Variant report

Variant	nsv827275
Chromosome Location	chr15:30110266-30115636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:691)
CpG islands
(count:855)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:691 , 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	chr15:30115339-30115686	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:30110302-30110578	K562	blood:	n/a	n/a
3	ARID3A	chr15:30113508-30113944	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:30113516-30113887	K562	blood:	n/a	n/a
5	ATF1	chr15:30113535-30113894	K562	blood:	n/a	n/a
6	ATF2	chr15:30113515-30113947	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:30113491-30113996	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr15:30113464-30113906	K562	blood:	n/a	n/a
9	ATF3	chr15:30113629-30113845	K562	blood:	n/a	n/a
10	BACH1	chr15:30112449-30113905	K562	blood:	n/a	n/a
11	BACH1	chr15:30113488-30115592	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr15:30113602-30113834	GM12878	blood:	n/a	n/a
13	BCL3	chr15:30114340-30115772	A549	lung:	n/a	n/a
14	BHLHE40	chr15:30113612-30115724	HepG2	liver:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
15	BHLHE40	chr15:30113347-30115139	K562	blood:	n/a	chr15:30114178-30114194 chr15:30113787-30113803 chr15:30113928-30113944
16	BRCA1	chr15:30114219-30114626	HepG2	liver:	n/a	n/a
17	BRCA1	chr15:30114822-30115569	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr15:30115035-30115474	HepG2	liver:	n/a	n/a
19	CCNT2	chr15:30113637-30115356	K562	blood:	n/a	n/a
20	CEBPB	chr15:30115046-30115390	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:30113501-30113992	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:30113604-30113855	K562	blood:	n/a	n/a
23	CEBPB	chr15:30114998-30115334	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr15:30114343-30114592	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:30113613-30113914	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:30113583-30113985	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr15:30113558-30113878	K562	blood:	n/a	n/a
28	CEBPD	chr15:30113554-30113972	K562	blood:	n/a	n/a
29	CEBPD	chr15:30114463-30114737	HepG2	liver:	n/a	n/a
30	CEBPD	chr15:30113483-30114006	K562	blood:	n/a	n/a
31	CHD1	chr15:30111618-30116068	IMR90	lung:	n/a	n/a
32	CHD1	chr15:30111661-30114675	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr15:30114126-30115069	K562	blood:	n/a	n/a
34	CHD2	chr15:30114199-30115126	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr15:30113207-30113949	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr15:30113537-30113897	HepG2	liver:	n/a	n/a
37	CHD2	chr15:30113529-30115182	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr15:30114207-30115738	HepG2	liver:	n/a	n/a
39	CREB1	chr15:30114105-30115392	A549	lung:	n/a	n/a
40	CREB1	chr15:30113501-30113970	A549	lung:	n/a	n/a
41	CREB1	chr15:30114082-30115601	HepG2	liver:	n/a	n/a
42	CREB1	chr15:30114474-30114737	A549	lung:	n/a	n/a
43	CREB1	chr15:30113591-30114010	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr15:30113579-30113957	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr15:30114913-30115349	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr15:30113701-30113931	MCF-7	breast:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
47	CTCF	chr15:30113740-30113890	AG04449	skin:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
48	CTCF	chr15:30113705-30113872	MCF-7	breast:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
49	CTCF	chr15:30113680-30113830	A549	lung:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815
50	CTCF	chr15:30113680-30113830	HepG2	liver:	n/a	chr15:30113803-30113816 chr15:30113800-30113813 chr15:30113797-30113815

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30114651-30114701	AG09309	skin:	n/a
2	chr15:30114651-30114701	AG09309	skin:	n/a
3	chr15:30110856-30110906	AG04449	skin:	fetal
4	chr15:30115147-30115197	NB4	blood:	n/a
5	chr15:30110856-30110906	HCPEpiC	choroid plexus:	n/a
6	chr15:30114295-30114345	IMR90	lung:	fetal
7	chr15:30114912-30114962	NHDF-neo	bronchial:	n/a
8	chr15:30110856-30110906	GM12891	blood:	n/a
9	chr15:30113651-30113701	HRPEpiC	eye:	n/a
10	chr15:30110856-30110906	NH-A	brain:	n/a
11	chr15:30114912-30114962	AG09309	skin:	n/a
12	chr15:30113651-30113701	H1-hESC	embryonic stem cell:	embryo
13	chr15:30113723-30113773	H1-hESC	embryonic stem cell:	embryo
14	chr15:30113651-30113701	HCM	heart:	n/a
15	chr15:30114651-30114701	HL-60	blood:	n/a
16	chr15:30114912-30114962	GM06990	blood:	n/a
17	chr15:30114651-30114701	AoSMC	blood vessel:	n/a
18	chr15:30114814-30114864	H1-hESC	embryonic stem cell:	embryo
19	chr15:30114651-30114701	GM06990	blood:	n/a
20	chr15:30114651-30114701	HCT-116	colon:	n/a
21	chr15:30113651-30113701	NHDF-neo	bronchial:	n/a
22	chr15:30113723-30113773	HEK293	kidney:	embryo
23	chr15:30114295-30114345	SAEC	small airway:	n/a
24	chr15:30113723-30113773	LNCaP	prostate:	n/a
25	chr15:30114295-30114345	BE2_C	brain:	n/a
26	chr15:30114816-30114866	GM12891	blood:	n/a
27	chr15:30114816-30114866	IMR90	lung:	fetal
28	chr15:30114871-30114921	HepG2	liver:	n/a
29	chr15:30110856-30110906	GM12878	blood:	n/a
30	chr15:30114814-30114864	PFSK-1	brain:	n/a
31	chr15:30113831-30113881	CMK	blood:	n/a
32	chr15:30113651-30113701	HL-60	blood:	n/a
33	chr15:30115147-30115197	HIPEpiC	eye:	n/a
34	chr15:30115147-30115197	NT2-D1	testis:	n/a
