Variant report

Variant	esv3362083
Chromosome Location	chr14:69618574-69620972
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:815)
CpG islands
(count:734)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:69619850-69620066	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:69619140-69619322	K562	blood:	n/a	n/a
3	ARID3A	chr14:69618186-69618663	HepG2	liver:	n/a	n/a
4	ATF2	chr14:69618070-69618628	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr14:69618293-69618767	GM12878	blood:	n/a	n/a
6	ATF2	chr14:69619614-69620078	GM12878	blood:	n/a	n/a
7	BACH1	chr14:69619825-69621001	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr14:69618326-69618640	GM12878	blood:	n/a	n/a
9	BCLAF1	chr14:69619667-69620530	GM12878	blood:	n/a	chr14:69620048-69620061 chr14:69619976-69619989 chr14:69619939-69619952
10	BCLAF1	chr14:69618260-69618802	GM12878	blood:	n/a	n/a
11	BCLAF1	chr14:69618101-69618874	GM12878	blood:	n/a	n/a
12	BCLAF1	chr14:69619699-69620129	GM12878	blood:	n/a	chr14:69620048-69620061 chr14:69619976-69619989 chr14:69619939-69619952
13	BHLHE40	chr14:69619591-69620118	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:69619622-69620311	HepG2	liver:	n/a	chr14:69620232-69620248 chr14:69620235-69620251
15	BHLHE40	chr14:69619657-69620131	K562	blood:	n/a	n/a
16	BHLHE40	chr14:69618292-69618638	K562	blood:	n/a	chr14:69618435-69618451
17	BHLHE40	chr14:69618286-69618638	HepG2	liver:	n/a	chr14:69618435-69618451
18	BHLHE40	chr14:69618233-69618743	GM12878	blood:	n/a	chr14:69618435-69618451
19	BRCA1	chr14:69619849-69620023	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr14:69619566-69619585	HepG2	liver:	n/a	n/a
21	BRCA1	chr14:69618459-69618854	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr14:69619886-69620071	HepG2	liver:	n/a	n/a
23	CBX3	chr14:69619700-69619992	K562	blood:	n/a	n/a
24	CCNT2	chr14:69619500-69620423	K562	blood:	n/a	chr14:69620011-69620020
25	CCNT2	chr14:69618217-69619015	K562	blood:	n/a	chr14:69618979-69618988 chr14:69618316-69618325
26	CEBPB	chr14:69618367-69618828	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:69618482-69618759	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:69618518-69618790	K562	blood:	n/a	n/a
29	CEBPB	chr14:69618551-69618830	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:69619801-69619971	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:69618385-69618606	HepG2	liver:	n/a	n/a
32	CEBPD	chr14:69618156-69618704	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:69619880-69620136	HepG2	liver:	n/a	n/a
34	CEBPD	chr14:69619296-69620285	HepG2	liver:	n/a	n/a
35	CHD1	chr14:69619149-69619355	GM12878	blood:	n/a	n/a
36	CHD1	chr14:69618154-69618847	GM12878	blood:	n/a	n/a
37	CHD1	chr14:69617893-69619333	IMR90	lung:	n/a	n/a
38	CHD1	chr14:69619077-69619301	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr14:69620204-69620708	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr14:69619774-69620667	GM12878	blood:	n/a	n/a
41	CHD1	chr14:69618435-69618738	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr14:69619841-69620146	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr14:69618320-69618631	HepG2	liver:	n/a	n/a
44	CHD2	chr14:69619765-69620122	HepG2	liver:	n/a	n/a
45	CHD2	chr14:69619067-69620121	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr14:69619117-69619238	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr14:69618219-69618789	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr14:69619185-69619392	GM12878	blood:	n/a	n/a
