1	chr17:17183895-17184234	A549	lung:	n/a	n/a
46	CREB1	chr17:17183847-17184950	K562	blood:	n/a	n/a
47	CTCF	chr17:17183900-17184050	Hela-S3	cervix:	n/a	chr17:17184018-17184031
48	CTCF	chr17:17185000-17185150	GM12873	blood:	n/a	n/a
49	CTCF	chr17:17183840-17183990	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr17:17183840-17183990	BJ	skin:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17184608-17184658	RPTEC	kidney:	n/a
2	chr17:17184578-17184628	HAEpiC	amniotic membrane:	n/a
3	chr17:17184997-17185047	GM12878	blood:	n/a
4	chr17:17184891-17184941	PFSK-1	brain:	n/a
5	chr17:17184689-17184739	A549	lung:	n/a
6	chr17:17185060-17185110	NT2-D1	testis:	n/a
7	chr17:17184692-17184742	LNCaP	prostate:	n/a
8	chr17:17185060-17185110	ovcar-3	ovarian:	n/a
9	chr17:17184658-17184708	PFSK-1	brain:	n/a
10	chr17:17184578-17184628	AG04449	skin:	fetal
11	chr17:17184369-17184419	HPAEpiC	pulmonary alveolar:	n/a
12	chr17:17184658-17184708	SKMC	muscle:	n/a
13	chr17:17184997-17185047	BJ	skin:	n/a
14	chr17:17184369-17184419	ProgFib	skin:	n/a
15	chr17:17184891-17184941	ECC-1	luminal epithelium:	n/a
16	chr17:17184578-17184628	HCT-116	colon:	n/a
17	chr17:17184369-17184419	SK-N-MC	brain:	n/a
18	chr17:17185060-17185110	HUVEC	blood vessel:	n/a
19	chr17:17184602-17184652	T-47D	breast:	n/a
20	chr17:17184578-17184628	MCF-7	breast:	n/a
21	chr17:17184990-17185040	SK-N-SH_RA	brain:	n/a
22	chr17:17184602-17184652	GM12892	blood:	n/a
23	chr17:17184990-17185040	SKMC	muscle:	n/a
24	chr17:17185060-17185110	HRPEpiC	eye:	n/a
25	chr17:17184602-17184652	AG04449	skin:	fetal
26	chr17:17184692-17184742	PrEC	prostate:	n/a
27	chr17:17185060-17185110	HRE	kidney:	n/a
28	chr17:17185060-17185110	AG09319	gingival:	n/a
29	chr17:17184608-17184658	HEEpiC	esophagus:	n/a
30	chr17:17184692-17184742	GM12891	blood:	n/a
31	chr17:17185060-17185110	Jurkat	blood:	n/a
32	chr17:17184151-17184201	PrEC	prostate:	n/a
33	chr17:17184692-17184742	HPAEpiC	pulmonary alveolar:	n/a
34	chr17:17184891-17184941	HIPEpiC	eye:	n/a
35	chr17:17185060-17185110	NH-A	brain:	n/a
36	chr17:17184608-17184658	HRCEpiC	kidney:	n/a
37	chr17:17184632-17184682	ovcar-3	ovarian:	n/a
38	chr17:17184891-17184941	MCF10A-Er-Src	breast:	n/a
39	chr17:17184990-17185040	BJ	skin:	n/a
40	chr17:17184440-17184490	HNPCEpiC	eye:	n/a
41	chr17:17184602-17184652	SK-N-SH_RA	brain:	n/a
42	chr17:17184891-17184941	U87	brain:	n/a
43	chr17:17184578-17184628	HIPEpiC	eye:	n/a
44	chr17:17184632-17184682	HNPCEpiC	eye:	n/a
45	chr17:17184440-17184490	HPAEpiC	pulmonary alveolar:	n/a
46	chr17:17184151-17184201	ProgFib	skin:	n/a
47	chr17:17184602-17184652	HUVEC	blood vessel:	n/a
48	chr17:17184602-17184652	U87	brain:	n/a
49	chr17:17184578-17184628	SK-N-MC	brain:	n/a
50	chr17:17184151-17184201	Hela-S3	cervix:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17177648..17180936-chr17:17181197..17184729,6	MCF-7	breast:
2	chr15:65596820..65597667-chr17:17184161..17184674,2	Hela-S3	cervix:
3	chr17:17139508..17142367-chr17:17182538..17186121,3	MCF-7	breast:
4	chr11:62609146..62609719-chr17:17184144..17184739,2	NB4	blood:
5	chr17:17173847..17176636-chr17:17182577..17185189,4	MCF-7	breast:
6	chr1:92763984..92764912-chr17:17184143..17184722,2	Hela-S3	cervix:
7	chr17:17183059..17186537-chr17:17204352..17209458,5	K562	blood:
8	chr14:60558608..60559155-chr17:17184009..17184723,2	Hela-S3	cervix:
9	chr17:17185180..17188227-chr17:17188770..17192072,3	K562	blood:
10	chr17:17181690..17186423-chr17:17204352..17210529,13	K562	blood:
11	chr17:17185679..17187797-chr17:17192655..17194477,2	K562	blood:
12	chr17:17183415..17186229-chr17:17206165..17209020,3	MCF-7	breast:
13	chr17:17139412..17141506-chr17:17180331..17182233,2	K562	blood:
14	chr1:225117293..225117949-chr17:17184296..17185001,2	Hela-S3	cervix:
15	chr17:17108079..17111792-chr17:17180254..17184300,4	K562	blood:
16	chr17:17138280..17141930-chr17:17183181..17187644,4	MCF-7	breast:
17	chr17:17179863..17182572-chr17:17182928..17185820,4	K562	blood:
18	chr17:17109460..17111792-chr17:17182647..17184300,2	K562	blood:
19	chr17:17086210..17088657-chr17:17181524..17183953,3	K562	blood:
20	chr17:17132573..17135085-chr17:17184051..17185920,2	K562	blood:
21	chr17:17175034..17177881-chr17:17182376..17183909,2	K562	blood:
22	chr17:17182421..17186483-chr17:17204152..17209830,5	MCF-7	breast:
23	chr17:17179045..17181973-chr17:17206782..17208341,2	MCF-7	breast:
24	chr17:17166616..17168183-chr17:17181241..17182822,2	MCF-7	breast:
