Variant report

Variant	esv3368118
Chromosome Location	chr9:108006181-108008254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:926)
CpG islands
(count:306)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:108006571-108006804	K562	blood:	n/a	n/a
2	ARID3A	chr9:108006506-108006916	HepG2	liver:	n/a	n/a
3	ATF2	chr9:108006462-108006810	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:108006290-108006898	GM12878	blood:	n/a	n/a
5	ATF2	chr9:108006222-108006848	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:108006351-108006826	GM12878	blood:	n/a	n/a
7	ATF3	chr9:108006253-108006974	A549	lung:	n/a	chr9:108006752-108006761
8	ATF3	chr9:108006379-108006912	A549	lung:	n/a	chr9:108006752-108006761
9	BACH1	chr9:108007355-108008138	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:108006600-108006691	K562	blood:	n/a	n/a
11	BACH1	chr9:108006452-108006840	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:108006468-108006793	GM12878	blood:	n/a	n/a
13	BCL3	chr9:108006255-108006860	A549	lung:	n/a	chr9:108006667-108006680
14	BCL3	chr9:108006483-108006930	GM12878	blood:	n/a	chr9:108006667-108006680
15	BCL3	chr9:108006330-108006927	A549	lung:	n/a	chr9:108006667-108006680
16	BCLAF1	chr9:108006323-108007446	GM12878	blood:	n/a	chr9:108006667-108006680 chr9:108007203-108007216
17	BCLAF1	chr9:108006279-108006939	GM12878	blood:	n/a	chr9:108006667-108006680
18	BCLAF1	chr9:108006464-108006994	K562	blood:	n/a	chr9:108006667-108006680
19	BCLAF1	chr9:108006399-108006886	K562	blood:	n/a	chr9:108006667-108006680
20	BHLHE40	chr9:108006183-108007382	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:108006378-108007331	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:108006335-108006860	K562	blood:	n/a	n/a
23	BRCA1	chr9:108007494-108008290	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr9:108007462-108007698	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr9:108006434-108006821	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr9:108006372-108006849	GM12878	blood:	n/a	n/a
27	BRCA1	chr9:108006458-108006869	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:108006153-108006835	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr9:108006154-108007059	HCT-116	colon:	n/a	n/a
30	CBX3	chr9:108006467-108006812	K562	blood:	n/a	n/a
31	CBX3	chr9:108006125-108007159	HCT-116	colon:	n/a	n/a
32	CBX3	chr9:108006169-108006907	K562	blood:	n/a	n/a
33	CCNT2	chr9:108006550-108007369	K562	blood:	n/a	chr9:108006752-108006761
34	CEBPB	chr9:108007843-108008312	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:108006323-108006966	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:108006243-108006937	GM12878	blood:	n/a	n/a
37	CEBPB	chr9:108006478-108006917	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr9:108006335-108006825	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr9:108006652-108006685	K562	blood:	n/a	n/a
40	CEBPB	chr9:108006337-108006947	A549	lung:	n/a	n/a
41	CEBPD	chr9:108006457-108006943	HepG2	liver:	n/a	n/a
42	CEBPD	chr9:108006498-108006820	HepG2	liver:	n/a	n/a
43	CHD1	chr9:108007227-108008086	H1-hESC	embryonic stem cell:	n/a	chr9:108007384-108007391
44	CHD1	chr9:108005094-108008425	IMR90	lung:	n/a	chr9:108007384-108007391 chr9:108006753-108006763
45	CHD1	chr9:108007937-108007983	GM12878	blood:	n/a	n/a
46	CHD1	chr9:108006132-108006762	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr9:108006540-108006835	GM12878	blood:	n/a	chr9:108006753-108006763
48	CHD1	chr9:108007256-108007401	GM12878	blood:	n/a	chr9:108007384-108007391
49	CHD2	chr9:108006480-108006892	K562	blood:	n/a	chr9:108006753-108006763
50	CHD2	chr9:108007631-108007841	HepG2	liver:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:108006611-108006661	T-47D	breast:	n/a
2	chr9:108006611-108006661	T-47D	breast:	n/a
3	chr9:108006776-108006826	HIPEpiC	eye:	n/a
