Variant report

Variant	nsv907865
Chromosome Location	chr17:19558722-19575721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:244)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:244 , 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	ARID3A	chr17:19560630-19561122	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:19575285-19576052	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:19562682-19562978	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:19563346-19564460	HepG2	liver:	n/a	n/a
5	CEBPB	chr17:19562650-19563024	ECC-1	luminal epithelium:	n/a	chr17:19562802-19562813
6	CEBPB	chr17:19575341-19575662	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr17:19562620-19563174	HepG2	liver:	n/a	chr17:19562802-19562813
8	CEBPB	chr17:19575320-19575786	HepG2	liver:	n/a	chr17:19575699-19575711
9	CEBPB	chr17:19562580-19563054	ECC-1	luminal epithelium:	n/a	chr17:19562802-19562813
10	CEBPB	chr17:19573735-19573768	HepG2	liver:	n/a	n/a
11	CEBPB	chr17:19562541-19563111	A549	lung:	n/a	chr17:19562802-19562813
12	CEBPB	chr17:19562660-19563010	MCF-7	breast:	n/a	chr17:19562802-19562813
13	CEBPB	chr17:19562565-19562882	HepG2	liver:	n/a	chr17:19562802-19562813
14	CEBPB	chr17:19562649-19562936	Hela-S3	cervix:	n/a	chr17:19562802-19562813
15	CEBPB	chr17:19562637-19562976	A549	lung:	n/a	chr17:19562802-19562813
16	CEBPB	chr17:19562673-19562951	IMR90	lung:	n/a	chr17:19562802-19562813
17	CEBPB	chr17:19563569-19564208	HepG2	liver:	n/a	chr17:19563895-19563906 chr17:19563863-19563875
18	CEBPB	chr17:19562619-19562996	HepG2	liver:	n/a	chr17:19562802-19562813
19	CEBPB	chr17:19575325-19575662	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr17:19563682-19564228	HepG2	liver:	n/a	chr17:19563895-19563906 chr17:19563863-19563875
21	CEBPB	chr17:19575390-19575639	HepG2	liver:	n/a	n/a
22	CEBPB	chr17:19574862-19575817	HepG2	liver:	n/a	chr17:19575699-19575711 chr17:19574983-19574996
23	CEBPB	chr17:19575256-19575733	HepG2	liver:	n/a	chr17:19575699-19575711
24	CEBPB	chr17:19562697-19562890	H1-hESC	embryonic stem cell:	n/a	chr17:19562802-19562813
25	CEBPB	chr17:19562653-19562906	HepG2	liver:	n/a	chr17:19562802-19562813
26	CEBPB	chr17:19562645-19562935	K562	blood:	n/a	chr17:19562802-19562813
27	CEBPB	chr17:19563666-19564041	HepG2	liver:	n/a	chr17:19563895-19563906 chr17:19563863-19563875
28	CEBPD	chr17:19575262-19575592	HepG2	liver:	n/a	n/a
29	CHD2	chr17:19559477-19559560	HepG2	liver:	n/a	n/a
30	CHD2	chr17:19567306-19567424	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr17:19575704-19576160	HCT-116	colon:	n/a	n/a
32	CTCF	chr17:19571570-19571607	GM10248	blood:	n/a	n/a
33	CTCF	chr17:19574840-19574990	AG09319	gingival:	n/a	n/a
34	CTCF	chr17:19575720-19575970	HAc	cerebellar:	n/a	n/a
35	CTCF	chr17:19575460-19575610	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr17:19574840-19574990	AG10803	skin:	n/a	n/a
37	CTCF	chr17:19574880-19575030	AG09319	gingival:	n/a	n/a
38	CTCF	chr17:19574900-19575050	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr17:19575520-19575670	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr17:19575240-19575390	AG10803	skin:	n/a	n/a
41	E2F4	chr17:19561393-19561619	MCF10A-Er-Src	breast:	n/a	n/a
42	ELF1	chr17:19575437-19576029	HepG2	liver:	n/a	chr17:19575896-19575907
43	ELF1	chr17:19563729-19564061	HepG2	liver:	n/a	n/a
44	EP300	chr17:19562537-19563028	HepG2	liver:	n/a	n/a
45	EP300	chr17:19563343-19564416	HepG2	liver:	n/a	chr17:19563816-19563826
46	EP300	chr17:19575271-19575846	HepG2	liver:	n/a	n/a
47	EP300	chr17:19559974-19560717	ECC-1	luminal epithelium:	n/a	n/a
48	EP300	chr17:19563471-19564304	HepG2	liver:	n/a	chr17:19563816-19563826
49	EP300	chr17:19562557-19562910	HepG2	liver:	n/a	n/a
50	EP300	chr17:19575085-19576021	HepG2	liver:	n/a	chr17:19575898-19575907

