Variant report

Variant	nsv10514
Chromosome Location	chr4:68789515-69015886
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:875)
CpG islands
(count:794)
Chromatin interactive
region (count:62)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:68995505-68995878	K562	blood:	n/a	n/a
2	ATF1	chr4:69014644-69014829	K562	blood:	n/a	n/a
3	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
4	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
5	ATF1	chr4:68794343-68794570	K562	blood:	n/a	n/a
6	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
7	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
10	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
12	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
13	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
14	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
15	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
16	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
17	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:68854271-68854605	Hela-S3	cervix:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
19	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
20	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
21	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
22	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
24	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
25	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
26	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
27	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
28	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
30	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
31	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a
32	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
33	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
34	CEBPB	chr4:68886657-68887443	HCT-116	colon:	n/a	n/a
35	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
36	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
37	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
39	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
41	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
42	CEBPB	chr4:68894925-68895100	HepG2	liver:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
43	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
44	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
46	CEBPB	chr4:69014530-69014780	K562	blood:	n/a	n/a
47	CEBPB	chr4:69015863-69016001	K562	blood:	n/a	chr4:69015942-69015953
48	CEBPB	chr4:68888023-68888100	HepG2	liver:	n/a	chr4:68888044-68888055
49	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
50	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68801145-68801195	HRCEpiC	kidney:	n/a
2	chr4:68801145-68801195	HRCEpiC	kidney:	n/a
3	chr4:68830227-68830277	K562	blood:	n/a
4	chr4:68929020-68929070	ovcar-3	ovarian:	n/a
5	chr4:68929020-68929070	HNPCEpiC	eye:	n/a
6	chr4:68995759-68995809	PANC-1	pancreas:	n/a
7	chr4:68801145-68801195	HAEpiC	amniotic membrane:	n/a
8	chr4:68900280-68900330	NHBE	bronchial:	n/a
9	chr4:68904160-68904210	AG04449	skin:	fetal
10	chr4:68930433-68930483	PANC-1	pancreas:	n/a
11	chr4:68919575-68919625	NHBE	bronchial:	n/a
12	chr4:68929005-68929055	HEK293	kidney:	embryo
13	chr4:68928981-68929031	HL-60	blood:	n/a
14	chr4:68801145-68801195	U87	brain:	n/a
15	chr4:68900280-68900330	AG04450	lung:	fetal
16	chr4:68829101-68829151	ECC-1	luminal epithelium:	n/a
17	chr4:68929413-68929463	RPTEC	kidney:	n/a
18	chr4:68801145-68801195	ProgFib	skin:	n/a
19	chr4:68830227-68830277	AG09319	gingival:	n/a
20	chr4:68928981-68929031	ECC-1	luminal epithelium:	n/a
21	chr4:68995995-68996045	AG10803	skin:	n/a
22	chr4:68801145-68801195	MCF10A-Er-Src	breast:	n/a
23	chr4:68929020-68929070	HepG2	liver:	n/a
24	chr4:68929413-68929463	BE2_C	brain:	n/a
25	chr4:68801145-68801195	BJ	skin:	n/a
26	chr4:68995759-68995809	HEK293	kidney:	embryo
27	chr4:68904160-68904210	MCF10A-Er-Src	breast:	n/a
28	chr4:68929005-68929055	BJ	skin:	n/a
29	chr4:68995759-68995809	PrEC	prostate:	n/a
30	chr4:68929005-68929055	HCM	heart:	n/a
31	chr4:68904160-68904210	GM06990	blood:	n/a
32	chr4:68995759-68995809	AG09319	gingival:	n/a
33	chr4:68929020-68929070	Jurkat	blood:	n/a
34	chr4:68829101-68829151	HL-60	blood:	n/a
35	chr4:68929020-68929070	PFSK-1	brain:	n/a
36	chr4:68904160-68904210	HL-60	blood:	n/a
37	chr4:68830227-68830277	HUVEC	blood vessel:	n/a
38	chr4:68928981-68929031	NT2-D1	testis:	n/a
39	chr4:68995995-68996045	HRCEpiC	kidney:	n/a
40	chr4:68801145-68801195	HEK293	kidney:	embryo
41	chr4:68930433-68930483	HL-60	blood:	n/a
42	chr4:68928981-68929031	Hepatocyte	liver:	n/a
43	chr4:68929413-68929463	HUVEC	blood vessel:	n/a
44	chr4:68900280-68900330	BJ	skin:	n/a
45	chr4:68995759-68995809	AG09309	skin:	n/a
46	chr4:68929005-68929055	GM12892	blood:	n/a
47	chr4:68904160-68904210	SAEC	small airway:	n/a
48	chr4:68829101-68829151	NT2-D1	testis:	n/a
49	chr4:68919575-68919625	HUVEC	blood vessel:	n/a
50	chr4:68801145-68801195	HPAEpiC	pulmonary alveolar:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
2	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
3	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
4	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
5	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
6	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
7	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
8	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
9	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
10	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
11	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
12	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
13	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
14	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
15	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
16	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
17	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
18	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
19	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
20	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
21	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
22	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
23	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
24	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
25	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
26	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
27	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
28	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
29	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
30	chr4:68577504..68578308-chr4:68794030..68794919,2	MCF-7	breast:
31	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
32	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
33	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
34	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
35	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
36	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
37	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
38	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
39	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
40	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
41	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
42	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
43	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
44	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
45	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
46	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
47	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
48	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
49	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
50	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11A-2	chr4:68928266-68928986	NONHSAT147287
2	lnc-TMPRSS11A-2	chr4:68926328-68927569	NONHSAT096721
3	lnc-TMPRSS11A-2	chr4:68927540-68928987	NONHSAT096722
4	lnc-TMPRSS11E-1	chr4:68938823-68938951	NONHSAT096719
5	lnc-TMPRSS11E-1	chr4:68943181-68943348	ENSG00000248049
6	lnc-TMPRSS11E-1	chr4:68945839-68946363	ENSG00000248049
7	lnc-TMPRSS11E-1	chr4:68928325-68928939	ENSG00000248049
8	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096720
9	lnc-TMPRSS11E-1	chr4:68942997-68943139	ENSG00000248049
10	lnc-TMPRSS11E-1	chr4:68919226-68919276	NONHSAT096719
11	lnc-TMPRSS11E-1	chr4:68928801-68928939	ENSG00000248049
12	lnc-TMPRSS11E-1	chr4:68945839-68946670	ENSG00000248049
13	lnc-TMPRSS11A-2	chr4:68926583-68927569	NONHSAT096720
14	lnc-TMPRSS11E-1	chr4:68928780-68928939	ENSG00000248049
15	lnc-TMPRSS11E-1	chr4:68945839-68945944	ENSG00000248049
16	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096721
17	lnc-TMPRSS11A-2	chr4:68926312-68926518	NONHSAT096720
18	lnc-TMPRSS11E-1	chr4:68926333-68928939	NONHSAT096719

