Variant report

Variant	nsv524708
Chromosome Location	chr15:33357262-33365334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:254)
CpG islands
(count:489)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:33363674-33363871	HepG2	liver:	n/a	n/a
2	CEBPB	chr15:33360849-33361025	HepG2	liver:	n/a	n/a
3	CEBPB	chr15:33360670-33361334	MCF-7	breast:	n/a	n/a
4	CEBPB	chr15:33357108-33357454	IMR90	lung:	n/a	n/a
5	CEBPB	chr15:33360682-33361274	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr15:33360791-33361140	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr15:33360281-33361313	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:33360532-33361302	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr15:33360750-33361298	MCF-7	breast:	n/a	n/a
10	CEBPB	chr15:33360844-33361186	A549	lung:	n/a	n/a
11	CEBPB	chr15:33360683-33361294	A549	lung:	n/a	n/a
12	CEBPB	chr15:33359562-33359958	IMR90	lung:	n/a	n/a
13	CHD2	chr15:33360739-33361294	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr15:33359012-33359019	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr15:33360898-33361178	A549	lung:	n/a	n/a
16	CTCF	chr15:33359500-33359650	BJ	skin:	n/a	n/a
17	CTCF	chr15:33359640-33359790	GM12872	blood:	n/a	n/a
18	CTCF	chr15:33358391-33358422	MCF-7	breast:	n/a	n/a
19	CTCF	chr15:33360060-33360210	AG04449	skin:	n/a	n/a
20	CTCF	chr15:33359460-33359610	AG10803	skin:	n/a	n/a
21	CTCF	chr15:33361420-33361570	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr15:33360460-33360610	AG04449	skin:	n/a	chr15:33360490-33360499
23	CTCF	chr15:33359680-33359830	AG10803	skin:	n/a	n/a
24	CTCF	chr15:33361600-33361750	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr15:33359480-33359630	AG09319	gingival:	n/a	n/a
26	CTCF	chr15:33359480-33359630	AG10803	skin:	n/a	n/a
27	CTCF	chr15:33360080-33360230	AG10803	skin:	n/a	n/a
28	CTCF	chr15:33359920-33360070	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr15:33361480-33361630	A549	lung:	n/a	n/a
30	CTCF	chr15:33359060-33359210	AG04449	skin:	n/a	n/a
31	CTCF	chr15:33359520-33359670	AG09319	gingival:	n/a	n/a
32	E2F4	chr15:33360932-33361152	MCF10A-Er-Src	breast:	n/a	n/a
33	ELF1	chr15:33360043-33361496	MCF-7	breast:	n/a	chr15:33360256-33360267
34	ELF1	chr15:33360134-33360647	HepG2	liver:	n/a	chr15:33360256-33360267
35	ELF1	chr15:33360789-33361423	MCF-7	breast:	n/a	n/a
36	ELF1	chr15:33360085-33360617	HepG2	liver:	n/a	chr15:33360256-33360267
37	ELF1	chr15:33359919-33360750	MCF-7	breast:	n/a	chr15:33360256-33360267
38	EP300	chr15:33359635-33361383	ECC-1	luminal epithelium:	n/a	chr15:33361205-33361212 chr15:33361033-33361043 chr15:33360216-33360226
39	EP300	chr15:33359884-33360582	MCF-7	breast:	n/a	chr15:33360216-33360226
40	EP300	chr15:33357058-33357504	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr15:33359476-33361657	ECC-1	luminal epithelium:	n/a	chr15:33361205-33361212 chr15:33361033-33361043 chr15:33360216-33360226
42	EP300	chr15:33357040-33357445	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr15:33356445-33357545	SK-N-SH	brain:	n/a	n/a
44	EP300	chr15:33359888-33360534	MCF-7	breast:	n/a	chr15:33360216-33360226
45	EP300	chr15:33356968-33357573	SK-N-SH	brain:	n/a	n/a
46	EP300	chr15:33359888-33360502	T-47D	breast:	n/a	chr15:33360216-33360226
47	EP300	chr15:33360950-33361306	SK-N-SH_RA	brain:	n/a	chr15:33361205-33361212 chr15:33361033-33361043
48	EP300	chr15:33360669-33361338	MCF-7	breast:	n/a	chr15:33361205-33361212 chr15:33361033-33361043
49	EP300	chr15:33360689-33361432	MCF-7	breast:	n/a	chr15:33361205-33361212 chr15:33361033-33361043
50	EP300	chr15:33360632-33361373	A549	lung:	n/a	chr15:33361205-33361212 chr15:33361033-33361043

