Variant report

Variant	nsv1049915
Chromosome Location	chr11:74052264-74126319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1026)
CpG islands
(count:915)
Chromatin interactive
region (count:65)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:74109673-74110168	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:74099773-74100111	K562	blood:	n/a	n/a
3	ARID3A	chr11:74099776-74100062	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:74109792-74110550	K562	blood:	n/a	n/a
5	ATF1	chr11:74058616-74058871	K562	blood:	n/a	n/a
6	ATF1	chr11:74109795-74110168	K562	blood:	n/a	n/a
7	ATF2	chr11:74109517-74110209	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr11:74109553-74110141	GM12878	blood:	n/a	n/a
9	ATF3	chr11:74109530-74109947	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr11:74109589-74109956	K562	blood:	n/a	n/a
11	ATF3	chr11:74109518-74110053	K562	blood:	n/a	n/a
12	BACH1	chr11:74109922-74110097	K562	blood:	n/a	n/a
13	BCL3	chr11:74109563-74110310	A549	lung:	n/a	n/a
14	BCL3	chr11:74109533-74110328	A549	lung:	n/a	n/a
15	BCL3	chr11:74082537-74083207	A549	lung:	n/a	n/a
16	BCLAF1	chr11:74109528-74110174	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:74109642-74110284	A549	lung:	n/a	n/a
18	BHLHE40	chr11:74109612-74110226	K562	blood:	n/a	n/a
19	BHLHE40	chr11:74109503-74110380	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:74109625-74110115	HepG2	liver:	n/a	n/a
21	BHLHE40	chr11:74099785-74099970	K562	blood:	n/a	n/a
22	BRCA1	chr11:74109586-74110384	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:74099752-74099992	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr11:74109737-74110106	GM12878	blood:	n/a	n/a
25	CBX3	chr11:74109835-74110231	K562	blood:	n/a	n/a
26	CBX3	chr11:74109585-74110277	K562	blood:	n/a	n/a
27	CBX3	chr11:74099641-74100130	HCT-116	colon:	n/a	n/a
28	CCNT2	chr11:74109014-74109417	K562	blood:	n/a	chr11:74109254-74109263
29	CCNT2	chr11:74109642-74110269	K562	blood:	n/a	n/a
30	CEBPB	chr11:74082634-74083270	A549	lung:	n/a	n/a
31	CEBPB	chr11:74109560-74109855	HepG2	liver:	n/a	chr11:74109657-74109668
32	CEBPB	chr11:74109483-74109982	H1-hESC	embryonic stem cell:	n/a	chr11:74109657-74109668
33	CEBPB	chr11:74109464-74109880	HepG2	liver:	n/a	chr11:74109657-74109668
34	CEBPB	chr11:74109534-74109936	A549	lung:	n/a	chr11:74109657-74109668
35	CEBPB	chr11:74109504-74109997	K562	blood:	n/a	chr11:74109657-74109668
36	CEBPB	chr11:74109400-74110119	A549	lung:	n/a	chr11:74109657-74109668
37	CEBPB	chr11:74109476-74110008	K562	blood:	n/a	chr11:74109657-74109668
38	CEBPB	chr11:74109476-74110042	A549	lung:	n/a	chr11:74109657-74109668
39	CEBPB	chr11:74114001-74114035	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:74082822-74083137	A549	lung:	n/a	n/a
41	CEBPB	chr11:74109519-74109782	K562	blood:	n/a	chr11:74109657-74109668
42	CEBPB	chr11:74109462-74110084	Hela-S3	cervix:	n/a	chr11:74109657-74109668
43	CEBPB	chr11:74109478-74110006	IMR90	lung:	n/a	chr11:74109657-74109668
44	CEBPD	chr11:74109424-74109892	HepG2	liver:	n/a	chr11:74109656-74109667
45	CHD1	chr11:74099836-74100036	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr11:74109651-74110140	GM12878	blood:	n/a	n/a
47	CHD2	chr11:74108975-74110284	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr11:74109288-74110074	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr11:74109249-74109351	HepG2	liver:	n/a	n/a
50	CHD2	chr11:74109293-74110276	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74109076-74109126	AG04449	skin:	fetal
2	chr11:74109904-74109954	AG09319	gingival:	n/a
3	chr11:74109904-74109954	IMR90	lung:	fetal
4	chr11:74109221-74109271	PANC-1	pancreas:	n/a
5	chr11:74109510-74109560	NHBE	bronchial:	n/a
6	chr11:74109076-74109126	GM12892	blood:	n/a
7	chr11:74110106-74110156	BJ	skin:	n/a
8	chr11:74109971-74110021	NH-A	brain:	n/a
9	chr11:74105865-74105915	BE2_C	brain:	n/a
10	chr11:74109674-74109724	RPTEC	kidney:	n/a
11	chr11:74109971-74110021	SAEC	small airway:	n/a
12	chr11:74098949-74098999	SAEC	small airway:	n/a
13	chr11:74108683-74108733	AG09309	skin:	n/a
14	chr11:74109510-74109560	HRCEpiC	kidney:	n/a
15	chr11:74110223-74110273	GM12878	blood:	n/a
16	chr11:74109221-74109271	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:74109560-74109610	PANC-1	pancreas:	n/a
18	chr11:74108683-74108733	AoSMC	blood vessel:	n/a
19	chr11:74110145-74110195	Jurkat	blood:	n/a
20	chr11:74105865-74105915	NHDF-neo	bronchial:	n/a
21	chr11:74109221-74109271	ECC-1	luminal epithelium:	n/a
22	chr11:74110106-74110156	ECC-1	luminal epithelium:	n/a
23	chr11:74109674-74109724	SKMC	muscle:	n/a
24	chr11:74110145-74110195	AG09319	gingival:	n/a
