Variant report

Variant	nsv1043176
Chromosome Location	chr15:55010228-55563000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3262)
CpG islands
(count:1467)
Chromatin interactive
region (count:246)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:3262 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55529100-55530323	K562	blood:	n/a	n/a
2	ARID3A	chr15:55494186-55494335	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:55460540-55460930	K562	blood:	n/a	n/a
4	ARID3A	chr15:55488876-55489789	HepG2	liver:	n/a	chr15:55489665-55489681 chr15:55489664-55489680
5	ARID3A	chr15:55490006-55490197	K562	blood:	n/a	n/a
6	ARID3A	chr15:55552870-55553285	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:55401183-55401328	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:55513290-55513722	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:55559634-55560031	K562	blood:	n/a	n/a
10	ARID3A	chr15:55526466-55527155	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:55401059-55401442	K562	blood:	n/a	n/a
12	ARID3A	chr15:55542686-55542931	K562	blood:	n/a	n/a
13	ARID3A	chr15:55509887-55510127	K562	blood:	n/a	n/a
14	ARID3A	chr15:55530654-55532559	K562	blood:	n/a	n/a
15	ARID3A	chr15:55550744-55550788	K562	blood:	n/a	n/a
16	ARID3A	chr15:55542492-55543043	HepG2	liver:	n/a	n/a
17	ARID3A	chr15:55527826-55528022	K562	blood:	n/a	n/a
18	ARID3A	chr15:55509833-55510139	HepG2	liver:	n/a	n/a
19	ARID3A	chr15:55547675-55547685	K562	blood:	n/a	n/a
20	ARID3A	chr15:55460484-55460926	HepG2	liver:	n/a	n/a
21	ATF1	chr15:55309260-55309314	K562	blood:	n/a	n/a
22	ATF1	chr15:55514846-55515135	K562	blood:	n/a	n/a
23	ATF1	chr15:55405564-55405581	K562	blood:	n/a	n/a
24	ATF1	chr15:55509853-55510124	K562	blood:	n/a	n/a
25	ATF1	chr15:55531712-55532710	K562	blood:	n/a	n/a
26	ATF1	chr15:55529617-55530115	K562	blood:	n/a	n/a
27	ATF1	chr15:55527854-55528080	K562	blood:	n/a	n/a
28	ATF1	chr15:55547268-55547416	K562	blood:	n/a	n/a
29	ATF1	chr15:55488973-55489508	K562	blood:	n/a	n/a
30	ATF1	chr15:55513452-55513853	K562	blood:	n/a	n/a
31	ATF2	chr15:55516813-55517609	GM12878	blood:	n/a	n/a
32	ATF2	chr15:55509734-55510174	GM12878	blood:	n/a	n/a
33	ATF2	chr15:55488798-55489435	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr15:55401149-55401766	GM12878	blood:	n/a	n/a
35	ATF2	chr15:55128557-55128968	GM12878	blood:	n/a	n/a
36	ATF2	chr15:55547721-55548440	GM12878	blood:	n/a	n/a
37	ATF2	chr15:55513439-55513945	GM12878	blood:	n/a	n/a
38	ATF2	chr15:55488665-55489468	GM12878	blood:	n/a	n/a
39	ATF2	chr15:55513407-55514139	GM12878	blood:	n/a	n/a
40	ATF2	chr15:55516942-55517584	GM12878	blood:	n/a	n/a
41	ATF2	chr15:55488786-55489603	GM12878	blood:	n/a	n/a
42	ATF2	chr15:55514723-55515204	GM12878	blood:	n/a	n/a
43	ATF2	chr15:55488774-55489321	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF3	chr15:55529616-55530176	K562	blood:	n/a	n/a
45	ATF3	chr15:55488761-55489398	K562	blood:	n/a	chr15:55488948-55488957
46	ATF3	chr15:55488733-55489551	A549	lung:	n/a	chr15:55488948-55488957
47	ATF3	chr15:55488694-55489633	A549	lung:	n/a	chr15:55488948-55488957
48	ATF3	chr15:55489010-55489248	K562	blood:	n/a	n/a
49	ATF3	chr15:55559648-55559988	K562	blood:	n/a	n/a
50	BACH1	chr15:55509968-55510092	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55489241-55489291	NHDF-neo	bronchial:	n/a
2	chr15:55473630-55473680	LNCaP	prostate:	n/a
3	chr15:55562699-55562749	AG04450	lung:	fetal
4	chr15:55489241-55489291	NHDF-neo	bronchial:	n/a
5	chr15:55473630-55473680	LNCaP	prostate:	n/a
6	chr15:55562699-55562749	AG04450	lung:	fetal
7	chr15:55543264-55543314	HEEpiC	esophagus:	n/a
8	chr15:55489235-55489285	NHBE	bronchial:	n/a
9	chr15:55489544-55489594	HEEpiC	esophagus:	n/a
10	chr15:55489544-55489594	HNPCEpiC	eye:	n/a
11	chr15:55559759-55559809	HepG2	liver:	n/a
12	chr15:55485089-55485139	SK-N-SH_RA	brain:	n/a
13	chr15:55489235-55489285	AG10803	skin:	n/a
14	chr15:55489541-55489591	HepG2	liver:	n/a
15	chr15:55074274-55074324	A549	lung:	n/a
16	chr15:55513621-55513671	HNPCEpiC	eye:	n/a
17	chr15:55489120-55489170	HIPEpiC	eye:	n/a
