Variant report

Variant	nsv881342
Chromosome Location	chr4:152363772-152560449
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:152443367-152443482	HepG2	liver:	n/a	n/a
2	ATF2	chr4:152405480-152406188	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:152405446-152406295	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:152410658-152411028	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:152405961-152406194	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:152405613-152406248	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:152459478-152459498	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:152470311-152470372	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:152410762-152410960	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:152488330-152488532	GM12878	blood:	n/a	n/a
11	BATF	chr4:152488331-152488574	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:152405884-152406142	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr4:152405934-152406177	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr4:152488300-152488541	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:152488306-152488634	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:152470637-152470868	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr4:152457378-152457504	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:152461855-152463032	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:152459606-152459805	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr4:152461870-152462341	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:152405800-152406344	HCT-116	colon:	n/a	chr4:152406332-152406343
22	CBX3	chr4:152405804-152406321	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:152469912-152470196	K562	blood:	n/a	n/a
24	CBX3	chr4:152461730-152462436	HCT-116	colon:	n/a	n/a
25	CBX3	chr4:152469835-152470243	K562	blood:	n/a	n/a
26	CEBPB	chr4:152390191-152390711	MCF-7	breast:	n/a	chr4:152390361-152390372 chr4:152390438-152390449 chr4:152390359-152390370 chr4:152390438-152390451 chr4:152390359-152390372 chr4:152390438-152390451
27	CEBPB	chr4:152521033-152521392	HepG2	liver:	n/a	chr4:152521257-152521270 chr4:152521204-152521215
28	CEBPB	chr4:152390353-152390655	A549	lung:	n/a	chr4:152390361-152390372 chr4:152390438-152390449 chr4:152390359-152390370 chr4:152390438-152390451 chr4:152390359-152390372 chr4:152390438-152390451
29	CEBPB	chr4:152390218-152390712	ECC-1	luminal epithelium:	n/a	chr4:152390361-152390372 chr4:152390438-152390449 chr4:152390359-152390370 chr4:152390438-152390451 chr4:152390359-152390372 chr4:152390438-152390451
30	CEBPB	chr4:152407325-152407470	HepG2	liver:	n/a	chr4:152407430-152407441
31	CEBPB	chr4:152393893-152394240	IMR90	lung:	n/a	chr4:152394063-152394074 chr4:152394065-152394074 chr4:152394063-152394076 chr4:152394065-152394074 chr4:152394065-152394074 chr4:152394065-152394076 chr4:152394063-152394076 chr4:152394065-152394074
32	CEBPB	chr4:152405715-152406306	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:152453205-152453458	A549	lung:	n/a	chr4:152453416-152453427 chr4:152453418-152453427 chr4:152453416-152453429
34	CEBPB	chr4:152479893-152480229	K562	blood:	n/a	chr4:152480049-152480060 chr4:152480049-152480062 chr4:152480024-152480037 chr4:152480050-152480061 chr4:152480051-152480060 chr4:152479966-152479977
35	CEBPB	chr4:152521033-152521408	IMR90	lung:	n/a	chr4:152521257-152521270 chr4:152521204-152521215
36	CEBPB	chr4:152458872-152459191	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:152390238-152390676	HepG2	liver:	n/a	chr4:152390361-152390372 chr4:152390438-152390449 chr4:152390359-152390370 chr4:152390438-152390451 chr4:152390359-152390372 chr4:152390438-152390451
38	CEBPB	chr4:152521063-152521392	Hela-S3	cervix:	n/a	chr4:152521257-152521270 chr4:152521204-152521215
39	CEBPB	chr4:152393906-152394313	MCF-7	breast:	n/a	chr4:152394063-152394074 chr4:152394065-152394074 chr4:152394063-152394076 chr4:152394065-152394074 chr4:152394065-152394074 chr4:152394065-152394076 chr4:152394063-152394076 chr4:152394065-152394074
40	CEBPB	chr4:152458940-152459236	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr4:152548579-152548837	K562	blood:	n/a	chr4:152548700-152548711 chr4:152548701-152548712
42	CEBPB	chr4:152453244-152453421	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr4:152479918-152480218	HepG2	liver:	n/a	chr4:152480049-152480060 chr4:152480049-152480062 chr4:152480024-152480037 chr4:152480050-152480061 chr4:152480051-152480060 chr4:152479966-152479977
44	CEBPB	chr4:152462553-152462904	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:152516823-152517052	HepG2	liver:	n/a	chr4:152516990-152517001
46	CEBPB	chr4:152458860-152459225	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:152521066-152521400	K562	blood:	n/a	chr4:152521257-152521270 chr4:152521204-152521215
48	CEBPB	chr4:152479982-152480182	H1-hESC	embryonic stem cell:	n/a	chr4:152480049-152480060 chr4:152480049-152480062 chr4:152480024-152480037 chr4:152480050-152480061 chr4:152480051-152480060
