Variant report

Variant	nsv427954
Chromosome Location	chr15:30292944-30458813
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	chr15:30318705-30318959	K562	blood:	n/a	n/a
2	BACH1	chr15:30396041-30396079	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr15:30411972-30412280	GM12878	blood:	n/a	n/a
4	BATF	chr15:30402704-30403029	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
5	BATF	chr15:30412052-30412331	GM12878	blood:	n/a	n/a
6	BATF	chr15:30389801-30390448	GM12878	blood:	n/a	n/a
7	BATF	chr15:30442191-30442458	GM12878	blood:	n/a	n/a
8	BATF	chr15:30402631-30402999	GM12878	blood:	n/a	chr15:30402836-30402847 chr15:30402837-30402847 chr15:30402841-30402851
9	BATF	chr15:30411642-30411805	GM12878	blood:	n/a	n/a
10	BATF	chr15:30428014-30428211	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:30402711-30402962	GM12878	blood:	n/a	chr15:30402839-30402848 chr15:30402794-30402803
12	BCL11A	chr15:30402651-30402946	GM12878	blood:	n/a	chr15:30402839-30402848 chr15:30402794-30402803
13	BCL11A	chr15:30411977-30412278	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:30441259-30441499	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:30390006-30390348	GM12878	blood:	n/a	chr15:30390232-30390245
16	BCL11A	chr15:30389938-30390215	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:30348379-30348447	K562	blood:	n/a	n/a
18	BRCA1	chr15:30333944-30334068	GM12878	blood:	n/a	n/a
19	BRCA1	chr15:30299806-30299977	GM12878	blood:	n/a	n/a
20	CEBPB	chr15:30357445-30357725	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
21	CEBPB	chr15:30343011-30343208	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:30357467-30357767	K562	blood:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
23	CEBPB	chr15:30373008-30373220	A549	lung:	n/a	n/a
24	CEBPB	chr15:30422283-30422484	IMR90	lung:	n/a	chr15:30422424-30422435
25	CEBPB	chr15:30422311-30422460	Hela-S3	cervix:	n/a	chr15:30422424-30422435
26	CEBPB	chr15:30422277-30422508	K562	blood:	n/a	chr15:30422424-30422435
27	CEBPB	chr15:30324857-30325057	HepG2	liver:	n/a	chr15:30324984-30324995
28	CEBPB	chr15:30357423-30357772	H1-hESC	embryonic stem cell:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
29	CEBPB	chr15:30357281-30357870	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
30	CEBPB	chr15:30320812-30320869	A549	lung:	n/a	n/a
31	CEBPB	chr15:30357417-30357754	HepG2	liver:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
32	CEBPB	chr15:30357266-30357793	Hela-S3	cervix:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
33	CEBPB	chr15:30306024-30306117	A549	lung:	n/a	n/a
34	CEBPB	chr15:30422222-30422557	K562	blood:	n/a	chr15:30422424-30422435
35	CEBPB	chr15:30357402-30357757	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
36	CEBPB	chr15:30357425-30357791	IMR90	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
37	CEBPB	chr15:30331155-30331602	Hela-S3	cervix:	n/a	chr15:30331295-30331307
38	CEBPB	chr15:30422311-30422503	A549	lung:	n/a	chr15:30422424-30422435
39	CEBPB	chr15:30422303-30422505	H1-hESC	embryonic stem cell:	n/a	chr15:30422424-30422435
40	CHD1	chr15:30330953-30331153	GM12878	blood:	n/a	n/a
41	CHD1	chr15:30320265-30320466	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr15:30347814-30348022	GM12878	blood:	n/a	n/a
43	CHD1	chr15:30335445-30335601	GM12878	blood:	n/a	n/a
44	CHD2	chr15:30331324-30331787	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr15:30348847-30348886	Lung_OC	lung:	n/a	n/a
46	CTCF	chr15:30367260-30367410	HPF	lung:	n/a	n/a
