Variant report

Variant	nsv1042989
Chromosome Location	chr14:45774194-46489107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2309)
CpG islands
(count:550)
Chromatin interactive
region (count:56)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2309 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
4	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
5	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:46368023-46368235	GM12878	blood:	n/a	n/a
7	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
8	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
9	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
10	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
11	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
12	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:46337474-46337979	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:46338183-46338481	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:46337580-46337867	GM12878	blood:	n/a	n/a
16	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
17	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
18	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
21	CBX3	chr14:46256472-46256659	K562	blood:	n/a	n/a
22	CBX3	chr14:46213002-46213438	HCT-116	colon:	n/a	n/a
23	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
24	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
25	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
26	CEBPB	chr14:45990474-45990674	IMR90	lung:	n/a	chr14:45990587-45990604
27	CEBPB	chr14:46031190-46031458	HepG2	liver:	n/a	chr14:46031347-46031358
28	CEBPB	chr14:46441175-46441403	HepG2	liver:	n/a	chr14:46441316-46441327
29	CEBPB	chr14:45902380-45902544	A549	lung:	n/a	n/a
30	CEBPB	chr14:46094194-46094315	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr14:45810697-45810951	A549	lung:	n/a	n/a
32	CEBPB	chr14:46242906-46243113	HepG2	liver:	n/a	chr14:46243004-46243015
33	CEBPB	chr14:46388459-46388948	MCF-7	breast:	n/a	chr14:46388709-46388720
34	CEBPB	chr14:46055949-46056230	HepG2	liver:	n/a	chr14:46056048-46056059
35	CEBPB	chr14:46232907-46233168	HepG2	liver:	n/a	n/a
36	CEBPB	chr14:46270324-46270772	HepG2	liver:	n/a	chr14:46270518-46270529
37	CEBPB	chr14:46477968-46478185	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:45902392-45902559	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr14:46441220-46441420	H1-hESC	embryonic stem cell:	n/a	chr14:46441316-46441327
40	CEBPB	chr14:46000477-46000804	HepG2	liver:	n/a	chr14:46000620-46000631
41	CEBPB	chr14:46441158-46441496	A549	lung:	n/a	chr14:46441316-46441327
42	CEBPB	chr14:46270325-46270606	IMR90	lung:	n/a	chr14:46270518-46270529
43	CEBPB	chr14:46170313-46170577	HepG2	liver:	n/a	chr14:46170421-46170432
44	CEBPB	chr14:45893200-45893264	A549	lung:	n/a	n/a
45	CEBPB	chr14:46388507-46388949	MCF-7	breast:	n/a	chr14:46388709-46388720
46	CEBPB	chr14:46242879-46243131	IMR90	lung:	n/a	chr14:46243004-46243015
47	CEBPB	chr14:45902361-45902662	IMR90	lung:	n/a	n/a
48	CEBPB	chr14:45781555-45781799	A549	lung:	n/a	chr14:45781644-45781655
49	CEBPB	chr14:46248535-46248671	HepG2	liver:	n/a	chr14:46248607-46248618
50	CEBPB	chr14:45784842-45784985	H1-hESC	embryonic stem cell:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46241576-46241626	U87	brain:	n/a
2	chr14:46241576-46241626	U87	brain:	n/a
3	chr14:46358139-46358189	HIPEpiC	eye:	n/a
4	chr14:46300358-46300408	SK-N-SH	brain:	n/a
5	chr14:45930824-45930874	HUVEC	blood vessel:	n/a
6	chr14:45840127-45840177	AG04450	lung:	fetal
7	chr14:45870299-45870349	AG09319	gingival:	n/a
8	chr14:46300358-46300408	GM06990	blood:	n/a
9	chr14:45930824-45930874	AG04449	skin:	fetal
10	chr14:45870299-45870349	GM19239	blood:	n/a
11	chr14:46241576-46241626	SK-N-SH_RA	brain:	n/a
12	chr14:46283172-46283222	Caco-2	colon:	n/a
13	chr14:46241576-46241626	NT2-D1	testis:	n/a
14	chr14:46241576-46241626	AG09319	gingival:	n/a
15	chr14:45870299-45870349	BE2_C	brain:	n/a
16	chr14:45930824-45930874	SK-N-SH_RA	brain:	n/a
17	chr14:46358279-46358329	SK-N-MC	brain:	n/a
18	chr14:46358279-46358329	NHBE	bronchial:	n/a
19	chr14:45870299-45870349	HCPEpiC	choroid plexus:	n/a
20	chr14:46358279-46358329	HRE	kidney:	n/a
21	chr14:46283172-46283222	PrEC	prostate:	n/a
22	chr14:46283172-46283222	A549	lung:	n/a
23	chr14:46300358-46300408	AG10803	skin:	n/a
24	chr14:46358279-46358329	NB4	blood:	n/a
25	chr14:46283172-46283222	HAEpiC	amniotic membrane:	n/a
26	chr14:46283172-46283222	U87	brain:	n/a
27	chr14:46300358-46300408	ECC-1	luminal epithelium:	n/a
28	chr14:46358139-46358189	LNCaP	prostate:	n/a
29	chr14:46358139-46358189	HL-60	blood:	n/a
30	chr14:45840127-45840177	IMR90	lung:	fetal
31	chr14:46358279-46358329	U87	brain:	n/a
32	chr14:46300358-46300408	AG04450	lung:	fetal
33	chr14:45840127-45840177	HRE	kidney:	n/a
34	chr14:46358139-46358189	ProgFib	skin:	n/a
35	chr14:46358279-46358329	K562	blood:	n/a
36	chr14:45930824-45930874	NB4	blood:	n/a
37	chr14:45930824-45930874	GM12891	blood:	n/a
