Variant report

Variant	nsv904421
Chromosome Location	chr15:78041789-78129964
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1227)
CpG islands
(count:1162)
Chromatin interactive
region (count:79)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1227 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78077195-78077543	K562	blood:	n/a	n/a
2	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:78112581-78112794	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr15:78088327-78088760	GM12878	blood:	n/a	n/a
5	BCL3	chr15:78088304-78088829	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:78113815-78114121	K562	blood:	n/a	chr15:78113828-78113844
7	BHLHE40	chr15:78113211-78113483	K562	blood:	n/a	chr15:78113370-78113391 chr15:78113374-78113387
8	BHLHE40	chr15:78095857-78096131	K562	blood:	n/a	n/a
9	BHLHE40	chr15:78102084-78102117	K562	blood:	n/a	n/a
10	BHLHE40	chr15:78089629-78089938	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:78112561-78112947	K562	blood:	n/a	n/a
12	BHLHE40	chr15:78104173-78104542	K562	blood:	n/a	chr15:78104303-78104324 chr15:78104308-78104317 chr15:78104309-78104318 chr15:78104310-78104319 chr15:78104309-78104318 chr15:78104307-78104320
13	BHLHE40	chr15:78096532-78096945	K562	blood:	n/a	n/a
14	BHLHE40	chr15:78045537-78045939	K562	blood:	n/a	n/a
15	BHLHE40	chr15:78101143-78101495	K562	blood:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
16	BHLHE40	chr15:78077441-78077584	K562	blood:	n/a	n/a
17	BHLHE40	chr15:78101148-78101512	HepG2	liver:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
18	BRCA1	chr15:78116340-78116364	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr15:78077171-78077598	K562	blood:	n/a	n/a
20	CBX3	chr15:78052152-78052709	HCT-116	colon:	n/a	n/a
21	CCNT2	chr15:78112531-78112910	K562	blood:	n/a	n/a
22	CEBPB	chr15:78097862-78098204	HepG2	liver:	n/a	chr15:78098032-78098043
23	CEBPB	chr15:78097872-78098202	A549	lung:	n/a	chr15:78098032-78098043
24	CEBPB	chr15:78097972-78098198	Hela-S3	cervix:	n/a	chr15:78098032-78098043
25	CEBPB	chr15:78097885-78098211	K562	blood:	n/a	chr15:78098032-78098043
26	CEBPB	chr15:78044703-78044893	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:78077418-78077509	K562	blood:	n/a	n/a
28	CEBPB	chr15:78056910-78057263	K562	blood:	n/a	n/a
29	CEBPB	chr15:78048679-78048924	HepG2	liver:	n/a	chr15:78048788-78048799
30	CEBPB	chr15:78048637-78048925	A549	lung:	n/a	chr15:78048788-78048799
31	CEBPB	chr15:78097916-78098237	MCF-7	breast:	n/a	chr15:78098032-78098043
32	CEBPB	chr15:78097866-78098207	IMR90	lung:	n/a	chr15:78098032-78098043
33	CEBPB	chr15:78044923-78044935	K562	blood:	n/a	n/a
34	CEBPB	chr15:78097908-78098155	H1-hESC	embryonic stem cell:	n/a	chr15:78098032-78098043
35	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:78114017-78114116	K562	blood:	n/a	n/a
37	CHD2	chr15:78122597-78122722	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr15:78112768-78112882	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr15:78095843-78096168	K562	blood:	n/a	n/a
40	CHD2	chr15:78112731-78112878	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr15:78058928-78058962	K562	blood:	n/a	n/a
42	CHD2	chr15:78089582-78089843	GM12878	blood:	n/a	n/a
43	CHD2	chr15:78093119-78093139	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr15:78128582-78129087	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr15:78077295-78077568	A549	lung:	n/a	n/a
46	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
47	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr15:78112651-78112918	H1-hESC	embryonic stem cell:	n/a	chr15:78112771-78112781
49	CTCF	chr15:78060548-78060777	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr15:78112640-78112790	MCF-7	breast:	n/a	chr15:78112771-78112781

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78103228-78103278	CMK	blood:	n/a
2	chr15:78112818-78112868	MCF10A-Er-Src	breast:	n/a
3	chr15:78114278-78114328	HRE	kidney:	n/a
4	chr15:78103228-78103278	CMK	blood:	n/a
5	chr15:78112818-78112868	MCF10A-Er-Src	breast:	n/a
6	chr15:78114278-78114328	HRE	kidney:	n/a
7	chr15:78108562-78108612	SK-N-SH	brain:	n/a
8	chr15:78114888-78114938	SK-N-SH	brain:	n/a
9	chr15:78112818-78112868	HIPEpiC	eye:	n/a
10	chr15:78111196-78111246	MCF-7	breast:	n/a
11	chr15:78110903-78110953	CMK	blood:	n/a
12	chr15:78111830-78111880	PFSK-1	brain:	n/a
13	chr15:78077656-78077706	HCPEpiC	choroid plexus:	n/a
14	chr15:78114278-78114328	HCM	heart:	n/a
15	chr15:78112026-78112076	GM12892	blood:	n/a
16	chr15:78112026-78112076	HRE	kidney:	n/a
17	chr15:78109450-78109500	HMEC	breast:	n/a
