Variant report

Variant	nsv545395
Chromosome Location	chr1:10584672-10613660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10585313-10585425	K562	blood:	n/a	n/a
2	ATF1	chr1:10599523-10599788	K562	blood:	n/a	n/a
3	ATF1	chr1:10588458-10588700	K562	blood:	n/a	n/a
4	ATF1	chr1:10602899-10602927	K562	blood:	n/a	n/a
5	ATF2	chr1:10590276-10590762	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:10590356-10590765	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:10589305-10589454	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:10597631-10597675	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr1:10588384-10588799	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:10588377-10589047	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:10597474-10597880	ECC-1	luminal epithelium:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
12	CEBPB	chr1:10597402-10597922	MCF-7	breast:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
13	CEBPB	chr1:10597540-10597792	HepG2	liver:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
14	CEBPB	chr1:10597521-10597849	A549	lung:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
15	CEBPB	chr1:10597487-10597859	K562	blood:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
16	CEBPB	chr1:10590405-10590680	H1-hESC	embryonic stem cell:	n/a	chr1:10590406-10590419
17	CEBPB	chr1:10597292-10597978	HCT-116	colon:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
18	CEBPB	chr1:10597483-10597856	IMR90	lung:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
19	CEBPB	chr1:10597556-10597862	A549	lung:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
20	CEBPB	chr1:10597441-10597889	HCT-116	colon:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
21	CEBPB	chr1:10597520-10597825	HepG2	liver:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
22	CEBPB	chr1:10611071-10611295	HepG2	liver:	n/a	chr1:10611177-10611188 chr1:10611177-10611186 chr1:10611175-10611188
23	CEBPB	chr1:10606900-10606956	K562	blood:	n/a	n/a
24	CEBPB	chr1:10597481-10597847	HepG2	liver:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
25	CEBPB	chr1:10599102-10599306	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:10597429-10597875	MCF-7	breast:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
27	CEBPB	chr1:10588227-10589086	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:10597485-10597862	ECC-1	luminal epithelium:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
29	CEBPB	chr1:10597480-10597836	Hela-S3	cervix:	n/a	chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597663-10597674 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597662-10597675 chr1:10597664-10597673 chr1:10597664-10597673 chr1:10597662-10597673
30	CEBPD	chr1:10597533-10597741	HepG2	liver:	n/a	chr1:10597664-10597673
31	CHD1	chr1:10590380-10590641	H1-hESC	embryonic stem cell:	n/a	chr1:10590608-10590618
32	CHD2	chr1:10588387-10589129	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr1:10590459-10590715	H1-hESC	embryonic stem cell:	n/a	chr1:10590608-10590618
34	CTCF	chr1:10590436-10590568	HepG2	liver:	n/a	chr1:10590532-10590545
35	CTCF	chr1:10596340-10596490	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr1:10590364-10590624	HUVEC	blood vessel:	n/a	chr1:10590532-10590545
37	CTCF	chr1:10590324-10590688	K562	blood:	n/a	chr1:10590532-10590545
38	CTCF	chr1:10590360-10590510	HVMF	connective:	n/a	n/a
39	CTCF	chr1:10596366-10596452	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:10601220-10601370	GM12872	blood:	n/a	n/a
41	CTCF	chr1:10590400-10590550	HBMEC	blood vessel:	n/a	chr1:10590532-10590545
42	CTCF	chr1:10590540-10590690	GM12878	blood:	n/a	n/a
43	CTCF	chr1:10596260-10596550	HRE	kidney:	n/a	n/a
44	CTCF	chr1:10596322-10596473	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:10590480-10590630	AG09309	skin:	n/a	chr1:10590532-10590545
46	CTCF	chr1:10590400-10590550	GM12873	blood:	n/a	chr1:10590532-10590545
47	CTCF	chr1:10596280-10596430	BE2_C	brain:	n/a	n/a
48	CTCF	chr1:10590460-10590610	HRPEpiC	eye:	n/a	chr1:10590532-10590545
49	CTCF	chr1:10590373-10590655	GM19238	blood:	n/a	chr1:10590532-10590545
50	CTCF	chr1:10590440-10590590	GM12867	blood:	n/a	chr1:10590532-10590545

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10595970-10596020	HCF	heart:	n/a