35	chr15:30114651-30114701	A549	lung:	n/a
36	chr15:30114814-30114864	PrEC	prostate:	n/a
37	chr15:30114871-30114921	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:30114816-30114866	AG09319	gingival:	n/a
39	chr15:30113723-30113773	ProgFib	skin:	n/a
40	chr15:30115149-30115199	MCF10A-Er-Src	breast:	n/a
41	chr15:30113723-30113773	RPTEC	kidney:	n/a
42	chr15:30114871-30114921	HUVEC	blood vessel:	n/a
43	chr15:30110856-30110906	CMK	blood:	n/a
44	chr15:30114814-30114864	HCT-116	colon:	n/a
45	chr15:30113651-30113701	AG10803	skin:	n/a
46	chr15:30114816-30114866	PFSK-1	brain:	n/a
47	chr15:30115299-30115349	PFSK-1	brain:	n/a
48	chr15:30115147-30115197	U87	brain:	n/a
49	chr15:30114912-30114962	ProgFib	skin:	n/a
50	chr15:30114295-30114345	HMEC	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30104335..30106670-chr15:30108797..30110344,3	MCF-7	breast:
2	chr15:30051900..30054307-chr15:30111477..30113324,2	K562	blood:
3	chr15:30113418..30114284-chr5:10249625..10250242,2	Hela-S3	cervix:
4	chr12:57913766..57914507-chr15:30113406..30114143,2	Hela-S3	cervix:
5	chr15:30110373..30112075-chr15:30112692..30115321,2	MCF-7	breast:
6	chr15:30114363..30114879-chr5:162931957..162932799,2	Hela-S3	cervix:
7	chr15:30033909..30035507-chr15:30113047..30114881,2	MCF-7	breast:
8	chr15:30114291..30114811-chr19:3762538..3763244,2	HCT-116	colon:
9	chr15:30115117..30117286-chr15:30127029..30129725,2	K562	blood:
10	chr12:6862162..6862757-chr15:30114314..30115083,2	HCT-116	colon:
11	chr15:30111283..30113750-chr22:19879705..19881456,2	K562	blood:
12	chr15:30113789..30114693-chr6:31795054..31795835,2	Hela-S3	cervix:
13	chr15:30104918..30110272-chr15:30111258..30116596,7	MCF-7	breast:
14	chr1:52521763..52522611-chr15:30114227..30114914,2	Hela-S3	cervix:
15	chr15:30113746..30114342-chr16:31191095..31191723,2	Hela-S3	cervix:
16	chr15:30114003..30114757-chr17:34900104..34900989,2	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
ENSG00000150756	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000183617	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000117862	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000089693	chromatin interactions
ENSG00000104067	chromatin interactions
ENSG00000038274	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000134717	chromatin interactions
ENSG00000259523	chromatin interactions
ENSG00000005955	chromatin interactions

Extended variants
information (count: 203 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:203 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536295759	chr15:30110296-30110297	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs534499853	chr15:30110325-30110326	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552596723	chr15:30110404-30110405	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371432452	chr15:30110405-30110406	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200215490	chr15:30110425-30110426	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536712047	chr15:30110432-30110433	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554248854	chr15:30110488-30110489	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556711977	chr15:30110538-30110539	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192984982	chr15:30110541-30110542	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576239488	chr15:30110547-30110548	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs539066029	chr15:30110558-30110559	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559278364	chr15:30110593-30110594	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571226135	chr15:30110602-30110603	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572739536	chr15:30110643-30110644	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145817052	chr15:30110644-30110645	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs118092617	chr15:30110665-30110666	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531800399	chr15:30110668-30110669	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538319031	chr15:30110679-30110680	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs185273481	chr15:30110691-30110692	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141738498	chr15:30110694-30110695	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531959058	chr15:30110701-30110702	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551786679	chr15:30110709-30110710	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369015243	chr15:30110724-30110725	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528431450	chr15:30110746-30110747	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113800651	chr15:30110771-30110772	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs8032316	chr15:30110776-30110777	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs568214084	chr15:30110777-30110778	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556692971	chr15:30110872-30110873	Enhancers Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs543559082	chr15:30110874-30110875	Enhancers Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs143424887	chr15:30110891-30110892	Enhancers Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11312672	chr15:30110892-30110893	Enhancers Weak transcription Strong transcription Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs190510539	