Variant report

Variant	nsv974544
Chromosome Location	chr15:30338551-30373033
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	BHLHE40	chr15:30348379-30348447	K562	blood:	n/a	n/a
2	CEBPB	chr15:30357266-30357793	Hela-S3	cervix:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
3	CEBPB	chr15:30357423-30357772	H1-hESC	embryonic stem cell:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
4	CEBPB	chr15:30357402-30357757	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
5	CEBPB	chr15:30357467-30357767	K562	blood:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
6	CEBPB	chr15:30357445-30357725	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
7	CEBPB	chr15:30373008-30373220	A549	lung:	n/a	n/a
8	CEBPB	chr15:30357417-30357754	HepG2	liver:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
9	CEBPB	chr15:30343011-30343208	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:30357425-30357791	IMR90	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
11	CEBPB	chr15:30357281-30357870	A549	lung:	n/a	chr15:30357588-30357599 chr15:30357569-30357581
12	CHD1	chr15:30347814-30348022	GM12878	blood:	n/a	n/a
13	CTCF	chr15:30367600-30367750	WI-38	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
14	CTCF	chr15:30367580-30367730	GM12871	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
15	CTCF	chr15:30367565-30367788	GM12878	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
16	CTCF	chr15:30367560-30367710	AG10803	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
17	CTCF	chr15:30367566-30367794	Hela-S3	cervix:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
18	CTCF	chr15:30367551-30367808	HUVEC	blood vessel:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
19	CTCF	chr15:30367656-30367764	GM20000	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
20	CTCF	chr15:30367620-30367770	AG09309	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
21	CTCF	chr15:30367580-30367730	GM12867	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
22	CTCF	chr15:30367571-30367797	LNCaP	prostate:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
23	CTCF	chr15:30367600-30367750	GM12869	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
24	CTCF	chr15:30367580-30367730	HCM	heart:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
25	CTCF	chr15:30367500-30367650	GM12870	blood:	n/a	n/a
26	CTCF	chr15:30367560-30367710	HEK293	kidney:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
27	CTCF	chr15:30367620-30367770	HL-60	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
28	CTCF	chr15:30367435-30367871	HepG2	liver:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
29	CTCF	chr15:30341480-30341630	A549	lung:	n/a	n/a
30	CTCF	chr15:30367596-30367709	GM19239	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
31	CTCF	chr15:30367120-30367270	NHLF	lung:	n/a	n/a
32	CTCF	chr15:30348847-30348886	Lung_OC	lung:	n/a	n/a
33	CTCF	chr15:30367573-30367701	GM19238	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
34	CTCF	chr15:30367260-30367410	AG04449	skin:	n/a	n/a
35	CTCF	chr15:30367700-30367850	WI-38	lung:	n/a	n/a
36	CTCF	chr15:30367603-30367667	MCF-7	breast:	n/a	n/a
37	CTCF	chr15:30367550-30367758	A549	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
38	CTCF	chr15:30367620-30367770	AG10803	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
39	CTCF	chr15:30367332-30367954	HCT-116	colon:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
40	CTCF	chr15:30367560-30367710	GM12864	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
41	CTCF	chr15:30367600-30367750	HRPEpiC	eye:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
42	CTCF	chr15:30371660-30371810	A549	lung:	n/a	n/a
43	CTCF	chr15:30367580-30367730	NHLF	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
44	CTCF	chr15:30367560-30367710	AG09319	gingival:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
45	CTCF	chr15:30367580-30367736	NHEK	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
46	CTCF	chr15:30367600-30367750	HCT-116	colon:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
47	CTCF	chr15:30367620-30367770	HPF	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
48	CTCF	chr15:30367321-30367779	HCT-116	colon:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
49	CTCF	chr15:30367490-30367848	H1-hESC	embryonic stem cell:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
50	CTCF	chr15:30367604-30367767	GM10266	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30366335-30366385	A549	lung:	n/a
2	chr15:30365409-30365459	LNCaP	prostate:	n/a
3	chr15:30339875-30339925	GM06990	blood:	n/a
4	chr15:30366335-30366385	PFSK-1	brain:	n/a
5	chr15:30365409-30365459	HCPEpiC	choroid plexus:	n/a
6	chr15:30366335-30366385	RPTEC	kidney:	n/a
7	chr15:30365409-30365459	SK-N-SH	brain:	n/a
8	chr15:30339875-30339925	HepG2	liver:	n/a
9	chr15:30365409-30365459	AG04449	skin:	fetal
10	chr15:30366335-30366385	GM12878	blood:	n/a
11	chr15:30339875-30339925	SK-N-MC	brain:	n/a
12	chr15:30366335-30366385	HNPCEpiC	eye:	n/a
13	chr15:30366335-30366385	PrEC	prostate:	n/a
14	chr15:30366335-30366385	HEK293	kidney:	embryo
