Variant report

Variant	nsv1048462
Chromosome Location	chr14:97421360-97804598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2449)
CpG islands
(count:2691)
Chromatin interactive
region (count:85)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2449 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:97651703-97651733	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:97733069-97733416	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:97643549-97643645	K562	blood:	n/a	n/a
4	ATF1	chr14:97543698-97544043	K562	blood:	n/a	n/a
5	ATF1	chr14:97488156-97488552	K562	blood:	n/a	n/a
6	ATF1	chr14:97487417-97487693	K562	blood:	n/a	n/a
7	ATF1	chr14:97540916-97541439	K562	blood:	n/a	n/a
8	ATF2	chr14:97572438-97572907	GM12878	blood:	n/a	n/a
9	ATF2	chr14:97772459-97773711	GM12878	blood:	n/a	n/a
10	ATF2	chr14:97506016-97506519	GM12878	blood:	n/a	n/a
11	ATF2	chr14:97772403-97773440	GM12878	blood:	n/a	n/a
12	ATF2	chr14:97543619-97544056	GM12878	blood:	n/a	n/a
13	ATF2	chr14:97506138-97506479	GM12878	blood:	n/a	n/a
14	ATF2	chr14:97586908-97587209	GM12878	blood:	n/a	n/a
15	ATF2	chr14:97781997-97782498	GM12878	blood:	n/a	n/a
16	ATF3	chr14:97488136-97488408	GM12878	blood:	n/a	n/a
17	ATF3	chr14:97488155-97488490	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr14:97488189-97488393	K562	blood:	n/a	n/a
19	ATF3	chr14:97646673-97646904	K562	blood:	n/a	n/a
20	ATF3	chr14:97732914-97733516	HCT-116	colon:	n/a	n/a
21	ATF3	chr14:97488193-97488420	GM12878	blood:	n/a	n/a
22	BACH1	chr14:97629084-97629190	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr14:97499841-97500082	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr14:97743843-97745369	H1-hESC	embryonic stem cell:	n/a	chr14:97744283-97744297
25	BACH1	chr14:97685638-97685991	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr14:97683519-97684107	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr14:97634867-97634986	K562	blood:	n/a	n/a
28	BACH1	chr14:97543668-97544023	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr14:97477209-97477387	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:97609169-97609307	K562	blood:	n/a	n/a
31	BACH1	chr14:97744125-97744325	K562	blood:	n/a	chr14:97744283-97744297
32	BACH1	chr14:97543681-97544052	K562	blood:	n/a	n/a
33	BATF	chr14:97604107-97604401	GM12878	blood:	n/a	n/a
34	BATF	chr14:97772798-97773068	GM12878	blood:	n/a	n/a
35	BATF	chr14:97586900-97587132	GM12878	blood:	n/a	chr14:97586998-97587009
36	BATF	chr14:97773112-97773428	GM12878	blood:	n/a	chr14:97773205-97773215
37	BATF	chr14:97543703-97543944	GM12878	blood:	n/a	chr14:97543871-97543881
38	BATF	chr14:97772460-97772771	GM12878	blood:	n/a	chr14:97772627-97772638 chr14:97772628-97772638
39	BATF	chr14:97604134-97604435	GM12878	blood:	n/a	n/a
40	BATF	chr14:97772496-97772707	GM12878	blood:	n/a	chr14:97772627-97772638 chr14:97772628-97772638
41	BATF	chr14:97643968-97644228	GM12878	blood:	n/a	n/a
42	BATF	chr14:97773100-97773527	GM12878	blood:	n/a	chr14:97773205-97773215
43	BCL11A	chr14:97543753-97543975	GM12878	blood:	n/a	n/a
44	BCL3	chr14:97774613-97774972	GM12878	blood:	n/a	n/a
45	BCL3	chr14:97619544-97619824	GM12878	blood:	n/a	n/a
46	BCL3	chr14:97643910-97644241	GM12878	blood:	n/a	n/a
47	BCL3	chr14:97772470-97773676	GM12878	blood:	n/a	chr14:97773207-97773216 chr14:97773208-97773217
48	BCL3	chr14:97632935-97633166	GM12878	blood:	n/a	chr14:97633102-97633111
49	BCL3	chr14:97518351-97518629	GM12878	blood:	n/a	n/a
50	BCL3	chr14:97506126-97506394	GM12878	blood:	n/a	chr14:97506271-97506280

(count:2691 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:97673803-97673853	HUVEC	blood vessel:	n/a
2	chr14:97500175-97500225	HUVEC	blood vessel:	n/a
3	chr14:97673803-97673853	LNCaP	prostate:	n/a
4	chr14:97688014-97688064	SKMC	muscle:	n/a
5	chr14:97499987-97500037	T-47D	breast:	n/a
6	chr14:97684772-97684822	Hela-S3	cervix:	n/a
7	chr14:97673471-97673521	HEK293	kidney:	embryo
8	chr14:97673803-97673853	HUVEC	blood vessel:	n/a