49	CEBPB	chr4:152380497-152381013	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:152407290-152407617	IMR90	lung:	n/a	chr4:152407430-152407441

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152475308-152475358	NHBE	bronchial:	n/a
2	chr4:152475308-152475358	NHBE	bronchial:	n/a
3	chr4:152543520-152543570	HEEpiC	esophagus:	n/a
4	chr4:152405174-152405224	HRPEpiC	eye:	n/a
5	chr4:152424074-152424124	HRCEpiC	kidney:	n/a
6	chr4:152424074-152424124	ovcar-3	ovarian:	n/a
7	chr4:152493081-152493131	HCPEpiC	choroid plexus:	n/a
8	chr4:152543520-152543570	PANC-1	pancreas:	n/a
9	chr4:152424074-152424124	HCF	heart:	n/a
10	chr4:152364959-152365009	GM12892	blood:	n/a
11	chr4:152424074-152424124	AoSMC	blood vessel:	n/a
12	chr4:152543520-152543570	ovcar-3	ovarian:	n/a
13	chr4:152364959-152365009	ovcar-3	ovarian:	n/a
14	chr4:152432509-152432559	HRE	kidney:	n/a
15	chr4:152475308-152475358	SK-N-MC	brain:	n/a
16	chr4:152424074-152424124	NT2-D1	testis:	n/a
17	chr4:152543520-152543570	Hepatocyte	liver:	n/a
18	chr4:152475308-152475358	HRCEpiC	kidney:	n/a
19	chr4:152424074-152424124	SK-N-SH_RA	brain:	n/a
20	chr4:152462020-152462070	HCPEpiC	choroid plexus:	n/a
21	chr4:152364959-152365009	A549	lung:	n/a
22	chr4:152405174-152405224	PFSK-1	brain:	n/a
23	chr4:152364959-152365009	HIPEpiC	eye:	n/a
24	chr4:152364959-152365009	IMR90	lung:	fetal
25	chr4:152543520-152543570	U87	brain:	n/a
26	chr4:152493081-152493131	SAEC	small airway:	n/a
27	chr4:152462020-152462070	HNPCEpiC	eye:	n/a
28	chr4:152405174-152405224	H1-hESC	embryonic stem cell:	embryo
29	chr4:152424074-152424124	HCM	heart:	n/a
30	chr4:152424074-152424124	SK-N-MC	brain:	n/a
31	chr4:152376761-152376811	HAEpiC	amniotic membrane:	n/a
32	chr4:152364959-152365009	LNCaP	prostate:	n/a
33	chr4:152432509-152432559	GM12878	blood:	n/a
34	chr4:152432509-152432559	Hepatocyte	liver:	n/a
35	chr4:152424074-152424124	MCF-7	breast:	n/a
36	chr4:152493081-152493131	GM12892	blood:	n/a
37	chr4:152475308-152475358	Hela-S3	cervix:	n/a
38	chr4:152376761-152376811	SK-N-MC	brain:	n/a
39	chr4:152475308-152475358	NH-A	brain:	n/a
40	chr4:152493081-152493131	HRE	kidney:	n/a
41	chr4:152475308-152475358	A549	lung:	n/a
42	chr4:152376761-152376811	SKMC	muscle:	n/a
43	chr4:152543520-152543570	HRE	kidney:	n/a
44	chr4:152432509-152432559	HEK293	kidney:	embryo
45	chr4:152493081-152493131	HRCEpiC	kidney:	n/a
46	chr4:152462020-152462070	ECC-1	luminal epithelium:	n/a
47	chr4:152493081-152493131	GM12891	blood:	n/a
48	chr4:152364959-152365009	HCPEpiC	choroid plexus:	n/a
49	chr4:152405174-152405224	NHDF-neo	bronchial:	n/a
50	chr4:152424074-152424124	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:152451680..152452632-chr4:152566818..152567655,2	K562	blood:
2	chr4:152392114..152395056-chr4:152400714..152402332,2	MCF-7	breast:
3	chr4:152371542..152374443-chr4:152375598..152378565,2	MCF-7	breast:
4	chr4:152493503..152497006-chr4:152497328..152500411,3	MCF-7	breast:
5	chr4:152329894..152331826-chr4:152444189..152446160,2	MCF-7	breast:
6	chr4:152478771..152481740-chr4:152484056..152486219,2	MCF-7	breast:
7	chr4:152389958..152393083-chr4:152394251..152396843,3	K562	blood:
8	chr4:152405946..152407616-chr4:152409141..152411607,2	MCF-7	breast:
9	chr4:152329111..152331152-chr4:152461032..152463159,2	MCF-7	breast:
10	chr4:152451909..152453994-chr4:152457176..152459826,2	K562	blood:
11	chr4:152451448..152452616-chr4:152525138..152526027,3	MCF-7	breast:
12	chr4:152451909..152453994-chr4:152457176..152459826,2	K562	blood:
13	chr4:152389958..152392173-chr4:152395343..152398079,2	K562	blood:
14	chr4:152392114..152395056-chr4:152400714..152402332,2	MCF-7	breast:
15	chr4:152034136..152036286-chr4:152523781..152526720,2	K562	blood:
16	chr4:152283616..152284269-chr4:152525183..152526125,3	K562	blood:
17	chr4:152391915..152393876-chr4:152394170..152396250,2	MCF-7	breast:
18	chr4:152405946..152407616-chr4:152409141..152411607,2	MCF-7	breast:
19	chr4:152371542..152374443-chr4:152375598..152378565,2	MCF-7	breast:
20	chr4:152452273..152454102-chr4:152495162..152497210,2	MCF-7	breast:
21	chr4:152328008..152330909-chr4:152463220..152466219,3	MCF-7	breast:
22	chr4:152547828..152549705-chr4:152551466..152554040,2	MCF-7	breast:
23	chr4:152393445..152396231-chr4:152399034..152401565,3	MCF-7	breast:
24	chr4:152478771..152481740-chr4:152484056..152486219,2	MCF-7	breast:
25	chr4:152547828..152549705-chr4:152551466..152554040,2	MCF-7	breast:
26	chr4:152458335..152459868-chr4:152462212..152465147,2	K562	blood:
27	chr4:152330012..152332003-chr4:152378597..152381385,2	MCF-7	breast:
28	chr4:152389958..152392173-chr4:152395343..152398079,2	K562	blood:
29	chr4:152389958..152393083-chr4:152394251..152396843,3	K562	blood:
30	chr4:152329199..152330989-chr4:152430941..152433845,2	MCF-7	breast:
31	chr4:152391915..152393876-chr4:152394170..152396250,2	MCF-7	breast:
32	chr16:50936343..50936843-chr4:152377370..152378176,2	K562	blood:
33	chr4:152451448..152452616-chr4:152525138..152526027,3	MCF-7	breast:
34	chr4:152410378..152410940-chr4:152525127..152525930,2	MCF-7	breast:
35	chr4:152421016..152422529-chr4:152424814..152426344,2	K562	blood:
36	chr4:152452273..152454102-chr4:152495162..152497210,2	MCF-7	breast:
37	chr4:152424956..152426757-chr4:152427452..152429748,2	K562	blood:
38	chr4:152283972..152284521-chr4:152533392..152534267,2	MCF-7	breast:
39	chr4:152443577..152445745-chr4:152452980..152455004,2	MCF-7	breast:
40	chr4:152451927..152452872-chr4:152533925..152534665,2	MCF-7	breast:
41	chr4:152553489..152556475-chr4:152557193..152559882,2	MCF-7	breast:
42	chr4:152458335..152459868-chr4:152462212..152465147,2	K562	blood:
43	chr4:152497358..152500298-chr4:152502845..152505045,2	K562	blood:
44	chr4:152451927..152452872-chr4:152533925..152534665,2	MCF-7	breast:
45	chr4:152421016..152422529-chr4:152424814..152426344,2	K562	blood:
46	chr4:152197795..152198565-chr4:152533473..152534113,3	MCF-7	breast:
47	chr4:152410378..152410940-chr4:152525127..152525930,2	MCF-7	breast:
48	chr4:152480645..152483966-chr4:152488462..152492385,3	MCF-7	breast:
49	chr4:152424956..152426757-chr4:152427452..152429748,2	K562	blood:
50	chr4:152480645..152483966-chr4:152488462..152492385,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PET112-3	chr4:152542740-152543080	l_2754_chr4:152493858-152548475_thyroid
2	lnc-FAM160A1-8	chr4:152375853-152375960	NONHSAT098760
3	lnc-PET112-3	chr4:152493859-152493983	l_2754_chr4:152493858-152548475_thyroid
4	lnc-FAM160A1-8	chr4:152375853-152375960	NONHSAT098761
5	lnc-FAM160A1-8	chr4:152403676-152403800	NONHSAT098760
6	lnc-FAM160A1-8	chr4:152487290-152487410	NONHSAT098760
7	lnc-FAM160A1-8	chr4:152455847-152455928	NONHSAT098761
8	lnc-PET112-3	chr4:152548091-152548475	l_2754_chr4:152493858-152548475_thyroid
9	lnc-PET112-3	chr4:152546122-152546210	l_2754_chr4:152493858-152548475_thyroid

Variant related genes	Relation type
FAM160A1	TF binding region
RN7SKP35	TF binding region
ENSG00000221657	TF binding region
FAM160A1	CpG island
RN7SKP35	CpG island
ENSG00000221657	CpG island
ENSG00000164142	chromatin interactions
ENSG00000189050	chromatin interactions
ENSG00000189099	chromatin interactions
ENSG00000267302	chromatin interactions
ENSG00000251611	chromatin interactions
ENSG00000253019	chromatin interactions

Extended variants
information (count: 6575 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6575 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2709815	chr4:152363772-152363773	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544847840	chr4:152363796-152363797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571865095	chr4:152363912-152363913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148728423	chr4:152363960-152363961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142300505	chr4:152363972-152363973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545582266	chr4:152363979-152363980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576145187	chr4:152364005-152364006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147905677	chr4:152364110-152364111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141714372	chr4:152364119-152364120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563983878	chr4:152364147-152364148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116034216	chr4:152364157-152364158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182480555	chr4:152364160-152364161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186950163	chr4:152364171-152364172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77648943	chr4:152364243-152364244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552209440	chr4:152364247-152364248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147093920	chr4:152364269-152364270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537957876	chr4:152364285-152364286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533125994	chr4:152364288-152364289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76618862	chr4:152364311-152364312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192389012	chr4:152364360-152364361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368383184	chr4:152364373-152364374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79842871	chr4:152364374-152364375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565649130	chr4:152364429-152364430	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs539415432	chr4:152364441-152364442	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs541100391	chr4:152364482-152364483	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557753195	chr4:152364547-152364548	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs147726040	chr4:152364571-152364572	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs543544557	chr4:152364637-152364638	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555672491	chr4:152364643-152364644	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs78999366	chr4:152364644-152364645	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs541266698	chr4:152364674-152364675	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs201969605	chr4:152364769-152364770	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs549769943	chr4:152364770-152364771	