Variant report

Variant	nsv1018926
Chromosome Location	chr9:965006-1014141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1288)
CpG islands
(count:2501)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:1009225-1009309	K562	blood:	n/a	n/a
2	ATF1	chr9:1013083-1013384	K562	blood:	n/a	n/a
3	BACH1	chr9:971586-971900	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:1005054-1005459	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:969420-970114	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:971010-971040	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr9:972119-972583	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:976333-976475	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr9:998447-999060	GM12878	blood:	n/a	n/a
10	BATF	chr9:998485-999029	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:998478-999038	GM12878	blood:	n/a	n/a
12	BCL11A	chr9:998476-999059	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:1009111-1009469	HepG2	liver:	n/a	chr9:1009235-1009251
14	BHLHE40	chr9:1009153-1009539	GM12878	blood:	n/a	chr9:1009235-1009251
15	BHLHE40	chr9:1009121-1009447	K562	blood:	n/a	chr9:1009235-1009251
16	BHLHE40	chr9:998476-999116	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:1005037-1005437	GM12878	blood:	n/a	n/a
18	BRCA1	chr9:1009179-1009384	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:1009140-1009395	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:968034-968190	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr9:998488-999102	K562	blood:	n/a	n/a
22	CBX3	chr9:998426-999145	K562	blood:	n/a	n/a
23	CEBPB	chr9:967405-967773	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr9:1007275-1007605	HepG2	liver:	n/a	chr9:1007420-1007431
25	CEBPB	chr9:1006646-1006667	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:1007270-1007577	IMR90	lung:	n/a	chr9:1007420-1007431
27	CEBPB	chr9:1005104-1005356	HepG2	liver:	n/a	n/a
28	CEBPB	chr9:1007119-1007701	MCF-7	breast:	n/a	chr9:1007420-1007431
29	CEBPB	chr9:1005027-1005521	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:1008255-1008623	IMR90	lung:	n/a	n/a
31	CEBPB	chr9:1007173-1007672	MCF-7	breast:	n/a	chr9:1007420-1007431
32	CEBPB	chr9:1009159-1009464	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:1008314-1008607	A549	lung:	n/a	n/a
34	CEBPB	chr9:1005051-1005367	A549	lung:	n/a	n/a
35	CEBPB	chr9:1005008-1005372	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:1007275-1007607	A549	lung:	n/a	chr9:1007420-1007431
37	CHD1	chr9:975419-975456	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr9:1009154-1009437	GM12878	blood:	n/a	n/a
39	CHD1	chr9:977536-977736	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr9:976980-977174	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr9:974839-975039	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:1009169-1009480	HepG2	liver:	n/a	n/a
43	CHD2	chr9:967533-968215	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr9:1009154-1009544	GM12878	blood:	n/a	n/a
45	CHD2	chr9:972108-972282	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr9:976157-976788	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr9:971492-971716	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr9:970707-970888	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr9:977073-977522	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr9:971321-971843	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2501 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:973198-973248	LNCaP	prostate:	n/a
2	chr9:969473-969523	NHBE	bronchial:	n/a
3	chr9:990260-990310	AG04449	skin:	fetal
4	chr9:995579-995629	HAEpiC	amniotic membrane:	n/a
5	chr9:990618-990668	GM12878	blood:	n/a
6	chr9:997475-997525	SK-N-MC	brain:	n/a
7	chr9:970882-970932	SK-N-SH	brain:	n/a
8	chr9:969530-969580	ProgFib	skin:	n/a
9	chr9:974533-974583	CMK	blood:	n/a
10	chr9:975856-975906	HNPCEpiC	eye:	n/a
11	chr9:990692-990742	GM19239	blood:	n/a
12	chr9:970297-970347	U87	brain:	n/a
13	chr9:977109-977159	NT2-D1	testis:	n/a
14	chr9:971046-971096	SAEC	small airway:	n/a
15	chr9:971046-971096	AG09309	skin:	n/a
16	chr9:976634-976684	Caco-2	colon:	n/a
17	chr9:998533-998583	SK-N-SH	brain:	n/a
18	chr9:972520-972570	HCM	heart:	n/a
19	chr9:998533-998583	AG10803	skin:	n/a
20	chr9:970297-970347	HL-60	blood:	n/a
21	chr9:972622-972672	GM19239	blood:	n/a
22	chr9:990692-990742	HIPEpiC	eye:	n/a
23	chr9:975997-976047	HRCEpiC	kidney:	n/a
