Variant report

Variant	nsv542292
Chromosome Location	chr15:29729596-29784023
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	ARID3A	chr15:29731449-29731827	HepG2	liver:	n/a	n/a
2	BACH1	chr15:29743463-29743737	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr15:29731483-29731800	HepG2	liver:	n/a	n/a
4	CEBPB	chr15:29762540-29762872	MCF-7	breast:	n/a	n/a
5	CEBPB	chr15:29731407-29731804	MCF-7	breast:	n/a	n/a
6	CEBPB	chr15:29762438-29763384	MCF-7	breast:	n/a	n/a
7	CEBPB	chr15:29762542-29762826	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:29763080-29763249	A549	lung:	n/a	n/a
9	CEBPB	chr15:29731336-29731761	MCF-7	breast:	n/a	n/a
10	CEBPB	chr15:29762583-29762824	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr15:29762999-29763242	MCF-7	breast:	n/a	n/a
12	CHD2	chr15:29743623-29743633	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr15:29743427-29743712	A549	lung:	n/a	n/a
14	CTCF	chr15:29743497-29743750	HepG2	liver:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
15	CTCF	chr15:29743540-29743690	SK-N-SH_RA	brain:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
16	CTCF	chr15:29743441-29743762	MCF-7	breast:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
17	CTCF	chr15:29743523-29743651	NHEK	skin:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
18	CTCF	chr15:29743510-29743685	GM12878	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
19	CTCF	chr15:29743474-29743703	K562	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
20	CTCF	chr15:29743500-29743650	A549	lung:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
21	CTCF	chr15:29743520-29743670	AG04450	lung:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
22	CTCF	chr15:29772673-29772676	GM12878	blood:	n/a	n/a
23	CTCF	chr15:29743452-29743720	H1-hESC	embryonic stem cell:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
24	CTCF	chr15:29772626-29772717	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:29743520-29743670	WERI-Rb-1	eye:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
26	CTCF	chr15:29743460-29743610	GM12865	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
27	CTCF	chr15:29743540-29743690	HA-sp	spinal cord:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
28	CTCF	chr15:29743500-29743650	BE2_C	brain:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
29	CTCF	chr15:29743504-29743683	K562	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
30	CTCF	chr15:29743441-29743824	MCF-7	breast:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
31	CTCF	chr15:29743352-29743741	MCF-7	breast:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601 chr15:29743383-29743392
32	CTCF	chr15:29743500-29743650	HepG2	liver:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
33	CTCF	chr15:29743620-29743770	HCM	heart:	n/a	n/a
34	CTCF	chr15:29743554-29743619	Medullo	brain:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
35	CTCF	chr15:29743523-29743644	ProgFib	skin:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
36	CTCF	chr15:29743520-29743670	MCF-7	breast:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
37	CTCF	chr15:29743511-29743664	LNCaP	prostate:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
38	CTCF	chr15:29743480-29743630	GM12866	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
39	CTCF	chr15:29743520-29743670	RPTEC	kidney:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
40	CTCF	chr15:29743520-29743670	GM12873	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
41	CTCF	chr15:29769151-29769213	GM13976	blood:	n/a	n/a
42	CTCF	chr15:29743480-29743630	HFF-Myc	foreskin:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
43	CTCF	chr15:29743520-29743670	HCPEpiC	choroid plexus:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
44	CTCF	chr15:29743520-29743670	HBMEC	blood vessel:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
45	CTCF	chr15:29743520-29743670	HepG2	liver:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
46	CTCF	chr15:29773317-29773355	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:29743490-29743707	Gliobla	brain:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
48	CTCF	chr15:29743540-29743690	GM12865	blood:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
49	CTCF	chr15:29743500-29743650	AG04449	skin:	n/a	chr15:29743586-29743599 chr15:29743586-29743594 chr15:29743583-29743601
50	CTCF	chr15:29772520-29772670	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:29744853-29744903	RPTEC	kidney:	n/a
2	chr15:29773425-29773475	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:29773425-29773475	SK-N-SH	brain:	n/a
4	chr15:29763183-29763233	NB4	blood:	n/a
5	chr15:29773425-29773475	AG09309	skin:	n/a
6	chr15:29773425-29773475	NT2-D1	testis:	n/a
7	chr15:29744853-29744903	K562	blood:	n/a
8	chr15:29773425-29773475	RPTEC	kidney:	n/a
9	chr15:29763183-29763233	Jurkat	blood:	n/a
10	chr15:29773425-29773475	CMK	blood:	n/a
11	chr15:29773425-29773475	BE2_C	brain:	n/a
12	chr15:29744853-29744903	AG04449	skin:	fetal
13	chr15:29773425-29773475	A549	lung:	n/a
14	chr15:29763183-29763233	IMR90	lung:	fetal
15	chr15:29744853-29744903	Hepatocyte	liver:	n/a
16	chr15:29763183-29763233	PANC-1	pancreas:	n/a
17	chr15:29763183-29763233	BJ	skin:	n/a
18	chr15:29744853-29744903	HAEpiC	amniotic membrane:	n/a
19	chr15:29763183-29763233	AG04449	skin:	fetal
20	chr15:29744853-29744903	Jurkat	blood:	n/a
21	chr15:29744853-29744903	MCF-7	breast:	n/a
22	chr15:29773425-29773475	AG04450	lung:	fetal