25	chr17:17138181..17140588-chr17:17182569..17184810,2	K562	blood:
26	chr17:17159982..17161623-chr17:17181233..17182802,2	K562	blood:

No data

Variant related genes	Relation type
COPS3	TF binding region
COPS3	CpG island
ENSG00000185842	chromatin interactions
ENSG00000126773	chromatin interactions
ENSG00000154803	chromatin interactions
ENSG00000205309	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000122484	chromatin interactions
ENSG00000141030	chromatin interactions
ENSG00000264187	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000266498	chromatin interactions
ENSG00000179598	chromatin interactions

Extended variants
information (count: 246 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:246 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531431346	chr17:17181627-17181628	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs551643030	chr17:17181639-17181640	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs368441537	chr17:17181647-17181648	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs571453174	chr17:17181663-17181664	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs534111895	chr17:17181676-17181677	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs76118135	chr17:17181686-17181687	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs142983559	chr17:17181750-17181751	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs535843937	chr17:17181751-17181752	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs571619946	chr17:17181794-17181795	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs555474183	chr17:17181804-17181805	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs575371947	chr17:17181887-17181888	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs111657379	chr17:17181902-17181903	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs146143686	chr17:17181933-17181934	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs140188299	chr17:17181947-17181948	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs557956055	chr17:17181956-17181957	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs577836216	chr17:17182058-17182059	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs80281653	chr17:17182121-17182122	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs560851215	chr17:17182145-17182146	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs574208116	chr17:17182169-17182170	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs542656661	chr17:17182187-17182188	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs577107290	chr17:17182211-17182212	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs149760971	chr17:17182251-17182252	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs531469879	chr17:17182256-17182257	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs545104099	chr17:17182271-17182272	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs564948026	chr17:17182310-17182311	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs145710793	chr17:17182313-17182314	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs141996620	chr17:17182343-17182344	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545774087	chr17:17182413-17182414	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556359748	chr17:17182431-17182432	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs547227900	chr17:17182436-17182437	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs567597344	chr17:17182440-17182441	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs566640890	chr17:17182466-17182467	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs9890700	chr17:17182513-17182514	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549390713	chr17:17182522-17182523	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs78389992	chr17:17182546-17182547	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs151070856	chr17:17182553-17182554	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs141305917	chr17:17182590-17182591	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs12935953	chr17:17182614-17182615	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs534409600	chr17:17182625-17182626	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs146987820	chr17:17182628-17182629	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs147630824	chr17:17182672-17182673	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs190568816	