Variant report

Variant	nsv832331
Chromosome Location	chr12:11925095-12114451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2717)
CpG islands
(count:1041)
Chromatin interactive
region (count:90)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2717 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11951813-11952010	K562	blood:	n/a	n/a
2	ARID3A	chr12:11993393-11993652	K562	blood:	n/a	n/a
3	ARID3A	chr12:12038224-12038257	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:11958602-11958995	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:12038550-12039011	HepG2	liver:	n/a	n/a
6	ATF1	chr12:11991969-11992503	K562	blood:	n/a	chr12:11992098-11992112
7	ATF1	chr12:11948475-11949402	K562	blood:	n/a	n/a
8	ATF1	chr12:11993336-11993695	K562	blood:	n/a	n/a
9	ATF1	chr12:12080293-12080511	K562	blood:	n/a	n/a
10	ATF1	chr12:12050919-12051142	K562	blood:	n/a	n/a
11	ATF1	chr12:11951770-11952359	K562	blood:	n/a	n/a
12	ATF2	chr12:11974873-11975910	GM12878	blood:	n/a	n/a
13	ATF2	chr12:11983045-11983520	GM12878	blood:	n/a	n/a
14	ATF2	chr12:11988461-11990100	GM12878	blood:	n/a	n/a
15	ATF2	chr12:11988725-11990133	GM12878	blood:	n/a	n/a
16	ATF2	chr12:12047789-12049040	GM12878	blood:	n/a	n/a
17	ATF2	chr12:11963781-11964578	GM12878	blood:	n/a	n/a
18	ATF2	chr12:11924268-11925592	GM12878	blood:	n/a	n/a
19	ATF2	chr12:11965199-11966118	GM12878	blood:	n/a	n/a
20	ATF2	chr12:11983047-11983789	GM12878	blood:	n/a	n/a
21	ATF2	chr12:11984856-11985424	GM12878	blood:	n/a	n/a
22	ATF2	chr12:11931831-11932955	GM12878	blood:	n/a	chr12:11932509-11932520
23	ATF2	chr12:12111517-12112045	GM12878	blood:	n/a	n/a
24	ATF2	chr12:11926847-11927538	GM12878	blood:	n/a	n/a
25	ATF2	chr12:11984847-11985473	GM12878	blood:	n/a	n/a
26	ATF2	chr12:11974720-11976027	GM12878	blood:	n/a	n/a
27	ATF2	chr12:11933323-11934452	GM12878	blood:	n/a	n/a
28	ATF2	chr12:11931910-11932730	GM12878	blood:	n/a	chr12:11932509-11932520
29	ATF2	chr12:12035252-12035751	GM12878	blood:	n/a	n/a
30	ATF2	chr12:11965345-11965912	GM12878	blood:	n/a	n/a
31	ATF2	chr12:11933123-11934562	GM12878	blood:	n/a	n/a
32	ATF3	chr12:12038167-12039100	A549	lung:	n/a	n/a
33	BACH1	chr12:11959935-11959946	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr12:11989885-11990144	K562	blood:	n/a	n/a
35	BACH1	chr12:11980033-11980380	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr12:11966181-11966363	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr12:11989908-11990100	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr12:12028306-12028629	GM12878	blood:	n/a	n/a
39	BATF	chr12:11932150-11932649	GM12878	blood:	n/a	n/a
40	BATF	chr12:11989138-11989906	GM12878	blood:	n/a	n/a
41	BATF	chr12:11924906-11925473	GM12878	blood:	n/a	n/a
42	BATF	chr12:11989335-11989873	GM12878	blood:	n/a	n/a
43	BATF	chr12:12111617-12111933	GM12878	blood:	n/a	n/a
44	BATF	chr12:12046980-12047274	GM12878	blood:	n/a	chr12:12047129-12047140
45	BATF	chr12:11963992-11964236	GM12878	blood:	n/a	n/a
46	BATF	chr12:11974979-11975811	GM12878	blood:	n/a	n/a
47	BATF	chr12:11986904-11987490	GM12878	blood:	n/a	chr12:11987218-11987229
48	BATF	chr12:12015661-12016078	GM12878	blood:	n/a	chr12:12015874-12015883
49	BATF	chr12:11985023-11985318	GM12878	blood:	n/a	n/a
50	BATF	chr12:11985064-11985361	GM12878	blood:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12031304-12031354	ProgFib	skin:	n/a
2	chr12:12022652-12022702	HCF	heart:	n/a
3	chr12:12015769-12015819	SKMC	muscle:	n/a
4	chr12:11947968-11948018	HL-60	blood:	n/a
5	chr12:12031304-12031354	ProgFib	skin:	n/a
6	chr12:12022652-12022702	HCF	heart:	n/a
7	chr12:12015769-12015819	SKMC	muscle:	n/a
8	chr12:11947968-11948018	HL-60	blood:	n/a
9	chr12:11940936-11940986	Hepatocyte	liver:	n/a
10	chr12:11975515-11975565	BJ	skin:	n/a
11	chr12:11975515-11975565	HepG2	liver:	n/a
12	chr12:12015769-12015819	HRPEpiC	eye:	n/a
13	chr12:12008666-12008716	AG04450	lung:	fetal
14	chr12:12015769-12015819	H1-hESC	embryonic stem cell:	embryo
15	chr12:12015769-12015819	HNPCEpiC	eye:	n/a
16	chr12:11981922-11981972	BJ	skin:	n/a
17	chr12:11932089-11932139	MCF10A-Er-Src	breast:	n/a
18	chr12:11947968-11948018	NB4	blood:	n/a
19	chr12:12015769-12015819	AG04450	lung:	fetal
20	chr12:12111838-12111888	NHDF-neo	bronchial:	n/a
21	chr12:11981922-11981972	PANC-1	pancreas:	n/a
22	chr12:12111838-12111888	HRPEpiC	eye:	n/a
23	chr12:11992925-11992975	AG09319	gingival:	n/a
24	chr12:12015769-12015819	LNCaP	prostate:	n/a
25	chr12:11992925-11992975	Hela-S3	cervix:	n/a
26	chr12:12111838-12111888	HIPEpiC	eye:	n/a
27	chr12:12015769-12015819	Jurkat	blood:	n/a
