Variant report

Variant	nsv569543
Chromosome Location	chr15:56255774-56321854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1241)
CpG islands
(count:796)
Chromatin interactive
region (count:61)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:56290869-56290907	K562	blood:	n/a	n/a
2	ARID3A	chr15:56267850-56267851	K562	blood:	n/a	n/a
3	ARID3A	chr15:56286628-56286918	K562	blood:	n/a	n/a
4	ARID3A	chr15:56285729-56285953	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:56285218-56285455	K562	blood:	n/a	n/a
6	ATF1	chr15:56295967-56296197	K562	blood:	n/a	n/a
7	ATF1	chr15:56311295-56311472	K562	blood:	n/a	n/a
8	ATF1	chr15:56301135-56301199	K562	blood:	n/a	n/a
9	ATF1	chr15:56286965-56287213	K562	blood:	n/a	n/a
10	ATF3	chr15:56295943-56296234	K562	blood:	n/a	chr15:56296138-56296151
11	BACH1	chr15:56285350-56286282	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr15:56285172-56286542	K562	blood:	n/a	chr15:56285460-56285476
13	BHLHE40	chr15:56286927-56286969	K562	blood:	n/a	n/a
14	BHLHE40	chr15:56309879-56310348	K562	blood:	n/a	n/a
15	BHLHE40	chr15:56285538-56285951	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:56298674-56298896	HepG2	liver:	n/a	n/a
17	BHLHE40	chr15:56291015-56291031	K562	blood:	n/a	n/a
18	BHLHE40	chr15:56310014-56310402	HepG2	liver:	n/a	n/a
19	BRCA1	chr15:56285563-56285941	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr15:56320664-56320979	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr15:56285288-56285308	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr15:56290670-56291397	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr15:56285293-56285463	GM12878	blood:	n/a	n/a
24	CBX3	chr15:56285682-56285992	K562	blood:	n/a	n/a
25	CBX3	chr15:56306952-56307210	K562	blood:	n/a	n/a
26	CBX3	chr15:56306949-56307149	K562	blood:	n/a	n/a
27	CCNT2	chr15:56285239-56286486	K562	blood:	n/a	n/a
28	CEBPB	chr15:56298655-56298882	Hela-S3	cervix:	n/a	chr15:56298720-56298731
29	CEBPB	chr15:56269476-56269801	HepG2	liver:	n/a	chr15:56269633-56269644
30	CEBPB	chr15:56261769-56262184	MCF-7	breast:	n/a	n/a
31	CEBPB	chr15:56295963-56296294	Hela-S3	cervix:	n/a	chr15:56296117-56296128
32	CEBPB	chr15:56310153-56310358	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:56269501-56269801	IMR90	lung:	n/a	chr15:56269633-56269644
34	CEBPB	chr15:56290800-56290987	K562	blood:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
35	CEBPB	chr15:56297105-56297289	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr15:56290772-56291058	IMR90	lung:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
37	CEBPB	chr15:56315434-56315641	Hela-S3	cervix:	n/a	chr15:56315481-56315492
38	CEBPB	chr15:56297105-56297209	K562	blood:	n/a	n/a
39	CEBPB	chr15:56308913-56309113	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:56309053-56309130	K562	blood:	n/a	n/a
41	CEBPB	chr15:56269483-56269797	A549	lung:	n/a	chr15:56269633-56269644
42	CEBPB	chr15:56298629-56298888	HepG2	liver:	n/a	chr15:56298720-56298731
43	CEBPB	chr15:56285127-56285219	K562	blood:	n/a	n/a
44	CEBPB	chr15:56295986-56296186	IMR90	lung:	n/a	chr15:56296117-56296128
45	CEBPB	chr15:56265039-56265208	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:56309966-56310452	HepG2	liver:	n/a	n/a
47	CEBPB	chr15:56315347-56315649	HepG2	liver:	n/a	chr15:56315481-56315492
48	CEBPB	chr15:56295964-56296254	K562	blood:	n/a	chr15:56296117-56296128
49	CEBPB	chr15:56261819-56262052	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:56290772-56291097	K562	blood:	n/a	chr15:56290913-56290926 chr15:56290913-56290924

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56285741-56285791	HL-60	blood:	n/a
2	chr15:56286575-56286625	H1-hESC	embryonic stem cell:	embryo
3	chr15:56285484-56285534	HCT-116	colon:	n/a
4	chr15:56285741-56285791	HL-60	blood:	n/a
5	chr15:56286575-56286625	H1-hESC	embryonic stem cell:	embryo
6	chr15:56285484-56285534	HCT-116	colon:	n/a
7	chr15:56299380-56299430	AG09319	gingival:	n/a
8	chr15:56286336-56286386	PANC-1	pancreas:	n/a
9	chr15:56286336-56286386	AG10803	skin:	n/a
10	chr15:56286575-56286625	NHDF-neo	bronchial:	n/a
11	chr15:56282277-56282327	ECC-1	luminal epithelium:	n/a
12	chr15:56285761-56285811	GM12891	blood:	n/a
13	chr15:56290261-56290311	MCF10A-Er-Src	breast:	n/a
14	chr15:56286336-56286386	AG09309	skin:	n/a
15	chr15:56285741-56285791	HCT-116	colon:	n/a
16	chr15:56285484-56285534	GM19239	blood:	n/a
17	chr15:56299380-56299430	PANC-1	pancreas:	n/a
18	chr15:56286067-56286117	HL-60	blood:	n/a
19	chr15:56286283-56286333	RPTEC	kidney:	n/a