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33360262-33360312	Caco-2	colon:	n/a
2	chr15:33360262-33360312	Caco-2	colon:	n/a
3	chr15:33360195-33360245	A549	lung:	n/a
4	chr15:33360271-33360321	Jurkat	blood:	n/a
5	chr15:33360353-33360403	HMEC	breast:	n/a
6	chr15:33360195-33360245	GM06990	blood:	n/a
7	chr15:33360901-33360951	HRPEpiC	eye:	n/a
8	chr15:33360271-33360321	NT2-D1	testis:	n/a
9	chr15:33360262-33360312	PANC-1	pancreas:	n/a
10	chr15:33360262-33360312	LNCaP	prostate:	n/a
11	chr15:33360271-33360321	HRPEpiC	eye:	n/a
12	chr15:33360353-33360403	AG10803	skin:	n/a
13	chr15:33360353-33360403	PrEC	prostate:	n/a
14	chr15:33360195-33360245	AoSMC	blood vessel:	n/a
15	chr15:33360901-33360951	Jurkat	blood:	n/a
16	chr15:33360271-33360321	Hela-S3	cervix:	n/a
17	chr15:33360262-33360312	HEK293	kidney:	embryo
18	chr15:33360353-33360403	BJ	skin:	n/a
19	chr15:33360195-33360245	AG10803	skin:	n/a
20	chr15:33360485-33360535	Caco-2	colon:	n/a
21	chr15:33359788-33359838	SKMC	muscle:	n/a
22	chr15:33359788-33359838	NHDF-neo	bronchial:	n/a
23	chr15:33360485-33360535	AG09309	skin:	n/a
24	chr15:33360901-33360951	BE2_C	brain:	n/a
25	chr15:33360271-33360321	AG09319	gingival:	n/a
26	chr15:33360485-33360535	HNPCEpiC	eye:	n/a
27	chr15:33360262-33360312	IMR90	lung:	fetal
28	chr15:33359788-33359838	NH-A	brain:	n/a
29	chr15:33360214-33360264	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:33360195-33360245	HRE	kidney:	n/a
31	chr15:33360195-33360245	HCM	heart:	n/a
32	chr15:33359788-33359838	PrEC	prostate:	n/a
33	chr15:33360195-33360245	HAEpiC	amniotic membrane:	n/a
34	chr15:33360195-33360245	HEK293	kidney:	embryo
35	chr15:33360485-33360535	Jurkat	blood:	n/a
36	chr15:33360485-33360535	HEEpiC	esophagus:	n/a
37	chr15:33360262-33360312	HUVEC	blood vessel:	n/a
38	chr15:33360271-33360321	AG10803	skin:	n/a
39	chr15:33360262-33360312	HL-60	blood:	n/a
40	chr15:33360262-33360312	GM12892	blood:	n/a
41	chr15:33360353-33360403	MCF-7	breast:	n/a
42	chr15:33360214-33360264	HRCEpiC	kidney:	n/a
43	chr15:33360262-33360312	GM12878	blood:	n/a
44	chr15:33360485-33360535	HUVEC	blood vessel:	n/a
45	chr15:33360353-33360403	IMR90	lung:	fetal
46	chr15:33360901-33360951	HIPEpiC	eye:	n/a
47	chr15:33360195-33360245	NHBE	bronchial:	n/a
48	chr15:33360271-33360321	HepG2	liver:	n/a
49	chr15:33360271-33360321	BE2_C	brain:	n/a
50	chr15:33360262-33360312	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:33362639..33366197-chr15:33366478..33369547,3	K562	blood:
2	chr15:33317164..33319982-chr15:33363430..33365963,2	MCF-7	breast:
3	chr15:32960265..32963015-chr15:33359103..33361723,2	MCF-7	breast:
4	chr15:33362639..33365167-chr15:33367329..33369547,2	K562	blood:
5	chr15:33360297..33360858-chr2:122288120..122289062,2	Hela-S3	cervix:
6	chr15:33313321..33315541-chr15:33363936..33365487,2	MCF-7	breast:
7	chr15:33360408..33362379-chr15:33362981..33365485,2	MCF-7	breast:
8	chr15:33312296..33313936-chr15:33357129..33359638,2	MCF-7	breast:
9	chr15:33360408..33362379-chr15:33362981..33365485,2	MCF-7	breast:
10	chr15:33298321..33300066-chr15:33361018..33362893,2	MCF-7	breast:
11	chr15:33297830..33309224-chr15:33355310..33362883,25	MCF-7	breast:
12	chr15:33359729..33362501-chr7:80547999..80549877,2	MCF-7	breast:
13	chr15:33314218..33314802-chr15:33358026..33358783,2	MCF-7	breast:
14	chr15:33364817..33369587-chr15:33370489..33373626,4	MCF-7	breast:

No data

Variant related genes	Relation type
FMN1	TF binding region
FMN1	CpG island
ENSG00000075223	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000241818	chromatin interactions
ENSG00000259686	chromatin interactions

