Variant report

Variant	nsv1030526
Chromosome Location	chr5:29125802-29204186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:244)
Chromatin interactive
region (count:23)
LncRNA
region (count:114)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:29134593-29134792	K562	blood:	n/a	n/a
2	ATF1	chr5:29152180-29152302	K562	blood:	n/a	n/a
3	BRCA1	chr5:29197449-29199081	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr5:29134584-29134844	K562	blood:	n/a	n/a
5	CCNT2	chr5:29203655-29203807	K562	blood:	n/a	n/a
6	CEBPB	chr5:29146476-29146686	K562	blood:	n/a	chr5:29146478-29146489
7	CEBPB	chr5:29146405-29146644	HepG2	liver:	n/a	chr5:29146478-29146489
8	CEBPB	chr5:29167029-29167225	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:29158133-29158405	HepG2	liver:	n/a	chr5:29158266-29158277
10	CEBPB	chr5:29191878-29192092	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:29181470-29181778	A549	lung:	n/a	chr5:29181601-29181614 chr5:29181602-29181613 chr5:29181669-29181682
12	CEBPB	chr5:29134588-29134823	K562	blood:	n/a	n/a
13	CEBPB	chr5:29181472-29181748	HepG2	liver:	n/a	chr5:29181601-29181614 chr5:29181602-29181613 chr5:29181669-29181682
14	CEBPB	chr5:29180075-29180275	HepG2	liver:	n/a	chr5:29180117-29180130 chr5:29180162-29180171 chr5:29180161-29180172
15	CEBPB	chr5:29161604-29161751	HepG2	liver:	n/a	chr5:29161684-29161695 chr5:29161686-29161695
16	CEBPB	chr5:29181501-29181619	H1-hESC	embryonic stem cell:	n/a	chr5:29181601-29181614 chr5:29181602-29181613
17	CEBPB	chr5:29156459-29156660	HepG2	liver:	n/a	chr5:29156513-29156524
18	CEBPB	chr5:29179236-29179442	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:29181438-29181752	IMR90	lung:	n/a	chr5:29181601-29181614 chr5:29181602-29181613 chr5:29181669-29181682
20	CEBPB	chr5:29156421-29156644	A549	lung:	n/a	chr5:29156513-29156524
21	CEBPB	chr5:29146371-29146687	A549	lung:	n/a	chr5:29146478-29146489
22	CEBPB	chr5:29181451-29181743	K562	blood:	n/a	chr5:29181601-29181614 chr5:29181602-29181613 chr5:29181669-29181682
23	CEBPB	chr5:29156500-29156503	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:29130906-29131232	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:29197559-29198814	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:29134625-29134899	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:29170712-29171041	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:29162422-29162713	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:29134586-29134903	K562	blood:	n/a	n/a
30	CEBPB	chr5:29161539-29161867	HepG2	liver:	n/a	chr5:29161684-29161695 chr5:29161686-29161695
31	CHD2	chr5:29151100-29151303	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:29161875-29161886	LNCaP	prostate:	n/a	n/a
33	CTCF	chr5:29147100-29147250	Caco-2	colon:	n/a	n/a
34	CTCF	chr5:29147120-29147281	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:29161815-29161984	Hela-S3	cervix:	n/a	chr5:29161889-29161910
36	CTCF	chr5:29131300-29131450	HVMF	connective:	n/a	n/a
37	CTCF	chr5:29161824-29161949	Medullo	brain:	n/a	chr5:29161889-29161910
38	CTCF	chr5:29147160-29147310	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:29191940-29192025	GM20000	blood:	n/a	n/a
40	CTCF	chr5:29147140-29147290	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr5:29161820-29161970	BE2_C	brain:	n/a	chr5:29161889-29161910
42	CTCF	chr5:29146860-29147010	BE2_C	brain:	n/a	n/a
43	CTCF	chr5:29161860-29162010	MCF-7	breast:	n/a	chr5:29161889-29161910
44	CTCF	chr5:29127708-29127728	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr5:29147180-29147205	K562	blood:	n/a	n/a
46	CTCF	chr5:29147140-29147290	HEK293	kidney:	n/a	n/a
47	CTCF	chr5:29161827-29161925	LNCaP	prostate:	n/a	chr5:29161889-29161910
48	CTCF	chr5:29147020-29147170	BE2_C	brain:	n/a	n/a
49	CTCF	chr5:29126680-29126776	GM20000	blood:	n/a	n/a
50	CTCF	chr5:29147177-29147215	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:29150410-29150460	AG10803	skin:	n/a
2	chr5:29128011-29128061	PFSK-1	brain:	n/a
3	chr5:29191970-29192020	LNCaP	prostate:	n/a
4	chr5:29191970-29192020	HCF	heart:	n/a
5	chr5:29128011-29128061	HCM	heart:	n/a
6	chr5:29191970-29192020	ECC-1	luminal epithelium:	n/a
7	chr5:29128011-29128061	HIPEpiC	eye:	n/a
8	chr5:29128011-29128061	AG10803	skin:	n/a
9	chr5:29151828-29151878	GM19239	blood:	n/a
10	chr5:29150410-29150460	PrEC	prostate:	n/a
11	chr5:29151828-29151878	T-47D	breast:	n/a
12	chr5:29151828-29151878	HEEpiC	esophagus:	n/a
13	chr5:29151828-29151878	NB4	blood:	n/a
14	chr5:29191970-29192020	AoSMC	blood vessel:	n/a
15	chr5:29150410-29150460	BJ	skin:	n/a
16	chr5:29150410-29150460	HEEpiC	esophagus:	n/a
17	chr5:29191970-29192020	SK-N-MC	brain:	n/a
18	chr5:29151828-29151878	BE2_C	brain:	n/a
19	chr5:29150410-29150460	ProgFib	skin:	n/a
20	chr5:29191970-29192020	HRCEpiC	kidney:	n/a
