Variant report

Variant	nsv982312
Chromosome Location	chr9:86424154-86490046
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:528)
CpG islands
(count:366)
Chromatin interactive
region (count:9)
LncRNA
region (count:53)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr9:86464911-86465156	GM12878	blood:	n/a	n/a
2	BCL11A	chr9:86464843-86465149	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:86432167-86432635	GM12878	blood:	n/a	chr9:86432477-86432493
4	BHLHE40	chr9:86432260-86432688	K562	blood:	n/a	chr9:86432477-86432493
5	BHLHE40	chr9:86432362-86432520	HepG2	liver:	n/a	chr9:86432477-86432493
6	CCNT2	chr9:86432252-86432698	K562	blood:	n/a	chr9:86432668-86432677
7	CEBPB	chr9:86434689-86434833	K562	blood:	n/a	chr9:86434732-86434743
8	CEBPB	chr9:86437426-86437435	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:86427727-86427914	K562	blood:	n/a	n/a
10	CEBPB	chr9:86434682-86434882	HepG2	liver:	n/a	chr9:86434732-86434743
11	CHD1	chr9:86432239-86432282	GM12878	blood:	n/a	n/a
12	CHD1	chr9:86431789-86432598	IMR90	lung:	n/a	chr9:86432468-86432478 chr9:86431865-86431875
13	CHD2	chr9:86432265-86432364	GM12878	blood:	n/a	n/a
14	CHD2	chr9:86432810-86432972	GM12878	blood:	n/a	n/a
15	CHD2	chr9:86432754-86432816	Hela-S3	cervix:	n/a	n/a
16	CREB1	chr9:86432803-86432995	A549	lung:	n/a	n/a
17	CREB1	chr9:86432235-86433076	A549	lung:	n/a	n/a
18	CTCF	chr9:86432240-86432390	HCFaa	heart:	n/a	n/a
19	CTCF	chr9:86454750-86454778	MCF-7	breast:	n/a	n/a
20	CTCF	chr9:86454640-86454790	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr9:86432220-86432370	HPF	lung:	n/a	n/a
22	CTCF	chr9:86432291-86432433	MCF-7	breast:	n/a	n/a
23	CTCF	chr9:86432206-86432534	K562	blood:	n/a	n/a
24	CTCF	chr9:86454652-86454797	A549	lung:	n/a	n/a
25	CTCF	chr9:86445840-86445990	HCT-116	colon:	n/a	n/a
26	CTCF	chr9:86452095-86452311	IMR90	lung:	n/a	n/a
27	CTCF	chr9:86445720-86445870	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr9:86452121-86452246	GM20000	blood:	n/a	n/a
29	CTCF	chr9:86432268-86432444	GM12891	blood:	n/a	n/a
30	CTCF	chr9:86432280-86432411	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr9:86432280-86432430	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:86432780-86432930	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr9:86432280-86432430	NHEK	skin:	n/a	n/a
34	CTCF	chr9:86432240-86432390	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr9:86452017-86452323	GM13977	blood:	n/a	n/a
36	CTCF	chr9:86432316-86432421	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr9:86432262-86432460	GM10248	blood:	n/a	n/a
38	CTCF	chr9:86452071-86452313	A549	lung:	n/a	n/a
39	CTCF	chr9:86452000-86452150	AG09309	skin:	n/a	n/a
40	CTCF	chr9:86432280-86432430	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr9:86436457-86436501	GM10248	blood:	n/a	n/a
42	CTCF	chr9:86461178-86461266	Lung_OC	lung:	n/a	n/a
43	CTCF	chr9:86432260-86432410	HCT-116	colon:	n/a	n/a
44	CTCF	chr9:86451972-86452313	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:86452141-86452275	Fibrobl	skin:	n/a	n/a
46	CTCF	chr9:86432240-86432390	GM12867	blood:	n/a	n/a
47	CTCF	chr9:86432260-86432410	GM12872	blood:	n/a	n/a
48	CTCF	chr9:86452122-86452250	GM13976	blood:	n/a	n/a
49	CTCF	chr9:86452061-86452287	LNCaP	prostate:	n/a	n/a
50	CTCF	chr9:86445700-86445850	HEEpiC	esophagus:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:86481663-86481713	HIPEpiC	eye:	n/a
2	chr9:86432031-86432081	HEEpiC	esophagus:	n/a
3	chr9:86433764-86433814	ProgFib	skin:	n/a
4	chr9:86431343-86431393	U87	brain:	n/a
5	chr9:86432031-86432081	NHBE	bronchial:	n/a
6	chr9:86432031-86432081	SAEC	small airway:	n/a
7	chr9:86433081-86433131	Hepatocyte	liver:	n/a
8	chr9:86432854-86432904	HRPEpiC	eye:	n/a
9	chr9:86433764-86433814	HCM	heart:	n/a
10	chr9:86432854-86432904	U87	brain:	n/a
11	chr9:86481663-86481713	ECC-1	luminal epithelium:	n/a
12	chr9:86432031-86432081	RPTEC	kidney:	n/a
13	chr9:86431343-86431393	GM12878	blood:	n/a
14	chr9:86431343-86431393	ProgFib	skin:	n/a
15	chr9:86433764-86433814	SKMC	muscle:	n/a
16	chr9:86433764-86433814	HRCEpiC	kidney:	n/a
17	chr9:86433764-86433814	ovcar-3	ovarian:	n/a
18	chr9:86481663-86481713	HMEC	breast:	n/a
19	chr9:86431343-86431393	GM19239	blood:	n/a
20	chr9:86433764-86433814	Caco-2	colon:	n/a
21	chr9:86481663-86481713	NT2-D1	testis:	n/a
22	chr9:86432031-86432081	HPAEpiC	pulmonary alveolar:	n/a
23	chr9:86432854-86432904	PFSK-1	brain:	n/a