Extended variants
information (count: 442 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2306277	chr15:33357262-33357263	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370110054	chr15:33357280-33357281	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532819415	chr15:33357298-33357299	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372655081	chr15:33357302-33357303	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551650639	chr15:33357345-33357346	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs565781401	chr15:33357353-33357354	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150057803	chr15:33357368-33357369	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181068935	chr15:33357417-33357418	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375927761	chr15:33357422-33357423	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184866533	chr15:33357450-33357451	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564835221	chr15:33357463-33357464	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555423381	chr15:33357465-33357466	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs35328525	chr15:33357479-33357480	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373277725	chr15:33357486-33357487	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573591283	chr15:33357494-33357495	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs560229516	chr15:33357496-33357497	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147756568	chr15:33357518-33357519	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73378520	chr15:33357527-33357528	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs140920408	chr15:33357570-33357571	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527593270	chr15:33357578-33357579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563779860	chr15:33357603-33357604	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73378521	chr15:33357607-33357608	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530672270	chr15:33357619-33357620	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550372324	chr15:33357632-33357633	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs189590742	chr15:33357667-33357668	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147933837	chr15:33357676-33357677	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549170651	chr15:33357699-33357700	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10775202	chr15:33357723-33357724	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs10851823	chr15:33357755-33357756	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs532928094	chr15:33357795-33357796	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148947270	chr15:33357818-33357819	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs569730810	chr15:33357819-33357820	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536891819	chr15:33357849-33357850	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181537036	chr15:33357890-33357891	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370802757	chr15:33357919-33357920	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567228209	chr15:33357920-33357921	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143723431	chr15:33357982-33357983	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538696925	chr15:33358018-33358019	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185994103	chr15:33358053-33358054	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs4780074	chr15:33358079-33358080	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs151031686	chr15:33358081-33358082	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536976732	chr15:33358097-33358098	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113641209	chr15:33358108-33358109	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576264576	chr15:33358143-33358144	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369595538	chr15:33358190-33358191	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs191947460	chr15:33358255-33358256	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561437256	chr15:33358265-33358266	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573592264	chr15:33358278-33358279	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540959429	chr15:33358284-33358285	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140958080	chr15:33358286-33358287	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	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
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
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33337000-33358000	Weak transcription	Colonic Mucosa	Colon
2	chr15:33345600-33358200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr15:33348000-33358200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr15:33348200-33360000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:33350400-33358800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:33350400-33358800	Weak transcription	Pancreas	Pancrea
7	chr15:33350600-33358200	Weak transcription	Placenta	Placenta
8	chr15:33355000-33358600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr15:33355400-33360600	Weak transcription	Right Ventricle	heart
10	chr15:33355600-33358600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:33355600-33358800	Weak transcription	Small Intestine	intestine
12	chr15:33355600-33358800	Active TSS	Thymus	Thymus
13	chr15:33355800-33358600	Weak transcription	Gastric	stomach
14	chr15:33356000-33357600	Genic enhancers	HSMM	muscle
15	chr15:33356200-33357400	Enhancers	Fetal Kidney	kidney
16	chr15:33356200-33357400	Enhancers	NHDF-Ad	bronchial
17	chr15:33356400-33357400	Flanking Active TSS	Osteobl	bone
18	chr15:33356400-33357800	Flanking Active TSS	NH-A	brain
19	chr15:33356400-33359200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:33356600-33357400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr15:33356600-33357400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:33356600-33357400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr15:33356600-33357400	Active TSS	Stomach Mucosa	stomach
24	chr15:33356600-33358400	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr15:33356600-33359000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:33356600-33359800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr15:33356800-33357400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:33356800-33357400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:33356800-33357400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:33356800-33357400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:33356800-33357400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr15:33356800-33357400	Enhancers	Esophagus	oesophagus
33	chr15:33356800-33357400	Active TSS	Lung	lung
34	chr15:33356800-33357400	Enhancers	HMEC	breast
35	chr15:33356800-33357600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:33356800-33357600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr15:33356800-33358000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr15:33356800-33358000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:33356800-33358200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr15:33356800-33358400	Weak transcription	Hela-S3	cervix
41	chr15:33356800-33361000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr15:33357000-33357400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr15:33357000-33357400	Active TSS	NHLF	lung
44	chr15:33357000-33357600	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr15:33357000-33358200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr15:33357000-33358200	Weak transcription	HepG2	liver
47	chr15:33357000-33359200	Enhancers	Duodenum Mucosa	Duodenum
48	chr15:33357200-33357400	Flanking Active TSS	HSMMtube	muscle
49	chr15:33357200-33358200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr15:33357200-33358400	Weak transcription	Fetal Thymus	thymus

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