23	chr15:29763183-29763233	Hela-S3	cervix:	n/a
24	chr15:29744853-29744903	ovcar-3	ovarian:	n/a
25	chr15:29773425-29773475	ECC-1	luminal epithelium:	n/a
26	chr15:29763183-29763233	HRPEpiC	eye:	n/a
27	chr15:29773425-29773475	HCT-116	colon:	n/a
28	chr15:29744853-29744903	PFSK-1	brain:	n/a
29	chr15:29773425-29773475	HCPEpiC	choroid plexus:	n/a
30	chr15:29773425-29773475	GM19239	blood:	n/a
31	chr15:29744853-29744903	NT2-D1	testis:	n/a
32	chr15:29744853-29744903	U87	brain:	n/a
33	chr15:29744853-29744903	AG04450	lung:	fetal
34	chr15:29763183-29763233	NH-A	brain:	n/a
35	chr15:29744853-29744903	HNPCEpiC	eye:	n/a
36	chr15:29744853-29744903	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:29773425-29773475	LNCaP	prostate:	n/a
38	chr15:29763183-29763233	NHDF-neo	bronchial:	n/a
39	chr15:29773425-29773475	SK-N-SH_RA	brain:	n/a
40	chr15:29763183-29763233	T-47D	breast:	n/a
41	chr15:29773425-29773475	HL-60	blood:	n/a
42	chr15:29773425-29773475	SK-N-MC	brain:	n/a
43	chr15:29744853-29744903	HepG2	liver:	n/a
44	chr15:29763183-29763233	Caco-2	colon:	n/a
45	chr15:29744853-29744903	NH-A	brain:	n/a
46	chr15:29744853-29744903	HCT-116	colon:	n/a
47	chr15:29763183-29763233	K562	blood:	n/a
48	chr15:29773425-29773475	SKMC	muscle:	n/a
49	chr15:29744853-29744903	PrEC	prostate:	n/a
50	chr15:29773425-29773475	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:29394234..29397212-chr15:29740388..29743315,2	K562	blood:
2	chr15:29763109..29764996-chr15:29776827..29779007,2	MCF-7	breast:
3	chr15:29732499..29734253-chr15:29736470..29738645,2	MCF-7	breast:
4	chr15:29720284..29721871-chr15:29739978..29741969,2	K562	blood:
5	chr15:29750799..29752700-chr15:29760206..29762148,2	MCF-7	breast:
6	chr15:29732499..29734253-chr15:29736470..29738645,2	MCF-7	breast:
7	chr15:29749605..29750384-chr15:41312914..41313837,2	MCF-7	breast:
8	chr15:29749956..29752554-chr15:29753590..29755276,2	K562	blood:
9	chr15:29743489..29744057-chr15:29860766..29861643,3	MCF-7	breast:
10	chr15:29742588..29744530-chr15:29754721..29756773,2	K562	blood:
11	chr15:29749956..29752554-chr15:29753590..29755276,2	K562	blood:
12	chr15:29743174..29744066-chr15:29860740..29861596,5	MCF-7	breast:
13	chr15:29742588..29744530-chr15:29754721..29756773,2	K562	blood:
14	chr15:29750799..29752700-chr15:29760206..29762148,2	MCF-7	breast:
15	chr15:29763109..29764996-chr15:29776827..29779007,2	MCF-7	breast:

Variant related genes	Relation type
FAM189A1	TF binding region
FAM189A1	CpG island

Extended variants
information (count: 2370 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:2370 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527875333	chr15:29729679-29729680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548455333	chr15:29729730-29729731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140082248	chr15:29729766-29729767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567950649	chr15:29729813-29729814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12901720	chr15:29729815-29729816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs536504542	chr15:29729816-29729817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4780223	chr15:29729879-29729880	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191278047	chr15:29729887-29729888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145381432	chr15:29729901-29729902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183134018	chr15:29729960-29729961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371592551	chr15:29730051-29730052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76398873	chr15:29730053-29730054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541263712	chr15:29730106-29730107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545803192	chr15:29730129-29730130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4780224	chr15:29730152-29730153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146447511	chr15:29730186-29730187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140872400	chr15:29730234-29730235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115255612	chr15:29730243-29730244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545210897	chr15:29730265-29730266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565375051	chr15:29730290-29730291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115875471	chr15:29730326-29730327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547978488	chr15:29730356-29730357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367587090	chr15:29730381-29730382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145115941	chr15:29730401-29730402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138864631	chr15:29730471-29730472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17670574	chr15:29730473-29730474	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs56239648	chr15:29730498-29730499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538246750	chr15:29730505-29730506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558222591	chr15:29730540-29730541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73382136	chr15:29730548-29730549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs55976010	chr15:29730560-29730561	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs116533270	chr15:29730571-29730572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574664786	