Variant report

Variant	nsv1035925
Chromosome Location	chr14:35404661-35483420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1275)
CpG islands
(count:1285)
Chromatin interactive
region (count:75)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35456533-35456710	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35449799-35452898	HepG2	liver:	n/a	chr14:35452584-35452600
3	ARID3A	chr14:35450353-35450528	K562	blood:	n/a	n/a
4	ATF1	chr14:35451277-35452397	K562	blood:	n/a	chr14:35452182-35452196
5	ATF2	chr14:35451363-35452438	H1-hESC	embryonic stem cell:	n/a	chr14:35452182-35452196
6	ATF2	chr14:35451237-35452526	GM12878	blood:	n/a	chr14:35452182-35452196
7	ATF2	chr14:35451431-35452788	GM12878	blood:	n/a	chr14:35452182-35452196
8	ATF2	chr14:35451408-35452422	H1-hESC	embryonic stem cell:	n/a	chr14:35452182-35452196
9	ATF3	chr14:35451382-35452359	A549	lung:	n/a	n/a
10	ATF3	chr14:35451470-35452221	A549	lung:	n/a	n/a
11	BACH1	chr14:35451138-35451216	K562	blood:	n/a	n/a
12	BCL3	chr14:35451609-35452394	A549	lung:	n/a	chr14:35452052-35452061 chr14:35451657-35451665
13	BCL3	chr14:35451306-35452403	A549	lung:	n/a	chr14:35452052-35452061 chr14:35451657-35451665
14	BCL3	chr14:35451369-35452377	GM12878	blood:	n/a	chr14:35452052-35452061 chr14:35451657-35451665
15	BCLAF1	chr14:35450327-35450834	GM12878	blood:	n/a	n/a
16	BCLAF1	chr14:35451328-35452663	GM12878	blood:	n/a	chr14:35452052-35452061 chr14:35451657-35451665
17	BCLAF1	chr14:35451265-35452591	GM12878	blood:	n/a	chr14:35452052-35452061 chr14:35451657-35451665
18	BHLHE40	chr14:35451594-35452335	HepG2	liver:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
19	BHLHE40	chr14:35450405-35450477	K562	blood:	n/a	n/a
20	BHLHE40	chr14:35451084-35452554	HepG2	liver:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
21	BHLHE40	chr14:35451268-35452651	GM12878	blood:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
22	BHLHE40	chr14:35451309-35452916	K562	blood:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
23	BHLHE40	chr14:35450069-35450816	HepG2	liver:	n/a	n/a
24	BHLHE40	chr14:35451546-35452238	HepG2	liver:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
25	BHLHE40	chr14:35451435-35452177	A549	lung:	n/a	chr14:35451857-35451870 chr14:35451658-35451674
26	BRCA1	chr14:35450492-35450902	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr14:35451383-35452348	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:35451411-35452411	HepG2	liver:	n/a	n/a
29	BRCA1	chr14:35451531-35452399	GM12878	blood:	n/a	n/a
30	CBX3	chr14:35451395-35452317	K562	blood:	n/a	n/a
31	CBX3	chr14:35451766-35452184	K562	blood:	n/a	n/a
32	CCNT2	chr14:35451540-35452083	K562	blood:	n/a	chr14:35451839-35451848
33	CEBPB	chr14:35450038-35450400	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:35456395-35456756	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:35450265-35450786	K562	blood:	n/a	n/a
36	CEBPB	chr14:35456487-35456748	A549	lung:	n/a	n/a
37	CEBPB	chr14:35451580-35452355	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:35451543-35452401	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr14:35424166-35424264	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:35420615-35420711	K562	blood:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
41	CEBPB	chr14:35456490-35456754	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr14:35451594-35451964	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:35451247-35452497	GM12878	blood:	n/a	n/a
44	CEBPB	chr14:35443045-35443246	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:35450086-35450285	A549	lung:	n/a	n/a
46	CEBPB	chr14:35450096-35450845	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:35420493-35420854	IMR90	lung:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682
48	CEBPB	chr14:35450083-35450803	HepG2	liver:	n/a	n/a
49	CEBPB	chr14:35456404-35456746	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:35420425-35420947	MCF-7	breast:	n/a	chr14:35420669-35420680 chr14:35420666-35420683 chr14:35420669-35420682

