Variant report

Variant	esv3437718
Chromosome Location	chr15:30112685-30116033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:677)
CpG islands
(count:794)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30113508-30113944	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:30115339-30115686	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:30113516-30113887	K562	blood:	n/a	n/a
4	ATF1	chr15:30113535-30113894	K562	blood:	n/a	n/a
5	ATF2	chr15:30113491-30113996	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:30113515-30113947	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr15:30113464-30113906	K562	blood:	n/a	n/a
8	ATF3	chr15:30113629-30113845	K562	blood:	n/a	n/a
9	BACH1	chr15:30113488-30115592	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:30112449-30113905	K562	blood:	n/a	n/a
11	BATF	chr15:30113602-30113834	GM12878	blood:	n/a	n/a
12	BCL3	chr15:30114340-30115772	A549	lung:	n/a	n/a
13	BHLHE40	chr15:30113347-30115139	K562	blood:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
14	BHLHE40	chr15:30113612-30115724	HepG2	liver:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
15	BRCA1	chr15:30114219-30114626	HepG2	liver:	n/a	n/a
16	BRCA1	chr15:30114822-30115569	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr15:30115035-30115474	HepG2	liver:	n/a	n/a
18	CCNT2	chr15:30113637-30115356	K562	blood:	n/a	n/a
19	CEBPB	chr15:30113501-30113992	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr15:30115046-30115390	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:30114343-30114592	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:30113558-30113878	K562	blood:	n/a	n/a
23	CEBPB	chr15:30113613-30113914	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:30114998-30115334	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr15:30113604-30113855	K562	blood:	n/a	n/a
26	CEBPB	chr15:30113583-30113985	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr15:30114463-30114737	HepG2	liver:	n/a	n/a
28	CEBPD	chr15:30113483-30114006	K562	blood:	n/a	n/a
29	CEBPD	chr15:30113554-30113972	K562	blood:	n/a	n/a
30	CHD1	chr15:30111618-30116068	IMR90	lung:	n/a	n/a
31	CHD1	chr15:30111661-30114675	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr15:30113529-30115182	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr15:30114126-30115069	K562	blood:	n/a	n/a
34	CHD2	chr15:30113537-30113897	HepG2	liver:	n/a	n/a
35	CHD2	chr15:30114199-30115126	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:30114207-30115738	HepG2	liver:	n/a	n/a
37	CHD2	chr15:30113207-30113949	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr15:30114474-30114737	A549	lung:	n/a	n/a
39	CREB1	chr15:30113501-30113970	A549	lung:	n/a	n/a
40	CREB1	chr15:30113579-30113957	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr15:30113591-30114010	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr15:30114082-30115601	HepG2	liver:	n/a	n/a
43	CREB1	chr15:30114105-30115392	A549	lung:	n/a	n/a
44	CTBP2	chr15:30114913-30115349	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr15:30113705-30113872	MCF-7	breast:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
46	CTCF	chr15:30113576-30114290	IMR90	lung:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
47	CTCF	chr15:30113680-30113830	HRPEpiC	eye:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
48	CTCF	chr15:30113760-30113910	Caco-2	colon:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
49	CTCF	chr15:30113720-30113870	NHDF-neo	bronchial:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
