Variant report

Variant	nsv511593
Chromosome Location	chr17:18322349-18445526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:978)
Chromatin interactive
region (count:0)
LncRNA
region (count:74)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:18362390-18362672	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr17:18355389-18355575	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr17:18410950-18411370	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
4	BATF	chr17:18379801-18380128	GM12878	blood:	n/a	n/a
5	BATF	chr17:18396335-18396562	GM12878	blood:	n/a	chr17:18396479-18396490
6	BATF	chr17:18411051-18411300	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
7	BATF	chr17:18396259-18396664	GM12878	blood:	n/a	chr17:18396479-18396490
8	BATF	chr17:18379787-18380078	GM12878	blood:	n/a	n/a
9	BCL11A	chr17:18424410-18424651	GM12878	blood:	n/a	n/a
10	BCL11A	chr17:18379825-18380074	GM12878	blood:	n/a	n/a
11	BCL11A	chr17:18379766-18380162	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	chr17:18362210-18362602	Hela-S3	cervix:	n/a	chr17:18362363-18362376
16	CEBPB	chr17:18362356-18362662	IMR90	lung:	n/a	chr17:18362363-18362376
17	CEBPB	chr17:18322037-18322380	K562	blood:	n/a	n/a
18	CTCF	chr17:18345520-18345670	RPTEC	kidney:	n/a	n/a
19	CTCF	chr17:18428466-18428592	GM12892	blood:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
20	CTCF	chr17:18349102-18349152	LNCaP	prostate:	n/a	n/a
21	CTCF	chr17:18348546-18348582	LNCaP	prostate:	n/a	n/a
22	CTCF	chr17:18400380-18400530	BE2_C	brain:	n/a	n/a
23	CTCF	chr17:18403628-18403966	A549	lung:	n/a	n/a
24	CTCF	chr17:18428466-18428597	K562	blood:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
25	CTCF	chr17:18400800-18400858	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr17:18345573-18345708	Medullo	brain:	n/a	n/a
27	CTCF	chr17:18400380-18400530	GM06990	blood:	n/a	n/a
28	CTCF	chr17:18445044-18445201	Lung_OC	lung:	n/a	n/a
29	CTCF	chr17:18403979-18404072	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr17:18345580-18345730	HEK293	kidney:	n/a	n/a
31	CTCF	chr17:18380870-18380944	GM19239	blood:	n/a	n/a
32	CTCF	chr17:18345520-18345670	NB4	blood:	n/a	n/a
33	CTCF	chr17:18381253-18381295	Gliobla	brain:	n/a	chr17:18381256-18381277 chr17:18381261-18381279 chr17:18381264-18381274 chr17:18381262-18381278
34	CTCF	chr17:18345521-18345760	GM19239	blood:	n/a	n/a
35	CTCF	chr17:18345418-18345840	K562	blood:	n/a	n/a
36	CTCF	chr17:18428313-18428780	A549	lung:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
37	CTCF	chr17:18399629-18399702	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr17:18403707-18403887	GM19240	blood:	n/a	n/a
39	CTCF	chr17:18403674-18403912	Gliobla	brain:	n/a	n/a
40	CTCF	chr17:18428440-18428607	A549	lung:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
41	CTCF	chr17:18345484-18345792	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr17:18403713-18403867	GM12891	blood:	n/a	n/a
43	CTCF	chr17:18400495-18400662	MCF-7	breast:	n/a	n/a
44	CTCF	chr17:18418276-18418321	GM20000	blood:	n/a	n/a
45	CTCF	chr17:18400489-18400644	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr17:18345514-18345751	A549	lung:	n/a	n/a
47	CTCF	chr17:18403655-18404117	K562	blood:	n/a	n/a
48	CTCF	chr17:18345520-18345670	GM12872	blood:	n/a	n/a
49	CTCF	chr17:18428441-18428633	MCF-7	breast:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
50	CTCF	chr17:18400313-18400844	A549	lung:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18325001-18325051	U87	brain:	n/a
2	chr17:18397849-18397899	GM19239	blood:	n/a
3	chr17:18325001-18325051	U87	brain:	n/a
4	chr17:18397849-18397899	GM19239	blood:	n/a
5	chr17:18431043-18431093	Hela-S3	cervix:	n/a
6	chr17:18419896-18419946	NB4	blood:	n/a
7	chr17:18380159-18380209	AG09309	skin:	n/a
8	chr17:18428092-18428142	HCT-116	colon:	n/a
9	chr17:18380159-18380209	SK-N-MC	brain:	n/a
10	chr17:18430908-18430958	HCT-116	colon:	n/a
11	chr17:18378879-18378929	AG04450	lung:	fetal
12	chr17:18325001-18325051	SAEC	small airway:	n/a
13	chr17:18379129-18379179	SK-N-MC	brain:	n/a
14	chr17:18326064-18326114	GM19239	blood:	n/a
15	chr17:18326064-18326114	PrEC	prostate:	n/a
16	chr17:18380354-18380404	HRCEpiC	kidney:	n/a
17	chr17:18324790-18324840	HMEC	breast:	n/a
18	chr17:18428092-18428142	K562	blood:	n/a
19	chr17:18430908-18430958	HCPEpiC	choroid plexus:	n/a
20	chr17:18430908-18430958	ECC-1	luminal epithelium:	n/a
21	chr17:18397849-18397899	HIPEpiC	eye:	n/a
22	chr17:18324790-18324840	HCF	heart:	n/a
23	chr17:18430908-18430958	NHBE	bronchial:	n/a
24	chr17:18397849-18397899	HCF	heart:	n/a
25	chr17:18428092-18428142	HepG2	liver:	n/a
26	chr17:18428092-18428142	CMK	blood:	n/a
27	chr17:18429951-18430001	U87	brain:	n/a
28	chr17:18380354-18380404	HIPEpiC	eye:	n/a
29	chr17:18379129-18379179	HEEpiC	esophagus:	n/a
30	chr17:18380354-18380404	MCF10A-Er-Src	breast:	n/a
31	chr17:18431043-18431093	AG09319	gingival:	n/a
32	chr17:18326064-18326114	NHBE	bronchial:	n/a
33	chr17:18397849-18397899	HRPEpiC	eye:	n/a
34	chr17:18397849-18397899	SK-N-SH	brain:	n/a
35	chr17:18324790-18324840	SK-N-SH_RA	brain:	n/a
36	chr17:18428092-18428142	BJ	skin:	n/a
37	chr17:18421335-18421385	PrEC	prostate:	n/a
38	chr17:18429951-18430001	GM12878	blood:	n/a
39	chr17:18431043-18431093	GM12892	blood:	n/a
40	chr17:18379129-18379179	BE2_C	brain:	n/a
41	chr17:18325001-18325051	PFSK-1	brain:	n/a
42	chr17:18324895-18324945	ProgFib	skin:	n/a
43	chr17:18429951-18430001	MCF-7	breast:	n/a
44	chr17:18432149-18432199	HPAEpiC	pulmonary alveolar:	n/a
45	chr17:18432149-18432199	SK-N-SH	brain:	n/a
46	chr17:18419896-18419946	ovcar-3	ovarian:	n/a
47	chr17:18326064-18326114	SKMC	muscle:	n/a
48	chr17:18378879-18378929	AoSMC	blood vessel:	n/a
49	chr17:18324895-18324945	HEEpiC	esophagus:	n/a
50	chr17:18419896-18419946	HIPEpiC	eye:	n/a

