Variant report

Variant	nsv999153
Chromosome Location	chr2:20467929-20521954
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	chr2:20490861-20491084	HepG2	liver:	n/a	n/a
2	ATF3	chr2:20490803-20491174	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr2:20490827-20491181	K562	blood:	n/a	chr2:20491018-20491039
4	BHLHE40	chr2:20488765-20489108	K562	blood:	n/a	n/a
5	BHLHE40	chr2:20488804-20489055	A549	lung:	n/a	n/a
6	BHLHE40	chr2:20490870-20491140	HepG2	liver:	n/a	chr2:20491018-20491039
7	BRCA1	chr2:20515409-20515410	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr2:20490762-20491283	HCT-116	colon:	n/a	n/a
9	CBX3	chr2:20490814-20491206	K562	blood:	n/a	n/a
10	CEBPB	chr2:20504796-20505020	IMR90	lung:	n/a	n/a
11	CEBPB	chr2:20491592-20491831	HepG2	liver:	n/a	chr2:20491683-20491694
12	CEBPB	chr2:20488469-20489113	Hela-S3	cervix:	n/a	chr2:20488551-20488562
13	CEBPB	chr2:20492781-20493089	A549	lung:	n/a	chr2:20492914-20492931
14	CEBPB	chr2:20491523-20491698	K562	blood:	n/a	chr2:20491683-20491694
15	CEBPB	chr2:20488484-20488736	IMR90	lung:	n/a	chr2:20488551-20488562
16	CEBPB	chr2:20488454-20488711	K562	blood:	n/a	chr2:20488551-20488562
17	CEBPB	chr2:20491545-20491819	A549	lung:	n/a	chr2:20491683-20491694
18	CEBPB	chr2:20492813-20493078	IMR90	lung:	n/a	chr2:20492914-20492931
19	CEBPB	chr2:20491478-20491678	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:20488463-20488693	HepG2	liver:	n/a	chr2:20488551-20488562
21	CEBPB	chr2:20492766-20493106	HepG2	liver:	n/a	chr2:20492914-20492931
22	CEBPB	chr2:20486715-20487005	K562	blood:	n/a	n/a
23	CEBPB	chr2:20504901-20504928	HepG2	liver:	n/a	n/a
24	CHD2	chr2:20488773-20488971	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr2:20490801-20491093	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr2:20490881-20491091	GM10266	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
27	CTCF	chr2:20490713-20491199	HepG2	liver:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
28	CTCF	chr2:20490823-20491105	LNCaP	prostate:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
29	CTCF	chr2:20490940-20491090	NHDF-neo	bronchial:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
30	CTCF	chr2:20490900-20491050	HPAF	blood vessel:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
31	CTCF	chr2:20490900-20491050	HPF	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
32	CTCF	chr2:20491640-20491790	NB4	blood:	n/a	n/a
33	CTCF	chr2:20490880-20491030	HCT-116	colon:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
34	CTCF	chr2:20490810-20491185	A549	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
35	CTCF	chr2:20490696-20491149	K562	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
36	CTCF	chr2:20490880-20491030	GM12865	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
37	CTCF	chr2:20472720-20472870	K562	blood:	n/a	n/a
38	CTCF	chr2:20490900-20491050	GM12873	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
39	CTCF	chr2:20490860-20491010	HCT-116	colon:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
40	CTCF	chr2:20490920-20491070	AG09309	skin:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
41	CTCF	chr2:20490842-20491114	HepG2	liver:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
42	CTCF	chr2:20490900-20491050	AG09309	skin:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
43	CTCF	chr2:20490813-20491152	MCF-7	breast:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
44	CTCF	chr2:20490900-20491050	GM12801	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
45	CTCF	chr2:20490920-20491070	GM12873	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
46	CTCF	chr2:20490863-20491106	Lung_OC	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
47	CTCF	chr2:20490830-20491185	Gliobla	brain:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
48	CTCF	chr2:20490860-20491010	BE2_C	brain:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
49	CTCF	chr2:20490900-20491050	K562	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
50	CTCF	chr2:20490900-20491050	Caco-2	colon:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:20504345-20504395	GM12878	blood:	n/a
2	chr2:20504345-20504395	PrEC	prostate:	n/a
3	chr2:20515455-20515505	T-47D	breast:	n/a
4	chr2:20504345-20504395	BE2_C	brain:	n/a
5	chr2:20491052-20491102	HCM	heart:	n/a
6	chr2:20494247-20494297	LNCaP	prostate:	n/a
7	chr2:20494247-20494297	H1-hESC	embryonic stem cell:	embryo
8	chr2:20515455-20515505	HAEpiC	amniotic membrane:	n/a
9	chr2:20494247-20494297	Jurkat	blood:	n/a
10	chr2:20515455-20515505	HepG2	liver:	n/a
