Variant report

Variant	esv1843009
Chromosome Location	chr17:18293427-18465221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:958)
CpG islands
(count:1403)
Chromatin interactive
region (count:0)
LncRNA
region (count:87)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:18314118-18314356	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr17:18362390-18362672	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:18355389-18355575	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr17:18411051-18411300	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
5	BATF	chr17:18301531-18301764	GM12878	blood:	n/a	n/a
6	BATF	chr17:18379787-18380078	GM12878	blood:	n/a	n/a
7	BATF	chr17:18396335-18396562	GM12878	blood:	n/a	chr17:18396479-18396490
8	BATF	chr17:18410950-18411370	GM12878	blood:	n/a	chr17:18411156-18411166 chr17:18411155-18411166
9	BATF	chr17:18396259-18396664	GM12878	blood:	n/a	chr17:18396479-18396490
10	BATF	chr17:18379801-18380128	GM12878	blood:	n/a	n/a
11	BATF	chr17:18306836-18307314	GM12878	blood:	n/a	n/a
12	BATF	chr17:18306799-18307466	GM12878	blood:	n/a	n/a
13	BCL11A	chr17:18379825-18380074	GM12878	blood:	n/a	n/a
14	BCL11A	chr17:18306911-18307191	GM12878	blood:	n/a	n/a
15	BCL11A	chr17:18306873-18307246	GM12878	blood:	n/a	n/a
16	BCL11A	chr17:18424410-18424651	GM12878	blood:	n/a	n/a
17	BCL11A	chr17:18379766-18380162	GM12878	blood:	n/a	n/a
18	BCL11A	chr17:18378052-18378384	GM12878	blood:	n/a	n/a
19	BCL3	chr17:18314773-18315245	A549	lung:	n/a	n/a
20	BHLHE40	chr17:18424672-18424862	GM12878	blood:	n/a	n/a
21	BHLHE40	chr17:18396537-18396565	K562	blood:	n/a	n/a
22	CEBPB	chr17:18322037-18322380	K562	blood:	n/a	n/a
23	CEBPB	chr17:18362356-18362662	IMR90	lung:	n/a	chr17:18362363-18362376
24	CEBPB	chr17:18322055-18322251	K562	blood:	n/a	n/a
25	CEBPB	chr17:18318052-18318134	A549	lung:	n/a	chr17:18318100-18318113 chr17:18318102-18318113 chr17:18318102-18318111
26	CEBPB	chr17:18362210-18362602	Hela-S3	cervix:	n/a	chr17:18362363-18362376
27	CEBPB	chr17:18317946-18318165	IMR90	lung:	n/a	chr17:18318100-18318113 chr17:18318102-18318113 chr17:18318102-18318111
28	CEBPB	chr17:18322048-18322324	K562	blood:	n/a	n/a
29	CHD1	chr17:18315013-18315207	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr17:18314139-18314423	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr17:18339581-18339680	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr17:18400380-18400530	HVMF	connective:	n/a	n/a
33	CTCF	chr17:18355380-18355530	NHEK	skin:	n/a	chr17:18355490-18355499
34	CTCF	chr17:18428313-18428780	A549	lung:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
35	CTCF	chr17:18403725-18403883	ProgFib	skin:	n/a	n/a
36	CTCF	chr17:18345520-18345670	GM12868	blood:	n/a	n/a
37	CTCF	chr17:18391849-18391946	Lung_OC	lung:	n/a	n/a
38	CTCF	chr17:18345520-18345670	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr17:18345500-18345650	GM12865	blood:	n/a	n/a
40	CTCF	chr17:18345500-18345650	HPF	lung:	n/a	n/a
41	CTCF	chr17:18380879-18380969	Pancreas_OC	pancreas:	n/a	n/a