28	chr12:12022684-12022734	HAEpiC	amniotic membrane:	n/a
29	chr12:12038352-12038402	HCT-116	colon:	n/a
30	chr12:12022498-12022548	SK-N-SH	brain:	n/a
31	chr12:11932089-11932139	HEK293	kidney:	embryo
32	chr12:12008666-12008716	GM19239	blood:	n/a
33	chr12:12022684-12022734	HEEpiC	esophagus:	n/a
34	chr12:11932089-11932139	PrEC	prostate:	n/a
35	chr12:12038352-12038402	AG09309	skin:	n/a
36	chr12:11975515-11975565	HRPEpiC	eye:	n/a
37	chr12:11992925-11992975	SK-N-SH_RA	brain:	n/a
38	chr12:12044761-12044811	Hepatocyte	liver:	n/a
39	chr12:11947968-11948018	NHDF-neo	bronchial:	n/a
40	chr12:12044761-12044811	ProgFib	skin:	n/a
41	chr12:12008666-12008716	HCT-116	colon:	n/a
42	chr12:11940936-11940986	H1-hESC	embryonic stem cell:	embryo
43	chr12:12044761-12044811	AG04450	lung:	fetal
44	chr12:12022498-12022548	GM12892	blood:	n/a
45	chr12:12111838-12111888	SAEC	small airway:	n/a
46	chr12:12022684-12022734	Hepatocyte	liver:	n/a
47	chr12:12038352-12038402	K562	blood:	n/a
48	chr12:11966066-11966116	Caco-2	colon:	n/a
49	chr12:11992925-11992975	K562	blood:	n/a
50	chr12:12022498-12022548	HIPEpiC	eye:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:12056694..12059278-chr12:12764602..12766509,2	MCF-7	breast:
2	chr12:11948872..11951757-chr12:11956550..11958126,2	K562	blood:
3	chr12:12031401..12033657-chr12:12034507..12036670,2	K562	blood:
4	chr12:11980059..11983037-chr12:11983284..11986471,3	K562	blood:
5	chr12:11990397..11992859-chr12:11995396..11997268,2	K562	blood:
6	chr12:11928703..11930258-chr12:11944667..11947353,2	MCF-7	breast:
7	chr12:12103017..12105353-chr12:12107721..12110488,2	K562	blood:
8	chr12:11968088..11970752-chr12:11973780..11976134,2	MCF-7	breast:
9	chr12:11980059..11983037-chr12:11983284..11986471,3	K562	blood:
10	chr12:12028553..12032107-chr12:12033393..12035272,3	MCF-7	breast:
11	chr12:11800455..11804262-chr12:12036773..12041762,7	MCF-7	breast:
12	chr12:12043911..12046841-chr12:12047911..12050506,2	K562	blood:
13	chr12:12003194..12007907-chr12:12014129..12016810,4	K562	blood:
14	chr11:62608627..62609481-chr12:12025415..12025915,2	NB4	blood:
15	chr12:11947390..11949205-chr12:11950511..11952947,3	K562	blood:
16	chr12:11984588..11986522-chr12:11992006..11994443,2	K562	blood:
17	chr12:12031118..12033194-chr12:12036584..12038902,3	MCF-7	breast:
18	chr12:11933115..11935435-chr12:11937428..11939790,2	K562	blood:
19	chr12:11984588..11987060-chr12:11992006..11993729,2	K562	blood:
20	chr12:11947957..11949595-chr12:11953538..11956063,2	K562	blood:
21	chr12:12046000..12048958-chr12:12054696..12056752,2	MCF-7	breast:
22	chr12:11915800..11917603-chr12:11959606..11961755,2	MCF-7	breast:
23	chr12:11990610..11993601-chr12:12013404..12016369,2	K562	blood:
24	chr12:11800641..11803782-chr12:12029596..12032475,4	MCF-7	breast:
25	chr12:11965171..11967330-chr12:14922995..14925026,2	MCF-7	breast:
26	chr12:11990610..11993968-chr12:12013101..12016369,3	K562	blood:
27	chr12:12038004..12040734-chr12:12041723..12044015,2	MCF-7	breast:
28	chr12:11801130..11802885-chr12:11934926..11936924,2	MCF-7	breast:
29	chr12:12031401..12033657-chr12:12034507..12036670,2	K562	blood:
30	chr12:11984792..11986374-chr12:11987471..11989426,2	K562	blood:
31	chr12:11990610..11993601-chr12:12013404..12016369,2	K562	blood:
32	chr12:11972270..11974612-chr12:11976151..11979593,3	K562	blood:
33	chr12:11898044..11900698-chr12:11957221..11959288,2	MCF-7	breast:
34	chr12:11928703..11930258-chr12:11944667..11947353,2	MCF-7	breast:
35	chr12:11930876..11932594-chr12:11939826..11941565,2	MCF-7	breast:
36	chr12:11990610..11993968-chr12:12013101..12016369,3	K562	blood:
37	chr12:11947234..11949205-chr12:11950410..11952845,3	K562	blood:
38	chr12:11803344..11805107-chr12:11973209..11975681,2	MCF-7	breast:
39	chr12:11990397..11992859-chr12:11995396..11997268,2	K562	blood:
40	chr12:12091767..12093459-chr12:12099941..12102782,2	MCF-7	breast:
41	chr12:11947643..11948143-chr5:31886675..31887176,2	Hela-S3	cervix:
42	chr12:11984588..11986522-chr12:11992006..11994443,2	K562	blood:
43	chr12:11974834..11977419-chr12:11984759..11987051,2	K562	blood:
44	chr12:11968088..11970752-chr12:11973780..11976134,2	MCF-7	breast:
45	chr12:11958358..11962044-chr12:11963614..11966577,4	MCF-7	breast:
46	chr12:11974834..11977419-chr12:11984759..11987051,2	K562	blood:
47	chr12:12028150..12030746-chr12:12035648..12039846,3	MCF-7	breast:
48	chr12:11977943..11979982-chr12:11981933..11983586,2	K562	blood:
49	chr12:12072555..12074559-chr12:12078850..12081268,2	K562	blood:
50	chr12:12014231..12015148-chr12:12106678..12107204,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV6-2	chr12:12095997-12096048	ucscGeneNc_uc001rab_1
2	lnc-ETV6-2	chr12:12094065-12094155	ucscGeneNc_uc001rab_1
3	lnc-ETV6-2	chr12:12098809-12099970	ucscGeneNc_uc001rab_1

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ETV6	hsa-miR-129-5p	chr12:12048220-12048240
2	ETV6	hsa-miR-129-5p	chr12:12048216-12048222
3	ETV6	hsa-miR-129-5p	chr12:12048234-12048240
4	ETV6	hsa-miR-129-5p	chr12:12047654-12047674

Variant related genes	Relation type
ETV6	TF binding region
ETV6	CpG island
ENSG00000139083	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000111269	chromatin interactions

Extended variants
information (count: 7463 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:7463 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181207210	chr12:11925144-11925145	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs570561032	chr12:11925176-11925177	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs115058194	chr12:11925204-11925205	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs556369738	chr12:11925271-11925272	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143807270	chr12:11925290-11925291	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535703352	chr12:11925292-11925293	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs553886921	chr12:11925306-11925307	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs572357825	chr12:11925337-11925338	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs545789023	chr12:11925341-11925342	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs7973524	chr12:11925446-11925447	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576112346	chr12:11925448-11925449	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs543638041	chr12:11925462-11925463	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs146864364	chr12:11925505-11925506	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs536844512	chr12:11925521-11925522	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs529575802	chr12:11925540-11925541	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185474548	chr12:11925557-11925558	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559899015	chr12:11925623-11925624	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527331212	chr12:11925660-11925661	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553554917	chr12:11925686-11925687	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552195126	chr12:11925720-11925721	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573598668	chr12:11925725-11925726	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531029292	chr12:11925782-11925783	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs57093886	chr12:11925808-11925809	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs565616468	chr12:11925825-11925826	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543130383	chr12:11925826-11925827	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140746344	chr12:11925828-11925829	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2724597	chr12:11925854-11925855	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2724596	chr12:11925857-11925858	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535386421	chr12:11925861-11925862	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2723826	chr12:11925866-11925867	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572242109	chr12:11925894-11925895	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150400623	chr12:11925895-11925896	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145213693	chr12:11925896-11925897	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs57828340	chr12:11925927-11925928	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576151790	chr12:11925996-11925997	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543478965	chr12:11926002-11926003	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11609606	chr12:11926020-11926021	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574133037	chr12:11926032-11926033	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541264353	chr12:11926045-11926046	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550849159	chr12:11926053-11926054	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12425912	chr12:11926077-11926078	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7967177	chr12:11926101-11926102	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545833834	