49	CHD2	chr14:69618123-69618726	GM12878	blood:	n/a	n/a
50	CHD2	chr14:69618293-69618708	H1-hESC	embryonic stem cell:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69620129-69620179	AG09319	gingival:	n/a
2	chr14:69619456-69619506	Jurkat	blood:	n/a
3	chr14:69620129-69620179	AG09319	gingival:	n/a
4	chr14:69619456-69619506	Jurkat	blood:	n/a
5	chr14:69619456-69619506	AG04450	lung:	fetal
6	chr14:69619456-69619506	GM19239	blood:	n/a
7	chr14:69618982-69619032	HAEpiC	amniotic membrane:	n/a
8	chr14:69619916-69619966	NH-A	brain:	n/a
9	chr14:69620440-69620490	GM12891	blood:	n/a
10	chr14:69619846-69619896	HEK293	kidney:	embryo
11	chr14:69619846-69619896	A549	lung:	n/a
12	chr14:69619856-69619906	NT2-D1	testis:	n/a
13	chr14:69618982-69619032	HCT-116	colon:	n/a
14	chr14:69618595-69618645	HRE	kidney:	n/a
15	chr14:69619856-69619906	SKMC	muscle:	n/a
16	chr14:69619456-69619506	MCF-7	breast:	n/a
17	chr14:69620847-69620897	GM12878	blood:	n/a
18	chr14:69619916-69619966	AG10803	skin:	n/a
19	chr14:69619916-69619966	SKMC	muscle:	n/a
20	chr14:69620440-69620490	HRPEpiC	eye:	n/a
21	chr14:69620129-69620179	HL-60	blood:	n/a
22	chr14:69620434-69620484	MCF-7	breast:	n/a
23	chr14:69620440-69620490	HRE	kidney:	n/a
24	chr14:69620847-69620897	AG04450	lung:	fetal
25	chr14:69620847-69620897	ProgFib	skin:	n/a
26	chr14:69619856-69619906	AG04449	skin:	fetal
27	chr14:69620434-69620484	A549	lung:	n/a
28	chr14:69619856-69619906	HCF	heart:	n/a
29	chr14:69618595-69618645	SK-N-SH_RA	brain:	n/a
30	chr14:69620662-69620712	HCF	heart:	n/a
31	chr14:69619856-69619906	HRPEpiC	eye:	n/a
32	chr14:69619456-69619506	HUVEC	blood vessel:	n/a
33	chr14:69619456-69619506	SKMC	muscle:	n/a
34	chr14:69619856-69619906	HCM	heart:	n/a
35	chr14:69620129-69620179	HCM	heart:	n/a
36	chr14:69619916-69619966	GM12878	blood:	n/a
37	chr14:69620129-69620179	HNPCEpiC	eye:	n/a
38	chr14:69620662-69620712	SK-N-SH_RA	brain:	n/a
39	chr14:69620129-69620179	ProgFib	skin:	n/a
40	chr14:69619846-69619896	NHDF-neo	bronchial:	n/a
41	chr14:69619456-69619506	HIPEpiC	eye:	n/a
42	chr14:69620440-69620490	AG09309	skin:	n/a
43	chr14:69620662-69620712	CMK	blood:	n/a
44	chr14:69619846-69619896	GM12892	blood:	n/a
45	chr14:69619846-69619896	HAEpiC	amniotic membrane:	n/a
46	chr14:69619456-69619506	AG04449	skin:	fetal
47	chr14:69620662-69620712	LNCaP	prostate:	n/a
48	chr14:69620432-69620482	HIPEpiC	eye:	n/a
49	chr14:69619856-69619906	HepG2	liver:	n/a
50	chr14:69619846-69619896	K562	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69618202..69621032-chr14:69863576..69866501,3	MCF-7	breast:
2	chr14:69443112..69445265-chr14:69618639..69620966,2	K562	blood:
3	chr14:69614281..69621283-chr14:69656459..69660724,14	MCF-7	breast:
4	chr14:69618275..69624022-chr14:69655650..69660294,14	MCF-7	breast:
5	chr14:69617775..69618630-chr14:69709107..69709873,3	MCF-7	breast:
6	chr14:69618346..69620839-chr14:69725644..69728530,2	K562	blood:
7	chr14:69618542..69620239-chr14:69620857..69623470,2	MCF-7	breast:
8	chr14:69583942..69585536-chr14:69616276..69618691,2	MCF-7	breast:
9	chr14:69620237..69623204-chr14:69623601..69625436,2	MCF-7	breast:
10	chr14:69620081..69621700-chr14:69636572..69639368,2	MCF-7	breast:
11	chr14:69600414..69601969-chr14:69620394..69622104,2	K562	blood:
12	chr14:69620207..69622979-chr14:69654185..69655880,2	K562	blood:
13	chr14:69608197..69610454-chr14:69620173..69622020,3	MCF-7	breast:
14	chr14:69616886..69618828-chr14:69863511..69865491,2	K562	blood:
15	chr14:69616829..69621784-chr14:69657152..69660113,5	K562	blood:

No data

Variant related genes	Relation type
DCAF5	TF binding region
DCAF5	CpG island
ENSG00000072110	chromatin interactions
ENSG00000100626	chromatin interactions
ENSG00000081177	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000258520	chromatin interactions
ENSG00000139990	chromatin interactions
ENSG00000029364	chromatin interactions
ENSG00000258957	chromatin interactions

Extended variants
information (count: 74 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:74 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545045021	chr14:69618574-69618575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs548956850	chr14:69618637-69618638	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs567262495	chr14:69618691-69618692	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs534668660	chr14:69618726-69618727	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs553313672	chr14:69618749-69618750	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs546259750	chr14:69618774-69618775	Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs578098034	chr14:69618844-69618845	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs118030788	chr14:69618920-69618921	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs557260774	chr14:69618945-69618946	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs34817641	chr14:69619031-69619032	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs191785443	chr14:69619116-69619117	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs184373338	chr14:69619160-69619161	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs1275419	chr14:69619173-69619174	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs71102632	chr14:69619198-69619199	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs190044599	chr14:69619220-69619221	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs561288562	chr14:69619232-69619233	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs573277996	chr14:69619244-69619245	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs540685114	chr14:69619306-69619307	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs12879923	chr14:69619326-69619327	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs565216828	chr14:69619413-69619414	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs200017545	chr14:69619443-69619444	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs551597202	chr14:69619452-69619453	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs375667888	chr14:69619454-69619455	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs368388515	chr14:69619456-69619457	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs563617457	chr14:69619459-69619460	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs372758352	chr14:69619471-69619472	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs375952187	chr14:69619476-69619477	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs530786110	chr14:69619534-69619535	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs144556740	chr14:69619555-69619556	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs367687713	chr14:69619589-69619590	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs567227115	chr14:69619597-69619598	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs371828864	chr14:69619622-69619623	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs375118926	chr14:69619670-69619671	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs534434650	chr14:69619686-69619687	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs369260220	chr14:69619705-69619706	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs546710727	chr14:69619708-69619709	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs182272156	chr14:69619711-69619712	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs570988488	chr14:69619755-69619756	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs538886137	chr14:69619767-69619768	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs557091020	chr14:69619775-69619776	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs569211615	chr14:69619827-69619828	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs536923345	chr14:69619874-69619875	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs113615810	chr14:69619987-69619988	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs554679599	chr14:69620018-69620019	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs573220046	chr14:69620025-69620026	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs540241203	chr14:69620095-69620096	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs559053304	chr14:69620136-69620137	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs577409449	chr14:69620137-69620138	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs545234948	chr14:69620231-69620232	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs113260043	chr14:69620276-69620277	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69616400-69621600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:69617400-69620200	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr14:69617400-69620600	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr14:69617600-69620400	Active TSS	H1 Cell Line	embryonic stem cell
5	chr14:69617600-69620400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:69617600-69620600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr14:69617600-69620600	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr14:69617600-69620600	Active TSS	Brain Hippocampus Middle	brain
9	chr14:69617600-69621000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:69617600-69621000	Active TSS	Right Atrium	heart
11	chr14:69617600-69621200	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr14:69617800-69618600	Active TSS	Fetal Brain Female	brain
13	chr14:69617800-69620400	Active TSS	HSMM	muscle
14	chr14:69617800-69620400	Active TSS	K562	blood
15	chr14:69617800-69620600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr14:69617800-69620600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr14:69617800-69620600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr14:69617800-69620600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:69617800-69620600	Active TSS	Brain Angular Gyrus	brain
20	chr14:69617800-69620600	Active TSS	Brain Cingulate Gyrus	brain
21	chr14:69617800-69620600	Active TSS	Fetal Intestine Small	intestine
22	chr14:69617800-69620600	Active TSS	Sigmoid Colon	Sigmoid Colon
23	chr14:69617800-69620600	Active TSS	GM12878-XiMat	blood
24	chr14:69617800-69620800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr14:69617800-69620800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:69617800-69620800	Active TSS	Aorta	Aorta
27	chr14:69617800-69620800	Active TSS	Fetal Intestine Large	intestine
28	chr14:69617800-69620800	Active TSS	Ovary	ovary
29	chr14:69617800-69621000	Active TSS	H9 Cell Line	embryonic stem cell
30	chr14:69617800-69621000	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr14:69618000-69618600	Active TSS	Brain Germinal Matrix	brain
32	chr14:69618000-69619600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
33	chr14:69618000-69619600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr14:69618000-69620400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr14:69618000-69620400	Active TSS	iPS-18 Cell Line	embryonic stem cell
36	chr14:69618000-69620400	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr14:69618000-69620400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr14:69618000-69620400	Active TSS	HepG2	liver
39	chr14:69618000-69620600	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr14:69618000-69620600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:69618000-69620600	Active TSS	A549	lung
42	chr14:69618000-69620800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:69618000-69620800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr14:69618000-69620800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr14:69618000-69620800	Active TSS	Gastric	stomach
46	chr14:69618000-69620800	Active TSS	Left Ventricle	heart
47	chr14:69618000-69620800	Active TSS	Lung	lung
48	chr14:69618000-69620800	Active TSS	Pancreas	Pancrea
49	chr14:69618000-69621000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:69618000-69621000	Active TSS	Colon Smooth Muscle	Colon

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