15	chr15:30366335-30366385	GM19239	blood:	n/a
16	chr15:30365409-30365459	PANC-1	pancreas:	n/a
17	chr15:30365409-30365459	NH-A	brain:	n/a
18	chr15:30365409-30365459	HRPEpiC	eye:	n/a
19	chr15:30339875-30339925	BE2_C	brain:	n/a
20	chr15:30339875-30339925	AG04450	lung:	fetal
21	chr15:30365409-30365459	HRE	kidney:	n/a
22	chr15:30365409-30365459	H1-hESC	embryonic stem cell:	embryo
23	chr15:30339875-30339925	HNPCEpiC	eye:	n/a
24	chr15:30366335-30366385	AG04450	lung:	fetal
25	chr15:30339875-30339925	Hepatocyte	liver:	n/a
26	chr15:30366335-30366385	NB4	blood:	n/a
27	chr15:30339875-30339925	AG09309	skin:	n/a
28	chr15:30365409-30365459	SKMC	muscle:	n/a
29	chr15:30366335-30366385	U87	brain:	n/a
30	chr15:30339875-30339925	NHDF-neo	bronchial:	n/a
31	chr15:30365409-30365459	AoSMC	blood vessel:	n/a
32	chr15:30365409-30365459	NHDF-neo	bronchial:	n/a
33	chr15:30365409-30365459	HepG2	liver:	n/a
34	chr15:30339875-30339925	SKMC	muscle:	n/a
35	chr15:30339875-30339925	H1-hESC	embryonic stem cell:	embryo
36	chr15:30339875-30339925	GM12891	blood:	n/a
37	chr15:30366335-30366385	HIPEpiC	eye:	n/a
38	chr15:30366335-30366385	AoSMC	blood vessel:	n/a
39	chr15:30366335-30366385	HUVEC	blood vessel:	n/a
40	chr15:30339875-30339925	T-47D	breast:	n/a
41	chr15:30339875-30339925	SAEC	small airway:	n/a
42	chr15:30365409-30365459	GM12891	blood:	n/a
43	chr15:30366335-30366385	GM06990	blood:	n/a
44	chr15:30339875-30339925	MCF-7	breast:	n/a
45	chr15:30339875-30339925	AG04449	skin:	fetal
46	chr15:30366335-30366385	MCF10A-Er-Src	breast:	n/a
47	chr15:30366335-30366385	SAEC	small airway:	n/a
48	chr15:30365409-30365459	HCT-116	colon:	n/a
49	chr15:30365409-30365459	BJ	skin:	n/a
50	chr15:30339875-30339925	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
2	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
3	chr15:30039724..30040629-chr15:30367249..30368123,2	K562	blood:
4	chr15:30233133..30233805-chr15:30367233..30367920,2	MCF-7	breast:
5	chr15:29959926..29960944-chr15:30367131..30368208,4	K562	blood:

Variant related genes	Relation type
ENSG00000259647	TF binding region
ENSG00000229389	TF binding region
GOLGA8J	TF binding region
ENSG00000259647	CpG island
ENSG00000229389	CpG island
GOLGA8J	CpG island

Extended variants
information (count: 1258 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372609955	chr15:30338561-30338562	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377289331	chr15:30338599-30338600	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs183093665	chr15:30338613-30338614	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs577807948	chr15:30338616-30338617	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540050051	chr15:30338674-30338675	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs187428727	chr15:30338682-30338683	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs146960505	chr15:30338683-30338684	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574580806	chr15:30338694-30338695	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs541834596	chr15:30338713-30338714	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs193102972	chr15:30338742-30338743	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530795087	chr15:30338761-30338762	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs571282568	chr15:30338824-30338825	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs137964196	chr15:30338845-30338846	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs533623769	chr15:30338865-30338866	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546832815	chr15:30338877-30338878	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538701730	chr15:30338903-30338904	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs144018625	chr15:30338904-30338905	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs540263738	chr15:30338913-30338914	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555480025	chr15:30338989-30338990	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs568905796	chr15:30339005-30339006	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs185537408	chr15:30339037-30339038	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs558078021	chr15:30339148-30339149	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs577812976	chr15:30339235-30339236	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187757930	chr15:30339258-30339259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533998642	chr15:30339315-30339316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192633634	chr15:30339316-30339317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184106784	chr15:30339321-30339322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541951079	chr15:30339324-30339325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368736387	chr15:30339325-30339326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575277074	chr15:30339353-30339354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544279134	chr15:30339356-30339357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575154704	