(count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35451556-35451606	NHBE	bronchial:	n/a
2	chr14:35451984-35452034	AoSMC	blood vessel:	n/a
3	chr14:35451962-35452012	HNPCEpiC	eye:	n/a
4	chr14:35408689-35408739	HNPCEpiC	eye:	n/a
5	chr14:35451556-35451606	NHBE	bronchial:	n/a
6	chr14:35451984-35452034	AoSMC	blood vessel:	n/a
7	chr14:35451962-35452012	HNPCEpiC	eye:	n/a
8	chr14:35408689-35408739	HNPCEpiC	eye:	n/a
9	chr14:35450692-35450742	SAEC	small airway:	n/a
10	chr14:35450692-35450742	Jurkat	blood:	n/a
11	chr14:35452353-35452403	HNPCEpiC	eye:	n/a
12	chr14:35409083-35409133	SK-N-SH	brain:	n/a
13	chr14:35409083-35409133	AoSMC	blood vessel:	n/a
14	chr14:35408569-35408619	BE2_C	brain:	n/a
15	chr14:35409641-35409691	Caco-2	colon:	n/a
16	chr14:35447884-35447934	HEK293	kidney:	embryo
17	chr14:35452602-35452652	CMK	blood:	n/a
18	chr14:35452441-35452491	MCF10A-Er-Src	breast:	n/a
19	chr14:35452353-35452403	BJ	skin:	n/a
20	chr14:35409641-35409691	SAEC	small airway:	n/a
21	chr14:35452110-35452160	U87	brain:	n/a
22	chr14:35408569-35408619	SK-N-SH_RA	brain:	n/a
23	chr14:35408689-35408739	MCF10A-Er-Src	breast:	n/a
24	chr14:35409083-35409133	BE2_C	brain:	n/a
25	chr14:35408689-35408739	U87	brain:	n/a
26	chr14:35452110-35452160	HMEC	breast:	n/a
27	chr14:35451965-35452015	HCM	heart:	n/a
28	chr14:35451965-35452015	T-47D	breast:	n/a
29	chr14:35451556-35451606	AG04450	lung:	fetal
30	chr14:35452441-35452491	HL-60	blood:	n/a
31	chr14:35451914-35451964	RPTEC	kidney:	n/a
32	chr14:35451807-35451857	SK-N-MC	brain:	n/a
33	chr14:35451807-35451857	PFSK-1	brain:	n/a
34	chr14:35451984-35452034	HRPEpiC	eye:	n/a
35	chr14:35451962-35452012	LNCaP	prostate:	n/a
36	chr14:35452441-35452491	SKMC	muscle:	n/a
37	chr14:35452353-35452403	MCF-7	breast:	n/a
38	chr14:35408689-35408739	GM12878	blood:	n/a
39	chr14:35452110-35452160	A549	lung:	n/a
40	chr14:35451962-35452012	GM12892	blood:	n/a
41	chr14:35451965-35452015	GM06990	blood:	n/a
42	chr14:35451793-35451843	HCT-116	colon:	n/a
43	chr14:35452602-35452652	GM12878	blood:	n/a
44	chr14:35447884-35447934	PrEC	prostate:	n/a
45	chr14:35451914-35451964	HRPEpiC	eye:	n/a
46	chr14:35451807-35451857	RPTEC	kidney:	n/a
47	chr14:35451984-35452034	GM06990	blood:	n/a
48	chr14:35452602-35452652	HCPEpiC	choroid plexus:	n/a
49	chr14:35451556-35451606	A549	lung:	n/a
50	chr14:35452441-35452491	AG04450	lung:	fetal

