Variant report

Variant	esv3396463
Chromosome Location	chr14:104181449-104183347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:544)
CpG islands
(count:549)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:104181716-104182129	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:104181708-104182071	K562	blood:	n/a	n/a
3	ATF1	chr14:104181789-104182088	K562	blood:	n/a	n/a
4	BACH1	chr14:104182946-104182978	K562	blood:	n/a	n/a
5	BHLHE40	chr14:104181692-104182268	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:104181638-104182343	HepG2	liver:	n/a	n/a
7	BHLHE40	chr14:104181657-104182117	K562	blood:	n/a	n/a
8	BRCA1	chr14:104181658-104181667	HepG2	liver:	n/a	n/a
9	BRCA1	chr14:104181643-104181893	GM12878	blood:	n/a	n/a
10	BRCA1	chr14:104181922-104181946	HepG2	liver:	n/a	n/a
11	BRCA1	chr14:104181438-104182113	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr14:104181401-104182801	K562	blood:	n/a	n/a
13	CEBPB	chr14:104181826-104182082	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:104181783-104182156	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr14:104181515-104181550	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr14:104181912-104182319	HepG2	liver:	n/a	n/a
17	CEBPZ	chr14:104181718-104182101	HepG2	liver:	n/a	n/a
18	CHD1	chr14:104181412-104181948	GM12878	blood:	n/a	n/a
19	CHD1	chr14:104181449-104181686	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr14:104181403-104182354	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr14:104181628-104182218	K562	blood:	n/a	n/a
22	CHD2	chr14:104182941-104183242	GM12878	blood:	n/a	n/a
23	CHD2	chr14:104181502-104182209	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr14:104182838-104182860	HepG2	liver:	n/a	n/a
25	CHD2	chr14:104181619-104182140	HepG2	liver:	n/a	n/a
26	CHD2	chr14:104181607-104182281	GM12878	blood:	n/a	n/a
27	CREB1	chr14:104181319-104182512	HepG2	liver:	n/a	n/a
28	CREB1	chr14:104181396-104182398	A549	lung:	n/a	n/a
29	CREB1	chr14:104181581-104182318	GM12878	blood:	n/a	n/a
30	CREB1	chr14:104181657-104182366	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr14:104181528-104182377	HepG2	liver:	n/a	n/a
32	CREB1	chr14:104181491-104182372	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr14:104182224-104182261	GM12891	blood:	n/a	n/a
34	CTCF	chr14:104181777-104181786	Lung_OC	lung:	n/a	n/a
35	CTCF	chr14:104182164-104182234	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr14:104181655-104182115	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr14:104181843-104182089	GM12878	blood:	n/a	n/a
38	CTCF	chr14:104181743-104181921	K562	blood:	n/a	n/a
39	CTCF	chr14:104181847-104182022	Lung_OC	lung:	n/a	n/a
40	E2F1	chr14:104181542-104182140	Hela-S3	cervix:	n/a	chr14:104181782-104181794
41	E2F4	chr14:104181607-104182136	GM12878	blood:	n/a	chr14:104181758-104181769 chr14:104181782-104181794 chr14:104181781-104181792
42	E2F4	chr14:104181484-104182129	Hela-S3	cervix:	n/a	chr14:104181758-104181769 chr14:104181782-104181794 chr14:104181781-104181792
43	E2F4	chr14:104180846-104182172	MCF10A-Er-Src	breast:	n/a	chr14:104181758-104181769 chr14:104181782-104181794 chr14:104181781-104181792
44	E2F4	chr14:104181523-104182218	K562	blood:	n/a	chr14:104181758-104181769 chr14:104181782-104181794 chr14:104181781-104181792
45	E2F6	chr14:104181649-104181975	K562	blood:	n/a	chr14:104181782-104181794 chr14:104181781-104181792
46	E2F6	chr14:104181316-104181948	K562	blood:	n/a	chr14:104181782-104181794 chr14:104181781-104181792
47	E2F6	chr14:104182570-104182861	K562	blood:	n/a	n/a
48	E2F6	chr14:104181314-104182073	A549	lung:	n/a	chr14:104181782-104181794 chr14:104181781-104181792
49	E2F6	chr14:104182026-104182223	K562	blood:	n/a	n/a
50	E2F6	chr14:104181291-104183150	K562	blood:	n/a	chr14:104181782-104181794 chr14:104182507-104182519 chr14:104181781-104181792

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104181929-104181979	SK-N-SH	brain:	n/a
2	chr14:104181929-104181979	K562	blood:	n/a
3	chr14:104182045-104182095	NHDF-neo	bronchial:	n/a
4	chr14:104182836-104182886	MCF-7	breast:	n/a
5	chr14:104181875-104181925	Hela-S3	cervix:	n/a
6	chr14:104182175-104182225	CMK	blood:	n/a
7	chr14:104182045-104182095	GM12878	blood:	n/a
8	chr14:104182836-104182886	PANC-1	pancreas:	n/a
9	chr14:104181875-104181925	RPTEC	kidney:	n/a
10	chr14:104181924-104181974	PrEC	prostate:	n/a
11	chr14:104182945-104182995	Jurkat	blood:	n/a
12	chr14:104182836-104182886	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:104182836-104182886	IMR90	lung:	fetal
14	chr14:104181875-104181925	GM06990	blood:	n/a
15	chr14:104182074-104182124	NT2-D1	testis:	n/a
16	chr14:104182945-104182995	AG04450	lung:	fetal
17	chr14:104181929-104181979	MCF-7	breast:	n/a
18	chr14:104181924-104181974	T-47D	breast:	n/a
19	chr14:104182951-104183001	H1-hESC	embryonic stem cell:	embryo
20	chr14:104182951-104183001	HRE	kidney:	n/a
21	chr14:104181929-104181979	IMR90	lung:	fetal
22	chr14:104182951-104183001	GM12892	blood:	n/a
23	chr14:104182945-104182995	AoSMC	blood vessel:	n/a
24	chr14:104181929-104181979	BE2_C	brain:	n/a
25	chr14:104182045-104182095	Caco-2	colon:	n/a
26	chr14:104182951-104183001	HEK293	kidney:	embryo
27	chr14:104182945-104182995	ovcar-3	ovarian:	n/a
28	chr14:104181875-104181925	HRCEpiC	kidney:	n/a
29	chr14:104181875-104181925	HCPEpiC	choroid plexus:	n/a
30	chr14:104181924-104181974	SK-N-SH	brain:	n/a
31	chr14:104182175-104182225	NT2-D1	testis:	n/a
32	chr14:104182074-104182124	HMEC	breast:	n/a
33	chr14:104182074-104182124	HRPEpiC	eye:	n/a
34	chr14:104181929-104181979	ProgFib	skin:	n/a
35	chr14:104182175-104182225	AG09319	gingival:	n/a
