Variant report

Variant	nsv541989
Chromosome Location	chr14:21696056-21742729
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3049)
CpG islands
(count:855)
Chromatin interactive
region (count:100)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3049 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21712624-21712985	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21717162-21717278	K562	blood:	n/a	n/a
3	ARID3A	chr14:21711256-21711587	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21732200-21733006	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:21737436-21738247	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:21697647-21697673	K562	blood:	n/a	n/a
7	ARID3A	chr14:21736068-21736120	K562	blood:	n/a	n/a
8	ARID3A	chr14:21709409-21709593	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:21711963-21711985	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:21737195-21738158	K562	blood:	n/a	n/a
11	ATF1	chr14:21737526-21738185	K562	blood:	n/a	n/a
12	ATF2	chr14:21731973-21733035	GM12878	blood:	n/a	n/a
13	ATF2	chr14:21735629-21736731	GM12878	blood:	n/a	n/a
14	ATF2	chr14:21735362-21735856	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr14:21732138-21732971	GM12878	blood:	n/a	n/a
16	ATF2	chr14:21737251-21738411	GM12878	blood:	n/a	n/a
17	ATF2	chr14:21729052-21729484	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr14:21731544-21732278	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr14:21729447-21729836	GM12878	blood:	n/a	n/a
20	ATF2	chr14:21727624-21728013	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr14:21730290-21730933	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr14:21726892-21727596	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:21736929-21737878	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr14:21736898-21737748	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr14:21735848-21738400	GM12878	blood:	n/a	n/a
26	BACH1	chr14:21735698-21736021	K562	blood:	n/a	n/a
27	BATF	chr14:21731822-21732559	GM12878	blood:	n/a	chr14:21732455-21732465 chr14:21732451-21732461
28	BATF	chr14:21733926-21734221	GM12878	blood:	n/a	chr14:21734053-21734064
29	BATF	chr14:21732236-21732561	GM12878	blood:	n/a	chr14:21732455-21732465 chr14:21732451-21732461
30	BCL11A	chr14:21732207-21732610	GM12878	blood:	n/a	chr14:21732453-21732462 chr14:21732454-21732463
31	BCL3	chr14:21737194-21738062	A549	lung:	n/a	chr14:21737990-21738003
32	BCL3	chr14:21736964-21737430	A549	lung:	n/a	chr14:21737188-21737197
33	BCL3	chr14:21727073-21727426	K562	blood:	n/a	n/a
34	BCLAF1	chr14:21709359-21711746	GM12878	blood:	n/a	n/a
35	BCLAF1	chr14:21713989-21714387	GM12878	blood:	n/a	n/a
36	BCLAF1	chr14:21731491-21731826	GM12878	blood:	n/a	n/a
37	BCLAF1	chr14:21726752-21727540	GM12878	blood:	n/a	n/a
38	BCLAF1	chr14:21706763-21707518	GM12878	blood:	n/a	n/a
39	BCLAF1	chr14:21737799-21738615	GM12878	blood:	n/a	chr14:21738216-21738225 chr14:21737990-21738003
40	BCLAF1	chr14:21720323-21720739	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:21712549-21713102	GM12878	blood:	n/a	n/a
42	BCLAF1	chr14:21733808-21734347	GM12878	blood:	n/a	n/a
43	BCLAF1	chr14:21731848-21732313	K562	blood:	n/a	n/a
44	BCLAF1	chr14:21705331-21705994	GM12878	blood:	n/a	n/a
45	BCLAF1	chr14:21732126-21733056	GM12878	blood:	n/a	chr14:21732453-21732462 chr14:21732454-21732463
46	BCLAF1	chr14:21710768-21711305	GM12878	blood:	n/a	n/a
47	BCLAF1	chr14:21726818-21727567	K562	blood:	n/a	n/a
48	BCLAF1	chr14:21712564-21713058	GM12878	blood:	n/a	n/a
49	BCLAF1	chr14:21729129-21729488	GM12878	blood:	n/a	n/a
50	BCLAF1	chr14:21726995-21727466	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21725703-21725753	HMEC	breast:	n/a
2	chr14:21725703-21725753	HMEC	breast:	n/a
3	chr14:21737878-21737928	HIPEpiC	eye:	n/a
4	chr14:21737765-21737815	HEK293	kidney:	embryo
5	chr14:21727471-21727521	ECC-1	luminal epithelium:	n/a
6	chr14:21731063-21731113	ProgFib	skin:	n/a
7	chr14:21731063-21731113	ECC-1	luminal epithelium:	n/a
8	chr14:21731063-21731113	SK-N-SH	brain:	n/a
9	chr14:21737878-21737928	NHDF-neo	bronchial:	n/a
10	chr14:21704611-21704661	NHDF-neo	bronchial:	n/a
11	chr14:21738093-21738143	AoSMC	blood vessel:	n/a
12	chr14:21737935-21737985	HRCEpiC	kidney:	n/a
13	chr14:21731063-21731113	IMR90	lung:	fetal
14	chr14:21737252-21737302	HepG2	liver:	n/a
15	chr14:21725703-21725753	ovcar-3	ovarian:	n/a
16	chr14:21725703-21725753	PrEC	prostate:	n/a
17	chr14:21704611-21704661	GM12878	blood:	n/a
18	chr14:21704611-21704661	Hepatocyte	liver:	n/a
19	chr14:21734410-21734460	SK-N-SH_RA	brain:	n/a