21	chr5:29151828-29151878	HAEpiC	amniotic membrane:	n/a
22	chr5:29191970-29192020	IMR90	lung:	fetal
23	chr5:29128011-29128061	Hela-S3	cervix:	n/a
24	chr5:29151828-29151878	K562	blood:	n/a
25	chr5:29151828-29151878	NHBE	bronchial:	n/a
26	chr5:29128011-29128061	CMK	blood:	n/a
27	chr5:29151828-29151878	Caco-2	colon:	n/a
28	chr5:29151828-29151878	HIPEpiC	eye:	n/a
29	chr5:29150410-29150460	HRPEpiC	eye:	n/a
30	chr5:29128011-29128061	LNCaP	prostate:	n/a
31	chr5:29128011-29128061	GM12891	blood:	n/a
32	chr5:29128011-29128061	HRCEpiC	kidney:	n/a
33	chr5:29151828-29151878	U87	brain:	n/a
34	chr5:29150410-29150460	PANC-1	pancreas:	n/a
35	chr5:29150410-29150460	GM12878	blood:	n/a
36	chr5:29128011-29128061	HMEC	breast:	n/a
37	chr5:29191970-29192020	HRE	kidney:	n/a
38	chr5:29150410-29150460	SKMC	muscle:	n/a
39	chr5:29151828-29151878	AG04449	skin:	fetal
40	chr5:29151828-29151878	Hela-S3	cervix:	n/a
41	chr5:29128011-29128061	HEEpiC	esophagus:	n/a
42	chr5:29151828-29151878	AG04450	lung:	fetal
43	chr5:29150410-29150460	AG04450	lung:	fetal
44	chr5:29191970-29192020	GM12892	blood:	n/a
45	chr5:29151828-29151878	PFSK-1	brain:	n/a
46	chr5:29150410-29150460	SAEC	small airway:	n/a
47	chr5:29191970-29192020	PFSK-1	brain:	n/a
48	chr5:29191970-29192020	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:29151828-29151878	MCF-7	breast:	n/a
50	chr5:29191970-29192020	PrEC	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:29144474..29145271-chr5:133861804..133862472,2	Hela-S3	cervix:
2	chr5:29138046..29139623-chr5:29144117..29145732,2	K562	blood:
3	chr5:29144357..29145929-chr5:29148245..29150453,2	K562	blood:
4	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
5	chr5:29173081..29175967-chr5:29178841..29180963,2	K562	blood:
6	chr5:29191166..29194055-chr5:29197511..29200144,2	MCF-7	breast:
7	chr5:29161582..29162331-chr5:29218131..29218799,3	MCF-7	breast:
8	chr5:29195975..29198561-chr5:29201740..29203808,2	MCF-7	breast:
9	chr5:29144206..29145857-chr5:29147427..29149745,2	K562	blood:
10	chr5:29173081..29175967-chr5:29178841..29180963,2	K562	blood:
11	chr5:29192802..29195589-chr5:29735604..29737359,2	K562	blood:
12	chr5:29195975..29198561-chr5:29201740..29203808,2	MCF-7	breast:
13	chr5:29191166..29194055-chr5:29197511..29200144,2	MCF-7	breast:
14	chr5:29144206..29145857-chr5:29147427..29149745,2	K562	blood:
15	chr5:29145282..29146802-chr5:29147272..29149204,2	MCF-7	breast:
16	chr5:29158096..29160564-chr5:29163373..29164995,2	K562	blood:
17	chr5:29199626..29201396-chr5:29206824..29209711,2	K562	blood:
18	chr5:29145282..29146802-chr5:29147272..29149204,2	MCF-7	breast:
19	chr5:29176140..29178605-chr5:29180488..29182983,2	K562	blood:
20	chr5:29176140..29178605-chr5:29180488..29182983,2	K562	blood:
21	chr5:29138046..29139623-chr5:29144117..29145732,2	K562	blood:
22	chr5:28932533..28934760-chr5:29193358..29195088,2	K562	blood:
23	chr5:29144357..29145929-chr5:29148245..29150453,2	K562	blood:

(count:114 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-2	chr5:29164518-29164621	XLOC_004325
2	lnc-CDH9-7	chr5:29141837-29142353	XLOC_004764
3	lnc-CDH6-2	chr5:29169667-29169693	ENSG00000259786.2
4	lnc-CDH6-2	chr5:29169667-29169693	XLOC_004325
5	lnc-CDH6-2	chr5:29164513-29164621	NONHSAT100847
6	lnc-CDH6-2	chr5:29162523-29162763	XLOC_004325
7	lnc-CDH6-2	chr5:29176999-29177040	XLOC_004325
8	lnc-CDH6-2	chr5:29169666-29169720	NONHSAT100838
9	lnc-CDH6-2	chr5:29145854-29145981	NONHSAT100838
10	lnc-CDH6-2	chr5:29169667-29169693	XLOC_004325
11	lnc-CDH6-2	chr5:29162523-29162697	ENSG00000259786.1
12	lnc-CDH6-2	chr5:29183412-29183428	XLOC_004325
13	lnc-CDH6-2	chr5:29164513-29164621	NONHSAT100846
14	lnc-CDH6-2	chr5:29165037-29165153	ENSG00000259786.1
15	lnc-CDH6-2	chr5:29153566-29153802	ENSG00000259786.1
16	lnc-CDH6-2	chr5:29162523-29162698	NONHSAT100843
17	lnc-CDH6-2	chr5:29153566-29153727	ENSG00000259786.2
18	lnc-CDH6-2	chr5:29146378-29146568	ENSG00000259786.1
19	lnc-CDH6-2	chr5:29169667-29169693	XLOC_004325
20	lnc-CDH6-2	chr5:29172150-29172276	XLOC_004325
21	lnc-CDH6-2	chr5:29145855-29145981	XLOC_004325
22	lnc-CDH6-2	chr5:29172150-29172465	ENSG00000259786.2
23	lnc-CDH6-2	chr5:29164518-29164621	XLOC_004325
24	lnc-CDH6-2	chr5:29165037-29165091	XLOC_004325
25	lnc-CDH6-2	chr5:29162523-29162697	ENSG00000259786.2
26	lnc-CDH6-10	chr5:29198280-29198453	ucscGeneNc_uc003jhb_1
27	lnc-CDH6-10	chr5:29200794-29200910	ucscGeneNc_uc003jhb_1
28	lnc-CDH9-15	chr5:29179050-29179278	l_2894_chr5:29177610-29179278_testes
29	lnc-CDH6-2	chr5:29169667-29169693	ENSG00000259786.1
30	lnc-CDH6-2	chr5:29162522-29162847	NONHSAT100838
31	lnc-CDH6-2	chr5:29146378-29146568	XLOC_004325
32	lnc-CDH6-2	chr5:29164515-29164621	NONHSAT100838
33	lnc-CDH6-2	chr5:29176999-29177040	XLOC_004325
34	lnc-CDH6-2	chr5:29153566-29153907	XLOC_004325
