Variant report

Variant	nsv879219
Chromosome Location	chr4:68743032-69028913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1496)
CpG islands
(count:979)
Chromatin interactive
region (count:79)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1496 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	ARID3A	chr4:68776107-68776264	HepG2	liver:	n/a	n/a
3	ATF1	chr4:68794343-68794570	K562	blood:	n/a	n/a
4	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
5	ATF1	chr4:69014644-69014829	K562	blood:	n/a	n/a
6	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
7	ATF1	chr4:69018227-69018433	K562	blood:	n/a	n/a
8	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
9	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
12	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
15	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
16	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
17	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
18	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
19	CEBPB	chr4:68751495-68752334	IMR90	lung:	n/a	chr4:68752041-68752054
20	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:68775720-68775923	H1-hESC	embryonic stem cell:	n/a	chr4:68775829-68775840
22	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
23	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
24	CEBPB	chr4:68775659-68776005	Hela-S3	cervix:	n/a	chr4:68775829-68775840
25	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
26	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
27	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
28	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
29	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
31	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
32	CEBPB	chr4:68886657-68887443	HCT-116	colon:	n/a	n/a
33	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
34	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
35	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
36	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
37	CEBPB	chr4:68775691-68776000	A549	lung:	n/a	chr4:68775829-68775840
38	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
39	CEBPB	chr4:69014530-69014780	K562	blood:	n/a	n/a
40	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
42	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
43	CEBPB	chr4:68775653-68776022	IMR90	lung:	n/a	chr4:68775829-68775840
44	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
45	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
46	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
47	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
48	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
49	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
50	CEBPB	chr4:68775665-68776273	K562	blood:	n/a	chr4:68775829-68775840

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68751711-68751761	Jurkat	blood:	n/a
2	chr4:68904160-68904210	HEK293	kidney:	embryo
3	chr4:68919575-68919625	HCPEpiC	choroid plexus:	n/a
4	chr4:68751711-68751761	Jurkat	blood:	n/a
5	chr4:68904160-68904210	HEK293	kidney:	embryo
6	chr4:68919575-68919625	HCPEpiC	choroid plexus:	n/a
7	chr4:68750080-68750130	Jurkat	blood:	n/a
8	chr4:68928981-68929031	NHBE	bronchial:	n/a
9	chr4:68829101-68829151	AG04449	skin:	fetal
10	chr4:68929020-68929070	RPTEC	kidney:	n/a
11	chr4:68751711-68751761	AG09319	gingival:	n/a
12	chr4:68904160-68904210	HAEpiC	amniotic membrane:	n/a
13	chr4:68929020-68929070	MCF-7	breast:	n/a
14	chr4:68929413-68929463	MCF-7	breast:	n/a
15	chr4:68919575-68919625	RPTEC	kidney:	n/a
16	chr4:68904160-68904210	PANC-1	pancreas:	n/a
17	chr4:68776652-68776702	A549	lung:	n/a
18	chr4:68750080-68750130	GM12878	blood:	n/a
19	chr4:68751711-68751761	HCT-116	colon:	n/a
20	chr4:68829101-68829151	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:68919575-68919625	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:68900280-68900330	HIPEpiC	eye:	n/a
23	chr4:68829101-68829151	HRPEpiC	eye:	n/a
24	chr4:68929005-68929055	GM12878	blood:	n/a
25	chr4:68830227-68830277	HEEpiC	esophagus:	n/a
26	chr4:68829101-68829151	U87	brain:	n/a
27	chr4:68900280-68900330	HUVEC	blood vessel:	n/a
28	chr4:68904160-68904210	IMR90	lung:	fetal
29	chr4:68829101-68829151	NHDF-neo	bronchial:	n/a
30	chr4:68776652-68776702	H1-hESC	embryonic stem cell:	embryo
31	chr4:68995759-68995809	SK-N-SH	brain:	n/a
32	chr4:68928981-68929031	NB4	blood:	n/a
33	chr4:68830227-68830277	Jurkat	blood:	n/a
34	chr4:68776652-68776702	HCT-116	colon:	n/a
35	chr4:68830227-68830277	NB4	blood:	n/a
36	chr4:68751711-68751761	HCPEpiC	choroid plexus:	n/a
37	chr4:68929005-68929055	K562	blood:	n/a
38	chr4:68995759-68995809	HCM	heart:	n/a
39	chr4:68829101-68829151	HRE	kidney:	n/a
40	chr4:68919575-68919625	ProgFib	skin:	n/a
41	chr4:68928981-68929031	ProgFib	skin:	n/a
42	chr4:68829101-68829151	NH-A	brain:	n/a
43	chr4:68930433-68930483	AG04450	lung:	fetal
44	chr4:68900280-68900330	NHBE	bronchial:	n/a
45	chr4:68751711-68751761	HCM	heart:	n/a
46	chr4:68919575-68919625	HNPCEpiC	eye:	n/a
47	chr4:68801145-68801195	AG04450	lung:	fetal
48	chr4:68930433-68930483	GM06990	blood:	n/a
49	chr4:68750080-68750130	HEEpiC	esophagus:	n/a
50	chr4:68829101-68829151	HEK293	kidney:	embryo

