Variant report

Variant	esv1821068
Chromosome Location	chr15:30372282-30685516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:30396041-30396079	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr15:30402704-30403029	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
3	BATF	chr15:30412052-30412331	GM12878	blood:	n/a	n/a
4	BATF	chr15:30411642-30411805	GM12878	blood:	n/a	n/a
5	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
6	BATF	chr15:30389801-30390448	GM12878	blood:	n/a	n/a
7	BATF	chr15:30428014-30428211	GM12878	blood:	n/a	n/a
8	BATF	chr15:30458984-30459268	GM12878	blood:	n/a	n/a
9	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
10	BATF	chr15:30626371-30626674	GM12878	blood:	n/a	chr15:30626595-30626606
11	BATF	chr15:30442191-30442458	GM12878	blood:	n/a	n/a
12	BATF	chr15:30411972-30412280	GM12878	blood:	n/a	n/a
13	BATF	chr15:30402631-30402999	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
14	BATF	chr15:30459001-30459247	GM12878	blood:	n/a	n/a
15	BATF	chr15:30626382-30626790	GM12878	blood:	n/a	chr15:30626595-30626606
16	BCL11A	chr15:30411977-30412278	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:30626396-30626697	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:30469390-30469696	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:30402651-30402946	GM12878	blood:	n/a	chr15:30402839-30402848 chr15:30402794-30402803
20	BCL11A	chr15:30402711-30402962	GM12878	blood:	n/a	chr15:30402839-30402848 chr15:30402794-30402803
21	BCL11A	chr15:30626461-30626686	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:30678714-30679009	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
23	BCL11A	chr15:30678698-30678949	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
24	BCL11A	chr15:30389938-30390215	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:30441259-30441499	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:30390006-30390348	GM12878	blood:	n/a	chr15:30390232-30390245
27	BCL11A	chr15:30465220-30465511	GM12878	blood:	n/a	n/a
28	BCL3	chr15:30668118-30668389	GM12878	blood:	n/a	n/a
29	BCL3	chr15:30668077-30668421	GM12878	blood:	n/a	n/a
30	CEBPB	chr15:30422222-30422557	K562	blood:	n/a	chr15:30422424-30422435
31	CEBPB	chr15:30422283-30422484	IMR90	lung:	n/a	chr15:30422424-30422435
32	CEBPB	chr15:30422277-30422508	K562	blood:	n/a	chr15:30422424-30422435
33	CEBPB	chr15:30422303-30422505	H1-hESC	embryonic stem cell:	n/a	chr15:30422424-30422435
34	CEBPB	chr15:30422311-30422460	Hela-S3	cervix:	n/a	chr15:30422424-30422435
35	CEBPB	chr15:30373008-30373220	A549	lung:	n/a	n/a
36	CEBPB	chr15:30488906-30489076	IMR90	lung:	n/a	n/a
37	CEBPB	chr15:30422311-30422503	A549	lung:	n/a	chr15:30422424-30422435
38	CHD2	chr15:30465233-30465388	GM12878	blood:	n/a	n/a
39	CHD2	chr15:30618331-30618661	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:30506070-30506210	MCF-7	breast:	n/a	chr15:30506141-30506162 chr15:30506139-30506157
41	CTCF	chr15:30442146-30442260	GM12891	blood:	n/a	n/a
42	CTCF	chr15:30384987-30385071	Medullo	brain:	n/a	n/a
43	CTCF	chr15:30662267-30662405	K562	blood:	n/a	chr15:30662337-30662358 chr15:30662335-30662353
44	CTCF	chr15:30465340-30465490	GM12870	blood:	n/a	n/a
45	CTCF	chr15:30516226-30516273	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr15:30395920-30396070	AG04449	skin:	n/a	chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
47	CTCF	chr15:30396000-30396150	HCM	heart:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
48	CTCF	chr15:30457010-30457031	GM19239	blood:	n/a	n/a
49	CTCF	chr15:30465608-30465864	GM19240	blood:	n/a	chr15:30465736-30465754 chr15:30465731-30465752 chr15:30465730-30465737 chr15:30465737-30465753 chr15:30465738-30465751
50	CTCF	chr15:30602571-30602595	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30516422-30516472	SK-N-SH	brain:	n/a
2	chr15:30516422-30516472	SK-N-SH	brain:	n/a
3	chr15:30666736-30666786	A549	lung:	n/a
4	chr15:30654880-30654930	T-47D	breast:	n/a
5	chr15:30517601-30517651	HNPCEpiC	eye:	n/a
6	chr15:30517601-30517651	HEEpiC	esophagus:	n/a
7	chr15:30685198-30685248	AG04450	lung:	fetal