35	lnc-CDH6-2	chr5:29172150-29172465	XLOC_004325
36	lnc-CDH6-2	chr5:29164518-29164621	XLOC_004325
37	lnc-CDH6-2	chr5:29169667-29169693	NONHSAT100846
38	lnc-CDH6-2	chr5:29172149-29172465	NONHSAT100838
39	lnc-CDH6-2	chr5:29143618-29143836	XLOC_004325
40	lnc-CDH6-2	chr5:29143616-29143836	XLOC_004325
41	lnc-CDH6-2	chr5:29153643-29153840	ENSG00000259786.2
42	lnc-CDH6-2	chr5:29164524-29164621	ENSG00000259786.2
43	lnc-CDH6-11	chr5:29126624-29126682	NONHSAT100835
44	lnc-CDH6-2	chr5:29167715-29167904	ENSG00000259786.2
45	lnc-CDH6-2	chr5:29153566-29153840	NONHSAT100842
46	lnc-CDH6-2	chr5:29165037-29165091	NONHSAT100846
47	lnc-CDH6-2	chr5:29176998-29177040	NONHSAT100838
48	lnc-CDH6-2	chr5:29169667-29169720	XLOC_004325
49	lnc-CDH6-2	chr5:29153566-29153592	ENSG00000259786.2
50	lnc-CDH6-10	chr5:29200281-29200378	ucscGeneNc_uc003jhb_1

No data

Variant related genes	Relation type
ENSG00000259786	TF binding region
ENSG00000259786	CpG island
ENSG00000259786	chromatin interactions
ENSG00000043143	chromatin interactions
ARHGEF37	miRNA target sites
ARID4B	miRNA target sites
ITPRIP	miRNA target sites
RGPD5	miRNA target sites
RND3	miRNA target sites
PLOD2	miRNA target sites
C19orf30	miRNA target sites
RMND5A	miRNA target sites
ARHGEF4	miRNA target sites
MEF2C	miRNA target sites
MYOT	miRNA target sites
PRR5L	miRNA target sites
ARID5B	miRNA target sites
CYP19A1	miRNA target sites
PRR14L	miRNA target sites
ARIH2	miRNA target sites

Extended variants
information (count: 2207 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200870821	chr5:29126639-29126640	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs554343914	chr5:29126650-29126651	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs191978595	chr5:29126657-29126658	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs548090009	chr5:29126658-29126659	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs12697209	chr5:29128601-29128602	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573657417	chr5:29128614-29128615	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs71621755	chr5:29128628-29128629	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs544315414	chr5:29128667-29128668	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs562971190	chr5:29128722-29128723	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs376805867	chr5:29128756-29128757	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs533244544	chr5:29128772-29128773	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535874735	chr5:29128817-29128818	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs190232243	chr5:29128827-29128828	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs527632139	chr5:29128846-29128847	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549252367	chr5:29128850-29128851	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144126807	chr5:29128859-29128860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs2329987	chr5:29128888-29128889	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs160319	chr5:29128908-29128909	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143261770	chr5:29128941-29128942	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs148663105	chr5:29128968-29128969	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs539341767	chr5:29134005-29134006	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs575922533	chr5:29134011-29134012	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs180886622	chr5:29134026-29134027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs186134016	chr5:29134043-29134044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs141060561	chr5:29134124-29134125	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs309694	chr5:29134205-29134206	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575108598	chr5:29134216-29134217	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs536074774	chr5:29134237-29134238	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs557257762	chr5:29134252-29134253	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs367611674	chr5:29134275-29134276	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs575936299	chr5:29134282-29134283	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs546179412	chr5:29134292-29134293	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs564145334	chr5:29134306-29134307	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs73062350	chr5:29134352-29134353	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs371173876	chr5:29134365-29134366	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs116009742	chr5:29134382-29134383	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs529350953	chr5:29134400-29134401	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550790389	