Variant report

Variant	esv1807943
Chromosome Location	chr4:68806909-69013001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:732)
Chromatin interactive
region (count:39)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 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	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	chr4:69012824-69013135	K562	blood:	n/a	n/a
8	CBX3	chr4:69012748-69013185	K562	blood:	n/a	n/a
9	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
10	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
11	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
12	CEBPB	chr4:68856283-68856483	K562	blood:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
13	CEBPB	chr4:68857875-68858075	H1-hESC	embryonic stem cell:	n/a	chr4:68857997-68858014
14	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
15	CEBPB	chr4:68926854-68927085	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:68939433-68939695	HepG2	liver:	n/a	chr4:68939507-68939518
17	CEBPB	chr4:68854296-68854552	K562	blood:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
18	CEBPB	chr4:68867062-68867417	IMR90	lung:	n/a	chr4:68867240-68867257
19	CEBPB	chr4:68853094-68853163	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:68894997-68895022	K562	blood:	n/a	n/a
21	CEBPB	chr4:68855215-68855252	K562	blood:	n/a	n/a
22	CEBPB	chr4:68867077-68867408	HepG2	liver:	n/a	chr4:68867240-68867257
23	CEBPB	chr4:68867081-68867455	MCF-7	breast:	n/a	chr4:68867240-68867257
24	CEBPB	chr4:68926863-68927089	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:68856229-68856393	HepG2	liver:	n/a	chr4:68856321-68856332 chr4:68856323-68856334 chr4:68856323-68856332
26	CEBPB	chr4:68867136-68867337	Hela-S3	cervix:	n/a	chr4:68867240-68867257
27	CEBPB	chr4:68861899-68862052	HepG2	liver:	n/a	chr4:68861967-68861980 chr4:68861968-68861979
28	CEBPB	chr4:68854301-68854524	A549	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
29	CEBPB	chr4:68854271-68854605	Hela-S3	cervix:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
30	CEBPB	chr4:68855216-68855371	HepG2	liver:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
31	CEBPB	chr4:68854260-68854618	IMR90	lung:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
32	CEBPB	chr4:68867138-68867338	H1-hESC	embryonic stem cell:	n/a	chr4:68867240-68867257
33	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
34	CEBPB	chr4:68940147-68940530	Hela-S3	cervix:	n/a	chr4:68940343-68940354
35	CEBPB	chr4:68867084-68867396	A549	lung:	n/a	chr4:68867240-68867257
36	CEBPB	chr4:68854270-68854590	HepG2	liver:	n/a	chr4:68854428-68854439 chr4:68854428-68854441 chr4:68854428-68854441 chr4:68854429-68854440
37	CEBPB	chr4:68940212-68940475	HepG2	liver:	n/a	chr4:68940343-68940354
38	CEBPB	chr4:68886657-68887443	HCT-116	colon:	n/a	n/a
39	CEBPB	chr4:68888023-68888100	HepG2	liver:	n/a	chr4:68888044-68888055
40	CEBPB	chr4:68939459-68939688	IMR90	lung:	n/a	chr4:68939507-68939518
41	CEBPB	chr4:68855153-68855430	MCF-7	breast:	n/a	chr4:68855246-68855257 chr4:68855292-68855300 chr4:68855247-68855258
42	CEBPB	chr4:68894902-68895059	H1-hESC	embryonic stem cell:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
43	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
44	CEBPB	chr4:68894925-68895100	HepG2	liver:	n/a	chr4:68894994-68895007 chr4:68894996-68895005
45	CEBPB	chr4:68887982-68888143	A549	lung:	n/a	chr4:68888044-68888055
46	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
47	CEBPB	chr4:68940238-68940438	A549	lung:	n/a	chr4:68940343-68940354
48	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
49	CREB1	chr4:68989221-68989671	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr4:68989350-68989616	H1-hESC	embryonic stem cell:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68900280-68900330	U87	brain:	n/a
2	chr4:68829101-68829151	U87	brain:	n/a
3	chr4:68929413-68929463	NHDF-neo	bronchial:	n/a
4	chr4:68904160-68904210	LNCaP	prostate:	n/a
5	chr4:68930433-68930483	NT2-D1	testis:	n/a
6	chr4:68995995-68996045	PANC-1	pancreas:	n/a
7	chr4:68829101-68829151	HEK293	kidney:	embryo
8	chr4:68995759-68995809	GM19239	blood:	n/a
9	chr4:68929005-68929055	HRE	kidney:	n/a
10	chr4:68929005-68929055	Hela-S3	cervix:	n/a
11	chr4:68929413-68929463	HCPEpiC	choroid plexus:	n/a