4	chr9:108008079-108008129	Caco-2	colon:	n/a
5	chr9:108007124-108007174	BE2_C	brain:	n/a
6	chr9:108007124-108007174	AG04450	lung:	fetal
7	chr9:108007124-108007174	H1-hESC	embryonic stem cell:	embryo
8	chr9:108006974-108007024	U87	brain:	n/a
9	chr9:108008079-108008129	GM12878	blood:	n/a
10	chr9:108006776-108006826	ProgFib	skin:	n/a
11	chr9:108006776-108006826	MCF10A-Er-Src	breast:	n/a
12	chr9:108006776-108006826	GM19239	blood:	n/a
13	chr9:108008079-108008129	HCM	heart:	n/a
14	chr9:108006611-108006661	AG04450	lung:	fetal
15	chr9:108008079-108008129	HPAEpiC	pulmonary alveolar:	n/a
16	chr9:108006776-108006826	ECC-1	luminal epithelium:	n/a
17	chr9:108007124-108007174	HCF	heart:	n/a
18	chr9:108006611-108006661	GM12891	blood:	n/a
19	chr9:108007124-108007174	HRE	kidney:	n/a
20	chr9:108007124-108007174	PrEC	prostate:	n/a
21	chr9:108008079-108008129	HEK293	kidney:	embryo
22	chr9:108007124-108007174	HepG2	liver:	n/a
23	chr9:108008079-108008129	GM06990	blood:	n/a
24	chr9:108007124-108007174	NB4	blood:	n/a
25	chr9:108006611-108006661	NB4	blood:	n/a
26	chr9:108007124-108007174	U87	brain:	n/a
27	chr9:108008079-108008129	NT2-D1	testis:	n/a
28	chr9:108006974-108007024	AG04450	lung:	fetal
29	chr9:108008079-108008129	RPTEC	kidney:	n/a
30	chr9:108006776-108006826	NB4	blood:	n/a
31	chr9:108006611-108006661	HepG2	liver:	n/a
32	chr9:108006776-108006826	PANC-1	pancreas:	n/a
33	chr9:108006974-108007024	SK-N-MC	brain:	n/a
34	chr9:108006611-108006661	H1-hESC	embryonic stem cell:	embryo
35	chr9:108006776-108006826	Hepatocyte	liver:	n/a
36	chr9:108007124-108007174	GM19239	blood:	n/a
37	chr9:108006974-108007024	CMK	blood:	n/a
38	chr9:108008079-108008129	HCPEpiC	choroid plexus:	n/a
39	chr9:108007124-108007174	SKMC	muscle:	n/a
40	chr9:108006776-108006826	NHBE	bronchial:	n/a
41	chr9:108008079-108008129	T-47D	breast:	n/a
42	chr9:108006776-108006826	HRPEpiC	eye:	n/a
43	chr9:108006776-108006826	BE2_C	brain:	n/a
44	chr9:108006974-108007024	SK-N-SH_RA	brain:	n/a
45	chr9:108007124-108007174	PFSK-1	brain:	n/a
46	chr9:108008079-108008129	NH-A	brain:	n/a
47	chr9:108006611-108006661	Hepatocyte	liver:	n/a
48	chr9:108008079-108008129	IMR90	lung:	fetal
49	chr9:108006776-108006826	HCF	heart:	n/a
50	chr9:108006974-108007024	AG09319	gingival:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:107631539..107633067-chr9:108007173..108009446,2	MCF-7	breast:
2	chr9:107687369..107691649-chr9:108006197..108009884,7	MCF-7	breast:
3	chr9:107948857..107951560-chr9:108005097..108008240,3	MCF-7	breast:
4	chr9:108005738..108008360-chr9:108117762..108120177,2	MCF-7	breast:
5	chr9:107986788..107989562-chr9:108004560..108006596,2	K562	blood:
6	chr9:108006932..108009449-chr9:108036462..108038843,2	MCF-7	breast:
7	chr9:108007303..108009573-chr9:108053805..108056055,2	MCF-7	breast:
8	chr9:108007022..108007998-chr9:108122682..108123316,3	MCF-7	breast:
9	chr9:108007262..108007998-chr9:108175454..108176410,3	MCF-7	breast:
10	chr9:107904194..107906765-chr9:108007305..108010272,2	MCF-7	breast:
11	chr9:108004369..108006903-chr9:108106116..108108591,2	MCF-7	breast:
12	chr9:107986434..107988530-chr9:108007277..108010113,2	MCF-7	breast:
13	chr2:130939236..130940096-chr9:108006055..108006614,2	NB4	blood:
14	chr9:107964013..107966115-chr9:108007069..108009049,2	MCF-7	breast:
15	chr9:108005319..108006844-chr9:108176651..108179101,2	MCF-7	breast:
16	chr9:108007121..108007988-chr9:108175578..108176396,3	MCF-7	breast:
17	chr9:108003331..108004862-chr9:108007062..108008730,2	MCF-7	breast:
18	chr9:108007148..108008877-chr9:108174581..108177913,4	MCF-7	breast:
19	chr9:108006963..108009238-chr9:108022447..108024092,2	MCF-7	breast:
20	chr9:108006964..108008816-chr9:108165166..108168105,2	MCF-7	breast:
21	chr6:26031886..26032421-chr9:108007272..108008250,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSD1L-3	chr9:108006929-108007185	NONHSAT133813