9	chr14:97500175-97500225	HUVEC	blood vessel:	n/a
10	chr14:97673803-97673853	LNCaP	prostate:	n/a
11	chr14:97688014-97688064	SKMC	muscle:	n/a
12	chr14:97499987-97500037	T-47D	breast:	n/a
13	chr14:97684772-97684822	Hela-S3	cervix:	n/a
14	chr14:97673471-97673521	HEK293	kidney:	embryo
15	chr14:97432390-97432440	AG04450	lung:	fetal
16	chr14:97673803-97673853	K562	blood:	n/a
17	chr14:97674219-97674269	GM19239	blood:	n/a
18	chr14:97431137-97431187	HCT-116	colon:	n/a
19	chr14:97685274-97685324	NH-A	brain:	n/a
20	chr14:97647221-97647271	HCPEpiC	choroid plexus:	n/a
21	chr14:97502302-97502352	HCF	heart:	n/a
22	chr14:97432390-97432440	Hepatocyte	liver:	n/a
23	chr14:97674065-97674115	SAEC	small airway:	n/a
24	chr14:97432390-97432440	HL-60	blood:	n/a
25	chr14:97765260-97765310	GM12878	blood:	n/a
26	chr14:97685551-97685601	PFSK-1	brain:	n/a
27	chr14:97673471-97673521	LNCaP	prostate:	n/a
28	chr14:97491613-97491663	IMR90	lung:	fetal
29	chr14:97685386-97685436	HEEpiC	esophagus:	n/a
30	chr14:97499987-97500037	Caco-2	colon:	n/a
31	chr14:97432390-97432440	NT2-D1	testis:	n/a
32	chr14:97744285-97744335	SAEC	small airway:	n/a
33	chr14:97499484-97499534	GM12892	blood:	n/a
34	chr14:97493395-97493445	AG04450	lung:	fetal
35	chr14:97492191-97492241	IMR90	lung:	fetal
36	chr14:97744285-97744335	U87	brain:	n/a
37	chr14:97446061-97446111	MCF10A-Er-Src	breast:	n/a
38	chr14:97499987-97500037	HAEpiC	amniotic membrane:	n/a
39	chr14:97499987-97500037	NHDF-neo	bronchial:	n/a
40	chr14:97685158-97685208	HRCEpiC	kidney:	n/a
41	chr14:97674065-97674115	HEEpiC	esophagus:	n/a
42	chr14:97673726-97673776	HCT-116	colon:	n/a
43	chr14:97538227-97538277	AoSMC	blood vessel:	n/a
44	chr14:97500345-97500395	U87	brain:	n/a
45	chr14:97673726-97673776	LNCaP	prostate:	n/a
46	chr14:97685657-97685707	PrEC	prostate:	n/a
47	chr14:97685657-97685707	MCF-7	breast:	n/a
48	chr14:97431088-97431138	IMR90	lung:	fetal
49	chr14:97685657-97685707	HIPEpiC	eye:	n/a
50	chr14:97685576-97685626	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:97050494..97051205-chr14:97646447..97647466,5	MCF-7	breast:
2	chr14:97434498..97437074-chr14:97441838..97443445,2	K562	blood:
3	chr14:97596048..97598203-chr14:97603765..97605393,2	K562	blood:
4	chr14:97423279..97425568-chr14:97429181..97431047,2	K562	blood:
5	chr14:97651095..97652058-chr14:97739587..97740524,3	MCF-7	breast:
6	chr14:97751007..97753663-chr14:97754837..97757487,2	K562	blood:
7	chr14:97596048..97598203-chr14:97603765..97605393,2	K562	blood:
8	chr14:97456234..97458409-chr14:97461531..97463727,2	K562	blood:
9	chr14:97651280..97652184-chr14:97764384..97765754,4	MCF-7	breast:
10	chr14:97456234..97458409-chr14:97461531..97463727,2	K562	blood:
11	chr14:97745906..97747938-chr14:97751482..97753019,2	K562	blood:
12	chr14:97477675..97482203-chr14:97483753..97489139,4	K562	blood:
13	chr14:97787267..97788972-chr14:97792409..97794274,2	K562	blood:
14	chr14:97050610..97051137-chr14:97605232..97605759,2	MCF-7	breast:
15	chr14:97050353..97051095-chr14:97764453..97765380,2	MCF-7	breast:
16	chr14:97697038..97699980-chr14:97703722..97706302,2	MCF-7	breast:
17	chr14:97553286..97555382-chr14:97558626..97561527,2	K562	blood:
18	chr14:97450622..97452449-chr14:97455717..97457862,2	K562	blood:
19	chr14:97764275..97766451-chr14:97769406..97772010,2	K562	blood:
20	chr14:97671104..97673006-chr14:97674619..97676270,2	K562	blood:
21	chr14:97606953..97609487-chr14:97610383..97611884,2	K562	blood:
22	chr14:97639064..97641431-chr14:97643207..97645082,2	K562	blood:
23	chr14:97450622..97452449-chr14:97455717..97457862,2	K562	blood:
24	chr14:97549993..97552425-chr14:97577946..97579457,2	K562	blood:
25	chr14:97651485..97652238-chr14:98050652..98051540,4	MCF-7	breast:
26	chr14:97450949..97452696-chr14:97456362..97458662,2	K562	blood:
27	chr14:97460388..97463151-chr14:97509528..97512144,2	K562	blood:
28	chr14:97745906..97747938-chr14:97751482..97753019,2	K562	blood:
29	chr14:97671104..97673006-chr14:97674619..97676270,2	K562	blood:
30	chr14:97651671..97652701-chr14:99740847..99741626,3	MCF-7	breast:
31	chr14:97440996..97441496-chr19:13263555..13264058,2	Hela-S3	cervix:
32	chr14:97544852..97547266-chr14:97555136..97557458,2	MCF-7	breast:
33	chr14:97697038..97699980-chr14:97703722..97706302,2	MCF-7	breast:
34	chr14:97643292..97643925-chr14:97717949..97718598,2	MCF-7	breast:
35	chr14:97773582..97775840-chr14:97784279..97786173,2	K562	blood:
36	chr14:97639064..97641431-chr14:97643207..97645082,2	K562	blood:
37	chr14:97024529..97026540-chr14:97633465..97635443,2	K562	blood:
38	chr14:97612641..97614798-chr14:97625949..97628536,2	K562	blood:
39	chr14:97460420..97462846-chr14:97464837..97466683,2	K562	blood:
40	chr14:97269964..97272713-chr14:97520420..97522820,2	K562	blood:
41	chr14:97539439..97541387-chr14:97544260..97546200,2	K562	blood:
42	chr14:97023617..97026546-chr14:97637896..97640052,3	K562	blood:
43	chr14:97585815..97588251-chr14:97591300..97593311,2	K562	blood:
44	chr14:97665245..97667832-chr14:97669943..97672541,2	MCF-7	breast:
45	chr14:97450949..97452696-chr14:97456362..97458662,2	K562	blood:
46	chr14:97717920..97718671-chr14:98050570..98051161,2	MCF-7	breast:
47	chr14:97670920..97672473-chr14:97709312..97711136,2	K562	blood:
48	chr14:97539439..97541387-chr14:97544260..97546200,2	K562	blood:
49	chr14:97767536..97770149-chr14:97771082..97773749,2	MCF-7	breast:
50	chr14:97507620..97510431-chr14:97512096..97514121,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK1-4	chr14:97621194-97621506	ENSG00000259110.1
2	lnc-VRK1-3	chr14:97582692-97582928	ENSG00000258393.1
3	lnc-ATG2B-3	chr14:97473837-97474117	NONHSAT039560
4	lnc-RP11-204N11.1.1-4	chr14:97584079-97584223	ENSG00000259026
5	lnc-ATG2B-3	chr14:97471607-97471891	NONHSAT039555
6	lnc-ATG2B-10	chr14:97494020-97495910	ucscGeneNc_uc001yfy_1
7	lnc-VRK1-8	chr14:97698536-97698658	l_1054_chr14:97672173-97698658_whiteBloodCell
8	lnc-VRK1-8	chr14:97672174-97672287	l_1054_chr14:97672173-97698658_whiteBloodCell
9	lnc-ATG2B-10	chr14:97496353-97496507	ucscGeneNc_uc001yfy_1
10	lnc-VRK1-3	chr14:97584711-97584878	ENSG00000258393.1
11	lnc-RP11-204N11.1.1-4	chr14:97579919-97580010	ENSG00000259026
12	lnc-VRK1-3	chr14:97587582-97587838	ENSG00000258393.1
13	lnc-ATG2B-3	chr14:97472218-97472504	NONHSAT039560
14	lnc-RP11-204N11.1.1-4	chr14:97578348-97578413	ENSG00000259026
15	lnc-RP11-204N11.1.1-4	chr14:97585408-97585584	ENSG00000259026
16	lnc-ATG2B-3	chr14:97471963-97472504	NONHSAT039559
17	lnc-VRK1-6	chr14:97431367-97431619	NONHSAT140175
18	lnc-VRK1-3	chr14:97585952-97586129	ENSG00000258393.1
19	lnc-ATG2B-3	chr14:97473838-97474120	NONHSAT039559
20	lnc-ATG2B-10	chr14:97505363-97505637	ucscGeneNc_uc001yfy_1
21	lnc-ATG2B-3	chr14:97551110-97551878	NONHSAT039555
22	lnc-ATG2B-3	chr14:97471905-97471999	NONHSAT039555
23	lnc-VRK1-4	chr14:97624942-97625073	ENSG00000259110.1
24	lnc-ATG2B-3	chr14:97472219-97472504	XLOC_011115
25	lnc-RP11-204N11.1.1-4	chr14:97576753-97577199	ENSG00000259026
26	lnc-VRK1-7	chr14:97459201-97462938	NONHSAT039558
27	lnc-ATG2B-3	chr14:97473838-97474117	XLOC_011115
28	lnc-ATG2B-3	chr14:97515530-97515875	NONHSAT039555
29	lnc-ATG2B-10	chr14:97514067-97514200	ucscGeneNc_uc001yfy_1
30	lnc-RP11-204N11.1.1-4	chr14:97584122-97584570	ENSG00000259026

No data

Variant related genes	Relation type
ENSG00000259026	TF binding region
ENSG00000259110	TF binding region
ENSG00000258393	TF binding region
ENSG00000259026	CpG island
ENSG00000259110	CpG island
ENSG00000258393	CpG island
ENSG00000259026	chromatin interactions
ADAM17	miRNA target sites
YES1	miRNA target sites

Extended variants