18	chr15:55543264-55543314	ECC-1	luminal epithelium:	n/a
19	chr15:55488809-55488859	IMR90	lung:	fetal
20	chr15:55543264-55543314	GM06990	blood:	n/a
21	chr15:55489544-55489594	T-47D	breast:	n/a
22	chr15:55356396-55356446	AG09319	gingival:	n/a
23	chr15:55562773-55562823	PrEC	prostate:	n/a
24	chr15:55489563-55489613	HNPCEpiC	eye:	n/a
25	chr15:55489084-55489134	H1-hESC	embryonic stem cell:	embryo
26	chr15:55489544-55489594	HMEC	breast:	n/a
27	chr15:55489544-55489594	HCF	heart:	n/a
28	chr15:55489293-55489343	AG09319	gingival:	n/a
29	chr15:55489563-55489613	AG04449	skin:	fetal
30	chr15:55562699-55562749	HepG2	liver:	n/a
31	chr15:55489563-55489613	Jurkat	blood:	n/a
32	chr15:55485089-55485139	BE2_C	brain:	n/a
33	chr15:55559759-55559809	AG04450	lung:	fetal
34	chr15:55562403-55562453	HCT-116	colon:	n/a
35	chr15:55473630-55473680	Jurkat	blood:	n/a
36	chr15:55489374-55489424	Jurkat	blood:	n/a
37	chr15:55131855-55131905	CMK	blood:	n/a
38	chr15:55562699-55562749	U87	brain:	n/a
39	chr15:55356396-55356446	AG04449	skin:	fetal
40	chr15:55562699-55562749	T-47D	breast:	n/a
41	chr15:55489293-55489343	HEK293	kidney:	embryo
42	chr15:55489541-55489591	GM12891	blood:	n/a
43	chr15:55074274-55074324	T-47D	breast:	n/a
44	chr15:55489544-55489594	Hepatocyte	liver:	n/a
45	chr15:55510003-55510053	NH-A	brain:	n/a
46	chr15:55489235-55489285	RPTEC	kidney:	n/a
47	chr15:55489235-55489285	A549	lung:	n/a
48	chr15:55489235-55489285	HCM	heart:	n/a
49	chr15:55489120-55489170	GM19239	blood:	n/a
50	chr15:55510003-55510053	PFSK-1	brain:	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr15:55532146..55535139-chr15:55535159..55539232,4	K562	blood:
2	chr15:55327619..55328387-chr15:55460369..55461213,2	MCF-7	breast:
3	chr15:55532304..55535313-chr15:55545055..55548758,3	K562	blood:
4	chr15:55542912..55546349-chr15:55547649..55552018,4	K562	blood:
5	chr15:55555230..55557590-chr15:55561714..55563308,2	K562	blood:
6	chr15:55514943..55517401-chr15:55527045..55529673,2	K562	blood:
7	chr15:54268785..54269712-chr15:55460337..55461244,4	MCF-7	breast:
8	chr15:55557767..55561627-chr15:55569250..55572425,4	K562	blood:
9	chr15:55529763..55532078-chr15:55535534..55537821,2	K562	blood:
10	chr15:55441978..55444770-chr15:55453903..55455710,2	K562	blood:
11	chr15:55400894..55401490-chr15:65197977..65198492,2	MCF-7	breast:
12	chr15:55468427..55470541-chr15:55470610..55476298,5	K562	blood:
13	chr15:54374784..54375687-chr15:55460665..55461171,2	MCF-7	breast:
14	chr15:55505618..55507168-chr15:55508897..55511690,2	K562	blood:
15	chr15:55540071..55542542-chr15:55580150..55582152,2	K562	blood:
16	chr15:55470856..55473009-chr15:55473749..55475937,3	K562	blood:
17	chr15:55487591..55491418-chr15:55506365..55509165,4	MCF-7	breast:
18	chr15:55530995..55533093-chr15:55578497..55580439,2	K562	blood:
19	chr15:55487577..55489204-chr15:55541881..55543410,2	MCF-7	breast:
20	chr15:54268702..54269681-chr15:55400788..55401575,2	MCF-7	breast:
21	chr15:55533451..55535034-chr15:55546175..55548758,2	K562	blood:
22	chr15:55519854..55522805-chr15:55537341..55539230,2	MCF-7	breast:
23	chr15:55416875..55419348-chr15:55422802..55424971,2	K562	blood:
24	chr15:55509687..55510456-chr15:55700271..55700912,2	MCF-7	breast:
25	chr15:55470856..55473009-chr15:55473749..55475937,3	K562	blood:
26	chr15:55545838..55548100-chr15:55559043..55560883,2	K562	blood:
27	chr15:55488317..55491579-chr15:55501093..55504631,4	K562	blood:
28	chr15:55469036..55471417-chr15:55477962..55479850,2	K562	blood:
29	chr15:55528450..55530631-chr15:55610596..55613298,2	K562	blood:
30	chr15:55499294..55501265-chr15:55504444..55506030,2	K562	blood:
31	chr15:55549763..55552169-chr15:55552285..55555168,2	K562	blood:
32	chr15:55499151..55502246-chr15:55504126..55506184,4	K562	blood:
33	chr15:55528399..55531795-chr15:55570084..55572608,4	K562	blood:
34	chr15:55514943..55517401-chr15:55527045..55529673,2	K562	blood:
35	chr15:55531824..55533387-chr15:55558858..55561281,2	K562	blood:
36	chr15:55541209..55543610-chr15:55545999..55547542,2	K562	blood:
37	chr15:55531824..55534011-chr15:55559781..55562269,2	K562	blood:
38	chr15:55484699..55490442-chr15:55579270..55584640,8	K562	blood:
39	chr15:55507956..55509832-chr15:55511265..55513326,2	K562	blood:
40	chr15:55508422..55515195-chr15:55580692..55586566,10	MCF-7	breast:
41	chr15:55488918..55489744-chr9:128003531..128004033,2	Hela-S3	cervix:
42	chr15:55416875..55419348-chr15:55422802..55424971,2	K562	blood:
43	chr15:55473058..55474936-chr15:55475651..55479463,4	K562	blood:
44	chr15:55463428..55465333-chr15:55485353..55487968,3	K562	blood:
45	chr15:55485173..55489207-chr15:55609824..55611374,3	K562	blood:
46	chr15:55524517..55526709-chr15:55528227..55531220,3	MCF-7	breast:
47	chr15:55536038..55538706-chr15:55541637..55544470,3	K562	blood:
48	chr15:55108183..55110175-chr15:55112199..55114608,2	K562	blood:
49	chr15:55510048..55513584-chr15:55529255..55531820,4	K562	blood:
50	chr15:55489108..55489798-chr16:89626508..89627135,2	NB4	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGB-1	chr15:55383073-55384107	ucscGeneNc_uc010bfv_1
2	lnc-PIGB-1	chr15:55384055-55384371	ENSG00000260937.1
3	lnc-RSL24D1-2	chr15:55530316-55530689	NONHSAT043984
4	lnc-RSL24D1-3	chr15:55212817-55213114	ucExp_388_-
5	lnc-RSL24D1-1	chr15:55469323-55470373	ENSG00000248800
6	lnc-PIGB-1	chr15:55385907-55386558	ucscGeneNc_uc010bfv_1
7	lnc-PIGB-2	chr15:55482151-55482204	ucscGeneNc_uc002aeh_2
8	lnc-PIGB-3	chr15:55403336-55403422	l_1161_chr15:55398420-55404514_testes
9	lnc-PIGB-1	chr15:55384055-55384319	XLOC_011261
10	lnc-PIGB-1	chr15:55348947-55349110	NONHSAT043978
11	lnc-PIGB-2	chr15:55456636-55456655	ucscGeneNc_uc002aeh_2
12	lnc-RSL24D1-1	chr15:55464171-55468937	ENSG00000248800
13	lnc-RSL24D1-2	chr15:55562363-55562482	NONHSAT043984
14	lnc-UNC13C-3	chr15:55212817-55213114	ucExp_388_+
15	lnc-PIGB-1	chr15:55384054-55384319	NONHSAT043978
16	lnc-PIGB-3	chr15:55404340-55404514	l_1161_chr15:55398420-55404514_testes
17	lnc-PIGB-3	chr15:55402395-55402617	l_1161_chr15:55398420-55404514_testes
18	lnc-PIGB-2	chr15:55486463-55486766	ucscGeneNc_uc002aeh_2
19	lnc-PIGB-2	chr15:55485456-55485554	ucscGeneNc_uc002aeh_2
20	lnc-PIGB-1	chr15:55387032-55387257	ucscGeneNc_uc010bfv_1
21	lnc-PIGB-2	chr15:55477831-55477920	ucscGeneNc_uc002aeh_2
22	lnc-PIGB-3	chr15:55398421-55398946	l_1161_chr15:55398420-55404514_testes
23	lnc-PIGB-2	chr15:55476414-55476596	ucscGeneNc_uc002aeh_2
24	lnc-PIGB-2	chr15:55473443-55473581	ucscGeneNc_uc002aeh_2
25	lnc-PIGB-2	chr15:55481509-55481528	ucscGeneNc_uc002aeh_2
26	lnc-PIGB-1	chr15:55380197-55380231	ENSG00000260937.1
27	lnc-RSL24D1-2	chr15:55561992-55562482	NONHSAT043985
28	lnc-PIGB-1	chr15:55348948-55349110	XLOC_011261

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	RAB27A	hsa-miR-124-3p	chr15:55497468-55497487
2	RAB27A	hsa-miR-124-3p	chr15:55497474-55497467
3	RAB27A	hsa-miR-26b-5p	chr15:55496283-55496303

Variant related genes	Relation type
ENSG00000260937	TF binding region
RSL24D1	TF binding region
RAB27A	TF binding region
ENSG00000260937	CpG island
RSL24D1	CpG island
RAB27A	CpG island
ENSG00000144560	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000044574	chromatin interactions
ENSG00000259669	chromatin interactions
ENSG00000164062	chromatin interactions
ENSG00000267296	chromatin interactions
ENSG00000260916	chromatin interactions
ENSG00000230259	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000239705	chromatin interactions
ENSG00000245848	chromatin interactions
ENSG00000261652	chromatin interactions
ENSG00000167526	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000133316	chromatin interactions
ANKRD17	miRNA target sites
KLHL2	miRNA target sites
MAP3K3	miRNA target sites

Extended variants
information (count: 12899 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:12899 , 50 per page) page: 1 2 3 4 5 6 7 ... 258