25	chr11:74109221-74109271	U87	brain:	n/a
26	chr11:74109674-74109724	ProgFib	skin:	n/a
27	chr11:74110145-74110195	AG09309	skin:	n/a
28	chr11:74109971-74110021	AG04450	lung:	fetal
29	chr11:74105865-74105915	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:74109560-74109610	NT2-D1	testis:	n/a
31	chr11:74098949-74098999	HIPEpiC	eye:	n/a
32	chr11:74109560-74109610	HCF	heart:	n/a
33	chr11:74110223-74110273	RPTEC	kidney:	n/a
34	chr11:74110223-74110273	HepG2	liver:	n/a
35	chr11:74110145-74110195	HEK293	kidney:	embryo
36	chr11:74098949-74098999	ovcar-3	ovarian:	n/a
37	chr11:74109608-74109658	IMR90	lung:	fetal
38	chr11:74110145-74110195	PrEC	prostate:	n/a
39	chr11:74109608-74109658	NHDF-neo	bronchial:	n/a
40	chr11:74110106-74110156	HEK293	kidney:	embryo
41	chr11:74108683-74108733	NHDF-neo	bronchial:	n/a
42	chr11:74098949-74098999	HUVEC	blood vessel:	n/a
43	chr11:74109674-74109724	HIPEpiC	eye:	n/a
44	chr11:74110145-74110195	IMR90	lung:	fetal
45	chr11:74110106-74110156	T-47D	breast:	n/a
46	chr11:74109971-74110021	HepG2	liver:	n/a
47	chr11:74109221-74109271	HIPEpiC	eye:	n/a
48	chr11:74109560-74109610	AG04450	lung:	fetal
49	chr11:74098949-74098999	HRPEpiC	eye:	n/a
50	chr11:74109221-74109271	PFSK-1	brain:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:74097699..74100088-chr11:74103636..74105838,4	MCF-7	breast:
2	chr11:74081090..74083546-chr11:74085874..74088231,2	MCF-7	breast:
3	chr11:74091071..74093515-chr11:74095775..74098618,2	K562	blood:
4	chr11:74085550..74088254-chr11:74088597..74091470,2	K562	blood:
5	chr11:74053944..74055887-chr11:74058250..74060555,2	MCF-7	breast:
6	chr11:74102477..74106045-chr11:74107152..74109674,4	K562	blood:
7	chr11:74043932..74046437-chr11:74097322..74099844,2	K562	blood:
8	chr11:74107664..74111808-chr11:74126117..74130270,5	MCF-7	breast:
9	chr11:74092361..74094901-chr11:74100930..74103322,2	K562	blood:
10	chr11:74085418..74089578-chr11:74097575..74099669,3	MCF-7	breast:
11	chr11:73966846..73967553-chr11:74099341..74100160,2	MCF-7	breast:
12	chr11:74122725..74125748-chr11:74128034..74129993,3	MCF-7	breast:
13	chr11:74081090..74083546-chr11:74085874..74088231,2	MCF-7	breast:
14	chr11:74108659..74110537-chr11:74118206..74120213,2	K562	blood:
15	chr11:74041581..74043351-chr11:74050387..74052312,2	MCF-7	breast:
16	chr11:74099780..74100392-chr11:74281311..74282210,2	K562	blood:
17	chr11:74093796..74096757-chr11:74106676..74108506,3	K562	blood:
18	chr11:74092775..74094919-chr11:74115876..74118809,2	MCF-7	breast:
19	chr11:74085418..74089578-chr11:74097575..74099669,3	MCF-7	breast:
20	chr11:74085550..74088254-chr11:74088597..74091470,2	K562	blood:
21	chr11:73942988..73945702-chr11:74054339..74056814,2	K562	blood:
22	chr11:74107693..74110555-chr11:74110829..74112804,2	MCF-7	breast:
23	chr11:74109269..74109802-chr15:74907719..74908512,2	Hela-S3	cervix:
24	chr11:74104017..74106054-chr11:74107838..74110081,3	K562	blood:
25	chr11:74099650..74100358-chr11:74160062..74160991,4	MCF-7	breast:
26	chr11:74102528..74107005-chr11:74107093..74111376,8	MCF-7	breast:
27	chr11:74100543..74103930-chr11:74153911..74157152,3	MCF-7	breast:
28	chr11:74099950..74102299-chr11:74108209..74110170,3	K562	blood:
29	chr11:74099483..74099994-chr11:74153863..74154588,2	MCF-7	breast:
30	chr11:74087058..74089421-chr11:74090926..74093848,2	MCF-7	breast:
31	chr11:74099388..74100488-chr11:74160054..74161057,5	MCF-7	breast:
32	chr11:74090302..74094852-chr11:74107852..74111115,4	MCF-7	breast:
33	chr11:74092361..74094901-chr11:74100930..74103322,2	K562	blood:
34	chr11:74091071..74093515-chr11:74095775..74098618,2	K562	blood:
35	chr11:74092349..74095078-chr11:74103770..74106282,2	MCF-7	breast:
36	chr11:74092775..74094919-chr11:74115876..74118809,2	MCF-7	breast:
37	chr11:74108659..74110537-chr11:74118206..74120213,2	K562	blood:
38	chr11:74050053..74052444-chr11:74059467..74061186,2	K562	blood:
39	chr11:74050053..74052444-chr11:74059467..74061186,2	K562	blood:
40	chr11:74041592..74044323-chr11:74054058..74056372,2	MCF-7	breast:
41	chr11:74111193..74112861-chr11:74116086..74118546,2	K562	blood:
42	chr11:74099429..74100351-chr11:74159564..74161010,6	K562	blood:
43	chr11:74087058..74089421-chr11:74090926..74093848,2	MCF-7	breast:
44	chr11:74010289..74013142-chr11:74079571..74081272,2	K562	blood:
45	chr11:74092349..74095078-chr11:74103770..74106282,2	MCF-7	breast:
46	chr11:74104263..74106385-chr11:74107787..74109498,2	MCF-7	breast:
47	chr11:74113820..74116685-chr11:74117117..74119605,4	MCF-7	breast:
48	chr11:74107862..74112061-chr11:74124805..74130360,12	MCF-7	breast:
49	chr11:74097699..74100088-chr11:74103636..74105838,4	MCF-7	breast:
50	chr11:74099605..74100422-chr11:74153909..74154835,7	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPME1-3	chr11:74065488-74066765	NONHSAT022895
2	lnc-POLD3-4	chr11:74108698-74108714	ENSG00000254631.1
3	lnc-POLD3-4	chr11:74108594-74108714	ENSG00000254631.1
4	lnc-POLD3-4	chr11:74108814-74108950	ENSG00000254631.1
5	lnc-POLD3-4	chr11:74108814-74108950	ENSG00000254631.1
6	lnc-KCNE3-1	chr11:74108791-74109453	NONHSAT022898
7	lnc-POLD3-3	chr11:74120105-74120210	ENSG00000255440

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548al	chr11:74110346-74110367	MIMAT0019024

No data

Variant related genes	Relation type
MIR548AL	TF binding region
ENSG00000254631	TF binding region
ENSG00000255440	TF binding region
HNRNPA1P40	TF binding region
PGM2L1	TF binding region
MIR548AL	CpG island
ENSG00000254631	CpG island
ENSG00000255440	CpG island
HNRNPA1P40	CpG island
PGM2L1	CpG island
ENSG00000254631	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000179335	chromatin interactions
ENSG00000264402	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000165434	chromatin interactions
ENSG00000271380	chromatin interactions
ENSG00000255440	chromatin interactions
ENSG00000260919	chromatin interactions

Extended variants
information (count: 2595 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2595 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41349744	chr11:74052264-74052265	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537725512	chr11:74052354-74052355	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571447625	chr11:74052356-74052357	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs574278747	chr11:74052357-74052358	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184059801	chr11:74052396-74052397	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76567502	chr11:74052402-74052403	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553299275	chr11:74052453-74052454	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201790256	chr11:74052462-74052463	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11236062	chr11:74052463-74052464	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540786700	chr11:74052465-74052466	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372533236	chr11:74052502-74052503	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187998688	chr11:74052503-74052504	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180817116	chr11:74052547-74052548	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7122900	chr11:74052582-74052583	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114650095	chr11:74052612-74052613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548720345	chr11:74052696-74052697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183797884	chr11:74052724-74052725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370576343	chr11:74052741-74052742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs397777854	chr11:74052761-74052762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528551169	chr11:74052811-74052812	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189248759	chr11:74052845-74052846	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs687063	chr11:74052870-74052871	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs537487105	chr11:74052923-74052924	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557675349	chr11:74052925-74052926	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138571753	chr11:74053090-74053091	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182255118	chr11:74053231-74053232	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553499030	chr11:74053258-74053259	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375608958	chr11:74053282-74053283	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535801119	chr11:74053284-74053285	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573394162	chr11:74053329-74053330	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566348190	chr11:74053330-74053331	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541102760	chr11:74053339-74053340	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557614954	chr11:74053396-74053397	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577210483	chr11:74053429-74053430	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542974717	chr11:74053439-74053440	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554155289	chr11:74053479-74053480	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200147693	chr11:74053486-74053487	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542528424	chr11:74053492-74053493	