Variant report

Variant	nsv907780
Chromosome Location	chr17:18317188-18445923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:1037)
Chromatin interactive
region (count:0)
LncRNA
region (count:77)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:18355389-18355575	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr17:18362390-18362672	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr17:18411051-18411300	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
4	BATF	chr17:18396259-18396664	GM12878	blood:	n/a	chr17:18396479-18396490
5	BATF	chr17:18379787-18380078	GM12878	blood:	n/a	n/a
6	BATF	chr17:18396335-18396562	GM12878	blood:	n/a	chr17:18396479-18396490
7	BATF	chr17:18410950-18411370	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
8	BATF	chr17:18379801-18380128	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:18379825-18380074	GM12878	blood:	n/a	n/a
10	BCL11A	chr17:18379766-18380162	GM12878	blood:	n/a	n/a
11	BCL11A	chr17:18424410-18424651	GM12878	blood:	n/a	n/a
12	BCL11A	chr17:18378052-18378384	GM12878	blood:	n/a	n/a
13	BHLHE40	chr17:18396537-18396565	K562	blood:	n/a	n/a
14	BHLHE40	chr17:18424672-18424862	GM12878	blood:	n/a	n/a
15	CEBPB	chr17:18318052-18318134	A549	lung:	n/a	chr17:18318100-18318113 chr17:18318102-18318113 chr17:18318102-18318111
16	CEBPB	chr17:18362210-18362602	Hela-S3	cervix:	n/a	chr17:18362363-18362376
17	CEBPB	chr17:18322055-18322251	K562	blood:	n/a	n/a
18	CEBPB	chr17:18362356-18362662	IMR90	lung:	n/a	chr17:18362363-18362376
19	CEBPB	chr17:18322048-18322324	K562	blood:	n/a	n/a
20	CEBPB	chr17:18322037-18322380	K562	blood:	n/a	n/a
21	CEBPB	chr17:18317946-18318165	IMR90	lung:	n/a	chr17:18318100-18318113 chr17:18318102-18318113 chr17:18318102-18318111
22	CTCF	chr17:18345872-18345996	GM10266	blood:	n/a	n/a
23	CTCF	chr17:18350694-18350758	GM13976	blood:	n/a	n/a
24	CTCF	chr17:18400595-18400599	GM13976	blood:	n/a	n/a
25	CTCF	chr17:18345514-18345751	A549	lung:	n/a	n/a
26	CTCF	chr17:18345520-18345670	NHLF	lung:	n/a	n/a
27	CTCF	chr17:18403698-18403880	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:18345520-18345670	HVMF	connective:	n/a	n/a
29	CTCF	chr17:18400495-18400709	IMR90	lung:	n/a	n/a
30	CTCF	chr17:18345500-18345650	HepG2	liver:	n/a	n/a
31	CTCF	chr17:18345520-18345670	GM12873	blood:	n/a	n/a
32	CTCF	chr17:18400380-18400530	GM06990	blood:	n/a	n/a
33	CTCF	chr17:18345520-18345670	NB4	blood:	n/a	n/a
34	CTCF	chr17:18400514-18400622	GM12878	blood:	n/a	n/a
35	CTCF	chr17:18381227-18381311	NHEK	skin:	n/a	chr17:18381256-18381277 chr17:18381261-18381279 chr17:18381264-18381274 chr17:18381262-18381278
36	CTCF	chr17:18400495-18400662	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:18428453-18428620	GM10248	blood:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
38	CTCF	chr17:18429619-18429651	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr17:18403663-18403997	A549	lung:	n/a	n/a
