Variant report

Variant	esv2759697
Chromosome Location	chr9:79365865-79673907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2542)
CpG islands
(count:2503)
Chromatin interactive
region (count:103)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2542 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:79425348-79425631	HepG2	liver:	n/a	n/a
2	ATF1	chr9:79527598-79527798	K562	blood:	n/a	n/a
3	ATF2	chr9:79370415-79371134	GM12878	blood:	n/a	n/a
4	ATF2	chr9:79497594-79498091	GM12878	blood:	n/a	n/a
5	ATF2	chr9:79521106-79521455	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:79626799-79627535	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:79370494-79370857	GM12878	blood:	n/a	n/a
8	ATF3	chr9:79371309-79371591	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:79370515-79370738	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:79630515-79631464	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:79626979-79627104	K562	blood:	n/a	n/a
12	BACH1	chr9:79628877-79629047	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:79520702-79521451	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:79634381-79634430	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:79633780-79633914	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:79645069-79645110	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:79643416-79643828	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr9:79626898-79627699	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr9:79635610-79635797	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:79629535-79629842	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:79370445-79370745	GM12878	blood:	n/a	chr9:79370630-79370641
22	BATF	chr9:79370397-79370831	GM12878	blood:	n/a	chr9:79370630-79370641
23	BATF	chr9:79372198-79372549	GM12878	blood:	n/a	chr9:79372361-79372372
24	BCL3	chr9:79497679-79498015	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:79370453-79370951	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:79521051-79521251	HepG2	liver:	n/a	chr9:79521086-79521102
27	BHLHE40	chr9:79502439-79502703	GM12878	blood:	n/a	n/a
28	CBX3	chr9:79432963-79433704	HCT-116	colon:	n/a	n/a
29	CEBPB	chr9:79561129-79561279	K562	blood:	n/a	n/a
30	CEBPB	chr9:79594343-79594618	IMR90	lung:	n/a	chr9:79594442-79594453
31	CEBPB	chr9:79600454-79600702	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:79432362-79432804	MCF-7	breast:	n/a	n/a
33	CEBPB	chr9:79370501-79370832	H1-hESC	embryonic stem cell:	n/a	chr9:79370674-79370685
34	CEBPB	chr9:79488014-79488369	IMR90	lung:	n/a	chr9:79488197-79488208
35	CEBPB	chr9:79425363-79425667	A549	lung:	n/a	n/a
36	CEBPB	chr9:79488053-79488641	H1-hESC	embryonic stem cell:	n/a	chr9:79488197-79488208
37	CEBPB	chr9:79516842-79517063	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr9:79480843-79481043	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:79433198-79433543	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:79485641-79485971	HepG2	liver:	n/a	chr9:79485810-79485821
41	CEBPB	chr9:79371214-79371585	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:79626933-79627598	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr9:79485635-79485977	A549	lung:	n/a	chr9:79485810-79485821
44	CEBPB	chr9:79488071-79488276	HepG2	liver:	n/a	chr9:79488197-79488208
45	CEBPB	chr9:79450477-79450738	A549	lung:	n/a	n/a
46	CEBPB	chr9:79371238-79371465	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:79594333-79594611	A549	lung:	n/a	chr9:79594442-79594453
48	CEBPB	chr9:79521370-79521385	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:79481694-79482082	IMR90	lung:	n/a	n/a
50	CEBPB	chr9:79470870-79471076	HepG2	liver:	n/a	n/a

