Variant report

Variant	nsv904250
Chromosome Location	chr15:57225766-57294085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:305)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57226209-57226854	K562	blood:	n/a	n/a
2	ARID3A	chr15:57264390-57264853	K562	blood:	n/a	n/a
3	ARID3A	chr15:57257894-57258148	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57252427-57252618	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57275254-57275472	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57262164-57262398	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57249593-57250337	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:57281407-57282155	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:57225655-57226003	K562	blood:	n/a	n/a
10	ARID3A	chr15:57271204-57271795	HepG2	liver:	n/a	chr15:57271527-57271543
11	ARID3A	chr15:57263403-57263635	K562	blood:	n/a	n/a
12	ARID3A	chr15:57280562-57280984	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:57281883-57282101	K562	blood:	n/a	n/a
14	ATF1	chr15:57225612-57225773	K562	blood:	n/a	n/a
15	ATF1	chr15:57226517-57226869	K562	blood:	n/a	n/a
16	ATF1	chr15:57264660-57264913	K562	blood:	n/a	n/a
17	ATF2	chr15:57252057-57252784	GM12878	blood:	n/a	n/a
18	ATF2	chr15:57243166-57243752	GM12878	blood:	n/a	n/a
19	ATF2	chr15:57243165-57243623	GM12878	blood:	n/a	n/a
20	ATF2	chr15:57256206-57256858	GM12878	blood:	n/a	n/a
21	ATF2	chr15:57252188-57252761	GM12878	blood:	n/a	n/a
22	BACH1	chr15:57226542-57226590	K562	blood:	n/a	n/a
23	BACH1	chr15:57265992-57266005	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr15:57252297-57252772	GM12878	blood:	n/a	chr15:57252539-57252550
25	BATF	chr15:57243148-57243483	GM12878	blood:	n/a	n/a
26	BATF	chr15:57252379-57252719	GM12878	blood:	n/a	chr15:57252539-57252550
27	BCL11A	chr15:57252328-57252744	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:57243148-57243555	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:57243289-57243499	GM12878	blood:	n/a	n/a
30	BCL3	chr15:57256319-57256601	GM12878	blood:	n/a	n/a
31	BCL3	chr15:57252199-57252677	GM12878	blood:	n/a	n/a
32	BCL3	chr15:57271054-57271868	A549	lung:	n/a	n/a
33	BCLAF1	chr15:57243099-57243697	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:57252291-57252683	GM12878	blood:	n/a	n/a
35	BHLHE40	chr15:57281904-57282089	K562	blood:	n/a	n/a
36	BHLHE40	chr15:57263440-57263705	K562	blood:	n/a	n/a
37	BHLHE40	chr15:57233777-57234029	K562	blood:	n/a	n/a
38	BHLHE40	chr15:57250100-57250554	HepG2	liver:	n/a	n/a
39	BHLHE40	chr15:57243277-57243596	GM12878	blood:	n/a	n/a
40	CBX3	chr15:57238369-57238650	K562	blood:	n/a	n/a
41	CBX3	chr15:57263356-57263717	K562	blood:	n/a	n/a
42	CCNT2	chr15:57264654-57264949	K562	blood:	n/a	n/a
43	CCNT2	chr15:57256118-57256675	K562	blood:	n/a	chr15:57256585-57256605
44	CEBPB	chr15:57263316-57263616	MCF-7	breast:	n/a	n/a
45	CEBPB	chr15:57240649-57241022	A549	lung:	n/a	chr15:57240831-57240842 chr15:57240830-57240843
46	CEBPB	chr15:57263090-57263751	A549	lung:	n/a	n/a
47	CEBPB	chr15:57240552-57241099	A549	lung:	n/a	chr15:57240831-57240842 chr15:57240830-57240843
48	CEBPB	chr15:57240644-57241020	K562	blood:	n/a	chr15:57240831-57240842 chr15:57240830-57240843
49	CEBPB	chr15:57263253-57263630	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:57240741-57241009	HepG2	liver:	n/a	chr15:57240831-57240842 chr15:57240830-57240843

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57250375-57250425	SK-N-MC	brain:	n/a
2	chr15:57250375-57250425	HRE	kidney:	n/a
3	chr15:57250375-57250425	LNCaP	prostate:	n/a
4	chr15:57277634-57277684	Hepatocyte	liver:	n/a
5	chr15:57250375-57250425	Hela-S3	cervix:	n/a
6	chr15:57272441-57272491	SK-N-MC	brain:	n/a
7	chr15:57272441-57272491	IMR90	lung:	fetal
8	chr15:57277634-57277684	BE2_C	brain:	n/a
9	chr15:57272441-57272491	NHDF-neo	bronchial:	n/a
10	chr15:57251471-57251521	U87	brain:	n/a
11	chr15:57251471-57251521	AG10803	skin:	n/a
12	chr15:57250375-57250425	SK-N-SH	brain:	n/a
13	chr15:57251471-57251521	Hepatocyte	liver:	n/a
14	chr15:57256372-57256422	HUVEC	blood vessel:	n/a
15	chr15:57277634-57277684	MCF10A-Er-Src	breast:	n/a
16	chr15:57251471-57251521	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:57250375-57250425	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:57250375-57250425	AG10803	skin:	n/a
19	chr15:57256372-57256422	PrEC	prostate:	n/a
20	chr15:57256372-57256422	HCT-116	colon:	n/a