11	chr2:20515455-20515505	PANC-1	pancreas:	n/a
12	chr2:20494247-20494297	HRCEpiC	kidney:	n/a
13	chr2:20504345-20504395	U87	brain:	n/a
14	chr2:20504345-20504395	T-47D	breast:	n/a
15	chr2:20515455-20515505	Caco-2	colon:	n/a
16	chr2:20515455-20515505	ProgFib	skin:	n/a
17	chr2:20494247-20494297	HNPCEpiC	eye:	n/a
18	chr2:20494247-20494297	ProgFib	skin:	n/a
19	chr2:20504345-20504395	NHBE	bronchial:	n/a
20	chr2:20494247-20494297	HMEC	breast:	n/a
21	chr2:20504345-20504395	HAEpiC	amniotic membrane:	n/a
22	chr2:20504345-20504395	HL-60	blood:	n/a
23	chr2:20494247-20494297	K562	blood:	n/a
24	chr2:20504345-20504395	AG09319	gingival:	n/a
25	chr2:20494247-20494297	Hela-S3	cervix:	n/a
26	chr2:20515455-20515505	A549	lung:	n/a
27	chr2:20494247-20494297	HRE	kidney:	n/a
28	chr2:20494247-20494297	HCPEpiC	choroid plexus:	n/a
29	chr2:20494247-20494297	HL-60	blood:	n/a
30	chr2:20515455-20515505	HCF	heart:	n/a
31	chr2:20504345-20504395	HCT-116	colon:	n/a
32	chr2:20491052-20491102	IMR90	lung:	fetal
33	chr2:20515455-20515505	HCM	heart:	n/a
34	chr2:20504345-20504395	A549	lung:	n/a
35	chr2:20504345-20504395	HEEpiC	esophagus:	n/a
36	chr2:20491052-20491102	A549	lung:	n/a
37	chr2:20491052-20491102	NB4	blood:	n/a
38	chr2:20504345-20504395	HRE	kidney:	n/a
39	chr2:20494247-20494297	U87	brain:	n/a
40	chr2:20504345-20504395	SAEC	small airway:	n/a
41	chr2:20515455-20515505	GM12878	blood:	n/a
42	chr2:20491052-20491102	ECC-1	luminal epithelium:	n/a
43	chr2:20515455-20515505	RPTEC	kidney:	n/a
44	chr2:20515455-20515505	BJ	skin:	n/a
45	chr2:20504345-20504395	HRPEpiC	eye:	n/a
46	chr2:20491052-20491102	HEEpiC	esophagus:	n/a
47	chr2:20515455-20515505	K562	blood:	n/a
48	chr2:20494247-20494297	SKMC	muscle:	n/a
49	chr2:20504345-20504395	BJ	skin:	n/a
50	chr2:20504345-20504395	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:20489518..20491306-chr2:20498308..20500639,2	MCF-7	breast:
2	chr2:20496655..20499171-chr2:20500184..20502040,2	MCF-7	breast:
3	chr2:20155021..20155807-chr2:20490528..20491423,2	MCF-7	breast:
4	chr2:20484989..20487523-chr2:20496339..20498014,2	K562	blood:
5	chr2:20478789..20484582-chr2:20484927..20489294,7	K562	blood:
6	chr2:20472858..20474518-chr2:20518038..20520813,2	K562	blood:
7	chr2:20422753..20425256-chr2:20490607..20493628,3	MCF-7	breast:
8	chr2:20500817..20502817-chr2:20508534..20510980,2	K562	blood:
9	chr2:20461979..20463748-chr2:20470148..20471678,2	K562	blood:
10	chr2:20481278..20483845-chr2:20486511..20488232,4	MCF-7	breast:
11	chr2:20467246..20470350-chr2:20472212..20474237,3	K562	blood:
12	chr2:20506314..20508608-chr2:20513176..20516092,2	K562	blood:
13	chr2:20482981..20486539-chr2:20487663..20489842,4	MCF-7	breast:
14	chr2:20500817..20502817-chr2:20508534..20510980,2	K562	blood:
15	chr2:20467246..20470350-chr2:20472212..20474237,3	K562	blood:
16	chr2:20496655..20499171-chr2:20500184..20502040,2	MCF-7	breast:
17	chr2:20494958..20496619-chr2:20499621..20501776,2	MCF-7	breast:
18	chr2:20510407..20513116-chr2:20513569..20515907,2	K562	blood:
19	chr2:20475766..20478628-chr2:20479027..20481170,2	MCF-7	breast:
20	chr2:20515520..20519760-chr2:20526136..20528429,4	K562	blood:
21	chr2:20497505..20499547-chr2:20501441..20503193,2	K562	blood:
22	chr2:20512988..20515103-chr2:20550103..20552554,2	MCF-7	breast:
23	chr2:20520628..20522961-chr2:20529239..20532212,2	K562	blood:
24	chr2:20487646..20490086-chr2:20519151..20521903,2	K562	blood:
25	chr2:20100256..20102732-chr2:20505788..20508709,2	K562	blood:
26	chr2:20466339..20468775-chr2:20471320..20473308,2	MCF-7	breast:
27	chr2:20475845..20477677-chr2:20489513..20491458,2	K562	blood:
28	chr2:20421775..20427916-chr2:20486064..20491550,11	MCF-7	breast:
29	chr2:20506531..20509283-chr2:20510739..20513407,2	MCF-7	breast:
30	chr2:20463108..20465491-chr2:20466450..20468569,2	K562	blood:
31	chr2:20484550..20486934-chr2:20490044..20492996,3	MCF-7	breast:
32	chr2:20503251..20505625-chr2:20506483..20510190,4	K562	blood:
33	chr2:20215401..20215928-chr2:20490512..20491468,2	K562	blood:
34	chr2:20497505..20499547-chr2:20501441..20503193,2	K562	blood:
35	chr2:20503251..20505156-chr2:20505532..20508254,2	K562	blood:
36	chr2:20354974..20357549-chr2:20502769..20504637,2	MCF-7	breast:
37	chr2:20473741..20476352-chr2:20478752..20483600,5	MCF-7	breast:
38	chr2:20481278..20483845-chr2:20486511..20488232,4	MCF-7	breast:
39	chr2:20495005..20497847-chr2:20502307..20504684,2	MCF-7	breast:
40	chr2:20477908..20478887-chr2:20491028..20491640,2	K562	blood:
41	chr2:20422501..20424749-chr2:20493123..20495327,2	MCF-7	breast:
42	chr2:20498204..20500485-chr2:20550867..20552472,2	K562	blood:
43	chr2:20475238..20477975-chr2:20479251..20482026,2	K562	blood:
44	chr2:20424404..20426434-chr2:20494387..20495933,2	MCF-7	breast:
45	chr2:20466339..20468775-chr2:20471320..20473308,2	MCF-7	breast:
46	chr2:20521709..20523416-chr2:20549735..20551920,2	MCF-7	breast:
47	chr2:20474838..20476628-chr2:20486157..20488618,2	K562	blood:
48	chr2:20474838..20476628-chr2:20486157..20488618,2	K562	blood:
49	chr2:20503251..20505156-chr2:20505532..20508254,2	K562	blood:
50	chr2:20503262..20504823-chr2:20520357..20523063,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOB-10	chr2:20514284-20514382	NONHSAT069436
2	lnc-RHOB-10	chr2:20515981-20516189	NONHSAT069436

Variant related genes	Relation type
PUM2	TF binding region
PUM2	CpG island
ENSG00000223247	chromatin interactions
ENSG00000143878	chromatin interactions
ENSG00000055917	chromatin interactions
ENSG00000183891	chromatin interactions
ENSG00000271991	chromatin interactions
ENSG00000213729	chromatin interactions
ENSG00000115884	chromatin interactions

Extended variants
information (count: 2109 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2109 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4666299	chr2:20467929-20467930	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182561429	chr2:20467935-20467936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74335625	chr2:20467941-20467942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75005157	chr2:20467943-20467944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557348764	chr2:20467964-20467965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72787404	chr2:20467968-20467969	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536978128	chr2:20467980-20467981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543980376	chr2:20467991-20467992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561002566	chr2:20468005-20468006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186889932	chr2:20468009-20468010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540072677	chr2:20468016-20468017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368485892	chr2:20468100-20468101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550837320	chr2:20468166-20468167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532319947	chr2:20468214-20468215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552403776	chr2:20468248-20468249	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs13393733	chr2:20468271-20468272	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142379843	chr2:20468272-20468273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550820052	chr2:20468274-20468275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191329311	chr2:20468311-20468312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533216669	chr2:20468343-20468344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563797008	chr2:20468355-20468356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs151312710	chr2:20468357-20468358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553640089	chr2:20468365-20468366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199759550	chr2:20468395-20468396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200920954	chr2:20468398-20468399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374048255	chr2:20468402-20468403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72044779	chr2:20468403-20468404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188730233	chr2:20468404-20468405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79084837	chr2:20468418-20468419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376740339	chr2:20468447-20468448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559242399	chr2:20468453-20468454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34145581	chr2:20468457-20468458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13409830	chr2:20468470-20468471	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs575146219	chr2:20468498-20468499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544166704	chr2:20468511-20468512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554253096	chr2:20468571-20468572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574234418	chr2:20468575-20468576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539938172	chr2:20468598-20468599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140598970	chr2:20468608-20468609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367637649	chr2:20468639-20468640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371893571	