Variant report

Variant	nsv904133
Chromosome Location	chr15:42528982-42681057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1630)
CpG islands
(count:2019)
Chromatin interactive
region (count:81)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1630 , 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	chr15:42663368-42663711	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:42567248-42567519	K562	blood:	n/a	n/a
3	ARID3A	chr15:42606957-42607251	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:42631456-42631554	K562	blood:	n/a	n/a
5	ARID3A	chr15:42565103-42566342	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:42578419-42579027	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:42566680-42567011	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:42663297-42663692	K562	blood:	n/a	n/a
9	ATF1	chr15:42668273-42668516	K562	blood:	n/a	n/a
10	ATF1	chr15:42565151-42566153	K562	blood:	n/a	n/a
11	ATF1	chr15:42677714-42678028	K562	blood:	n/a	n/a
12	ATF2	chr15:42565220-42565693	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr15:42565086-42565735	GM12878	blood:	n/a	n/a
14	ATF2	chr15:42565128-42565962	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr15:42565240-42566091	GM12878	blood:	n/a	n/a
16	BACH1	chr15:42566258-42566267	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:42663204-42663778	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:42580032-42580034	K562	blood:	n/a	n/a
19	BACH1	chr15:42565191-42565854	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:42571559-42571922	K562	blood:	n/a	n/a
21	BACH1	chr15:42663343-42663771	K562	blood:	n/a	n/a
22	BCL3	chr15:42565289-42565851	A549	lung:	n/a	n/a
23	BCL3	chr15:42565205-42565682	A549	lung:	n/a	n/a
24	BCLAF1	chr15:42565086-42566518	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:42565125-42566650	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:42668048-42668449	K562	blood:	n/a	n/a
27	BHLHE40	chr15:42678662-42678785	K562	blood:	n/a	n/a
28	BHLHE40	chr15:42677791-42678051	K562	blood:	n/a	n/a
29	BHLHE40	chr15:42605738-42605826	K562	blood:	n/a	n/a
30	BHLHE40	chr15:42565191-42567220	K562	blood:	n/a	n/a
31	BHLHE40	chr15:42571337-42572085	K562	blood:	n/a	n/a
32	BHLHE40	chr15:42565232-42566680	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:42565375-42566126	HepG2	liver:	n/a	n/a
34	BRCA1	chr15:42564758-42566829	Hela-S3	cervix:	n/a	chr15:42565231-42565238
35	BRCA1	chr15:42564908-42565775	H1-hESC	embryonic stem cell:	n/a	chr15:42565231-42565238
36	BRCA1	chr15:42566532-42566636	HepG2	liver:	n/a	n/a
37	BRCA1	chr15:42655615-42656507	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr15:42565405-42565896	HepG2	liver:	n/a	n/a
39	BRCA1	chr15:42566234-42566325	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr15:42565071-42566044	K562	blood:	n/a	n/a
41	CBX3	chr15:42670146-42670519	K562	blood:	n/a	n/a
42	CBX3	chr15:42544053-42544417	K562	blood:	n/a	n/a
43	CBX3	chr15:42571335-42572016	K562	blood:	n/a	n/a
44	CCNT2	chr15:42565279-42566034	K562	blood:	n/a	chr15:42565403-42565412 chr15:42565344-42565353 chr15:42565934-42565943
45	CCNT2	chr15:42566384-42566666	K562	blood:	n/a	n/a
46	CCNT2	chr15:42578655-42578985	K562	blood:	n/a	chr15:42578948-42578968
47	CEBPB	chr15:42577834-42578033	K562	blood:	n/a	n/a
48	CEBPB	chr15:42577310-42577543	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:42577265-42577578	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:42568246-42568548	HepG2	liver:	n/a	n/a

(count:2019 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42550398-42550448	NHDF-neo	bronchial:	n/a
2	chr15:42565830-42565880	AG04450	lung:	fetal
3	chr15:42564634-42564684	HepG2	liver:	n/a
4	chr15:42566272-42566322	ProgFib	skin:	n/a
5	chr15:42651086-42651136	AG04449	skin:	fetal
6	chr15:42565284-42565334	AoSMC	blood vessel:	n/a
7	chr15:42550398-42550448	NHDF-neo	bronchial:	n/a
8	chr15:42565830-42565880	AG04450	lung:	fetal
9	chr15:42564634-42564684	HepG2	liver:	n/a
10	chr15:42566272-42566322	ProgFib	skin:	n/a
11	chr15:42651086-42651136	AG04449	skin:	fetal
12	chr15:42565284-42565334	AoSMC	blood vessel:	n/a
13	chr15:42566151-42566201	GM19239	blood:	n/a
14	chr15:42650662-42650712	SK-N-MC	brain:	n/a
15	chr15:42640316-42640366	AoSMC	blood vessel:	n/a
16	chr15:42550398-42550448	HEEpiC	esophagus:	n/a
17	chr15:42651086-42651136	HCM	heart:	n/a
18	chr15:42562638-42562688	MCF10A-Er-Src	breast:	n/a
19	chr15:42639458-42639508	GM06990	blood:	n/a
20	chr15:42566662-42566712	BE2_C	brain:	n/a
21	chr15:42650760-42650810	MCF-7	breast:	n/a
22	chr15:42566151-42566201	GM12878	blood:	n/a
23	chr15:42565790-42565840	HCPEpiC	choroid plexus:	n/a
24	chr15:42565651-42565701	SK-N-SH	brain:	n/a
25	chr15:42566662-42566712	HCPEpiC	choroid plexus:	n/a
26	chr15:42565701-42565751	AG10803	skin:	n/a
27	chr15:42566343-42566393	HCF	heart:	n/a
28	chr15:42565790-42565840	HMEC	breast:	n/a
