Variant report

Variant	nsv876740
Chromosome Location	chr3:46656980-46748453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1982)
CpG islands
(count:2628)
Chromatin interactive
region (count:157)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1982 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:46661623-46661869	K562	blood:	n/a	n/a
2	ATF1	chr3:46684585-46684909	K562	blood:	n/a	n/a
3	ATF2	chr3:46746461-46746813	GM12878	blood:	n/a	n/a
4	ATF2	chr3:46671272-46671937	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:46671292-46671865	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr3:46671400-46671857	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr3:46671409-46671780	K562	blood:	n/a	n/a
8	ATF3	chr3:46671570-46671752	GM12878	blood:	n/a	n/a
9	BACH1	chr3:46671292-46671750	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:46746558-46746758	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:46735430-46735744	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:46734048-46734515	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr3:46720127-46720375	GM12878	blood:	n/a	n/a
14	BATF	chr3:46720130-46720422	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:46671448-46671810	GM12878	blood:	n/a	chr3:46671654-46671670
16	BHLHE40	chr3:46734263-46734269	A549	lung:	n/a	n/a
17	BHLHE40	chr3:46671422-46671839	K562	blood:	n/a	chr3:46671654-46671670
18	BHLHE40	chr3:46736761-46737392	K562	blood:	n/a	n/a
19	BHLHE40	chr3:46736984-46737365	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:46746528-46746852	K562	blood:	n/a	n/a
21	BHLHE40	chr3:46735446-46735593	K562	blood:	n/a	n/a
22	BHLHE40	chr3:46734493-46734748	K562	blood:	n/a	n/a
23	BRCA1	chr3:46746485-46746854	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr3:46700658-46700720	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr3:46746601-46746847	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr3:46746586-46746696	HepG2	liver:	n/a	n/a
27	BRCA1	chr3:46708976-46709045	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr3:46734876-46735076	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr3:46693497-46693764	K562	blood:	n/a	n/a
30	CBX3	chr3:46671216-46671805	K562	blood:	n/a	n/a
31	CCNT2	chr3:46671310-46671777	K562	blood:	n/a	n/a
32	CCNT2	chr3:46734819-46735516	K562	blood:	n/a	n/a
33	CEBPB	chr3:46732340-46732540	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:46737591-46737781	HepG2	liver:	n/a	chr3:46737680-46737691 chr3:46737682-46737693 chr3:46737680-46737693 chr3:46737682-46737691
35	CEBPB	chr3:46684497-46684838	HepG2	liver:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
36	CEBPB	chr3:46689225-46689389	K562	blood:	n/a	n/a
37	CEBPB	chr3:46674341-46674550	K562	blood:	n/a	chr3:46674459-46674470
38	CEBPB	chr3:46684495-46684810	K562	blood:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
39	CEBPB	chr3:46746392-46746831	GM12878	blood:	n/a	n/a
40	CEBPB	chr3:46684537-46684825	Hela-S3	cervix:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
41	CEBPB	chr3:46674353-46674610	Hela-S3	cervix:	n/a	chr3:46674459-46674470
42	CEBPB	chr3:46702387-46702777	MCF-7	breast:	n/a	n/a
43	CEBPB	chr3:46720185-46720372	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:46737527-46737719	Hela-S3	cervix:	n/a	chr3:46737680-46737691 chr3:46737682-46737693 chr3:46737680-46737693 chr3:46737682-46737691
45	CEBPB	chr3:46684472-46684933	K562	blood:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
46	CEBPB	chr3:46685349-46685566	A549	lung:	n/a	n/a
47	CEBPB	chr3:46674348-46674548	HepG2	liver:	n/a	chr3:46674459-46674470
48	CEBPB	chr3:46684501-46684834	A549	lung:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
49	CEBPB	chr3:46684576-46684850	H1-hESC	embryonic stem cell:	n/a	chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684663-46684676 chr3:46684665-46684674 chr3:46684665-46684674
50	CEBPB	chr3:46670495-46670689	HepG2	liver:	n/a	chr3:46670542-46670553

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46742865-46742915	SK-N-SH	brain:	n/a
2	chr3:46734393-46734443	NHBE	bronchial:	n/a
3	chr3:46687388-46687438	ProgFib	skin:	n/a
4	chr3:46735009-46735059	HUVEC	blood vessel:	n/a
5	chr3:46687388-46687438	NT2-D1	testis:	n/a
6	chr3:46742865-46742915	SK-N-SH	brain:	n/a
7	chr3:46734393-46734443	NHBE	bronchial:	n/a
8	chr3:46687388-46687438	ProgFib	skin:	n/a
9	chr3:46735009-46735059	HUVEC	blood vessel:	n/a
10	chr3:46687388-46687438	NT2-D1	testis:	n/a
11	chr3:46742491-46742541	AoSMC	blood vessel:	n/a
12	chr3:46746779-46746829	ProgFib	skin:	n/a
13	chr3:46718941-46718991	Hela-S3	cervix:	n/a
14	chr3:46735801-46735851	AG09319	gingival:	n/a
15	chr3:46742703-46742753	K562	blood:	n/a
