Variant report

Variant	nsv564730
Chromosome Location	chr14:46122141-46729024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2023)
CpG islands
(count:366)
Chromatin interactive
region (count:34)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2023 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
4	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
5	BACH1	chr14:46559473-46559585	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
8	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
9	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
10	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
11	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
12	BATF	chr14:46368023-46368235	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	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
17	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
18	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
19	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
20	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
21	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
22	CBX3	chr14:46256472-46256659	K562	blood:	n/a	n/a
23	CBX3	chr14:46213002-46213438	HCT-116	colon:	n/a	n/a
24	CBX3	chr14:46517423-46517924	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:46134262-46134552	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr14:46523694-46524102	IMR90	lung:	n/a	n/a
27	CEBPB	chr14:46624384-46624661	A549	lung:	n/a	n/a
28	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr14:46477968-46478185	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:46688925-46689144	IMR90	lung:	n/a	chr14:46689036-46689047
31	CEBPB	chr14:46388556-46388893	A549	lung:	n/a	chr14:46388709-46388720
32	CEBPB	chr14:46242879-46243131	IMR90	lung:	n/a	chr14:46243004-46243015
33	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
34	CEBPB	chr14:46688915-46689127	HepG2	liver:	n/a	chr14:46689036-46689047
35	CEBPB	chr14:46270325-46270606	IMR90	lung:	n/a	chr14:46270518-46270529
36	CEBPB	chr14:46560063-46560127	K562	blood:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
37	CEBPB	chr14:46170313-46170577	HepG2	liver:	n/a	chr14:46170421-46170432
38	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
39	CEBPB	chr14:46441220-46441420	H1-hESC	embryonic stem cell:	n/a	chr14:46441316-46441327
40	CEBPB	chr14:46441175-46441403	HepG2	liver:	n/a	chr14:46441316-46441327
41	CEBPB	chr14:46587638-46587921	HepG2	liver:	n/a	chr14:46587769-46587780
42	CEBPB	chr14:46629835-46630166	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
44	CEBPB	chr14:46673638-46673846	HepG2	liver:	n/a	chr14:46673736-46673749 chr14:46673736-46673747 chr14:46673736-46673749
45	CEBPB	chr14:46248535-46248671	HepG2	liver:	n/a	chr14:46248607-46248618
46	CEBPB	chr14:46134164-46134582	MCF-7	breast:	n/a	n/a
47	CEBPB	chr14:46559920-46560194	A549	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
48	CEBPB	chr14:46559908-46560222	IMR90	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
49	CEBPB	chr14:46232907-46233168	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:46504563-46504826	IMR90	lung:	n/a	chr14:46504676-46504687

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46300358-46300408	HRE	kidney:	n/a
2	chr14:46241576-46241626	AG04449	skin:	fetal
3	chr14:46358139-46358189	AoSMC	blood vessel:	n/a
4	chr14:46358139-46358189	SK-N-MC	brain:	n/a
5	chr14:46283172-46283222	HepG2	liver:	n/a
6	chr14:46283172-46283222	MCF-7	breast:	n/a
7	chr14:46358279-46358329	ECC-1	luminal epithelium:	n/a
8	chr14:46358139-46358189	K562	blood:	n/a
9	chr14:46358279-46358329	NB4	blood:	n/a
10	chr14:46358279-46358329	AG10803	skin:	n/a
11	chr14:46241576-46241626	Hepatocyte	liver:	n/a
12	chr14:46300358-46300408	Jurkat	blood:	n/a
13	chr14:46300358-46300408	SK-N-SH	brain:	n/a
14	chr14:46283172-46283222	Hela-S3	cervix:	n/a
15	chr14:46358279-46358329	HepG2	liver:	n/a
16	chr14:46358279-46358329	ProgFib	skin:	n/a
17	chr14:46358279-46358329	PANC-1	pancreas:	n/a
18	chr14:46283117-46283167	Hepatocyte	liver:	n/a
19	chr14:46241576-46241626	RPTEC	kidney:	n/a
20	chr14:46358139-46358189	PANC-1	pancreas:	n/a
21	chr14:46358279-46358329	MCF10A-Er-Src	breast:	n/a
22	chr14:46283117-46283167	PFSK-1	brain:	n/a
23	chr14:46300358-46300408	AG04449	skin:	fetal
24	chr14:46300358-46300408	NH-A	brain:	n/a
25	chr14:46358279-46358329	AG04449	skin:	fetal
26	chr14:46283117-46283167	IMR90	lung:	fetal
27	chr14:46283172-46283222	BE2_C	brain:	n/a
28	chr14:46358279-46358329	HCPEpiC	choroid plexus:	n/a
29	chr14:46300358-46300408	HCF	heart:	n/a
30	chr14:46300358-46300408	HCT-116	colon:	n/a