No data

(count:74 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM106A-2	chr17:18427091-18427711	ENSG00000273018.1
2	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
3	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
4	lnc-AL353997.5.1-4	chr17:18343220-18343625	NONHSAT146373
5	lnc-FAM106A-2	chr17:18427091-18427191	ENSG00000273018.1
6	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
7	lnc-FAM106A-2	chr17:18426379-18426609	NONHSAT146382
8	lnc-FAM106A-2	chr17:18445402-18445501	ENSG00000273018.1
9	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
10	lnc-AL353997.5.1-1	chr17:18328108-18328411	ENSG00000205266.5
11	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
12	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
13	lnc-AL353997.5.1-4	chr17:18344268-18344334	NONHSAT146373
14	lnc-FAM106A-2	chr17:18422796-18422988	NONHSAT146382
15	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
16	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
17	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
18	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
19	lnc-FAM106A-2	chr17:18420604-18420787	NONHSAT146381
20	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
21	lnc-FAM106A-2	chr17:18420604-18420787	ENSG00000273018.1
22	lnc-FAM106A-2	chr17:18426965-18427191	ENSG00000273018.1
23	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
24	lnc-FAM106A-2	chr17:18444241-18444277	NONHSAT146384
25	lnc-FAM106A-2	chr17:18431887-18432298	ENSG00000273018.1
26	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
27	lnc-FAM106A-2	chr17:18436661-18436946	ENSG00000273018.1
28	lnc-FAM106A-2	chr17:18436395-18436705	NONHSAT146384
29	lnc-FAM106A-2	chr17:18422958-18422988	ENSG00000273018.1
30	lnc-AL353997.5.1-1	chr17:18327635-18327951	ENSG00000205266.5
31	lnc-FAM106A-2	chr17:18436661-18436852	ENSG00000273018.1
32	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
33	lnc-FAM106A-2	chr17:18436661-18437376	ENSG00000273018.1
34	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
35	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
36	lnc-FAM106A-2	chr17:18424393-18424459	ENSG00000273018.1
37	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
38	lnc-FAM106A-2	chr17:18431887-18432126	NONHSAT146381
39	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
40	lnc-FAM106A-2	chr17:18427457-18427714	ENSG00000273018.1
41	lnc-FAM106A-2	chr17:18427091-18427191	ENSG00000273018.1
42	lnc-AL353997.5.1-6	chr17:18395483-18395859	NONHSAT146378
43	lnc-FAM106A-2	chr17:18430884-18431074	ENSG00000273018.1
44	lnc-FAM106A-2	chr17:18430884-18431074	ENSG00000273018.1
45	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
46	lnc-FAM106A-2	chr17:18431887-18432642	ENSG00000273018.1
47	lnc-AL353997.5.1-4	chr17:18343740-18343831	NONHSAT146373
48	lnc-FAM106A-2	chr17:18445402-18445501	ENSG00000273018.1
49	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
50	lnc-FAM106A-2	chr17:18431900-18432061	ENSG00000273018.1