42	CTCF	chr17:18331698-18331751	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr17:18297461-18297539	GM10248	blood:	n/a	chr17:18297501-18297509
44	CTCF	chr17:18428446-18428609	K562	blood:	n/a	chr17:18428545-18428561 chr17:18428546-18428567
45	CTCF	chr17:18322636-18322684	GM13976	blood:	n/a	n/a
46	CTCF	chr17:18345500-18345650	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr17:18400513-18400623	HepG2	liver:	n/a	n/a
48	CTCF	chr17:18381234-18381345	Pancreas_OC	pancreas:	n/a	chr17:18381256-18381277 chr17:18381261-18381279 chr17:18381264-18381274 chr17:18381262-18381278
49	CTCF	chr17:18345500-18345650	HRE	kidney:	n/a	n/a
50	CTCF	chr17:18400403-18400659	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18397849-18397899	H1-hESC	embryonic stem cell:	embryo
2	chr17:18380354-18380404	SAEC	small airway:	n/a
3	chr17:18324895-18324945	HRPEpiC	eye:	n/a
4	chr17:18295503-18295553	HRE	kidney:	n/a
5	chr17:18421335-18421385	AG09309	skin:	n/a
6	chr17:18378879-18378929	SK-N-SH_RA	brain:	n/a
7	chr17:18380159-18380209	Hepatocyte	liver:	n/a
8	chr17:18421335-18421385	HCT-116	colon:	n/a
9	chr17:18428092-18428142	NH-A	brain:	n/a
10	chr17:18295431-18295481	RPTEC	kidney:	n/a
11	chr17:18324790-18324840	AG04449	skin:	fetal
12	chr17:18432149-18432199	RPTEC	kidney:	n/a
13	chr17:18429951-18430001	HUVEC	blood vessel:	n/a
14	chr17:18313048-18313098	Jurkat	blood:	n/a
15	chr17:18317909-18317959	GM12892	blood:	n/a
16	chr17:18428092-18428142	AG04449	skin:	fetal
17	chr17:18313048-18313098	PFSK-1	brain:	n/a
18	chr17:18378879-18378929	AG10803	skin:	n/a
19	chr17:18326064-18326114	SK-N-MC	brain:	n/a
20	chr17:18379129-18379179	U87	brain:	n/a
21	chr17:18432149-18432199	AoSMC	blood vessel:	n/a
22	chr17:18380354-18380404	ProgFib	skin:	n/a
23	chr17:18431043-18431093	AG09319	gingival:	n/a
24	chr17:18380354-18380404	HNPCEpiC	eye:	n/a
25	chr17:18302510-18302560	AG04449	skin:	fetal
26	chr17:18325001-18325051	NHBE	bronchial:	n/a
27	chr17:18430908-18430958	NT2-D1	testis:	n/a
28	chr17:18428092-18428142	MCF-7	breast:	n/a
29	chr17:18378879-18378929	MCF10A-Er-Src	breast:	n/a
30	chr17:18313048-18313098	AG09319	gingival:	n/a
31	chr17:18380354-18380404	U87	brain:	n/a
32	chr17:18428092-18428142	SK-N-MC	brain:	n/a
33	chr17:18326064-18326114	SAEC	small airway:	n/a
34	chr17:18429951-18430001	HCF	heart:	n/a
35	chr17:18324895-18324945	HCM	heart:	n/a
36	chr17:18380159-18380209	HCF	heart:	n/a
37	chr17:18305305-18305355	HRE	kidney:	n/a
38	chr17:18432149-18432199	HEK293	kidney:	embryo
39	chr17:18419896-18419946	AG09309	skin:	n/a
40	chr17:18317909-18317959	T-47D	breast:	n/a
41	chr17:18302510-18302560	NT2-D1	testis:	n/a
42	chr17:18379129-18379179	GM06990	blood:	n/a
43	chr17:18326064-18326114	BE2_C	brain:	n/a
44	chr17:18313048-18313098	Hepatocyte	liver:	n/a
45	chr17:18313121-18313171	BE2_C	brain:	n/a
46	chr17:18295431-18295481	HCT-116	colon:	n/a
47	chr17:18397849-18397899	IMR90	lung:	fetal
48	chr17:18429951-18430001	SAEC	small airway:	n/a
49	chr17:18305305-18305355	HPAEpiC	pulmonary alveolar:	n/a
50	chr17:18428092-18428142	HEEpiC	esophagus:	n/a