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
2	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
3	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
4	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
5	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
6	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
7	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
8	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
9	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
10	chr4:68784466..68787667-chr4:69042128..69044915,3	MCF-7	breast:
11	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
12	chr4:68747971..68750609-chr4:68750969..68752547,2	MCF-7	breast:
13	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
14	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
15	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
16	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
17	chr4:68783821..68784619-chr4:69040970..69041992,6	MCF-7	breast:
18	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
19	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
20	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
21	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
22	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
23	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
24	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
25	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
26	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
27	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
28	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
29	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
30	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
31	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
32	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
33	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
34	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
35	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
36	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
37	chr4:68414627..68415373-chr4:68775821..68776638,2	MCF-7	breast:
38	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
39	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
40	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
41	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
42	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
43	chr4:68737188..68737967-chr4:68783944..68784741,2	MCF-7	breast:
44	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
45	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
46	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
47	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
48	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
49	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
50	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS11E-1	chr4:68928780-68928939	ENSG00000248049
2	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096720
3	lnc-TMPRSS11E-1	chr4:68945839-68946670	ENSG00000248049
4	lnc-TMPRSS11A-2	chr4:68927540-68928987	NONHSAT096722
5	lnc-TMPRSS11E-1	chr4:68945839-68946363	ENSG00000248049
6	lnc-TMPRSS11A-2	chr4:68926583-68927569	NONHSAT096720
7	lnc-TMPRSS11E-1	chr4:68938823-68938951	NONHSAT096719
8	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096721
9	lnc-GNRHR-5	chr4:68749644-68749719	NONHSAT096713
10	lnc-GNRHR-5	chr4:68749644-68749678	NONHSAT096715
11	lnc-GNRHR-5	chr4:68749644-68749716	NONHSAT096714
12	lnc-TMPRSS11A-2	chr4:68926312-68926518	NONHSAT096720
13	lnc-TMPRSS11E-1	chr4:68945839-68945944	ENSG00000248049
14	lnc-TMPRSS11A-2	chr4:68928266-68928986	NONHSAT147287
15	lnc-TMPRSS11E-1	chr4:68942997-68943139	ENSG00000248049
16	lnc-TMPRSS11E-1	chr4:68919226-68919276	NONHSAT096719
17	lnc-TMPRSS11E-1	chr4:68928325-68928939	ENSG00000248049
18	lnc-TMPRSS11E-1	chr4:68926333-68928939	NONHSAT096719
19	lnc-TMPRSS11A-2	chr4:68926328-68927569	NONHSAT096721
20	lnc-TMPRSS11E-1	chr4:68928801-68928939	ENSG00000248049
21	lnc-TMPRSS11E-1	chr4:68943181-68943348	ENSG00000248049

No data

Variant related genes	Relation type
TMPRSS11D	TF binding region
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
TMPRSS11D	CpG island
GCOM2	CpG island
SYT14L	CpG island
TMPRSS11A	CpG island
UBA6-AS1	CpG island
RNU6-95P	CpG island
TMPRSS11F	CpG island
TMPRSS11GP	CpG island
ENSG00000153802	chromatin interactions
ENSG00000248049	chromatin interactions
ENSG00000198092	chromatin interactions
ENSG00000175582	chromatin interactions
ENSG00000270228	chromatin interactions
ENSG00000033178	chromatin interactions
BCL2L11	miRNA target sites
BRD1	miRNA target sites
DICER1	miRNA target sites
GOLGA6A	miRNA target sites
KLHL15	miRNA target sites
ASPH	miRNA target sites
DDX50	miRNA target sites
RALGPS2	miRNA target sites

