Variant report

Variant	esv1792054
Chromosome Location	chr17:15934025-16010920
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:612)
CpG islands
(count:123)
Chromatin interactive
region (count:27)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15946193-15946249	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:16009878-16010075	K562	blood:	n/a	n/a
3	ARID3A	chr17:15942859-15943125	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:15943987-15944643	HepG2	liver:	n/a	n/a
5	ATF1	chr17:16009815-16010155	K562	blood:	n/a	n/a
6	BACH1	chr17:15995090-15995456	K562	blood:	n/a	n/a
7	BACH1	chr17:15995089-15995466	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr17:15973666-15973854	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr17:15990257-15990528	GM12878	blood:	n/a	n/a
10	BHLHE40	chr17:16010701-16010761	K562	blood:	n/a	n/a
11	BHLHE40	chr17:16009819-16010168	K562	blood:	n/a	n/a
12	BHLHE40	chr17:15990365-15990449	GM12878	blood:	n/a	n/a
13	CBX3	chr17:15995175-15995382	K562	blood:	n/a	n/a
14	CBX3	chr17:15984887-15985173	K562	blood:	n/a	n/a
15	CCNT2	chr17:15992643-15992843	K562	blood:	n/a	n/a
16	CEBPB	chr17:15971654-15971888	K562	blood:	n/a	chr17:15971821-15971834
17	CEBPB	chr17:15974932-15975199	IMR90	lung:	n/a	n/a
18	CEBPB	chr17:15954495-15954714	K562	blood:	n/a	chr17:15954611-15954622
19	CEBPB	chr17:15979148-15979711	A549	lung:	n/a	chr17:15979463-15979474
20	CEBPB	chr17:15954451-15954743	A549	lung:	n/a	chr17:15954611-15954622
21	CEBPB	chr17:15974912-15975173	K562	blood:	n/a	n/a
22	CEBPB	chr17:15988407-15988944	IMR90	lung:	n/a	n/a
23	CEBPB	chr17:15979290-15979645	Hela-S3	cervix:	n/a	chr17:15979463-15979474
24	CEBPB	chr17:15954476-15954738	IMR90	lung:	n/a	chr17:15954611-15954622
25	CEBPB	chr17:15942854-15943210	HepG2	liver:	n/a	chr17:15943029-15943040
26	CEBPB	chr17:15937172-15937240	A549	lung:	n/a	n/a
27	CEBPB	chr17:15991998-15992145	A549	lung:	n/a	n/a
28	CEBPB	chr17:15937093-15937286	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr17:15968830-15969099	HepG2	liver:	n/a	n/a
30	CEBPB	chr17:15979281-15979649	K562	blood:	n/a	chr17:15979463-15979474
31	CEBPB	chr17:15971645-15971982	IMR90	lung:	n/a	chr17:15971821-15971834
32	CEBPB	chr17:15974993-15975366	A549	lung:	n/a	chr17:15975243-15975254
33	CEBPB	chr17:15974994-15975370	HepG2	liver:	n/a	chr17:15975243-15975254
34	CEBPB	chr17:15979288-15979647	IMR90	lung:	n/a	chr17:15979463-15979474
35	CEBPB	chr17:15954462-15954772	HepG2	liver:	n/a	chr17:15954611-15954622
36	CEBPB	chr17:15945745-15946059	HepG2	liver:	n/a	n/a
37	CEBPB	chr17:16009839-16010093	K562	blood:	n/a	n/a
38	CEBPB	chr17:15979293-15979632	H1-hESC	embryonic stem cell:	n/a	chr17:15979463-15979474
39	CEBPB	chr17:15954596-15954704	H1-hESC	embryonic stem cell:	n/a	chr17:15954611-15954622