8	chr15:30666736-30666786	NH-A	brain:	n/a
9	chr15:30483519-30483569	Jurkat	blood:	n/a
10	chr15:30487914-30487964	Hepatocyte	liver:	n/a
11	chr15:30487914-30487964	AG04449	skin:	fetal
12	chr15:30516422-30516472	SK-N-SH_RA	brain:	n/a
13	chr15:30484753-30484803	Hela-S3	cervix:	n/a
14	chr15:30515844-30515894	GM06990	blood:	n/a
15	chr15:30486767-30486817	U87	brain:	n/a
16	chr15:30520018-30520068	SK-N-SH_RA	brain:	n/a
17	chr15:30435199-30435249	HRE	kidney:	n/a
18	chr15:30677804-30677854	HMEC	breast:	n/a
19	chr15:30677804-30677854	MCF10A-Er-Src	breast:	n/a
20	chr15:30677804-30677854	PFSK-1	brain:	n/a
21	chr15:30520018-30520068	NHBE	bronchial:	n/a
22	chr15:30515162-30515212	PrEC	prostate:	n/a
23	chr15:30396121-30396171	RPTEC	kidney:	n/a
24	chr15:30487914-30487964	AoSMC	blood vessel:	n/a
25	chr15:30516906-30516956	PANC-1	pancreas:	n/a
26	chr15:30666736-30666786	T-47D	breast:	n/a
27	chr15:30484033-30484083	HEEpiC	esophagus:	n/a
28	chr15:30487914-30487964	HEK293	kidney:	embryo
29	chr15:30515162-30515212	GM06990	blood:	n/a
30	chr15:30435199-30435249	Caco-2	colon:	n/a
31	chr15:30396121-30396171	AG09319	gingival:	n/a
32	chr15:30434661-30434711	HCT-116	colon:	n/a
33	chr15:30484033-30484083	MCF10A-Er-Src	breast:	n/a
34	chr15:30489014-30489064	CMK	blood:	n/a
35	chr15:30434661-30434711	BE2_C	brain:	n/a
36	chr15:30484033-30484083	HUVEC	blood vessel:	n/a
37	chr15:30396500-30396550	GM12892	blood:	n/a
38	chr15:30517601-30517651	NH-A	brain:	n/a
39	chr15:30520018-30520068	HCF	heart:	n/a
40	chr15:30517601-30517651	MCF10A-Er-Src	breast:	n/a
41	chr15:30654880-30654930	HCPEpiC	choroid plexus:	n/a
42	chr15:30515844-30515894	MCF-7	breast:	n/a
43	chr15:30654880-30654930	HCF	heart:	n/a
44	chr15:30520018-30520068	MCF-7	breast:	n/a
45	chr15:30486767-30486817	PrEC	prostate:	n/a
46	chr15:30517589-30517639	RPTEC	kidney:	n/a
47	chr15:30517601-30517651	GM12892	blood:	n/a
48	chr15:30483519-30483569	HRCEpiC	kidney:	n/a
49	chr15:30486767-30486817	HMEC	breast:	n/a
50	chr15:30484753-30484803	ECC-1	luminal epithelium:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.3
2	lnc-CHRFAM7A-2	chr15:30649969-30650976	ENSG00000270173.1
3	lnc-CHRFAM7A-1	chr15:30462766-30462831	ENSG00000259906.1
4	lnc-RP5-1086D14.3.1-1	chr15:30502611-30503009	ENSG00000225930.2
5	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.2
6	lnc-RP11-382B18.2.1-2	chr15:30672556-30672602	NONHSAT041347
7	lnc-CHRFAM7A-1	chr15:30462912-30462975	ENSG00000259906.1
8	lnc-AC120045.3-2	chr15:30435925-30436203	NONHSAT041332
9	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.3
10	lnc-RP5-1086D14.3.1-1	chr15:30502620-30506743	ENSG00000225930.3
11	lnc-RP11-382B18.2.1-2	chr15:30673906-30674079	NONHSAT041347
12	lnc-RP11-382B18.2.1-2	chr15:30679066-30679190	NONHSAT041348
13	lnc-AC120045.3-4	chr15:30383854-30384132	NONHSAT041327
14	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.2
15	lnc-RP11-382B18.2.1-2	chr15:30679087-30679190	NONHSAT041347
16	lnc-RP11-382B18.2.1-2	chr15:30675247-30675585	NONHSAT041348
17	lnc-CHRFAM7A-1	chr15:30471212-30471332	ENSG00000259906.1
18	lnc-RP5-1086D14.3.1-1	chr15:30502620-30504471	ENSG00000225930.2
19	lnc-CHRFAM7A-1	chr15:30471079-30472146	ENSG00000259906.1
20	lnc-RP11-382B18.2.1-2	chr15:30675522-30675585	NONHSAT041347

Variant related genes	Relation type
ULK4P3	TF binding region
RNU6-17P	TF binding region
RN7SL469P	TF binding region
ENSG00000238519	TF binding region
ENSG00000238783	TF binding region
ENSG00000263070	TF binding region
ENSG00000225930	TF binding region
ENSG00000270173	TF binding region
ENSG00000221785	TF binding region
CHRFAM7A	TF binding region
ENSG00000261747	TF binding region
ENSG00000221250	TF binding region
ENSG00000207432	TF binding region
RN7SL673P	TF binding region
GOLGA8T	TF binding region
DNM1P30	TF binding region
ENSG00000259906	TF binding region
GOLGA8J	TF binding region
DNM1P28	TF binding region
ENSG00000270955	TF binding region
ENSG00000259993	TF binding region
ULK4P3	CpG island
RNU6-17P	CpG island
RN7SL469P	CpG island
ENSG00000238519	CpG island
ENSG00000238783	CpG island
ENSG00000263070	CpG island