16	chr3:46672436-46672486	AG09309	skin:	n/a
17	chr3:46672436-46672486	SK-N-MC	brain:	n/a
18	chr3:46735801-46735851	NT2-D1	testis:	n/a
19	chr3:46742898-46742948	A549	lung:	n/a
20	chr3:46743199-46743249	AG09319	gingival:	n/a
21	chr3:46741492-46741542	HRCEpiC	kidney:	n/a
22	chr3:46733475-46733525	HCF	heart:	n/a
23	chr3:46727805-46727855	HEEpiC	esophagus:	n/a
24	chr3:46742898-46742948	SKMC	muscle:	n/a
25	chr3:46742703-46742753	HEK293	kidney:	embryo
26	chr3:46735782-46735832	HNPCEpiC	eye:	n/a
27	chr3:46742865-46742915	HEEpiC	esophagus:	n/a
28	chr3:46747930-46747980	HCT-116	colon:	n/a
29	chr3:46671334-46671384	T-47D	breast:	n/a
30	chr3:46734393-46734443	HUVEC	blood vessel:	n/a
31	chr3:46735801-46735851	Jurkat	blood:	n/a
32	chr3:46669290-46669340	HEK293	kidney:	embryo
33	chr3:46727805-46727855	LNCaP	prostate:	n/a
34	chr3:46735154-46735204	Caco-2	colon:	n/a
35	chr3:46735009-46735059	RPTEC	kidney:	n/a
36	chr3:46735338-46735388	HCT-116	colon:	n/a
37	chr3:46735152-46735202	HEK293	kidney:	embryo
38	chr3:46735695-46735745	NHBE	bronchial:	n/a
39	chr3:46719625-46719675	AG09319	gingival:	n/a
40	chr3:46735154-46735204	T-47D	breast:	n/a
41	chr3:46718990-46719040	AG04449	skin:	fetal
42	chr3:46742491-46742541	LNCaP	prostate:	n/a
43	chr3:46735695-46735745	HEK293	kidney:	embryo
44	chr3:46735801-46735851	SK-N-MC	brain:	n/a
45	chr3:46735319-46735369	SK-N-MC	brain:	n/a
46	chr3:46669290-46669340	HAEpiC	amniotic membrane:	n/a
47	chr3:46719834-46719884	A549	lung:	n/a
48	chr3:46671563-46671613	K562	blood:	n/a
49	chr3:46719834-46719884	Caco-2	colon:	n/a
50	chr3:46742491-46742541	HCT-116	colon:	n/a

(count:157 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:46745129..46746095-chr3:46936433..46937176,2	MCF-7	breast:
2	chr3:46712670..46714568-chr3:46716862..46719583,2	K562	blood:
3	chr3:46701509..46703825-chr3:47020121..47022596,2	MCF-7	breast:
4	chr3:46738781..46740669-chr3:46750489..46752316,2	K562	blood:
5	chr3:46703608..46706840-chr3:46708905..46711367,3	K562	blood:
6	chr3:46589952..46592593-chr3:46732036..46734467,2	K562	blood:
7	chr3:46733801..46735413-chr3:46924430..46926212,2	MCF-7	breast:
8	chr3:46722742..46724325-chr3:46733459..46735116,2	K562	blood:
9	chr3:46675056..46675850-chr3:46708207..46708731,2	MCF-7	breast:
10	chr3:46599516..46600466-chr3:46671185..46672080,3	MCF-7	breast:
11	chr3:46675056..46675850-chr3:46708207..46708731,2	MCF-7	breast:
12	chr3:46735218..46737600-chr3:46738787..46741218,2	K562	blood:
13	chr3:46707782..46708419-chr3:46950685..46951647,2	MCF-7	breast:
14	chr3:46703608..46706840-chr3:46708905..46711367,3	K562	blood:
15	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
16	chr3:46529944..46530794-chr3:46705110..46706015,2	K562	blood:
17	chr3:46746461..46747137-chr3:46936122..46936835,3	MCF-7	breast:
18	chr3:46697148..46699057-chr3:46702525..46705499,2	K562	blood:
19	chr3:46733050..46735013-chr3:46736523..46739104,3	K562	blood:
20	chr3:46503615..46504280-chr3:46671186..46672162,2	MCF-7	breast:
21	chr3:46748228..46751973-chr3:46757589..46759527,3	MCF-7	breast:
22	chr3:46679942..46681539-chr3:46683800..46686351,2	K562	blood:
23	chr3:46476162..46478897-chr3:46745088..46748069,2	K562	blood:
24	chr3:46723220..46725442-chr3:46727287..46728789,2	K562	blood:
25	chr3:46650273..46651172-chr3:46707945..46708857,6	MCF-7	breast:
26	chr3:46711200..46713596-chr3:46721127..46724340,3	MCF-7	breast:
27	chr3:46735218..46737600-chr3:46738787..46741218,2	K562	blood:
28	chr3:46702436..46704815-chr3:46735975..46737913,2	MCF-7	breast:
29	chr3:46436315..46436954-chr3:46671328..46672082,2	K562	blood:
30	chr3:46723115..46726062-chr3:46732632..46735169,2	MCF-7	breast:
31	chr3:46732249..46733917-chr3:46887547..46889689,2	MCF-7	breast:
32	chr3:46658701..46661042-chr3:46905477..46908148,2	MCF-7	breast:
33	chr3:46736001..46738313-chr3:46739420..46741660,3	MCF-7	breast:
34	chr3:46551542..46553996-chr3:46670081..46671656,2	K562	blood:
35	chr17:43393907..43394635-chr3:46734362..46735110,2	Hela-S3	cervix:
36	chr3:46704689..46705566-chr3:46936603..46937451,3	MCF-7	breast:
37	chr3:46709508..46711743-chr3:46776427..46778541,2	K562	blood:
38	chr3:46711657..46716189-chr3:46730133..46733448,4	MCF-7	breast:
39	chr3:46737124..46738860-chr3:46743430..46745835,2	K562	blood:
40	chr3:46670811..46674020-chr3:46675061..46678300,4	K562	blood:
41	chr3:46529884..46530839-chr3:46671105..46672532,19	MCF-7	breast:
42	chr3:46707418..46709371-chr3:46712225..46713806,2	K562	blood:
43	chr3:46735288..46735975-chr3:46746178..46746698,2	K562	blood:
44	chr3:46679942..46681539-chr3:46683800..46686351,2	K562	blood:
45	chr3:46720300..46721832-chr3:46725360..46727686,2	K562	blood:
46	chr3:46699829..46702382-chr3:46705244..46707445,2	K562	blood:
47	chr3:46715976..46718963-chr3:46721062..46722912,2	MCF-7	breast:
48	chr3:46650761..46651345-chr3:46671138..46672058,2	MCF-7	breast:
49	chr3:46634709..46635296-chr3:46671423..46672075,2	MCF-7	breast:
50	chr3:46724809..46726431-chr3:46731600..46733617,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RTP3-2	chr3:46658673-46658716	NONHSAT089450
2	lnc-TMIE-1	chr3:46667272-46667698	NONHSAT089452

No data

Variant related genes	Relation type
ALS2CL	TF binding region
ENSG00000251967	TF binding region
ENSG00000256354	TF binding region
TMIE	TF binding region
ALS2CL	CpG island
ENSG00000251967	CpG island
ENSG00000256354	CpG island
TMIE	CpG island
ENSG00000113558	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000006062	chromatin interactions
ENSG00000241186	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000206549	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000178038	chromatin interactions
ENSG00000160799	chromatin interactions
ENSG00000181585	chromatin interactions
ENSG00000264306	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000160796	chromatin interactions
ENSG00000261603	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000160801	chromatin interactions

Extended variants
information (count: 3763 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3763 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1106665	chr3:46656980-46656981	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568075878	chr3:46656983-46656984	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs111474803	chr3:46656991-46656992	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556981834	chr3:46656999-46657000	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs116143467	chr3:46657043-46657044	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs577946370	chr3:46657115-46657116	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs375253393	chr3:46657122-46657123	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs75118686	chr3:46657123-46657124	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs545130283	chr3:46657138-46657139	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs1106664	chr3:46657162-46657163	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs74351380	chr3:46657167-46657168	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs73077560	chr3:46657202-46657203	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs555463888	chr3:46657227-46657228	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs79036361	chr3:46657271-46657272	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs544303732	chr3:46657322-46657323	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs192719974	chr3:46657331-46657332	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs201281577	chr3:46657336-46657337	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs137999277	chr3:46657340-46657341	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs111864834	chr3:46657341-46657342	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs563717700	chr3:46657359-46657360	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs150578746	chr3:46657427-46657428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73077561	chr3:46657428-46657429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs80118899	chr3:46657498-46657499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77691508	chr3:46657500-46657501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373582063	chr3:46657523-46657524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559121174	chr3:46657545-46657546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72904204	chr3:46657578-46657579	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs546906131	chr3:46657582-46657583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189636294	chr3:46657608-46657609	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs528850547	chr3:46657612-46657613	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs550306175	chr3:46657615-46657616	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs116545523	chr3:46657623-46657624	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs374135073	chr3:46657675-46657676	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs577507495	chr3:46657696-46657697	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs192067157	chr3:46657698-46657699	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs551984580	chr3:46657742-46657743	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs567107097	chr3:46657749-46657750	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs373720216	