Variant report

Variant	nsv541986
Chromosome Location	chr14:21692703-21735893
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2550)
CpG islands
(count:305)
Chromatin interactive
region (count:85)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2550 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21711963-21711985	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21711256-21711587	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21717162-21717278	K562	blood:	n/a	n/a
4	ARID3A	chr14:21732200-21733006	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:21709409-21709593	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:21697647-21697673	K562	blood:	n/a	n/a
7	ARID3A	chr14:21712624-21712985	HepG2	liver:	n/a	n/a
8	ATF2	chr14:21730290-21730933	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr14:21731973-21733035	GM12878	blood:	n/a	n/a
10	ATF2	chr14:21735362-21735856	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr14:21729052-21729484	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:21726892-21727596	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr14:21732138-21732971	GM12878	blood:	n/a	n/a
14	ATF2	chr14:21735629-21736731	GM12878	blood:	n/a	n/a
15	ATF2	chr14:21735848-21738400	GM12878	blood:	n/a	n/a
16	ATF2	chr14:21729447-21729836	GM12878	blood:	n/a	n/a
17	ATF2	chr14:21731544-21732278	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr14:21727624-21728013	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr14:21735698-21736021	K562	blood:	n/a	n/a
20	BATF	chr14:21733926-21734221	GM12878	blood:	n/a	chr14:21734053-21734064
21	BATF	chr14:21731822-21732559	GM12878	blood:	n/a	chr14:21732455-21732465 chr14:21732451-21732461
22	BATF	chr14:21732236-21732561	GM12878	blood:	n/a	chr14:21732455-21732465 chr14:21732451-21732461
23	BCL11A	chr14:21732207-21732610	GM12878	blood:	n/a	chr14:21732453-21732462 chr14:21732454-21732463
24	BCL3	chr14:21727073-21727426	K562	blood:	n/a	n/a
25	BCLAF1	chr14:21732126-21733056	GM12878	blood:	n/a	chr14:21732453-21732462 chr14:21732454-21732463
26	BCLAF1	chr14:21705331-21705994	GM12878	blood:	n/a	n/a
27	BCLAF1	chr14:21726818-21727567	K562	blood:	n/a	n/a
28	BCLAF1	chr14:21733808-21734347	GM12878	blood:	n/a	n/a
29	BCLAF1	chr14:21713989-21714387	GM12878	blood:	n/a	n/a
30	BCLAF1	chr14:21709359-21711746	GM12878	blood:	n/a	n/a
31	BCLAF1	chr14:21726752-21727540	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:21720323-21720739	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:21729129-21729488	GM12878	blood:	n/a	n/a
34	BCLAF1	chr14:21712549-21713102	GM12878	blood:	n/a	n/a
35	BCLAF1	chr14:21728983-21729484	K562	blood:	n/a	n/a
36	BCLAF1	chr14:21723447-21724382	GM12878	blood:	n/a	n/a
37	BCLAF1	chr14:21712564-21713058	GM12878	blood:	n/a	n/a
38	BCLAF1	chr14:21731848-21732313	K562	blood:	n/a	n/a
39	BCLAF1	chr14:21706763-21707518	GM12878	blood:	n/a	n/a
40	BCLAF1	chr14:21710768-21711305	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:21726995-21727466	K562	blood:	n/a	n/a
42	BCLAF1	chr14:21731491-21731826	GM12878	blood:	n/a	n/a
43	BCLAF1	chr14:21724730-21725441	GM12878	blood:	n/a	n/a
44	BHLHE40	chr14:21731802-21731811	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:21733964-21734185	GM12878	blood:	n/a	n/a
46	BRCA1	chr14:21730667-21730856	GM12878	blood:	n/a	n/a
47	BRCA1	chr14:21709394-21709761	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr14:21727172-21727553	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr14:21699415-21699501	GM12878	blood:	n/a	n/a
50	CCNT2	chr14:21727232-21727439	K562	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21704611-21704661	SK-N-SH_RA	brain:	n/a
2	chr14:21727471-21727521	AG10803	skin:	n/a
3	chr14:21704611-21704661	HCT-116	colon:	n/a
4	chr14:21731063-21731113	SK-N-SH	brain:	n/a
5	chr14:21731063-21731113	ovcar-3	ovarian:	n/a
6	chr14:21725703-21725753	ovcar-3	ovarian:	n/a
7	chr14:21734410-21734460	NT2-D1	testis:	n/a
8	chr14:21731063-21731113	GM12892	blood:	n/a
9	chr14:21734410-21734460	HCF	heart:	n/a
10	chr14:21704611-21704661	HRPEpiC	eye:	n/a
11	chr14:21734410-21734460	GM12892	blood:	n/a
12	chr14:21734410-21734460	A549	lung:	n/a
13	chr14:21704611-21704661	HNPCEpiC	eye:	n/a
14	chr14:21731063-21731113	Hepatocyte	liver:	n/a
15	chr14:21727471-21727521	NB4	blood:	n/a
16	chr14:21727471-21727521	HCF	heart:	n/a
17	chr14:21734410-21734460	HepG2	liver:	n/a
18	chr14:21725703-21725753	Hela-S3	cervix:	n/a
19	chr14:21725703-21725753	HRE	kidney:	n/a
20	chr14:21731063-21731113	HRE	kidney:	n/a