information (count: 11086 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:11086 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535243253	chr14:97421374-97421375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547295089	chr14:97421421-97421422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs710263	chr14:97421498-97421499	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs533973312	chr14:97421500-97421501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190243606	chr14:97421503-97421504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75230356	chr14:97421517-97421518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144459665	chr14:97421587-97421588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145611667	chr14:97421605-97421606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575108666	chr14:97421634-97421635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148911332	chr14:97421637-97421638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs56363380	chr14:97421638-97421639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542323850	chr14:97421671-97421672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572770724	chr14:97421676-97421677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs5810787	chr14:97421725-97421726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs33936435	chr14:97421726-97421727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57463578	chr14:97421727-97421728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573874934	chr14:97421754-97421755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572465263	chr14:97421755-97421756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182818340	chr14:97421785-97421786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531301201	chr14:97421827-97421828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543173989	chr14:97421845-97421846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150937052	chr14:97421883-97421884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34783098	chr14:97421948-97421949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529064836	chr14:97421960-97421961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547181636	chr14:97422047-97422048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540395889	chr14:97422118-97422119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140866629	chr14:97422157-97422158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532234955	chr14:97422165-97422166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552578100	chr14:97422236-97422237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79491969	chr14:97422249-97422250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562141772	chr14:97422319-97422320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs710264	chr14:97422377-97422378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs710265	chr14:97422389-97422390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568556240	chr14:97422431-97422432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144682551	chr14:97422447-97422448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187206015	chr14:97422476-97422477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34324821	chr14:97422526-97422527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371798557	chr14:97422579-97422580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138376170	chr14:97422583-97422584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs856267	chr14:97422603-97422604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558401230	chr14:97422610-97422611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3953101	chr14:97422619-97422620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575950017	chr14:97422637-97422638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142954120	chr14:97422663-97422664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4017426	chr14:97422702-97422703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2370031	chr14:97422730-97422731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74076808	chr14:97422731-97422732	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs9671876	chr14:97422767-97422768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189667890	chr14:97422814-97422815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117046791	chr14:97422818-97422819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1695 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97408600-97428600	Weak transcription	Thymus	Thymus