12	chr4:68904160-68904210	NT2-D1	testis:	n/a
13	chr4:68928981-68929031	GM12892	blood:	n/a
14	chr4:68919575-68919625	HepG2	liver:	n/a
15	chr4:68995759-68995809	GM12892	blood:	n/a
16	chr4:68829101-68829151	Hepatocyte	liver:	n/a
17	chr4:68919575-68919625	AG04449	skin:	fetal
18	chr4:68900280-68900330	SK-N-MC	brain:	n/a
19	chr4:68900280-68900330	NT2-D1	testis:	n/a
20	chr4:68904160-68904210	HepG2	liver:	n/a
21	chr4:68930433-68930483	NHDF-neo	bronchial:	n/a
22	chr4:68995759-68995809	H1-hESC	embryonic stem cell:	embryo
23	chr4:68928981-68929031	H1-hESC	embryonic stem cell:	embryo
24	chr4:68995995-68996045	GM06990	blood:	n/a
25	chr4:68928981-68929031	GM19239	blood:	n/a
26	chr4:68995995-68996045	ovcar-3	ovarian:	n/a
27	chr4:68919575-68919625	GM12892	blood:	n/a
28	chr4:68929005-68929055	RPTEC	kidney:	n/a
29	chr4:68930433-68930483	SK-N-MC	brain:	n/a
30	chr4:68928981-68929031	MCF10A-Er-Src	breast:	n/a
31	chr4:68928981-68929031	HRPEpiC	eye:	n/a
32	chr4:68930433-68930483	HCF	heart:	n/a
33	chr4:68904160-68904210	MCF10A-Er-Src	breast:	n/a
34	chr4:68904160-68904210	HRPEpiC	eye:	n/a
35	chr4:68929005-68929055	MCF-7	breast:	n/a
36	chr4:68995759-68995809	NHDF-neo	bronchial:	n/a
37	chr4:68830227-68830277	A549	lung:	n/a
38	chr4:68929020-68929070	AG04449	skin:	fetal
39	chr4:68930433-68930483	BE2_C	brain:	n/a
40	chr4:68904160-68904210	A549	lung:	n/a
41	chr4:68830227-68830277	AoSMC	blood vessel:	n/a
42	chr4:68929020-68929070	HRCEpiC	kidney:	n/a
43	chr4:68930433-68930483	Caco-2	colon:	n/a
44	chr4:68919575-68919625	AG09319	gingival:	n/a
45	chr4:68929413-68929463	HAEpiC	amniotic membrane:	n/a
46	chr4:68904160-68904210	Caco-2	colon:	n/a
47	chr4:68995995-68996045	AG09309	skin:	n/a
48	chr4:68930433-68930483	Jurkat	blood:	n/a
49	chr4:68929020-68929070	RPTEC	kidney:	n/a
50	chr4:68904160-68904210	HPAEpiC	pulmonary alveolar:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
2	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
3	chr4:68784089..68784796-chr4:68853790..68854411,2	MCF-7	breast:
4	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
5	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
6	chr11:73471645..73472154-chr4:68919136..68920088,2	MCF-7	breast:
7	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
8	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
9	chr4:68945279..68946241-chr4:69040966..69041537,2	K562	blood:
10	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
11	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
12	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
13	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
14	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
15	chr4:68883089..68884997-chr4:68887701..68890688,2	MCF-7	breast:
16	chr4:68941684..68942576-chr4:69041048..69041788,2	K562	blood:
17	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
18	chr4:68854585..68857401-chr4:68944516..68946087,2	MCF-7	breast:
19	chr4:69012983..69014956-chr4:69018521..69020057,2	K562	blood:
20	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
21	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
22	chr4:68913890..68916498-chr4:68916992..68918591,2	MCF-7	breast:
23	chr4:68911783..68913982-chr4:68917527..68919121,2	K562	blood:
24	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:
25	chr4:68853837..68854799-chr4:69040919..69041918,3	MCF-7	breast:
26	chr4:68941725..68942553-chr4:69040855..69041893,4	MCF-7	breast:
27	chr4:68945761..68946581-chr4:69040992..69041794,2	MCF-7	breast:
28	chr4:68854785..68855326-chr4:69041026..69041997,2	MCF-7	breast:
29	chr4:68915001..68917748-chr4:68918946..68921356,2	MCF-7	breast:
30	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:
31	chr4:68853962..68854562-chr4:69041076..69041834,2	K562	blood:
32	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
33	chr4:68924336..68926843-chr4:68931083..68932839,2	MCF-7	breast:
34	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
35	chr4:68782884..68785601-chr4:68941722..68943617,2	MCF-7	breast:
36	chr4:68887827..68889608-chr4:68891154..68893430,2	K562	blood:
37	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
38	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
39	chr4:68919044..68921969-chr4:68924326..68927015,2	K562	blood:

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

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

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

Extended variants
information (count: 3150 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3150 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6849403	chr4:68806909-68806910	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375193866	chr4:68806910-68806911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187866373	chr4:68806936-68806937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571031037	chr4:68807004-68807005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534125084	chr4:68807046-68807047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74854413	chr4:68807063-68807064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573386486	chr4:68807084-68807085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34739465	chr4:68807132-68807133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538212104	chr4:68807165-68807166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113315846	chr4:68807185-68807186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192941339	chr4:68807198-68807199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs61494642	chr4:68807254-68807255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111443497	chr4:68807294-68807295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369721043	chr4:68807310-68807311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527521881	chr4:68807378-68807379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541208968	chr4:68807393-68807394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536946075	chr4:68807408-68807409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188947151	chr4:68807409-68807410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529344677	chr4:68807423-68807424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561601208	chr4:68807522-68807523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142487824	chr4:68807582-68807583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549376518	chr4:68807584-68807585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569119824	chr4:68807587-68807588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532037263	chr4:68807608-68807609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79841300	chr4:68807620-68807621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181687554	chr4:68807631-68807632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59758356	chr4:68807639-68807640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113619546	chr4:68807644-68807645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553926345	chr4:68807669-68807670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567370763	chr4:68807672-68807673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148079014	chr4:68807683-68807684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111696872	chr4:68807687-68807688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73823372	chr4:68807718-68807719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs6854601	chr4:68807747-68807748	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs146148126	chr4:68807757-68807758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs72851239	chr4:68807772-68807773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376585407	chr4:68807821-68807822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561033832	chr4:68807832-68807833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369524783	chr4:68807852-68807853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112552896	chr4:68807907-68807908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114674866	chr4:68807965-68807966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573851710	chr4:68808006-68808007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184658703	chr4:68808007-68808008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189451824	chr4:68808035-68808036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142140370	chr4:68808068-68808069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72851240	chr4:68808079-68808080	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs180776440	chr4:68808098-68808099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547594127	chr4:68808106-68808107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186180878	chr4:68808168-68808169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189440547	chr4:68808257-68808258	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
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:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68806600-68807000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:68806800-68818600	Weak transcription	Esophagus	oesophagus
3	chr4:68810600-68811000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:68810600-68811600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:68811000-68811800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:68811600-68812000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:68811800-68812600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:68812000-68812400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr4:68818800-68819000	Enhancers	Esophagus	oesophagus
10	chr4:68827400-68827600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:68827400-68828800	Active TSS	Esophagus	oesophagus
12	chr4:68829000-68829200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:68839200-68839600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr4:68848800-68849800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:68849000-68849800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:68849000-68849800	Enhancers	HMEC	breast
17	chr4:68849000-68849800	Enhancers	NHEK	skin
18	chr4:68849400-68849800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:68849400-68849800	Enhancers	Hela-S3	cervix
20	chr4:68849800-68854600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:68854600-68854800	Enhancers	HMEC	breast
22	chr4:68854600-68855000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:68854600-68855600	Enhancers	NH-A	brain
24	chr4:68854800-68855400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:68855400-68856000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:68856000-68856600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:68856200-68856600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:68856400-68856600	Enhancers	Dnd41	blood
29	chr4:68856600-68856800	Active TSS	Primary hematopoietic stem cells	blood
30	chr4:68856600-68856800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:68856600-68857000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:68856600-68857000	Flanking Active TSS	Dnd41	blood
33	chr4:68856800-68857000	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr4:68856800-68857000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr4:68857000-68857400	Enhancers	Dnd41	blood
36	chr4:68884600-68884800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:68885000-68886600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:68886600-68887400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:68886600-68887400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:68886600-68887600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:68886600-68887600	Enhancers	NHEK	skin
42	chr4:68886800-68887600	Enhancers	HMEC	breast
43	chr4:68886800-68888000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:68887000-68889600	Weak transcription	Brain Substantia Nigra	brain
45	chr4:68915600-68916600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:68915800-68916600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:68915800-68916600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:68916600-68920000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr4:68916600-68920000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:68916600-68920400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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