40	CTCF	chr17:18403702-18403899	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr17:18324863-18325061	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr17:18400484-18400661	GM19238	blood:	n/a	n/a
43	CTCF	chr17:18345500-18345650	GM12875	blood:	n/a	n/a
44	CTCF	chr17:18400380-18400530	A549	lung:	n/a	n/a
45	CTCF	chr17:18355273-18355644	NHEK	skin:	n/a	chr17:18355490-18355499
46	CTCF	chr17:18400380-18400530	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr17:18400528-18400575	GM13976	blood:	n/a	n/a
48	CTCF	chr17:18348704-18348814	GM13976	blood:	n/a	n/a
49	CTCF	chr17:18391475-18391562	GM19238	blood:	n/a	n/a
50	CTCF	chr17:18403626-18403896	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18428092-18428142	HCPEpiC	choroid plexus:	n/a
2	chr17:18397849-18397899	GM06990	blood:	n/a
3	chr17:18378879-18378929	BJ	skin:	n/a
4	chr17:18431043-18431093	K562	blood:	n/a
5	chr17:18317909-18317959	SAEC	small airway:	n/a
6	chr17:18380354-18380404	LNCaP	prostate:	n/a
7	chr17:18432149-18432199	RPTEC	kidney:	n/a
8	chr17:18432149-18432199	HIPEpiC	eye:	n/a
9	chr17:18324790-18324840	RPTEC	kidney:	n/a
10	chr17:18380159-18380209	GM19239	blood:	n/a
11	chr17:18379129-18379179	PANC-1	pancreas:	n/a
12	chr17:18432149-18432199	Jurkat	blood:	n/a
13	chr17:18317909-18317959	ovcar-3	ovarian:	n/a
14	chr17:18421335-18421385	AG09309	skin:	n/a
15	chr17:18421335-18421385	NHDF-neo	bronchial:	n/a
16	chr17:18324895-18324945	T-47D	breast:	n/a
17	chr17:18379129-18379179	AG09319	gingival:	n/a
18	chr17:18397849-18397899	AG10803	skin:	n/a
19	chr17:18317909-18317959	T-47D	breast:	n/a
20	chr17:18432149-18432199	HepG2	liver:	n/a
21	chr17:18432149-18432199	LNCaP	prostate:	n/a
22	chr17:18429951-18430001	SK-N-MC	brain:	n/a
23	chr17:18324895-18324945	ECC-1	luminal epithelium:	n/a
24	chr17:18380354-18380404	HPAEpiC	pulmonary alveolar:	n/a
25	chr17:18317909-18317959	MCF10A-Er-Src	breast:	n/a
26	chr17:18397849-18397899	K562	blood:	n/a
27	chr17:18419896-18419946	SAEC	small airway:	n/a
28	chr17:18419896-18419946	SK-N-MC	brain:	n/a
29	chr17:18324895-18324945	ovcar-3	ovarian:	n/a
30	chr17:18397849-18397899	HCT-116	colon:	n/a
31	chr17:18430908-18430958	LNCaP	prostate:	n/a
32	chr17:18429951-18430001	HL-60	blood:	n/a
33	chr17:18380159-18380209	T-47D	breast:	n/a
34	chr17:18378879-18378929	HepG2	liver:	n/a
35	chr17:18428092-18428142	AoSMC	blood vessel:	n/a
36	chr17:18380159-18380209	BE2_C	brain:	n/a
37	chr17:18397849-18397899	HMEC	breast:	n/a
38	chr17:18430908-18430958	HMEC	breast:	n/a
39	chr17:18430908-18430958	SK-N-SH_RA	brain:	n/a
40	chr17:18421335-18421385	SKMC	muscle:	n/a
41	chr17:18419896-18419946	PFSK-1	brain:	n/a
42	chr17:18317909-18317959	PrEC	prostate:	n/a
43	chr17:18429951-18430001	MCF-7	breast:	n/a
44	chr17:18428092-18428142	HAEpiC	amniotic membrane:	n/a
45	chr17:18429951-18430001	SK-N-SH	brain:	n/a
46	chr17:18421335-18421385	ECC-1	luminal epithelium:	n/a
47	chr17:18379129-18379179	GM06990	blood:	n/a
48	chr17:18432149-18432199	U87	brain:	n/a
49	chr17:18324790-18324840	Hepatocyte	liver:	n/a
50	chr17:18419896-18419946	BE2_C	brain:	n/a