No data

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

Extended variants
information (count: 2472 )
Associated
traits (count: 169 )

Variant overlapped rSNPs/rCNVs (count:2472 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550722317	chr17:18322356-18322357	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs188865676	chr17:18324830-18324831	Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs547009001	chr17:18324844-18324845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566986190	chr17:18324871-18324872	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs535928617	chr17:18324891-18324892	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs556015081	chr17:18324898-18324899	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
7	rs9912832	chr17:18324900-18324901	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
8	rs146699416	chr17:18324901-18324902	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
9	rs558389239	chr17:18324906-18324907	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
10	rs193221006	chr17:18324917-18324918	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
11	rs543301	chr17:18324946-18324947	Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs573901213	chr17:18324996-18324997	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs554225780	chr17:18325002-18325003	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
14	rs574109452	chr17:18325003-18325004	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
15	rs543103971	chr17:18325016-18325017	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
16	rs562881252	chr17:18325030-18325031	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
17	rs142037918	chr17:18325047-18325048	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs56076360	chr17:18325051-18325052	Enhancers	TF binding region CpG island	2 gene(s)	Overlapped CNVs	mRNA abundance
19	rs544875873	chr17:18325074-18325075	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs4924860	chr17:18325085-18325086	Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs368736834	chr17:18325086-18325087	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs527594680	chr17:18325118-18325119	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs547319998	chr17:18325135-18325136	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs566902416	chr17:18325151-18325152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529689576	chr17:18325167-18325168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549838657	chr17:18325215-18325216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569661082	chr17:18325245-18325246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538391228	chr17:18325348-18325349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558093532	chr17:18325375-18325376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560454275	chr17:18325377-18325378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544981288	chr17:18325415-18325416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149215767	chr17:18325420-18325421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386795973	chr17:18325457-18325458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187355169	chr17:18325486-18325487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554550800	chr17:18325492-18325493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200143874	chr17:18325591-18325592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574071167	chr17:18325615-18325616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542662869	chr17:18325618-18325619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556574335	chr17:18325661-18325662	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
40	rs201036868	chr17:18325667-18325668	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
41	rs545153982	chr17:18325714-18325715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564721386	chr17:18325729-18325730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527512920	chr17:18325730-18325731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540924338	chr17:18325768-18325769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560890288	chr17:18325834-18325835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs202002856	chr17:18325870-18325871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529603728	chr17:18325871-18325872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549516754	chr17:18325879-18325880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569708029	chr17:18325907-18325908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532125386	chr17:18325925-18325926	Enhancers	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:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18324800-18326200	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr17:18324800-18326400	Enhancers	Fetal Thymus	thymus
3	chr17:18333000-18333400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr17:18339400-18339800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr17:18351000-18351400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr17:18351200-18351400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr17:18351200-18351400	Enhancers	NHEK	skin
8	chr17:18351400-18352800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr17:18351400-18353000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr17:18351400-18355400	Weak transcription	NHEK	skin
11	chr17:18352800-18353400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr17:18353000-18353200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr17:18353200-18353600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr17:18353400-18353600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr17:18353600-18354400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr17:18353600-18354600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr17:18354400-18354600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr17:18354600-18355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr17:18354600-18355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr17:18355400-18355600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr17:18355400-18355600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr17:18355400-18355800	Enhancers	NHEK	skin
23	chr17:18355600-18355800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr17:18355600-18355800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr17:18361000-18362400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr17:18361600-18361800	Enhancers	Hela-S3	cervix
27	chr17:18361600-18362000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr17:18362000-18362400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr17:18362200-18362600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr17:18362200-18362600	Active TSS	A549	lung
31	chr17:18362200-18362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr17:18362400-18362600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:18362400-18362600	Bivalent Enhancer	Fetal Lung	lung
34	chr17:18362400-18362600	Active TSS	Hela-S3	cervix
35	chr17:18362400-18362800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr17:18362400-18362800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr17:18362400-18362800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr17:18362400-18362800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr17:18362400-18362800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr17:18362400-18363400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr17:18362600-18362800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr17:18362600-18362800	Enhancers	Muscle Satellite Cultured Cells	--
43	chr17:18362600-18362800	Flanking Active TSS	Hela-S3	cervix
44	chr17:18362600-18362800	Enhancers	Osteobl	bone
45	chr17:18362600-18372000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr17:18367200-18367400	Enhancers	Fetal Intestine Large	intestine
47	chr17:18370000-18380000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr17:18370400-18370600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr17:18370600-18371000	Enhancers	Esophagus	oesophagus
50	chr17:18371000-18372000	Weak transcription	Esophagus	oesophagus

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