Variant report

Variant	nsv1050614
Chromosome Location	chr11:46414720-46496732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:891)
CpG islands
(count:673)
Chromatin interactive
region (count:82)
LncRNA
region (count:0)
Mature miRNA
region (count: 4)
miRNA target
sites (count:1)

(count:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46448994-46449194	K562	blood:	n/a	n/a
2	ARID3A	chr11:46467186-46467376	K562	blood:	n/a	n/a
3	ARID3A	chr11:46443227-46443395	K562	blood:	n/a	n/a
4	ARID3A	chr11:46483191-46483473	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:46474922-46475094	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:46473416-46473664	K562	blood:	n/a	n/a
7	ATF1	chr11:46473454-46473653	K562	blood:	n/a	n/a
8	ATF1	chr11:46494354-46494426	K562	blood:	n/a	n/a
9	BACH1	chr11:46448756-46449380	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:46448745-46449320	K562	blood:	n/a	n/a
11	BATF	chr11:46477484-46477705	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:46448992-46449140	K562	blood:	n/a	n/a
13	BHLHE40	chr11:46442812-46443109	K562	blood:	n/a	n/a
14	BHLHE40	chr11:46474788-46474802	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:46494379-46494394	HepG2	liver:	n/a	n/a
16	BRCA1	chr11:46444397-46444477	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr11:46448838-46449313	K562	blood:	n/a	n/a
18	CEBPB	chr11:46450045-46450119	K562	blood:	n/a	n/a
19	CEBPB	chr11:46474761-46475028	HepG2	liver:	n/a	chr11:46474871-46474882
20	CEBPB	chr11:46487210-46487578	HepG2	liver:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
21	CEBPB	chr11:46479228-46479578	K562	blood:	n/a	n/a
22	CEBPB	chr11:46477865-46478200	H1-hESC	embryonic stem cell:	n/a	chr11:46478003-46478014 chr11:46478003-46478016
23	CEBPB	chr11:46485651-46485732	HepG2	liver:	n/a	chr11:46485679-46485692 chr11:46485680-46485691 chr11:46485679-46485690 chr11:46485679-46485690
24	CEBPB	chr11:46479301-46479501	K562	blood:	n/a	n/a
25	CEBPB	chr11:46487332-46487483	HepG2	liver:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
26	CEBPB	chr11:46487263-46487534	K562	blood:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
27	CEBPB	chr11:46479298-46479572	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:46487256-46487572	HepG2	liver:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
29	CEBPB	chr11:46487322-46487514	Hela-S3	cervix:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
30	CEBPB	chr11:46474744-46475024	HepG2	liver:	n/a	chr11:46474871-46474882
31	CEBPB	chr11:46487242-46487604	HepG2	liver:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
32	CEBPB	chr11:46487249-46487551	A549	lung:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
33	CEBPB	chr11:46417551-46417656	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr11:46430788-46430919	HepG2	liver:	n/a	chr11:46430806-46430817
35	CEBPB	chr11:46474784-46474922	HepG2	liver:	n/a	chr11:46474871-46474882
36	CEBPB	chr11:46430792-46430830	A549	lung:	n/a	chr11:46430806-46430817
37	CEBPB	chr11:46487244-46487545	IMR90	lung:	n/a	chr11:46487389-46487398 chr11:46487387-46487398 chr11:46487388-46487399
38	CEBPB	chr11:46479256-46479569	IMR90	lung:	n/a	n/a
39	CEBPB	chr11:46479263-46479564	K562	blood:	n/a	n/a
40	CHD2	chr11:46414090-46414804	H1-hESC	embryonic stem cell:	n/a	chr11:46414282-46414292
41	CHD2	chr11:46430124-46430324	HepG2	liver:	n/a	n/a
42	CREB1	chr11:46466697-46467184	GM12878	blood:	n/a	n/a
43	CREB1	chr11:46414055-46414810	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr11:46431683-46431793	GM13976	blood:	n/a	n/a
45	CTCF	chr11:46431654-46431849	A549	lung:	n/a	chr11:46431787-46431800
46	CTCF	chr11:46431654-46431830	Gliobla	brain:	n/a	chr11:46431787-46431800
47	CTCF	chr11:46468200-46468350	WI-38	lung:	n/a	n/a
48	CTCF	chr11:46431671-46431825	GM12878	blood:	n/a	chr11:46431787-46431800
49	CTCF	chr11:46431700-46431850	HA-sp	spinal cord:	n/a	chr11:46431787-46431800
50	CTCF	chr11:46431679-46431814	ProgFib	skin:	n/a	chr11:46431787-46431800

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46418140-46418190	HL-60	blood:	n/a
2	chr11:46450417-46450467	HUVEC	blood vessel:	n/a
3	chr11:46418140-46418190	HL-60	blood:	n/a
4	chr11:46450417-46450467	HUVEC	blood vessel:	n/a
5	chr11:46448921-46448971	SK-N-MC	brain:	n/a
6	chr11:46467232-46467282	AG09309	skin:	n/a
7	chr11:46486318-46486368	AG10803	skin:	n/a
8	chr11:46448921-46448971	NB4	blood:	n/a
9	chr11:46415316-46415366	BJ	skin:	n/a
10	chr11:46439420-46439470	Hela-S3	cervix:	n/a
11	chr11:46467232-46467282	NH-A	brain:	n/a
12	chr11:46418140-46418190	HepG2	liver:	n/a
13	chr11:46448921-46448971	GM06990	blood:	n/a
14	chr11:46467232-46467282	Hepatocyte	liver:	n/a
15	chr11:46450256-46450306	HepG2	liver:	n/a