38	chr14:45930824-45930874	Caco-2	colon:	n/a
39	chr14:46241576-46241626	CMK	blood:	n/a
40	chr14:46283117-46283167	GM19239	blood:	n/a
41	chr14:45930824-45930874	K562	blood:	n/a
42	chr14:46241576-46241626	HCPEpiC	choroid plexus:	n/a
43	chr14:46283172-46283222	HUVEC	blood vessel:	n/a
44	chr14:45930824-45930874	AG09309	skin:	n/a
45	chr14:45930824-45930874	AG04450	lung:	fetal
46	chr14:46358139-46358189	HMEC	breast:	n/a
47	chr14:45930824-45930874	RPTEC	kidney:	n/a
48	chr14:45930824-45930874	NH-A	brain:	n/a
49	chr14:46283172-46283222	HCF	heart:	n/a
50	chr14:45870299-45870349	H1-hESC	embryonic stem cell:	embryo

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
2	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
3	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
4	chr14:45774667..45776638-chr14:45777456..45779936,2	MCF-7	breast:
5	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
6	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
7	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
8	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
9	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
10	chr14:45895702..45896616-chr14:45996086..45997189,11	MCF-7	breast:
11	chr14:45827598..45829425-chr14:45832240..45834984,2	MCF-7	breast:
12	chr14:45980303..45983033-chr14:45994308..45996794,2	MCF-7	breast:
13	chr14:46120979..46122575-chr14:46124329..46126907,2	K562	blood:
14	chr14:46139668..46140618-chr4:151721697..151722558,2	MCF-7	breast:
15	chr14:46038732..46040536-chr14:46054530..46057374,2	K562	blood:
16	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
17	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
18	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
19	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
20	chr14:45932172..45934812-chr14:45938386..45940699,2	K562	blood:
21	chr14:45773220..45776127-chr14:45776332..45778274,2	K562	blood:
22	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
23	chr14:45973970..45976424-chr14:45980516..45983044,2	MCF-7	breast:
24	chr14:46182590..46185086-chr14:46185381..46187428,2	MCF-7	breast:
25	chr14:45602740..45605100-chr14:45878381..45880365,2	MCF-7	breast:
26	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
27	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
28	chr14:46120979..46122575-chr14:46124329..46126907,2	K562	blood:
29	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
30	chr14:46147083..46148164-chr14:46409225..46410271,4	MCF-7	breast:
31	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
32	chr14:46185365..46185918-chr14:46409681..46410218,2	MCF-7	breast:
33	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
34	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
35	chr14:45833660..45834242-chr14:45996510..45997327,3	MCF-7	breast:
36	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
37	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
38	chr10:29154738..29155346-chr14:46193775..46194564,2	MCF-7	breast:
39	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
40	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
41	chr12:122908054..122908892-chr14:46408991..46409734,2	MCF-7	breast:
42	chr14:46038732..46040536-chr14:46054530..46057374,2	K562	blood:
43	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
44	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
45	chr14:45980303..45983033-chr14:45994308..45996794,2	MCF-7	breast:
46	chr14:45835845..45838000-chr14:45843048..45845340,2	K562	blood:
47	chr14:45895709..45896868-chr14:45996158..45997180,10	MCF-7	breast:
48	chr14:45833828..45835787-chr14:45839702..45842192,2	K562	blood:
49	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
50	chr14:46090382..46092001-chr17:58682515..58685367,2	MCF-7	breast:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-5	chr14:46241339-46241424	XLOC_010816
2	lnc-FANCM-5	chr14:46217809-46217860	XLOC_010816
3	lnc-MIS18BP1-1	chr14:46183506-46183653	NONHSAT036669
4	lnc-MIS18BP1-1	chr14:46184553-46184894	ENSG00000258616
5	lnc-MIS18BP1-1	chr14:46181102-46181156	ENSG00000258616
6	lnc-MIS18BP1-1	chr14:46175461-46175705	ENSG00000258616
7	lnc-MIS18BP1-1	chr14:46177039-46177101	ENSG00000258616
8	lnc-MIS18BP1-1	chr14:46175495-46175705	XLOC_011012
9	lnc-FANCM-5	chr14:46217809-46217893	NONHSAT036668
10	lnc-MIS18BP1-1	chr14:46183487-46183623	ENSG00000258616
11	lnc-MIS18BP1-1	chr14:46175461-46175705	ENSG00000258616
12	lnc-FANCM-5	chr14:46241613-46241659	XLOC_010816
13	lnc-MIS18BP1-1	chr14:46183487-46183656	ENSG00000258616
14	lnc-FANCM-4	chr14:46037729-46038272	ENSG00000258845
15	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
16	lnc-FANCM-10	chr14:46483700-46483934	NONHSAT036677
17	lnc-FANCM-5	chr14:46213325-46213370	XLOC_010816
18	lnc-MIS18BP1-1	chr14:46175453-46175705	ENSG00000258616
19	lnc-FANCM-5	chr14:46179124-46179145	NONHSAT036668
20	lnc-MIS18BP1-1	chr14:46183487-46183634	ENSG00000258616
21	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036668