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73407659	chr15:55019010-55019011	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191647035	chr15:55019021-55019022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111611412	chr15:55019067-55019068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557467335	chr15:55019069-55019070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184882919	chr15:55019104-55019105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538827279	chr15:55019111-55019112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558420462	chr15:55019151-55019152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2414375	chr15:55019158-55019159	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs540935692	chr15:55019162-55019163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11071115	chr15:55019174-55019175	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574075545	chr15:55019209-55019210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543050352	chr15:55019245-55019246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563037263	chr15:55019248-55019249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535613706	chr15:55019281-55019282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188344958	chr15:55019310-55019311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192189849	chr15:55019367-55019368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559647551	chr15:55019403-55019404	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528697661	chr15:55019436-55019437	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76941815	chr15:55019438-55019439	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568762783	chr15:55019467-55019468	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141673029	chr15:55019469-55019470	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551035535	chr15:55019505-55019506	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571196207	chr15:55019507-55019508	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539901552	chr15:55019516-55019517	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553449683	chr15:55019523-55019524	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79814212	chr15:55019563-55019564	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534849284	chr15:55019578-55019579	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116703677	chr15:55019633-55019634	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574435109	chr15:55019648-55019649	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538932173	chr15:55019649-55019650	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562894739	chr15:55019655-55019656	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576436587	chr15:55019691-55019692	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74014867	chr15:55019702-55019703	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559418433	chr15:55019706-55019707	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528655413	chr15:55019721-55019722	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530055942	chr15:55019722-55019723	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562359810	chr15:55019732-55019733	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531278900	chr15:55019738-55019739	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs28679864	chr15:55019753-55019754	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147995738	chr15:55019772-55019773	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141635929	chr15:55019784-55019785	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546757255	chr15:55019785-55019786	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150501167	chr15:55019787-55019788	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548498296	chr15:55019801-55019802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11071116	chr15:55019870-55019871	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs372182603	chr15:55019872-55019873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376501921	chr15:55019887-55019888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554799564	chr15:55019899-55019900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369071828	chr15:55019908-55019909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537252588	chr15:55019935-55019936	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	17440070	CNVD