2	chr1:10595970-10596020	HCF	heart:	n/a
3	chr1:10601833-10601883	A549	lung:	n/a
4	chr1:10600222-10600272	NT2-D1	testis:	n/a
5	chr1:10600222-10600272	HCT-116	colon:	n/a
6	chr1:10604446-10604496	HEK293	kidney:	embryo
7	chr1:10611109-10611159	HCF	heart:	n/a
8	chr1:10601833-10601883	SK-N-MC	brain:	n/a
9	chr1:10590481-10590531	HCF	heart:	n/a
10	chr1:10600222-10600272	Caco-2	colon:	n/a
11	chr1:10590481-10590531	AG09319	gingival:	n/a
12	chr1:10601595-10601645	PFSK-1	brain:	n/a
13	chr1:10600222-10600272	HCM	heart:	n/a
14	chr1:10595970-10596020	GM06990	blood:	n/a
15	chr1:10595970-10596020	HEK293	kidney:	embryo
16	chr1:10601833-10601883	GM12892	blood:	n/a
17	chr1:10604446-10604496	HCPEpiC	choroid plexus:	n/a
18	chr1:10601595-10601645	HCPEpiC	choroid plexus:	n/a
19	chr1:10601389-10601439	HL-60	blood:	n/a
20	chr1:10611109-10611159	ProgFib	skin:	n/a
21	chr1:10601833-10601883	ECC-1	luminal epithelium:	n/a
22	chr1:10600222-10600272	HRE	kidney:	n/a
23	chr1:10601579-10601629	Jurkat	blood:	n/a
24	chr1:10590672-10590722	PFSK-1	brain:	n/a
25	chr1:10604446-10604496	GM12891	blood:	n/a
26	chr1:10590672-10590722	Hela-S3	cervix:	n/a
27	chr1:10595970-10596020	SK-N-SH_RA	brain:	n/a
28	chr1:10595970-10596020	AG04449	skin:	fetal
29	chr1:10601579-10601629	HRE	kidney:	n/a
30	chr1:10601833-10601883	K562	blood:	n/a
31	chr1:10590481-10590531	HL-60	blood:	n/a
32	chr1:10601579-10601629	PANC-1	pancreas:	n/a
33	chr1:10595970-10596020	HRCEpiC	kidney:	n/a
34	chr1:10601579-10601629	Hela-S3	cervix:	n/a
35	chr1:10601389-10601439	GM12891	blood:	n/a
36	chr1:10604446-10604496	BE2_C	brain:	n/a
37	chr1:10611109-10611159	HCM	heart:	n/a
38	chr1:10600222-10600272	A549	lung:	n/a
39	chr1:10595970-10596020	NH-A	brain:	n/a
40	chr1:10601595-10601645	HRCEpiC	kidney:	n/a
41	chr1:10601389-10601439	AoSMC	blood vessel:	n/a
42	chr1:10604446-10604496	ECC-1	luminal epithelium:	n/a
43	chr1:10601595-10601645	MCF-7	breast:	n/a
44	chr1:10601595-10601645	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:10601833-10601883	HCM	heart:	n/a
46	chr1:10601595-10601645	K562	blood:	n/a
47	chr1:10589400-10589450	RPTEC	kidney:	n/a
48	chr1:10595970-10596020	GM19239	blood:	n/a
49	chr1:10601833-10601883	HNPCEpiC	eye:	n/a
50	chr1:10601595-10601645	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:10589309..10591508-chr1:10651161..10652770,2	MCF-7	breast:
2	chr1:10588129..10591030-chr1:10598382..10599942,2	K562	blood:
3	chr1:10612660..10614592-chr1:10614870..10616805,2	K562	blood:
4	chr1:10595945..10600298-chr1:10602356..10606682,5	K562	blood:
5	chr1:10583207..10584998-chr1:10614672..10617008,2	K562	blood:
6	chr1:10589102..10590636-chr1:10751361..10753054,2	MCF-7	breast:
7	chr1:10588978..10590692-chr1:10934341..10936990,2	MCF-7	breast:
8	chr1:10570481..10573299-chr1:10599222..10600978,2	K562	blood:
9	chr1:10568543..10570422-chr1:10582522..10585336,2	K562	blood:
10	chr1:10599611..10603439-chr1:10608820..10611916,3	K562	blood:
11	chr1:10612128..10614249-chr1:11118816..11121304,2	MCF-7	breast:
12	chr1:10601514..10603833-chr1:10611610..10614031,2	K562	blood:
13	chr1:10581501..10583988-chr1:10587081..10589695,2	MCF-7	breast:
14	chr1:10589627..10591241-chr1:10607715..10610040,2	K562	blood:
15	chr1:10604158..10605695-chr1:10610029..10612944,2	K562	blood:
16	chr1:10585162..10588309-chr1:10589608..10593566,5	K562	blood:
17	chr1:10591577..10594181-chr1:10600029..10602001,2	K562	blood:
18	chr1:10608473..10610056-chr1:10690153..10691726,2	MCF-7	breast:
19	chr1:10579090..10582212-chr1:10583289..10585385,3	K562	blood:
20	chr1:10591577..10594181-chr1:10600029..10602001,2	K562	blood:
21	chr1:10586788..10588823-chr1:10605231..10607555,2	K562	blood:
22	chr1:10586788..10588823-chr1:10605231..10607555,2	K562	blood:
23	chr1:10591516..10593262-chr1:10606474..10609056,2	K562	blood:
24	chr1:10576515..10578710-chr1:10584102..10586640,2	K562	blood:
25	chr1:10589627..10591241-chr1:10607715..10610040,2	K562	blood:
26	chr1:10613182..10615278-chr1:10634059..10635850,2	MCF-7	breast:
27	chr1:10610347..10612190-chr1:10616959..10619144,2	K562	blood:
28	chr1:10594251..10596401-chr1:10598205..10601279,3	K562	blood:
29	chr1:10601514..10603833-chr1:10611610..10614031,2	K562	blood:
30	chr1:10585162..10588309-chr1:10589608..10593566,5	K562	blood:
