Variant report

Variant	nsv1029876
Chromosome Location	chr9:2526760-2633562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1225)
CpG islands
(count:611)
Chromatin interactive
region (count:22)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:2570935-2570937	HepG2	liver:	n/a	n/a
2	ATF1	chr9:2570654-2571097	K562	blood:	n/a	n/a
3	ATF2	chr9:2602570-2603228	GM12878	blood:	n/a	n/a
4	ATF2	chr9:2602546-2603254	GM12878	blood:	n/a	n/a
5	ATF2	chr9:2616716-2617355	GM12878	blood:	n/a	n/a
6	ATF2	chr9:2570491-2571088	GM12878	blood:	n/a	n/a
7	ATF2	chr9:2570575-2571089	GM12878	blood:	n/a	n/a
8	ATF3	chr9:2623434-2623749	H1-hESC	embryonic stem cell:	n/a	chr9:2623474-2623494
9	BACH1	chr9:2568840-2568890	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:2621410-2621682	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:2621293-2621482	GM12878	blood:	n/a	n/a
12	BATF	chr9:2602261-2602493	GM12878	blood:	n/a	n/a
13	BATF	chr9:2570619-2571066	GM12878	blood:	n/a	n/a
14	BATF	chr9:2621265-2621528	GM12878	blood:	n/a	n/a
15	BATF	chr9:2570593-2570937	GM12878	blood:	n/a	n/a
16	BATF	chr9:2617015-2617371	GM12878	blood:	n/a	n/a
17	BATF	chr9:2602596-2603221	GM12878	blood:	n/a	n/a
18	BATF	chr9:2617020-2617395	GM12878	blood:	n/a	n/a
19	BATF	chr9:2602600-2603204	GM12878	blood:	n/a	n/a
20	BATF	chr9:2617416-2617678	GM12878	blood:	n/a	n/a
21	BATF	chr9:2617423-2617686	GM12878	blood:	n/a	n/a
22	BCL11A	chr9:2570653-2571002	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:2602637-2602848	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:2602578-2603142	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:2616785-2617375	GM12878	blood:	n/a	chr9:2617113-2617122
26	BCL11A	chr9:2616999-2617318	GM12878	blood:	n/a	chr9:2617113-2617122
27	BCL3	chr9:2601903-2602131	GM12878	blood:	n/a	n/a
28	BCL3	chr9:2570621-2571006	GM12878	blood:	n/a	n/a
29	BCL3	chr9:2602568-2602933	GM12878	blood:	n/a	n/a
30	BCLAF1	chr9:2570647-2571008	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:2570676-2571086	GM12878	blood:	n/a	n/a
32	BHLHE40	chr9:2570762-2571109	K562	blood:	n/a	n/a
33	BHLHE40	chr9:2621256-2621931	GM12878	blood:	n/a	chr9:2621658-2621674 chr9:2621798-2621814 chr9:2621583-2621599 chr9:2621799-2621815
34	BHLHE40	chr9:2621446-2621718	K562	blood:	n/a	chr9:2621658-2621674 chr9:2621583-2621599
35	BHLHE40	chr9:2623320-2623869	HepG2	liver:	n/a	chr9:2623484-2623493 chr9:2623485-2623494 chr9:2623485-2623494
36	BHLHE40	chr9:2621241-2621747	HepG2	liver:	n/a	chr9:2621658-2621674 chr9:2621583-2621599
37	BHLHE40	chr9:2623345-2623847	A549	lung:	n/a	chr9:2623484-2623493 chr9:2623485-2623494 chr9:2623485-2623494
38	BHLHE40	chr9:2622428-2622971	GM12878	blood:	n/a	chr9:2622781-2622797 chr9:2622746-2622762
39	BHLHE40	chr9:2602783-2603189	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:2623210-2623849	GM12878	blood:	n/a	chr9:2623484-2623493 chr9:2623485-2623494 chr9:2623485-2623494
41	BRCA1	chr9:2623380-2623503	HepG2	liver:	n/a	n/a
42	BRCA1	chr9:2570638-2571415	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr9:2570525-2571114	HCT-116	colon:	n/a	n/a
44	CCNT2	chr9:2621423-2621804	K562	blood:	n/a	n/a
45	CCNT2	chr9:2583456-2583656	K562	blood:	n/a	n/a
46	CEBPB	chr9:2621212-2621491	K562	blood:	n/a	n/a
47	CEBPB	chr9:2609838-2609957	H1-hESC	embryonic stem cell:	n/a	chr9:2609864-2609875
48	CEBPB	chr9:2602592-2603169	Hela-S3	cervix:	n/a	chr9:2602944-2602955
49	CEBPB	chr9:2621155-2621549	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:2570528-2571233	HCT-116	colon:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:2621918-2621968	ProgFib	skin:	n/a
2	chr9:2621918-2621968	ProgFib	skin:	n/a
3	chr9:2621918-2621968	T-47D	breast:	n/a
4	chr9:2623146-2623196	PrEC	prostate:	n/a
5	chr9:2623146-2623196	AG09309	skin:	n/a
6	chr9:2623684-2623734	MCF10A-Er-Src	breast:	n/a
7	chr9:2626347-2626397	GM12878	blood:	n/a
8	chr9:2623684-2623734	GM19239	blood:	n/a
9	chr9:2626347-2626397	HNPCEpiC	eye:	n/a
10	chr9:2623562-2623612	PANC-1	pancreas:	n/a
11	chr9:2619314-2619364	HUVEC	blood vessel:	n/a
12	chr9:2619314-2619364	Hela-S3	cervix:	n/a
13	chr9:2621379-2621429	SK-N-SH	brain:	n/a
14	chr9:2621094-2621144	SAEC	small airway:	n/a
15	chr9:2623684-2623734	SK-N-SH_RA	brain:	n/a
16	chr9:2619314-2619364	HL-60	blood:	n/a
17	chr9:2626347-2626397	SAEC	small airway:	n/a
18	chr9:2619314-2619364	BJ	skin:	n/a
19	chr9:2622584-2622634	BJ	skin:	n/a