20	chr14:21738093-21738143	NHDF-neo	bronchial:	n/a
21	chr14:21727471-21727521	HepG2	liver:	n/a
22	chr14:21738303-21738353	BJ	skin:	n/a
23	chr14:21737765-21737815	BE2_C	brain:	n/a
24	chr14:21704611-21704661	Jurkat	blood:	n/a
25	chr14:21738473-21738523	T-47D	breast:	n/a
26	chr14:21704611-21704661	IMR90	lung:	fetal
27	chr14:21734410-21734460	SAEC	small airway:	n/a
28	chr14:21734410-21734460	PFSK-1	brain:	n/a
29	chr14:21737878-21737928	AG09309	skin:	n/a
30	chr14:21737878-21737928	CMK	blood:	n/a
31	chr14:21725703-21725753	Hela-S3	cervix:	n/a
32	chr14:21738093-21738143	BE2_C	brain:	n/a
33	chr14:21737765-21737815	HCT-116	colon:	n/a
34	chr14:21738473-21738523	Caco-2	colon:	n/a
35	chr14:21737935-21737985	Jurkat	blood:	n/a
36	chr14:21737252-21737302	HL-60	blood:	n/a
37	chr14:21704611-21704661	H1-hESC	embryonic stem cell:	embryo
38	chr14:21734410-21734460	A549	lung:	n/a
39	chr14:21737765-21737815	HRPEpiC	eye:	n/a
40	chr14:21737751-21737801	HCF	heart:	n/a
41	chr14:21727471-21727521	T-47D	breast:	n/a
42	chr14:21737765-21737815	HCF	heart:	n/a
43	chr14:21727471-21727521	GM06990	blood:	n/a
44	chr14:21738303-21738353	GM12892	blood:	n/a
45	chr14:21738093-21738143	HCM	heart:	n/a
46	chr14:21737765-21737815	A549	lung:	n/a
47	chr14:21734410-21734460	MCF10A-Er-Src	breast:	n/a
48	chr14:21738473-21738523	NT2-D1	testis:	n/a
49	chr14:21704611-21704661	RPTEC	kidney:	n/a
50	chr14:21725703-21725753	HepG2	liver:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:21704014..21706045-chr14:21718733..21720971,2	K562	blood:
2	chr14:21732878..21735093-chr14:21822568..21824225,2	K562	blood:
3	chr14:21713934..21716894-chr14:21726084..21727992,2	MCF-7	breast:
4	chr14:21707926..21709527-chr14:21851833..21853917,2	MCF-7	breast:
5	chr14:21711515..21716714-chr14:21717085..21720110,6	K562	blood:
6	chr14:21702152..21704976-chr14:21712747..21715545,2	MCF-7	breast:
7	chr14:21725191..21730004-chr14:21826474..21830888,4	K562	blood:
8	chr14:21715199..21716841-chr14:21736566..21738722,2	MCF-7	breast:
9	chr14:21702152..21704976-chr14:21712747..21715545,2	MCF-7	breast:
10	chr14:21708482..21710752-chr14:21732706..21735405,2	MCF-7	breast:
11	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
12	chr14:21701295..21703897-chr14:21842847..21844816,2	K562	blood:
13	chr14:21708563..21711469-chr14:21841010..21843260,2	K562	blood:
14	chr14:21736080..21739636-chr14:21765775..21769584,7	MCF-7	breast:
15	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
16	chr14:21731613..21734582-chr14:21826282..21828114,3	MCF-7	breast:
17	chr14:21727857..21729371-chr14:21850635..21853386,2	MCF-7	breast:
18	chr14:21727224..21727734-chr6:45404153..45404890,2	NB4	blood:
19	chr14:21731325..21733922-chr14:21791322..21794128,2	MCF-7	breast:
20	chr14:21737031..21737660-chr17:29297639..29298182,2	NB4	blood:
21	chr14:21720243..21722004-chr14:21769243..21771035,2	K562	blood:
22	chr14:21702039..21704805-chr14:21710008..21711834,2	MCF-7	breast:
23	chr14:21708836..21711408-chr14:21737080..21738669,2	MCF-7	breast:
24	chr14:21670001..21672457-chr14:21706378..21709017,2	K562	blood:
25	chr14:21704014..21706045-chr14:21718733..21720971,2	K562	blood:
26	chr14:21702039..21704805-chr14:21710008..21711834,2	MCF-7	breast:
27	chr14:21729320..21731037-chr14:21850307..21852347,2	K562	blood:
28	chr14:21709944..21712875-chr14:21904000..21906310,2	MCF-7	breast:
29	chr14:21709126..21711410-chr14:21715324..21718061,2	MCF-7	breast:
30	chr14:21734081..21737638-chr14:21753111..21756446,3	K562	blood:
31	chr14:21709126..21711410-chr14:21715324..21718061,2	MCF-7	breast:
32	chr14:21736096..21738321-chr14:38062641..38065635,3	MCF-7	breast:
33	chr14:21731095..21732813-chr14:21767081..21768936,2	K562	blood:
34	chr14:21709277..21713584-chr14:21714708..21717034,3	K562	blood:
35	chr14:21687620..21689527-chr14:21733855..21735500,2	MCF-7	breast:
36	chr14:21725390..21727095-chr14:21852518..21854130,2	K562	blood:
37	chr14:21725675..21728735-chr14:21786792..21790773,3	K562	blood:
38	chr14:21726630..21729193-chr14:21742611..21744564,2	MCF-7	breast:
39	chr1:151429381..151432201-chr14:21736244..21738881,2	MCF-7	breast:
40	chr14:21698033..21699942-chr14:21736432..21738329,2	MCF-7	breast:
41	chr14:21735788..21737662-chr17:57969823..57971989,2	MCF-7	breast:
42	chr14:21737121..21738626-chr14:21850627..21853188,2	K562	blood:
43	chr14:21731892..21738562-chr14:21850801..21854193,10	MCF-7	breast:
44	chr14:21737105..21737803-chr17:79008561..79009062,2	Hela-S3	cervix:
45	chr14:21696071..21699064-chr14:21715465..21718444,2	MCF-7	breast:
46	chr14:21709759..21712361-chr14:21720311..21725270,5	K562	blood:
47	chr14:21705854..21707392-chr14:21708475..21711254,2	K562	blood:
48	chr14:21690598..21692490-chr14:21705492..21708066,2	MCF-7	breast:
49	chr14:21736749..21737624-chr20:42086408..42086970,2	Hela-S3	cervix:
50	chr14:21709277..21713584-chr14:21714708..21717034,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUPT16H-3	chr14:21730762-21730857	NONHSAT035669
2	lnc-SUPT16H-3	chr14:21731152-21731988	NONHSAT035670
3	lnc-SUPT16H-3	chr14:21731470-21731988	NONHSAT035669
4	lnc-SUPT16H-3	chr14:21737457-21737548	NONHSAT035670
5	lnc-SUPT16H-3	chr14:21737457-21737601	NONHSAT035669

No data

Variant related genes	Relation type
HNRNPC	TF binding region
HNRNPC	CpG island
ENSG00000124193	chromatin interactions
ENSG00000092200	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000175866	chromatin interactions
ENSG00000181481	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000109919	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000102096	chromatin interactions
ENSG00000162415	chromatin interactions
ENSG00000100888	chromatin interactions

Extended variants
information (count: 2003 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547845954	chr14:21696062-21696063	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570801893	chr14:21696078-21696079	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557177552	chr14:21696091-21696092	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs539571057	chr14:21696118-21696119	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372155617	chr14:21696156-21696157	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs147574744	chr14:21696175-21696176	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535603566	chr14:21696185-21696186	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555536952	chr14:21696216-21696217	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572443283	chr14:21696245-21696246	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571948752	chr14:21696279-21696280	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539080991	chr14:21696280-21696281	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140772548	chr14:21696293-21696294	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553512420	chr14:21696342-21696343	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116773770	chr14:21696356-21696357	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545592190	chr14:21696401-21696402	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114852709	chr14:21696439-21696440	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531431255	chr14:21696454-21696455	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562432720	chr14:21696504-21696505	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542087176	chr14:21696505-21696506	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376833437	chr14:21696528-21696529	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561851359	chr14:21696542-21696543	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527610263	chr14:21696543-21696544	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555325570	chr14:21696553-21696554	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116956603	chr14:21696555-21696556	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181098050	chr14:21696564-21696565	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531215522	chr14:21696614-21696615	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55645943	chr14:21696663-21696664	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550007612	chr14:21696694-21696695	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570176651	chr14:21696698-21696699	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186593563	chr14:21696702-21696703	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150104265	chr14:21696725-21696726	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191344342	chr14:21696776-21696777	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79579021	chr14:21696857-21696858	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114937503	chr14:21696880-21696881	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558392996	chr14:21696915-21696916	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576767030	chr14:21696916-21696917	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180856993	chr14:21696933-21696934	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115598005	chr14:21696938-21696939	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185413414	chr14:21696940-21696941	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547992816	