chr12:11926138-11926139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56695427	chr12:11926142-11926143	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536104965	chr12:11926143-11926144	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200025402	chr12:11926146-11926147	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201109154	chr12:11926147-11926148	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549799549	chr12:11926158-11926159	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12369776	chr12:11926178-11926179	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12369777	chr12:11926182-11926183	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21680795	CNVD
Cancer	17440070	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Acute lymphoblastic leukemia	19129520	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	21088497	CNVD
Myelodysplastic syndrome	22875624	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:6409 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11908600-11931800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:11909600-11932400	Genic enhancers	Fetal Thymus	thymus
3	chr12:11914400-11925400	Genic enhancers	Dnd41	blood
4	chr12:11914400-11925800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:11915400-11938000	Weak transcription	NHEK	skin
6	chr12:11915600-11938000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:11918000-11936000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:11919400-11926800	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:11919400-11935000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:11919600-11926800	Weak transcription	Psoas Muscle	Psoas
11	chr12:11919600-11927600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:11919600-11932000	Weak transcription	HSMM	muscle
13	chr12:11919600-11936200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:11919600-11936800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr12:11919800-11926600	Weak transcription	Brain Anterior Caudate	brain
16	chr12:11919800-11927600	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr12:11919800-11929400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:11919800-11931400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:11919800-11932400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:11920000-11926400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr12:11920000-11927800	Weak transcription	Brain Substantia Nigra	brain
22	chr12:11920000-11929600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:11920000-11931800	Weak transcription	HSMMtube	muscle
24	chr12:11920000-11937800	Weak transcription	NHLF	lung
25	chr12:11920200-11926600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr12:11920600-11926800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr12:11921000-11925800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:11921000-11926800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr12:11921200-11930800	Weak transcription	Fetal Lung	lung
30	chr12:11921200-11931200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:11921400-11926400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr12:11921400-11927200	Weak transcription	Brain Angular Gyrus	brain
33	chr12:11921400-11927200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr12:11921600-11926600	Weak transcription	Brain Hippocampus Middle	brain
35	chr12:11921600-11927000	Weak transcription	Fetal Intestine Large	intestine
36	chr12:11921800-11926600	Weak transcription	Gastric	stomach
37	chr12:11921800-11926800	Weak transcription	Small Intestine	intestine
38	chr12:11921800-11946600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:11922000-11926400	Weak transcription	Liver	Liver
40	chr12:11922000-11926800	Weak transcription	HepG2	liver
41	chr12:11922000-11928600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:11922000-11929000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr12:11922000-11948200	Weak transcription	Colonic Mucosa	Colon
44	chr12:11922400-11925400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr12:11922600-11925400	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr12:11922600-11925400	Enhancers	Thymus	Thymus
47	chr12:11922800-11925200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr12:11923000-11926600	Weak transcription	Aorta	Aorta
49	chr12:11923000-11928000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:11923200-11926600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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