29	chr15:42566662-42566712	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:42566343-42566393	HNPCEpiC	eye:	n/a
31	chr15:42566318-42566368	SK-N-SH_RA	brain:	n/a
32	chr15:42566272-42566322	GM06990	blood:	n/a
33	chr15:42562638-42562688	PANC-1	pancreas:	n/a
34	chr15:42640283-42640333	ECC-1	luminal epithelium:	n/a
35	chr15:42640316-42640366	HAEpiC	amniotic membrane:	n/a
36	chr15:42639458-42639508	AG09309	skin:	n/a
37	chr15:42564634-42564684	SK-N-SH	brain:	n/a
38	chr15:42565284-42565334	RPTEC	kidney:	n/a
39	chr15:42640316-42640366	NT2-D1	testis:	n/a
40	chr15:42565522-42565572	SK-N-SH_RA	brain:	n/a
41	chr15:42566264-42566314	HL-60	blood:	n/a
42	chr15:42566662-42566712	NHBE	bronchial:	n/a
43	chr15:42565284-42565334	IMR90	lung:	fetal
44	chr15:42568411-42568461	NT2-D1	testis:	n/a
45	chr15:42639458-42639508	HEK293	kidney:	embryo
46	chr15:42565872-42565922	SK-N-MC	brain:	n/a
47	chr15:42565651-42565701	HCF	heart:	n/a
48	chr15:42650760-42650810	NHBE	bronchial:	n/a
49	chr15:42566151-42566201	K562	blood:	n/a
50	chr15:42565903-42565953	Hela-S3	cervix:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:42581427..42583072-chr15:42583575..42585107,2	K562	blood:
2	chr15:42563255..42565132-chr15:42636659..42638368,2	K562	blood:
3	chr15:42559733..42563310-chr15:42678634..42681534,3	K562	blood:
4	chr15:42554958..42556524-chr15:42720183..42722144,2	K562	blood:
5	chr15:42581427..42583072-chr15:42583575..42585107,2	K562	blood:
6	chr15:42544904..42547005-chr15:42561537..42563318,2	K562	blood:
7	chr15:42563158..42565885-chr15:42567865..42572400,4	MCF-7	breast:
8	chr15:42584658..42587621-chr15:42618841..42621037,2	K562	blood:
9	chr15:42678390..42681163-chr15:42692112..42694875,2	K562	blood:
10	chr15:42568979..42570543-chr15:42572513..42574015,2	K562	blood:
11	chr15:42677853..42678408-chr15:42942399..42943222,2	K562	blood:
12	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
13	chr11:34073237..34073837-chr15:42565350..42566240,2	Hela-S3	cervix:
14	chr15:42573833..42576317-chr15:42582410..42584049,2	K562	blood:
15	chr15:42532284..42534911-chr15:42549043..42552041,2	K562	blood:
16	chr15:42564714..42568797-chr15:42571510..42577176,8	K562	blood:
17	chr15:42565275..42567071-chr15:42601912..42604080,2	MCF-7	breast:
18	chr15:42563951..42566890-chr15:42577773..42583283,5	K562	blood:
19	chr13:96328903..96329487-chr15:42565285..42566134,2	Hela-S3	cervix:
20	chr15:42453296..42455922-chr15:42565346..42568176,2	K562	blood:
21	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
22	chr15:42565191..42565693-chr4:25378475..25379333,2	Hela-S3	cervix:
23	chr15:42632246..42634380-chr15:42651943..42654549,2	K562	blood:
24	chr15:42679521..42681202-chr15:42684595..42687043,2	MCF-7	breast:
25	chr15:42657935..42659641-chr15:42660404..42662394,2	K562	blood:
26	chr15:42564260..42567137-chr15:42576635..42580359,3	MCF-7	breast:
27	chr15:42564172..42566903-chr15:42569265..42571976,2	MCF-7	breast:
28	chr15:42565354..42567848-chr15:42584150..42585706,2	MCF-7	breast:
29	chr15:42672860..42675186-chr15:42675250..42677559,2	K562	blood:
30	chr15:42565221..42567445-chr15:42597344..42599463,2	MCF-7	breast:
31	chr15:42565452..42566007-chr6:13328640..13329262,2	Hela-S3	cervix:
32	chr11:62554539..62555349-chr15:42565272..42566248,2	Hela-S3	cervix:
33	chr14:77923503..77924384-chr15:42565241..42565896,2	NB4	blood:
34	chr1:155903773..155904358-chr15:42565120..42565881,2	Hela-S3	cervix:
35	chr15:42679543..42681444-chr15:42683292..42685260,2	K562	blood:
36	chr15:42550561..42553177-chr15:42566692..42569235,2	K562	blood:
37	chr15:42547199..42549905-chr15:42563424..42565633,2	K562	blood:
38	chr15:42565726..42566604-chr15:65588308..65589204,2	Hela-S3	cervix:
39	chr15:42573833..42576317-chr15:42582410..42584049,2	K562	blood:
40	chr11:71814032..71814862-chr15:42565436..42566128,2	NB4	blood:
41	chr1:115212876..115213635-chr15:42565277..42565911,2	Hela-S3	cervix:
42	chr15:42429166..42430382-chr15:42677434..42678387,4	K562	blood:
43	chr15:42544015..42546634-chr15:42547457..42549970,2	K562	blood:
44	chr15:42564636..42566534-chr15:42781561..42783413,2	K562	blood:
45	chr15:42660141..42662692-chr15:42684785..42686595,2	K562	blood:
46	chr15:42533593..42536142-chr15:42545624..42547945,2	K562	blood:
47	chr15:42565305..42567163-chr15:42839364..42842481,3	K562	blood:
48	chr15:42636103..42638509-chr15:42640210..42643122,3	K562	blood:
49	chr15:42563158..42565885-chr15:42567865..42572400,4	MCF-7	breast:
50	chr15:42565172..42565968-chr3:20227231..20227766,2	Hela-S3	cervix:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPN3-3	chr15:42605885-42605983	NONHSAT042004
2	lnc-CAPN3-3	chr15:42606186-42606584	NONHSAT042004
3	lnc-TMEM87A-2	chr15:42615533-42616353	ucscGeneNc_uc001ztu_2
4	lnc-TMEM87A-2	chr15:42613996-42614964	ucscGeneNc_uc001ztu_2
5	lnc-CAPN3-2	chr15:42607911-42608280	expReg_chr15_2472_+

No data

