Variant report

Variant	nsv542368
Chromosome Location	chr15:43056145-43262736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1629)
CpG islands
(count:1284)
Chromatin interactive
region (count:71)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1629 , 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	chr15:43212851-43213468	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43084973-43084978	K562	blood:	n/a	n/a
3	ARID3A	chr15:43201623-43201823	K562	blood:	n/a	n/a
4	ARID3A	chr15:43203332-43203532	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:43210078-43210609	K562	blood:	n/a	n/a
6	ARID3A	chr15:43195629-43195773	K562	blood:	n/a	n/a
7	ARID3A	chr15:43211191-43212159	K562	blood:	n/a	n/a
8	ARID3A	chr15:43149379-43149394	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:43218927-43219225	K562	blood:	n/a	n/a
10	ARID3A	chr15:43218923-43219234	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:43232723-43232915	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:43213015-43213273	K562	blood:	n/a	n/a
13	ARID3A	chr15:43211757-43212427	HepG2	liver:	n/a	n/a
14	ATF1	chr15:43249174-43249360	K562	blood:	n/a	n/a
15	ATF1	chr15:43212928-43213441	K562	blood:	n/a	n/a
16	ATF2	chr15:43212845-43213483	GM12878	blood:	n/a	n/a
17	ATF2	chr15:43182779-43183086	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:43063754-43063800	K562	blood:	n/a	n/a
19	BACH1	chr15:43200945-43201043	K562	blood:	n/a	n/a
20	BACH1	chr15:43249047-43249355	K562	blood:	n/a	n/a
21	BACH1	chr15:43213330-43213542	K562	blood:	n/a	n/a
22	BACH1	chr15:43213051-43213935	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr15:43196188-43196507	GM12878	blood:	n/a	n/a
24	BATF	chr15:43196217-43196391	GM12878	blood:	n/a	n/a
25	BATF	chr15:43211580-43211917	GM12878	blood:	n/a	n/a
26	BATF	chr15:43186195-43186482	GM12878	blood:	n/a	n/a
27	BATF	chr15:43183826-43184145	GM12878	blood:	n/a	chr15:43183946-43183957
28	BATF	chr15:43211598-43211905	GM12878	blood:	n/a	n/a
29	BCLAF1	chr15:43212867-43213317	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:43212956-43213479	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:43212327-43212625	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:43212878-43213387	K562	blood:	n/a	n/a
33	BHLHE40	chr15:43212105-43212527	K562	blood:	n/a	n/a
34	BHLHE40	chr15:43212312-43213509	HepG2	liver:	n/a	n/a
35	BHLHE40	chr15:43218918-43219249	GM12878	blood:	n/a	n/a
36	BRCA1	chr15:43235587-43235646	HepG2	liver:	n/a	n/a
37	BRCA1	chr15:43212975-43213476	HepG2	liver:	n/a	n/a
38	BRCA1	chr15:43213027-43213572	GM12878	blood:	n/a	n/a
39	BRCA1	chr15:43212946-43213494	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr15:43218950-43219226	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr15:43248812-43249305	K562	blood:	n/a	n/a
42	CBX3	chr15:43136108-43136415	K562	blood:	n/a	n/a
43	CBX3	chr15:43212871-43213571	K562	blood:	n/a	n/a
44	CBX3	chr15:43135978-43136424	K562	blood:	n/a	n/a
45	CCNT2	chr15:43249078-43249284	K562	blood:	n/a	n/a
46	CCNT2	chr15:43212150-43213369	K562	blood:	n/a	chr15:43212614-43212623 chr15:43212528-43212537
47	CEBPB	chr15:43249014-43249233	K562	blood:	n/a	chr15:43249128-43249139
48	CEBPB	chr15:43249025-43249277	A549	lung:	n/a	chr15:43249128-43249139
49	CEBPB	chr15:43120859-43120958	K562	blood:	n/a	n/a
50	CEBPB	chr15:43124721-43125181	IMR90	lung:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43213095-43213145	AoSMC	blood vessel:	n/a
2	chr15:43210848-43210898	NHBE	bronchial:	n/a
3	chr15:43213993-43214043	BE2_C	brain:	n/a
4	chr15:43213095-43213145	AoSMC	blood vessel:	n/a
5	chr15:43210848-43210898	NHBE	bronchial:	n/a
6	chr15:43213993-43214043	BE2_C	brain:	n/a
7	chr15:43213095-43213145	HRPEpiC	eye:	n/a
8	chr15:43236857-43236907	LNCaP	prostate:	n/a
9	chr15:43213114-43213164	SK-N-SH_RA	brain:	n/a
10	chr15:43213993-43214043	HNPCEpiC	eye:	n/a
11	chr15:43094585-43094635	HUVEC	blood vessel:	n/a
12	chr15:43213022-43213072	NB4	blood:	n/a
13	chr15:43236857-43236907	HUVEC	blood vessel:	n/a
14	chr15:43213593-43213643	RPTEC	kidney:	n/a
15	chr15:43208721-43208771	GM12892	blood:	n/a
16	chr15:43183056-43183106	HCF	heart:	n/a
17	chr15:43213993-43214043	SK-N-SH	brain:	n/a
18	chr15:43213593-43213643	NT2-D1	testis:	n/a
19	chr15:43213195-43213245	ProgFib	skin:	n/a
20	chr15:43213095-43213145	HL-60	blood:	n/a
21	chr15:43212417-43212467	HRPEpiC	eye:	n/a
22	chr15:43213357-43213407	GM12878	blood:	n/a
23	chr15:43212363-43212413	HCM	heart:	n/a
24	chr15:43211292-43211342	HRCEpiC	kidney:	n/a