2	chr14:97416400-97425600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr14:97416600-97425000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr14:97417800-97426400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr14:97420200-97430800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:97420600-97426600	Weak transcription	Dnd41	blood
7	chr14:97422400-97422600	Enhancers	Fetal Muscle Trunk	muscle
8	chr14:97423600-97424000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr14:97424400-97424600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:97424600-97426200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:97425000-97426600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr14:97425400-97427000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr14:97425600-97428600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr14:97426000-97428200	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr14:97426200-97426400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:97426200-97427400	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr14:97426200-97431400	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr14:97426400-97427000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:97426400-97428600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr14:97426400-97430200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr14:97426400-97431200	Enhancers	Primary B cells from peripheral blood	blood
22	chr14:97426600-97427200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr14:97426600-97427400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr14:97426600-97427400	Strong transcription	Dnd41	blood
25	chr14:97426600-97428800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr14:97426800-97427000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:97427000-97427200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:97427000-97427200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr14:97427000-97427200	Enhancers	Fetal Muscle Trunk	muscle
30	chr14:97427000-97427600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr14:97427000-97428200	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
32	chr14:97427000-97428400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr14:97427000-97428600	Enhancers	Primary B cells from cord blood	blood
34	chr14:97427000-97428600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr14:97427200-97427600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:97427200-97427800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr14:97427200-97432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr14:97427400-97427800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr14:97427400-97427800	ZNF genes & repeats	Dnd41	blood
40	chr14:97427400-97428200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr14:97427600-97428200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr14:97427600-97431800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:97427800-97428200	Weak transcription	Dnd41	blood
44	chr14:97427800-97428400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr14:97427800-97428400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr14:97428200-97428400	Enhancers	Primary T cells from cord blood	blood
47	chr14:97428200-97428400	Enhancers	Dnd41	blood
48	chr14:97428200-97428600	Enhancers	Primary T cells fromperipheralblood	blood
49	chr14:97428200-97429400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr14:97428200-97429400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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