Variant report

Variant	esv3693408
Chromosome Location	chr14:65292670-65358576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:924)
CpG islands
(count:976)
Chromatin interactive
region (count:115)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:65358532-65358848	K562	blood:	n/a	n/a
2	ARID3A	chr14:65307911-65308213	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:65358561-65358873	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:65309260-65309553	K562	blood:	n/a	n/a
5	ARID3A	chr14:65311740-65312063	K562	blood:	n/a	n/a
6	ARID3A	chr14:65312352-65312843	K562	blood:	n/a	n/a
7	ARID3A	chr14:65346612-65346812	K562	blood:	n/a	n/a
8	ARID3A	chr14:65307849-65308792	K562	blood:	n/a	n/a
9	ATF1	chr14:65308104-65308831	K562	blood:	n/a	n/a
10	ATF1	chr14:65358514-65358786	K562	blood:	n/a	n/a
11	ATF1	chr14:65311705-65312044	K562	blood:	n/a	n/a
12	ATF1	chr14:65298746-65298946	K562	blood:	n/a	n/a
13	ATF1	chr14:65315109-65315305	K562	blood:	n/a	n/a
14	ATF2	chr14:65314902-65315324	GM12878	blood:	n/a	n/a
15	ATF2	chr14:65314902-65315304	GM12878	blood:	n/a	n/a
16	ATF3	chr14:65307861-65308200	K562	blood:	n/a	n/a
17	BACH1	chr14:65346136-65346313	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:65328674-65328939	H1-hESC	embryonic stem cell:	n/a	n/a
19	BHLHE40	chr14:65308481-65308897	K562	blood:	n/a	n/a
20	BHLHE40	chr14:65347197-65347386	K562	blood:	n/a	n/a
21	BHLHE40	chr14:65346586-65346932	K562	blood:	n/a	chr14:65346870-65346886 chr14:65346601-65346617 chr14:65346610-65346626
22	BHLHE40	chr14:65311700-65312005	K562	blood:	n/a	n/a
23	BRCA1	chr14:65328763-65328908	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr14:65358566-65358821	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr14:65332696-65333135	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr14:65339404-65339774	K562	blood:	n/a	n/a
27	CBX3	chr14:65307747-65308174	K562	blood:	n/a	n/a
28	CBX3	chr14:65346602-65346868	K562	blood:	n/a	n/a
29	CBX3	chr14:65307700-65308344	K562	blood:	n/a	n/a
30	CBX3	chr14:65308496-65309078	K562	blood:	n/a	n/a
31	CCNT2	chr14:65345877-65347531	K562	blood:	n/a	chr14:65347261-65347270
32	CCNT2	chr14:65308107-65308923	K562	blood:	n/a	n/a
33	CCNT2	chr14:65311703-65312147	K562	blood:	n/a	n/a
34	CCNT2	chr14:65342120-65342468	K562	blood:	n/a	n/a
35	CEBPB	chr14:65331086-65331300	IMR90	lung:	n/a	chr14:65331117-65331128
36	CEBPB	chr14:65293497-65293887	HepG2	liver:	n/a	chr14:65293680-65293691 chr14:65293677-65293694 chr14:65293680-65293693
37	CEBPB	chr14:65340452-65341041	MCF-7	breast:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
38	CEBPB	chr14:65293534-65293838	Hela-S3	cervix:	n/a	chr14:65293680-65293691 chr14:65293677-65293694 chr14:65293680-65293693
39	CEBPB	chr14:65340621-65340878	A549	lung:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
40	CEBPB	chr14:65293600-65293779	HepG2	liver:	n/a	chr14:65293680-65293691 chr14:65293677-65293694 chr14:65293680-65293693
41	CEBPB	chr14:65340464-65340990	MCF-7	breast:	n/a	chr14:65340754-65340765 chr14:65340754-65340767
42	CEBPB	chr14:65312642-65312884	IMR90	lung:	n/a	n/a
43	CEBPB	chr14:65311733-65312383	K562	blood:	n/a	n/a
44	CEBPB	chr14:65293535-65293871	IMR90	lung:	n/a	chr14:65293680-65293691 chr14:65293677-65293694 chr14:65293680-65293693
45	CEBPB	chr14:65308007-65308792	K562	blood:	n/a	chr14:65308254-65308267
46	CEBPB	chr14:65357433-65357786	K562	blood:	n/a	n/a
47	CEBPB	chr14:65311670-65312086	K562	blood:	n/a	n/a
48	CEBPB	chr14:65308083-65308922	K562	blood:	n/a	chr14:65308254-65308267
49	CEBPB	chr14:65331094-65331247	HepG2	liver:	n/a	chr14:65331117-65331128
50	CEBPB	chr14:65340559-65340951	Hela-S3	cervix:	n/a	chr14:65340754-65340765 chr14:65340754-65340767

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65347275-65347325	NH-A	brain:	n/a
2	chr14:65345681-65345731	ECC-1	luminal epithelium:	n/a
3	chr14:65346628-65346678	IMR90	lung:	fetal
4	chr14:65347345-65347395	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:65308247-65308297	GM19239	blood:	n/a
6	chr14:65323467-65323517	NHBE	bronchial:	n/a
7	chr14:65342922-65342972	AG09319	gingival:	n/a
8	chr14:65346490-65346540	SK-N-SH_RA	brain:	n/a
9	chr14:65346628-65346678	HepG2	liver:	n/a
10	chr14:65347345-65347395	HRCEpiC	kidney:	n/a
11	chr14:65308247-65308297	GM12891	blood:	n/a
12	chr14:65347138-65347188	IMR90	lung:	fetal
13	chr14:65346148-65346198	GM06990	blood:	n/a
14	chr14:65346686-65346736	H1-hESC	embryonic stem cell:	embryo
15	chr14:65345681-65345731	CMK	blood:	n/a
16	chr14:65347275-65347325	NHDF-neo	bronchial:	n/a