Variant related genes	Relation type
CAPN3	TF binding region
ENSG00000258461	TF binding region
GANC	TF binding region
TMEM87A	TF binding region
ENSG00000260571	TF binding region
CAPN3	CpG island
ENSG00000258461	CpG island
GANC	CpG island
TMEM87A	CpG island
ENSG00000260571	CpG island
ENSG00000199568	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000105879	chromatin interactions
ENSG00000137814	chromatin interactions
ENSG00000241764	chromatin interactions
ENSG00000053900	chromatin interactions
ENSG00000175984	chromatin interactions
ENSG00000103994	chromatin interactions
ENSG00000185475	chromatin interactions
ENSG00000166887	chromatin interactions
ENSG00000132680	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000163378	chromatin interactions
ENSG00000135387	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000102580	chromatin interactions
ENSG00000244513	chromatin interactions
ENSG00000122952	chromatin interactions
ENSG00000261002	chromatin interactions
ENSG00000247400	chromatin interactions
ENSG00000100591	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000092529	chromatin interactions
ENSG00000180979	chromatin interactions
ENSG00000151445	chromatin interactions
ENSG00000188089	chromatin interactions
ENSG00000130479	chromatin interactions
ENSG00000105479	chromatin interactions

Extended variants
information (count: 6204 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6204 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12440087	chr15:42528982-42528983	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562443504	chr15:42528988-42528989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573528743	chr15:42528989-42528990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191429363	chr15:42528993-42528994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182526668	chr15:42529055-42529056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550344010	chr15:42529167-42529168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544775974	chr15:42529205-42529206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1712409	chr15:42529207-42529208	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530411146	chr15:42529225-42529226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570198301	chr15:42529285-42529286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150368011	chr15:42529298-42529299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1712408	chr15:42529312-42529313	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145128650	chr15:42529328-42529329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1679011	chr15:42529402-42529403	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs114301408	chr15:42529451-42529452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539167971	chr15:42529455-42529456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372765708	chr15:42529464-42529465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558770388	chr15:42529470-42529471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186153354	chr15:42529516-42529517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534379864	chr15:42529551-42529552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372870744	chr15:42529597-42529598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537826110	chr15:42529601-42529602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377209095	chr15:42529612-42529613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115529956	chr15:42529619-42529620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374132576	chr15:42529620-42529621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141414167	chr15:42529664-42529665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149080105	chr15:42529665-42529666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377564643	chr15:42529666-42529667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35187134	chr15:42529695-42529696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369339663	chr15:42529721-42529722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372661450	chr15:42529733-42529734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116844280	chr15:42529739-42529740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376919652	chr15:42529752-42529753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138319789	chr15:42529765-42529766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552673339	chr15:42529771-42529772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112218370	chr15:42529803-42529804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553180130	chr15:42529831-42529832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200096627	chr15:42529845-42529846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545123517	chr15:42529850-42529851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs66512609	