Variant report

Variant	nsv518620
Chromosome Location	chr17:15563393-15608194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1008)
CpG islands
(count:977)
Chromatin interactive
region (count:9)
LncRNA
region (count:44)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15602736-15603024	HepG2	liver:	n/a	n/a
2	ATF1	chr17:15602817-15603017	K562	blood:	n/a	n/a
3	ATF2	chr17:15602639-15603127	GM12878	blood:	n/a	n/a
4	BACH1	chr17:15602905-15603025	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr17:15587367-15587738	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr17:15587522-15587574	K562	blood:	n/a	n/a
7	BATF	chr17:15602698-15603139	GM12878	blood:	n/a	n/a
8	BCL11A	chr17:15602570-15603218	GM12878	blood:	n/a	n/a
9	BCL3	chr17:15587434-15587831	A549	lung:	n/a	chr17:15587623-15587632
10	BHLHE40	chr17:15587520-15587720	GM12878	blood:	n/a	n/a
11	BHLHE40	chr17:15602795-15603168	GM12878	blood:	n/a	n/a
12	BHLHE40	chr17:15602827-15603100	K562	blood:	n/a	n/a
13	BRCA1	chr17:15602708-15603099	GM12878	blood:	n/a	chr17:15602870-15602879
14	BRCA1	chr17:15602639-15603141	Hela-S3	cervix:	n/a	chr17:15602870-15602879
15	BRCA1	chr17:15587530-15587649	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr17:15602711-15603054	H1-hESC	embryonic stem cell:	n/a	chr17:15602870-15602879
17	BRCA1	chr17:15602716-15603056	HepG2	liver:	n/a	chr17:15602870-15602879
18	CBX3	chr17:15602574-15603183	K562	blood:	n/a	n/a
19	CEBPB	chr17:15588349-15588353	IMR90	lung:	n/a	n/a
20	CEBPB	chr17:15590473-15590661	HepG2	liver:	n/a	n/a
21	CEBPB	chr17:15602806-15603183	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr17:15577101-15577343	K562	blood:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
23	CEBPB	chr17:15577092-15577369	IMR90	lung:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
24	CEBPB	chr17:15577095-15577347	HepG2	liver:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
25	CEBPB	chr17:15577097-15577313	Hela-S3	cervix:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
26	CEBPB	chr17:15577110-15577369	K562	blood:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
27	CEBPB	chr17:15577155-15577293	H1-hESC	embryonic stem cell:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
28	CEBPB	chr17:15577095-15577345	A549	lung:	n/a	chr17:15577231-15577242 chr17:15577231-15577244
29	CEBPD	chr17:15587439-15587708	HepG2	liver:	n/a	n/a
30	CEBPD	chr17:15602980-15603199	HepG2	liver:	n/a	n/a
31	CEBPD	chr17:15602664-15602922	HepG2	liver:	n/a	n/a
32	CHD2	chr17:15602651-15603116	H1-hESC	embryonic stem cell:	n/a	chr17:15602870-15602879
33	CHD2	chr17:15602653-15603124	K562	blood:	n/a	chr17:15602870-15602879
34	CHD2	chr17:15602655-15603159	HepG2	liver:	n/a	chr17:15602870-15602879
35	CHD2	chr17:15587535-15587604	HepG2	liver:	n/a	n/a
36	CHD2	chr17:15602649-15603183	GM12878	blood:	n/a	chr17:15602870-15602879
37	CHD2	chr17:15587448-15587799	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr17:15587599-15587642	K562	blood:	n/a	n/a
39	CHD2	chr17:15602572-15603200	Hela-S3	cervix:	n/a	chr17:15602870-15602879
40	CREB1	chr17:15602714-15603177	A549	lung:	n/a	n/a
41	CREB1	chr17:15602820-15603076	HepG2	liver:	n/a	n/a
42	CREB1	chr17:15602822-15603091	GM12878	blood:	n/a	n/a
43	CREB1	chr17:15602741-15603081	A549	lung:	n/a	n/a
44	CTCF	chr17:15573080-15573230	A549	lung:	n/a	n/a
45	CTCF	chr17:15573000-15573150	HAc	cerebellar:	n/a	chr17:15573027-15573040 chr17:15573036-15573057 chr17:15573041-15573059
46	CTCF	chr17:15587240-15587390	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr17:15572977-15573119	GM12892	blood:	n/a	chr17:15573027-15573040 chr17:15573036-15573057 chr17:15573041-15573059
48	CTCF	chr17:15573000-15573150	AG09309	skin:	n/a	chr17:15573027-15573040 chr17:15573036-15573057 chr17:15573041-15573059
49	CTCF	chr17:15587240-15587390	NHEK	skin:	n/a	n/a
50	CTCF	chr17:15587169-15587189	MCF-7	breast:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15603030-15603080	MCF10A-Er-Src	breast:	n/a
2	chr17:15603030-15603080	MCF10A-Er-Src	breast:	n/a
3	chr17:15600659-15600709	SK-N-SH_RA	brain:	n/a
4	chr17:15608033-15608083	ECC-1	luminal epithelium:	n/a
5	chr17:15603030-15603080	LNCaP	prostate:	n/a
6	chr17:15586426-15586476	K562	blood:	n/a
7	chr17:15602714-15602764	H1-hESC	embryonic stem cell:	embryo
8	chr17:15607775-15607825	PFSK-1	brain:	n/a
9	chr17:15586426-15586476	PANC-1	pancreas:	n/a
10	chr17:15600659-15600709	RPTEC	kidney:	n/a
11	chr17:15587124-15587174	MCF-7	breast:	n/a
12	chr17:15587147-15587197	HCF	heart:	n/a
13	chr17:15603030-15603080	NHDF-neo	bronchial:	n/a
14	chr17:15608091-15608141	PrEC	prostate:	n/a