20	chr15:56285261-56285311	GM12891	blood:	n/a
21	chr15:56286575-56286625	GM12891	blood:	n/a
22	chr15:56286067-56286117	GM12892	blood:	n/a
23	chr15:56286575-56286625	HCPEpiC	choroid plexus:	n/a
24	chr15:56285484-56285534	SKMC	muscle:	n/a
25	chr15:56299380-56299430	HRE	kidney:	n/a
26	chr15:56286150-56286200	A549	lung:	n/a
27	chr15:56285484-56285534	ProgFib	skin:	n/a
28	chr15:56286336-56286386	GM12891	blood:	n/a
29	chr15:56286150-56286200	HRPEpiC	eye:	n/a
30	chr15:56286575-56286625	AG04450	lung:	fetal
31	chr15:56286283-56286333	HNPCEpiC	eye:	n/a
32	chr15:56285261-56285311	Hela-S3	cervix:	n/a
33	chr15:56284168-56284218	SK-N-SH	brain:	n/a
34	chr15:56286575-56286625	U87	brain:	n/a
35	chr15:56286067-56286117	HRCEpiC	kidney:	n/a
36	chr15:56290261-56290311	GM12892	blood:	n/a
37	chr15:56299380-56299430	PrEC	prostate:	n/a
38	chr15:56284168-56284218	HAEpiC	amniotic membrane:	n/a
39	chr15:56286575-56286625	AoSMC	blood vessel:	n/a
40	chr15:56285761-56285811	NHDF-neo	bronchial:	n/a
41	chr15:56290261-56290311	NHBE	bronchial:	n/a
42	chr15:56286150-56286200	GM19239	blood:	n/a
43	chr15:56285261-56285311	GM06990	blood:	n/a
44	chr15:56286336-56286386	K562	blood:	n/a
45	chr15:56290261-56290311	IMR90	lung:	fetal
46	chr15:56286067-56286117	NHDF-neo	bronchial:	n/a
47	chr15:56299380-56299430	Jurkat	blood:	n/a
48	chr15:56286283-56286333	PFSK-1	brain:	n/a
49	chr15:56285741-56285791	CMK	blood:	n/a
50	chr15:56299380-56299430	Hepatocyte	liver:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:56286056..56286943-chr15:56344508..56345311,2	MCF-7	breast:
2	chr15:56282892..56284804-chr15:56387312..56388901,2	MCF-7	breast:
3	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
4	chr1:109234674..109235306-chr15:56285708..56286287,2	Hela-S3	cervix:
5	chr15:56260979..56263208-chr15:56266401..56268573,2	MCF-7	breast:
6	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:
7	chr15:56276877..56278529-chr15:56290959..56293005,2	MCF-7	breast:
8	chr15:56288413..56291274-chr15:56330655..56333525,2	MCF-7	breast:
9	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
10	chr15:56257143..56259328-chr15:56260984..56263123,2	K562	blood:
11	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
12	chr15:56283971..56286834-chr15:56291176..56293680,2	K562	blood:
13	chr15:56299007..56301700-chr15:56309609..56311858,2	MCF-7	breast:
14	chr15:56283238..56284535-chr15:56344426..56345460,6	MCF-7	breast:
15	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
16	chr15:56251937..56254023-chr15:56256235..56258687,3	K562	blood:
17	chr15:56286068..56286594-chr15:56344895..56345645,2	MCF-7	breast:
18	chr1:233748980..233749780-chr15:56285541..56286277,2	Hela-S3	cervix:
19	chr15:56309924..56310815-chr15:56344688..56345628,4	MCF-7	breast:
20	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
21	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
22	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
23	chr15:56286939..56288503-chr15:56293657..56295210,2	K562	blood:
24	chr15:56254403..56256035-chr15:56332964..56335048,2	MCF-7	breast:
25	chr15:56259678..56262217-chr15:56262455..56264913,2	MCF-7	breast:
26	chr15:56285499..56287418-chr15:56534884..56536553,2	K562	blood:
27	chr15:56259678..56262217-chr15:56262455..56264913,2	MCF-7	breast:
28	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
29	chr15:56308090..56310952-chr15:56323916..56326374,2	MCF-7	breast:
30	chr15:56286939..56288503-chr15:56293657..56295210,2	K562	blood:
31	chr15:56250089..56252612-chr15:56259045..56261387,2	MCF-7	breast:
32	chr15:56274993..56280197-chr15:56282390..56286830,6	MCF-7	breast:
33	chr15:56284668..56287599-chr15:56288074..56291098,3	K562	blood:
34	chr15:56281435..56283774-chr15:56390486..56392704,2	MCF-7	breast:
35	chr15:56260979..56263208-chr15:56266401..56268573,2	MCF-7	breast:
36	chr1:28994985..28995485-chr15:56285972..56286627,2	Hela-S3	cervix:
37	chr15:56269452..56273528-chr15:56284245..56287674,5	MCF-7	breast:
38	chr14:55737712..55738366-chr15:56285235..56286222,2	Hela-S3	cervix:
39	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
40	chr15:56282050..56287467-chr15:56534024..56538662,8	MCF-7	breast:
41	chr15:56292596..56295463-chr15:56332389..56335036,2	MCF-7	breast:
42	chr15:56309948..56310461-chr15:56538175..56538871,2	MCF-7	breast:
43	chr15:56285724..56286656-chr8:8559373..8559873,2	Hela-S3	cervix:
44	chr15:56282101..56284524-chr15:56536077..56539290,3	MCF-7	breast:
45	chr15:56279620..56282017-chr15:56535404..56538288,2	MCF-7	breast:
46	chr15:56271720..56275778-chr15:56283975..56286935,4	K562	blood:
47	chr15:56271136..56275778-chr15:56283975..56288276,6	K562	blood:
48	chr15:56284954..56286880-chr15:56299616..56301777,2	K562	blood:
49	chr15:56285803..56286769-chr7:144532503..144533132,2	HCT-116	colon:
50	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFX7-2	chr15:56305102-56305262	l_1162_chr15:56293600-56416163_liver
2	lnc-RFX7-3	chr15:56285709-56285811	NONHSAT044012
3	lnc-RFX7-3	chr15:56279929-56280199	NONHSAT044012
4	lnc-RFX7-2	chr15:56321306-56321486	l_1162_chr15:56293600-56416163_liver
5	lnc-RFX7-2	chr15:56293601-56293799	l_1162_chr15:56293600-56416163_liver

No data

Variant related genes	Relation type
CNOT6LP1	TF binding region
NEDD4	TF binding region
CNOT6LP1	CpG island
NEDD4	CpG island
ENSG00000176305	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000230183	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000151575	chromatin interactions
ENSG00000135750	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000196511	chromatin interactions
ENSG00000134186	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000162419	chromatin interactions

Extended variants
information (count: 2460 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2460 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4774837	chr15:56255774-56255775	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs66493820	chr15:56255794-56255795	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs188365134	chr15:56255807-56255808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs66540128	chr15:56255811-56255812	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs572636309	chr15:56255988-56255989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369744901	chr15:56255999-56256000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs67620259	chr15:56256099-56256100	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540285831	chr15:56256130-56256131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146406058	chr15:56256147-56256148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529682676	chr15:56256148-56256149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543428724	chr15:56256225-56256226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs58703788	chr15:56256264-56256265	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs60760787	chr15:56256277-56256278	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs139811523	chr15:56256291-56256292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58047840	chr15:56256302-56256303	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs181337918	chr15:56256305-56256306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565417967	chr15:56256312-56256313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568029674	chr15:56256379-56256380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs60646551	chr15:56256381-56256382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62045215	chr15:56256393-56256394	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556260473	chr15:56256415-56256416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184523872	chr15:56256436-56256437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538746223	chr15:56256485-56256486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151125420	chr15:56256486-56256487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77913535	chr15:56256487-56256488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs398070669	chr15:56256508-56256509	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557459987	chr15:56256550-56256551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550295714	chr15:56256562-56256563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570506136	chr15:56256573-56256574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572623285	chr15:56256587-56256588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532958080	chr15:56256592-56256593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546677135	chr15:56256641-56256642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534490803	chr15:56256661-56256662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs57472279	chr15:56256757-56256758	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555238818	chr15:56256846-56256847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35996825	chr15:56256848-56256849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375226645	chr15:56256849-56256850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34169831	chr15:56256850-56256851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59224264	