No data

Variant related genes	Relation type
GCOM2	TF binding region
SYT14L	TF binding region
TMPRSS11A	TF binding region
UBA6-AS1	TF binding region
RNU6-95P	TF binding region
TMPRSS11F	TF binding region
TMPRSS11GP	TF binding region
GCOM2	CpG island
SYT14L	CpG island
TMPRSS11A	CpG island
UBA6-AS1	CpG island
RNU6-95P	CpG island
TMPRSS11F	CpG island
TMPRSS11GP	CpG island
ENSG00000270228	chromatin interactions
ENSG00000198092	chromatin interactions
ENSG00000033178	chromatin interactions
ENSG00000175582	chromatin interactions
ENSG00000248049	chromatin interactions
KLHL15	miRNA target sites
RALGPS2	miRNA target sites
DDX50	miRNA target sites
ASPH	miRNA target sites
BRD1	miRNA target sites
GOLGA6A	miRNA target sites
BCL2L11	miRNA target sites
DICER1	miRNA target sites

Extended variants
information (count: 3951 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3951 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189458159	chr4:68789567-68789568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534280937	chr4:68789603-68789604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553902795	chr4:68789608-68789609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567620170	chr4:68789618-68789619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531376273	chr4:68789674-68789675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149179048	chr4:68789694-68789695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200548724	chr4:68789695-68789696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536556027	chr4:68789707-68789708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376145918	chr4:68789709-68789710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576325246	chr4:68789721-68789722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180796856	chr4:68789722-68789723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545238566	chr4:68789728-68789729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558711606	chr4:68789732-68789733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571835474	chr4:68789739-68789740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80321743	chr4:68789748-68789749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6839279	chr4:68789778-68789779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186038072	chr4:68789799-68789800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376811083	chr4:68789824-68789825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369884437	chr4:68789833-68789834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373447572	chr4:68789853-68789854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144009146	chr4:68789866-68789867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200746363	chr4:68789906-68789907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370139605	chr4:68789909-68789910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201795879	chr4:68789916-68789917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566293897	chr4:68789961-68789962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563617746	chr4:68789976-68789977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142521133	chr4:68790017-68790018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552432223	chr4:68790036-68790037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565352774	chr4:68790058-68790059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28434494	chr4:68790066-68790067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs527801981	chr4:68790082-68790083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547831857	chr4:68790090-68790091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191279730	chr4:68790143-68790144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536697648	chr4:68790167-68790168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549757175	chr4:68790179-68790180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112923771	chr4:68790184-68790185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367916263	chr4:68790194-68790195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538923149	chr4:68790269-68790270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143366965	chr4:68790281-68790282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572565294	chr4:68790305-68790306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373395792	chr4:68790323-68790324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534428226	chr4:68790347-68790348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554599631	chr4:68790425-68790426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115994432	chr4:68790429-68790430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76068672	chr4:68790444-68790445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181302678	chr4:68790502-68790503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185898235	chr4:68790629-68790630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546086920	chr4:68790633-68790634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559600198	chr4:68790650-68790651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148005544	chr4:68790675-68790676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68779800-68792200	Weak transcription	Esophagus	oesophagus
2	chr4:68792200-68792400	ZNF genes & repeats	Esophagus	oesophagus
3	chr4:68792200-68793400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:68792400-68793200	Genic enhancers	Esophagus	oesophagus
5	chr4:68792600-68793400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:68792600-68793600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:68793000-68793200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:68793000-68793400	Enhancers	Spleen	Spleen
9	chr4:68793200-68793400	ZNF genes & repeats	Esophagus	oesophagus
10	chr4:68793200-68794400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
12	chr4:68793600-68794800	Enhancers	Primary hematopoietic stem cells	blood
13	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
18	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:68794400-68796000	Enhancers	HMEC	breast
21	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:68794400-68797800	Enhancers	NHEK	skin
23	chr4:68794600-68795200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:68797800-68800200	Weak transcription	NHEK	skin
33	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:68798600-68802000	Enhancers	Dnd41	blood
35	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
48	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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