Cancer	20164919	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
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD

Chromatin state (count:3089 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55019000-55020000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr15:55019200-55019400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:55019400-55019800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:55020000-55020400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:55020400-55021000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr15:55021000-55022200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:55022200-55023000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:55030400-55031000	ZNF genes & repeats	Adipose Nuclei	Adipose
9	chr15:55030400-55031000	ZNF genes & repeats	Aorta	Aorta
10	chr15:55037600-55037800	Weak transcription	Aorta	Aorta
11	chr15:55037800-55038200	ZNF genes & repeats	Aorta	Aorta
12	chr15:55038200-55041600	Weak transcription	Aorta	Aorta
13	chr15:55041800-55042000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:55055800-55056200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:55056200-55057200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr15:55057200-55057800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:55057800-55058000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr15:55062000-55062800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr15:55062000-55062800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr15:55062200-55062600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr15:55062200-55062800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr15:55062400-55062800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr15:55062600-55064400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr15:55062800-55064400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:55062800-55064800	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr15:55064400-55065000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr15:55064400-55065600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr15:55064800-55065000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:55065000-55065400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:55065000-55070200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr15:55065600-55065800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr15:55068000-55068200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr15:55068400-55068600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:55070400-55070600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:55079600-55082400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:55079800-55082800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:55080200-55081600	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr15:55081400-55082000	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr15:55081600-55082000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr15:55081600-55082000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr15:55081600-55082400	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr15:55082000-55082800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr15:55082400-55082600	Active TSS	Fetal Heart	heart
44	chr15:55082600-55090400	Weak transcription	Fetal Heart	heart
45	chr15:55084600-55085000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr15:55084600-55085000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr15:55084600-55085200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr15:55089600-55090800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:55089800-55090200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr15:55090200-55095600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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