20	chr9:2571396-2571446	AG04449	skin:	fetal
21	chr9:2621094-2621144	HCM	heart:	n/a
22	chr9:2621918-2621968	LNCaP	prostate:	n/a
23	chr9:2623684-2623734	HEK293	kidney:	embryo
24	chr9:2623562-2623612	NHDF-neo	bronchial:	n/a
25	chr9:2619314-2619364	ECC-1	luminal epithelium:	n/a
26	chr9:2623562-2623612	NB4	blood:	n/a
27	chr9:2619314-2619364	HCF	heart:	n/a
28	chr9:2622584-2622634	HepG2	liver:	n/a
29	chr9:2623684-2623734	HCT-116	colon:	n/a
30	chr9:2619314-2619364	NB4	blood:	n/a
31	chr9:2571396-2571446	SKMC	muscle:	n/a
32	chr9:2622584-2622634	HMEC	breast:	n/a
33	chr9:2623146-2623196	ECC-1	luminal epithelium:	n/a
34	chr9:2623146-2623196	NHBE	bronchial:	n/a
35	chr9:2623146-2623196	LNCaP	prostate:	n/a
36	chr9:2621094-2621144	ovcar-3	ovarian:	n/a
37	chr9:2623562-2623612	HEEpiC	esophagus:	n/a
38	chr9:2621094-2621144	NT2-D1	testis:	n/a
39	chr9:2621379-2621429	AG04449	skin:	fetal
40	chr9:2621918-2621968	HEEpiC	esophagus:	n/a
41	chr9:2623562-2623612	HRPEpiC	eye:	n/a
42	chr9:2621379-2621429	Caco-2	colon:	n/a
43	chr9:2571396-2571446	HRCEpiC	kidney:	n/a
44	chr9:2622584-2622634	T-47D	breast:	n/a
45	chr9:2619314-2619364	HMEC	breast:	n/a
46	chr9:2621094-2621144	GM12878	blood:	n/a
47	chr9:2623562-2623612	RPTEC	kidney:	n/a
48	chr9:2623146-2623196	A549	lung:	n/a
49	chr9:2622584-2622634	RPTEC	kidney:	n/a
50	chr9:2571396-2571446	ECC-1	luminal epithelium:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:2613986..2615496-chr9:2621852..2624711,2	MCF-7	breast:
2	chr9:2228114..2228719-chr9:2625246..2626097,2	MCF-7	breast:
3	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
4	chr9:2619846..2622881-chr9:2631771..2635491,3	MCF-7	breast:
5	chr9:2611403..2613342-chr9:2621748..2624247,2	MCF-7	breast:
6	chr9:2620203..2621987-chr9:2627062..2629533,2	MCF-7	breast:
7	chr9:2613768..2615804-chr9:2618805..2621446,2	K562	blood:
8	chr9:2567610..2570420-chr9:2620713..2623138,2	MCF-7	breast:
9	chr9:2621566..2623636-chr9:2638581..2641950,3	MCF-7	breast:
10	chr9:2624771..2627181-chr9:2629101..2631938,2	MCF-7	breast:
11	chr9:2616577..2619117-chr9:2619974..2622873,2	MCF-7	breast:
12	chr9:2620987..2624573-chr9:2639977..2643677,3	MCF-7	breast:
13	chr9:2618162..2620045-chr9:2621820..2624612,2	K562	blood:
14	chr9:2624771..2627181-chr9:2629101..2631938,2	MCF-7	breast:
15	chr9:2573981..2575628-chr9:2620967..2623639,2	MCF-7	breast:
16	chr9:2598816..2601731-chr9:2621895..2624839,2	MCF-7	breast:
17	chr9:2617041..2619621-chr9:2621235..2624621,3	MCF-7	breast:
18	chr9:2622798..2625667-chr9:2640741..2642429,2	K562	blood:
19	chr9:2621586..2624495-chr9:2626376..2628188,2	K562	blood:
20	chr9:2549233..2551309-chr9:2562434..2565091,2	K562	blood:
21	chr10:27845465..27846029-chr9:2600388..2600977,2	MCF-7	breast:
22	chr9:2255030..2255773-chr9:2600478..2601011,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
2	lnc-KIAA0020-1	chr9:2535652-2536015	ENSG00000236404
3	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404.4
4	lnc-VLDLR-1	chr9:2541548-2541635	XLOC_007267
5	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
6	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404.4
7	lnc-KIAA0020-1	chr9:2535652-2536015	ENSG00000236404
8	lnc-KIAA0020-1	chr9:2621229-2621413	ENSG00000236404.4
9	lnc-KIAA0020-1	chr9:2539399-2539552	NONHSAT129997
10	lnc-VLDLR-3	chr9:2531097-2531214	NONHSAT129998
11	lnc-KIAA0020-1	chr9:2536359-2536453	ENSG00000236404
12	lnc-KIAA0020-1	chr9:2621229-2621413	ENSG00000236404
13	lnc-KIAA0020-1	chr9:2619998-2621792	NONHSAT130002
14	lnc-KIAA0020-1	chr9:2535724-2536015	NONHSAT129997
15	lnc-KIAA0020-1	chr9:2570622-2570754	ENSG00000236404
16	lnc-KIAA0020-1	chr9:2539399-2539552	NR_015375
17	lnc-KIAA0020-1	chr9:2536359-2536453	NONHSAT129997
18	lnc-KIAA0020-1	chr9:2536359-2536453	NR_015375
19	lnc-KIAA0020-1	chr9:2529289-2529552	l_3727_chr9:2411588-2611526_ovary
20	lnc-KIAA0020-1	chr9:2535655-2536015	NR_015375
21	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404
22	lnc-KIAA0020-1	chr9:2611229-2611526	l_3727_chr9:2411588-2611526_ovary
23	lnc-KIAA0020-1	chr9:2560622-2560842	l_3727_chr9:2411588-2611526_ovary
24	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404
25	lnc-KIAA0020-1	chr9:2539399-2539552	ENSG00000236404
26	lnc-KIAA0020-1	chr9:2622100-2622373	NR_015375
27	lnc-KIAA0020-1	chr9:2622100-2622373	ENSG00000236404
28	lnc-VLDLR-1	chr9:2541097-2541214	XLOC_007267