chr2:20468676-20468677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566824538	chr2:20468729-20468730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147123164	chr2:20468731-20468732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545796448	chr2:20468777-20468778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112131626	chr2:20468836-20468837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531482831	chr2:20468868-20468869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550985287	chr2:20468942-20468943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567652024	chr2:20468945-20468946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535169803	chr2:20468951-20468952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534926011	chr2:20468953-20468954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	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
Breast cancer	22522925	CNVD

Chromatin state (count:1821 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20442000-20491000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:20442800-20474800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:20444400-20489000	Weak transcription	Stomach Mucosa	stomach
4	chr2:20445400-20473800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:20446400-20473600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:20447000-20468600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr2:20447000-20470200	Strong transcription	Dnd41	blood
8	chr2:20452000-20481600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr2:20454200-20471600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:20454200-20480800	Weak transcription	Aorta	Aorta
11	chr2:20454200-20480800	Weak transcription	Psoas Muscle	Psoas
12	chr2:20454200-20482800	Weak transcription	Pancreas	Pancrea
13	chr2:20454200-20488800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:20454200-20490800	Weak transcription	Right Ventricle	heart
15	chr2:20454200-20491000	Weak transcription	Gastric	stomach
16	chr2:20454200-20491000	Weak transcription	Spleen	Spleen
17	chr2:20454200-20499600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:20454400-20481600	Weak transcription	Brain Angular Gyrus	brain
19	chr2:20455400-20481600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:20455400-20482600	Weak transcription	Ovary	ovary
21	chr2:20455800-20481600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr2:20455800-20485000	Weak transcription	Colonic Mucosa	Colon
23	chr2:20456400-20482600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr2:20456400-20488800	Weak transcription	Small Intestine	intestine
25	chr2:20456600-20477800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr2:20458000-20491000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr2:20459800-20478000	Weak transcription	Fetal Heart	heart
28	chr2:20459800-20480800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:20459800-20481600	Weak transcription	Brain Anterior Caudate	brain
30	chr2:20459800-20481600	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:20460000-20476600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr2:20460000-20480600	Weak transcription	Brain Hippocampus Middle	brain
33	chr2:20460200-20481000	Weak transcription	HMEC	breast
34	chr2:20460200-20528600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:20460800-20471800	Weak transcription	HSMMtube	muscle
36	chr2:20460800-20480600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr2:20460800-20481600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr2:20460800-20485800	Weak transcription	Fetal Brain Male	brain
39	chr2:20461000-20480000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr2:20461000-20481800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr2:20461800-20469600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr2:20461800-20477800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr2:20462200-20480800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr2:20462200-20482400	Weak transcription	Brain Germinal Matrix	brain
45	chr2:20462400-20480800	Weak transcription	Left Ventricle	heart
46	chr2:20462600-20477200	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr2:20462600-20480800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:20462600-20482200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:20463000-20468600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr2:20463000-20476600	Weak transcription	Duodenum Smooth Muscle	Duodenum

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