17	chr14:65346148-65346198	HIPEpiC	eye:	n/a
18	chr14:65346490-65346540	HCF	heart:	n/a
19	chr14:65346148-65346198	HNPCEpiC	eye:	n/a
20	chr14:65345681-65345731	U87	brain:	n/a
21	chr14:65346628-65346678	MCF-7	breast:	n/a
22	chr14:65347345-65347395	MCF10A-Er-Src	breast:	n/a
23	chr14:65342922-65342972	HEEpiC	esophagus:	n/a
24	chr14:65347138-65347188	A549	lung:	n/a
25	chr14:65345381-65345431	ProgFib	skin:	n/a
26	chr14:65323467-65323517	NB4	blood:	n/a
27	chr14:65346628-65346678	HCT-116	colon:	n/a
28	chr14:65346633-65346683	PANC-1	pancreas:	n/a
29	chr14:65347275-65347325	HUVEC	blood vessel:	n/a
30	chr14:65346721-65346771	HCPEpiC	choroid plexus:	n/a
31	chr14:65346633-65346683	H1-hESC	embryonic stem cell:	embryo
32	chr14:65342922-65342972	GM12892	blood:	n/a
33	chr14:65323467-65323517	AoSMC	blood vessel:	n/a
34	chr14:65308247-65308297	IMR90	lung:	fetal
35	chr14:65345381-65345431	GM12892	blood:	n/a
36	chr14:65346628-65346678	Hepatocyte	liver:	n/a
37	chr14:65346148-65346198	HepG2	liver:	n/a
38	chr14:65323467-65323517	HRPEpiC	eye:	n/a
39	chr14:65346875-65346925	Hepatocyte	liver:	n/a
40	chr14:65308247-65308297	ECC-1	luminal epithelium:	n/a
41	chr14:65342922-65342972	SK-N-SH	brain:	n/a
42	chr14:65323467-65323517	PANC-1	pancreas:	n/a
43	chr14:65323467-65323517	RPTEC	kidney:	n/a
44	chr14:65347345-65347395	U87	brain:	n/a
45	chr14:65346148-65346198	HL-60	blood:	n/a
46	chr14:65347345-65347395	ECC-1	luminal epithelium:	n/a
47	chr14:65346721-65346771	LNCaP	prostate:	n/a
48	chr14:65308247-65308297	HRCEpiC	kidney:	n/a
49	chr14:65308247-65308297	PANC-1	pancreas:	n/a
50	chr14:65346148-65346198	PrEC	prostate:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:65293736..65296089-chr14:65308632..65311499,2	K562	blood:
2	chr14:65307919..65310275-chr14:65380643..65382616,2	K562	blood:
3	chr14:65346776..65351606-chr14:65355142..65358604,5	K562	blood:
4	chr14:65311733..65313591-chr14:65343114..65345431,2	K562	blood:
5	chr14:65306058..65308869-chr14:65317790..65319964,2	MCF-7	breast:
6	chr14:65310132..65313690-chr14:65314321..65317713,3	K562	blood:
7	chr14:65289524..65290526-chr14:65358021..65359324,8	K562	blood:
8	chr14:65344538..65346383-chr14:65347730..65349628,3	K562	blood:
9	chr14:65289183..65290767-chr14:65349424..65351043,2	K562	blood:
10	chr14:65311733..65313591-chr14:65343114..65345431,2	K562	blood:
11	chr14:65302136..65304869-chr14:65306448..65308856,2	MCF-7	breast:
12	chr14:65238323..65239708-chr14:65358202..65359292,7	MCF-7	breast:
13	chr14:65317600..65319919-chr14:65379346..65381872,2	MCF-7	breast:
14	chr14:65289311..65290700-chr14:65357720..65359432,13	MCF-7	breast:
15	chr14:65324493..65326622-chr14:65332005..65334164,2	MCF-7	breast:
16	chr14:65310132..65314457-chr14:65315119..65319141,7	K562	blood:
17	chr14:65302483..65304714-chr14:65308064..65309843,2	K562	blood:
18	chr14:65347870..65349476-chr14:65380923..65383635,2	MCF-7	breast:
19	chr14:65328178..65330456-chr14:65344505..65346586,2	K562	blood:
20	chr14:65324493..65326622-chr14:65332005..65334164,2	MCF-7	breast:
21	chr14:65294605..65296941-chr14:65298914..65301120,2	K562	blood:
22	chr14:65307162..65309690-chr14:65332529..65335458,2	K562	blood:
23	chr14:65307862..65310367-chr14:65313110..65315645,2	MCF-7	breast:
24	chr14:65335703..65338607-chr14:65380232..65382733,2	K562	blood:
25	chr14:65347011..65349276-chr14:65350145..65352997,3	MCF-7	breast:
26	chr14:65238831..65239785-chr14:65358174..65359063,5	MCF-7	breast:
27	chr14:65346776..65348701-chr14:65353935..65356642,2	K562	blood:
28	chr14:65308032..65309548-chr14:65310473..65312252,2	K562	blood:
29	chr14:65352038..65354745-chr14:65354823..65356401,2	MCF-7	breast:
30	chr14:65344538..65346383-chr14:65347730..65349628,3	K562	blood:
31	chr14:65333231..65337568-chr14:65342616..65346293,4	K562	blood:
32	chr12:57482006..57484279-chr14:65344658..65346177,2	MCF-7	breast:
33	chr14:65306551..65309829-chr14:65344865..65347134,3	K562	blood:
34	chr14:65333231..65337568-chr14:65342616..65346293,4	K562	blood:
35	chr14:65315994..65317932-chr14:65325129..65327129,2	K562	blood:
36	chr14:65313283..65315169-chr14:65321927..65324245,2	K562	blood:
37	chr14:65288738..65289433-chr14:65358177..65359166,2	K562	blood:
38	chr14:65293069..65296062-chr14:65321540..65323696,2	K562	blood:
39	chr14:65296488..65300322-chr14:65306337..65310294,4	K562	blood:
40	chr14:65346800..65348898-chr14:65351625..65354536,2	K562	blood:
41	chr14:65313751..65315359-chr14:65318780..65321450,2	MCF-7	breast:
42	chr14:65294605..65296941-chr14:65298914..65301120,2	K562	blood:
43	chr14:65335678..65337852-chr14:65340686..65343364,4	K562	blood:
44	chr14:65228221..65230600-chr14:65293367..65295100,2	MCF-7	breast:
45	chr14:65315994..65317932-chr14:65325129..65327129,2	K562	blood:
46	chr14:65301182..65304259-chr14:65304528..65307494,3	K562	blood:
47	chr14:65306477..65308569-chr14:65377752..65379840,2	MCF-7	breast:
48	chr14:65353028..65355615-chr14:65356230..65358479,2	K562	blood:
49	chr14:65308370..65310775-chr14:65344440..65346663,2	K562	blood:
50	chr14:65338313..65340623-chr14:65341723..65344715,3	K562	blood:

No data

Variant related genes	Relation type
SPTB	TF binding region
SPTB	CpG island
ENSG00000070182	chromatin interactions
ENSG00000126804	chromatin interactions
ENSG00000258289	chromatin interactions
ENSG00000257365	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000166886	chromatin interactions
ENSG00000125954	chromatin interactions

Extended variants
information (count: 2492 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2492 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11158561	chr14:65292670-65292671	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559990571	chr14:65292684-65292685	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184429533	chr14:65292750-65292751	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs548664320	chr14:65292752-65292753	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569146097	chr14:65292780-65292781	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190102147	chr14:65292879-65292880	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs533881556	chr14:65292907-65292908	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs551677158	chr14:65292976-65292977	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs77800976	chr14:65293015-65293016	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181286645	chr14:65293017-65293018	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553478243	chr14:65293018-65293019	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs138006168	chr14:65293036-65293037	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142590992	chr14:65293049-65293050	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs118183750	chr14:65293097-65293098	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575573228	chr14:65293101-65293102	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544539180	chr14:65293109-65293110	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558021729	chr14:65293121-65293122	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs577864979	chr14:65293198-65293199	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs540382664	chr14:65293201-65293202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs560204872	chr14:65293252-65293253	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs573618187	chr14:65293259-65293260	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540790067	chr14:65293264-65293265	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs186525620	chr14:65293266-65293267	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531315012	chr14:65293267-65293268	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs551739004	chr14:65293278-65293279	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs229617	chr14:65293386-65293387	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs527485300	chr14:65293406-65293407	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs149693534	chr14:65293448-65293449	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529301462	chr14:65293456-65293457	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs144427990	chr14:65293460-65293461	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs179337	chr14:65293469-65293470	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs574058955	chr14:65293475-65293476	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs191431329	chr14:65293506-65293507	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537848245	chr14:65293553-65293554	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs229616	chr14:65293556-65293557	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs180698582	chr14:65293559-65293560	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534142958	chr14:65293622-65293623	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs76435737	chr14:65293626-65293627	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574153431	chr14:65293648-65293649	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542390564	chr14:65293741-65293742	