31	chr1:10577532..10580475-chr1:10590665..10593408,2	K562	blood:
32	chr1:10591516..10593262-chr1:10606474..10609056,2	K562	blood:
33	chr1:10590066..10590945-chr1:10927189..10927789,2	K562	blood:
34	chr1:10604158..10605695-chr1:10610029..10612944,2	K562	blood:
35	chr1:10588129..10591030-chr1:10598382..10599942,2	K562	blood:
36	chr1:10597953..10600122-chr1:10755934..10757500,2	K562	blood:
37	chr1:10599611..10603439-chr1:10608820..10611916,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PEX14-1	chr1:10596270-10596629	NONHSAT000859

Variant related genes	Relation type
PEX14	TF binding region
PEX14	CpG island
ENSG00000116649	chromatin interactions
ENSG00000142655	chromatin interactions

Extended variants
information (count: 979 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2506887	chr1:10584672-10584673	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116518207	chr1:10584710-10584711	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113020709	chr1:10584734-10584735	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375042325	chr1:10584735-10584736	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2506888	chr1:10584738-10584739	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs543125926	chr1:10584742-10584743	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552335244	chr1:10584755-10584756	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533347141	chr1:10584809-10584810	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77228766	chr1:10584810-10584811	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371616337	chr1:10584863-10584864	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528010408	chr1:10584895-10584896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200352600	chr1:10584907-10584908	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142249382	chr1:10584924-10584925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567671952	chr1:10584945-10584946	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151254600	chr1:10584978-10584979	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190749990	chr1:10584980-10584981	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560865235	chr1:10585026-10585027	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112111830	chr1:10585034-10585035	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2480789	chr1:10585046-10585047	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs550293208	chr1:10585090-10585091	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571796098	chr1:10585115-10585116	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13375411	chr1:10585139-10585140	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs547582519	chr1:10585305-10585306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17035154	chr1:10585315-10585316	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs536553241	chr1:10585317-10585318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554228626	chr1:10585368-10585369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199862806	chr1:10585378-10585379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575625536	chr1:10585408-10585409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141578111	chr1:10585412-10585413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184188861	chr1:10585484-10585485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576565117	chr1:10585493-10585494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531352494	chr1:10585507-10585508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545237578	chr1:10585515-10585516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17035156	chr1:10585527-10585528	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs572610205	chr1:10585534-10585535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187805713	chr1:10585574-10585575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561613983	chr1:10585583-10585584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531713466	chr1:10585696-10585697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567949895	chr1:10585709-10585710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550232262	chr1:10585734-10585735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565340935	chr1:10585743-10585744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532658540	