21	chr15:57277634-57277684	SK-N-MC	brain:	n/a
22	chr15:57251471-57251521	MCF-7	breast:	n/a
23	chr15:57272441-57272491	RPTEC	kidney:	n/a
24	chr15:57272441-57272491	HepG2	liver:	n/a
25	chr15:57251471-57251521	AG04450	lung:	fetal
26	chr15:57256372-57256422	SK-N-MC	brain:	n/a
27	chr15:57277634-57277684	HCT-116	colon:	n/a
28	chr15:57251471-57251521	HCF	heart:	n/a
29	chr15:57272441-57272491	AG04450	lung:	fetal
30	chr15:57272441-57272491	HMEC	breast:	n/a
31	chr15:57250375-57250425	PFSK-1	brain:	n/a
32	chr15:57272441-57272491	HUVEC	blood vessel:	n/a
33	chr15:57256372-57256422	GM06990	blood:	n/a
34	chr15:57277634-57277684	MCF-7	breast:	n/a
35	chr15:57277634-57277684	Jurkat	blood:	n/a
36	chr15:57272441-57272491	GM19239	blood:	n/a
37	chr15:57256372-57256422	ovcar-3	ovarian:	n/a
38	chr15:57256372-57256422	CMK	blood:	n/a
39	chr15:57251471-57251521	RPTEC	kidney:	n/a
40	chr15:57272441-57272491	HCT-116	colon:	n/a
41	chr15:57277634-57277684	GM06990	blood:	n/a
42	chr15:57250375-57250425	HNPCEpiC	eye:	n/a
43	chr15:57272441-57272491	HEK293	kidney:	embryo
44	chr15:57277634-57277684	HCF	heart:	n/a
45	chr15:57256372-57256422	SAEC	small airway:	n/a
46	chr15:57272441-57272491	U87	brain:	n/a
47	chr15:57251471-57251521	T-47D	breast:	n/a
48	chr15:57251471-57251521	HCT-116	colon:	n/a
49	chr15:57250375-57250425	BJ	skin:	n/a
50	chr15:57272441-57272491	MCF-7	breast:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:57263359..57266200-chr15:57266241..57268315,2	K562	blood:
2	chr15:57222920..57225645-chr15:57236445..57240161,3	MCF-7	breast:
3	chr15:57179564..57182313-chr15:57232225..57234178,2	K562	blood:
4	chr15:57219695..57221734-chr15:57225928..57228525,2	K562	blood:
5	chr15:57269633..57272065-chr15:57273062..57274627,2	K562	blood:
6	chr15:57215422..57217856-chr15:57225443..57228595,3	K562	blood:
7	chr15:57253721..57256073-chr15:57262899..57264820,2	K562	blood:
8	chr15:57265601..57267263-chr15:57271593..57273612,2	K562	blood:
9	chr15:57263359..57266200-chr15:57266241..57268315,2	K562	blood:
10	chr15:57281787..57284402-chr15:57285432..57287690,2	K562	blood:
11	chr15:57213053..57214861-chr15:57239551..57242181,2	K562	blood:
12	chr15:57208964..57210715-chr15:57261991..57264737,2	K562	blood:
13	chr15:57209996..57212300-chr15:57225729..57228088,3	K562	blood:
14	chr15:57277263..57280006-chr15:57281828..57283970,2	K562	blood:
15	chr15:57254284..57256820-chr15:57279086..57281932,2	K562	blood:
16	chr15:57210017..57214406-chr15:57230340..57233852,4	K562	blood:
17	chr15:57208582..57210610-chr15:57249153..57251996,2	K562	blood:
18	chr15:57275197..57277151-chr15:57278136..57281602,3	K562	blood:
19	chr15:57210057..57212896-chr15:57260738..57263139,2	MCF-7	breast:
20	chr15:57286718..57288374-chr15:57289394..57292211,2	K562	blood:
21	chr15:57261844..57263544-chr15:57271380..57273128,2	K562	blood:
22	chr15:57210283..57211789-chr15:57264775..57267167,2	K562	blood:
23	chr15:57254284..57256820-chr15:57279086..57281932,2	K562	blood:
24	chr15:57269633..57272065-chr15:57273062..57274627,2	K562	blood:
25	chr15:57212275..57213860-chr15:57281190..57283282,2	K562	blood:
26	chr15:57210623..57212439-chr15:57268070..57269704,2	MCF-7	breast:
27	chr15:57286718..57288374-chr15:57289394..57292211,2	K562	blood:
28	chr15:57222937..57224563-chr15:57225257..57227921,2	K562	blood:
29	chr15:57222937..57225630-chr15:57226421..57228724,2	K562	blood:
30	chr15:57242148..57243813-chr15:57244143..57246252,2	MCF-7	breast:
31	chr15:57210198..57214861-chr15:57238728..57241582,5	K562	blood:
32	chr15:57261844..57263544-chr15:57271380..57273128,2	K562	blood:
33	chr15:57277206..57280483-chr15:57280538..57284418,3	K562	blood:
34	chr15:57227613..57229628-chr15:57229814..57231520,2	K562	blood:
35	chr15:57243814..57246675-chr15:57249324..57251467,2	K562	blood:
36	chr15:57262336..57264742-chr15:57265375..57267744,2	K562	blood:
37	chr15:57273239..57275335-chr15:57275612..57277322,2	K562	blood:
38	chr15:57243814..57246675-chr15:57249324..57251467,2	K562	blood:
39	chr15:57286745..57288660-chr15:57302090..57304157,2	MCF-7	breast:
40	chr15:57285454..57287142-chr15:57328507..57331190,2	K562	blood:
41	chr15:57227613..57229628-chr15:57229814..57231520,2	K562	blood:
42	chr15:57210716..57212486-chr15:57263351..57264921,2	K562	blood:
43	chr15:57273239..57275335-chr15:57275612..57277322,2	K562	blood:
44	chr15:57242148..57243813-chr15:57244143..57246252,2	MCF-7	breast:
45	chr15:57254985..57258076-chr15:57265765..57268821,3	K562	blood:
46	chr15:57265601..57267263-chr15:57271593..57273612,2	K562	blood:
47	chr15:57254985..57258076-chr15:57265765..57268821,3	K562	blood:
48	chr15:57253721..57256073-chr15:57262899..57264820,2	K562	blood:
49	chr15:57281787..57284402-chr15:57285432..57287690,2	K562	blood:
50	chr15:57277206..57280483-chr15:57280538..57284418,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000222586	TF binding region
ENSG00000222586	CpG island
ENSG00000140262	chromatin interactions
ENSG00000137871	chromatin interactions

Extended variants
information (count: 2775 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2775 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs213155	chr15:57225766-57225767	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs116135214	chr15:57225857-57225858	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559889506	chr15:57225872-57225873	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573271571	chr15:57225921-57225922	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534276135	chr15:57225927-57225928	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs542285045	chr15:57225930-57225931	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs538959702	chr15:57225959-57225960	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562230764	chr15:57225978-57225979	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531268698	chr15:57226007-57226008	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs73411254	chr15:57226029-57226030	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564671330	chr15:57226050-57226051	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533349069	chr15:57226053-57226054	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376235164	chr15:57226111-57226112	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546282177	chr15:57226160-57226161	Weak transcription Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs181202476	chr15:57226252-57226253	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371002672	chr15:57226267-57226268	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs185208157	chr15:57226296-57226297	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs146169438	chr15:57226326-57226327	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558859280	chr15:57226328-57226329	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs137888445	chr15:57226329-57226330	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs538116270	chr15:57226395-57226396	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557770808	chr15:57226446-57226447	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189689934	chr15:57226533-57226534	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183452244	chr15:57226542-57226543	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113665934	chr15:57226559-57226560	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191626687	chr15:57226591-57226592	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs34579450	chr15:57226611-57226612	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs16977155	chr15:57226614-57226615	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573401303	chr15:57226615-57226616	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183550541	chr15:57226645-57226646	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149474677	chr15:57226666-57226667	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs188281817	chr15:57226692-57226693	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs116113015	chr15:57226695-57226696	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564669946	chr15:57226716-57226717	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114484918	chr15:57226771-57226772	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556750144	chr15:57226786-57226787	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546820952	chr15:57226791-57226792	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs559802372	chr15:57226796-57226797	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12592486	chr15:57226814-57226815	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs143963103	chr15:57226863-57226864	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548828586	chr15:57226882-57226883	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs568789352	chr15:57226891-57226892	