Variant report

Variant	nsv974543
Chromosome Location	chr15:30327423-30336196
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	BRCA1	chr15:30333944-30334068	GM12878	blood:	n/a	n/a
2	CEBPB	chr15:30331155-30331602	Hela-S3	cervix:	n/a	chr15:30331295-30331307
3	CHD1	chr15:30335445-30335601	GM12878	blood:	n/a	n/a
4	CHD1	chr15:30330953-30331153	GM12878	blood:	n/a	n/a
5	CHD2	chr15:30331324-30331787	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr15:30335520-30335670	NHEK	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
7	CTCF	chr15:30335540-30335690	BJ	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
8	CTCF	chr15:30335580-30335697	MCF-7	breast:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
9	CTCF	chr15:30335680-30335830	HAc	cerebellar:	n/a	n/a
10	CTCF	chr15:30335570-30335690	SK-N-SH_RA	brain:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
11	CTCF	chr15:30335440-30335590	HMEC	breast:	n/a	n/a
12	CTCF	chr15:30335520-30335670	HCM	heart:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
13	CTCF	chr15:30335560-30335710	HCPEpiC	choroid plexus:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
14	CTCF	chr15:30335460-30335610	HVMF	connective:	n/a	n/a
15	CTCF	chr15:30335560-30335710	HPAF	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
16	CTCF	chr15:30335473-30335759	GM12878	blood:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
17	CTCF	chr15:30335520-30335670	HRPEpiC	eye:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
18	CTCF	chr15:30335640-30335790	RPTEC	kidney:	n/a	n/a
19	CTCF	chr15:30335377-30335724	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
20	CTCF	chr15:30335435-30335744	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
21	CTCF	chr15:30335560-30335710	NHDF-neo	bronchial:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
22	CTCF	chr15:30335280-30335430	AG04450	lung:	n/a	n/a
23	CTCF	chr15:30335300-30335450	HCM	heart:	n/a	n/a
24	CTCF	chr15:30335480-30335630	K562	blood:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
25	CTCF	chr15:30335425-30335690	ECC-1	luminal epithelium:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
26	CTCF	chr15:30335270-30335840	SK-N-SH	brain:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
27	CTCF	chr15:30335560-30335710	AG09319	gingival:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
28	CTCF	chr15:30335540-30335690	HFF-Myc	foreskin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
29	CTCF	chr15:30335291-30335859	HCT-116	colon:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
30	CTCF	chr15:30335500-30335650	NHEK	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
31	CTCF	chr15:30335490-30335726	LNCaP	prostate:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
32	CTCF	chr15:30335520-30335670	AG04449	skin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
33	CTCF	chr15:30335382-30335820	HCT-116	colon:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
34	CTCF	chr15:30335540-30335690	HPF	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
35	CTCF	chr15:30335440-30335590	HAc	cerebellar:	n/a	n/a
36	CTCF	chr15:30335373-30335821	MCF-7	breast:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
37	CTCF	chr15:30335611-30335683	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr15:30335640-30335790	HRE	kidney:	n/a	n/a
39	CTCF	chr15:30335569-30335696	Pancreas_OC	pancreas:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
40	CTCF	chr15:30335500-30335650	RPTEC	kidney:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
41	CTCF	chr15:30335520-30335670	AG09319	gingival:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
42	CTCF	chr15:30335580-30335730	AG04450	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
43	CTCF	chr15:30335527-30335726	MCF-7	breast:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
44	CTCF	chr15:30335540-30335690	HCM	heart:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
45	CTCF	chr15:30335540-30335690	AoAF	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
46	CTCF	chr15:30335460-30335690	BE2_C	brain:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
47	CTCF	chr15:30335395-30335799	A549	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
48	CTCF	chr15:30335560-30335710	HBMEC	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
49	CTCF	chr15:30335520-30335670	HFF	foreskin:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
50	CTCF	chr15:30335640-30335790	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30333911-30333961	BJ	skin:	n/a
2	chr15:30334898-30334948	HNPCEpiC	eye:	n/a
3	chr15:30334898-30334948	T-47D	breast:	n/a
4	chr15:30333911-30333961	HRPEpiC	eye:	n/a
5	chr15:30334898-30334948	LNCaP	prostate:	n/a
6	chr15:30334898-30334948	ECC-1	luminal epithelium:	n/a
7	chr15:30333911-30333961	HepG2	liver:	n/a
8	chr15:30334898-30334948	SK-N-MC	brain:	n/a
9	chr15:30333911-30333961	T-47D	breast:	n/a
10	chr15:30333911-30333961	HEEpiC	esophagus:	n/a
11	chr15:30333911-30333961	U87	brain:	n/a
12	chr15:30334898-30334948	ProgFib	skin:	n/a
13	chr15:30333911-30333961	Hela-S3	cervix:	n/a
14	chr15:30334898-30334948	PrEC	prostate:	n/a
15	chr15:30333911-30333961	NB4	blood:	n/a
16	chr15:30334898-30334948	HMEC	breast:	n/a
17	chr15:30334898-30334948	U87	brain:	n/a
18	chr15:30334898-30334948	NHDF-neo	bronchial:	n/a
19	chr15:30334898-30334948	Hepatocyte	liver:	n/a
20	chr15:30333911-30333961	SK-N-SH	brain:	n/a
21	chr15:30334898-30334948	HAEpiC	amniotic membrane:	n/a
22	chr15:30334898-30334948	SKMC	muscle:	n/a
23	chr15:30333911-30333961	HAEpiC	amniotic membrane:	n/a
24	chr15:30334898-30334948	GM06990	blood:	n/a
25	chr15:30333911-30333961	AoSMC	blood vessel:	n/a
26	chr15:30334898-30334948	HRPEpiC	eye:	n/a
27	chr15:30334898-30334948	NHBE	bronchial:	n/a
28	chr15:30334898-30334948	PANC-1	pancreas:	n/a
29	chr15:30333911-30333961	HCT-116	colon:	n/a
30	chr15:30334898-30334948	HCT-116	colon:	n/a
31	chr15:30333911-30333961	HL-60	blood:	n/a
32	chr15:30333911-30333961	AG10803	skin:	n/a
33	chr15:30333911-30333961	ovcar-3	ovarian:	n/a
34	chr15:30333911-30333961	A549	lung:	n/a
35	chr15:30333911-30333961	HMEC	breast:	n/a
36	chr15:30333911-30333961	PrEC	prostate:	n/a
37	chr15:30333911-30333961	HEK293	kidney:	embryo
38	chr15:30334898-30334948	H1-hESC	embryonic stem cell:	embryo
39	chr15:30334898-30334948	HL-60	blood:	n/a
40	chr15:30333911-30333961	HCPEpiC	choroid plexus:	n/a
41	chr15:30334898-30334948	HIPEpiC	eye:	n/a
42	chr15:30333911-30333961	NHDF-neo	bronchial:	n/a
43	chr15:30333911-30333961	H1-hESC	embryonic stem cell:	embryo
44	chr15:30334898-30334948	K562	blood:	n/a
45	chr15:30333911-30333961	BE2_C	brain:	n/a
46	chr15:30333911-30333961	HCF	heart:	n/a
47	chr15:30333911-30333961	SKMC	muscle:	n/a
48	chr15:30333911-30333961	PANC-1	pancreas:	n/a
49	chr15:30333911-30333961	K562	blood:	n/a
50	chr15:30334898-30334948	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:30234442..30235027-chr15:30335180..30335724,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260174	TF binding region
ENSG00000260174	CpG island