24	chr9:86431343-86431393	BJ	skin:	n/a
25	chr9:86433764-86433814	NH-A	brain:	n/a
26	chr9:86433081-86433131	BE2_C	brain:	n/a
27	chr9:86431343-86431393	HCM	heart:	n/a
28	chr9:86433764-86433814	GM12878	blood:	n/a
29	chr9:86431343-86431393	SK-N-MC	brain:	n/a
30	chr9:86433081-86433131	IMR90	lung:	fetal
31	chr9:86431343-86431393	HRCEpiC	kidney:	n/a
32	chr9:86431343-86431393	AG04450	lung:	fetal
33	chr9:86432031-86432081	AG04449	skin:	fetal
34	chr9:86432031-86432081	ECC-1	luminal epithelium:	n/a
35	chr9:86433764-86433814	Hela-S3	cervix:	n/a
36	chr9:86431343-86431393	NHBE	bronchial:	n/a
37	chr9:86432031-86432081	SK-N-MC	brain:	n/a
38	chr9:86433764-86433814	HEK293	kidney:	embryo
39	chr9:86432854-86432904	HPAEpiC	pulmonary alveolar:	n/a
40	chr9:86481663-86481713	SK-N-SH	brain:	n/a
41	chr9:86432031-86432081	HIPEpiC	eye:	n/a
42	chr9:86433081-86433131	AG04449	skin:	fetal
43	chr9:86431343-86431393	AoSMC	blood vessel:	n/a
44	chr9:86433764-86433814	HCPEpiC	choroid plexus:	n/a
45	chr9:86432854-86432904	AG04449	skin:	fetal
46	chr9:86433081-86433131	Jurkat	blood:	n/a
47	chr9:86433764-86433814	HRPEpiC	eye:	n/a
48	chr9:86433081-86433131	SK-N-SH_RA	brain:	n/a
49	chr9:86432031-86432081	NH-A	brain:	n/a
50	chr9:86481663-86481713	SK-N-SH_RA	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:86322196..86324871-chr9:86423684..86425224,2	MCF-7	breast:
2	chr9:86320718..86323719-chr9:86450162..86455199,6	MCF-7	breast:
3	chr9:86321555..86324208-chr9:86431445..86433817,2	MCF-7	breast:
4	chr9:86321607..86323730-chr9:86445405..86447358,2	MCF-7	breast:
5	chr9:86321469..86324662-chr9:86431245..86433854,3	MCF-7	breast:
6	chr9:86236750..86239117-chr9:86447566..86449894,2	MCF-7	breast:
7	chr9:86468995..86471879-chr9:86534830..86536450,2	MCF-7	breast:
8	chr9:86429346..86431861-chr9:86535994..86537805,2	MCF-7	breast:
9	chr9:86430622..86432919-chr9:86535075..86537489,2	MCF-7	breast:

(count:53 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RMI1-5	chr9:86474193-86474240	ENSG00000231616.4
2	lnc-RMI1-5	chr9:86463801-86463870	ENSG00000231616.4
3	lnc-RMI1-5	chr9:86473216-86474075	ENSG00000231616.4
4	lnc-RMI1-5	chr9:86473779-86474075	ENSG00000231616.4
5	lnc-RMI1-6	chr9:86434721-86434785	ENSG00000245608
6	lnc-RMI1-5	chr9:86473779-86474070	ENSG00000231616.4
7	lnc-RMI1-5	chr9:86463725-86463870	ENSG00000231616.4
8	lnc-RMI1-5	chr9:86451945-86452058	ENSG00000226877.3
9	lnc-RMI1-5	chr9:86445783-86445854	ENSG00000226877.1
10	lnc-RMI1-5	chr9:86473779-86474069	ENSG00000231616.4
11	lnc-RMI1-5	chr9:86474193-86474240	ENSG00000231616.4
12	lnc-RMI1-5	chr9:86482629-86483154	ENSG00000231616.4
13	lnc-RMI1-5	chr9:86464323-86464506	ENSG00000231616.4
14	lnc-RMI1-5	chr9:86446478-86446527	ENSG00000226877.3
15	lnc-RMI1-5	chr9:86444571-86444630	ENSG00000226877.1
16	lnc-RMI1-5	chr9:86446480-86446527	ENSG00000226877.1
17	lnc-RMI1-5	chr9:86452323-86452502	ENSG00000226877.1
18	lnc-RMI1-6	chr9:86442823-86443087	ENSG00000245608
19	lnc-RMI1-5	chr9:86474193-86474240	ENSG00000231616.4
20	lnc-RMI1-6	chr9:86434721-86434785	NONHSAT132748
21	lnc-RMI1-5	chr9:86451945-86452058	ENSG00000226877.1
22	lnc-RMI1-6	chr9:86434446-86434617	NONHSAT132748
23	lnc-RMI1-5	chr9:86450466-86450620	ENSG00000226877.1
24	lnc-RMI1-6	chr9:86432881-86432983	ENSG00000245608
25	lnc-RMI1-6	chr9:86435226-86435354	NONHSAT132748
26	lnc-RMI1-6	chr9:86442823-86443094	NONHSAT132748
27	lnc-RMI1-5	chr9:86469971-86470092	ENSG00000231616.4
28	lnc-RMI1-5	chr9:86452323-86452500	ENSG00000226877.1
29	lnc-RMI1-5	chr9:86451945-86452058	ENSG00000226877.1
30	lnc-RMI1-5	chr9:86473756-86474075	ENSG00000231616.4
31	lnc-RMI1-5	chr9:86464287-86464506	ENSG00000231616.4
32	lnc-RMI1-5	chr9:86474193-86474250	ENSG00000231616.4
33	lnc-RMI1-6	chr9:86433316-86433488	NONHSAT132748
34	lnc-RMI1-5	chr9:86452587-86452779	ENSG00000226877.1
35	lnc-KIF27-1	chr9:86432900-86433036	NONHSAT132747
36	lnc-RMI1-6	chr9:86435226-86435354	ENSG00000245608
37	lnc-RMI1-5	chr9:86474492-86475013	ENSG00000231616.4
38	lnc-RMI1-5	chr9:86474193-86474250	ENSG00000231616.4
39	lnc-RMI1-5	chr9:86463753-86463870	ENSG00000231616.4
40	lnc-RMI1-5	chr9:86482629-86483335	ENSG00000231616.4
41	lnc-RMI1-5	chr9:86464287-86464506	ENSG00000231616.4
42	lnc-RMI1-5	chr9:86473893-86474075	ENSG00000231616.4
43	lnc-KIF27-1	chr9:86431911-86432042	NONHSAT132747
44	lnc-RMI1-5	chr9:86452587-86452776	ENSG00000226877.3
45	lnc-RMI1-5	chr9:86446475-86446527	ENSG00000226877.1