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:35462942..35465025-chr14:35469219..35471008,2	MCF-7	breast:
2	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
3	chr1:6452943..6453799-chr14:35451965..35452803,2	Hela-S3	cervix:
4	chr14:35430162..35434482-chr14:35434976..35439153,5	K562	blood:
5	chr14:35022467..35024689-chr14:35444966..35447403,2	MCF-7	breast:
6	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
7	chr14:35466324..35467917-chr14:35470934..35473111,2	K562	blood:
8	chr14:35393659..35395682-chr14:35403132..35405921,2	K562	blood:
9	chr12:46766054..46766614-chr14:35451546..35452273,2	Hela-S3	cervix:
10	chr14:35452133..35453716-chr14:35873041..35875070,2	K562	blood:
11	chr14:35451620..35453361-chr14:35464939..35467575,2	MCF-7	breast:
12	chr14:35341122..35342965-chr14:35463628..35465327,2	K562	blood:
13	chr14:35023701..35025768-chr14:35449276..35451419,2	K562	blood:
14	chr14:35450376..35452323-chr14:35627573..35629639,2	K562	blood:
15	chr14:35465599..35469103-chr14:35471087..35474391,3	MCF-7	breast:
16	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
17	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
18	chr1:116518333..116519266-chr14:35451605..35452534,2	Hela-S3	cervix:
19	chr14:35456800..35459337-chr14:35464974..35467131,2	K562	blood:
20	chr14:35454836..35457264-chr14:35513196..35514987,2	K562	blood:
21	chr14:35405852..35407525-chr14:35456925..35458489,2	K562	blood:
22	chr14:35339842..35342583-chr14:35472313..35474482,2	K562	blood:
23	chr14:35451354..35452438-chr14:64971301..64972306,3	Hela-S3	cervix:
24	chr14:35462942..35465025-chr14:35469219..35471008,2	MCF-7	breast:
25	chr14:35017275..35019117-chr14:35456494..35458889,2	MCF-7	breast:
26	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
27	chr14:35456800..35459337-chr14:35464974..35467131,2	K562	blood:
28	chr14:35342877..35345707-chr14:35420662..35422275,2	MCF-7	breast:
29	chr14:35451366..35453471-chr14:35871625..35875238,3	MCF-7	breast:
30	chr14:35449790..35454325-chr14:35456141..35461309,8	K562	blood:
31	chr14:35450245..35452169-chr14:35590215..35593362,3	MCF-7	breast:
32	chr14:35455186..35457809-chr14:35509575..35512529,2	K562	blood:
33	chr14:35451287..35451881-chr19:3557480..3558017,2	Hela-S3	cervix:
34	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
35	chr1:161147107..161147971-chr14:35451769..35452587,2	Hela-S3	cervix:
36	chr14:35459374..35461110-chr8:86390877..86393712,2	MCF-7	breast:
37	chr14:35430162..35434482-chr14:35434976..35439153,5	K562	blood:
38	chr14:35426260..35429015-chr14:35450690..35452638,2	K562	blood:
39	chr12:57081062..57081966-chr14:35451425..35452037,2	HCT-116	colon:
40	chr14:35445006..35447808-chr14:35448445..35452722,4	MCF-7	breast:
41	chr14:35022824..35025797-chr14:35452600..35454659,2	MCF-7	breast:
42	chr14:35450099..35453742-chr14:35513316..35517237,10	K562	blood:
43	chr14:35451886..35454032-chr4:69771560..69773312,2	MCF-7	breast:
44	chr14:35346926..35348942-chr14:35435760..35437416,2	K562	blood:
45	chr14:35397975..35400662-chr14:35403521..35405781,3	K562	blood:
46	chr14:35449839..35454578-chr14:35513316..35515954,7	K562	blood:
47	chr14:35405852..35407525-chr14:35456925..35458489,2	K562	blood:
48	chr14:35441146..35443555-chr14:35874693..35876513,2	MCF-7	breast:
49	chr14:35451762..35452508-chr19:18111810..18112416,2	Hela-S3	cervix:
50	chr14:35449513..35454029-chr14:35868261..35874094,7	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRP54-3	chr14:35436212-35436294	NONHSAT036352
2	lnc-SRP54-3	chr14:35433120-35433246	NONHSAT036352
3	lnc-SRP54-5	chr14:35409128-35409702	NR_002937
4	lnc-BAZ1A-1	chr14:35449441-35452103	NONHSAT036355
5	lnc-SRP54-3	chr14:35438376-35438513	NONHSAT036352
6	lnc-SRP54-3	chr14:35435735-35436151	NONHSAT036352

No data

Variant related genes	Relation type
ENSG00000258704	TF binding region
SRP54	TF binding region
IGBP1P1	TF binding region
ENSG00000199980	TF binding region
ENSG00000258704	CpG island
SRP54	CpG island
IGBP1P1	CpG island
ENSG00000199980	CpG island
ENSG00000126804	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000161091	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000163393	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000088888	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000145623	chromatin interactions
ENSG00000206588	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000249740	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000267231	chromatin interactions
ENSG00000271746	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000097021	chromatin interactions