chr15:56256854-56256855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs60902586	chr15:56256870-56256871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150473505	chr15:56256871-56256872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149758664	chr15:56256874-56256875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71441417	chr15:56256876-56256877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576474513	chr15:56256889-56256890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200891809	chr15:56256891-56256892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145712820	chr15:56256900-56256901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs59116560	chr15:56256923-56256924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs58177503	chr15:56256925-56256926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60258159	chr15:56256928-56256929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377123486	chr15:56256929-56256930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56229400-56259000	Weak transcription	Ovary	ovary
2	chr15:56229400-56259400	Weak transcription	Small Intestine	intestine
3	chr15:56229600-56282600	Weak transcription	NHLF	lung
4	chr15:56229800-56259000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr15:56231400-56284200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr15:56231600-56260000	Weak transcription	Left Ventricle	heart
7	chr15:56232600-56257200	Weak transcription	Primary T cells from cord blood	blood
8	chr15:56236000-56258200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr15:56236000-56259000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr15:56236000-56261200	Weak transcription	Esophagus	oesophagus
11	chr15:56236200-56257000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:56236200-56257000	Weak transcription	Aorta	Aorta
13	chr15:56236200-56276000	Weak transcription	HUVEC	blood vessel
14	chr15:56236600-56257000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr15:56236800-56257000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr15:56236800-56282800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr15:56238200-56257000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr15:56241000-56261400	Weak transcription	Pancreas	Pancrea
19	chr15:56243000-56257000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr15:56243200-56256400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr15:56243200-56256400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr15:56243200-56276200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:56243400-56257000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr15:56244600-56257800	Weak transcription	Fetal Brain Male	brain
25	chr15:56247400-56257000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:56247600-56257400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr15:56248200-56285200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:56250000-56266600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr15:56250600-56257200	Weak transcription	Fetal Stomach	stomach
30	chr15:56251200-56258200	Weak transcription	A549	lung
31	chr15:56251600-56281600	Weak transcription	Osteobl	bone
32	chr15:56252200-56261800	Weak transcription	Spleen	Spleen
33	chr15:56252400-56261200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr15:56253200-56256400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:56253200-56256800	Weak transcription	Lung	lung
36	chr15:56253200-56259000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr15:56253200-56261200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:56253200-56261400	Weak transcription	HSMMtube	muscle
39	chr15:56253400-56257000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr15:56253400-56257000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:56253400-56257000	Weak transcription	HSMM	muscle
42	chr15:56253400-56259000	Weak transcription	Adipose Nuclei	Adipose
43	chr15:56253400-56261200	Weak transcription	Gastric	stomach
44	chr15:56253400-56261600	Weak transcription	Placenta	Placenta
45	chr15:56253400-56261800	Weak transcription	HMEC	breast
46	chr15:56253600-56257000	Weak transcription	Fetal Intestine Large	intestine
47	chr15:56253600-56257000	Weak transcription	NHEK	skin
48	chr15:56253600-56282400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr15:56253800-56256800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr15:56254000-56258200	Weak transcription	Muscle Satellite Cultured Cells	--

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