16	chr11:46467232-46467282	HAEpiC	amniotic membrane:	n/a
17	chr11:46450417-46450467	HCT-116	colon:	n/a
18	chr11:46448921-46448971	PFSK-1	brain:	n/a
19	chr11:46467232-46467282	SK-N-SH	brain:	n/a
20	chr11:46415316-46415366	NT2-D1	testis:	n/a
21	chr11:46478214-46478264	SK-N-SH	brain:	n/a
22	chr11:46486318-46486368	CMK	blood:	n/a
23	chr11:46415316-46415366	SK-N-MC	brain:	n/a
24	chr11:46418140-46418190	HCT-116	colon:	n/a
25	chr11:46450256-46450306	NHDF-neo	bronchial:	n/a
26	chr11:46450417-46450467	CMK	blood:	n/a
27	chr11:46450256-46450306	HRPEpiC	eye:	n/a
28	chr11:46448921-46448971	AG09319	gingival:	n/a
29	chr11:46448921-46448971	Caco-2	colon:	n/a
30	chr11:46478214-46478264	HL-60	blood:	n/a
31	chr11:46486318-46486368	HRCEpiC	kidney:	n/a
32	chr11:46467232-46467282	ProgFib	skin:	n/a
33	chr11:46426289-46426339	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:46486318-46486368	NHDF-neo	bronchial:	n/a
35	chr11:46418140-46418190	T-47D	breast:	n/a
36	chr11:46450417-46450467	H1-hESC	embryonic stem cell:	embryo
37	chr11:46418140-46418190	HCPEpiC	choroid plexus:	n/a
38	chr11:46439420-46439470	ovcar-3	ovarian:	n/a
39	chr11:46450417-46450467	HL-60	blood:	n/a
40	chr11:46486318-46486368	HCM	heart:	n/a
41	chr11:46426289-46426339	HCT-116	colon:	n/a
42	chr11:46448921-46448971	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:46478214-46478264	HRPEpiC	eye:	n/a
44	chr11:46426289-46426339	ECC-1	luminal epithelium:	n/a
45	chr11:46415316-46415366	U87	brain:	n/a
46	chr11:46418140-46418190	HEEpiC	esophagus:	n/a
47	chr11:46478214-46478264	HepG2	liver:	n/a
48	chr11:46478214-46478264	HRE	kidney:	n/a
49	chr11:46439420-46439470	HL-60	blood:	n/a
50	chr11:46467232-46467282	Caco-2	colon:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:46490909..46492549-chr11:46494181..46496864,2	K562	blood:
2	chr11:46461604..46463369-chr11:46465505..46467389,2	K562	blood:
3	chr11:46414393..46416737-chr11:46429746..46431617,2	K562	blood:
4	chr11:46450955..46452945-chr11:46454344..46456750,3	MCF-7	breast:
5	chr11:46431554..46433236-chr11:46435981..46438386,2	K562	blood:
6	chr11:46433892..46435607-chr11:46449879..46451873,2	MCF-7	breast:
7	chr11:46413148..46415878-chr11:46416015..46418632,3	MCF-7	breast:
8	chr11:46413333..46415363-chr11:46417315..46419574,2	MCF-7	breast:
9	chr11:46468131..46471544-chr11:46473469..46477776,3	K562	blood:
10	chr11:46477611..46479570-chr11:46639487..46642071,2	MCF-7	breast:
11	chr11:46473814..46475655-chr11:46477410..46480121,2	MCF-7	breast:
12	chr11:46443817..46445771-chr11:46447587..46449187,2	K562	blood:
13	chr11:46480834..46483230-chr11:46484591..46487303,2	K562	blood:
14	chr11:46449230..46453145-chr11:46464134..46466452,3	MCF-7	breast:
15	chr11:46449218..46452238-chr6:34392341..34394490,5	MCF-7	breast:
16	chr11:46468131..46471544-chr11:46473469..46477776,3	K562	blood:
17	chr11:46450238..46451231-chr6:34393265..34393905,3	MCF-7	breast:
18	chr11:46424684..46426472-chr11:46440604..46442113,2	K562	blood:
19	chr11:46411065..46412828-chr11:46420913..46422705,2	MCF-7	breast:
20	chr11:46440995..46443504-chr11:46446202..46449083,2	MCF-7	breast:
21	chr11:46473814..46475655-chr11:46477410..46480121,2	MCF-7	breast:
22	chr11:46452244..46454737-chr11:46456753..46459294,3	K562	blood:
23	chr11:46410113..46411901-chr11:46416140..46417772,2	K562	blood:
24	chr11:46437731..46440325-chr11:46455877..46458436,2	K562	blood:
25	chr11:46419265..46420850-chr11:46421932..46424415,2	K562	blood:
26	chr11:46450213..46450713-chr6:34392822..34393736,2	Hela-S3	cervix:
27	chr11:46495928..46497602-chr11:46509674..46511734,2	K562	blood:
28	chr11:46450734..46451351-chr6:34393375..34394080,2	Hela-S3	cervix:
29	chr11:46461604..46463369-chr11:46465505..46467389,2	K562	blood:
30	chr11:46483527..46486367-chr11:46487935..46489569,2	MCF-7	breast:
31	chr11:46450955..46452945-chr11:46454344..46456750,3	MCF-7	breast:
32	chr11:46412693..46415235-chr11:46560575..46563535,2	K562	blood:
33	chr11:46431554..46433236-chr11:46435981..46438386,2	K562	blood:
34	chr11:46448640..46452068-chr11:46454493..46457739,3	K562	blood:
35	chr11:46411121..46411885-chr11:46431663..46432191,2	MCF-7	breast:
36	chr11:46450731..46452237-chr6:34392318..34394068,7	MCF-7	breast:
37	chr11:46415996..46418970-chr11:46425126..46426689,2	K562	blood:
38	chr11:46461604..46464506-chr11:46464583..46467005,4	K562	blood:
39	chr11:46472755..46475296-chr11:46477098..46478709,2	K562	blood:
40	chr11:46461604..46464506-chr11:46464583..46467005,4	K562	blood:
41	chr11:46440995..46443504-chr11:46446202..46449083,2	MCF-7	breast:
42	chr11:46431292..46432224-chr11:46559060..46559954,4	MCF-7	breast:
43	chr11:46431419..46434415-chr11:46435571..46438386,5	K562	blood:
44	chr11:46414393..46416737-chr11:46429746..46431617,2	K562	blood:
45	chr11:46424684..46426472-chr11:46440604..46442113,2	K562	blood:
46	chr11:46413333..46415363-chr11:46417315..46419574,2	MCF-7	breast:
47	chr11:46461056..46463228-chr11:46472080..46474431,3	MCF-7	breast:
48	chr11:46468408..46470921-chr11:46496767..46499525,2	K562	blood:
49	chr11:46431419..46434415-chr11:46435571..46438386,5	K562	blood:
50	chr11:46429446..46431562-chr11:46432327..46435072,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3160-3p	chr11:46473408-46473429	MIMAT0015034_1
hsa-miR-3160-5p	chr11:46473406-46473427	MIMAT0019212
hsa-miR-3160-3p	chr11:46473365-46473386	MIMAT0015034
hsa-miR-3160-5p	chr11:46473367-46473388	MIMAT0019212_1

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AMBRA1	hsa-miR-339-5p	chr11:46418447-46418469

Variant related genes	Relation type
ENSG00000244313	TF binding region
AMBRA1	TF binding region
MIR3160-2	TF binding region
ENSG00000244313	CpG island
AMBRA1	CpG island
MIR3160-2	CpG island
ENSG00000124614	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000244313	chromatin interactions
ENSG00000265014	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000110492	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000110497	chromatin interactions

Extended variants
information (count: 2706 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2706 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140833591	chr11:46414750-46414751	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs535159259	chr11:46414900-46414901	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557146294	chr11:46414976-46414977	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567712546	chr11:46415002-46415003	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs535536130	chr11:46415007-46415008	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs79065248	chr11:46415038-46415039	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572097557	chr11:46415168-46415169	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191127444	chr11:46415169-46415170	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs557763146	chr11:46415179-46415180	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549598997	chr11:46415223-46415224	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144589243	chr11:46415240-46415241	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs535221289	chr11:46415252-46415253	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371386413	chr11:46415315-46415316	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538141221	chr11:46415319-46415320	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563508113	chr11:46415332-46415333	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556057820	chr11:46415361-46415362	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558521901	chr11:46415362-46415363	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573707984	chr11:46415477-46415478	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542807466	chr11:46415525-46415526	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs578171008	chr11:46415598-46415599	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559635250	chr11:46415639-46415640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528550924	chr11:46415658-46415659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551391555	chr11:46415721-46415722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564898874	chr11:46415743-46415744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531118299	chr11:46415749-46415750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550942938	chr11:46415755-46415756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567942427	chr11:46415776-46415777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537469828	chr11:46415791-46415792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557033632	chr11:46415846-46415847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574082859	chr11:46415998-46415999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565664326	chr11:46415999-46416000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184726407	chr11:46416005-46416006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373593133	chr11:46416049-46416050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189317501	chr11:46416060-46416061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181682887	chr11:46416091-46416092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577672682	chr11:46416155-46416156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112441668	chr11:46416245-46416246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537346511	chr11:46416258-46416259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35191892	