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559483556	chr11:74053507-74053508	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151007979	chr11:74053512-74053513	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140901450	chr11:74053533-74053534	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs592644	chr11:74053547-74053548	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs138854022	chr11:74053552-74053553	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371880752	chr11:74053553-74053554	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142735059	chr11:74053557-74053558	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146960261	chr11:74053573-74053574	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548955	chr11:74053587-74053588	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376494726	chr11:74053615-74053616	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369829875	chr11:74053620-74053621	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144486313	chr11:74053623-74053624	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74031200-74071200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74037000-74055400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:74037400-74078800	Weak transcription	Small Intestine	intestine
4	chr11:74037600-74052800	Weak transcription	A549	lung
5	chr11:74037800-74086200	Weak transcription	Brain Anterior Caudate	brain
6	chr11:74038000-74071200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr11:74038000-74077400	Weak transcription	Psoas Muscle	Psoas
8	chr11:74038000-74077600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr11:74038000-74084400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:74038200-74052800	Weak transcription	Ovary	ovary
11	chr11:74038200-74053600	Weak transcription	Spleen	Spleen
12	chr11:74038200-74058200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:74038200-74065000	Weak transcription	Aorta	Aorta
14	chr11:74038200-74071000	Weak transcription	Fetal Stomach	stomach
15	chr11:74038200-74071400	Weak transcription	Left Ventricle	heart
16	chr11:74038200-74071400	Weak transcription	Lung	lung
17	chr11:74038200-74082000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr11:74038200-74084400	Weak transcription	Colon Smooth Muscle	Colon
19	chr11:74038400-74052800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr11:74038400-74084400	Weak transcription	Liver	Liver
21	chr11:74038400-74086200	Weak transcription	Adipose Nuclei	Adipose
22	chr11:74038600-74071400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr11:74038800-74070600	Weak transcription	Fetal Brain Male	brain
24	chr11:74039000-74053000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:74039200-74055200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr11:74039400-74071400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr11:74039800-74066200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:74041600-74052800	Weak transcription	Fetal Lung	lung
29	chr11:74041800-74071200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:74041800-74071400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:74042000-74077600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:74042200-74065600	Weak transcription	Fetal Heart	heart
33	chr11:74042200-74081200	Weak transcription	Hela-S3	cervix
34	chr11:74042400-74053200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr11:74043200-74054000	Weak transcription	Right Ventricle	heart
36	chr11:74043800-74058200	Weak transcription	Osteobl	bone
37	chr11:74044800-74062000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:74044800-74079200	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr11:74045800-74071400	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr11:74045800-74073200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr11:74046000-74071800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr11:74046600-74054200	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr11:74046800-74055000	Strong transcription	HSMM	muscle
44	chr11:74046800-74057200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr11:74046800-74060000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:74046800-74062600	Strong transcription	Fetal Thymus	thymus
47	chr11:74047000-74053800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:74047000-74056800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:74047000-74056800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr11:74047000-74058200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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