22	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036670
23	lnc-MIS18BP1-1	chr14:46184553-46185155	ENSG00000258616
24	lnc-MIS18BP1-1	chr14:46181102-46181156	ENSG00000258616
25	lnc-FANCM-6	chr14:46410146-46410221	ENSG00000258700
26	lnc-MIS18BP1-1	chr14:46177058-46177101	NONHSAT036666
27	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675
28	lnc-MIS18BP1-1	chr14:46184553-46185114	NONHSAT036666
29	lnc-FANCM-4	chr14:46037198-46037298	ENSG00000258845
30	lnc-FANCM-5	chr14:46195358-46195474	NONHSAT036670
31	lnc-FANCM-5	chr14:46217539-46217865	NONHSAT036671
32	lnc-MIS18BP1-1	chr14:46175475-46175705	ENSG00000258616
33	lnc-MIS18BP1-1	chr14:46175463-46175705	ENSG00000258616
34	lnc-MIS18BP1-1	chr14:46184553-46185084	NONHSAT036669
35	lnc-FANCM-5	chr14:46241612-46241659	NONHSAT036671
36	lnc-MIS18BP1-1	chr14:46181102-46181226	XLOC_011012
37	lnc-FANCM-5	chr14:46241338-46241424	NONHSAT036671
38	lnc-FANCM-5	chr14:46217809-46217840	NONHSAT036670
39	lnc-MIS18BP1-1	chr14:46184553-46184690	ENSG00000258616
40	lnc-FANCM-5	chr14:46213166-46213370	NONHSAT036671
41	lnc-FANCM-10	chr14:46484296-46484458	NONHSAT036677

No data

Variant related genes	Relation type
ENSG00000260046	TF binding region
ENSG00000258746	TF binding region
ENSG00000258616	TF binding region
ENSG00000258845	TF binding region
ENSG00000264420	TF binding region
ENSG00000257900	TF binding region
LINC00871	TF binding region
ENSG00000260046	CpG island
ENSG00000258746	CpG island
ENSG00000258616	CpG island
ENSG00000258845	CpG island
ENSG00000264420	CpG island
ENSG00000257900	CpG island
LINC00871	CpG island
ENSG00000258616	chromatin interactions
ENSG00000100442	chromatin interactions
ENSG00000258700	chromatin interactions
IGF2BP3	miRNA target sites
CNOT6L	miRNA target sites

Extended variants
information (count: 10122 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:10122 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192125749	chr14:45774815-45774816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147612399	chr14:45774836-45774837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565661100	chr14:45774918-45774919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183869933	chr14:45774931-45774932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534942517	chr14:45774961-45774962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76893429	chr14:45774965-45774966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367635998	chr14:45774999-45775000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548498133	chr14:45775019-45775020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560232758	chr14:45775075-45775076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10149814	chr14:45775137-45775138	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs545812154	chr14:45775142-45775143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74721839	chr14:45775164-45775165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78269233	chr14:45775167-45775168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs118112483	chr14:45775187-45775188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567966014	chr14:45775196-45775197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142127160	chr14:45775262-45775263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187548143	chr14:45775343-45775344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145962625	chr14:45775354-45775355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs534016892	chr14:45775403-45775404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558945492	chr14:45775418-45775419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138427427	chr14:45775474-45775475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570875213	chr14:45775504-45775505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192012586	chr14:45775539-45775540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374080420	chr14:45775574-45775575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188384334	chr14:45783019-45783020	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs368046509	chr14:45783023-45783024	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs140923596	chr14:45783042-45783043	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs527767829	chr14:45783048-45783049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552639855	chr14:45783160-45783161	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570877228	chr14:45783168-45783169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs144597073	chr14:45783194-45783195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs550214722	chr14:45783236-45783237	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs192665313	chr14:45783283-45783284	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561712049	chr14:45783358-45783359	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs554321309	chr14:45783475-45783476	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs571842837	