Extended variants
information (count: 349 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577188828	chr15:30327474-30327475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34975920	chr15:30327487-30327488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111686594	chr15:30327489-30327490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553978894	chr15:30327523-30327524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567057087	chr15:30327552-30327553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114416441	chr15:30327613-30327614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372205737	chr15:30327623-30327624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72723283	chr15:30327625-30327626	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538422209	chr15:30327633-30327634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12101693	chr15:30327635-30327636	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs148260152	chr15:30327691-30327692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533820207	chr15:30327715-30327716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553754148	chr15:30327741-30327742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573860151	chr15:30327761-30327762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188129520	chr15:30327779-30327780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76255814	chr15:30327781-30327782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141550928	chr15:30327788-30327789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181570502	chr15:30327798-30327799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559768845	chr15:30327801-30327802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564280809	chr15:30327803-30327804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533207681	chr15:30327863-30327864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186342212	chr15:30327868-30327869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560503798	chr15:30327871-30327872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77993010	chr15:30327927-30327928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3923926	chr15:30328060-30328061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569437809	chr15:30328065-30328066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191999662	chr15:30328070-30328071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146171875	chr15:30328100-30328101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563915172	chr15:30328109-30328110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571366775	chr15:30328173-30328174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367655736	chr15:30328229-30328230	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553500547	chr15:30328230-30328231	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116597025	chr15:30328257-30328258	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142433706	chr15:30328258-30328259	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537511465	chr15:30328290-30328291	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531089395	chr15:30328311-30328312	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556455867	chr15:30328358-30328359	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534722548	chr15:30328383-30328384	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183371973	chr15:30328472-30328473	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs544849587	chr15:30328586-30328587	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558291369	chr15:30328645-30328646	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150678915	chr15:30328649-30328650	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs139870211	chr15:30328651-30328652	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs75073184	chr15:30328662-30328663	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs529324476	chr15:30328688-30328689	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs371874144	chr15:30328710-30328711	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs563244091	chr15:30328714-30328715	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs531997903	chr15:30328740-30328741	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs552011170	chr15:30328790-30328791	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs79681641	chr15:30328797-30328798	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