15	chr17:15587124-15587174	SAEC	small airway:	n/a
16	chr17:15608091-15608141	Caco-2	colon:	n/a
17	chr17:15603984-15604034	HEEpiC	esophagus:	n/a
18	chr17:15586426-15586476	AoSMC	blood vessel:	n/a
19	chr17:15606456-15606506	Hepatocyte	liver:	n/a
20	chr17:15602873-15602923	ECC-1	luminal epithelium:	n/a
21	chr17:15608033-15608083	NB4	blood:	n/a
22	chr17:15603984-15604034	GM12878	blood:	n/a
23	chr17:15587124-15587174	SK-N-SH_RA	brain:	n/a
24	chr17:15587124-15587174	CMK	blood:	n/a
25	chr17:15587147-15587197	HCPEpiC	choroid plexus:	n/a
26	chr17:15587124-15587174	HCT-116	colon:	n/a
27	chr17:15586170-15586220	A549	lung:	n/a
28	chr17:15587124-15587174	K562	blood:	n/a
29	chr17:15603984-15604034	ProgFib	skin:	n/a
30	chr17:15608091-15608141	LNCaP	prostate:	n/a
31	chr17:15603984-15604034	GM12892	blood:	n/a
32	chr17:15603030-15603080	NH-A	brain:	n/a
33	chr17:15602880-15602930	AG09319	gingival:	n/a
34	chr17:15602880-15602930	ovcar-3	ovarian:	n/a
35	chr17:15602714-15602764	NH-A	brain:	n/a
36	chr17:15587279-15587329	HRCEpiC	kidney:	n/a
37	chr17:15602873-15602923	AG09319	gingival:	n/a
38	chr17:15600659-15600709	PFSK-1	brain:	n/a
39	chr17:15587147-15587197	SK-N-SH_RA	brain:	n/a
40	chr17:15587147-15587197	HPAEpiC	pulmonary alveolar:	n/a
41	chr17:15603030-15603080	HCM	heart:	n/a
42	chr17:15602880-15602930	RPTEC	kidney:	n/a
43	chr17:15587147-15587197	ovcar-3	ovarian:	n/a
44	chr17:15600659-15600709	HCM	heart:	n/a
45	chr17:15607775-15607825	U87	brain:	n/a
46	chr17:15603984-15604034	SAEC	small airway:	n/a
47	chr17:15602880-15602930	HCPEpiC	choroid plexus:	n/a
48	chr17:15587147-15587197	HepG2	liver:	n/a
49	chr17:15606456-15606506	HCPEpiC	choroid plexus:	n/a
50	chr17:15607775-15607825	SAEC	small airway:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:15582137..15583945-chr17:15586739..15588630,2	MCF-7	breast:
2	chr17:15563102..15563727-chr17:15973385..15973964,2	MCF-7	breast:
3	chr17:15565672..15568468-chr17:15583905..15586616,2	MCF-7	breast:
4	chr17:15160810..15162326-chr17:15564040..15566649,2	K562	blood:
5	chr17:15603099..15603617-chr17:18585233..18585750,2	HCT-116	colon:
6	chr17:15081140..15081829-chr17:15562872..15563684,2	MCF-7	breast:
7	chr17:15561055..15565103-chr17:15565320..15567687,3	MCF-7	breast:
8	chr17:15555196..15556875-chr17:15562176..15564992,2	K562	blood:
9	chr17:15561055..15565103-chr17:15565320..15567687,3	MCF-7	breast:

(count:44 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145841
2	lnc-ZNF286A-7	chr17:15603054-15603091	NONHSAT145850
3	lnc-RP11-385D13.1.1-1	chr17:15580889-15581035	NONHSAT145843
4	lnc-ZNF286A-7	chr17:15603477-15603901	NONHSAT145853
5	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145843
6	lnc-ZNF286A-7	chr17:15602895-15603091	NONHSAT145849
7	lnc-ZSWIM7-1	chr17:15596563-15596608	ENSG00000248550
8	lnc-ZNF286A-7	chr17:15603449-15603680	NONHSAT145848
9	lnc-RP11-385D13.1.1-1	chr17:15580489-15580591	NONHSAT145843
10	lnc-RP11-385D13.1.1-1	chr17:15587510-15587589	NONHSAT145841
11	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145841
12	lnc-ZNF286A-7	chr17:15603449-15603991	NONHSAT145850
13	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145838
14	lnc-RP11-385D13.1.1-1	chr17:15587510-15587615	NONHSAT145843
15	lnc-ZNF286A-7	chr17:15604466-15604544	NONHSAT145853
16	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145840
17	lnc-RP11-385D13.1.1-1	chr17:15587510-15587613	NONHSAT145846
18	lnc-ZNF286A-7	chr17:15603362-15603853	NONHSAT145849
19	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145844
20	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145838
21	lnc-RP11-385D13.1.1-1	chr17:15586168-15586265	NONHSAT145840
22	lnc-RP11-385D13.1.1-1	chr17:15584365-15584536	NONHSAT145838
23	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145844
24	lnc-RP11-385D13.1.1-1	chr17:15580889-15580996	NONHSAT145844
25	lnc-RP11-385D13.1.1-1	chr17:15580945-15581035	NONHSAT145845
26	lnc-RP11-385D13.1.1-1	chr17:15587510-15587612	NONHSAT145845
27	lnc-RP11-385D13.1.1-1	chr17:15587510-15587580	NONHSAT145840
28	lnc-RP11-385D13.1.1-1	chr17:15584402-15584536	NONHSAT145846
29	lnc-RP11-385D13.1.1-1	chr17:15586168-15586278	NONHSAT145845
30	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145845
31	lnc-RP11-385D13.1.1-1	chr17:15587510-15587625	NONHSAT145847
32	lnc-RP11-385D13.1.1-1	chr17:15586350-15586685	NONHSAT145847
33	lnc-RP11-385D13.1.1-1	chr17:15587510-15587611	NONHSAT145838
34	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145843
35	lnc-ZNF286A-7	chr17:15604466-15604614	NONHSAT145848
36	lnc-RP11-385D13.1.1-1	chr17:15586168-15586265	NONHSAT145841