31	chr14:46358139-46358189	NHBE	bronchial:	n/a
32	chr14:46241576-46241626	HRCEpiC	kidney:	n/a
33	chr14:46283117-46283167	ECC-1	luminal epithelium:	n/a
34	chr14:46300358-46300408	GM12891	blood:	n/a
35	chr14:46358279-46358329	NT2-D1	testis:	n/a
36	chr14:46358139-46358189	H1-hESC	embryonic stem cell:	embryo
37	chr14:46283117-46283167	AG04450	lung:	fetal
38	chr14:46283172-46283222	K562	blood:	n/a
39	chr14:46283172-46283222	SK-N-SH	brain:	n/a
40	chr14:46241576-46241626	HIPEpiC	eye:	n/a
41	chr14:46241576-46241626	HRE	kidney:	n/a
42	chr14:46241576-46241626	SK-N-SH	brain:	n/a
43	chr14:46358279-46358329	HCF	heart:	n/a
44	chr14:46241576-46241626	AG09309	skin:	n/a
45	chr14:46283172-46283222	AG10803	skin:	n/a
46	chr14:46300358-46300408	PFSK-1	brain:	n/a
47	chr14:46283117-46283167	HCM	heart:	n/a
48	chr14:46283117-46283167	NH-A	brain:	n/a
49	chr14:46358139-46358189	BJ	skin:	n/a
50	chr14:46300358-46300408	RPTEC	kidney:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
2	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
3	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
4	chr14:46120979..46122575-chr14:46124329..46126907,2	K562	blood:
5	chr12:122908054..122908892-chr14:46408991..46409734,2	MCF-7	breast:
6	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
7	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
8	chr14:46538407..46539085-chr4:43195045..43195862,2	MCF-7	breast:
9	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
10	chr14:46147083..46148164-chr14:46409225..46410271,4	MCF-7	breast:
11	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
12	chr14:46185365..46185918-chr14:46409681..46410218,2	MCF-7	breast:
13	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
14	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
15	chr14:46182590..46185086-chr14:46185381..46187428,2	MCF-7	breast:
16	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
17	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
18	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
19	chr14:46718996..46719973-chr14:46813315..46814211,4	MCF-7	breast:
20	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
21	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
22	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
23	chr14:46120979..46122575-chr14:46124329..46126907,2	K562	blood:
24	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
25	chr14:46139668..46140618-chr4:151721697..151722558,2	MCF-7	breast:
26	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
27	chr14:46557288..46558270-chr17:53789584..53790485,2	MCF-7	breast:
28	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:
29	chr14:46719211..46719811-chr14:46813566..46814094,2	MCF-7	breast:
30	chr14:46517458..46517985-chr14:47049934..47050581,2	MCF-7	breast:
31	chr10:29154738..29155346-chr14:46193775..46194564,2	MCF-7	breast:
32	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
33	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
34	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700
2	lnc-FANCM-6	chr14:46680027-46680142	ENSG00000258700
3	lnc-FANCM-5	chr14:46241338-46241424	NONHSAT036671
4	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036678
5	lnc-FANCM-10	chr14:46483700-46483934	NONHSAT036677
6	lnc-MIS18BP1-1	chr14:46177039-46177101	ENSG00000258616
7	lnc-MIS18BP1-1	chr14:46184553-46185084	NONHSAT036669
8	lnc-MIS18BP1-1	chr14:46183487-46183623	ENSG00000258616
9	lnc-FANCM-5	chr14:46195358-46195474	NONHSAT036670
10	lnc-FANCM-10	chr14:46484296-46484458	NONHSAT036677
11	lnc-FANCM-5	chr14:46217809-46217860	XLOC_010816
12	lnc-MIS18BP1-1	chr14:46184553-46184690	ENSG00000258616
13	lnc-MIS18BP1-1	chr14:46175495-46175705	XLOC_011012
14	lnc-FANCM-5	chr14:46213325-46213370	XLOC_010816
15	lnc-FANCM-5	chr14:46241612-46241659	NONHSAT036671
16	lnc-MIS18BP1-1	chr14:46175453-46175705	ENSG00000258616
17	lnc-FANCM-5	chr14:46217539-46217865	NONHSAT036671
18	lnc-MIS18BP1-1	chr14:46181102-46181156	ENSG00000258616
19	lnc-FANCM-5	chr14:46241613-46241659	XLOC_010816
20	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036678
21	lnc-FANCM-5	chr14:46217809-46217893	NONHSAT036668
22	lnc-MIS18BP1-1	chr14:46184553-46184894	ENSG00000258616
23	lnc-MIS18BP1-1	chr14:46175463-46175705	ENSG00000258616
24	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036668
25	lnc-FANCM-5	chr14:46217809-46217840	NONHSAT036670
26	lnc-MIS18BP1-1	chr14:46181102-46181226	XLOC_011012
27	lnc-FANCM-5	chr14:46213235-46213370	NONHSAT036670
28	lnc-FANCM-6	chr14:46533362-46533419	ENSG00000258700
29	lnc-FANCM-6	chr14:46410146-46410221	ENSG00000258700