50	CTCF	chr15:30113701-30113931	MCF-7	breast:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30113831-30113881	NHBE	bronchial:	n/a
2	chr15:30113831-30113881	NHBE	bronchial:	n/a
3	chr15:30114816-30114866	A549	lung:	n/a
4	chr15:30114651-30114701	Hela-S3	cervix:	n/a
5	chr15:30114814-30114864	ProgFib	skin:	n/a
6	chr15:30114295-30114345	HRPEpiC	eye:	n/a
7	chr15:30115299-30115349	GM06990	blood:	n/a
8	chr15:30114295-30114345	AG04450	lung:	fetal
9	chr15:30113651-30113701	HCF	heart:	n/a
10	chr15:30115147-30115197	BJ	skin:	n/a
11	chr15:30114912-30114962	IMR90	lung:	fetal
12	chr15:30115299-30115349	SK-N-MC	brain:	n/a
13	chr15:30114474-30114524	AG09319	gingival:	n/a
14	chr15:30114871-30114921	H1-hESC	embryonic stem cell:	embryo
15	chr15:30113723-30113773	ProgFib	skin:	n/a
16	chr15:30114474-30114524	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:30115149-30115199	Jurkat	blood:	n/a
18	chr15:30113723-30113773	ovcar-3	ovarian:	n/a
19	chr15:30115149-30115199	MCF-7	breast:	n/a
20	chr15:30115147-30115197	SAEC	small airway:	n/a
21	chr15:30113651-30113701	K562	blood:	n/a
22	chr15:30115299-30115349	HepG2	liver:	n/a
23	chr15:30113723-30113773	GM06990	blood:	n/a
24	chr15:30113831-30113881	HCF	heart:	n/a
25	chr15:30113723-30113773	SAEC	small airway:	n/a
26	chr15:30114816-30114866	AG04450	lung:	fetal
27	chr15:30113723-30113773	PANC-1	pancreas:	n/a
28	chr15:30115149-30115199	HUVEC	blood vessel:	n/a
29	chr15:30114814-30114864	GM06990	blood:	n/a
30	chr15:30114912-30114962	HRE	kidney:	n/a
31	chr15:30114816-30114866	PrEC	prostate:	n/a
32	chr15:30114871-30114921	HCM	heart:	n/a
33	chr15:30115147-30115197	PANC-1	pancreas:	n/a
34	chr15:30114871-30114921	HCF	heart:	n/a
35	chr15:30114814-30114864	NH-A	brain:	n/a
36	chr15:30115147-30115197	K562	blood:	n/a
37	chr15:30114871-30114921	Hela-S3	cervix:	n/a
38	chr15:30114871-30114921	HCPEpiC	choroid plexus:	n/a
39	chr15:30114871-30114921	HRE	kidney:	n/a
40	chr15:30114814-30114864	HRE	kidney:	n/a
41	chr15:30115147-30115197	HCF	heart:	n/a
42	chr15:30114912-30114962	ovcar-3	ovarian:	n/a
43	chr15:30113651-30113701	Hela-S3	cervix:	n/a
44	chr15:30114295-30114345	NHDF-neo	bronchial:	n/a
45	chr15:30115299-30115349	HEEpiC	esophagus:	n/a
46	chr15:30115147-30115197	SK-N-SH_RA	brain:	n/a
47	chr15:30114295-30114345	ECC-1	luminal epithelium:	n/a
48	chr15:30113651-30113701	PFSK-1	brain:	n/a
49	chr15:30114912-30114962	HRCEpiC	kidney:	n/a
50	chr15:30115149-30115199	HRCEpiC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30113789..30114693-chr6:31795054..31795835,2	Hela-S3	cervix:
2	chr15:30114291..30114811-chr19:3762538..3763244,2	HCT-116	colon:
3	chr15:30115117..30117286-chr15:30127029..30129725,2	K562	blood:
4	chr15:30051900..30054307-chr15:30111477..30113324,2	K562	blood:
5	chr15:30111283..30113750-chr22:19879705..19881456,2	K562	blood:
6	chr1:52521763..52522611-chr15:30114227..30114914,2	Hela-S3	cervix:
7	chr12:57913766..57914507-chr15:30113406..30114143,2	Hela-S3	cervix:
8	chr15:30114363..30114879-chr5:162931957..162932799,2	Hela-S3	cervix:
9	chr15:30033909..30035507-chr15:30113047..30114881,2	MCF-7	breast:
10	chr15:30114003..30114757-chr17:34900104..34900989,2	Hela-S3	cervix:
11	chr12:6862162..6862757-chr15:30114314..30115083,2	HCT-116	colon:
12	chr15:30113418..30114284-chr5:10249625..10250242,2	Hela-S3	cervix:
13	chr15:30113746..30114342-chr16:31191095..31191723,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8J-2	chr15:30114834-30116284	ENSG00000259523.1
2	lnc-GOLGA8J-2	chr15:30115425-30115571	XLOC_011197