chr1:10585845-10585846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547231739	chr1:10585866-10585867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565879758	chr1:10585882-10585883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192423336	chr1:10585886-10585887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558463194	chr1:10585908-10585909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548078894	chr1:10585913-10585914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569643808	chr1:10585928-10585929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147756972	chr1:10585960-10585961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553638354	chr1:10585973-10585974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1148 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10570800-10595600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:10572000-10590000	Weak transcription	Spleen	Spleen
3	chr1:10572200-10598600	Weak transcription	Brain Anterior Caudate	brain
4	chr1:10572600-10587600	Weak transcription	Hela-S3	cervix
5	chr1:10572600-10587800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:10573400-10596000	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:10573800-10588000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:10573800-10588200	Weak transcription	Fetal Intestine Large	intestine
9	chr1:10575600-10588000	Weak transcription	NHLF	lung
10	chr1:10576000-10589200	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr1:10576400-10596000	Weak transcription	Dnd41	blood
12	chr1:10577000-10603600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:10577400-10587800	Weak transcription	Pancreas	Pancrea
14	chr1:10577400-10587800	Weak transcription	Right Atrium	heart
15	chr1:10577400-10587800	Weak transcription	HSMM	muscle
16	chr1:10577400-10588000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr1:10577400-10588000	Weak transcription	Lung	lung
18	chr1:10577400-10588000	Weak transcription	NHDF-Ad	bronchial
19	chr1:10577400-10596400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:10577600-10588000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:10577600-10588400	Weak transcription	Adipose Nuclei	Adipose
22	chr1:10577800-10587800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:10577800-10587800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr1:10577800-10590800	Weak transcription	Fetal Thymus	thymus
25	chr1:10578000-10587800	Weak transcription	HMEC	breast
26	chr1:10578000-10588000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:10578200-10587800	Weak transcription	NHEK	skin
28	chr1:10578200-10588400	Weak transcription	Fetal Kidney	kidney
29	chr1:10578200-10589800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:10578400-10590600	Weak transcription	Placenta	Placenta
31	chr1:10579400-10589200	Weak transcription	Gastric	stomach
32	chr1:10579400-10610200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr1:10579600-10587800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr1:10579600-10587800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:10579600-10587800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr1:10579600-10587800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:10579600-10587800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:10579600-10588000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr1:10579600-10590000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr1:10579600-10596200	Weak transcription	Fetal Muscle Trunk	muscle
41	chr1:10579800-10587000	Weak transcription	Left Ventricle	heart
42	chr1:10579800-10587600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr1:10579800-10587600	Weak transcription	A549	lung
44	chr1:10579800-10587800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:10579800-10587800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr1:10579800-10588000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr1:10579800-10588000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr1:10579800-10588000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:10579800-10588000	Weak transcription	Esophagus	oesophagus
50	chr1:10579800-10588000	Weak transcription	HSMMtube	muscle

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