Extended variants
information (count: 6060 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6060 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7670723	chr4:68743032-68743033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76728422	chr4:68743035-68743036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80128658	chr4:68743051-68743052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536700062	chr4:68743058-68743059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562554182	chr4:68743068-68743069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139903642	chr4:68743110-68743111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554059498	chr4:68743164-68743165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531876879	chr4:68743165-68743166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75931751	chr4:68743172-68743173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545413808	chr4:68743175-68743176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559576558	chr4:68743286-68743287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573088151	chr4:68743323-68743324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74668801	chr4:68743335-68743336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561779193	chr4:68743336-68743337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373237113	chr4:68743368-68743369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530736187	chr4:68743371-68743372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550265174	chr4:68743394-68743395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563795354	chr4:68743412-68743413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372040411	chr4:68743442-68743443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573733120	chr4:68743478-68743479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186594304	chr4:68743520-68743521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566356853	chr4:68743554-68743555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190270514	chr4:68743609-68743610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181923892	chr4:68743697-68743698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186240998	chr4:68743731-68743732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75650065	chr4:68743739-68743740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541089815	chr4:68743754-68743755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536697573	chr4:68743827-68743828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78866606	chr4:68743840-68743841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142174571	chr4:68743861-68743862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539404256	chr4:68743895-68743896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567575652	chr4:68743936-68743937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151269475	chr4:68743954-68743955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573089312	chr4:68743956-68743957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs114726310	chr4:68744006-68744007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555716176	chr4:68744094-68744095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575483919	chr4:68744108-68744109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1899219	chr4:68744117-68744118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs563756353	chr4:68744147-68744148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369725823	chr4:68744193-68744194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532697049	chr4:68744252-68744253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534436150	chr4:68744319-68744320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546177887	chr4:68744322-68744323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559443712	chr4:68744339-68744340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528493264	chr4:68744407-68744408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191046306	chr4:68744427-68744428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10023103	chr4:68744470-68744471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182127422	chr4:68744502-68744503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550796128	chr4:68744513-68744514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185165373	chr4:68744541-68744542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Depressive disorder	21152026	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	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
Schizophrenia	20967226	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68739000-68747000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:68739600-68747400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:68741200-68751400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:68741400-68746600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:68741400-68746800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr4:68741400-68746800	Weak transcription	NHDF-Ad	bronchial
7	chr4:68741400-68751800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr4:68741400-68752800	Weak transcription	Esophagus	oesophagus
9	chr4:68741600-68746600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:68741800-68746800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:68742000-68744800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:68744800-68745600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:68744800-68746000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr4:68744800-68746600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr4:68744800-68752800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr4:68745600-68746600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:68746000-68748800	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr4:68746400-68747200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:68746400-68747800	Enhancers	Brain Germinal Matrix	brain
20	chr4:68746400-68747800	Enhancers	Fetal Muscle Leg	muscle
21	chr4:68746600-68746800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:68746600-68747200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr4:68746600-68748200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:68746600-68749600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr4:68746800-68747600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:68746800-68747600	Enhancers	NHEK	skin
27	chr4:68746800-68747800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:68746800-68747800	Enhancers	NHDF-Ad	bronchial
29	chr4:68746800-68748200	Enhancers	HSMM	muscle
30	chr4:68747000-68747600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:68747200-68747600	Enhancers	NHLF	lung
32	chr4:68747200-68747800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:68747200-68747800	Enhancers	HSMMtube	muscle
34	chr4:68747200-68750200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:68747200-68751600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:68747400-68747800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:68747400-68747800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:68747600-68747800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr4:68747600-68748000	Flanking Active TSS	NHEK	skin
40	chr4:68747600-68751200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:68747600-68751600	Weak transcription	NHLF	lung
42	chr4:68747800-68750000	Weak transcription	NHDF-Ad	bronchial
43	chr4:68747800-68750200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:68747800-68750200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:68747800-68751600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:68747800-68751600	Weak transcription	HSMMtube	muscle
47	chr4:68748000-68748400	Enhancers	NHEK	skin
48	chr4:68748200-68748800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:68748200-68751400	Weak transcription	HSMM	muscle
50	chr4:68748400-68749600	Weak transcription	NHEK	skin

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