Variant report

Variant	esv1808788
Chromosome Location	chr4:68797487-69008251
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:735)
CpG islands
(count:794)
Chromatin interactive
region (count:44)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
4	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
5	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
7	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
8	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
9	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
10	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
11	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
12	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
13	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
14	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
15	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
16	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
17	CEBPB	chr4:68894925-68895100	HepG2	liver:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
18	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
19	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
20	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
21	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
22	CEBPB	chr4:68886657-68887443	HCT-116	colon:	n/a	n/a
23	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
24	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:68854271-68854605	Hela-S3	cervix:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
26	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
27	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
28	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
29	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:68856283-68856483	K562	blood:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
31	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
32	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
34	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
35	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
36	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
37	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
38	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
39	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
40	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
41	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
42	CEBPB	chr4:68888023-68888100	HepG2	liver:	n/a	chr4:68888044-68888055
43	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
44	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a
45	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
46	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
47	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
48	CREB1	chr4:68989350-68989616	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr4:68989221-68989671	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:68945663-68945828	K562	blood:	n/a	chr4:68945782-68945798 chr4:68945783-68945804 chr4:68945781-68945799

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68801145-68801195	CMK	blood:	n/a
2	chr4:68801145-68801195	CMK	blood:	n/a
3	chr4:68801145-68801195	NHBE	bronchial:	n/a
4	chr4:68830227-68830277	NHDF-neo	bronchial:	n/a
5	chr4:68904160-68904210	BJ	skin:	n/a
6	chr4:68900280-68900330	HCF	heart:	n/a
7	chr4:68829101-68829151	NHBE	bronchial:	n/a
8	chr4:68904160-68904210	NT2-D1	testis:	n/a
9	chr4:68928981-68929031	LNCaP	prostate:	n/a
10	chr4:68929020-68929070	PFSK-1	brain:	n/a
11	chr4:68801145-68801195	SK-N-SH	brain:	n/a
12	chr4:68900280-68900330	AG10803	skin:	n/a
13	chr4:68929020-68929070	NHBE	bronchial:	n/a
14	chr4:68830227-68830277	GM12878	blood:	n/a
15	chr4:68928981-68929031	MCF-7	breast:	n/a
16	chr4:68928981-68929031	MCF10A-Er-Src	breast:	n/a
17	chr4:68829101-68829151	HEEpiC	esophagus:	n/a
18	chr4:68929413-68929463	RPTEC	kidney:	n/a
19	chr4:68995995-68996045	AG04449	skin:	fetal
20	chr4:68900280-68900330	AG04450	lung:	fetal
21	chr4:68829101-68829151	SK-N-MC	brain:	n/a
22	chr4:68928981-68929031	Caco-2	colon:	n/a
23	chr4:68995759-68995809	HRE	kidney:	n/a
24	chr4:68930433-68930483	SK-N-SH_RA	brain:	n/a
25	chr4:68929005-68929055	HCPEpiC	choroid plexus:	n/a
26	chr4:68929020-68929070	SKMC	muscle:	n/a
27	chr4:68929005-68929055	GM12892	blood:	n/a
28	chr4:68929020-68929070	GM12892	blood:	n/a
29	chr4:68919575-68919625	NB4	blood:	n/a
30	chr4:68930433-68930483	HCF	heart:	n/a
31	chr4:68929005-68929055	IMR90	lung:	fetal
32	chr4:68929005-68929055	MCF10A-Er-Src	breast:	n/a
33	chr4:68930433-68930483	NHDF-neo	bronchial:	n/a
34	chr4:68995995-68996045	GM19239	blood:	n/a
35	chr4:68801145-68801195	HCPEpiC	choroid plexus:	n/a
36	chr4:68904160-68904210	HRE	kidney:	n/a
37	chr4:68928981-68929031	SKMC	muscle:	n/a
38	chr4:68928981-68929031	HNPCEpiC	eye:	n/a
39	chr4:68829101-68829151	CMK	blood:	n/a
40	chr4:68929020-68929070	HEK293	kidney:	embryo
41	chr4:68995995-68996045	HRPEpiC	eye:	n/a
42	chr4:68801145-68801195	AG04449	skin:	fetal
43	chr4:68829101-68829151	MCF-7	breast:	n/a
44	chr4:68830227-68830277	GM12891	blood:	n/a
45	chr4:68900280-68900330	Jurkat	blood:	n/a
46	chr4:68930433-68930483	HL-60	blood:	n/a
47	chr4:68900280-68900330	SK-N-SH_RA	brain:	n/a
48	chr4:68995995-68996045	NH-A	brain:	n/a
49	chr4:68830227-68830277	HUVEC	blood vessel:	n/a
50	chr4:68900280-68900330	AG09319	gingival:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
2	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
3	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
4	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
5	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
6	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
7	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
8	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
9	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
10	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
11	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
12	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
13	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
14	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
15	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
16	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
17	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
18	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
19	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
20	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
21	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
22	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
23	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
24	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
25	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
26	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
27	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
28	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
29	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
30	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
31	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
32	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
33	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
34	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
35	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
36	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
37	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
38	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
39	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
40	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
41	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
42	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
43	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
44	chr4:68796679..68798591-chr4:68806253..68807881,2	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	chr4:68928780-68928939	ENSG00000248049
3	lnc-TMPRSS11E-1	chr4:68945839-68946670	ENSG00000248049
4	lnc-TMPRSS11A-2	chr4:68927540-68928987	NONHSAT096722
5	lnc-TMPRSS11E-1	chr4:68928801-68928939	ENSG00000248049
6	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096720
7	lnc-TMPRSS11E-1	chr4:68926333-68928939	NONHSAT096719
8	lnc-TMPRSS11A-2	chr4:68926312-68926518	NONHSAT096720
9	lnc-TMPRSS11E-1	chr4:68928325-68928939	ENSG00000248049
10	lnc-TMPRSS11A-2	chr4:68928266-68928986	NONHSAT147287
11	lnc-TMPRSS11E-1	chr4:68938823-68938951	NONHSAT096719
12	lnc-TMPRSS11E-1	chr4:68945839-68946363	ENSG00000248049
13	lnc-TMPRSS11A-2	chr4:68926583-68927569	NONHSAT096720
14	lnc-TMPRSS11E-1	chr4:68945839-68945944	ENSG00000248049
15	lnc-TMPRSS11E-1	chr4:68943181-68943348	ENSG00000248049
16	lnc-TMPRSS11E-1	chr4:68919226-68919276	NONHSAT096719
17	lnc-TMPRSS11E-1	chr4:68942997-68943139	ENSG00000248049
18	lnc-TMPRSS11A-2	chr4:68927630-68929015	NONHSAT096721

