Variant report

Variant	esv1806791
Chromosome Location	chr4:68781695-69018980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1095)
CpG islands
(count:793)
Chromatin interactive
region (count:74)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1095 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	chr4:68799641-68799825	K562	blood:	n/a	n/a
3	ATF1	chr4:69014644-69014829	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	ATF1	chr4:69018227-69018433	K562	blood:	n/a	n/a
7	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
8	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
11	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
13	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
14	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
15	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
16	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
17	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
18	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
19	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
20	CEBPB	chr4:69014530-69014780	K562	blood:	n/a	n/a
21	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
22	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
23	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
24	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
25	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
26	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
27	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
28	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a
30	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
32	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
33	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
34	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
35	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
36	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
37	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
38	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
39	CEBPB	chr4:68856283-68856483	K562	blood:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
40	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
42	CEBPB	chr4:69015863-69016001	K562	blood:	n/a	chr4:69015942-69015953
43	CEBPB	chr4:69014522-69014797	K562	blood:	n/a	n/a
44	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:69015854-69016082	HepG2	liver:	n/a	chr4:69015942-69015953
46	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
47	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
48	CEBPB	chr4:68894925-68895100	HepG2	liver:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
49	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68904160-68904210	SAEC	small airway:	n/a
2	chr4:68904160-68904210	MCF10A-Er-Src	breast:	n/a
3	chr4:68919575-68919625	Caco-2	colon:	n/a
4	chr4:68929413-68929463	GM12878	blood:	n/a
5	chr4:68900280-68900330	ProgFib	skin:	n/a
6	chr4:68904160-68904210	MCF-7	breast:	n/a
7	chr4:68919575-68919625	GM12892	blood:	n/a
8	chr4:68929005-68929055	GM12878	blood:	n/a
9	chr4:68904160-68904210	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:68929005-68929055	HepG2	liver:	n/a
11	chr4:68995995-68996045	HIPEpiC	eye:	n/a
12	chr4:68900280-68900330	GM12892	blood:	n/a
13	chr4:68830227-68830277	GM19239	blood:	n/a
14	chr4:68930433-68930483	Caco-2	colon:	n/a
15	chr4:68829101-68829151	PrEC	prostate:	n/a
16	chr4:68929005-68929055	HCT-116	colon:	n/a
17	chr4:68995995-68996045	PrEC	prostate:	n/a
18	chr4:68930433-68930483	GM12878	blood:	n/a
19	chr4:68929413-68929463	Caco-2	colon:	n/a
20	chr4:68928981-68929031	HCM	heart:	n/a
21	chr4:68929413-68929463	NHDF-neo	bronchial:	n/a
22	chr4:68929020-68929070	HEK293	kidney:	embryo
23	chr4:68929020-68929070	SK-N-SH_RA	brain:	n/a
24	chr4:68801145-68801195	AG09309	skin:	n/a
25	chr4:68829101-68829151	HEEpiC	esophagus:	n/a
26	chr4:68801145-68801195	HCM	heart:	n/a
27	chr4:68930433-68930483	LNCaP	prostate:	n/a
28	chr4:68900280-68900330	ECC-1	luminal epithelium:	n/a
29	chr4:68900280-68900330	SAEC	small airway:	n/a
30	chr4:68830227-68830277	AG04450	lung:	fetal
31	chr4:68900280-68900330	HEEpiC	esophagus:	n/a
32	chr4:68929020-68929070	NHBE	bronchial:	n/a
33	chr4:68900280-68900330	HEK293	kidney:	embryo
34	chr4:68929413-68929463	Hela-S3	cervix:	n/a
35	chr4:68928981-68929031	T-47D	breast:	n/a
36	chr4:68995759-68995809	HCF	heart:	n/a
37	chr4:68830227-68830277	HMEC	breast:	n/a
38	chr4:68995995-68996045	NH-A	brain:	n/a
39	chr4:68995995-68996045	ProgFib	skin:	n/a
40	chr4:68995995-68996045	H1-hESC	embryonic stem cell:	embryo
41	chr4:68829101-68829151	ProgFib	skin:	n/a
42	chr4:68801145-68801195	GM12892	blood:	n/a
43	chr4:68801145-68801195	GM12891	blood:	n/a
44	chr4:68995995-68996045	Hela-S3	cervix:	n/a
45	chr4:68801145-68801195	U87	brain:	n/a
46	chr4:68900280-68900330	A549	lung:	n/a
47	chr4:68829101-68829151	K562	blood:	n/a
48	chr4:68830227-68830277	HIPEpiC	eye:	n/a
49	chr4:68995995-68996045	HRE	kidney:	n/a
50	chr4:68995995-68996045	AG09319	gingival:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
2	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
3	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
4	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
5	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
6	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
7	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
8	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
9	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
10	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
11	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
12	chr4:68784332..68784862-chr4:69040988..69041632,2	MCF-7	breast:
13	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
14	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
15	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
16	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
17	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
18	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
19	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
20	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
21	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
22	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
23	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
24	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
25	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
26	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
27	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
28	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
29	chr4:68577504..68578308-chr4:68794030..68794919,2	MCF-7	breast:
30	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
31	chr4:68784466..68787667-chr4:69042128..69044915,3	MCF-7	breast:
32	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
33	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
34	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
35	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
36	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
37	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