chr14:45783493-45783494	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs539160782	chr14:45783499-45783500	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs557402382	chr14:45783545-45783546	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs17115982	chr14:45783546-45783547	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569554717	chr14:45783587-45783588	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs537057623	chr14:45783607-45783608	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs146673274	chr14:45783609-45783610	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs561874218	chr14:45783639-45783640	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573876960	chr14:45783733-45783734	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs540899050	chr14:45783754-45783755	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs140713911	chr14:45783757-45783758	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs577919134	chr14:45784635-45784636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545212547	chr14:45784637-45784638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74320145	chr14:45784645-45784646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532923271	chr14:45784663-45784664	Enhancers	n/a	n/a	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21390271	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Cancer	19907438	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45774800-45775600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:45783000-45783800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:45784600-45785000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:45784600-45785000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:45784600-45785000	Enhancers	Pancreas	Pancrea
6	chr14:45784600-45785200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr14:45784600-45785200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:45784800-45785200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr14:45801200-45801800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:45801400-45802600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr14:45801800-45802200	Enhancers	Fetal Heart	heart
12	chr14:45801800-45802600	Enhancers	Left Ventricle	heart
13	chr14:45801800-45802800	Enhancers	Adipose Nuclei	Adipose
14	chr14:45802000-45802600	Enhancers	Psoas Muscle	Psoas
15	chr14:45809600-45810400	Enhancers	Colon Smooth Muscle	Colon
16	chr14:45813400-45813600	Enhancers	Gastric	stomach
17	chr14:45814600-45815200	Active TSS	Right Atrium	heart
18	chr14:45814800-45815400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr14:45815000-45815400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:45822400-45822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:45822400-45822800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr14:45822400-45822800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr14:45822400-45823000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr14:45822600-45823000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr14:45822600-45823400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:45830400-45831600	Enhancers	Fetal Heart	heart
27	chr14:45832200-45832400	Enhancers	Right Atrium	heart
28	chr14:45833200-45834200	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr14:45833800-45834400	Enhancers	Adipose Nuclei	Adipose
30	chr14:45833800-45834600	Enhancers	Right Atrium	heart
31	chr14:45837000-45837200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:45837200-45839800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr14:45837400-45841600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:45837600-45837800	Enhancers	H9 Cell Line	embryonic stem cell
35	chr14:45837800-45838000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr14:45837800-45838600	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr14:45838000-45839000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr14:45838600-45838800	Enhancers	H9 Cell Line	embryonic stem cell
39	chr14:45839000-45840400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr14:45839400-45840400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr14:45839600-45840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr14:45839600-45840400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr14:45839600-45840600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr14:45839800-45840600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:45839800-45840800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr14:45840000-45840400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr14:45840000-45840600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr14:45840200-45843200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr14:45840400-45842800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr14:45840400-45843000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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