30	lnc-MIS18BP1-1	chr14:46175461-46175705	ENSG00000258616
31	lnc-FANCM-5	chr14:46213166-46213370	NONHSAT036671
32	lnc-MIS18BP1-1	chr14:46184553-46185114	NONHSAT036666
33	lnc-MIS18BP1-1	chr14:46177058-46177101	NONHSAT036666
34	lnc-MIS18BP1-1	chr14:46183487-46183656	ENSG00000258616
35	lnc-MIS18BP1-1	chr14:46184553-46185155	ENSG00000258616
36	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675
37	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
38	lnc-FANCM-5	chr14:46241339-46241424	XLOC_010816
39	lnc-FANCM-6	chr14:46680950-46681007	NONHSAT036679
40	lnc-MIS18BP1-1	chr14:46183506-46183653	NONHSAT036669
41	lnc-MIS18BP1-1	chr14:46181102-46181156	ENSG00000258616
42	lnc-MIS18BP1-1	chr14:46175475-46175705	ENSG00000258616
43	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036678
44	lnc-FANCM-5	chr14:46179124-46179145	NONHSAT036668
45	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036679
46	lnc-MIS18BP1-1	chr14:46183487-46183634	ENSG00000258616
47	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
48	lnc-FANCM-6	chr14:46680950-46681007	ENSG00000258700
49	lnc-FANCM-6	chr14:46680027-46680142	NONHSAT036679
50	lnc-MIS18BP1-1	chr14:46175461-46175705	ENSG00000258616

No data

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

Extended variants
information (count: 7376 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:7376 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12895143	chr14:46122141-46122142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565397099	chr14:46122182-46122183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371135473	chr14:46122183-46122184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151179673	chr14:46122195-46122196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534347712	chr14:46122232-46122233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534332836	chr14:46122254-46122255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559198317	chr14:46122255-46122256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76095040	chr14:46122280-46122281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538564476	chr14:46122313-46122314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574336660	chr14:46122347-46122348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116565559	chr14:46122385-46122386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76231919	chr14:46127025-46127026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566439198	chr14:46127173-46127174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527240061	chr14:46127271-46127272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551800911	chr14:46127289-46127290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373678372	chr14:46127290-46127291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570443227	chr14:46127302-46127303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147969839	chr14:46127380-46127381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557249555	chr14:46127408-46127409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569402241	chr14:46127471-46127472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536458660	chr14:46127477-46127478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140605985	chr14:46127496-46127497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542385319	chr14:46127512-46127513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540629510	chr14:46127536-46127537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527638956	chr14:46127548-46127549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111295792	chr14:46127567-46127568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201242972	chr14:46127602-46127603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202156604	chr14:46127604-46127605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577251754	chr14:46127614-46127615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10144332	chr14:46127637-46127638	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs116562827	chr14:46127647-46127648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529864468	chr14:46127668-46127669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532050898	chr14:46127708-46127709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559104627	chr14:46127753-46127754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150445221	chr14:46127776-46127777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117011622	chr14:46127807-46127808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138281183	