46	lnc-RMI1-6	chr9:86434446-86434617	ENSG00000245608
47	lnc-RMI1-5	chr9:86446478-86446527	ENSG00000226877.1
48	lnc-RMI1-5	chr9:86451945-86452058	ENSG00000226877.1
49	lnc-RMI1-5	chr9:86474492-86474795	ENSG00000231616.4
50	lnc-RMI1-6	chr9:86432881-86432983	NONHSAT132748

No data

Variant related genes	Relation type
ENSG00000226877	TF binding region
ENSG00000231616	TF binding region
GKAP1	TF binding region
ENSG00000226877	CpG island
ENSG00000231616	CpG island
GKAP1	CpG island
ENSG00000254473	chromatin interactions
ENSG00000135018	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000148057	chromatin interactions
PDS5B	miRNA target sites
RUNX1	miRNA target sites
RNF182	miRNA target sites
FAM49B	miRNA target sites

Extended variants
information (count: 2342 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2342 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188019069	chr9:86424168-86424169	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs295282	chr9:86424198-86424199	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2780088	chr9:86424206-86424207	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34399155	chr9:86424221-86424222	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs71502720	chr9:86424274-86424275	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs2778329	chr9:86424275-86424276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs142400659	chr9:86424300-86424301	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2778328	chr9:86424304-86424305	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs548608278	chr9:86424323-86424324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546392510	chr9:86424343-86424344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs12553541	chr9:86424345-86424346	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567202587	chr9:86424354-86424355	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs2778327	chr9:86424404-86424405	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534384303	chr9:86424410-86424411	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs559229349	chr9:86424435-86424436	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570936668	chr9:86424439-86424440	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs295283	chr9:86424464-86424465	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs181993394	chr9:86424467-86424468	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs574752717	chr9:86424541-86424542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2780089	chr9:86424544-86424545	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs295284	chr9:86424566-86424567	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532313923	chr9:86424568-86424569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554857905	chr9:86424657-86424658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2780090	chr9:86424692-86424693	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs295285	chr9:86424714-86424715	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs295286	chr9:86424774-86424775	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531277957	chr9:86424787-86424788	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs186171118	chr9:86424813-86424814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs561683467	chr9:86424830-86424831	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs528880658	chr9:86424882-86424883	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547410442	chr9:86424889-86424890	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs550482721	chr9:86424898-86424899	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs192077336	chr9:86424910-86424911	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528020296	chr9:86424930-86424931	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552778875	chr9:86424949-86424950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183387067	chr9:86425004-86425005	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369900533	chr9:86425017-86425018	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556387035	chr9:86425047-86425048	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563380966	chr9:86425124-86425125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186813841	chr9:86425135-86425136	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554170053	chr9:86425153-86425154	