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:19568270-19568320	A549	lung:	n/a
2	chr17:19568270-19568320	AG10803	skin:	n/a
3	chr17:19568270-19568320	SK-N-SH_RA	brain:	n/a
4	chr17:19568270-19568320	HUVEC	blood vessel:	n/a
5	chr17:19568270-19568320	AG09319	gingival:	n/a
6	chr17:19568270-19568320	GM12892	blood:	n/a
7	chr17:19568270-19568320	H1-hESC	embryonic stem cell:	embryo
8	chr17:19568270-19568320	NB4	blood:	n/a
9	chr17:19568270-19568320	HRPEpiC	eye:	n/a
10	chr17:19568270-19568320	HCPEpiC	choroid plexus:	n/a
11	chr17:19568270-19568320	AG04449	skin:	fetal
12	chr17:19568270-19568320	U87	brain:	n/a
13	chr17:19568270-19568320	HL-60	blood:	n/a
14	chr17:19568270-19568320	NT2-D1	testis:	n/a
15	chr17:19568270-19568320	HPAEpiC	pulmonary alveolar:	n/a
16	chr17:19568270-19568320	PFSK-1	brain:	n/a
17	chr17:19568270-19568320	NH-A	brain:	n/a
18	chr17:19568270-19568320	GM12891	blood:	n/a
19	chr17:19568270-19568320	ECC-1	luminal epithelium:	n/a
20	chr17:19568270-19568320	LNCaP	prostate:	n/a
21	chr17:19568270-19568320	PrEC	prostate:	n/a
22	chr17:19568270-19568320	HCF	heart:	n/a
23	chr17:19568270-19568320	HIPEpiC	eye:	n/a
24	chr17:19568270-19568320	HNPCEpiC	eye:	n/a
25	chr17:19568270-19568320	IMR90	lung:	fetal
26	chr17:19568270-19568320	GM12878	blood:	n/a
27	chr17:19568270-19568320	HEK293	kidney:	embryo
28	chr17:19568270-19568320	HCT-116	colon:	n/a
29	chr17:19568270-19568320	SK-N-MC	brain:	n/a
30	chr17:19568270-19568320	HepG2	liver:	n/a
31	chr17:19568270-19568320	Jurkat	blood:	n/a
32	chr17:19568270-19568320	SAEC	small airway:	n/a
33	chr17:19568270-19568320	ProgFib	skin:	n/a
34	chr17:19568270-19568320	ovcar-3	ovarian:	n/a
35	chr17:19568270-19568320	BE2_C	brain:	n/a
36	chr17:19568270-19568320	Caco-2	colon:	n/a
37	chr17:19568270-19568320	GM19239	blood:	n/a
38	chr17:19568270-19568320	Hepatocyte	liver:	n/a
39	chr17:19568270-19568320	HEEpiC	esophagus:	n/a
40	chr17:19568270-19568320	HRE	kidney:	n/a
41	chr17:19568270-19568320	MCF10A-Er-Src	breast:	n/a
42	chr17:19568270-19568320	HAEpiC	amniotic membrane:	n/a
43	chr17:19568270-19568320	T-47D	breast:	n/a
44	chr17:19568270-19568320	RPTEC	kidney:	n/a
45	chr17:19568270-19568320	NHDF-neo	bronchial:	n/a
46	chr17:19568270-19568320	PANC-1	pancreas:	n/a
47	chr17:19568270-19568320	NHBE	bronchial:	n/a
48	chr17:19568270-19568320	HCM	heart:	n/a
49	chr17:19568270-19568320	SK-N-SH	brain:	n/a
50	chr17:19568270-19568320	MCF-7	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:19569611..19572312-chr17:19574479..19577295,2	MCF-7	breast:
2	chr17:19564551..19566163-chr17:19566583..19568566,2	MCF-7	breast:
3	chr17:19565101..19568606-chr17:19573068..19575796,3	MCF-7	breast:
4	chr17:19549675..19554690-chr17:19558689..19564889,9	MCF-7	breast:
5	chr17:19565101..19568606-chr17:19573068..19575796,3	MCF-7	breast:
6	chr17:19552797..19555708-chr17:19557293..19559431,2	MCF-7	breast:
7	chr17:19550266..19552397-chr17:19557719..19560014,2	MCF-7	breast:
8	chr17:19558329..19562006-chr17:19563141..19565959,3	MCF-7	breast:
9	chr17:19265895..19266829-chr17:19575547..19576368,3	MCF-7	breast:
10	chr17:19564551..19566163-chr17:19566583..19568566,2	MCF-7	breast:
11	chr17:19552711..19555521-chr17:19564350..19566731,2	MCF-7	breast:
12	chr17:19558329..19562006-chr17:19563141..19565959,3	MCF-7	breast:
13	chr17:19550468..19552548-chr17:19574981..19577039,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC115989.1.1-6	chr17:19575665-19575744	NONHSAT146516

No data

Variant related genes	Relation type
ALDH3A2	TF binding region
ENSG00000252349	TF binding region
ALDH3A2	CpG island
ENSG00000252349	CpG island
ENSG00000108641	chromatin interactions
ENSG00000252349	chromatin interactions
ENSG00000264932	chromatin interactions
ENSG00000072210	chromatin interactions