chr11:46416282-46416283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570430608	chr11:46416293-46416294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574589490	chr11:46416313-46416314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573872815	chr11:46416344-46416345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542494780	chr11:46416373-46416374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542760206	chr11:46416380-46416381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185230902	chr11:46416415-46416416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573025418	chr11:46416453-46416454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75483458	chr11:46416457-46416458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545057254	chr11:46416462-46416463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140184885	chr11:46416489-46416490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530857533	chr11:46416494-46416495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2927 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46410800-46415000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr11:46410800-46415000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr11:46411000-46414800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr11:46411400-46414800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
5	chr11:46412000-46415000	Enhancers	Lung	lung
6	chr11:46412400-46414800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr11:46412400-46415000	Active TSS	Brain Angular Gyrus	brain
8	chr11:46412600-46414800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
9	chr11:46412600-46414800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:46412800-46414800	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr11:46412800-46414800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr11:46412800-46415000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:46412800-46415000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:46412800-46415000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr11:46413000-46414800	Active TSS	H9 Cell Line	embryonic stem cell
16	chr11:46413000-46414800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:46413000-46425000	Weak transcription	Fetal Heart	heart
18	chr11:46413200-46414800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:46413200-46414800	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr11:46413200-46414800	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr11:46413200-46414800	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr11:46413200-46414800	Enhancers	Small Intestine	intestine
23	chr11:46413200-46415000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:46413400-46414800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:46413400-46414800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:46413400-46414800	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr11:46413400-46414800	Flanking Active TSS	Right Ventricle	heart
28	chr11:46413400-46415000	Flanking Bivalent TSS/Enh	Thymus	Thymus
29	chr11:46413600-46414800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:46413600-46414800	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr11:46413600-46414800	Flanking Active TSS	NH-A	brain
32	chr11:46413800-46414800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
33	chr11:46413800-46414800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr11:46413800-46414800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr11:46413800-46414800	Enhancers	GM12878-XiMat	blood
36	chr11:46414000-46414800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
37	chr11:46414000-46414800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:46414000-46414800	Enhancers	Brain Substantia Nigra	brain
39	chr11:46414000-46414800	Flanking Active TSS	Placenta	Placenta
40	chr11:46414000-46414800	Enhancers	Placenta Amnion	Placenta Amnion
41	chr11:46414000-46414800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
42	chr11:46414000-46415000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:46414000-46415000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
44	chr11:46414000-46415000	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr11:46414000-46415200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
46	chr11:46414200-46414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr11:46414200-46414800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr11:46414200-46414800	Flanking Active TSS	Primary T cells from cord blood	blood
49	chr11:46414200-46414800	Active TSS	Right Atrium	heart
50	chr11:46414200-46415000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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