25	chr15:43212363-43212413	GM12878	blood:	n/a
26	chr15:43210848-43210898	NB4	blood:	n/a
27	chr15:43213022-43213072	SK-N-MC	brain:	n/a
28	chr15:43213022-43213072	NT2-D1	testis:	n/a
29	chr15:43213095-43213145	ProgFib	skin:	n/a
30	chr15:43213357-43213407	HRPEpiC	eye:	n/a
31	chr15:43183056-43183106	T-47D	breast:	n/a
32	chr15:43215648-43215698	HIPEpiC	eye:	n/a
33	chr15:43213993-43214043	PANC-1	pancreas:	n/a
34	chr15:43213195-43213245	HAEpiC	amniotic membrane:	n/a
35	chr15:43212701-43212751	GM12878	blood:	n/a
36	chr15:43212701-43212751	K562	blood:	n/a
37	chr15:43213022-43213072	AG10803	skin:	n/a
38	chr15:43213114-43213164	K562	blood:	n/a
39	chr15:43213022-43213072	GM12891	blood:	n/a
40	chr15:43213015-43213065	Jurkat	blood:	n/a
41	chr15:43094585-43094635	MCF10A-Er-Src	breast:	n/a
42	chr15:43213022-43213072	NH-A	brain:	n/a
43	chr15:43183056-43183106	HAEpiC	amniotic membrane:	n/a
44	chr15:43210848-43210898	GM12878	blood:	n/a
45	chr15:43213257-43213307	GM12892	blood:	n/a
46	chr15:43213993-43214043	RPTEC	kidney:	n/a
47	chr15:43215648-43215698	Jurkat	blood:	n/a
48	chr15:43183056-43183106	U87	brain:	n/a
49	chr15:43183056-43183106	NB4	blood:	n/a
50	chr15:43213052-43213102	AG04449	skin:	fetal

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43121973..43125936-chr15:43126193..43128701,3	K562	blood:
2	chr15:43192591..43195469-chr15:43198395..43200582,2	K562	blood:
3	chr15:43234709..43237589-chr15:43247590..43250522,2	MCF-7	breast:
4	chr15:42996313..42997182-chr15:43218578..43219161,2	MCF-7	breast:
5	chr15:43234709..43237589-chr15:43247590..43250522,2	MCF-7	breast:
6	chr15:43141386..43143078-chr15:43144642..43146770,2	K562	blood:
7	chr15:43242538..43245839-chr15:43247604..43251014,3	K562	blood:
8	chr15:43204600..43210679-chr15:43210946..43214208,10	K562	blood:
9	chr15:43015023..43015967-chr15:43218682..43219556,3	MCF-7	breast:
10	chr15:43201061..43205182-chr15:43207494..43209457,4	K562	blood:
11	chr15:43102804..43105030-chr15:43109590..43112345,2	K562	blood:
12	chr15:43123371..43125082-chr15:43125965..43128701,2	K562	blood:
13	chr15:43212341..43214138-chr15:43216840..43218518,2	K562	blood:
14	chr15:43201553..43203286-chr15:43204467..43206953,2	K562	blood:
15	chr15:43073320..43075006-chr15:43078502..43081178,2	K562	blood:
16	chr15:43246670..43249589-chr15:43250577..43252629,2	K562	blood:
17	chr15:43068879..43071699-chr15:43077378..43080380,3	K562	blood:
18	chr15:43105622..43108101-chr15:43116852..43119781,2	K562	blood:
19	chr15:43102804..43105292-chr15:43108115..43111090,2	K562	blood:
20	chr15:43073320..43075006-chr15:43078502..43081178,2	K562	blood:
21	chr15:43032504..43034009-chr15:43211732..43214005,2	MCF-7	breast:
22	chr15:43105622..43108101-chr15:43116852..43119781,2	K562	blood:
23	chr15:43093067..43093836-chr15:43218523..43219050,2	MCF-7	breast:
24	chr15:43029256..43031403-chr15:43210732..43214178,4	K562	blood:
25	chr15:43214929..43217236-chr15:43217479..43219760,2	K562	blood:
26	chr15:43117816..43119740-chr15:43122004..43123832,2	MCF-7	breast:
27	chr15:43089428..43090276-chr15:43219004..43219572,2	MCF-7	breast:
28	chr15:43025909..43027534-chr15:43242943..43244599,2	K562	blood:
29	chr15:43017657..43020242-chr15:43257370..43259686,2	K562	blood:
30	chr15:43169823..43171405-chr15:43172916..43175738,2	K562	blood:
31	chr15:43227976..43230941-chr15:43258410..43260187,2	K562	blood:
32	chr15:43201061..43205182-chr15:43207494..43209457,4	K562	blood:
33	chr15:43246670..43249589-chr15:43250577..43252629,2	K562	blood:
34	chr15:43071141..43072690-chr15:43088507..43091296,2	K562	blood:
35	chr15:43102804..43105292-chr15:43108115..43111090,2	K562	blood:
36	chr15:43117816..43119740-chr15:43122004..43123832,2	MCF-7	breast:
37	chr15:43212538..43214244-chr15:43477789..43479955,2	K562	blood:
38	chr15:43194424..43196390-chr15:43210753..43213420,2	K562	blood:
39	chr15:43197523..43199091-chr15:43202841..43204475,2	K562	blood:
40	chr15:43196236..43198232-chr15:43199329..43201446,2	K562	blood:
41	chr15:43214929..43217236-chr15:43217479..43219760,2	K562	blood:
42	chr15:43234809..43237372-chr15:43248299..43250757,2	K562	blood:
43	chr15:43089428..43090276-chr15:43219004..43219572,2	MCF-7	breast:
44	chr15:43094398..43098116-chr15:43199741..43201552,3	K562	blood:
45	chr15:43089342..43090187-chr15:43218626..43219526,3	MCF-7	breast:
46	chr15:43067614..43069309-chr15:43072261..43074765,2	K562	blood:
47	chr15:43093067..43093836-chr15:43218523..43219050,2	MCF-7	breast:
48	chr15:43067614..43069309-chr15:43072261..43074765,2	K562	blood:
49	chr15:43141386..43143078-chr15:43144642..43146770,2	K562	blood:
50	chr15:43092442..43095088-chr15:43100736..43102794,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM62-1	chr15:43232579-43233666	NONHSAT042051

No data

Variant related genes	Relation type
UBR1	TF binding region
FDPSP4	TF binding region
TTBK2	TF binding region
KRT8P50	TF binding region
UBR1	CpG island
FDPSP4	CpG island
TTBK2	CpG island
KRT8P50	CpG island
ENSG00000140326	chromatin interactions
ENSG00000246283	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000260799	chromatin interactions
ENSG00000128881	chromatin interactions
ENSG00000166946	chromatin interactions

Extended variants
information (count: 6881 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6881 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62020671	chr15:43056151-43056152	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs532858673	chr15:43056189-43056190	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs62020672	chr15:43056210-43056211	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs549862975	chr15:43056212-43056213	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs149675754	chr15:43056214-43056215	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs73410981	chr15:43056329-43056330	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548857736	chr15:43056351-43056352	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs377563049	chr15:43056353-43056354	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs541091433	chr15:43056430-43056431	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs371124647	chr15:43056436-43056437	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs565598693	chr15:43056451-43056452	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs534920062	chr15:43056460-43056461	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs553855096	chr15:43056479-43056480	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs570842790	chr15:43056492-43056493	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs539538595	chr15:43056504-43056505	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs556648099	chr15:43056513-43056514	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs576704997	chr15:43056571-43056572	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs542481013	chr15:43056593-43056594	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs556004092	chr15:43056597-43056598	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs572728187	chr15:43056599-43056600	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs111357761	chr15:43056609-43056610	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148494580	chr15:43056634-43056635	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs532977876	chr15:43056642-43056643	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs543127775	chr15:43056653-43056654	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs28542286	chr15:43056658-43056659	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs568798379	chr15:43056671-43056672	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs111647882	chr15:43056685-43056686	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs565560190	chr15:43056707-43056708	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs147604858	chr15:43056711-43056712	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs142188475	chr15:43056758-43056759	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs539414088	chr15:43056809-43056810	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs145424460	chr15:43056845-43056846	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs556683323	chr15:43056850-43056851	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs570121897	chr15:43056859-43056860	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs535953971	chr15:43056860-43056861	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs189190173	chr15:43056876-43056877	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs533430341	chr15:43056980-43056981	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs534991202	chr15:43057002-43057003	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs151071869	chr15:43057004-43057005	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs577558168	chr15:43057022-43057023	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs543365823	chr15:43057034-43057035	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs562947907	chr15:43057058-43057059	