No data

Variant related genes	Relation type
SLC44A1	TF binding region
SLC44A1	CpG island
ENSG00000238208	chromatin interactions
ENSG00000070214	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000152082	chromatin interactions
ENSG00000165029	chromatin interactions
ENSG00000226334	chromatin interactions

Extended variants
information (count: 67 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:67 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377019262	chr9:108006191-108006192	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs578029871	chr9:108006338-108006339	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs74458447	chr9:108006381-108006382	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs186848476	chr9:108006408-108006409	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs575572117	chr9:108006420-108006421	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs542975081	chr9:108006442-108006443	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs191481197	chr9:108006453-108006454	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs11336701	chr9:108006456-108006457	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs367722562	chr9:108006539-108006540	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs528542825	chr9:108006549-108006550	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs551302571	chr9:108006568-108006569	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs145106337	chr9:108006581-108006582	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs565127901	chr9:108006591-108006592	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs528946176	chr9:108006596-108006597	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs532527204	chr9:108006608-108006609	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs537938243	chr9:108006627-108006628	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs377174856	chr9:108006638-108006639	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs113975509	chr9:108006642-108006643	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs569725953	chr9:108006694-108006695	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs548944986	chr9:108006700-108006701	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs116468181	chr9:108006742-108006743	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs534700808	chr9:108006744-108006745	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs553065067	chr9:108006745-108006746	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs571471299	chr9:108006800-108006801	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs538809231	chr9:108006809-108006810	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs533824297	chr9:108006865-108006866	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs556990635	chr9:108006882-108006883	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs575479655	chr9:108006922-108006923	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs390529	chr9:108006948-108006949	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185658288	chr9:108006950-108006951	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs538613882	chr9:108006959-108006960	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs555397265	chr9:108007006-108007007	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs540337099	chr9:108007109-108007110	Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs374043828	chr9:108007340-108007341	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs564989275	chr9:108007356-108007357	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs532587580	chr9:108007405-108007406	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs556270906	chr9:108007441-108007442	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs190028737	chr9:108007488-108007489	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs182098443	chr9:108007511-108007512	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs530421478	chr9:108007551-108007552	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs114907728	chr9:108007569-108007570	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs567266024	chr9:108007578-108007579	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs111638590	chr9:108007680-108007681	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs35485876	chr9:108007689-108007690	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs546741675	chr9:108007717-108007718	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs571331740	chr9:108007732-108007733	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs538871806	chr9:108007754-108007755	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs192405258	chr9:108007839-108007840	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs183786618	chr9:108007844-108007845	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs536536906	chr9:108007853-108007854	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108002400-108006200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:108002600-108006200	Weak transcription	Left Ventricle	heart
3	chr9:108003200-108006200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:108003200-108006200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr9:108003200-108006200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:108003400-108006200	Enhancers	Brain Substantia Nigra	brain
7	chr9:108003600-108006200	Enhancers	HepG2	liver
8	chr9:108003600-108006400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr9:108003800-108006400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr9:108003800-108006400	Enhancers	Placenta	Placenta
11	chr9:108004000-108006200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr9:108004000-108006200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr9:108004000-108006200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr9:108004000-108006200	Enhancers	HSMM	muscle
15	chr9:108004200-108006200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr9:108004200-108006400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:108004200-108006600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr9:108004400-108006200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr9:108004600-108006200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:108004600-108006200	Active TSS	NHLF	lung
21	chr9:108004600-108006400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr9:108004600-108006600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:108004600-108006600	Flanking Active TSS	Osteobl	bone
24	chr9:108004800-108006200	Weak transcription	Fetal Brain Male	brain
25	chr9:108004800-108006200	Enhancers	Fetal Brain Female	brain
26	chr9:108004800-108006600	Flanking Active TSS	HUVEC	blood vessel
27	chr9:108004800-108009400	Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr9:108005000-108006200	Enhancers	Brain Anterior Caudate	brain
29	chr9:108005000-108006200	Weak transcription	Fetal Lung	lung
30	chr9:108005000-108006200	Weak transcription	Rectal Smooth Muscle	rectum
31	chr9:108005000-108006200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr9:108005000-108009200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr9:108005200-108006200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr9:108005200-108006200	Weak transcription	Ovary	ovary
35	chr9:108005200-108006200	Weak transcription	Right Atrium	heart
36	chr9:108005200-108006200	Enhancers	Stomach Mucosa	stomach
37	chr9:108005400-108006200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:108005400-108006200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr9:108005400-108006200	Weak transcription	Aorta	Aorta
40	chr9:108005400-108006200	Enhancers	Fetal Thymus	thymus
41	chr9:108005400-108006200	Weak transcription	HSMMtube	muscle
42	chr9:108005400-108006200	Enhancers	K562	blood
43	chr9:108005400-108006400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr9:108005400-108006600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr9:108005600-108006200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:108005600-108006200	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr9:108005600-108006200	Enhancers	Adipose Nuclei	Adipose
48	chr9:108005600-108006200	Enhancers	Brain Cingulate Gyrus	brain
49	chr9:108005600-108006200	Weak transcription	Psoas Muscle	Psoas
50	chr9:108005600-108006200	Enhancers	NHEK	skin

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