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:79627672-79627722	HCT-116	colon:	n/a
2	chr9:79631748-79631798	HEEpiC	esophagus:	n/a
3	chr9:79627672-79627722	HCT-116	colon:	n/a
4	chr9:79631748-79631798	HEEpiC	esophagus:	n/a
5	chr9:79637730-79637780	GM12892	blood:	n/a
6	chr9:79635445-79635495	HNPCEpiC	eye:	n/a
7	chr9:79638896-79638946	HIPEpiC	eye:	n/a
8	chr9:79635912-79635962	U87	brain:	n/a
9	chr9:79371681-79371731	HRE	kidney:	n/a
10	chr9:79627672-79627722	GM12892	blood:	n/a
11	chr9:79631748-79631798	H1-hESC	embryonic stem cell:	embryo
12	chr9:79630305-79630355	CMK	blood:	n/a
13	chr9:79392434-79392484	Hela-S3	cervix:	n/a
14	chr9:79635445-79635495	GM12892	blood:	n/a
15	chr9:79634509-79634559	SK-N-MC	brain:	n/a
16	chr9:79627672-79627722	HIPEpiC	eye:	n/a
17	chr9:79638896-79638946	SK-N-MC	brain:	n/a
18	chr9:79628488-79628538	LNCaP	prostate:	n/a
19	chr9:79625269-79625319	BJ	skin:	n/a
20	chr9:79488657-79488707	GM12878	blood:	n/a
21	chr9:79634037-79634087	GM19239	blood:	n/a
22	chr9:79628488-79628538	GM12892	blood:	n/a
23	chr9:79632225-79632275	Jurkat	blood:	n/a
24	chr9:79633350-79633400	CMK	blood:	n/a
25	chr9:79633350-79633400	HIPEpiC	eye:	n/a
26	chr9:79379372-79379422	HL-60	blood:	n/a
27	chr9:79520720-79520770	PFSK-1	brain:	n/a
28	chr9:79637457-79637507	LNCaP	prostate:	n/a
29	chr9:79371681-79371731	HNPCEpiC	eye:	n/a
30	chr9:79493927-79493977	PANC-1	pancreas:	n/a
31	chr9:79633737-79633787	SK-N-SH_RA	brain:	n/a
32	chr9:79630127-79630177	Hepatocyte	liver:	n/a
33	chr9:79637730-79637780	RPTEC	kidney:	n/a
34	chr9:79521082-79521132	AG04450	lung:	fetal
35	chr9:79634037-79634087	HRPEpiC	eye:	n/a
36	chr9:79637457-79637507	SK-N-SH_RA	brain:	n/a
37	chr9:79629843-79629893	HUVEC	blood vessel:	n/a
38	chr9:79520720-79520770	AoSMC	blood vessel:	n/a
39	chr9:79631737-79631787	SK-N-SH_RA	brain:	n/a
40	chr9:79379216-79379266	HCPEpiC	choroid plexus:	n/a
41	chr9:79634861-79634911	LNCaP	prostate:	n/a
42	chr9:79635445-79635495	U87	brain:	n/a
43	chr9:79379216-79379266	NHDF-neo	bronchial:	n/a
44	chr9:79488657-79488707	HAEpiC	amniotic membrane:	n/a
45	chr9:79633650-79633700	HCPEpiC	choroid plexus:	n/a
46	chr9:79630305-79630355	SKMC	muscle:	n/a
47	chr9:79516862-79516912	NHDF-neo	bronchial:	n/a
48	chr9:79630987-79631037	AG10803	skin:	n/a
49	chr9:79633650-79633700	HIPEpiC	eye:	n/a
50	chr9:79638117-79638167	ECC-1	luminal epithelium:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:52104614..52105495-chr9:79531675..79532265,2	MCF-7	breast:
2	chr9:79441567..79444031-chr9:79444174..79447007,2	MCF-7	breast:
3	chr9:79511162..79513490-chr9:79600307..79602272,2	MCF-7	breast:
4	chr9:79487218..79489827-chr9:79491730..79493342,2	MCF-7	breast:
5	chr9:79472515..79478078-chr9:79478521..79482952,4	MCF-7	breast:
6	chr9:79472515..79478078-chr9:79478521..79482952,4	MCF-7	breast:
7	chr9:79625779..79628421-chr9:79629663..79632130,2	MCF-7	breast:
8	chr17:56084524..56085437-chr9:79514590..79515427,2	Hela-S3	cervix:
9	chr9:79409501..79411465-chr9:79413182..79416088,2	MCF-7	breast:
10	chr9:79530053..79532362-chr9:79593128..79595760,2	MCF-7	breast:
11	chr9:79548326..79550915-chr9:79552221..79555116,2	K562	blood:
12	chr9:79611352..79612404-chr9:79765639..79766376,3	MCF-7	breast:
13	chr9:79508740..79509437-chr9:79601965..79602807,2	MCF-7	breast:
14	chr9:79424817..79426017-chr9:79601845..79603257,16	MCF-7	breast:
15	chr9:79424892..79425947-chr9:79602304..79603212,5	MCF-7	breast:
16	chr9:79613098..79615953-chr9:79615990..79618127,2	MCF-7	breast:
17	chr9:79424817..79426017-chr9:79601845..79603257,16	MCF-7	breast:
18	chr9:79376487..79377278-chr9:79424771..79425462,2	MCF-7	breast:
19	chr9:79432283..79434030-chr9:79637446..79639799,2	K562	blood:
20	chr9:79511162..79513490-chr9:79600307..79602272,2	MCF-7	breast:
21	chr9:79426009..79426954-chr9:79602259..79603041,2	MCF-7	breast:
22	chr9:79370786..79371842-chr9:79602290..79603157,3	MCF-7	breast:
23	chr9:79394787..79396465-chr9:79404032..79405891,2	MCF-7	breast:
24	chr1:189389640..189390412-chr9:79530846..79531642,2	MCF-7	breast:
25	chr9:79424975..79425845-chr9:79765382..79765927,2	K562	blood:
26	chr9:79463198..79464986-chr9:79466037..79468315,2	MCF-7	breast:
27	chr9:79628756..79629740-chr9:79765428..79766530,5	MCF-7	breast:
28	chr9:79448266..79451222-chr9:79453871..79455788,2	MCF-7	breast:
29	chr9:79422523..79423024-chr9:79602271..79602842,2	MCF-7	breast:
30	chr9:79425032..79425795-chr9:79611194..79612314,3	K562	blood:
31	chr9:79508733..79509699-chr9:79602239..79603154,6	MCF-7	breast:
32	chr9:79629104..79630379-chr9:79686755..79687615,3	MCF-7	breast:
33	chr9:79376487..79377278-chr9:79424771..79425462,2	MCF-7	breast:
34	chr9:79424995..79425779-chr9:79504416..79504965,2	MCF-7	breast:
35	chr9:79625515..79628414-chr9:79637125..79639075,2	MCF-7	breast:
36	chr9:79425391..79425951-chr9:79626908..79627892,2	K562	blood:
37	chr9:79411398..79414162-chr9:79415943..79417893,2	MCF-7	breast:
38	chr9:79508740..79509437-chr9:79601965..79602807,2	MCF-7	breast:
39	chr9:79398419..79401088-chr9:79401408..79403553,2	MCF-7	breast:
40	chr9:79394787..79396465-chr9:79404032..79405891,2	MCF-7	breast:
41	chr9:79391171..79393954-chr9:79402209..79403866,2	MCF-7	breast:
42	chr9:79629203..79630149-chr9:79765195..79766383,5	MCF-7	breast:
43	chr9:79409501..79411465-chr9:79413182..79416088,2	MCF-7	breast:
44	chr9:79370822..79371805-chr9:79602182..79602729,2	K562	blood:
45	chr9:79398419..79401088-chr9:79401408..79403553,2	MCF-7	breast:
46	chr9:79376082..79377810-chr9:79602239..79603222,6	MCF-7	breast:
47	chr9:79625779..79628421-chr9:79629663..79632130,2	MCF-7	breast:
48	chr9:79400787..79402755-chr9:79404564..79406713,2	MCF-7	breast:
49	chr9:79522918..79525713-chr9:79529471..79531753,2	MCF-7	breast:
50	chr9:79503710..79505573-chr9:79595934..79597543,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXB2-1	chr9:79398621-79398803	ENSG00000225937.1
2	lnc-PRUNE2-1	chr9:79546177-79546982	NONHSAT131967
3	lnc-PRUNE2-2	chr9:79587583-79587641	NONHSAT131969
4	lnc-PRUNE2-2	chr9:79586882-79587024	NONHSAT131969
5	lnc-FOXB2-1	chr9:79398621-79398803	NONHSAT131964
6	lnc-FOXB2-3	chr9:79607712-79608024	NONHSAT131970
7	lnc-FOXB2-4	chr9:79585238-79585430	NONHSAT131968
8	lnc-FOXB2-1	chr9:79397584-79397748	ENSG00000225937.1
9	lnc-FOXB2-3	chr9:79607015-79607433	NONHSAT131970
10	lnc-FOXB2-1	chr9:79399032-79402485	ENSG00000225937.1
11	lnc-FOXB2-4	chr9:79585562-79585944	NONHSAT131968
12	lnc-FOXB2-1	chr9:79399032-79402465	NONHSAT131964
13	lnc-FOXB2-1	chr9:79379354-79379471	NONHSAT131964
14	lnc-FOXB2-1	chr9:79379352-79379471	ENSG00000225937.1