Extended variants
information (count: 622 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4646796	chr17:19558722-19558723	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs578057954	chr17:19558754-19558755	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs149506573	chr17:19558773-19558774	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs146039275	chr17:19558815-19558816	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs573845793	chr17:19558860-19558861	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs542549106	chr17:19558897-19558898	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs562322161	chr17:19558943-19558944	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs112996084	chr17:19558971-19558972	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs544819086	chr17:19558982-19558983	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs564786886	chr17:19558986-19558987	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs138744243	chr17:19559064-19559065	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs962801	chr17:19559095-19559096	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs560977763	chr17:19559107-19559108	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs114584482	chr17:19559126-19559127	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs549723691	chr17:19559132-19559133	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs569589874	chr17:19559155-19559156	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs5819686	chr17:19559185-19559186	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs531902653	chr17:19559215-19559216	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs575438894	chr17:19559219-19559220	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs186946645	chr17:19559228-19559229	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs571649890	chr17:19559262-19559263	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs551212203	chr17:19559293-19559294	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs141548563	chr17:19559328-19559329	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs538123586	chr17:19559336-19559337	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs553865407	chr17:19559359-19559360	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs146171081	chr17:19559362-19559363	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs536269001	chr17:19559370-19559371	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs2072333	chr17:19559371-19559372	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs575941724	chr17:19559373-19559374	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs962800	chr17:19559468-19559469	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs558763424	chr17:19559473-19559474	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs572036205	chr17:19559474-19559475	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs76113935	chr17:19559529-19559530	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs74978516	chr17:19559537-19559538	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs529684475	chr17:19559564-19559565	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs148429983	chr17:19559613-19559614	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs117135285	chr17:19559620-19559621	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs2072332	chr17:19559623-19559624	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs370983032	chr17:19559629-19559630	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs374403134	chr17:19559645-19559646	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs181290597	chr17:19559656-19559657	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs75565573	chr17:19559709-19559710	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs370609228	chr17:19559720-19559721	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs571845978	chr17:19559727-19559728	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs387906254	chr17:19559728-19559729	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs72547561	chr17:19559736-19559737	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs145431941	chr17:19559737-19559738	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs371478620	chr17:19559738-19559739	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs72547562	chr17:19559758-19559759	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs72547563	chr17:19559761-19559762	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	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
Colorectal cancer	16774939	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
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
Autism	22543975	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19553200-19566800	Weak transcription	Primary B cells from cord blood	blood
2	chr17:19553200-19577400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr17:19553200-19580000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr17:19553400-19566400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr17:19553800-19560000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr17:19554400-19559400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr17:19554800-19574400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr17:19555000-19560400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr17:19555000-19561400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
10	chr17:19555000-19561400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:19555000-19563400	Strong transcription	Fetal Stomach	stomach
12	chr17:19555000-19568800	Weak transcription	NH-A	brain
13	chr17:19555000-19581800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr17:19555000-19582800	Weak transcription	HUVEC	blood vessel
15	chr17:19555200-19559200	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr17:19555200-19566400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr17:19555200-19566600	Weak transcription	NHDF-Ad	bronchial
18	chr17:19555200-19569800	Strong transcription	Fetal Muscle Trunk	muscle
19	chr17:19555200-19576400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr17:19555400-19559000	Weak transcription	Psoas Muscle	Psoas
21	chr17:19555400-19570000	Strong transcription	Fetal Muscle Leg	muscle
22	chr17:19555600-19562200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr17:19555600-19567200	Weak transcription	Right Atrium	heart
24	chr17:19555600-19569800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr17:19555600-19578600	Weak transcription	Small Intestine	intestine
26	chr17:19555800-19559000	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr17:19555800-19559200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr17:19555800-19560800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
29	chr17:19555800-19560800	Strong transcription	Left Ventricle	heart
30	chr17:19555800-19561000	Strong transcription	Fetal Brain Female	brain
31	chr17:19555800-19561600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr17:19555800-19562400	Strong transcription	Brain Hippocampus Middle	brain
33	chr17:19556000-19561400	Strong transcription	Cortex derived primary cultured neurospheres	brain
34	chr17:19556200-19559200	Strong transcription	A549	lung
35	chr17:19556200-19560800	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr17:19556200-19561200	Strong transcription	Colonic Mucosa	Colon
37	chr17:19556200-19569800	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr17:19556400-19558800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr17:19556400-19559200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
40	chr17:19556400-19559800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr17:19556400-19559800	Strong transcription	Fetal Lung	lung
42	chr17:19556400-19561200	Strong transcription	Brain Inferior Temporal Lobe	brain
43	chr17:19556400-19563600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr17:19556600-19558800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
45	chr17:19556600-19562200	Strong transcription	Adipose Nuclei	Adipose
46	chr17:19556600-19569800	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr17:19556800-19558800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr17:19556800-19559200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr17:19556800-19560200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr17:19556800-19560800	Strong transcription	Sigmoid Colon	Sigmoid Colon

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