No data

(count:77 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
2	lnc-AL353997.5.1-1	chr17:18328108-18328411	ENSG00000205266.5
3	lnc-FAM106A-2	chr17:18422796-18422988	NONHSAT146382
4	lnc-FAM106A-2	chr17:18420604-18420787	NONHSAT146381
5	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
6	lnc-FAM106A-2	chr17:18436661-18437376	ENSG00000273018.1
7	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
8	lnc-FAM106A-2	chr17:18435820-18436348	ENSG00000273018.1
9	lnc-FAM106A-2	chr17:18427457-18427714	ENSG00000273018.1
10	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
11	lnc-FAM106A-2	chr17:18436395-18436705	NONHSAT146384
12	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
13	lnc-FAM106A-2	chr17:18431887-18431914	ENSG00000273018.1
14	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
15	lnc-FAM106A-2	chr17:18422958-18422988	ENSG00000273018.1
16	lnc-AL353997.5.1-2	chr17:18317464-18317702	XLOC_012131
17	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
18	lnc-FAM106A-2	chr17:18436661-18436852	ENSG00000273018.1
19	lnc-AL353997.5.1-6	chr17:18395483-18395859	NONHSAT146378
20	lnc-AL353997.5.1-6	chr17:18395939-18396053	NONHSAT146378
21	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
22	lnc-FAM106A-2	chr17:18435820-18436192	ENSG00000273018.1
23	lnc-FAM106A-2	chr17:18420633-18420787	NONHSAT146382
24	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
25	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
26	lnc-FAM106A-2	chr17:18445402-18445501	ENSG00000273018.1
27	lnc-AL353997.5.1-2	chr17:18317468-18317702	XLOC_012131
28	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
29	lnc-FAM106A-2	chr17:18436661-18436705	ENSG00000273018.1
30	lnc-FAM106A-2	chr17:18430884-18431074	ENSG00000273018.1
31	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
32	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
33	lnc-FAM106A-2	chr17:18427091-18427191	ENSG00000273018.1
34	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
35	lnc-FAM106A-2	chr17:18426965-18427191	ENSG00000273018.1
36	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
37	lnc-FAM106A-1	chr17:18427880-18430160	NR_026809
38	lnc-AL353997.5.1-4	chr17:18343740-18343831	NONHSAT146373
39	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
40	lnc-FAM106A-2	chr17:18445402-18445501	ENSG00000273018.1
41	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
42	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
43	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
44	lnc-FAM106A-2	chr17:18427120-18427191	ENSG00000273018.1
45	lnc-FAM106A-2	chr17:18420604-18420787	ENSG00000273018.1
46	lnc-FAM106A-2	chr17:18430884-18431074	ENSG00000273018.1
47	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
48	lnc-FAM106A-2	chr17:18444241-18444277	NONHSAT146384
49	lnc-FAM106A-2	chr17:18436661-18436946	ENSG00000273018.1
50	lnc-AL353997.5.1-2	chr17:18317464-18317623	XLOC_012131

No data

Variant related genes	Relation type
ENSG00000205266	TF binding region
USP32P2	TF binding region
ENSG00000267492	TF binding region
KRT16P1	TF binding region
YWHAEP2	TF binding region
KRT17P2	TF binding region
SRP68P2	TF binding region
NOS2P2	TF binding region
KRT16P4	TF binding region
LGALS9C	TF binding region
ENSG00000227919	TF binding region
TNPO1P2	TF binding region
ENSG00000240279	TF binding region
FAM106A	TF binding region
ENSG00000273018	TF binding region
ENSG00000205266	CpG island
USP32P2	CpG island
ENSG00000267492	CpG island
KRT16P1	CpG island
YWHAEP2	CpG island
KRT17P2	CpG island
SRP68P2	CpG island
NOS2P2	CpG island
KRT16P4	CpG island
LGALS9C	CpG island
ENSG00000227919	CpG island
TNPO1P2	CpG island
ENSG00000240279	CpG island
FAM106A	CpG island
ENSG00000273018	CpG island
KIAA0664	miRNA target sites

Extended variants
information (count: 2637 )
Associated
traits (count: 169 )