21	chr14:21725703-21725753	ECC-1	luminal epithelium:	n/a
22	chr14:21734410-21734460	SKMC	muscle:	n/a
23	chr14:21731063-21731113	ProgFib	skin:	n/a
24	chr14:21731063-21731113	HCM	heart:	n/a
25	chr14:21725703-21725753	SK-N-SH	brain:	n/a
26	chr14:21725703-21725753	ProgFib	skin:	n/a
27	chr14:21727471-21727521	HAEpiC	amniotic membrane:	n/a
28	chr14:21731063-21731113	HepG2	liver:	n/a
29	chr14:21734410-21734460	HCM	heart:	n/a
30	chr14:21731063-21731113	NB4	blood:	n/a
31	chr14:21734410-21734460	HL-60	blood:	n/a
32	chr14:21704611-21704661	ovcar-3	ovarian:	n/a
33	chr14:21725703-21725753	SKMC	muscle:	n/a
34	chr14:21727471-21727521	Caco-2	colon:	n/a
35	chr14:21704611-21704661	ECC-1	luminal epithelium:	n/a
36	chr14:21727471-21727521	GM12891	blood:	n/a
37	chr14:21725703-21725753	HCF	heart:	n/a
38	chr14:21704611-21704661	NT2-D1	testis:	n/a
39	chr14:21725703-21725753	LNCaP	prostate:	n/a
40	chr14:21731063-21731113	HL-60	blood:	n/a
41	chr14:21734410-21734460	HIPEpiC	eye:	n/a
42	chr14:21727471-21727521	T-47D	breast:	n/a
43	chr14:21704611-21704661	H1-hESC	embryonic stem cell:	embryo
44	chr14:21725703-21725753	HAEpiC	amniotic membrane:	n/a
45	chr14:21731063-21731113	HCT-116	colon:	n/a
46	chr14:21734410-21734460	BJ	skin:	n/a
47	chr14:21734410-21734460	BE2_C	brain:	n/a
48	chr14:21725703-21725753	BE2_C	brain:	n/a
49	chr14:21731063-21731113	SAEC	small airway:	n/a
50	chr14:21725703-21725753	GM12878	blood:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:21709944..21712875-chr14:21904000..21906310,2	MCF-7	breast:
2	chr14:21719014..21721564-chr14:21851971..21854155,2	K562	blood:
3	chr14:21682920..21686919-chr14:21693629..21695651,3	MCF-7	breast:
4	chr14:21720789..21724175-chr14:21848561..21851525,3	K562	blood:
5	chr14:21732878..21735093-chr14:21822568..21824225,2	K562	blood:
6	chr14:21689585..21692266-chr14:21692375..21695207,2	MCF-7	breast:
7	chr14:21707431..21709141-chr14:21735831..21737898,2	K562	blood:
8	chr14:21704009..21707025-chr14:21707040..21709471,4	MCF-7	breast:
9	chr14:21698033..21699942-chr14:21736432..21738329,2	MCF-7	breast:
10	chr14:21709277..21713584-chr14:21714708..21717034,3	K562	blood:
11	chr14:21704009..21707025-chr14:21707040..21709471,4	MCF-7	breast:
12	chr14:21720243..21722004-chr14:21769243..21771035,2	K562	blood:
13	chr14:21700872..21703141-chr14:21723886..21726612,2	K562	blood:
14	chr14:21725317..21729371-chr14:21774547..21778706,6	K562	blood:
15	chr14:21729320..21731037-chr14:21850307..21852347,2	K562	blood:
16	chr14:21687620..21689527-chr14:21733855..21735500,2	MCF-7	breast:
17	chr14:21670001..21672457-chr14:21706378..21709017,2	K562	blood:
18	chr14:21727359..21730774-chr14:21816654..21820383,4	K562	blood:
19	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
20	chr14:21702039..21704805-chr14:21710008..21711834,2	MCF-7	breast:
21	chr14:21730203..21732388-chr14:21795365..21797950,2	K562	blood:
22	chr14:21711515..21716714-chr14:21717085..21720110,6	K562	blood:
23	chr14:21694684..21697867-chr14:21700846..21706348,4	MCF-7	breast:
24	chr14:21678845..21680444-chr14:21704444..21707261,2	K562	blood:
25	chr14:21692662..21694223-chr14:21694596..21696164,2	MCF-7	breast:
26	chr14:21731325..21733922-chr14:21791322..21794128,2	MCF-7	breast:
27	chr14:21709578..21711363-chr14:21732079..21734857,2	MCF-7	breast:
28	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
29	chr14:21709759..21712361-chr14:21720311..21725270,5	K562	blood:
30	chr14:21708482..21710752-chr14:21732706..21735405,2	MCF-7	breast:
31	chr14:21696071..21699064-chr14:21715465..21718444,2	MCF-7	breast:
32	chr14:21733893..21736248-chr14:21775936..21778469,3	K562	blood:
33	chr14:21715199..21716841-chr14:21736566..21738722,2	MCF-7	breast:
34	chr14:21692662..21694223-chr14:21694596..21696164,2	MCF-7	breast:
35	chr14:21709126..21711410-chr14:21715324..21718061,2	MCF-7	breast:
36	chr14:21725773..21728367-chr14:21769503..21772392,2	MCF-7	breast:
37	chr14:21730988..21732970-chr14:21824045..21825778,2	K562	blood:
38	chr14:21691458..21693876-chr14:21698799..21700473,3	K562	blood:
39	chr14:21725191..21730004-chr14:21826474..21830888,4	K562	blood:
40	chr14:21713934..21716894-chr14:21726084..21727992,2	MCF-7	breast:
41	chr14:21731613..21734582-chr14:21826282..21828114,3	MCF-7	breast:
42	chr14:21735788..21737662-chr17:57969823..57971989,2	MCF-7	breast:
43	chr14:21726630..21729193-chr14:21742611..21744564,2	MCF-7	breast:
44	chr14:21700378..21702346-chr14:21819126..21821504,2	MCF-7	breast:
45	chr14:21707926..21709527-chr14:21851833..21853917,2	MCF-7	breast:
46	chr14:21709126..21711410-chr14:21715324..21718061,2	MCF-7	breast:
47	chr14:21729912..21732388-chr14:21794121..21797950,3	K562	blood:
48	chr14:21701295..21703897-chr14:21842847..21844816,2	K562	blood:
49	chr14:21732396..21736856-chr14:21795995..21798414,4	K562	blood:
50	chr14:21715916..21717624-chr14:21774839..21777114,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUPT16H-3	chr14:21731470-21731988	NONHSAT035669
2	lnc-SUPT16H-3	chr14:21730762-21730857	NONHSAT035669
3	lnc-SUPT16H-3	chr14:21731152-21731988	NONHSAT035670

No data

Variant related genes	Relation type
HNRNPC	TF binding region
HNRNPC	CpG island
ENSG00000108423	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000092200	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000108443	chromatin interactions

Extended variants
information (count: 1900 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1900 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565332258	chr14:21692739-21692740	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530905148	chr14:21692772-21692773	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551194781	chr14:21692879-21692880	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540232400	chr14:21692888-21692889	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567742774	chr14:21692900-21692901	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185837498	chr14:21692923-21692924	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs28441482	chr14:21692999-21693000	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565691845	chr14:21693044-21693045	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544487081	chr14:21693050-21693051	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562758425	chr14:21693051-21693052	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534554474	chr14:21693172-21693173	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557787442	chr14:21693179-21693180	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140193630	chr14:21693214-21693215	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536734445	chr14:21693246-21693247	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141924555	chr14:21693284-21693285	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573728260	chr14:21693308-21693309	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542528740	chr14:21693327-21693328	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs8022073	chr14:21693354-21693355	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146310491	chr14:21693368-21693369	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs3790069	chr14:21693385-21693386	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs78858852	chr14:21693438-21693439	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61979501	chr14:21693440-21693441	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545046895	chr14:21693446-21693447	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565124901	chr14:21693447-21693448	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374746613	chr14:21693469-21693470	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs367783920	chr14:21693475-21693476	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs370591344	chr14:21693478-21693479	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560642895	chr14:21693488-21693489	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531068279	chr14:21693492-21693493	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs118150555	chr14:21693494-21693495	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561551222	chr14:21693522-21693523	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530280456	chr14:21693523-21693524	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547323597	chr14:21693535-21693536	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567220634	chr14:21693551-21693552	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532847926	chr14:21693596-21693597	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11384025	chr14:21693599-21693600	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10672627	chr14:21693600-21693601	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs80148377	chr14:21693609-21693610	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34863617	chr14:21693610-21693611	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551392866	chr14:21693627-21693628	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370241494	chr14:21693635-21693636	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs8023220	chr14:21693662-21693663	