47	CTCF	chr15:30395806-30395979	GM20000	blood:	n/a	chr15:30395870-30395886
48	CTCF	chr15:30385019-30385025	K562	blood:	n/a	n/a
49	CTCF	chr15:30389968-30390458	K562	blood:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390439-30390457 chr15:30390273-30390289 chr15:30390278-30390287
50	CTCF	chr15:30457010-30457031	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30366335-30366385	GM12878	blood:	n/a
2	chr15:30366335-30366385	HEEpiC	esophagus:	n/a
3	chr15:30366335-30366385	GM12878	blood:	n/a
4	chr15:30366335-30366385	HEEpiC	esophagus:	n/a
5	chr15:30434661-30434711	GM12891	blood:	n/a
6	chr15:30333911-30333961	HAEpiC	amniotic membrane:	n/a
7	chr15:30396121-30396171	NHDF-neo	bronchial:	n/a
8	chr15:30434661-30434711	HepG2	liver:	n/a
9	chr15:30365409-30365459	IMR90	lung:	fetal
10	chr15:30434661-30434711	PFSK-1	brain:	n/a
11	chr15:30434661-30434711	GM12892	blood:	n/a
12	chr15:30336940-30336990	Jurkat	blood:	n/a
13	chr15:30337018-30337068	K562	blood:	n/a
14	chr15:30396500-30396550	GM12878	blood:	n/a
15	chr15:30337018-30337068	HMEC	breast:	n/a
16	chr15:30434661-30434711	BE2_C	brain:	n/a
17	chr15:30366335-30366385	NH-A	brain:	n/a
18	chr15:30333911-30333961	GM12878	blood:	n/a
19	chr15:30336940-30336990	SK-N-SH_RA	brain:	n/a
20	chr15:30333911-30333961	SK-N-SH_RA	brain:	n/a
21	chr15:30333911-30333961	HepG2	liver:	n/a
22	chr15:30435199-30435249	GM19239	blood:	n/a
23	chr15:30336915-30336965	A549	lung:	n/a
24	chr15:30334898-30334948	Jurkat	blood:	n/a
25	chr15:30336940-30336990	Hepatocyte	liver:	n/a
26	chr15:30336915-30336965	ovcar-3	ovarian:	n/a
27	chr15:30336678-30336728	ovcar-3	ovarian:	n/a
28	chr15:30366335-30366385	NB4	blood:	n/a
29	chr15:30336915-30336965	HCF	heart:	n/a
30	chr15:30337875-30337925	K562	blood:	n/a
31	chr15:30336940-30336990	AG10803	skin:	n/a
32	chr15:30337366-30337416	RPTEC	kidney:	n/a
33	chr15:30336940-30336990	GM19239	blood:	n/a
34	chr15:30333911-30333961	HRE	kidney:	n/a
35	chr15:30336915-30336965	HRCEpiC	kidney:	n/a
36	chr15:30396500-30396550	Hela-S3	cervix:	n/a
37	chr15:30396500-30396550	BJ	skin:	n/a
38	chr15:30396500-30396550	NB4	blood:	n/a
39	chr15:30336915-30336965	NT2-D1	testis:	n/a
40	chr15:30366335-30366385	MCF-7	breast:	n/a
41	chr15:30334898-30334948	NT2-D1	testis:	n/a
42	chr15:30434661-30434711	HUVEC	blood vessel:	n/a
43	chr15:30434661-30434711	GM19239	blood:	n/a
44	chr15:30333911-30333961	T-47D	breast:	n/a
45	chr15:30337366-30337416	ovcar-3	ovarian:	n/a
46	chr15:30336915-30336965	BE2_C	brain:	n/a
47	chr15:30339875-30339925	AG09309	skin:	n/a
48	chr15:30435199-30435249	HEEpiC	esophagus:	n/a
49	chr15:30396500-30396550	ECC-1	luminal epithelium:	n/a
50	chr15:30334898-30334948	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:29959926..29960944-chr15:30367131..30368208,4	K562	blood:
2	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
3	chr15:30234111..30234981-chr15:30322295..30322806,2	MCF-7	breast:
4	chr15:30232675..30233456-chr15:30322159..30323009,2	MCF-7	breast:
5	chr15:30039724..30040629-chr15:30367249..30368123,2	K562	blood:
6	chr15:30233133..30233805-chr15:30367233..30367920,2	MCF-7	breast:
7	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
8	chr15:30234442..30235027-chr15:30335180..30335724,2	MCF-7	breast:
9	chr15:29960081..29960738-chr15:30322588..30323155,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP1-1	chr15:30297646-30297992	ENSG00000259647.1
2	lnc-TJP1-1	chr15:30337914-30338051	ENSG00000259647.1
3	lnc-AC120045.3-4	chr15:30383854-30384132	NONHSAT041327
4	lnc-AC120045.3-2	chr15:30435925-30436203	NONHSAT041332