chr5:29134417-29134418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs562539274	chr5:29134453-29134454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533259959	chr5:29134477-29134478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190986862	chr5:29134524-29134525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566100426	chr5:29134548-29134549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533742521	chr5:29134552-29134553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150251688	chr5:29134556-29134557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567389448	chr5:29134557-29134558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73747196	chr5:29134584-29134585	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs557582598	chr5:29134596-29134597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370496159	chr5:29134603-29134604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569307921	chr5:29134657-29134658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs55892003	chr5:29134661-29134662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29128600-29129000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
2	chr5:29134000-29134400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:29134200-29135000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr5:29134400-29136000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:29135000-29143600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:29143600-29144000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:29143600-29144000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:29143600-29144000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr5:29143600-29144000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr5:29144000-29148000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:29144000-29148600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:29144000-29150600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:29146800-29150600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr5:29148000-29148200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:29148000-29151400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:29148400-29149400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:29148600-29149000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr5:29148600-29151400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:29148800-29149000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr5:29148800-29149000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:29148800-29149200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:29148800-29150800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr5:29148800-29151000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:29149000-29149600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr5:29149000-29150200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr5:29149000-29150200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr5:29149000-29151600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:29149200-29153400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:29149400-29151400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr5:29149600-29150800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr5:29150000-29151400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr5:29150200-29151400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr5:29150200-29151400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr5:29150600-29150800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr5:29150600-29150800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:29150800-29151000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr5:29150800-29151200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:29150800-29151400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:29150800-29151400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:29150800-29151400	Enhancers	Colon Smooth Muscle	Colon
41	chr5:29151000-29151200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:29151000-29153200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr5:29151200-29151400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr5:29151400-29152800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr5:29151400-29153000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr5:29151400-29153400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr5:29151400-29153400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr5:29151400-29157600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr5:29151600-29157600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:29152800-29154000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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