chr15:29730572-29730573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568623043	chr15:29730611-29730612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs55984022	chr15:29730670-29730671	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559576790	chr15:29730690-29730691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576551535	chr15:29730707-29730708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78387080	chr15:29730730-29730731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368586628	chr15:29730763-29730764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372671750	chr15:29730809-29730810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565092090	chr15:29730848-29730849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572516021	chr15:29730854-29730855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574690073	chr15:29730866-29730867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80042956	chr15:29730889-29730890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575964745	chr15:29730914-29730915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561172030	chr15:29730917-29730918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540148340	chr15:29730951-29730952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530214993	chr15:29730970-29730971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550109012	chr15:29730972-29730973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11634762	chr15:29730996-29730997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:160)

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
idiopathic generalized epilepsy	19843651	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
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
Epilepsy	20502679	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	CNVD
Autism	20841430	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
Melanoma	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29725200-29735200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:29726200-29729800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr15:29727200-29730400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:29728400-29730200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:29729000-29730000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:29729200-29733000	Enhancers	Placenta	Placenta
7	chr15:29730000-29730200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr15:29730000-29730800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr15:29730200-29730600	Enhancers	Esophagus	oesophagus
10	chr15:29730200-29730800	Enhancers	Pancreas	Pancrea
11	chr15:29730200-29731400	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr15:29730200-29732000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr15:29730400-29731200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr15:29730600-29731200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr15:29730800-29731800	Weak transcription	Pancreas	Pancrea
16	chr15:29730800-29732200	Enhancers	Liver	Liver
17	chr15:29731000-29731400	Weak transcription	Stomach Mucosa	stomach
18	chr15:29731200-29731600	Enhancers	Small Intestine	intestine
19	chr15:29731200-29733200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:29731400-29731800	Enhancers	Stomach Mucosa	stomach
21	chr15:29731400-29732000	Enhancers	HepG2	liver
22	chr15:29731800-29732200	Enhancers	Pancreas	Pancrea
23	chr15:29731800-29732600	Weak transcription	Stomach Mucosa	stomach
24	chr15:29732000-29732800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr15:29732800-29733000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr15:29733200-29733600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr15:29735200-29735800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:29735400-29735600	Bivalent/Poised TSS	Hela-S3	cervix
29	chr15:29735800-29743400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:29737600-29738200	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr15:29741000-29741200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr15:29741200-29745200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr15:29743400-29745000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:29743400-29745200	Enhancers	Lung	lung
35	chr15:29743400-29745600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr15:29743600-29743800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:29743600-29743800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:29743600-29743800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr15:29743600-29743800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr15:29743600-29744000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:29743600-29745200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr15:29743600-29745400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:29743600-29745600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr15:29743600-29745800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr15:29743600-29745800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr15:29743800-29744400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:29743800-29744400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr15:29743800-29744800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr15:29743800-29745400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:29743800-29745400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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