Variant report

Variant	nsv949528
Chromosome Location	chr15:54041154-54281981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1610)
CpG islands
(count:916)
Chromatin interactive
region (count:46)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:54210484-54211065	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:54122872-54124852	HepG2	liver:	n/a	chr15:54124032-54124048
3	ARID3A	chr15:54100317-54100664	HepG2	liver:	n/a	chr15:54100560-54100576
4	ARID3A	chr15:54125132-54126029	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:54161924-54162226	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:54136050-54137124	HepG2	liver:	n/a	n/a
7	BACH1	chr15:54270443-54270603	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:54255417-54255420	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr15:54269100-54269383	GM12878	blood:	n/a	chr15:54269243-54269254
10	BCL3	chr15:54124056-54124467	A549	lung:	n/a	n/a
11	BCL3	chr15:54123951-54124626	A549	lung:	n/a	n/a
12	BHLHE40	chr15:54210429-54210824	HepG2	liver:	n/a	n/a
13	BHLHE40	chr15:54270556-54270727	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:54269170-54269333	HepG2	liver:	n/a	n/a
15	BHLHE40	chr15:54123267-54123462	HepG2	liver:	n/a	n/a
16	BHLHE40	chr15:54267062-54267260	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:54269065-54269371	GM12878	blood:	n/a	n/a
18	CEBPB	chr15:54211234-54211565	IMR90	lung:	n/a	n/a
19	CEBPB	chr15:54213553-54213869	A549	lung:	n/a	chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213724-54213737
20	CEBPB	chr15:54254561-54254881	IMR90	lung:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
21	CEBPB	chr15:54202264-54202783	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:54125524-54125854	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:54213626-54213826	H1-hESC	embryonic stem cell:	n/a	chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213724-54213737
24	CEBPB	chr15:54213590-54213884	IMR90	lung:	n/a	chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213726-54213735 chr15:54213724-54213737
25	CEBPB	chr15:54123168-54123538	HepG2	liver:	n/a	chr15:54123338-54123349
26	CEBPB	chr15:54063100-54063415	HepG2	liver:	n/a	chr15:54063268-54063279
27	CEBPB	chr15:54254557-54254885	A549	lung:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
28	CEBPB	chr15:54080501-54080573	A549	lung:	n/a	chr15:54080531-54080544
29	CEBPB	chr15:54063126-54063389	A549	lung:	n/a	chr15:54063268-54063279
30	CEBPB	chr15:54202350-54202790	MCF-7	breast:	n/a	n/a
31	CEBPB	chr15:54075082-54075175	K562	blood:	n/a	n/a
32	CEBPB	chr15:54211248-54211523	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr15:54123158-54123539	HepG2	liver:	n/a	chr15:54123338-54123349
34	CEBPB	chr15:54254620-54254904	K562	blood:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
35	CEBPB	chr15:54264954-54265172	HepG2	liver:	n/a	chr15:54265094-54265107 chr15:54265094-54265105 chr15:54265096-54265107
36	CEBPB	chr15:54210598-54210895	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:54078654-54078952	HepG2	liver:	n/a	chr15:54078793-54078804
38	CEBPB	chr15:54254551-54254923	HepG2	liver:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
39	CEBPB	chr15:54206106-54206325	IMR90	lung:	n/a	chr15:54206161-54206172 chr15:54206224-54206232
40	CEBPB	chr15:54250295-54250528	HepG2	liver:	n/a	chr15:54250456-54250467
41	CEBPB	chr15:54202309-54202822	A549	lung:	n/a	n/a
42	CEBPB	chr15:54063214-54063311	H1-hESC	embryonic stem cell:	n/a	chr15:54063268-54063279
43	CEBPB	chr15:54254502-54254970	MCF-7	breast:	n/a	chr15:54254727-54254740 chr15:54254727-54254738 chr15:54254729-54254740 chr15:54254727-54254740
44	CEBPB	chr15:54202466-54202778	HepG2	liver:	n/a	n/a
45	CEBPB	chr15:54272984-54273248	HepG2	liver:	n/a	chr15:54273084-54273095
46	CEBPB	chr15:54123151-54123440	A549	lung:	n/a	chr15:54123338-54123349
47	CEBPB	chr15:54123212-54123404	HepG2	liver:	n/a	chr15:54123338-54123349
48	CEBPB	chr15:54202204-54202821	MCF-7	breast:	n/a	n/a
49	CEBPB	chr15:54136388-54136773	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:54197905-54198090	HepG2	liver:	n/a	chr15:54198031-54198042

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54049269-54049319	HEK293	kidney:	embryo
2	chr15:54049269-54049319	HEK293	kidney:	embryo
3	chr15:54052305-54052355	HRPEpiC	eye:	n/a
4	chr15:54051239-54051289	AG04449	skin:	fetal
5	chr15:54270947-54270997	GM19239	blood:	n/a
6	chr15:54055336-54055386	NHBE	bronchial:	n/a
7	chr15:54270661-54270711	AoSMC	blood vessel:	n/a
8	chr15:54051543-54051593	HCT-116	colon:	n/a
9	chr15:54051239-54051289	PrEC	prostate:	n/a
10	chr15:54270947-54270997	PANC-1	pancreas:	n/a
11	chr15:54051543-54051593	GM19239	blood:	n/a
12	chr15:54051901-54051951	AG04450	lung:	fetal
13	chr15:54055336-54055386	Hela-S3	cervix:	n/a
14	chr15:54270947-54270997	GM06990	blood:	n/a
15	chr15:54051901-54051951	MCF10A-Er-Src	breast:	n/a