No data

Variant related genes	Relation type
FOXB2	TF binding region
ENSG00000229857	TF binding region
PCA3	TF binding region
ENSG00000236604	TF binding region
ENSG00000230335	TF binding region
ATP5J2P3	TF binding region
PRUNE2	TF binding region
FOXB2	CpG island
ENSG00000229857	CpG island
PCA3	CpG island
ENSG00000236604	CpG island
ENSG00000230335	CpG island
ATP5J2P3	CpG island
PRUNE2	CpG island
ENSG00000230335	chromatin interactions
ENSG00000233526	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000232851	chromatin interactions
ENSG00000065978	chromatin interactions
ENSG00000197969	chromatin interactions

Extended variants
information (count: 9898 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:9898 , 50 per page) page: 1 2 3 4 5 6 7 ... 198

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546783981	chr9:79365879-79365880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557548011	chr9:79365949-79365950	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116545246	chr9:79365964-79365965	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138144071	chr9:79365975-79365976	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577078354	chr9:79365980-79365981	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12340384	chr9:79365991-79365992	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573482619	chr9:79366005-79366006	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538666819	chr9:79366021-79366022	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185026243	chr9:79366022-79366023	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562423693	chr9:79366032-79366033	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545551805	chr9:79366086-79366087	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371331170	chr9:79366167-79366168	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35700337	chr9:79366168-79366169	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3048276	chr9:79366188-79366189	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62565565	chr9:79366189-79366190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201819597	chr9:79366191-79366192	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530798570	chr9:79366225-79366226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550997712	chr9:79366226-79366227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143135419	chr9:79366229-79366230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190275621	chr9:79366231-79366232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148256909	chr9:79366244-79366245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141201394	chr9:79366269-79366270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180979559	chr9:79366488-79366489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548847897	chr9:79366507-79366508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185801304	chr9:79366514-79366515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572272809	chr9:79366535-79366536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575527070	chr9:79366550-79366551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559124126	chr9:79366572-79366573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116889766	chr9:79366577-79366578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150752404	chr9:79366586-79366587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117203000	chr9:79366623-79366624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372671811	chr9:79366663-79366664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561658484	chr9:79366670-79366671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7868392	chr9:79366709-79366710	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533827514	chr9:79366731-79366732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9696512	chr9:79366824-79366825	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs573442251	chr9:79366837-79366838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542478995	chr9:79366838-79366839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373279097	chr9:79366865-79366866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112782171	chr9:79366894-79366895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555780300	chr9:79366924-79366925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575932211	chr9:79366944-79366945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544584569	chr9:79366950-79366951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11401508	chr9:79366952-79366953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs200952896	chr9:79366955-79366956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs201339182	chr9:79366956-79366957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs199959004	chr9:79366957-79366958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371822674	chr9:79366958-79366959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564456496	chr9:79366971-79366972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9314855	chr9:79366979-79366980	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:3554 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79333200-79370000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr9:79348200-79370200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:79348400-79370200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr9:79348400-79370200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr9:79358400-79370800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:79361200-79396600	Weak transcription	Aorta	Aorta
7	chr9:79362200-79370400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr9:79364000-79366000	Enhancers	Fetal Muscle Leg	muscle
9	chr9:79364400-79372000	Weak transcription	Brain Hippocampus Middle	brain
10	chr9:79364600-79371200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr9:79364600-79371200	Weak transcription	Brain Substantia Nigra	brain
12	chr9:79364600-79371400	Weak transcription	Brain Angular Gyrus	brain
13	chr9:79364600-79387000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr9:79364800-79370600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr9:79364800-79373600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:79364800-79374800	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:79365400-79366000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:79365400-79366200	Enhancers	Primary B cells from peripheral blood	blood
19	chr9:79365400-79366600	Enhancers	HSMMtube	muscle
20	chr9:79365600-79366000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr9:79365600-79366200	Enhancers	Fetal Kidney	kidney
22	chr9:79365600-79366200	Enhancers	Ovary	ovary
23	chr9:79365600-79366200	Strong transcription	HSMM	muscle
24	chr9:79365800-79367000	Enhancers	Primary B cells from cord blood	blood
25	chr9:79366000-79370200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr9:79366000-79370400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr9:79366000-79371200	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:79366200-79368800	Weak transcription	Primary B cells from peripheral blood	blood
29	chr9:79366200-79370000	Weak transcription	HSMM	muscle
30	chr9:79366600-79370000	Weak transcription	HSMMtube	muscle
31	chr9:79367000-79370200	Weak transcription	Primary B cells from cord blood	blood
32	chr9:79368800-79370400	Enhancers	Primary B cells from peripheral blood	blood
33	chr9:79369000-79370400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:79370000-79370600	Enhancers	HSMMtube	muscle
35	chr9:79370000-79371400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr9:79370000-79371600	Enhancers	HSMM	muscle
37	chr9:79370200-79370600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr9:79370200-79370800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:79370200-79371000	Active TSS	GM12878-XiMat	blood
40	chr9:79370200-79372800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:79370200-79375800	Enhancers	Primary B cells from cord blood	blood
42	chr9:79370400-79370800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:79370400-79370800	Enhancers	Osteobl	bone
44	chr9:79370400-79371000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr9:79370400-79371000	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr9:79370400-79371600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr9:79370400-79371600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr9:79370400-79371600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr9:79370400-79371600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr9:79370400-79372800	Enhancers	Brain Germinal Matrix	brain

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