chr14:21696987-21696988	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541923698	chr14:21697014-21697015	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561885635	chr14:21697021-21697022	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572237057	chr14:21697051-21697052	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540976630	chr14:21697060-21697061	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190959566	chr14:21697061-21697062	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138463158	chr14:21697096-21697097	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550187119	chr14:21697136-21697137	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563324041	chr14:21697224-21697225	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529370098	chr14:21697245-21697246	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs11848510	chr14:21697259-21697260	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

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
Breast cancer	22522925	CNVD
Ewing''s sarcoma	18628472	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

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	chr14:21672400-21709000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:21672600-21703000	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr14:21672800-21699400	Strong transcription	Duodenum Mucosa	Duodenum
8	chr14:21672800-21699400	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr14:21672800-21709000	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr14:21672800-21725200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr14:21673000-21702600	Strong transcription	Cortex derived primary cultured neurospheres	brain
12	chr14:21673000-21702800	Strong transcription	Fetal Intestine Large	intestine
13	chr14:21673200-21709200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr14:21673600-21706000	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr14:21674000-21696200	Weak transcription	Fetal Brain Male	brain
16	chr14:21674200-21698600	Strong transcription	Dnd41	blood
17	chr14:21674600-21698000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr14:21677000-21700400	Strong transcription	Liver	Liver
19	chr14:21677800-21727000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr14:21681000-21714000	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr14:21681200-21697000	Weak transcription	Right Ventricle	heart
22	chr14:21681600-21698000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
23	chr14:21682400-21703400	Strong transcription	Fetal Muscle Leg	muscle
24	chr14:21684000-21702600	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:21684400-21705200	Strong transcription	Primary B cells from peripheral blood	blood
26	chr14:21684800-21699000	Strong transcription	Fetal Thymus	thymus
27	chr14:21685400-21696600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr14:21685600-21702400	Strong transcription	Thymus	Thymus
29	chr14:21685800-21698000	Strong transcription	Fetal Lung	lung
30	chr14:21685800-21703400	Strong transcription	GM12878-XiMat	blood
31	chr14:21686200-21702600	Strong transcription	H9 Cell Line	embryonic stem cell
32	chr14:21686400-21704400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:21686800-21699400	Weak transcription	Right Atrium	heart
34	chr14:21686800-21700000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
35	chr14:21687400-21699400	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr14:21687600-21696400	Strong transcription	K562	blood
37	chr14:21687600-21698400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr14:21687600-21706400	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr14:21687600-21723200	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr14:21688200-21698600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr14:21688200-21712800	Strong transcription	HMEC	breast
42	chr14:21688200-21725200	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr14:21688400-21696200	Weak transcription	Fetal Heart	heart
44	chr14:21688400-21704200	Strong transcription	HSMM	muscle
45	chr14:21688400-21712800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr14:21688600-21696200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr14:21688600-21702400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:21688600-21707000	Strong transcription	Placenta	Placenta
49	chr14:21689000-21699800	Strong transcription	Brain Germinal Matrix	brain
50	chr14:21689000-21702600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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