Variant report

Variant	esv2759257
Chromosome Location	chr4:68777006-69028913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1120)
CpG islands
(count:793)
Chromatin interactive
region (count:74)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr4:68794343-68794570	K562	blood:	n/a	n/a
4	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
5	ATF1	chr4:68799641-68799825	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	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:68990022-68990381	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	chr4:69012748-69013185	K562	blood:	n/a	n/a
13	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:69012824-69013135	K562	blood:	n/a	n/a
15	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
16	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
17	CEBPB	chr4:69014522-69014797	K562	blood:	n/a	n/a
18	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
19	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
21	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
22	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
24	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
26	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
28	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
29	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
30	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
31	CEBPB	chr4:69015854-69016082	HepG2	liver:	n/a	chr4:69015942-69015953
32	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
33	CEBPB	chr4:68888023-68888100	HepG2	liver:	n/a	chr4:68888044-68888055
34	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
35	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
36	CEBPB	chr4:68794230-68794706	MCF-7	breast:	n/a	n/a
37	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
38	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
39	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
40	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
42	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
43	CEBPB	chr4:69014530-69014780	K562	blood:	n/a	n/a
44	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
45	CEBPB	chr4:69015863-69016001	K562	blood:	n/a	chr4:69015942-69015953
46	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
47	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
48	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
50	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68919575-68919625	GM19239	blood:	n/a
2	chr4:68995759-68995809	BJ	skin:	n/a
3	chr4:68830227-68830277	HAEpiC	amniotic membrane:	n/a
4	chr4:68929005-68929055	IMR90	lung:	fetal
5	chr4:68995995-68996045	HL-60	blood:	n/a
6	chr4:68929020-68929070	SAEC	small airway:	n/a
7	chr4:68830227-68830277	MCF-7	breast:	n/a
8	chr4:68919575-68919625	H1-hESC	embryonic stem cell:	embryo
9	chr4:68929020-68929070	CMK	blood:	n/a
10	chr4:68830227-68830277	SK-N-SH	brain:	n/a
11	chr4:68904160-68904210	HRCEpiC	kidney:	n/a
12	chr4:68930433-68930483	MCF10A-Er-Src	breast:	n/a
13	chr4:68930433-68930483	PrEC	prostate:	n/a
14	chr4:68929005-68929055	HAEpiC	amniotic membrane:	n/a
15	chr4:68929005-68929055	NH-A	brain:	n/a
16	chr4:68929005-68929055	GM19239	blood:	n/a
17	chr4:68930433-68930483	CMK	blood:	n/a
18	chr4:68829101-68829151	A549	lung:	n/a
19	chr4:68904160-68904210	NHDF-neo	bronchial:	n/a
20	chr4:68801145-68801195	HIPEpiC	eye:	n/a
21	chr4:68904160-68904210	HCM	heart:	n/a
22	chr4:68830227-68830277	CMK	blood:	n/a
23	chr4:68900280-68900330	SAEC	small airway:	n/a
24	chr4:68919575-68919625	AoSMC	blood vessel:	n/a
25	chr4:68829101-68829151	HCM	heart:	n/a
26	chr4:68929413-68929463	SK-N-MC	brain:	n/a
27	chr4:68900280-68900330	HCPEpiC	choroid plexus:	n/a
28	chr4:68929020-68929070	IMR90	lung:	fetal
29	chr4:68904160-68904210	ECC-1	luminal epithelium:	n/a
30	chr4:68930433-68930483	HepG2	liver:	n/a
31	chr4:68929020-68929070	BJ	skin:	n/a
32	chr4:68995995-68996045	GM12891	blood:	n/a
33	chr4:68829101-68829151	AoSMC	blood vessel:	n/a
34	chr4:68995759-68995809	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:68830227-68830277	H1-hESC	embryonic stem cell:	embryo
36	chr4:68929020-68929070	LNCaP	prostate:	n/a
37	chr4:68929020-68929070	HEK293	kidney:	embryo
38	chr4:68928981-68929031	NT2-D1	testis:	n/a
39	chr4:68919575-68919625	AG04450	lung:	fetal
40	chr4:68995995-68996045	HRCEpiC	kidney:	n/a
41	chr4:68929005-68929055	SK-N-SH_RA	brain:	n/a
42	chr4:68930433-68930483	IMR90	lung:	fetal
43	chr4:68928981-68929031	HIPEpiC	eye:	n/a
44	chr4:68929005-68929055	NT2-D1	testis:	n/a
45	chr4:68929020-68929070	AG10803	skin:	n/a
46	chr4:68929413-68929463	AG04450	lung:	fetal
47	chr4:68900280-68900330	AoSMC	blood vessel:	n/a
48	chr4:68829101-68829151	BE2_C	brain:	n/a
49	chr4:68928981-68929031	HepG2	liver:	n/a
50	chr4:68929413-68929463	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
2	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
3	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
4	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
5	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:
6	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
7	chr4:68737188..68737967-chr4:68783944..68784741,2	MCF-7	breast:
8	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
9	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
10	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
11	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
12	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
13	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
14	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
15	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
16	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
17	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
18	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
19	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
20	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
21	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
22	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
23	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
24	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
25	chr4:69014952..69016678-chr4:69016935..69018473,2	K562	blood:
26	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
27	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
28	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
29	chr4:68784332..68784862-chr4:69040988..69041632,2	MCF-7	breast:
30	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
31	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
32	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
33	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
34	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
35	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
36	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
37	chr4:68785311..68788293-chr4:68790779..68793140,2	MCF-7	breast:
38	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
39	chr4:68783821..68784619-chr4:69040970..69041992,6	MCF-7	breast:
40	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
41	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
42	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
43	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
44	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
45	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
46	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
47	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
48	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
49	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
50	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:

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

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

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
ENSG00000248049	chromatin interactions
ENSG00000033178	chromatin interactions
ENSG00000198092	chromatin interactions
ENSG00000270228	chromatin interactions
ENSG00000175582	chromatin interactions
RALGPS2	miRNA target sites
BRD1	miRNA target sites
DICER1	miRNA target sites
KLHL15	miRNA target sites
ASPH	miRNA target sites
BCL2L11	miRNA target sites
DDX50	miRNA target sites
GOLGA6A	miRNA target sites

Extended variants
information (count: 4860 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4860 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368829002	chr4:68777022-68777023	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548530297	chr4:68777024-68777025	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114594588	chr4:68777041-68777042	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs12646286	chr4:68777054-68777055	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs371262351	chr4:68777055-68777056	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375027937	chr4:68777063-68777064	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562773026	chr4:68777091-68777092	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369203246	chr4:68777092-68777093	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373272353	chr4:68777105-68777106	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376494815	chr4:68777129-68777130	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201118203	chr4:68777157-68777158	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148638761	chr4:68777174-68777175	Active TSS Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372154196	chr4:68777204-68777205	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199876613	chr4:68777260-68777261	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539133310	chr4:68777318-68777319	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77398428	chr4:68777323-68777324	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572132189	chr4:68777358-68777359	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373636400	chr4:68777383-68777384	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77085778	chr4:68777410-68777411	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554793161	chr4:68777427-68777428	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554879249	chr4:68777454-68777455	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574685013	chr4:68777464-68777465	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184071694	chr4:68777515-68777516	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75578795	chr4:68777548-68777549	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576827613	chr4:68777588-68777589	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545902526	chr4:68777644-68777645	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573220625	chr4:68777649-68777650	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117664968	chr4:68777659-68777660	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375721600	chr4:68777665-68777666	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185779324	chr4:68777683-68777684	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189710557	chr4:68777684-68777685	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111874831	chr4:68777761-68777762	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76126216	chr4:68777766-68777767	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530829872	chr4:68777783-68777784	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565192915	chr4:68777792-68777793	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143409469	chr4:68777814-68777815	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146814916	chr4:68777861-68777862	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs182341212	chr4:68777887-68777888	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112191739	chr4:68777994-68777995	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs72285357	chr4:68778000-68778001	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs398107464	chr4:68778001-68778002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74888390	chr4:68778023-68778024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113318206	chr4:68778024-68778025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77564468	chr4:68778025-68778026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186958088	chr4:68778039-68778040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541786808	chr4:68778055-68778056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191806087	chr4:68778144-68778145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140633251	chr4:68778169-68778170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534739121	chr4:68778170-68778171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145702886	chr4:68778185-68778186	Weak transcription Enhancers	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
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
Schizophrenia	20967226	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68773800-68779000	Weak transcription	Esophagus	oesophagus
2	chr4:68776800-68777200	Enhancers	Stomach Mucosa	stomach
3	chr4:68776800-68778000	Weak transcription	Fetal Intestine Small	intestine
4	chr4:68777000-68777200	Flanking Active TSS	Duodenum Mucosa	Duodenum
5	chr4:68777000-68778000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:68777800-68778600	Enhancers	Fetal Intestine Large	intestine
7	chr4:68778000-68778400	Enhancers	Fetal Intestine Small	intestine
8	chr4:68779000-68779800	ZNF genes & repeats	Esophagus	oesophagus
9	chr4:68779800-68792200	Weak transcription	Esophagus	oesophagus
10	chr4:68780200-68781000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:68781000-68782000	Enhancers	Dnd41	blood
12	chr4:68781200-68781600	Enhancers	Fetal Thymus	thymus
13	chr4:68785400-68785800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:68785800-68786000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr4:68785800-68788400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:68788200-68788800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:68788400-68788800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:68788400-68789000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:68788600-68789000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr4:68792200-68792400	ZNF genes & repeats	Esophagus	oesophagus
21	chr4:68792200-68793400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:68792400-68793200	Genic enhancers	Esophagus	oesophagus
23	chr4:68792600-68793400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr4:68792600-68793600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:68793000-68793200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:68793000-68793400	Enhancers	Spleen	Spleen
27	chr4:68793200-68793400	ZNF genes & repeats	Esophagus	oesophagus
28	chr4:68793200-68794400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
30	chr4:68793600-68794800	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
36	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:68794400-68796000	Enhancers	HMEC	breast
39	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:68794400-68797800	Enhancers	NHEK	skin
41	chr4:68794600-68795200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:68797800-68800200	Weak transcription	NHEK	skin

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