Variant overlapped rSNPs/rCNVs (count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56402445	chr17:18317188-18317189	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs531863936	chr17:18317278-18317279	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs551251293	chr17:18317328-18317329	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565073130	chr17:18317482-18317483	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs527518718	chr17:18317492-18317493	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs552904305	chr17:18317494-18317495	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs200303201	chr17:18317533-18317534	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs567266974	chr17:18317551-18317552	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs535807705	chr17:18317552-18317553	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs549371412	chr17:18317628-18317629	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs569384779	chr17:18317677-18317678	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs538742646	chr17:18317690-18317691	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs201303311	chr17:18317745-18317746	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374782601	chr17:18317760-18317761	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139128307	chr17:18317789-18317790	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs534167638	chr17:18317838-18317839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554464891	chr17:18317846-18317847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185169890	chr17:18317870-18317871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543015047	chr17:18317934-18317935	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs562884203	chr17:18317939-18317940	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs576390522	chr17:18318029-18318030	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs367657991	chr17:18318035-18318036	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs565280164	chr17:18318040-18318041	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs188743495	chr17:18318101-18318102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs547286332	chr17:18318127-18318128	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs191646081	chr17:18318153-18318154	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs529962173	chr17:18318171-18318172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201087969	chr17:18318172-18318173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60708150	chr17:18318173-18318174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183782612	chr17:18318177-18318178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140594109	chr17:18318184-18318185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565366825	chr17:18318186-18318187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188468028	chr17:18318196-18318197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534355502	chr17:18318216-18318217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554428319	chr17:18318251-18318252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs567924509	chr17:18318310-18318311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180853810	chr17:18318324-18318325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556922276	chr17:18318347-18318348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576379948	chr17:18318368-18318369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545110857	chr17:18318369-18318370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373970179	chr17:18318439-18318440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558970822	chr17:18318495-18318496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112973336	chr17:18318521-18318522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148908109	chr17:18318593-18318594	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs199866995	chr17:18318610-18318611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371720577	chr17:18318700-18318701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201667602	chr17:18318734-18318735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572452880	chr17:18318802-18318803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528031842	chr17:18318884-18318885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540801731	chr17:18318890-18318891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:169)

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
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
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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Sezary syndrome	18413736	CNVD
Medulloblastoma	16783165	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Tetralogy of Fallot	22912587	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18316200-18317400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr17:18316600-18317400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr17:18316600-18318000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr17:18316800-18317200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr17:18316800-18317200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr17:18316800-18317200	Weak transcription	Fetal Thymus	thymus
7	chr17:18316800-18317400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr17:18316800-18317600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr17:18317000-18317200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr17:18317000-18317200	Flanking Active TSS	Dnd41	blood
11	chr17:18317000-18317400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr17:18317200-18317400	Enhancers	Fetal Thymus	thymus
13	chr17:18317200-18317600	Enhancers	Dnd41	blood
14	chr17:18317200-18318000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr17:18317400-18317600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr17:18317600-18318000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr17:18317600-18318000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr17:18317600-18319800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr17:18318000-18318200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr17:18318000-18320000	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr17:18320200-18320400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr17:18320400-18320600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:18320400-18320600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr17:18324800-18326200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr17:18324800-18326400	Enhancers	Fetal Thymus	thymus
26	chr17:18333000-18333400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr17:18339400-18339800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr17:18351000-18351400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr17:18351200-18351400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr17:18351200-18351400	Enhancers	NHEK	skin
31	chr17:18351400-18352800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr17:18351400-18353000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:18351400-18355400	Weak transcription	NHEK	skin
34	chr17:18352800-18353400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:18353000-18353200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr17:18353200-18353600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr17:18353400-18353600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:18353600-18354400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr17:18353600-18354600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr17:18354400-18354600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr17:18354600-18355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr17:18354600-18355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr17:18355400-18355600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr17:18355400-18355600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr17:18355400-18355800	Enhancers	NHEK	skin
46	chr17:18355600-18355800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:18355600-18355800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr17:18361000-18362400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr17:18361600-18361800	Enhancers	Hela-S3	cervix
50	chr17:18361600-18362000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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