chr15:42529892-42529893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71108153	chr15:42529907-42529908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71431845	chr15:42529925-42529926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562470384	chr15:42529928-42529929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190526052	chr15:42529932-42529933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183487021	chr15:42529935-42529936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560829889	chr15:42529939-42529940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530418845	chr15:42529965-42529966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146052864	chr15:42529975-42529976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567867872	chr15:42529989-42529990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188981770	chr15:42530014-42530015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Intracranial arachnoid cysts	20187927	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	20164919	CNVD

Chromatin state (count:4105 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42500800-42563200	Weak transcription	Stomach Mucosa	stomach
2	chr15:42501000-42534800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr15:42501000-42536600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:42501000-42536800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr15:42501000-42538000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr15:42501200-42532400	Strong transcription	Fetal Muscle Trunk	muscle
7	chr15:42501800-42536800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr15:42502000-42535000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:42502200-42534000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:42502200-42536600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr15:42502800-42535200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:42502800-42536400	Strong transcription	Fetal Muscle Leg	muscle
13	chr15:42503200-42544000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:42506800-42532000	Strong transcription	Placenta	Placenta
15	chr15:42508000-42532200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr15:42509400-42535200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr15:42511800-42536800	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr15:42513200-42532200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:42513800-42534800	Strong transcription	Liver	Liver
20	chr15:42514000-42534800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr15:42514000-42535200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr15:42514200-42532400	Strong transcription	Adipose Nuclei	Adipose
23	chr15:42514200-42535200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:42514200-42535200	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr15:42514400-42531800	Strong transcription	Primary T cells from cord blood	blood
26	chr15:42514400-42533600	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr15:42514400-42534800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr15:42514400-42535000	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr15:42514400-42535000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr15:42514400-42536400	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr15:42514400-42536400	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr15:42514400-42537200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr15:42514600-42535000	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr15:42514800-42532000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:42515000-42535400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr15:42515000-42544600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr15:42515200-42534800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:42515400-42535400	Strong transcription	Primary T helper cells PMA-I stimulated	--
39	chr15:42515600-42530400	Strong transcription	NH-A	brain
40	chr15:42515600-42532600	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr15:42515600-42535000	Strong transcription	Primary B cells from cord blood	blood
42	chr15:42515800-42532400	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr15:42516000-42535200	Strong transcription	Primary B cells from peripheral blood	blood
44	chr15:42519200-42536400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:42519200-42543800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr15:42519200-42543800	Weak transcription	Gastric	stomach
47	chr15:42519400-42532000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr15:42519400-42562800	Weak transcription	Fetal Heart	heart
49	chr15:42520200-42530200	Weak transcription	Aorta	Aorta
50	chr15:42520200-42561000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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