40	CEBPB	chr17:15979277-15979646	HepG2	liver:	n/a	chr17:15979463-15979474
41	CEBPB	chr17:15979276-15979642	A549	lung:	n/a	chr17:15979463-15979474
42	CHD2	chr17:15944064-15944590	HepG2	liver:	n/a	n/a
43	CHD2	chr17:15990452-15990454	GM12878	blood:	n/a	n/a
44	CTCF	chr17:15961773-15961907	MCF-7	breast:	n/a	n/a
45	CTCF	chr17:15961728-15961959	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr17:15961800-15961950	GM12873	blood:	n/a	n/a
47	CTCF	chr17:16004140-16004290	AG10803	skin:	n/a	n/a
48	CTCF	chr17:16004171-16004341	GM12878	blood:	n/a	n/a
49	CTCF	chr17:16004200-16004350	GM12873	blood:	n/a	n/a
50	CTCF	chr17:15961584-15962014	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15970327-15970377	AG10803	skin:	n/a
2	chr17:15970327-15970377	AG10803	skin:	n/a
3	chr17:15947312-15947362	NH-A	brain:	n/a
4	chr17:15947312-15947362	HepG2	liver:	n/a
5	chr17:15970327-15970377	HUVEC	blood vessel:	n/a
6	chr17:15970327-15970377	HEEpiC	esophagus:	n/a
7	chr17:15947312-15947362	GM12878	blood:	n/a
8	chr17:15970327-15970377	H1-hESC	embryonic stem cell:	embryo
9	chr17:15970327-15970377	HAEpiC	amniotic membrane:	n/a
10	chr17:15970327-15970377	MCF-7	breast:	n/a
11	chr17:15970327-15970377	SAEC	small airway:	n/a
12	chr17:15970327-15970377	NB4	blood:	n/a
13	chr17:15947312-15947362	GM06990	blood:	n/a
14	chr17:15947312-15947362	ovcar-3	ovarian:	n/a
15	chr17:15970327-15970377	NT2-D1	testis:	n/a
16	chr17:15970327-15970377	GM06990	blood:	n/a
17	chr17:15970327-15970377	MCF10A-Er-Src	breast:	n/a
18	chr17:15970327-15970377	ProgFib	skin:	n/a
19	chr17:15947312-15947362	HRCEpiC	kidney:	n/a
20	chr17:15970327-15970377	HEK293	kidney:	embryo
21	chr17:15970327-15970377	PANC-1	pancreas:	n/a
22	chr17:15970327-15970377	AoSMC	blood vessel:	n/a
23	chr17:15970327-15970377	AG04449	skin:	fetal
24	chr17:15947312-15947362	GM12892	blood:	n/a
25	chr17:15970327-15970377	PFSK-1	brain:	n/a
26	chr17:15970327-15970377	NHBE	bronchial:	n/a
27	chr17:15970327-15970377	HRE	kidney:	n/a
28	chr17:15970327-15970377	HCF	heart:	n/a
29	chr17:15947312-15947362	HRPEpiC	eye:	n/a
30	chr17:15970327-15970377	AG04450	lung:	fetal
31	chr17:15947312-15947362	IMR90	lung:	fetal
32	chr17:15947312-15947362	Caco-2	colon:	n/a
33	chr17:15947312-15947362	Jurkat	blood:	n/a
34	chr17:15970327-15970377	Caco-2	colon:	n/a
35	chr17:15947312-15947362	HRE	kidney:	n/a
36	chr17:15970327-15970377	SK-N-SH	brain:	n/a
37	chr17:15947312-15947362	HEEpiC	esophagus:	n/a
38	chr17:15970327-15970377	BJ	skin:	n/a
39	chr17:15970327-15970377	Hepatocyte	liver:	n/a
40	chr17:15947312-15947362	SKMC	muscle:	n/a
41	chr17:15970327-15970377	Jurkat	blood:	n/a
42	chr17:15947312-15947362	HUVEC	blood vessel:	n/a
43	chr17:15947312-15947362	HCPEpiC	choroid plexus:	n/a