29	lnc-VLDLR-3	chr9:2531548-2531635	NONHSAT129998

No data

Variant related genes	Relation type
ENSG00000236404	TF binding region
ENSG00000231052	TF binding region
VLDLR	TF binding region
ENSG00000236404	CpG island
ENSG00000231052	CpG island
VLDLR	CpG island
ENSG00000236404	chromatin interactions
ENSG00000147852	chromatin interactions
PRKAR1A	miRNA target sites
CCNE2	miRNA target sites
SPRED1	miRNA target sites
PTEN	miRNA target sites
SLC19A2	miRNA target sites
DZIP3	miRNA target sites
ZBTB34	miRNA target sites

Extended variants
information (count: 5237 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:5237 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1015469	chr9:2526760-2526761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186554717	chr9:2526768-2526769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551745691	chr9:2526781-2526782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551294417	chr9:2526787-2526788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377045648	chr9:2526847-2526848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1537191	chr9:2526890-2526891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs147304913	chr9:2526899-2526900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554386061	chr9:2526900-2526901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1571816	chr9:2526961-2526962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs191338764	chr9:2527001-2527002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369293483	chr9:2527057-2527058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183829805	chr9:2527068-2527069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571135124	chr9:2527095-2527096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77137951	chr9:2527120-2527121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569730451	chr9:2527138-2527139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558948160	chr9:2527190-2527191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75408615	chr9:2527255-2527256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369219352	chr9:2527281-2527282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571374358	chr9:2527287-2527288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541504042	chr9:2527335-2527336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10812201	chr9:2527369-2527370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566079856	chr9:2527373-2527374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376304893	chr9:2527392-2527393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543649504	chr9:2527423-2527424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533972165	chr9:2527426-2527427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377666092	chr9:2527434-2527435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112852656	chr9:2527437-2527438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563947122	chr9:2527454-2527455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10738707	chr9:2527460-2527461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs148971140	chr9:2527481-2527482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539757772	chr9:2527517-2527518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386731715	chr9:2527525-2527526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111598081	chr9:2527554-2527555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568038489	chr9:2527588-2527589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193144382	chr9:2527592-2527593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185332238	chr9:2527629-2527630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374376630	chr9:2527635-2527636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570666299	chr9:2527673-2527674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10966785	chr9:2527712-2527713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7037427	chr9:2527752-2527753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140443781	chr9:2527757-2527758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10812202	chr9:2527766-2527767	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554993215	chr9:2527772-2527773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116915937	chr9:2527776-2527777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7021521	chr9:2527792-2527793	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115220938	chr9:2527819-2527820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577042131	chr9:2527881-2527882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546051464	chr9:2527884-2527885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7021724	chr9:2527900-2527901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs542223210	chr9:2527940-2527941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