36	chr14:104182945-104182995	GM06990	blood:	n/a
37	chr14:104182045-104182095	Hepatocyte	liver:	n/a
38	chr14:104181924-104181974	HRPEpiC	eye:	n/a
39	chr14:104182836-104182886	HIPEpiC	eye:	n/a
40	chr14:104182836-104182886	T-47D	breast:	n/a
41	chr14:104182045-104182095	Hela-S3	cervix:	n/a
42	chr14:104182074-104182124	Hela-S3	cervix:	n/a
43	chr14:104181924-104181974	HCM	heart:	n/a
44	chr14:104181875-104181925	HCT-116	colon:	n/a
45	chr14:104181924-104181974	CMK	blood:	n/a
46	chr14:104182074-104182124	Hepatocyte	liver:	n/a
47	chr14:104182074-104182124	NHDF-neo	bronchial:	n/a
48	chr14:104181929-104181979	HCT-116	colon:	n/a
49	chr14:104181929-104181979	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:104181924-104181974	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:104026026..104030833-chr14:104180410..104184978,6	MCF-7	breast:
2	chr14:104040497..104046116-chr14:104179984..104183762,7	MCF-7	breast:
3	chr14:104178608..104186342-chr14:104186894..104193138,16	K562	blood:
4	chr14:104181859..104182379-chr6:86353323..86354107,2	Hela-S3	cervix:
5	chr14:104027886..104033252-chr14:104178637..104183670,7	MCF-7	breast:
6	chr14:104095098..104097162-chr14:104179460..104182190,3	K562	blood:
7	chr14:104181282..104181917-chr6:30457138..30457957,2	Hela-S3	cervix:
8	chr14:104182047..104187446-chr14:104194338..104198036,7	K562	blood:
9	chr14:104093419..104097122-chr14:104180603..104183015,4	K562	blood:
10	chr14:103987454..103990068-chr14:104178702..104181671,2	K562	blood:
11	chr14:104180818..104182685-chr14:104312303..104315136,2	MCF-7	breast:
12	chr14:104181418..104182379-chr9:114393418..114394033,2	Hela-S3	cervix:
13	chr14:104182057..104182674-chr14:104195813..104196536,2	MCF-7	breast:
14	chr14:104092649..104097026-chr14:104179930..104185119,7	MCF-7	breast:
15	chr14:103993654..103996154-chr14:104180669..104183057,2	K562	blood:
16	chr14:104181470..104182117-chr8:125486026..125486841,2	Hela-S3	cervix:
17	chr14:104091773..104098220-chr14:104179036..104183968,10	MCF-7	breast:
18	chr14:104181509..104182182-chr6:26031441..26032296,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
XRCC3	TF binding region
ZFYVE21	TF binding region
XRCC3	CpG island
ZFYVE21	CpG island
ENSG00000166166	chromatin interactions
ENSG00000126214	chromatin interactions
ENSG00000166165	chromatin interactions
ENSG00000059769	chromatin interactions
ENSG00000260285	chromatin interactions
ENSG00000256053	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000264904	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000204592	chromatin interactions
ENSG00000244115	chromatin interactions
ENSG00000253096	chromatin interactions
ENSG00000166170	chromatin interactions
ENSG00000088808	chromatin interactions
ENSG00000258735	chromatin interactions
ENSG00000204173	chromatin interactions
ENSG00000100711	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569862257	chr14:104181507-104181508	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
2	rs372268622	chr14:104181511-104181512	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
3	rs535732816	chr14:104181524-104181525	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
4	rs555626546	chr14:104181582-104181583	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
5	rs572252050	chr14:104181593-104181594	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs534771872	chr14:104181594-104181595	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
7	rs554326307	chr14:104181676-104181677	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
8	rs577363748	chr14:104181685-104181686	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
9	rs373669204	chr14:104181700-104181701	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
10	rs3212023	chr14:104181715-104181716	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
11	rs3212022	chr14:104181728-104181729	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
12	rs562891274	chr14:104181729-104181730	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
13	rs576710393	chr14:104181732-104181733	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
14	rs542488367	chr14:104181751-104181752	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
15	rs561980080	chr14:104181783-104181784	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
16	rs527896479	chr14:104181789-104181790	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
17	rs191212781	chr14:104181898-104181899	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
18	rs530943223	chr14:104181909-104181910	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
19	rs141204284	chr14:104181913-104181914	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
20	rs533007674	chr14:104181923-104181924	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
21	rs549553526	chr14:104181948-104181949	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
22	rs569633005	chr14:104181993-104181994	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
23	rs535416171	chr14:104182029-104182030	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
24	rs545574172	chr14:104182102-104182103	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
25	rs549311776	chr14:104182109-104182110	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
26	rs368713701	chr14:104182142-104182143	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