37	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145845
38	lnc-RP11-385D13.1.1-1	chr17:15586168-15586265	NONHSAT145846
39	lnc-RP11-385D13.1.1-1	chr17:15587510-15587613	NONHSAT145844
40	lnc-RP11-385D13.1.1-1	chr17:15586168-15586265	NONHSAT145847
41	lnc-RP11-385D13.1.1-1	chr17:15584179-15584267	NONHSAT145840
42	lnc-RP11-385D13.1.1-1	chr17:15586168-15586265	NONHSAT145844
43	lnc-RP11-385D13.1.1-1	chr17:15586350-15586471	NONHSAT145846
44	lnc-ZNF286A-7	chr17:15602891-15603091	NONHSAT145848

No data

Variant related genes	Relation type
ENSG00000187607	TF binding region
TRIM16	TF binding region
ZNF29P	TF binding region
ZNF286A	TF binding region
ENSG00000187607	CpG island
TRIM16	CpG island
ZNF29P	CpG island
ZNF286A	CpG island
ENSG00000249459	chromatin interactions
ENSG00000221926	chromatin interactions
PHF17	miRNA target sites

Extended variants
information (count: 1360 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:1360 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202176441	chr17:15563393-15563394	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73272123	chr17:15563525-15563526	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566143454	chr17:15563580-15563581	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535187011	chr17:15563614-15563615	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555338769	chr17:15563676-15563677	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4792645	chr17:15563726-15563727	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs559632506	chr17:15563741-15563742	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200629360	chr17:15563747-15563748	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112532685	chr17:15563753-15563754	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372571665	chr17:15563756-15563757	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576894646	chr17:15563780-15563781	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148605003	chr17:15563785-15563786	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58508798	chr17:15563790-15563791	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564170502	chr17:15563833-15563834	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142229783	chr17:15563925-15563926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572162437	chr17:15563938-15563939	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540811677	chr17:15563941-15563942	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560876076	chr17:15563978-15563979	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187128075	chr17:15563994-15563995	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549403597	chr17:15564005-15564006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566591079	chr17:15564022-15564023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532082632	chr17:15564028-15564029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552003732	chr17:15564069-15564070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs58075329	chr17:15564084-15564085	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534937322	chr17:15564104-15564105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548799365	chr17:15564128-15564129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568811499	chr17:15564135-15564136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532927063	chr17:15564167-15564168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373574103	chr17:15564188-15564189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs80174715	chr17:15564216-15564217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550489491	chr17:15564235-15564236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545227028	chr17:15564261-15564262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56104277	chr17:15564271-15564272	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146996309	chr17:15564314-15564315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553224101	chr17:15564334-15564335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111303364	chr17:15564338-15564339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112953124	chr17:15564355-15564356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540874819	chr17:15564390-15564391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554331145	chr17:15564395-15564396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574249194	chr17:15564464-15564465	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191943698	chr17:15564483-15564484	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1476728	