16	chr15:54270947-54270997	HepG2	liver:	n/a
17	chr15:54052305-54052355	BJ	skin:	n/a
18	chr15:54055336-54055386	ovcar-3	ovarian:	n/a
19	chr15:54051880-54051930	GM06990	blood:	n/a
20	chr15:54052740-54052790	GM12878	blood:	n/a
21	chr15:54124220-54124270	U87	brain:	n/a
22	chr15:54270693-54270743	HCF	heart:	n/a
23	chr15:54051239-54051289	HUVEC	blood vessel:	n/a
24	chr15:54270693-54270743	HCT-116	colon:	n/a
25	chr15:54124220-54124270	Hela-S3	cervix:	n/a
26	chr15:54049269-54049319	AG09309	skin:	n/a
27	chr15:54270557-54270607	GM06990	blood:	n/a
28	chr15:54051901-54051951	IMR90	lung:	fetal
29	chr15:54051901-54051951	HCT-116	colon:	n/a
30	chr15:54049269-54049319	MCF-7	breast:	n/a
31	chr15:54051239-54051289	HPAEpiC	pulmonary alveolar:	n/a
32	chr15:54270947-54270997	ECC-1	luminal epithelium:	n/a
33	chr15:54051543-54051593	GM12891	blood:	n/a
34	chr15:54051239-54051289	RPTEC	kidney:	n/a
35	chr15:54051239-54051289	K562	blood:	n/a
36	chr15:54049269-54049319	T-47D	breast:	n/a
37	chr15:54124220-54124270	AoSMC	blood vessel:	n/a
38	chr15:54051901-54051951	HL-60	blood:	n/a
39	chr15:54055336-54055386	LNCaP	prostate:	n/a
40	chr15:54051747-54051797	HL-60	blood:	n/a
41	chr15:54270947-54270997	MCF10A-Er-Src	breast:	n/a
42	chr15:54051880-54051930	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:54270947-54270997	HRPEpiC	eye:	n/a
44	chr15:54049269-54049319	Hela-S3	cervix:	n/a
45	chr15:54051901-54051951	AG09319	gingival:	n/a
46	chr15:54051880-54051930	CMK	blood:	n/a
47	chr15:54271167-54271217	NH-A	brain:	n/a
48	chr15:54055336-54055386	IMR90	lung:	fetal
49	chr15:54051747-54051797	Caco-2	colon:	n/a
50	chr15:54051901-54051951	BE2_C	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54034974..54037119-chr15:54039892..54041894,2	MCF-7	breast:
2	chr15:54194862..54196938-chr15:54208486..54210997,2	MCF-7	breast:
3	chr15:54242646..54244179-chr15:54244228..54246313,2	MCF-7	breast:
4	chr15:54113534..54116285-chr15:54122883..54124924,2	MCF-7	breast:
5	chr15:54166889..54167944-chr15:54254910..54255478,3	MCF-7	breast:
6	chr15:54266407..54270072-chr15:55486535..55491034,4	MCF-7	breast:
7	chr15:54103478..54104302-chr15:54255062..54255563,2	MCF-7	breast:
8	chr15:54050503..54054059-chr15:54055807..54059339,3	MCF-7	breast:
9	chr15:54254908..54255701-chr15:55489106..55489772,3	MCF-7	breast:
10	chr15:54166967..54168008-chr15:54254966..54255810,4	MCF-7	breast:
11	chr15:54242646..54244179-chr15:54244228..54246313,2	MCF-7	breast:
12	chr15:54198099..54200218-chr15:54201016..54202612,2	MCF-7	breast:
13	chr15:54254831..54255689-chr15:55400781..55401468,2	MCF-7	breast:
14	chr15:54198099..54200218-chr15:54201016..54202612,2	MCF-7	breast:
15	chr15:54103478..54104302-chr15:54255062..54255563,2	MCF-7	breast:
16	chr15:54077990..54080956-chr15:54224851..54227112,2	MCF-7	breast:
17	chr15:54207936..54209663-chr15:54213507..54215025,2	MCF-7	breast:
18	chr15:54207577..54208228-chr6:107100580..107101438,2	MCF-7	breast:
19	chr15:54131232..54133067-chr15:54139996..54141988,3	MCF-7	breast:
20	chr15:54116856..54119680-chr15:54121215..54123914,2	MCF-7	breast:
21	chr15:54164441..54166381-chr15:54167099..54170073,2	MCF-7	breast:
22	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
23	chr15:54103533..54104375-chr15:54255060..54255801,2	MCF-7	breast:
24	chr1:181074348..181075243-chr15:54127964..54128671,2	MCF-7	breast:
25	chr15:54254706..54255764-chr15:54268796..54269699,6	MCF-7	breast:
26	chr15:54254685..54255342-chr15:54375170..54375703,2	MCF-7	breast:
27	chr15:54166967..54168008-chr15:54254966..54255810,4	MCF-7	breast:
28	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
29	chr15:54050503..54054059-chr15:54055807..54059339,3	MCF-7	breast:
30	chr15:54207936..54209663-chr15:54213507..54215025,2	MCF-7	breast:
31	chr15:54254851..54255818-chr15:55460244..55461151,4	MCF-7	breast:
32	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
33	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
34	chr15:54194862..54196938-chr15:54208486..54210997,2	MCF-7	breast:
35	chr15:54254977..54255831-chr15:54374717..54376166,5	MCF-7	breast:
36	chr15:54100067..54100735-chr15:54254841..54255517,2	MCF-7	breast:
37	chr15:54121587..54123725-chr15:55486823..55489231,2	MCF-7	breast:
38	chr15:54077990..54080956-chr15:54224851..54227112,2	MCF-7	breast:
39	chr15:54164441..54166381-chr15:54167099..54170073,2	MCF-7	breast:
40	chr15:54116856..54119680-chr15:54121215..54123914,2	MCF-7	breast:
41	chr15:54100067..54100735-chr15:54254841..54255517,2	MCF-7	breast:
42	chr15:54254945..54255611-chr15:55399622..55400326,2	MCF-7	breast:
43	chr15:54131232..54133067-chr15:54139996..54141988,3	MCF-7	breast:
44	chr15:54113534..54116285-chr15:54122883..54124924,2	MCF-7	breast:
45	chr15:54103533..54104375-chr15:54255060..54255801,2	MCF-7	breast:
46	chr15:54166889..54167944-chr15:54254910..54255478,3	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-1	chr15:54240343-54240805	ENSG00000259669.1
2	lnc-WDR72-1	chr15:54239821-54240033	ENSG00000259669.1
3	lnc-WDR72-1	chr15:54267015-54267136	ENSG00000259669.1
4	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
5	lnc-WDR72-1	chr15:54240403-54240805	ENSG00000259669.1
6	lnc-WDR72-1	chr15:54260199-54260347	ENSG00000259669.1
7	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
8	lnc-WDR72-1	chr15:54240686-54240805	ENSG00000259669.1
9	lnc-WDR72-1	chr15:54267015-54267165	ENSG00000259669.1
10	lnc-WDR72-1	chr15:54268965-54269105	ENSG00000259669.1
11	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
12	lnc-WDR72-3	chr15:54129468-54129757	NONHSAT043971
13	lnc-WDR72-1	chr15:54264872-54264981	NONHSAT140240
14	lnc-WDR72-1	chr15:54267015-54267206	NONHSAT140240
15	lnc-WDR72-1	chr15:54267015-54267147	ENSG00000259669.1
16	lnc-WDR72-1	chr15:54260199-54260347	ENSG00000259669.1
17	lnc-WDR72-1	chr15:54247966-54248028	ENSG00000259669.1
18	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
19	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1

No data

Variant related genes	Relation type
ENSG00000259301	TF binding region
ENSG00000259669	TF binding region
RNU6-449P	TF binding region
WDR72	TF binding region
ENSG00000259301	CpG island
ENSG00000259669	CpG island
RNU6-449P	CpG island
WDR72	CpG island
ENSG00000137876	chromatin interactions
ENSG00000166415	chromatin interactions
ENSG00000259669	chromatin interactions
ENSG00000206641	chromatin interactions

Extended variants
information (count: 6067 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6067 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560728	chr15:54041154-54041155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550417465	chr15:54041175-54041176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570407355	chr15:54041203-54041204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192721552	chr15:54041205-54041206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546369856	chr15:54041259-54041260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74015923	chr15:54041271-54041272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184545782	chr15:54041294-54041295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375602843	chr15:54041364-54041365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189279035	chr15:54041440-54041441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192679834	chr15:54041442-54041443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369345664	chr15:54041456-54041457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537861240	chr15:54041462-54041463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140292227	chr15:54041504-54041505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578244403	chr15:54041534-54041535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540961270	chr15:54041544-54041545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554371190	chr15:54041604-54041605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555000566	chr15:54041651-54041652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150062182	chr15:54041755-54041756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145383940	chr15:54041792-54041793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76945083	chr15:54041870-54041871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543805484	chr15:54041891-54041892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184249505	chr15:54041914-54041915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533044774	chr15:54041923-54041924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs59972881	chr15:54041949-54041950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149195191	chr15:54041951-54041952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142387425	chr15:54041965-54041966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549417492	chr15:54041966-54041967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190374594	chr15:54041982-54041983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569242910	chr15:54042025-54042026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2126188	chr15:54042026-54042027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs146839662	chr15:54042053-54042054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571682471	chr15:54042079-54042080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553610259	chr15:54042110-54042111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140631183	chr15:54042211-54042212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554171029	chr15:54042242-54042243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145687433	chr15:54042272-54042273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58173594	chr15:54042294-54042295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs556766564	