44	chr17:15970327-15970377	CMK	blood:	n/a
45	chr17:15947312-15947362	Hela-S3	cervix:	n/a
46	chr17:15970327-15970377	GM12892	blood:	n/a
47	chr17:15947312-15947362	HL-60	blood:	n/a
48	chr17:15970327-15970377	GM12891	blood:	n/a
49	chr17:15947312-15947362	HAEpiC	amniotic membrane:	n/a
50	chr17:15970327-15970377	BE2_C	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:15924357..15928221-chr17:15933368..15936168,3	K562	blood:
2	chr17:15935922..15937736-chr17:15946128..15948484,2	K562	blood:
3	chr17:15987048..15989365-chr17:16117375..16120147,2	MCF-7	breast:
4	chr17:15926454..15928435-chr17:15932440..15934895,2	MCF-7	breast:
5	chr17:15962217..15964355-chr17:15964514..15967478,2	K562	blood:
6	chr17:15944048..15946944-chr17:15948607..15950482,2	K562	blood:
7	chr17:15962217..15964355-chr17:15964514..15967478,2	K562	blood:
8	chr17:16000342..16002762-chr17:16006571..16009952,3	K562	blood:
9	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
10	chr17:15963401..15966357-chr17:16012433..16014400,2	K562	blood:
11	chr17:15931616..15933917-chr17:15935615..15938072,3	K562	blood:
12	chr17:15943040..15946944-chr17:15948607..15952058,5	K562	blood:
13	chr17:15968961..15972036-chr17:15974016..15976149,3	K562	blood:
14	chr17:7860807..7861740-chr17:15973359..15973862,2	MCF-7	breast:
15	chr17:15968719..15971375-chr17:15978183..15980041,2	K562	blood:
16	chr17:15958547..15961749-chr17:15963827..15966828,3	MCF-7	breast:
17	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
18	chr17:15943040..15946944-chr17:15948607..15952058,5	K562	blood:
19	chr17:15979525..15982244-chr17:16118246..16120149,2	K562	blood:
20	chr17:15941280..15942886-chr17:15944806..15947115,2	MCF-7	breast:
21	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
22	chr17:15972800..15974994-chr17:15979206..15981179,2	MCF-7	breast:
23	chr17:15081168..15081829-chr17:15973460..15974306,2	MCF-7	breast:
24	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
25	chr17:15972800..15974994-chr17:15979206..15981179,2	MCF-7	breast:
26	chr17:15563102..15563727-chr17:15973385..15973964,2	MCF-7	breast:
27	chr17:15992643..15994988-chr17:16118980..16121101,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM7-6	chr17:15960288-15961051	NONHSAT145890
2	lnc-AC002553.1-2	chr17:15947935-15948275	NONHSAT145887
3	lnc-ZSWIM7-4	chr17:15948169-15948278	NONHSAT145886
4	lnc-AC002553.1-1	chr17:15943786-15944587	NONHSAT145885
5	lnc-ZSWIM7-1	chr17:15948896-15948923	NONHSAT145888
6	lnc-ZSWIM7-1	chr17:15949364-15949795	NONHSAT145888
7	lnc-ZSWIM7-1	chr17:15949376-15949795	ENSG00000248550
8	lnc-ZSWIM7-4	chr17:15947766-15948163	NONHSAT145886
9	lnc-ZSWIM7-6	chr17:15961221-15961249	NONHSAT145890
10	lnc-TTC19-1	chr17:15987356-15987695	NONHSAT145891