chr14:46127809-46127810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551739359	chr14:46127840-46127841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570454042	chr14:46127885-46127886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75371852	chr14:46127906-46127907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543832114	chr14:46127929-46127930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs60824579	chr14:46127943-46127944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376411333	chr14:46127944-46127945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs368975234	chr14:46127945-46127946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184763016	chr14:46127954-46127955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1266286	chr14:46127969-46127970	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs377609795	chr14:46128004-46128005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80086865	chr14:46128059-46128060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187534381	chr14:46128090-46128091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192150600	chr14:46128109-46128110	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21390271	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46122000-46122400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr14:46127000-46128400	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr14:46127800-46128200	Enhancers	Rectal Smooth Muscle	rectum
4	chr14:46128000-46128200	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr14:46146400-46146800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:46146800-46147000	Enhancers	NHEK	skin
7	chr14:46146800-46149800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr14:46147200-46148200	Weak transcription	NHEK	skin
9	chr14:46147600-46151200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr14:46148000-46148600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr14:46148000-46150600	Enhancers	HSMM	muscle
12	chr14:46148200-46148400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:46148200-46148400	Enhancers	HSMMtube	muscle
14	chr14:46148200-46149000	Enhancers	NHEK	skin
15	chr14:46148200-46149600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:46148200-46150400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:46148200-46150600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:46148200-46150800	Enhancers	HUVEC	blood vessel
19	chr14:46148200-46152200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:46148600-46148800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:46148600-46148800	Enhancers	NHLF	lung
22	chr14:46148600-46149000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr14:46148600-46149200	Enhancers	HMEC	breast
24	chr14:46148600-46149400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:46148600-46150400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:46148800-46149400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr14:46148800-46149400	Enhancers	Rectal Smooth Muscle	rectum
28	chr14:46148800-46149600	Enhancers	Colon Smooth Muscle	Colon
29	chr14:46148800-46149800	Weak transcription	NHLF	lung
30	chr14:46148800-46150400	Enhancers	NH-A	brain
31	chr14:46148800-46150600	Enhancers	Osteobl	bone
32	chr14:46149000-46149200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:46149000-46149200	Flanking Active TSS	NHEK	skin
34	chr14:46149000-46149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr14:46149000-46149400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr14:46149000-46150000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr14:46149000-46150600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:46149200-46149400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:46149200-46149400	Enhancers	NHEK	skin
40	chr14:46149200-46150200	Weak transcription	HMEC	breast
41	chr14:46149400-46149600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr14:46149400-46149600	Flanking Active TSS	NHEK	skin
43	chr14:46149400-46149800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr14:46149400-46149800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:46149400-46150200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr14:46149400-46150400	Weak transcription	Rectal Smooth Muscle	rectum
47	chr14:46149600-46150600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr14:46149600-46150600	Enhancers	NHEK	skin
49	chr14:46149800-46150000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:46149800-46150400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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