18	chr15:78110106-78110156	HL-60	blood:	n/a
19	chr15:78060295-78060345	MCF-7	breast:	n/a
20	chr15:78060295-78060345	GM12891	blood:	n/a
21	chr15:78110857-78110907	U87	brain:	n/a
22	chr15:78112026-78112076	HCM	heart:	n/a
23	chr15:78118816-78118866	HRPEpiC	eye:	n/a
24	chr15:78114888-78114938	Caco-2	colon:	n/a
25	chr15:78110903-78110953	NT2-D1	testis:	n/a
26	chr15:78112818-78112868	AoSMC	blood vessel:	n/a
27	chr15:78114278-78114328	Hepatocyte	liver:	n/a
28	chr15:78111196-78111246	NT2-D1	testis:	n/a
29	chr15:78110903-78110953	H1-hESC	embryonic stem cell:	embryo
30	chr15:78108562-78108612	SKMC	muscle:	n/a
31	chr15:78077656-78077706	GM12878	blood:	n/a
32	chr15:78111390-78111440	PFSK-1	brain:	n/a
33	chr15:78111830-78111880	Hepatocyte	liver:	n/a
34	chr15:78114278-78114328	ECC-1	luminal epithelium:	n/a
35	chr15:78113237-78113287	HRE	kidney:	n/a
36	chr15:78110903-78110953	HAEpiC	amniotic membrane:	n/a
37	chr15:78103228-78103278	BJ	skin:	n/a
38	chr15:78112818-78112868	H1-hESC	embryonic stem cell:	embryo
39	chr15:78111390-78111440	HUVEC	blood vessel:	n/a
40	chr15:78108562-78108612	AG04449	skin:	fetal
41	chr15:78114888-78114938	CMK	blood:	n/a
42	chr15:78110903-78110953	Hela-S3	cervix:	n/a
43	chr15:78111196-78111246	HPAEpiC	pulmonary alveolar:	n/a
44	chr15:78114278-78114328	HL-60	blood:	n/a
45	chr15:78114888-78114938	SKMC	muscle:	n/a
46	chr15:78113237-78113287	A549	lung:	n/a
47	chr15:78103228-78103278	NHBE	bronchial:	n/a
48	chr15:78112818-78112868	SK-N-SH_RA	brain:	n/a
49	chr15:78112818-78112868	GM12892	blood:	n/a
50	chr15:78113667-78113717	MCF-7	breast:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:77835732..77836546-chr15:78113747..78114395,2	MCF-7	breast:
2	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
3	chr15:78129825..78131680-chr15:78135529..78137556,2	K562	blood:
4	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
5	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
6	chr15:78049442..78052366-chr15:78052707..78054607,2	MCF-7	breast:
7	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
8	chr15:78039556..78042296-chr15:78046861..78049587,2	K562	blood:
9	chr15:77411244..77411752-chr15:78113897..78114465,2	K562	blood:
10	chr15:77951815..77952789-chr15:78075941..78076556,2	K562	blood:
11	chr15:78088888..78092011-chr15:78092368..78096073,3	K562	blood:
12	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
13	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
14	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
15	chr15:77951754..77952701-chr15:78076956..78077942,7	K562	blood:
16	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:
17	chr15:78049309..78052245-chr15:78054880..78058301,3	K562	blood:
18	chr15:77925249..77927257-chr15:78113205..78115049,24	MCF-7	breast:
19	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
20	chr15:78039556..78042296-chr15:78046861..78049587,2	K562	blood:
21	chr15:77951840..77952665-chr15:78112887..78114250,4	MCF-7	breast:
22	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
23	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
24	chr15:78125331..78127542-chr15:78130355..78132025,2	K562	blood:
25	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
26	chr15:77951783..77952314-chr15:78066187..78066759,2	MCF-7	breast:
27	chr15:78116064..78118754-chr15:78122840..78125004,2	MCF-7	breast:
28	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
29	chr15:78029860..78033858-chr15:78038839..78041859,3	K562	blood:
30	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
31	chr15:78086471..78089118-chr20:52208956..52211312,2	MCF-7	breast:
32	chr15:78107758..78109313-chr15:78111361..78113671,2	K562	blood:
33	chr15:78045800..78048382-chr15:78053626..78056901,3	K562	blood:
34	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
35	chr15:78115470..78116424-chr15:78167241..78167877,2	MCF-7	breast:
36	chr15:78115466..78118484-chr15:78120011..78123409,3	MCF-7	breast:
37	chr15:77925491..77927003-chr15:78065547..78066951,12	MCF-7	breast:
38	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:
39	chr15:78103078..78104823-chr15:78106896..78108558,2	K562	blood:
40	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
41	chr15:78049309..78052245-chr15:78054880..78058301,3	K562	blood:
42	chr15:78049442..78052366-chr15:78052707..78054607,2	MCF-7	breast:
43	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
44	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
45	chr15:78045800..78048382-chr15:78053626..78056901,3	K562	blood:
46	chr15:77951738..77952728-chr15:78113529..78114461,5	K562	blood:
47	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:
48	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
49	chr15:78041656..78043427-chr15:78100097..78102130,2	MCF-7	breast:
50	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2D7-5	chr15:78080414-78080487	ENSG00000259213.1
2	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047458
3	lnc-SH2D7-5	chr15:78080723-78081016	ENSG00000259213.1
4	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458
5	lnc-SH2D7-5	chr15:78080231-78081011	XLOC_011317
6	lnc-SH2D7-5	chr15:78079529-78079589	XLOC_011317
7	lnc-SH2D7-5	chr15:78079535-78079589	ENSG00000259213.1
8	lnc-SH2D7-5	chr15:78080231-78080917	ENSG00000259213.1
9	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460
10	lnc-TBC1D2B-7	chr15:78113121-78113196	NONHSAT047459
11	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047460
12	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047459

No data

Variant related genes	Relation type
ENSG00000259213	TF binding region
LINGO1	TF binding region
ENSG00000259213	CpG island
LINGO1	CpG island
ENSG00000259281	chromatin interactions
ENSG00000259213	chromatin interactions
ENSG00000169783	chromatin interactions
ENSG00000171940	chromatin interactions

Extended variants
information (count: 3517 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3517 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11072670	chr15:78041789-78041790	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569059652	chr15:78041812-78041813	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12593505	chr15:78041829-78041830	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs34919191	chr15:78041866-78041867	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558058090	chr15:78041899-78041900	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572802146	chr15:78041947-78041948	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533517113	chr15:78041977-78041978	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555336160	chr15:78041978-78041979	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573699441	chr15:78042020-78042021	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186586483	chr15:78042032-78042033	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563572669	chr15:78042072-78042073	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77251372	chr15:78042138-78042139	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143477230	chr15:78042157-78042158	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190210329	chr15:78042182-78042183	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528495177	chr15:78042215-78042216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181422465	chr15:78042216-78042217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185608841	chr15:78042221-78042222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs59248409	chr15:78042240-78042241	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs551062198	chr15:78042254-78042255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569094754	chr15:78042259-78042260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138129707	chr15:78042302-78042303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376017448	chr15:78042328-78042329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564413106	chr15:78042392-78042393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528631248	chr15:78042413-78042414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566697706	chr15:78042474-78042475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368896432	chr15:78042484-78042485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555094624	chr15:78042485-78042486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573564014	chr15:78042558-78042559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116380241	chr15:78042578-78042579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555809682	chr15:78042580-78042581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189974218	chr15:78042588-78042589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182144275	chr15:78042640-78042641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143599830	chr15:78042686-78042687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs36027456	chr15:78042695-78042696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573487439	chr15:78042696-78042697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55655049	chr15:78042708-78042709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559014122	chr15:78042744-78042745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370303444	