chr15:30110926-30110927	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567049669	chr15:30110996-30110997	Enhancers Weak transcription Strong transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115535408	chr15:30111042-30111043	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550279461	chr15:30111051-30111052	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs147740369	chr15:30111057-30111058	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541216838	chr15:30111059-30111060	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs8023974	chr15:30111078-30111079	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs559040734	chr15:30111084-30111085	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs529923505	chr15:30111107-30111108	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs182332536	chr15:30111109-30111110	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554977650	chr15:30111131-30111132	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574948000	chr15:30111167-30111168	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142367390	chr15:30111177-30111178	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs563026729	chr15:30111182-30111183	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563497497	chr15:30111207-30111208	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374392583	chr15:30111234-30111235	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576567402	chr15:30111265-30111266	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs186131885	chr15:30111297-30111298	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559252387	chr15:30111301-30111302	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 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:568 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30082400-30113600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:30092600-30111400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr15:30098000-30111600	Weak transcription	Fetal Muscle Leg	muscle
4	chr15:30098000-30112400	Weak transcription	Fetal Stomach	stomach
5	chr15:30098400-30111600	Weak transcription	HSMMtube	muscle
6	chr15:30105200-30111800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:30105600-30112000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:30106200-30112000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr15:30106200-30112200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr15:30106400-30111600	Weak transcription	HSMM	muscle
11	chr15:30106600-30110400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:30106800-30112200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr15:30107200-30112600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr15:30108000-30111600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:30108000-30111600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:30108000-30111600	Weak transcription	Hela-S3	cervix
17	chr15:30108200-30111400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr15:30108200-30111400	Weak transcription	NHLF	lung
19	chr15:30108200-30111600	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr15:30108200-30111800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr15:30108200-30111800	Weak transcription	HMEC	breast
22	chr15:30108200-30112000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:30108200-30112000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr15:30108200-30113000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr15:30108400-30110400	Weak transcription	Fetal Kidney	kidney
26	chr15:30108400-30110600	Weak transcription	Right Ventricle	heart
27	chr15:30108400-30111000	Weak transcription	Brain Substantia Nigra	brain
28	chr15:30108400-30111400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr15:30108400-30111600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:30108400-30111600	Weak transcription	Adipose Nuclei	Adipose
31	chr15:30108400-30111600	Weak transcription	Osteobl	bone
32	chr15:30108400-30111800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:30108400-30111800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:30108400-30111800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:30108400-30111800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr15:30108400-30112200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr15:30108400-30112400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr15:30108400-30112800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr15:30108400-30113000	Weak transcription	Esophagus	oesophagus
40	chr15:30108600-30110400	Weak transcription	Right Atrium	heart
41	chr15:30108600-30110600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr15:30108600-30110800	Weak transcription	Left Ventricle	heart
43	chr15:30108600-30111000	Weak transcription	Lung	lung
44	chr15:30108600-30111200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:30108600-30111600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:30108600-30111600	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr15:30108600-30111600	Weak transcription	Psoas Muscle	Psoas
48	chr15:30108600-30111600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr15:30108600-30111800	Weak transcription	Aorta	Aorta
50	chr15:30108600-30111800	Weak transcription	Fetal Intestine Small	intestine

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