Melanoma	18172304	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
Ovarian cancer	21720365	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
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
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Schizophrenia	23813976	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	20967226	CNVD
Maculopathy	22355348	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1455 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2487400-2533400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr9:2493400-2529000	Weak transcription	Pancreas	Pancrea
3	chr9:2503400-2541000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr9:2506600-2528800	Weak transcription	Left Ventricle	heart
5	chr9:2506600-2559200	Weak transcription	Adipose Nuclei	Adipose
6	chr9:2520400-2537400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr9:2522200-2542600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:2522600-2538200	Weak transcription	Ovary	ovary
9	chr9:2524800-2527400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr9:2526200-2526800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr9:2526400-2526800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr9:2526600-2526800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr9:2527400-2539600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:2529200-2549800	Weak transcription	Aorta	Aorta
15	chr9:2530800-2537600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr9:2531600-2532400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:2532200-2532600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:2532400-2537400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:2532600-2536000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr9:2533000-2541800	Weak transcription	Brain Substantia Nigra	brain
21	chr9:2533400-2533600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr9:2534200-2537000	Weak transcription	Left Ventricle	heart
23	chr9:2535600-2539400	Weak transcription	Fetal Brain Female	brain
24	chr9:2537000-2537200	Enhancers	Left Ventricle	heart
25	chr9:2537000-2537400	Enhancers	Fetal Heart	heart
26	chr9:2537200-2556000	Weak transcription	Left Ventricle	heart
27	chr9:2537400-2538800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr9:2537600-2537800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr9:2538200-2538600	Strong transcription	Ovary	ovary
30	chr9:2538200-2538800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr9:2538600-2549800	Weak transcription	Ovary	ovary
32	chr9:2538800-2540600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:2539600-2541200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:2540000-2541000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:2540600-2540800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:2541800-2542400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr9:2542400-2559200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr9:2542600-2542800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:2542800-2549200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:2545800-2546600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:2545800-2546600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:2545800-2546600	Enhancers	Brain Anterior Caudate	brain
43	chr9:2545800-2546800	Enhancers	Brain Substantia Nigra	brain
44	chr9:2546000-2546200	Enhancers	Psoas Muscle	Psoas
45	chr9:2546000-2546200	Enhancers	Stomach Mucosa	stomach
46	chr9:2546000-2546600	Enhancers	Brain Hippocampus Middle	brain
47	chr9:2546200-2546400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:2546200-2546800	Enhancers	Brain Angular Gyrus	brain
49	chr9:2546200-2551800	Weak transcription	Psoas Muscle	Psoas
50	chr9:2546400-2547000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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