chr17:15564546-15564547	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs532046714	chr17:15564613-15564614	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140996338	chr17:15564669-15564670	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559232281	chr17:15564768-15564769	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77222473	chr17:15564783-15564784	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73272127	chr17:15564810-15564811	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs568674749	chr17:15564855-15564856	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531099598	chr17:15564856-15564857	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535733749	chr17:15564861-15564862	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
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
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
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
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15552200-15564600	Weak transcription	HepG2	liver
2	chr17:15554600-15571200	Weak transcription	Liver	Liver
3	chr17:15555000-15587000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr17:15555000-15587000	Weak transcription	Gastric	stomach
5	chr17:15555200-15564400	Weak transcription	GM12878-XiMat	blood
6	chr17:15555200-15567000	Weak transcription	Lung	lung
7	chr17:15555200-15567200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:15555200-15587000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:15555400-15564400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr17:15555400-15564600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr17:15555400-15565200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr17:15555400-15566800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr17:15555400-15567000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr17:15555400-15568200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr17:15555400-15568200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr17:15555400-15569000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr17:15555400-15576800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr17:15555400-15585800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr17:15555400-15586600	Weak transcription	Brain Angular Gyrus	brain
20	chr17:15555400-15586600	Weak transcription	Thymus	Thymus
21	chr17:15555400-15587000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr17:15555600-15564600	Weak transcription	Brain Hippocampus Middle	brain
23	chr17:15555600-15565800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr17:15555600-15566400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr17:15555600-15566400	Weak transcription	NHLF	lung
26	chr17:15555600-15567000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr17:15555600-15586800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr17:15555600-15586800	Weak transcription	NHDF-Ad	bronchial
29	chr17:15555600-15587000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr17:15555600-15587200	Weak transcription	Aorta	Aorta
31	chr17:15555800-15565800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr17:15556000-15563800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr17:15556600-15587000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr17:15557800-15564800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr17:15558200-15563600	Enhancers	Stomach Mucosa	stomach
36	chr17:15558600-15565400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr17:15558800-15564400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:15558800-15564400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr17:15558800-15565000	Weak transcription	Fetal Thymus	thymus
40	chr17:15558800-15566000	Weak transcription	Osteobl	bone
41	chr17:15558800-15567000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr17:15558800-15567200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:15558800-15567400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr17:15558800-15586600	Weak transcription	Brain Germinal Matrix	brain
45	chr17:15558800-15587000	Weak transcription	Ovary	ovary
46	chr17:15558800-15587000	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr17:15558800-15587000	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr17:15559000-15565600	Weak transcription	Fetal Intestine Large	intestine
49	chr17:15559000-15566800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr17:15559000-15585800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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