chr15:54042387-54042388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531688240	chr15:54042446-54042447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575230093	chr15:54042501-54042502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138266931	chr15:54042510-54042511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78726254	chr15:54042537-54042538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532788411	chr15:54042561-54042562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575048560	chr15:54042582-54042583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181150559	chr15:54042583-54042584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186649453	chr15:54042638-54042639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542436371	chr15:54042709-54042710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115061137	chr15:54042754-54042755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141171346	chr15:54042791-54042792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569068338	chr15:54042808-54042809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54039800-54047800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:54040600-54050000	Weak transcription	Fetal Kidney	kidney
3	chr15:54047800-54048000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr15:54048000-54048400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr15:54048400-54048600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr15:54050000-54051000	Active TSS	Fetal Kidney	kidney
7	chr15:54050200-54050400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:54050200-54050600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
9	chr15:54050400-54050600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:54050400-54050600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:54050400-54051200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:54050600-54050800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
13	chr15:54050600-54050800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr15:54050600-54050800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr15:54050600-54051000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr15:54050600-54052200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:54050800-54051200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
18	chr15:54050800-54051400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
19	chr15:54050800-54052200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
20	chr15:54050800-54052400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr15:54051000-54051200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
22	chr15:54051000-54051200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr15:54051000-54051400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr15:54051000-54051400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:54051000-54051400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:54051000-54051400	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr15:54051000-54051800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr15:54051000-54051800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr15:54051000-54052200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr15:54051000-54052200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
31	chr15:54051000-54052200	Bivalent/Poised TSS	Fetal Kidney	kidney
32	chr15:54051000-54052400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
33	chr15:54051200-54051400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:54051200-54051400	Enhancers	Liver	Liver
35	chr15:54051200-54051400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr15:54051200-54051600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:54051200-54051600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr15:54051200-54051600	Bivalent Enhancer	Fetal Intestine Large	intestine
39	chr15:54051200-54051600	Enhancers	Pancreas	Pancrea
40	chr15:54051200-54051800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
41	chr15:54051200-54051800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:54051200-54051800	Active TSS	Duodenum Mucosa	Duodenum
43	chr15:54051200-54052000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
44	chr15:54051200-54052400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
45	chr15:54051400-54051600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr15:54051400-54051600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:54051400-54051600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
48	chr15:54051400-54051600	Bivalent Enhancer	Adipose Nuclei	Adipose
49	chr15:54051400-54051600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
50	chr15:54051400-54051600	Bivalent Enhancer	Fetal Lung	lung

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