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527734363	chr14:21693685-21693686	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573162323	chr14:21693688-21693689	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571136465	chr14:21693708-21693709	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537172814	chr14:21693710-21693711	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191037623	chr14:21693715-21693716	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567132924	chr14:21693717-21693718	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs183672218	chr14:21693732-21693733	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150019632	chr14:21693772-21693773	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Ewing''s sarcoma	18628472	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21670400-21697600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:21670800-21702400	Strong transcription	Fetal Muscle Trunk	muscle
3	chr14:21671200-21732000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:21672200-21696600	Strong transcription	Primary B cells from cord blood	blood
5	chr14:21672400-21696000	Strong transcription	Adipose Nuclei	Adipose
6	chr14:21672400-21709000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:21672600-21703000	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr14:21672800-21699400	Strong transcription	Duodenum Mucosa	Duodenum
9	chr14:21672800-21699400	Strong transcription	Rectal Mucosa Donor 29	rectum
10	chr14:21672800-21709000	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr14:21672800-21725200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr14:21673000-21702600	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr14:21673000-21702800	Strong transcription	Fetal Intestine Large	intestine
14	chr14:21673200-21709200	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr14:21673600-21706000	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr14:21674000-21696200	Weak transcription	Fetal Brain Male	brain
17	chr14:21674200-21695400	Strong transcription	Fetal Kidney	kidney
18	chr14:21674200-21698600	Strong transcription	Dnd41	blood
19	chr14:21674600-21698000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:21677000-21700400	Strong transcription	Liver	Liver
21	chr14:21677800-21727000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr14:21681000-21714000	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr14:21681200-21697000	Weak transcription	Right Ventricle	heart
24	chr14:21681600-21698000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
25	chr14:21682200-21693800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:21682400-21694000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
27	chr14:21682400-21703400	Strong transcription	Fetal Muscle Leg	muscle
28	chr14:21684000-21702600	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr14:21684400-21705200	Strong transcription	Primary B cells from peripheral blood	blood
30	chr14:21684800-21693600	Weak transcription	Colonic Mucosa	Colon
31	chr14:21684800-21699000	Strong transcription	Fetal Thymus	thymus
32	chr14:21685400-21696600	Strong transcription	Primary hematopoietic stem cells	blood
33	chr14:21685600-21693200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:21685600-21694000	Genic enhancers	A549	lung
35	chr14:21685600-21702400	Strong transcription	Thymus	Thymus
36	chr14:21685800-21698000	Strong transcription	Fetal Lung	lung
37	chr14:21685800-21703400	Strong transcription	GM12878-XiMat	blood
38	chr14:21686200-21702600	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr14:21686400-21704400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr14:21686800-21699400	Weak transcription	Right Atrium	heart
41	chr14:21686800-21700000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
42	chr14:21687000-21694200	Weak transcription	Gastric	stomach
43	chr14:21687400-21699400	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:21687600-21696400	Strong transcription	K562	blood
45	chr14:21687600-21698400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr14:21687600-21706400	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr14:21687600-21723200	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr14:21687800-21693200	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr14:21687800-21693200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr14:21688200-21693400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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