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

Extended variants
information (count: 3533 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3533 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577195480	chr4:68797502-68797503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546008068	chr4:68797504-68797505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373495749	chr4:68797548-68797549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150589169	chr4:68797562-68797563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190772151	chr4:68797566-68797567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182309325	chr4:68797634-68797635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530085196	chr4:68797643-68797644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529825761	chr4:68797649-68797650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75592724	chr4:68797664-68797665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138571655	chr4:68797675-68797676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371040022	chr4:68797703-68797704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142955442	chr4:68797710-68797711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs151094571	chr4:68797711-68797712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370242991	chr4:68797727-68797728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112827609	chr4:68797740-68797741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376258886	chr4:68797791-68797792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374454980	chr4:68797806-68797807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552757290	chr4:68797808-68797809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73823321	chr4:68797827-68797828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534724742	chr4:68797851-68797852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554657884	chr4:68797887-68797888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538913317	chr4:68797920-68797921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537083701	chr4:68797949-68797950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10518046	chr4:68797982-68797983	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs373440493	chr4:68797984-68797985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149301743	chr4:68797991-68797992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186924350	chr4:68797992-68797993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553141358	chr4:68798028-68798029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191765351	chr4:68798065-68798066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144723929	chr4:68798134-68798135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561088223	chr4:68798141-68798142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375721556	chr4:68798180-68798181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140008305	chr4:68798213-68798214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569150092	chr4:68798329-68798330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543438051	chr4:68798377-68798378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563311700	chr4:68798380-68798381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28469855	chr4:68798413-68798414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549216049	chr4:68798444-68798445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566265662	chr4:68798480-68798481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147234931	chr4:68798494-68798495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548789133	chr4:68798506-68798507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140717177	chr4:68798531-68798532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182760708	chr4:68798533-68798534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142442568	chr4:68798536-68798537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs151330778	chr4:68798629-68798630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188404420	chr4:68798630-68798631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553042051	chr4:68798648-68798649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554756994	chr4:68798658-68798659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573085297	chr4:68798661-68798662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139351850	chr4:68798681-68798682	Weak transcription Enhancers	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Oral cancer	21386901	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

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
2	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:68794400-68797800	Enhancers	NHEK	skin
5	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:68797800-68800200	Weak transcription	NHEK	skin
13	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:68798600-68802000	Enhancers	Dnd41	blood
15	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
19	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
28	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:68800000-68801000	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:68800000-68801200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:68800000-68801200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:68800200-68800400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:68800200-68800800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:68800200-68800800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr4:68800200-68800800	Enhancers	NHEK	skin
38	chr4:68800200-68801200	Enhancers	Fetal Intestine Small	intestine
39	chr4:68800400-68800600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:68800400-68800800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:68800400-68800800	Enhancers	Brain Germinal Matrix	brain
42	chr4:68800400-68800800	Enhancers	Thymus	Thymus
43	chr4:68800400-68801000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:68800600-68800800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr4:68800600-68801000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr4:68800800-68801200	Enhancers	H9 Cell Line	embryonic stem cell
47	chr4:68800800-68801200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:68800800-68801200	Enhancers	Fetal Kidney	kidney
49	chr4:68800800-68801800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:68800800-68802000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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