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NCOR1	hsa-let-7b-5p	chr17:15934835-15934829

Variant related genes	Relation type
NCOR1	TF binding region
ENSG00000227782	TF binding region
RPLP1P11	TF binding region
RNU6-314P	TF binding region
ENSG00000233979	TF binding region
NCOR1	CpG island
ENSG00000227782	CpG island
RPLP1P11	CpG island
RNU6-314P	CpG island
ENSG00000233979	CpG island
ENSG00000252383	chromatin interactions
ENSG00000243686	chromatin interactions
ENSG00000227782	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000108474	chromatin interactions
BDH2	miRNA target sites

Extended variants
information (count: 2857 )
Associated
traits (count: 171 )

Variant overlapped rSNPs/rCNVs (count:2857 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12952466	chr17:15934025-15934026	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574909127	chr17:15934031-15934032	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538119972	chr17:15934070-15934071	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs13464	chr17:15934089-15934090	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369839389	chr17:15934107-15934108	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148551325	chr17:15934127-15934128	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188146077	chr17:15934134-15934135	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs578117979	chr17:15934244-15934245	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142125677	chr17:15934253-15934254	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560614268	chr17:15934282-15934283	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192735281	chr17:15934296-15934297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs116576373	chr17:15934298-15934299	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114088671	chr17:15934305-15934306	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531743770	chr17:15934339-15934340	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73981416	chr17:15934361-15934362	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs151176987	chr17:15934368-15934369	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534153199	chr17:15934382-15934383	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575604313	chr17:15934549-15934550	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77866703	chr17:15934788-15934789	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs566212236	chr17:15934834-15934835	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561036342	chr17:15934999-15935000	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs140182822	chr17:15935084-15935085	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115708449	chr17:15935092-15935093	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568466974	chr17:15935100-15935101	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537450963	chr17:15935116-15935117	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558425966	chr17:15935117-15935118	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571876782	chr17:15935158-15935159	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs534389826	chr17:15935183-15935184	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144012237	chr17:15935235-15935236	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185021409	chr17:15935322-15935323	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556706003	chr17:15935326-15935327	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576498237	chr17:15935359-15935360	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545117066	chr17:15935402-15935403	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188055326	chr17:15935421-15935422	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs533107019	chr17:15935447-15935448	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73981417	chr17:15935456-15935457	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559888118	chr17:15935487-15935488	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561209424	chr17:15935506-15935507	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529056639	chr17:15935525-15935526	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191456771	chr17:15935534-15935535	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12946339	chr17:15935558-15935559	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368886666	chr17:15935570-15935571	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112840784	chr17:15935574-15935575	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370706061	chr17:15935578-15935579	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1802210	chr17:15935608-15935609	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373779692	chr17:15935631-15935632	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532511938	chr17:15935636-15935637	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531315363	chr17:15935649-15935650	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552151209	chr17:15935675-15935676	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs199638814	chr17:15935705-15935706	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:171)

Disease	PMID	Source
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
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
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
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
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:2560 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15905000-15939600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr17:15905000-15946400	Strong transcription	HUES48 Cell Line	embryonic stem cell
3	chr17:15905200-15986400	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr17:15905400-15946600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr17:15906400-15939400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:15907800-15935600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:15913800-15990800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr17:15915400-15998000	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr17:15917400-15952800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr17:15921000-15946600	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr17:15921000-15991000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr17:15921000-15991200	Strong transcription	Primary B cells from peripheral blood	blood
13	chr17:15921400-15944400	Strong transcription	Duodenum Mucosa	Duodenum
14	chr17:15921400-15947000	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr17:15921400-15955000	Strong transcription	Dnd41	blood
16	chr17:15921600-15939200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr17:15921600-15941000	Strong transcription	Placenta	Placenta
18	chr17:15921600-15952400	Strong transcription	Primary T cells from cord blood	blood
19	chr17:15922600-15939800	Strong transcription	Liver	Liver
20	chr17:15923400-15941400	Weak transcription	Psoas Muscle	Psoas
21	chr17:15923800-15998000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr17:15924000-15944000	Strong transcription	Rectal Mucosa Donor 31	rectum
23	chr17:15924600-15936400	Strong transcription	Fetal Lung	lung
24	chr17:15925200-15952800	Strong transcription	Primary B cells from cord blood	blood
25	chr17:15925400-15943600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr17:15925600-15948000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr17:15926600-15944000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr17:15926800-15944000	Strong transcription	Fetal Intestine Large	intestine
29	chr17:15926800-15952600	Strong transcription	Adipose Nuclei	Adipose
30	chr17:15926800-15985400	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr17:15926800-15987600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr17:15927000-15944200	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr17:15927000-15945000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr17:15927000-15953400	Strong transcription	Primary T cells fromperipheralblood	blood
35	chr17:15927200-15942600	Strong transcription	HepG2	liver
36	chr17:15927200-15943400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr17:15927200-15956000	Strong transcription	Fetal Muscle Leg	muscle
38	chr17:15927200-15976400	Strong transcription	Fetal Muscle Trunk	muscle
39	chr17:15927600-15941400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr17:15927800-15934800	Strong transcription	Fetal Kidney	kidney
41	chr17:15927800-15943400	Strong transcription	Stomach Smooth Muscle	stomach
42	chr17:15927800-15954400	Strong transcription	Fetal Thymus	thymus
43	chr17:15927800-15971600	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr17:15927800-15987800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr17:15928200-15936000	Strong transcription	Fetal Brain Male	brain
46	chr17:15928200-15938800	Strong transcription	Brain Inferior Temporal Lobe	brain
47	chr17:15928200-15939600	Strong transcription	Primary hematopoietic stem cells	blood
48	chr17:15928200-15940600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr17:15928200-15952800	Strong transcription	Thymus	Thymus
50	chr17:15928200-15953000	Strong transcription	Left Ventricle	heart

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