Variant report

Variant	esv1807198
Chromosome Location	chr4:68865442-69009703
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:611)
Chromatin interactive
region (count:29)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr4:68995507-68995848	K562	blood:	n/a	n/a
3	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
4	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
6	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
8	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
9	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
11	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
12	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:68886657-68887443	HCT-116	colon:	n/a	n/a
14	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
15	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
16	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
17	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
18	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
19	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
20	CEBPB	chr4:68888023-68888100	HepG2	liver:	n/a	chr4:68888044-68888055
21	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
22	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
23	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
25	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
26	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
27	CEBPB	chr4:68894925-68895100	HepG2	liver:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
28	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
29	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
30	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a
31	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
32	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
33	CREB1	chr4:68989221-68989671	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr4:68989350-68989616	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:68942070-68942199	NHEK	skin:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
36	CTCF	chr4:68942085-68942141	LNCaP	prostate:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
37	CTCF	chr4:68942047-68942200	MCF-7	breast:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
38	CTCF	chr4:68942020-68942170	RPTEC	kidney:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
39	CTCF	chr4:68942080-68942230	NHEK	skin:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
40	CTCF	chr4:68941963-68942290	K562	blood:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
41	CTCF	chr4:68946174-68946197	Lung_OC	lung:	n/a	n/a
42	CTCF	chr4:68945840-68945990	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:68942051-68942156	LNCaP	prostate:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
44	CTCF	chr4:68966963-68967066	GM20000	blood:	n/a	n/a
45	CTCF	chr4:68989739-68989777	Lung_OC	lung:	n/a	n/a
46	CTCF	chr4:68866932-68866990	ProgFib	skin:	n/a	n/a
47	CTCF	chr4:68945720-68945870	HCT-116	colon:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799
48	CTCF	chr4:68933580-68933730	HMEC	breast:	n/a	n/a
49	CTCF	chr4:68942054-68942203	GM12878	blood:	n/a	chr4:68942111-68942132 chr4:68942109-68942127
50	CTCF	chr4:68942025-68942215	SK-N-SH_RA	brain:	n/a	chr4:68942111-68942132 chr4:68942109-68942127

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68995995-68996045	BE2_C	brain:	n/a
2	chr4:68995995-68996045	BE2_C	brain:	n/a
3	chr4:68919575-68919625	SKMC	muscle:	n/a
4	chr4:68995995-68996045	NHDF-neo	bronchial:	n/a
5	chr4:68929005-68929055	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:68919575-68919625	ECC-1	luminal epithelium:	n/a
7	chr4:68929005-68929055	GM06990	blood:	n/a
8	chr4:68929413-68929463	SK-N-SH_RA	brain:	n/a
9	chr4:68930433-68930483	HUVEC	blood vessel:	n/a
10	chr4:68929020-68929070	Caco-2	colon:	n/a
11	chr4:68930433-68930483	HL-60	blood:	n/a
12	chr4:68930433-68930483	MCF10A-Er-Src	breast:	n/a
13	chr4:68900280-68900330	ProgFib	skin:	n/a
14	chr4:68995759-68995809	NHBE	bronchial:	n/a
15	chr4:68929020-68929070	HMEC	breast:	n/a
16	chr4:68929413-68929463	RPTEC	kidney:	n/a
17	chr4:68929020-68929070	HL-60	blood:	n/a
18	chr4:68904160-68904210	A549	lung:	n/a
19	chr4:68900280-68900330	AG09309	skin:	n/a
20	chr4:68995759-68995809	Hepatocyte	liver:	n/a
21	chr4:68930433-68930483	HepG2	liver:	n/a
22	chr4:68929413-68929463	AG04449	skin:	fetal
23	chr4:68995995-68996045	HCT-116	colon:	n/a
24	chr4:68929413-68929463	HCM	heart:	n/a
25	chr4:68929020-68929070	AG04450	lung:	fetal
26	chr4:68904160-68904210	SK-N-SH_RA	brain:	n/a
27	chr4:68900280-68900330	GM19239	blood:	n/a
28	chr4:68928981-68929031	AG04449	skin:	fetal
29	chr4:68929413-68929463	HNPCEpiC	eye:	n/a
30	chr4:68930433-68930483	RPTEC	kidney:	n/a
31	chr4:68929413-68929463	HRPEpiC	eye:	n/a
32	chr4:68919575-68919625	SAEC	small airway:	n/a
33	chr4:68904160-68904210	HCF	heart:	n/a
34	chr4:68995759-68995809	HRCEpiC	kidney:	n/a
35	chr4:68929020-68929070	HCF	heart:	n/a
36	chr4:68995995-68996045	NB4	blood:	n/a
37	chr4:68995995-68996045	Hepatocyte	liver:	n/a
38	chr4:68928981-68929031	GM12892	blood:	n/a
39	chr4:68995759-68995809	AG04449	skin:	fetal
40	chr4:68900280-68900330	NHDF-neo	bronchial:	n/a
41	chr4:68929413-68929463	HCPEpiC	choroid plexus:	n/a
42	chr4:68930433-68930483	Hepatocyte	liver:	n/a
43	chr4:68919575-68919625	H1-hESC	embryonic stem cell:	embryo
44	chr4:68929413-68929463	H1-hESC	embryonic stem cell:	embryo
45	chr4:68904160-68904210	HMEC	breast:	n/a
46	chr4:68928981-68929031	HUVEC	blood vessel:	n/a
47	chr4:68929413-68929463	U87	brain:	n/a
48	chr4:68995995-68996045	SK-N-SH	brain:	n/a
49	chr4:68995759-68995809	HCF	heart:	n/a
50	chr4:68929020-68929070	CMK	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
2	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
3	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
4	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
5	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
6	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
7	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
8	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
9	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
10	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
11	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
12	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
13	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
14	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
15	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
16	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
17	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
18	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
19	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
20	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
21	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
22	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
23	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
24	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
25	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
26	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
27	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
28	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