24	chr9:990618-990668	H1-hESC	embryonic stem cell:	embryo
25	chr9:972520-972570	PrEC	prostate:	n/a
26	chr9:969473-969523	U87	brain:	n/a
27	chr9:976947-976997	H1-hESC	embryonic stem cell:	embryo
28	chr9:977490-977540	NHBE	bronchial:	n/a
29	chr9:972622-972672	HCPEpiC	choroid plexus:	n/a
30	chr9:976645-976695	RPTEC	kidney:	n/a
31	chr9:975825-975875	GM12878	blood:	n/a
32	chr9:998533-998583	PANC-1	pancreas:	n/a
33	chr9:976947-976997	HEEpiC	esophagus:	n/a
34	chr9:971757-971807	HCF	heart:	n/a
35	chr9:976645-976695	Jurkat	blood:	n/a
36	chr9:990260-990310	SAEC	small airway:	n/a
37	chr9:972622-972672	GM06990	blood:	n/a
38	chr9:970654-970704	AG10803	skin:	n/a
39	chr9:991047-991097	GM19239	blood:	n/a
40	chr9:977109-977159	Hepatocyte	liver:	n/a
41	chr9:970297-970347	PFSK-1	brain:	n/a
42	chr9:998547-998597	SAEC	small airway:	n/a
43	chr9:968090-968140	U87	brain:	n/a
44	chr9:973184-973234	ProgFib	skin:	n/a
45	chr9:972622-972672	HUVEC	blood vessel:	n/a
46	chr9:977770-977820	GM12878	blood:	n/a
47	chr9:972520-972570	AG10803	skin:	n/a
48	chr9:975997-976047	H1-hESC	embryonic stem cell:	embryo
49	chr9:991047-991097	PFSK-1	brain:	n/a
50	chr9:970654-970704	BJ	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:890713..892471-chr9:1006171..1008763,2	MCF-7	breast:
2	chr9:994727..996463-chr9:998360..1001251,2	K562	blood:
3	chr9:978343..980542-chr9:980897..983519,2	K562	blood:
4	chr9:979709..982475-chr9:990921..992536,2	MCF-7	breast:
5	chr9:960997..962745-chr9:963158..965869,2	MCF-7	breast:
6	chr9:978343..980542-chr9:980897..983519,2	K562	blood:
7	chr9:892914..894635-chr9:997792..999398,19	MCF-7	breast:
8	chr9:893739..894732-chr9:1008819..1009733,5	MCF-7	breast:
9	chr9:950930..953777-chr9:967112..968787,2	MCF-7	breast:
10	chr9:998424..999235-chr9:1008893..1009451,2	MCF-7	breast:
11	chr9:979709..982475-chr9:990921..992536,2	MCF-7	breast:
12	chr9:962191..965396-chr9:970150..972525,3	MCF-7	breast:
13	chr9:899986..901721-chr9:992328..994954,2	MCF-7	breast:
14	chr9:979898..983032-chr9:983503..985277,3	MCF-7	breast:
15	chr9:958309..961593-chr9:963098..965708,4	MCF-7	breast:
16	chr9:971648..973169-chr9:976261..977886,2	MCF-7	breast:
17	chr9:892531..895372-chr9:1005273..1008806,3	MCF-7	breast:
18	chr9:959751..962676-chr9:970259..973174,2	K562	blood:
19	chr9:893804..894399-chr9:1008894..1009774,3	K562	blood:
20	chr9:967263..969449-chr9:973261..974895,2	MCF-7	breast:
21	chr9:891599..892777-chr9:998523..999622,4	MCF-7	breast:
22	chr9:893903..894431-chr9:1004790..1005383,2	K562	blood:
23	chr9:1009051..1010072-chr9:1017840..1018709,4	MCF-7	breast:
24	chr9:892827..894783-chr9:997829..1000001,46	MCF-7	breast:
25	chr9:893937..894571-chr9:1000555..1001318,2	MCF-7	breast:
26	chr9:763938..764768-chr9:1004823..1005723,3	MCF-7	breast:
27	chr9:889496..890427-chr9:998557..999062,2	MCF-7	breast:
28	chr9:967263..969449-chr9:973261..974895,2	MCF-7	breast:
29	chr9:887794..889918-chr9:1005357..1008295,2	MCF-7	breast:
30	chr9:893523..894096-chr9:1008794..1009361,2	MCF-7	breast:
31	chr9:994727..996463-chr9:998360..1001251,2	K562	blood:
32	chr9:982152..984016-chr9:986443..989260,2	MCF-7	breast:
33	chr9:892287..894400-chr9:997529..999081,2	MCF-7	breast:
34	chr9:982152..984016-chr9:986443..989260,2	MCF-7	breast:
35	chr9:947744..949483-chr9:965915..968744,2	MCF-7	breast:
36	chr9:979898..983032-chr9:983503..985277,3	MCF-7	breast:
37	chr9:982598..984781-chr9:987934..990176,2	MCF-7	breast:
38	chr9:893090..895102-chr9:997642..1000257,3	MCF-7	breast:
39	chr9:910762..911411-chr9:998511..999239,3	MCF-7	breast:
40	chr9:385756..386457-chr9:1008777..1009377,2	MCF-7	breast:
41	chr9:968342..970313-chr9:973554..975096,2	K562	blood:
42	chr9:1007423..1009287-chr9:1045081..1047981,2	MCF-7	breast:
43	chr9:826413..827016-chr9:1004866..1005745,2	MCF-7	breast:
44	chr9:970488..973347-chr9:974585..976403,2	K562	blood:
45	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
46	chr12:97384088..97385884-chr9:964414..966557,2	MCF-7	breast:
47	chr9:892413..895344-chr9:995955..997519,2	MCF-7	breast:
48	chr2:238421116..238421980-chr9:998514..999134,2	MCF-7	breast:
49	chr9:988079..991446-chr9:991820..996186,5	MCF-7	breast:
50	chr9:970488..973347-chr9:974585..976403,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMRT3-1	chr9:974188-974410	NONHSAT129952
2	lnc-DMRT3-4	chr9:1011085-1011386	NONHSAT129956
3	lnc-DMRT3-4	chr9:1011710-1011799	NONHSAT129956