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571984300	chr9:86425175-86425176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373789926	chr9:86425188-86425189	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs138028020	chr9:86425195-86425196	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs557494491	chr9:86425207-86425208	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs191188024	chr9:86425215-86425216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs543066640	chr9:86425220-86425221	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561620498	chr9:86425259-86425260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143123190	chr9:86425291-86425292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545204611	chr9:86425332-86425333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86350000-86431600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:86353000-86432000	Weak transcription	Lung	lung
3	chr9:86363800-86431200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr9:86377200-86432000	Weak transcription	Gastric	stomach
5	chr9:86380200-86431600	Weak transcription	Fetal Kidney	kidney
6	chr9:86383600-86425800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr9:86389000-86431600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr9:86392000-86431600	Weak transcription	Psoas Muscle	Psoas
9	chr9:86392000-86431800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr9:86394400-86431600	Weak transcription	Colon Smooth Muscle	Colon
11	chr9:86399000-86431000	Weak transcription	A549	lung
12	chr9:86399400-86431000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr9:86399400-86431200	Weak transcription	Fetal Stomach	stomach
14	chr9:86399400-86431400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr9:86399400-86431600	Weak transcription	Right Ventricle	heart
16	chr9:86399400-86431800	Weak transcription	Esophagus	oesophagus
17	chr9:86399400-86431800	Weak transcription	Pancreas	Pancrea
18	chr9:86402800-86431600	Weak transcription	Fetal Brain Female	brain
19	chr9:86407000-86431600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:86408200-86431200	Weak transcription	Dnd41	blood
21	chr9:86409800-86431600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr9:86410400-86432000	Weak transcription	Small Intestine	intestine
23	chr9:86411200-86431400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr9:86412200-86432000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:86412600-86431000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr9:86413200-86431200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr9:86413800-86431000	Weak transcription	Aorta	Aorta
28	chr9:86413800-86431200	Weak transcription	Brain Hippocampus Middle	brain
29	chr9:86413800-86431600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr9:86413800-86431600	Weak transcription	Fetal Muscle Trunk	muscle
31	chr9:86414000-86430400	Weak transcription	HepG2	liver
32	chr9:86414000-86431200	Weak transcription	Primary B cells from peripheral blood	blood
33	chr9:86414200-86431000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr9:86414200-86431000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr9:86414200-86431000	Weak transcription	Brain Cingulate Gyrus	brain
36	chr9:86414200-86431000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:86414200-86431200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr9:86414200-86431200	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr9:86414200-86431400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr9:86414200-86431400	Weak transcription	Brain Anterior Caudate	brain
41	chr9:86414200-86431400	Weak transcription	Fetal Muscle Leg	muscle
42	chr9:86414200-86431600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr9:86414200-86431600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr9:86414600-86431200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr9:86416200-86431000	Weak transcription	Fetal Heart	heart
46	chr9:86417800-86431800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:86418000-86431000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:86418000-86431000	Weak transcription	Fetal Intestine Small	intestine
49	chr9:86418800-86426200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:86419200-86431600	Weak transcription	Fetal Intestine Large	intestine

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