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

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30325400-30327600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:30325600-30327600	Weak transcription	Brain Angular Gyrus	brain
3	chr15:30326400-30327600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:30326400-30327800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:30326400-30328000	Weak transcription	Brain Anterior Caudate	brain
6	chr15:30326400-30328200	Weak transcription	Brain Substantia Nigra	brain
7	chr15:30326600-30328200	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:30327600-30328200	Enhancers	Brain Angular Gyrus	brain
9	chr15:30327600-30328400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr15:30327600-30328800	Enhancers	Brain Cingulate Gyrus	brain
11	chr15:30327600-30329800	Enhancers	Fetal Brain Male	brain
12	chr15:30327800-30328400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr15:30327800-30328400	Enhancers	Fetal Brain Female	brain
14	chr15:30327800-30329000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr15:30328000-30328200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:30328000-30328200	Enhancers	Brain Anterior Caudate	brain
17	chr15:30328200-30328400	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr15:30328200-30328400	Enhancers	Brain Substantia Nigra	brain
19	chr15:30328200-30328600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:30328200-30328600	Enhancers	Brain Hippocampus Middle	brain
21	chr15:30328200-30331200	Weak transcription	Brain Angular Gyrus	brain
22	chr15:30328400-30328800	Active TSS	Brain Anterior Caudate	brain
23	chr15:30328400-30328800	Active TSS	Fetal Brain Female	brain
24	chr15:30328400-30331000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr15:30328400-30331200	Weak transcription	Brain Substantia Nigra	brain
26	chr15:30328400-30333600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr15:30328600-30331200	Weak transcription	Brain Hippocampus Middle	brain
28	chr15:30328800-30329200	Enhancers	Fetal Brain Female	brain
29	chr15:30328800-30331200	Weak transcription	Brain Anterior Caudate	brain
30	chr15:30328800-30333400	Weak transcription	Brain Cingulate Gyrus	brain
31	chr15:30329000-30331200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:30329400-30329600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr15:30329600-30337400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr15:30329800-30330800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr15:30330400-30332400	Enhancers	Liver	Liver
36	chr15:30330600-30331800	Enhancers	Colonic Mucosa	Colon
37	chr15:30330600-30331800	Enhancers	Hela-S3	cervix
38	chr15:30330600-30332000	Enhancers	Duodenum Mucosa	Duodenum
39	chr15:30330800-30331200	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr15:30330800-30332000	Enhancers	Adipose Nuclei	Adipose
41	chr15:30330800-30332200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr15:30331000-30331600	Enhancers	Ovary	ovary
43	chr15:30331000-30331800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr15:30331000-30331800	Enhancers	Pancreas	Pancrea
45	chr15:30331200-30331400	Enhancers	Fetal Lung	lung
46	chr15:30331200-30331600	Enhancers	Brain Substantia Nigra	brain
47	chr15:30331200-30331600	Enhancers	Left Ventricle	heart
48	chr15:30331200-30331800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr15:30331200-30331800	Enhancers	Brain Angular Gyrus	brain
50	chr15:30331200-30331800	Enhancers	Brain Anterior Caudate	brain

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