29	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 2113 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2113 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142760853	chr4:68865987-68865988	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs137976728	chr4:68866031-68866032	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs200094771	chr4:68866033-68866034	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs540780739	chr4:68866059-68866060	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs561081385	chr4:68866072-68866073	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs35647446	chr4:68866084-68866085	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs72647125	chr4:68866265-68866266	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs552399787	chr4:68866266-68866267	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs536191505	chr4:68866295-68866296	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs35848639	chr4:68866307-68866308	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs534857747	chr4:68866312-68866313	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs112212801	chr4:68866329-68866330	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs139447412	chr4:68866345-68866346	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs567786311	chr4:68866361-68866362	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs75503531	chr4:68866386-68866387	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs556609994	chr4:68866391-68866392	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs73825314	chr4:68866392-68866393	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs182955669	chr4:68866426-68866427	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs538969331	chr4:68866453-68866454	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs374893406	chr4:68866467-68866468	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs1438411	chr4:68866487-68866488	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1438413	chr4:68866977-68866978	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs13152133	chr4:68867106-68867107	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35289404	chr4:68867119-68867120	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs13120265	chr4:68867120-68867121	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372940045	chr4:68867226-68867227	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs376698053	chr4:68867231-68867232	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs1438414	chr4:68867256-68867257	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs550143952	chr4:68867282-68867283	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs568154823	chr4:68867307-68867308	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs190169283	chr4:68867412-68867413	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs4860879	chr4:68867432-68867433	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139241297	chr4:68867859-68867860	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs1370838	chr4:68867863-68867864	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528969215	chr4:68867892-68867893	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs187383682	chr4:68867893-68867894	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs149995275	chr4:68867910-68867911	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs568403773	chr4:68867930-68867931	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs35471695	chr4:68867939-68867940	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs1370839	chr4:68867956-68867957	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192287103	chr4:68867962-68867963	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs185527809	chr4:68867967-68867968	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs189205668	chr4:68867981-68867982	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs192240852	chr4:68867983-68867984	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs542156598	chr4:68868002-68868003	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs562005063	chr4:68868006-68868007	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs535713423	chr4:68882040-68882041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186128405	chr4:68882962-68882963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs17088953	chr4:68883006-68883007	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs533527047	chr4:68883015-68883016	Inactive region	TF binding region	1 gene(s)	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68884600-68884800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:68885000-68886600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:68886600-68887400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:68886600-68887400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:68886600-68887600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:68886600-68887600	Enhancers	NHEK	skin
7	chr4:68886800-68887600	Enhancers	HMEC	breast
8	chr4:68886800-68888000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:68887000-68889600	Weak transcription	Brain Substantia Nigra	brain
10	chr4:68915600-68916600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:68915800-68916600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr4:68915800-68916600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:68916600-68920000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr4:68916600-68920000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr4:68916600-68920400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr4:68916800-68920200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr4:68920000-68920800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:68920000-68921000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:68920000-68921200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:68920200-68920800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:68920400-68921000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:68920400-68921200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:68920600-68921200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:68927400-68929000	Active TSS	Brain Anterior Caudate	brain
25	chr4:68927600-68928600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:68928000-68928800	Active TSS	Brain Angular Gyrus	brain
27	chr4:68928000-68928800	Active TSS	Brain Cingulate Gyrus	brain
28	chr4:68928000-68928800	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr4:68928000-68929000	Active TSS	Brain Hippocampus Middle	brain
30	chr4:68928200-68928600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:68928200-68928600	Active TSS	K562	blood
32	chr4:68928200-68928800	Active TSS	Brain Substantia Nigra	brain
33	chr4:68932200-68943600	Weak transcription	Esophagus	oesophagus
34	chr4:68936000-68936600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:68936000-68939400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:68936200-68936400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:68936200-68936800	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr4:68936400-68936600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:68936400-68938400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr4:68936600-68937400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr4:68936800-68938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr4:68937200-68938200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:68937400-68939600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr4:68938000-68939600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:68938200-68938400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr4:68938200-68938600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:68938200-68939000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:68938200-68939600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:68938200-68939600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:68938200-68939600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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