No data

(count:87 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM106A-2	chr17:18446183-18446301	ENSG00000273018.1
2	lnc-FAM106A-2	chr17:18422796-18422988	NONHSAT146381
3	lnc-FAM106A-2	chr17:18427091-18427191	ENSG00000273018.1
4	lnc-FAM106A-2	chr17:18446987-18447029	ENSG00000273018.1
5	lnc-AL353997.5.1-5	chr17:18380114-18380207	NONHSAT146376
6	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
7	lnc-FAM106A-2	chr17:18420604-18420787	ENSG00000273018.1
8	lnc-FAM106A-2	chr17:18431887-18432642	ENSG00000273018.1
9	lnc-AL353997.5.1-4	chr17:18343220-18343625	NONHSAT146373
10	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
11	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
12	lnc-FAM106A-2	chr17:18426965-18427191	ENSG00000273018.1
13	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
14	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
15	lnc-FAM106A-1	chr17:18427880-18430160	NR_026809
16	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
17	lnc-FAM106A-2	chr17:18422958-18422988	ENSG00000273018.1
18	lnc-FAM106A-2	chr17:18435820-18435911	ENSG00000273018.1
19	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
20	lnc-FAM106A-2	chr17:18420633-18420787	NONHSAT146382
21	lnc-AL353997.5.1-1	chr17:18328108-18328411	ENSG00000205266.5
22	lnc-FAM106A-2	chr17:18435820-18436348	ENSG00000273018.1
23	lnc-AL353997.5.1-5	chr17:18387189-18387649	NONHSAT146376
24	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
25	lnc-FAM106A-2	chr17:18435820-18436192	ENSG00000273018.1
26	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
27	lnc-AL353997.5.1-1	chr17:18327635-18327951	ENSG00000205266.5
28	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
29	lnc-AL353997.5.1-2	chr17:18315789-18316112	XLOC_012131
30	lnc-AL353997.5.1-2	chr17:18317468-18317702	XLOC_012131
31	lnc-FAM106A-2	chr17:18454820-18454999	ENSG00000273018.1
32	lnc-FAM106A-2	chr17:18422796-18422988	NONHSAT146382
33	lnc-AL353997.5.1-2	chr17:18317464-18317702	XLOC_012131
34	lnc-FAM106A-2	chr17:18422796-18422988	ENSG00000273018.1
35	lnc-FAM106A-2	chr17:18446987-18447029	ENSG00000273018.1
36	lnc-FAM106A-2	chr17:18436661-18436946	ENSG00000273018.1
37	lnc-FAM106A-2	chr17:18445402-18445501	ENSG00000273018.1
38	lnc-FAM106A-2	chr17:18444241-18444277	NONHSAT146384
39	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
40	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
41	lnc-AL353997.5.1-2	chr17:18315660-18315823	XLOC_012131
42	lnc-FAM106A-2	chr17:18430884-18431074	ENSG00000273018.1
43	lnc-FAM106A-2	chr17:18431887-18432061	ENSG00000273018.1
44	lnc-FAM106A-2	chr17:18454820-18455019	ENSG00000273018.1
45	lnc-AL353997.5.1-6	chr17:18395939-18396053	NONHSAT146378
46	lnc-FAM106A-2	chr17:18431887-18432298	ENSG00000273018.1
47	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
48	lnc-FAM106A-2	chr17:18424393-18424459	ENSG00000273018.1
49	lnc-FAM106A-2	chr17:18420696-18420787	ENSG00000273018.1
50	lnc-FAM106A-2	chr17:18436661-18437376	ENSG00000273018.1

No data

Variant related genes	Relation type
ENSG00000205266	TF binding region
USP32P2	TF binding region
KRT16P4	TF binding region
LGALS9C	TF binding region
ENSG00000227919	TF binding region
ENSG00000267492	TF binding region
KRT16P1	TF binding region
TNPO1P2	TF binding region
ENSG00000240279	TF binding region
YWHAEP2	TF binding region
FAM106A	TF binding region
KRT17P2	TF binding region
SRP68P2	TF binding region
ENSG00000220161	TF binding region
NOS2P2	TF binding region
TBC1D3P4	TF binding region
ENSG00000264177	TF binding region
CCDC144B	TF binding region
ENSG00000273018	TF binding region
ENSG00000205266	CpG island
USP32P2	CpG island
KRT16P4	CpG island
LGALS9C	CpG island
ENSG00000227919	CpG island
ENSG00000267492	CpG island
KRT16P1	CpG island
TNPO1P2	CpG island
ENSG00000240279	CpG island
YWHAEP2	CpG island
FAM106A	CpG island
KRT17P2	CpG island
SRP68P2	CpG island
ENSG00000220161	CpG island
NOS2P2	CpG island
TBC1D3P4	CpG island
ENSG00000264177	CpG island
CCDC144B	CpG island
ENSG00000273018	CpG island
KIAA0664	miRNA target sites
KIAA0528	miRNA target sites

Extended variants
information (count: 3541 )
Associated
traits (count: 169 )