Extended variants
information (count: 3025 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3025 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113621432	chr14:35404678-35404679	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs538201194	chr14:35404681-35404682	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs201386783	chr14:35404717-35404718	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs55891655	chr14:35404743-35404744	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs578134437	chr14:35404749-35404750	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs545859603	chr14:35404751-35404752	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs190146580	chr14:35404833-35404834	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs548905342	chr14:35404841-35404842	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs56342879	chr14:35404879-35404880	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs567144773	chr14:35404905-35404906	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs55885312	chr14:35404912-35404913	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs56335256	chr14:35404917-35404918	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs117139067	chr14:35404944-35404945	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs541800792	chr14:35404967-35404968	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs80131210	chr14:35404982-35404983	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs182417692	chr14:35404993-35404994	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs72680616	chr14:35405073-35405074	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs571332919	chr14:35405080-35405081	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs375824048	chr14:35405085-35405086	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs370434695	chr14:35405086-35405087	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs12893875	chr14:35405089-35405090	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs55966918	chr14:35405113-35405114	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs200068505	chr14:35405114-35405115	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs550637271	chr14:35405123-35405124	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs564287417	chr14:35405137-35405138	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs111931980	chr14:35405138-35405139	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs532956853	chr14:35405153-35405154	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs546791582	chr14:35405174-35405175	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186166366	chr14:35405180-35405181	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs528295675	chr14:35405185-35405186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs190887378	chr14:35405227-35405228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs799462	chr14:35405244-35405245	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs56301301	chr14:35405251-35405252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12894471	chr14:35405256-35405257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568949480	chr14:35405263-35405264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs799463	chr14:35405274-35405275	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs182767846	chr14:35405278-35405279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534494690	chr14:35405300-35405301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188937246	chr14:35405307-35405308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12894634	chr14:35405312-35405313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534098654	chr14:35405333-35405334	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs12894658	chr14:35405351-35405352	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs375533983	chr14:35405380-35405381	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs572972529	chr14:35405381-35405382	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs192500641	chr14:35405388-35405389	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs78295796	chr14:35405401-35405402	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs59337361	chr14:35405421-35405422	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs56355867	chr14:35405424-35405425	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs60653654	chr14:35405429-35405430	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs527946426	chr14:35405436-35405437	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Autism	22495311	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2005 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35381400-35412200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:35389600-35411400	Weak transcription	Aorta	Aorta
3	chr14:35390000-35412600	Weak transcription	Ovary	ovary
4	chr14:35394600-35424000	Weak transcription	Fetal Lung	lung
5	chr14:35396400-35425200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr14:35396600-35424800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:35397200-35412800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr14:35397800-35420600	Weak transcription	Thymus	Thymus
9	chr14:35398000-35408200	Weak transcription	Liver	Liver
10	chr14:35398800-35410600	Weak transcription	Fetal Brain Male	brain
11	chr14:35399000-35412200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr14:35399400-35406800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr14:35399600-35412200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:35400600-35427000	Weak transcription	Primary B cells from cord blood	blood
15	chr14:35400800-35412200	Weak transcription	Adipose Nuclei	Adipose
16	chr14:35401000-35411200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:35401000-35421400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr14:35401000-35428800	Weak transcription	GM12878-XiMat	blood
19	chr14:35401000-35440400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr14:35401200-35404800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
21	chr14:35401200-35408800	Weak transcription	Primary T cells from cord blood	blood
22	chr14:35401400-35412200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr14:35401400-35412200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr14:35401400-35412600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:35401400-35428800	Weak transcription	Stomach Mucosa	stomach
26	chr14:35401800-35411600	Weak transcription	Brain Angular Gyrus	brain
27	chr14:35402800-35408200	Weak transcription	HepG2	liver
28	chr14:35402800-35412600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:35403000-35423800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:35403200-35425200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr14:35403600-35425200	Weak transcription	Gastric	stomach
32	chr14:35404400-35405200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr14:35404400-35406000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr14:35404600-35404800	Enhancers	Left Ventricle	heart
35	chr14:35404600-35405000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr14:35405000-35406200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr14:35405200-35407200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr14:35405800-35412800	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr14:35406200-35412600	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr14:35406800-35407000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr14:35406800-35407000	Enhancers	Spleen	Spleen
42	chr14:35407000-35408800	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr14:35407000-35425000	Weak transcription	Spleen	Spleen
44	chr14:35408200-35409000	Strong transcription	Liver	Liver
45	chr14:35408200-35409800	Strong transcription	HepG2	liver
46	chr14:35408200-35425400	Weak transcription	Stomach Smooth Muscle	stomach
47	chr14:35408800-35409600	Strong transcription	Primary T cells from cord blood	blood
48	chr14:35409000-35419000	Weak transcription	Liver	Liver
49	chr14:35409600-35411400	Weak transcription	Primary T cells from cord blood	blood
50	chr14:35409800-35412600	Weak transcription	HepG2	liver

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