No data

Variant related genes	Relation type
ENSG00000259523	TF binding region
TJP1	TF binding region
ENSG00000259523	CpG island
TJP1	CpG island
ENSG00000089693	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000038274	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000005955	chromatin interactions
ENSG00000117862	chromatin interactions
ENSG00000183617	chromatin interactions
ENSG00000134717	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000104067	chromatin interactions

Extended variants
information (count: 116 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371474926	chr15:30112702-30112703	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs548663645	chr15:30112730-30112731	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs45510691	chr15:30112734-30112735	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530837044	chr15:30112747-30112748	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186877587	chr15:30112759-30112760	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs143873965	chr15:30112768-30112769	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12909418	chr15:30112798-30112799	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs12898473	chr15:30112806-30112807	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs540017574	chr15:30112815-30112816	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs192071337	chr15:30112833-30112834	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12913219	chr15:30112843-30112844	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs12913221	chr15:30112845-30112846	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs560448902	chr15:30112858-30112859	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12913232	chr15:30112865-30112866	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs41280060	chr15:30112896-30112897	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs183443319	chr15:30112952-30112953	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs76649990	chr15:30113003-30113004	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs546439066	chr15:30113053-30113054	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs187778607	chr15:30113076-30113077	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558068132	chr15:30113101-30113102	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375936960	chr15:30113104-30113105	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577899262	chr15:30113105-30113106	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs45527439	chr15:30113106-30113107	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs560041021	chr15:30113126-30113127	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs45456792	chr15:30113167-30113168	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541922260	chr15:30113188-30113189	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs552876377	chr15:30113232-30113233	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561877010	chr15:30113235-30113236	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs530801050	chr15:30113258-30113259	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574688559	chr15:30113262-30113263	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs6495935	chr15:30113264-30113265	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs373925613	chr15:30113276-30113277	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369322267	chr15:30113281-30113282	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533412096	chr15:30113284-30113285	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs547281899	chr15:30113330-30113331	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566917724	chr15:30113451-30113452	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs191469501	chr15:30113454-30113455	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs75773681	chr15:30113472-30113473	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs41280062	chr15:30113497-30113498	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs569006235	chr15:30113498-30113499	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs530772403	chr15:30113536-30113537	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs117556647	chr15:30113552-30113553	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs557832821	chr15:30113554-30113555	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs577566123	chr15:30113567-30113568	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs533802975	chr15:30113597-30113598	Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs554047805	chr15:30113603-30113604	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs556263683	chr15:30113621-30113622	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs374112281	chr15:30113635-30113636	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs564289211	chr15:30113660-30113661	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs573724339	chr15:30113679-30113680	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	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
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Schizophrenia	19197363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Mental retardation	17124404	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Schizophrenia	23813976	CNVD
Cognitive impairment	21505072	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	CNVD
Autism	20841430	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Attention deficit hyperactivity disorder	22420046	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30082400-30113600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:30108200-30113000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr15:30108400-30112800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:30108400-30113000	Weak transcription	Esophagus	oesophagus
5	chr15:30108600-30113600	Weak transcription	Pancreas	Pancrea
6	chr15:30108800-30112800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr15:30108800-30112800	Weak transcription	Stomach Mucosa	stomach
8	chr15:30110400-30115400	Active TSS	Right Atrium	heart
9	chr15:30111200-30113000	Weak transcription	Lung	lung
10	chr15:30111200-30113600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:30111400-30115000	Active TSS	NHLF	lung
12	chr15:30111400-30115600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr15:30111600-30112800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr15:30111600-30112800	Flanking Active TSS	Fetal Kidney	kidney
15	chr15:30111600-30113000	Flanking Active TSS	HUVEC	blood vessel
16	chr15:30111600-30113200	Active TSS	Duodenum Mucosa	Duodenum
17	chr15:30111600-30114400	Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr15:30111600-30115000	Active TSS	Fetal Muscle Leg	muscle
19	chr15:30111600-30115000	Active TSS	HSMM	muscle
20	chr15:30111600-30115000	Active TSS	K562	blood
21	chr15:30111600-30115000	Active TSS	NH-A	brain
22	chr15:30111600-30115200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:30111600-30115200	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr15:30111600-30115200	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr15:30111600-30115200	Active TSS	Right Ventricle	heart
26	chr15:30111600-30115400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:30111600-30115400	Active TSS	Psoas Muscle	Psoas
28	chr15:30111600-30115400	Active TSS	Stomach Smooth Muscle	stomach
29	chr15:30111800-30113000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr15:30111800-30113000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:30111800-30113200	Flanking Active TSS	Liver	Liver
32	chr15:30111800-30113200	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr15:30111800-30114800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:30111800-30115200	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr15:30111800-30115200	Active TSS	Colon Smooth Muscle	Colon
36	chr15:30111800-30115200	Active TSS	HSMMtube	muscle
37	chr15:30111800-30115400	Active TSS	Aorta	Aorta
38	chr15:30111800-30115600	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr15:30111800-30115600	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr15:30112000-30112800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr15:30112000-30113000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:30112000-30113000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:30112000-30113000	Flanking Active TSS	NHEK	skin
44	chr15:30112000-30113800	Active TSS	Fetal Heart	heart
45	chr15:30112000-30115000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:30112000-30115000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr15:30112000-30115000	Active TSS	Placenta	Placenta
48	chr15:30112000-30115000	Active TSS	HMEC	breast
49	chr15:30112000-30115200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:30112000-30115200	Active TSS	Brain Inferior Temporal Lobe	brain

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