No data

Variant related genes	Relation type
ENSG00000228783	TF binding region
RNU6-1073P	TF binding region
DMRT3	TF binding region
ENSG00000228783	CpG island
RNU6-1073P	CpG island
DMRT3	CpG island
ENSG00000173253	chromatin interactions
ENSG00000064218	chromatin interactions

Extended variants
information (count: 2039 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:2039 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553891741	chr9:965400-965401	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs573685638	chr9:965415-965416	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs186709879	chr9:965436-965437	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs538352314	chr9:965446-965447	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs554627275	chr9:965468-965469	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs376199038	chr9:965469-965470	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs79875714	chr9:965527-965528	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs576624118	chr9:965575-965576	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs574780021	chr9:965590-965591	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs545691746	chr9:965629-965630	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565429158	chr9:965648-965649	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527933460	chr9:965703-965704	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146379006	chr9:965710-965711	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540559870	chr9:965777-965778	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560445521	chr9:965790-965791	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80132297	chr9:965794-965795	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548672552	chr9:965811-965812	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139652655	chr9:965831-965832	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144515898	chr9:965834-965835	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551309620	chr9:965838-965839	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571101245	chr9:965918-965919	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533775500	chr9:965961-965962	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs35750597	chr9:965972-965973	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191660006	chr9:965989-965990	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567396269	chr9:966028-966029	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4742604	chr9:966042-966043	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73382420	chr9:966058-966059	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146624886	chr9:966089-966090	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538957381	chr9:966100-966101	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74968864	chr9:966154-966155	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376238451	chr9:966172-966173	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140034024	chr9:966200-966201	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs279897	chr9:966257-966258	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541674042	chr9:966274-966275	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561487593	chr9:966287-966288	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72701073	chr9:966305-966306	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78657742	chr9:966321-966322	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546384538	chr9:966351-966352	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562342462	chr9:966358-966359	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531378565	chr9:966361-966362	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182680815	chr9:966396-966397	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377223064	chr9:966410-966411	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72701074	chr9:966420-966421	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564866236	chr9:966435-966436	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145700739	chr9:966488-966489	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539136074	chr9:966514-966515	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369779925	chr9:966518-966519	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367663770	chr9:966538-966539	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374482698	chr9:966563-966564	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187055410	chr9:966571-966572	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	21272361	CNVD
Non-small cell lung cancer	16651412	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Ovarian cancer	21781307	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD

Chromatin state (count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:965400-965600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:965400-966000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:965400-966000	Bivalent Enhancer	Fetal Kidney	kidney
4	chr9:965400-966800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:965600-965800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr9:965600-965800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr9:965600-965800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:965600-966000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
9	chr9:965600-967600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
10	chr9:965800-966000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr9:965800-966000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr9:965800-966000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr9:965800-966000	Bivalent Enhancer	Brain Hippocampus Middle	brain
14	chr9:966000-967000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:966800-967000	Bivalent Enhancer	Fetal Kidney	kidney
16	chr9:966800-967400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr9:966800-967400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr9:966800-967400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
19	chr9:966800-967600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:966800-967600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr9:966800-968000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
22	chr9:966800-968400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr9:967000-967200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
24	chr9:967000-967400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:967000-967400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
26	chr9:967000-967600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr9:967000-967800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr9:967000-967800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
29	chr9:967200-967600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr9:967400-967600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr9:967400-967600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
32	chr9:967400-968000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
33	chr9:967400-968400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
34	chr9:967600-967800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:967600-967800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:967600-967800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:967600-967800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:967600-967800	Bivalent Enhancer	Fetal Brain Female	brain
39	chr9:967600-968000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
40	chr9:967600-968000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
41	chr9:967600-968200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
42	chr9:967600-968200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:967600-968400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
44	chr9:967600-969000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr9:967800-968000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:967800-968000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr9:967800-968000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
48	chr9:967800-968200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
49	chr9:967800-968200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:967800-968200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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