38	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
39	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
40	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
41	chr4:68774616..68776298-chr4:68783211..68785677,2	K562	blood:
42	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
43	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
44	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
45	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
46	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
47	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
48	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
49	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
50	chr4:68783821..68784619-chr4:69040970..69041992,6	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 4349 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4349 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs353169	chr4:68781714-68781715	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558712442	chr4:68781735-68781736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543713998	chr4:68781757-68781758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs353168	chr4:68781760-68781761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183306207	chr4:68781829-68781830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139311355	chr4:68781887-68781888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs60057735	chr4:68781889-68781890	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs562995733	chr4:68781934-68781935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371083474	chr4:68781958-68781959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188160818	chr4:68781969-68781970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559662435	chr4:68781989-68781990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529367239	chr4:68782022-68782023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545319541	chr4:68782032-68782033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565122630	chr4:68782046-68782047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376294991	chr4:68782102-68782103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145257518	chr4:68782124-68782125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527413664	chr4:68782175-68782176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71669184	chr4:68782191-68782192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71219074	chr4:68782214-68782215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199575200	chr4:68782223-68782224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547060860	chr4:68782261-68782262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs116131379	chr4:68782268-68782269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566055123	chr4:68782269-68782270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149134828	chr4:68782288-68782289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569896783	chr4:68782310-68782311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367651967	chr4:68782355-68782356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371769708	chr4:68782399-68782400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552434167	chr4:68782413-68782414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565854261	chr4:68782415-68782416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534306721	chr4:68782418-68782419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376639914	chr4:68782429-68782430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143251015	chr4:68782438-68782439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151324849	chr4:68782450-68782451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534987887	chr4:68782475-68782476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536298450	chr4:68782493-68782494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79481134	chr4:68782618-68782619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576700088	chr4:68782645-68782646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72643693	chr4:68782699-68782700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372864948	chr4:68782705-68782706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78529076	chr4:68782758-68782759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571926487	chr4:68782804-68782805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140641091	chr4:68782823-68782824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540735982	chr4:68782894-68782895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533590883	chr4:68782963-68782964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115531109	chr4:68783065-68783066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4860865	chr4:68783072-68783073	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs80140581	chr4:68783083-68783084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532329329	chr4:68783098-68783099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552469524	chr4:68783217-68783218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191798365	chr4:68783241-68783242	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:276 , 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	chr4:68781000-68782000	Enhancers	Dnd41	blood
3	chr4:68785400-68785800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:68785800-68786000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:68785800-68788400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:68788200-68788800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:68788400-68788800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:68788400-68789000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:68788600-68789000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr4:68792200-68792400	ZNF genes & repeats	Esophagus	oesophagus
11	chr4:68792200-68793400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:68792400-68793200	Genic enhancers	Esophagus	oesophagus
13	chr4:68792600-68793400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:68792600-68793600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:68793000-68793200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:68793000-68793400	Enhancers	Spleen	Spleen
17	chr4:68793200-68793400	ZNF genes & repeats	Esophagus	oesophagus
18	chr4:68793200-68794400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
20	chr4:68793600-68794800	Enhancers	Primary hematopoietic stem cells	blood
21	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
26	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:68794400-68796000	Enhancers	HMEC	breast
29	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:68794400-68797800	Enhancers	NHEK	skin
31	chr4:68794600-68795200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:68797800-68800200	Weak transcription	NHEK	skin
41	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:68798600-68802000	Enhancers	Dnd41	blood
43	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
47	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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