ENSG00000225930	CpG island
ENSG00000270173	CpG island
ENSG00000221785	CpG island
CHRFAM7A	CpG island
ENSG00000261747	CpG island
ENSG00000221250	CpG island
ENSG00000207432	CpG island
RN7SL673P	CpG island
GOLGA8T	CpG island
DNM1P30	CpG island
ENSG00000259906	CpG island
GOLGA8J	CpG island
DNM1P28	CpG island
ENSG00000270955	CpG island
ENSG00000259993	CpG island

Extended variants
information (count: 1050 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546410665	chr15:30372282-30372283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566294558	chr15:30372313-30372314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150609807	chr15:30372319-30372320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528570716	chr15:30372357-30372358	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs548344830	chr15:30372364-30372365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs568486949	chr15:30372413-30372414	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs202085516	chr15:30372426-30372427	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs537037807	chr15:30372438-30372439	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs4275831	chr15:30372459-30372460	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199975592	chr15:30372463-30372464	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs4448915	chr15:30372466-30372467	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs7176620	chr15:30372473-30372474	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573427971	chr15:30372475-30372476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs9708145	chr15:30372480-30372481	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs7177988	chr15:30372495-30372496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544898267	chr15:30372502-30372503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200341648	chr15:30372505-30372506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12592895	chr15:30372512-30372513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146760384	chr15:30372517-30372518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372260511	chr15:30372555-30372556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572066160	chr15:30372556-30372557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74011040	chr15:30372571-30372572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs74011041	chr15:30372573-30372574	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs192147507	chr15:30372606-30372607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529048556	chr15:30372612-30372613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201720145	chr15:30372618-30372619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71397299	chr15:30372653-30372654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140663819	chr15:30372697-30372698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531009005	chr15:30372721-30372722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550717693	chr15:30372726-30372727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570822494	chr15:30372727-30372728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150115085	chr15:30372738-30372739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185077074	chr15:30372751-30372752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4587953	chr15:30372763-30372764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35731182	chr15:30372822-30372823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372624113	chr15:30372834-30372835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555466597	chr15:30372838-30372839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112770904	chr15:30372862-30372863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34132155	chr15:30372876-30372877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs34121900	chr15:30372882-30372883	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs147084802	chr15:30372921-30372922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540180260	chr15:30372942-30372943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560004251	