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192976240	chr15:57226923-57226924	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537452832	chr15:57226926-57226927	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576560007	chr15:57226945-57226946	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs541370403	chr15:57226979-57226980	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs551644218	chr15:57226997-57226998	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs148658161	chr15:57227016-57227017	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs533951213	chr15:57227031-57227032	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182629730	chr15:57227037-57227038	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Pancreatic cancer	17952125	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57212400-57230400	Weak transcription	Lung	lung
2	chr15:57212400-57233400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:57212400-57256000	Weak transcription	Pancreas	Pancrea
4	chr15:57212600-57241000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr15:57212800-57227200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr15:57213000-57227400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr15:57213200-57256000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr15:57213400-57226800	Weak transcription	Brain Germinal Matrix	brain
9	chr15:57215600-57227400	Weak transcription	Fetal Brain Female	brain
10	chr15:57216400-57241800	Weak transcription	Fetal Brain Male	brain
11	chr15:57220000-57226000	Enhancers	Fetal Intestine Large	intestine
12	chr15:57220200-57226200	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr15:57220400-57226800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr15:57220400-57236400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:57220800-57226200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:57221000-57226000	Enhancers	Duodenum Mucosa	Duodenum
17	chr15:57221000-57226600	Enhancers	Fetal Intestine Small	intestine
18	chr15:57221200-57226600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:57221400-57226600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr15:57221400-57227200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr15:57221600-57226400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr15:57221600-57226600	Weak transcription	HSMMtube	muscle
23	chr15:57221800-57226800	Enhancers	Brain Anterior Caudate	brain
24	chr15:57222000-57225800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr15:57222200-57225800	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr15:57222200-57226000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr15:57222200-57226200	Weak transcription	NHEK	skin
28	chr15:57222400-57227000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr15:57222400-57227400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr15:57222400-57229600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr15:57222400-57231200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr15:57222600-57226600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr15:57222600-57228800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:57222600-57229000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr15:57222600-57231200	Weak transcription	Osteobl	bone
36	chr15:57222600-57231800	Weak transcription	HSMM	muscle
37	chr15:57222600-57233000	Weak transcription	Right Ventricle	heart
38	chr15:57222600-57250200	Weak transcription	NH-A	brain
39	chr15:57222800-57231800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr15:57222800-57232600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:57222800-57240800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr15:57222800-57255000	Weak transcription	HMEC	breast
43	chr15:57223000-57226200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr15:57223000-57227400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:57223000-57236800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr15:57223200-57226400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr15:57223200-57226600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr15:57223200-57226600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:57223200-57227000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:57223200-57227400	Enhancers	Brain Hippocampus Middle	brain

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