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs573374536	chr15:43057082-43057083	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs371499992	chr15:43057088-43057089	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs542332422	chr15:43057096-43057097	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs531506275	chr15:43057123-43057124	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs559109075	chr15:43057132-43057133	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs528318726	chr15:43057157-43057158	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs551386117	chr15:43057276-43057277	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs565222239	chr15:43057330-43057331	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	19492091	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:3543 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43029800-43071000	Weak transcription	Pancreas	Pancrea
2	chr15:43030000-43066200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:43030000-43067200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:43030000-43093600	Weak transcription	Colonic Mucosa	Colon
5	chr15:43038400-43067400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr15:43044800-43066400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:43045000-43065600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr15:43045400-43062800	Weak transcription	Colon Smooth Muscle	Colon
9	chr15:43045400-43068000	Weak transcription	Fetal Heart	heart
10	chr15:43045600-43074400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:43045800-43064800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr15:43046000-43062600	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:43051800-43064000	Weak transcription	Left Ventricle	heart
14	chr15:43051800-43064400	Weak transcription	Fetal Stomach	stomach
15	chr15:43051800-43065200	Weak transcription	Placenta	Placenta
16	chr15:43051800-43066200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:43051800-43069400	Weak transcription	Gastric	stomach
18	chr15:43051800-43070600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr15:43051800-43074600	Weak transcription	Right Ventricle	heart
20	chr15:43051800-43075000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:43051800-43083800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:43052000-43063800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr15:43052000-43065800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr15:43052000-43065800	Weak transcription	Thymus	Thymus
25	chr15:43052000-43066000	Weak transcription	Spleen	Spleen
26	chr15:43052000-43066600	Weak transcription	Ovary	ovary
27	chr15:43052000-43074600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:43052800-43057600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr15:43053600-43112200	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:43053800-43066400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:43054000-43064400	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr15:43054000-43066000	Weak transcription	Brain Angular Gyrus	brain
33	chr15:43054000-43066200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr15:43054000-43066400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr15:43054000-43074600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr15:43054000-43080200	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr15:43054400-43064000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr15:43054600-43064200	Weak transcription	Liver	Liver
39	chr15:43054600-43067200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr15:43054600-43068600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr15:43054800-43056400	Weak transcription	Brain Germinal Matrix	brain
42	chr15:43054800-43058200	Weak transcription	Primary B cells from peripheral blood	blood
43	chr15:43054800-43063600	Weak transcription	Primary B cells from cord blood	blood
44	chr15:43054800-43064000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr15:43054800-43064000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr15:43054800-43064000	Weak transcription	Dnd41	blood
47	chr15:43054800-43064600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:43054800-43066400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:43054800-43067200	Weak transcription	Duodenum Mucosa	Duodenum
50	chr15:43054800-43146000	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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