27	rs565949736	chr14:104182172-104182173	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs552342705	chr14:104182178-104182179	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs534812523	chr14:104182183-104182184	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs557943184	chr14:104182211-104182212	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs376966619	chr14:104182267-104182268	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs371389100	chr14:104182274-104182275	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs570894992	chr14:104182358-104182359	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs539917931	chr14:104182365-104182366	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs556311493	chr14:104182466-104182467	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs576371486	chr14:104182558-104182559	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs541787562	chr14:104182570-104182571	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs555662088	chr14:104182631-104182632	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs116404895	chr14:104182677-104182678	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs559103824	chr14:104182711-104182712	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs541238009	chr14:104182782-104182783	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs564332087	chr14:104182812-104182813	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs532932754	chr14:104182848-104182849	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs3212021	chr14:104182876-104182877	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs370257037	chr14:104182887-104182888	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs570633207	chr14:104182903-104182904	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs543487564	chr14:104182909-104182910	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs563201609	chr14:104182928-104182929	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs182673740	chr14:104182937-104182938	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs548950044	chr14:104182940-104182941	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104180400-104183200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr14:104180400-104183600	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr14:104180400-104183800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr14:104180600-104181600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
5	chr14:104180600-104181600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr14:104180600-104181600	Flanking Active TSS	Brain Germinal Matrix	brain
7	chr14:104180600-104181800	Flanking Active TSS	Stomach Smooth Muscle	stomach
8	chr14:104180600-104181800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr14:104180600-104182800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr14:104180600-104183200	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr14:104180600-104183200	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr14:104180600-104183600	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr14:104180600-104184000	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr14:104180800-104181600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:104180800-104181600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
16	chr14:104180800-104181600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
17	chr14:104180800-104182600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:104180800-104182600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr14:104180800-104182800	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr14:104180800-104182800	Active TSS	H1 Cell Line	embryonic stem cell
21	chr14:104180800-104182800	Weak transcription	Stomach Mucosa	stomach
22	chr14:104180800-104182800	Active TSS	NH-A	brain
23	chr14:104180800-104183000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr14:104180800-104183000	Active TSS	GM12878-XiMat	blood
25	chr14:104180800-104183800	Active TSS	Right Ventricle	heart
26	chr14:104181000-104181600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
27	chr14:104181000-104181600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
28	chr14:104181000-104181600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:104181000-104181800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:104181000-104182800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:104181000-104182800	Active TSS	Primary T cells from cord blood	blood
32	chr14:104181000-104182800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr14:104181000-104182800	Active TSS	Muscle Satellite Cultured Cells	--
34	chr14:104181000-104182800	Weak transcription	Fetal Heart	heart
35	chr14:104181000-104182800	Active TSS	Rectal Mucosa Donor 31	rectum
36	chr14:104181000-104182800	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr14:104181000-104182800	Active TSS	Thymus	Thymus
38	chr14:104181000-104182800	Active TSS	Dnd41	blood
39	chr14:104181000-104182800	Active TSS	HMEC	breast
40	chr14:104181000-104182800	Active TSS	HUVEC	blood vessel
41	chr14:104181000-104183000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:104181000-104183000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:104181000-104183000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr14:104181000-104183000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:104181000-104183000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:104181000-104183000	Active TSS	A549	lung
47	chr14:104181000-104183000	Active TSS	Hela-S3	cervix
48	chr14:104181000-104183000	Active TSS	NHLF	lung
49	chr14:104181000-104183000	Active TSS	Osteobl	bone
50	chr14:104181000-104183200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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