chr15:30372947-30372948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573530835	chr15:30372959-30372960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533527486	chr15:30372962-30372963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542480738	chr15:30372974-30372975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200413394	chr15:30372975-30372976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192356804	chr15:30373032-30373033	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530920917	chr15:30373047-30373048	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs551005884	chr15:30373055-30373056	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
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
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
idiopathic generalized epilepsy	19843651	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	20502679	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30367600-30372600	Weak transcription	HSMM	muscle
2	chr15:30372600-30372800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr15:30372600-30373000	Enhancers	HSMM	muscle
4	chr15:30372600-30373600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr15:30372800-30373400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:30372800-30373600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr15:30373200-30373400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:30373200-30373400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:30373200-30373400	Enhancers	HSMMtube	muscle
10	chr15:30373200-30373400	Enhancers	Osteobl	bone
11	chr15:30395800-30396000	Active TSS	HMEC	breast
12	chr15:30395800-30396200	Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr15:30395800-30396200	Active TSS	Primary B cells from peripheral blood	blood
14	chr15:30395800-30396200	Active TSS	Colonic Mucosa	Colon
15	chr15:30395800-30396200	Active TSS	Gastric	stomach
16	chr15:30395800-30396400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:30395800-30396400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr15:30395800-30396400	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr15:30395800-30396400	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr15:30395800-30396400	Active TSS	Muscle Satellite Cultured Cells	--
21	chr15:30395800-30396400	Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr15:30395800-30396400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:30395800-30396400	Active TSS	Adipose Nuclei	Adipose
26	chr15:30395800-30396400	Active TSS	Esophagus	oesophagus
27	chr15:30395800-30396400	Active TSS	Fetal Brain Female	brain
28	chr15:30395800-30396400	Bivalent/Poised TSS	Fetal Stomach	stomach
29	chr15:30395800-30396400	Active TSS	Left Ventricle	heart
30	chr15:30395800-30396400	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr15:30395800-30396400	Active TSS	Right Atrium	heart
32	chr15:30395800-30396400	Active TSS	Right Ventricle	heart
33	chr15:30395800-30396400	Active TSS	Thymus	Thymus
34	chr15:30395800-30396400	Active TSS	Spleen	Spleen
35	chr15:30395800-30396400	Active TSS	HepG2	liver
36	chr15:30395800-30396400	Active TSS	Monocytes-CD14+_RO01746	blood
37	chr15:30395800-30396600	Active TSS	H1 Cell Line	embryonic stem cell
38	chr15:30395800-30396600	Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr15:30395800-30396600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:30395800-30396600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:30395800-30396600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr15:30395800-30396600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:30395800-30396600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr15:30395800-30396600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:30395800-30396600	Active TSS	Pancreas	Pancrea
48	chr15:30395800-30396600	Active TSS	HUVEC	blood vessel
49	chr15:30395800-30396800	Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr15:30395800-30396800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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