chr15:30339400-30339401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564806211	chr15:30339411-30339412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113517923	chr15:30339422-30339423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188599537	chr15:30339473-30339474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547188750	chr15:30339553-30339554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560694838	chr15:30339635-30339636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529495412	chr15:30339698-30339699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549138179	chr15:30339756-30339757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11634754	chr15:30339758-30339759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs573019071	chr15:30339770-30339771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540317808	chr15:30339796-30339797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537849725	chr15:30339844-30339845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561871735	chr15:30339875-30339876	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs111506258	chr15:30339956-30339957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529050043	chr15:30340034-30340035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571531329	chr15:30340092-30340093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533814824	chr15:30340124-30340125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546438942	chr15:30340182-30340183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573537209	chr15:30340192-30340193	Weak transcription	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:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30335400-30338600	Weak transcription	HSMM	muscle
2	chr15:30335600-30338600	Weak transcription	Fetal Kidney	kidney
3	chr15:30335600-30338800	Weak transcription	A549	lung
4	chr15:30335600-30341200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:30335600-30342400	Weak transcription	Liver	Liver
6	chr15:30337800-30338800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr15:30337800-30339000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:30338000-30338600	Weak transcription	Brain Substantia Nigra	brain
9	chr15:30338000-30338800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr15:30338000-30338800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr15:30338000-30339000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr15:30338200-30338800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr15:30338600-30338800	Enhancers	Brain Substantia Nigra	brain
14	chr15:30338600-30339000	Enhancers	HSMM	muscle
15	chr15:30338600-30339200	Enhancers	Fetal Kidney	kidney
16	chr15:30338800-30339000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:30338800-30339000	Enhancers	Brain Angular Gyrus	brain
18	chr15:30338800-30339000	Enhancers	A549	lung
19	chr15:30341200-30342800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:30342200-30342600	Enhancers	Brain Anterior Caudate	brain
21	chr15:30342400-30343200	Enhancers	Liver	Liver
22	chr15:30345200-30345400	Enhancers	Pancreas	Pancrea
23	chr15:30345400-30356400	Weak transcription	Pancreas	Pancrea
24	chr15:30346600-30347200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:30347600-30347800	Enhancers	Brain Cingulate Gyrus	brain
26	chr15:30347600-30347800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr15:30347800-30348400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr15:30347800-30348400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr15:30348000-30348200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr15:30348200-30348400	Weak transcription	Fetal Kidney	kidney
31	chr15:30348400-30348600	Enhancers	Brain Cingulate Gyrus	brain
32	chr15:30348400-30348600	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr15:30348400-30348600	Enhancers	Fetal Kidney	kidney
34	chr15:30348600-30351600	Weak transcription	Brain Cingulate Gyrus	brain
35	chr15:30348600-30351800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr15:30348600-30357200	Weak transcription	Fetal Kidney	kidney
37	chr15:30349200-30350000	Enhancers	Fetal Brain Male	brain
38	chr15:30349400-30352000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr15:30350000-30351200	Weak transcription	Fetal Brain Male	brain
40	chr15:30351200-30352200	Enhancers	Fetal Brain Male	brain
41	chr15:30351600-30352600	Enhancers	Brain Cingulate Gyrus	brain
42	chr15:30351800-30352400	Enhancers	Brain Angular Gyrus	brain
43	chr15:30351800-30352800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr15:30352000-30352200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr15:30352000-30352200	Enhancers	Brain Hippocampus Middle	brain
46	chr15:30352000-30352400	Enhancers	Brain Substantia Nigra	brain
47	chr15:30352200-30352600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:30352200-30352600	Weak transcription	Fetal Brain Male	brain
49	chr15:30352200-30355600	Weak transcription	Brain Hippocampus Middle	brain
50	chr15:30352400-30355200	Weak transcription	Brain Substantia Nigra	brain

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