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs559953491	chr4:152364779-152364780	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs527522983	chr4:152364788-152364789	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs201303516	chr4:152364837-152364838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72003901	chr4:152364838-152364839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368864713	chr4:152364839-152364840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533681080	chr4:152364847-152364848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545785139	chr4:152364869-152364870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202015153	chr4:152364873-152364874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs57147339	chr4:152364875-152364876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370363970	chr4:152364876-152364877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141088575	chr4:152364927-152364928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531427263	chr4:152364960-152364961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549897629	chr4:152365013-152365014	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543344336	chr4:152365072-152365073	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184927224	chr4:152365133-152365134	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114817554	chr4:152365205-152365206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374665851	chr4:152365233-152365234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152354400-152364200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr4:152354800-152364200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr4:152357600-152364200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:152357800-152364200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr4:152357800-152364200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr4:152360000-152364800	Weak transcription	Pancreas	Pancrea
7	chr4:152361000-152364200	Weak transcription	Fetal Brain Male	brain
8	chr4:152362000-152365000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:152362200-152364200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:152362200-152364400	Weak transcription	Left Ventricle	heart
11	chr4:152362800-152364000	Enhancers	NHEK	skin
12	chr4:152363200-152364400	Enhancers	Psoas Muscle	Psoas
13	chr4:152363200-152364400	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr4:152363600-152363800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:152364000-152379200	Weak transcription	NHEK	skin
16	chr4:152364200-152364400	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:152364200-152364400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:152364200-152364400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr4:152364200-152365000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:152364200-152365200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:152364200-152365400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:152364200-152365400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:152364200-152365400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:152364200-152365400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr4:152364200-152365400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:152364200-152365400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:152364200-152365400	Enhancers	Fetal Brain Male	brain
28	chr4:152364200-152366400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:152364400-152364600	Enhancers	Left Ventricle	heart
30	chr4:152364400-152364800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr4:152364400-152364800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr4:152364400-152364800	Enhancers	Brain Germinal Matrix	brain
33	chr4:152364400-152365000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr4:152364400-152365000	Weak transcription	Psoas Muscle	Psoas
35	chr4:152364400-152365000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr4:152364400-152365200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:152364400-152365800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:152364400-152366800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:152364600-152364800	Enhancers	HepG2	liver
40	chr4:152364600-152365200	Weak transcription	Left Ventricle	heart
41	chr4:152364800-152365200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr4:152364800-152365200	Enhancers	Pancreas	Pancrea
43	chr4:152364800-152365400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr4:152364800-152366000	Weak transcription	HepG2	liver
45	chr4:152365000-152365200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:152365000-152365200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr4:152365000-152365200	Enhancers	Psoas Muscle	Psoas
48	chr4:152365000-152365200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr4:152365000-152365400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr4:152365000-152365400	Enhancers	Right Atrium	heart

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