Variant overlapped rSNPs/rCNVs (count:3541 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138442138	chr17:18293427-18293428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115604883	chr17:18293444-18293445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559457562	chr17:18293481-18293482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559762363	chr17:18293489-18293490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs632347	chr17:18293510-18293511	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs632348	chr17:18293513-18293514	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs11652393	chr17:18293542-18293543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111413621	chr17:18293562-18293563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs632759	chr17:18293568-18293569	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs181617310	chr17:18293656-18293657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185049835	chr17:18293666-18293667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76741146	chr17:18293672-18293673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189892788	chr17:18293687-18293688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546701518	chr17:18293739-18293740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181117428	chr17:18293747-18293748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566599118	chr17:18293774-18293775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186544447	chr17:18293778-18293779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555212043	chr17:18293805-18293806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562347640	chr17:18293901-18293902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574986513	chr17:18293917-18293918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144671157	chr17:18293929-18293930	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs557041579	chr17:18293933-18293934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74557586	chr17:18293963-18293964	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
24	rs190018837	chr17:18294001-18294002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372674779	chr17:18294017-18294018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs180810375	chr17:18294078-18294079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573039958	chr17:18294142-18294143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541582187	chr17:18294163-18294164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1682237	chr17:18294168-18294169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561921012	chr17:18294182-18294183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186529134	chr17:18294186-18294187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1682238	chr17:18294190-18294191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564257388	chr17:18294216-18294217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538733457	chr17:18294219-18294220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190922505	chr17:18294221-18294222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4003480	chr17:18294287-18294288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142626816	chr17:18294298-18294299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570871230	chr17:18294299-18294300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4003479	chr17:18294300-18294301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566534255	chr17:18294325-18294326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535548052	chr17:18294336-18294337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548466500	chr17:18294337-18294338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575176412	chr17:18294347-18294348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4003478	chr17:18294374-18294375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4003477	chr17:18294386-18294387	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
46	rs4003476	chr17:18294402-18294403	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs557613531	chr17:18294408-18294409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577515676	chr17:18294517-18294518	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs2386447	chr17:18294537-18294538	Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs4003475	chr17:18294546-18294547	Enhancers	TF binding region	2 gene(s)	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Tetralogy of Fallot	22912587	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18291800-18293600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr17:18292200-18294400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr17:18293400-18293600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr17:18293400-18293600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr17:18293400-18293600	Enhancers	Fetal Muscle Trunk	muscle
6	chr17:18294400-18294600	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr17:18306600-18306800	Enhancers	GM12878-XiMat	blood
8	chr17:18306800-18314200	Weak transcription	GM12878-XiMat	blood
9	chr17:18307600-18308000	Enhancers	Primary B cells from peripheral blood	blood
10	chr17:18308000-18312400	Weak transcription	Primary B cells from peripheral blood	blood
11	chr17:18311600-18312800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr17:18312000-18312200	Enhancers	Fetal Thymus	thymus
13	chr17:18312200-18312400	Enhancers	Primary hematopoietic stem cells	blood
14	chr17:18312200-18312400	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr17:18312200-18312400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr17:18312200-18312400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:18312200-18312400	Enhancers	Brain Cingulate Gyrus	brain
18	chr17:18312200-18312600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr17:18312200-18312600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr17:18312200-18312600	Active TSS	Fetal Brain Female	brain
21	chr17:18312200-18312600	Flanking Active TSS	Fetal Thymus	thymus
22	chr17:18312200-18312800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr17:18312200-18312800	Enhancers	Fetal Lung	lung
24	chr17:18312200-18313000	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr17:18312200-18313000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr17:18312200-18313000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr17:18312200-18313000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr17:18312200-18313200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr17:18312200-18313200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr17:18312200-18313200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr17:18312200-18313200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr17:18312200-18313200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:18312200-18313200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr17:18312200-18313400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr17:18312200-18313600	Enhancers	A549	lung
36	chr17:18312200-18313600	Enhancers	Dnd41	blood
37	chr17:18312200-18314000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr17:18312200-18314400	Enhancers	Primary T cells from cord blood	blood
39	chr17:18312400-18312600	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr17:18312400-18312600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr17:18312400-18312600	Flanking Active TSS	Thymus	Thymus
42	chr17:18312400-18312800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr17:18312400-18312800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr17:18312400-18313000	Enhancers	Primary B cells from peripheral blood	blood
45	chr17:18312400-18313200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr17:18312400-18313600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr17:18312400-18313800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr17:18312400-18314000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:18312400-18314000	Enhancers	NHEK	skin
50	chr17:18312400-18314200	Weak transcription	Primary hematopoietic stem cells	blood

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