chr3:46657775-46657776	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs573560978	chr3:46657825-46657826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574254175	chr3:46657855-46657856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538198646	chr3:46657903-46657904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs117864426	chr3:46657907-46657908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184661897	chr3:46657929-46657930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75048420	chr3:46657941-46657942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563922271	chr3:46658009-46658010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114323879	chr3:46658033-46658034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2139635	chr3:46658044-46658045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs368883567	chr3:46658063-46658064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2139636	chr3:46658112-46658113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs77364475	chr3:46658116-46658117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2331 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46651600-46671200	Weak transcription	Right Atrium	heart
2	chr3:46651800-46658000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:46652000-46661000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr3:46652000-46661200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:46654200-46659400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr3:46654400-46657000	Weak transcription	Brain Substantia Nigra	brain
7	chr3:46654400-46663000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:46656600-46657000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:46656600-46657400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr3:46656600-46657600	Enhancers	Fetal Muscle Leg	muscle
11	chr3:46656600-46657800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:46656600-46657800	Enhancers	Fetal Lung	lung
13	chr3:46657000-46657200	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr3:46657000-46657600	Enhancers	Fetal Heart	heart
15	chr3:46657000-46657800	Enhancers	Brain Substantia Nigra	brain
16	chr3:46657000-46659200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:46657400-46657800	Enhancers	Fetal Muscle Trunk	muscle
18	chr3:46657600-46657800	Bivalent Enhancer	Fetal Muscle Leg	muscle
19	chr3:46658800-46661200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr3:46659200-46659400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:46659200-46659800	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr3:46659400-46659600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr3:46659400-46659600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:46659400-46659800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr3:46659600-46659800	Flanking Active TSS	Spleen	Spleen
26	chr3:46659600-46661200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:46659800-46660800	Weak transcription	Spleen	Spleen
28	chr3:46659800-46661000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:46660800-46661000	Enhancers	Spleen	Spleen
30	chr3:46661000-46661600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:46661000-46661800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr3:46661000-46661800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr3:46661200-46661800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr3:46661200-46661800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr3:46661200-46662400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr3:46661200-46662400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr3:46661400-46661800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr3:46661400-46661800	Enhancers	Fetal Muscle Trunk	muscle
39	chr3:46661400-46662000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:46661400-46662000	Enhancers	Adipose Nuclei	Adipose
41	chr3:46661400-46662400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:46661600-46661800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:46661600-46661800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:46661600-46661800	Bivalent Enhancer	Fetal Stomach	stomach
45	chr3:46661600-46661800	Bivalent Enhancer	NH-A	brain
46	chr3:46661600-46662200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:46661600-46662200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr3:46661600-46662200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr3:46661600-46670200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr3:46661800-46666200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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