chr15:78042751-78042752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35292095	chr15:78042758-78042759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs187562336	chr15:78042765-78042766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551100970	chr15:78042767-78042768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562931045	chr15:78042781-78042782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147187672	chr15:78042782-78042783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369605580	chr15:78042784-78042785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74676874	chr15:78042879-78042880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550843113	chr15:78042896-78042897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191793853	chr15:78042897-78042898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs527621544	chr15:78042930-78042931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114263547	chr15:78042981-78042982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76253314	chr15:78043015-78043016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78032600-78042200	Weak transcription	Fetal Brain Female	brain
2	chr15:78036800-78045800	Weak transcription	Right Atrium	heart
3	chr15:78039200-78042200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:78039400-78041800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr15:78039800-78042000	Enhancers	Esophagus	oesophagus
6	chr15:78040400-78045200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78040400-78046200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr15:78040800-78041800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr15:78040800-78042800	Weak transcription	Spleen	Spleen
10	chr15:78041600-78041800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:78041600-78042200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:78041800-78042000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
13	chr15:78041800-78042000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr15:78041800-78042000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr15:78041800-78042200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chr15:78041800-78042200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr15:78042000-78042200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr15:78042200-78042400	Enhancers	Fetal Brain Female	brain
19	chr15:78042400-78042800	Weak transcription	Fetal Brain Female	brain
20	chr15:78042800-78043000	Enhancers	Fetal Brain Female	brain
21	chr15:78042800-78043400	Enhancers	Spleen	Spleen
22	chr15:78043000-78044400	Weak transcription	Fetal Brain Female	brain
23	chr15:78043400-78045000	Weak transcription	Spleen	Spleen
24	chr15:78044400-78046200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:78044400-78047400	Enhancers	Fetal Brain Female	brain
26	chr15:78044600-78044800	Bivalent Enhancer	Brain Germinal Matrix	brain
27	chr15:78045000-78045600	ZNF genes & repeats	Spleen	Spleen
28	chr15:78045200-78045400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr15:78045200-78046000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:78045400-78046000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:78045600-78047600	Enhancers	Fetal Brain Male	brain
32	chr15:78045600-78048800	Weak transcription	Spleen	Spleen
33	chr15:78045800-78046000	Bivalent Enhancer	Brain Germinal Matrix	brain
34	chr15:78045800-78046200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:78046000-78046200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:78046000-78047200	Enhancers	Brain Germinal Matrix	brain
37	chr15:78046200-78046600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:78046200-78046600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr15:78046200-78048600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:78046600-78046800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:78046600-78051400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr15:78046800-78055200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:78047400-78047800	Weak transcription	Fetal Brain Female	brain
44	chr15:78047600-78051400	Weak transcription	Fetal Brain Male	brain
45	chr15:78047800-78048000	Enhancers	Fetal Brain Female	brain
46	chr15:78048000-78051800	Weak transcription	Fetal Brain Female	brain
47	chr15:78048600-78048800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr15:78048800-78049400	Enhancers	Spleen	Spleen
49	chr15:78051400-78051600	Enhancers	Fetal Brain Male	brain
50	chr15:78051400-78052200	Enhancers	Brain Inferior Temporal Lobe	brain

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