Variant related genes	Relation type
ENSG00000259647	TF binding region
ULK4P3	TF binding region
RN7SL469P	TF binding region
ENSG00000221785	TF binding region
ENSG00000261747	TF binding region
ENSG00000221250	TF binding region
ENSG00000207432	TF binding region
ENSG00000259749	TF binding region
RN7SL673P	TF binding region
GOLGA8T	TF binding region
DNM1P30	TF binding region
ENSG00000229389	TF binding region
GOLGA8J	TF binding region
DNM1P28	TF binding region
ENSG00000260174	TF binding region
ENSG00000259647	CpG island
ULK4P3	CpG island
RN7SL469P	CpG island
ENSG00000221785	CpG island
ENSG00000261747	CpG island
ENSG00000221250	CpG island
ENSG00000207432	CpG island
ENSG00000259749	CpG island
RN7SL673P	CpG island
GOLGA8T	CpG island
DNM1P30	CpG island
ENSG00000229389	CpG island
GOLGA8J	CpG island
DNM1P28	CpG island
ENSG00000260174	CpG island

Extended variants
information (count: 2737 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:2737 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74542312	chr15:30292954-30292955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576786211	chr15:30292985-30292986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545749224	chr15:30293002-30293003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559070837	chr15:30293105-30293106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528431874	chr15:30293110-30293111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528869620	chr15:30293125-30293126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561552861	chr15:30293206-30293207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181820707	chr15:30293217-30293218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201435778	chr15:30293297-30293298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139117347	chr15:30293312-30293313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570236499	chr15:30293318-30293319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72521250	chr15:30293319-30293320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs67726956	chr15:30293320-30293321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7403398	chr15:30293321-30293322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553620169	chr15:30293326-30293327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7403400	chr15:30293328-30293329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs67832672	chr15:30293331-30293332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549882503	chr15:30293363-30293364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562519582	chr15:30293386-30293387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112520392	chr15:30293387-30293388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185410725	chr15:30293397-30293398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190607294	chr15:30293402-30293403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551570594	chr15:30293484-30293485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535383517	chr15:30293536-30293537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147909543	chr15:30293570-30293571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575091297	chr15:30293618-30293619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71416447	chr15:30293630-30293631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537614839	chr15:30293705-30293706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140479864	chr15:30293709-30293710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560473307	chr15:30293730-30293731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545575970	chr15:30293771-30293772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4374114	chr15:30293789-30293790	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150149296	chr15:30293855-30293856	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs181411219	chr15:30293863-30293864	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs561617803	chr15:30293864-30293865	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563555052	chr15:30293910-30293911	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs369737561	chr15:30293977-30293978	Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550784379	chr15:30294052-30294053	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs564102204	chr15:30294055-30294056	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186322154	chr15:30294136-30294137	Bivalent Enhancer Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs77096950	chr15:30294235-30294236	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs79239832	chr15:30294278-30294279	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs537808657	chr15:30294358-30294359	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs534972784	chr15:30294400-30294401	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs548921384	chr15:30294483-30294484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138576991	chr15:30294505-30294506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537725902	chr15:30294511-30294512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557560440	chr15:30294538-30294539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76177214	chr15:30294552-30294553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539527998	chr15:30294636-30294637	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

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
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
idiopathic generalized epilepsy	19843651	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
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

Chromatin state (count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30281400-30293600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr15:30283600-30293000	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:30286600-30293200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:30290200-30293800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr15:30292600-30294200	Enhancers	Brain Anterior Caudate	brain
6	chr15:30292600-30298000	Enhancers	Brain Substantia Nigra	brain
7	chr15:30293000-30295800	Enhancers	Brain Hippocampus Middle	brain
8	chr15:30293200-30293400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr15:30293400-30294000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr15:30293400-30294800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:30293600-30294600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:30293600-30294800	Enhancers	Brain Cingulate Gyrus	brain
13	chr15:30293600-30295000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr15:30293800-30294000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:30293800-30294200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr15:30293800-30294800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr15:30293800-30294800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr15:30294000-30294200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr15:30294200-30294400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:30294200-30294400	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr15:30294200-30294600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr15:30294200-30294800	Enhancers	Brain Angular Gyrus	brain
23	chr15:30294400-30294800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr15:30294400-30294800	Enhancers	Brain Anterior Caudate	brain
25	chr15:30294800-30295200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:30294800-30296000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:30294800-30296800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:30294800-30297000	Weak transcription	Brain Anterior Caudate	brain
29	chr15:30294800-30297000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr15:30295000-30297000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr15:30295200-30295600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr15:30295800-30297000	Weak transcription	Brain Hippocampus Middle	brain
33	chr15:30296000-30296200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:30296200-30296600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:30296600-30297200	Enhancers	Fetal Lung	lung
36	chr15:30296600-30298000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:30296800-30298000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr15:30297000-30298000	Enhancers	Brain Anterior Caudate	brain
39	chr15:30297000-30298000	Enhancers	Brain Cingulate Gyrus	brain
40	chr15:30297000-30298000	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr15:30297000-30298400	Enhancers	Brain Hippocampus Middle	brain
42	chr15:30298000-30299200	Weak transcription	Brain Substantia Nigra	brain
43	chr15:30298000-30300600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:30298400-30299400	Weak transcription	Brain Hippocampus Middle	brain
45	chr15:30299200-30299400	Enhancers	Brain Substantia Nigra	brain
46	chr15:30299400-30299600	Enhancers	Brain Hippocampus Middle	brain
47	chr15:30300000-30300400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr15:30300400-30300800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr15:30300400-30301000	Enhancers	HSMM	muscle
50	chr15:30300800-30301400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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