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185133026	chr14:65293742-65293743	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2173556	chr14:65293788-65293789	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576152420	chr14:65293798-65293799	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2173557	chr14:65293809-65293810	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2173558	chr14:65293815-65293816	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544974517	chr14:65293816-65293817	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142449616	chr14:65293850-65293851	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190771422	chr14:65293854-65293855	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547647821	chr14:65293897-65293898	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs560958568	chr14:65293974-65293975	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Malignant peripheral nerve sheath tumor	18522746	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
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164920	CNVD

Chromatin state (count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65289600-65293600	Enhancers	Fetal Heart	heart
2	chr14:65289800-65295200	Enhancers	Left Ventricle	heart
3	chr14:65290000-65295200	Enhancers	Psoas Muscle	Psoas
4	chr14:65290400-65292800	Weak transcription	Gastric	stomach
5	chr14:65290400-65293400	Weak transcription	Spleen	Spleen
6	chr14:65290600-65294400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr14:65291000-65295600	Enhancers	Fetal Muscle Leg	muscle
8	chr14:65291600-65296000	Enhancers	K562	blood
9	chr14:65292000-65292800	Weak transcription	Right Atrium	heart
10	chr14:65292000-65293000	Enhancers	Colon Smooth Muscle	Colon
11	chr14:65292000-65297800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:65292200-65292800	Bivalent Enhancer	Fetal Stomach	stomach
13	chr14:65292200-65292800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr14:65292200-65293000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr14:65292400-65292800	Weak transcription	Right Ventricle	heart
16	chr14:65292400-65293200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr14:65292400-65294800	Enhancers	Fetal Muscle Trunk	muscle
18	chr14:65292600-65293800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr14:65292600-65297800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:65292800-65293000	Enhancers	Right Ventricle	heart
21	chr14:65292800-65293400	Enhancers	HSMMtube	muscle
22	chr14:65292800-65294000	Enhancers	Right Atrium	heart
23	chr14:65292800-65294000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr14:65292800-65294000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:65292800-65295000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:65293000-65294800	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr14:65293000-65294800	Weak transcription	Right Ventricle	heart
28	chr14:65293200-65293600	Enhancers	Primary B cells from cord blood	blood
29	chr14:65293200-65293600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:65293200-65293600	Bivalent Enhancer	Osteobl	bone
31	chr14:65293400-65293600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr14:65293400-65293600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr14:65293400-65293600	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr14:65293400-65293600	Flanking Active TSS	HSMMtube	muscle
35	chr14:65293400-65293800	Enhancers	Spleen	Spleen
36	chr14:65293600-65293800	Enhancers	HMEC	breast
37	chr14:65293600-65294600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr14:65293600-65295600	Enhancers	HSMMtube	muscle
39	chr14:65293600-65297400	Weak transcription	Fetal Heart	heart
40	chr14:65293800-65294400	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr14:65293800-65294400	Weak transcription	HMEC	breast
42	chr14:65294000-65294400	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr14:65294000-65294600	Weak transcription	Right Atrium	heart
44	chr14:65294000-65297800	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr14:65294400-65294800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr14:65294400-65295000	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr14:65294400-65295000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr14:65294400-65295000	Enhancers	HMEC	breast
49	chr14:65294400-65295200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:65294600-65295200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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