chr17:17182751-17182752	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs181721683	chr17:17182780-17182781	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs9891435	chr17:17182819-17182820	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs576130008	chr17:17182827-17182828	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs557912071	chr17:17182835-17182836	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs544978559	chr17:17182902-17182903	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs6502569	chr17:17182961-17182962	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs527391699	chr17:17182978-17182979	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs541260824	chr17:17182979-17182980	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:162)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Autism	22543975	CNVD

Chromatin state (count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17160400-17181800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:17163600-17182600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr17:17169800-17183200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr17:17171600-17182400	Weak transcription	Fetal Heart	heart
5	chr17:17171800-17183000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr17:17174200-17182400	Weak transcription	HMEC	breast
7	chr17:17174400-17182600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr17:17174600-17182400	Weak transcription	Psoas Muscle	Psoas
9	chr17:17174600-17182400	Weak transcription	Stomach Mucosa	stomach
10	chr17:17174600-17182400	Weak transcription	NHEK	skin
11	chr17:17174600-17183400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr17:17174800-17182600	Weak transcription	HSMMtube	muscle
13	chr17:17174800-17183000	Weak transcription	HSMM	muscle
14	chr17:17177000-17182000	Weak transcription	NHDF-Ad	bronchial
15	chr17:17177400-17182000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr17:17177400-17182400	Weak transcription	Fetal Brain Male	brain
17	chr17:17177400-17182400	Weak transcription	NH-A	brain
18	chr17:17177400-17182600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr17:17177400-17182600	Weak transcription	NHLF	lung
20	chr17:17177400-17182800	Weak transcription	Fetal Lung	lung
21	chr17:17177400-17183200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr17:17177600-17181800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr17:17177600-17182000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr17:17177600-17183000	Weak transcription	Small Intestine	intestine
25	chr17:17177800-17182400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr17:17177800-17182600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr17:17177800-17182600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr17:17177800-17182600	Weak transcription	Brain Substantia Nigra	brain
29	chr17:17177800-17182600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr17:17178200-17182600	Weak transcription	Osteobl	bone
31	chr17:17178400-17182400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr17:17178400-17182600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr17:17178400-17182600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr17:17178400-17182600	Weak transcription	HUVEC	blood vessel
35	chr17:17178400-17182800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr17:17178400-17183200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr17:17178600-17183000	Weak transcription	Colonic Mucosa	Colon
38	chr17:17178600-17183200	Weak transcription	Esophagus	oesophagus
39	chr17:17178800-17181800	Weak transcription	Brain Anterior Caudate	brain
40	chr17:17178800-17182400	Weak transcription	Gastric	stomach
41	chr17:17178800-17182400	Weak transcription	Lung	lung
42	chr17:17178800-17182800	Weak transcription	Fetal Kidney	kidney
43	chr17:17178800-17183000	Weak transcription	Spleen	Spleen
44	chr17:17178800-17183200	Weak transcription	Left Ventricle	heart
45	chr17:17179000-17182000	Weak transcription	Thymus	Thymus
46	chr17:17179000-17182600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr17:17179000-17182600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr17:17179000-17182600	Weak transcription	Brain Hippocampus Middle	brain
49	chr17:17179000-17183600	Weak transcription	Aorta	Aorta
50	chr17:17179200-17182000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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