Variant report

Variant	nsv1044255
Chromosome Location	chr15:31391226-31424185
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	chr15:31421507-31421736	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr15:31423548-31423765	GM12878	blood:	n/a	n/a
3	BCL3	chr15:31396399-31396673	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:31417481-31417552	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:31409068-31409078	HepG2	liver:	n/a	n/a
6	CHD2	chr15:31421338-31421752	HepG2	liver:	n/a	n/a
7	CTCF	chr15:31391620-31391770	HMF	breast:	n/a	n/a
8	CTCF	chr15:31421500-31421849	Spleen_OC	spleen:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
9	CTCF	chr15:31421600-31421750	GM12864	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
10	CTCF	chr15:31421600-31421750	AG04449	skin:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
11	CTCF	chr15:31421600-31421750	AG09309	skin:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
12	CTCF	chr15:31391600-31391750	GM12865	blood:	n/a	n/a
13	CTCF	chr15:31421957-31422033	GM12878	blood:	n/a	n/a
14	CTCF	chr15:31421569-31421800	GM13976	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
15	CTCF	chr15:31421494-31421824	GM19240	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
16	CTCF	chr15:31421490-31421854	A549	lung:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
17	CTCF	chr15:31421389-31421971	GM12878	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
18	CTCF	chr15:31421600-31421750	HUVEC	blood vessel:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
19	CTCF	chr15:31422260-31422410	AG09319	gingival:	n/a	n/a
20	CTCF	chr15:31421356-31421417	K562	blood:	n/a	n/a
21	CTCF	chr15:31421537-31421824	GM10266	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
22	CTCF	chr15:31391640-31391790	GM12868	blood:	n/a	n/a
23	CTCF	chr15:31402713-31402750	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr15:31421538-31421796	MCF-7	breast:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
25	CTCF	chr15:31421459-31421824	K562	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
26	CTCF	chr15:31391560-31391710	HMF	breast:	n/a	n/a
27	CTCF	chr15:31421600-31421750	HVMF	connective:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
28	CTCF	chr15:31421397-31421825	H1-hESC	embryonic stem cell:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
29	CTCF	chr15:31421620-31421770	HL-60	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
30	CTCF	chr15:31421580-31421730	HUVEC	blood vessel:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
31	CTCF	chr15:31421600-31421750	WERI-Rb-1	eye:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
32	CTCF	chr15:31391580-31391730	HMEC	breast:	n/a	n/a
33	CTCF	chr15:31391600-31391750	AG10803	skin:	n/a	n/a
34	CTCF	chr15:31396327-31396395	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:31391660-31391810	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr15:31421240-31421390	AG04449	skin:	n/a	n/a
37	CTCF	chr15:31391560-31391710	HCM	heart:	n/a	n/a
38	CTCF	chr15:31421537-31421823	GM13977	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
39	CTCF	chr15:31421620-31421770	GM12878	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
40	CTCF	chr15:31421600-31421750	HRPEpiC	eye:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
41	CTCF	chr15:31421160-31421310	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr15:31422020-31422170	GM12875	blood:	n/a	n/a
43	CTCF	chr15:31421600-31421750	GM12868	blood:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
44	CTCF	chr15:31421200-31421350	AG04450	lung:	n/a	n/a
45	CTCF	chr15:31396323-31396425	GM19239	blood:	n/a	n/a
46	CTCF	chr15:31421940-31422090	AG04449	skin:	n/a	n/a
47	CTCF	chr15:31421600-31421750	HCPEpiC	choroid plexus:	n/a	chr15:31421665-31421678 chr15:31421663-31421681
48	CTCF	chr15:31391620-31391770	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr15:31391620-31391770	GM12878	blood:	n/a	n/a
50	CTCF	chr15:31421260-31421410	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31391491-31391541	PANC-1	pancreas:	n/a
2	chr15:31420951-31421001	NB4	blood:	n/a
3	chr15:31394188-31394238	BJ	skin:	n/a
4	chr15:31394021-31394071	HNPCEpiC	eye:	n/a
5	chr15:31395221-31395271	HRE	kidney:	n/a
6	chr15:31394021-31394071	PFSK-1	brain:	n/a
7	chr15:31395221-31395271	LNCaP	prostate:	n/a
8	chr15:31394021-31394071	Jurkat	blood:	n/a
9	chr15:31394285-31394335	K562	blood:	n/a
10	chr15:31420951-31421001	HCM	heart:	n/a
11	chr15:31420951-31421001	A549	lung:	n/a
12	chr15:31394021-31394071	HEEpiC	esophagus:	n/a
13	chr15:31394285-31394335	HCT-116	colon:	n/a
14	chr15:31393845-31393895	CMK	blood:	n/a
15	chr15:31394021-31394071	SAEC	small airway:	n/a
16	chr15:31394021-31394071	HCT-116	colon:	n/a
17	chr15:31393845-31393895	SAEC	small airway:	n/a
18	chr15:31394285-31394335	GM12878	blood:	n/a
19	chr15:31393845-31393895	HCT-116	colon:	n/a
20	chr15:31391491-31391541	GM12878	blood:	n/a
21	chr15:31394021-31394071	PrEC	prostate:	n/a
22	chr15:31395221-31395271	IMR90	lung:	fetal
23	chr15:31391491-31391541	HMEC	breast:	n/a
24	chr15:31420951-31421001	AG09309	skin:	n/a
25	chr15:31393845-31393895	HCPEpiC	choroid plexus:	n/a
26	chr15:31394021-31394071	GM19239	blood:	n/a
27	chr15:31394188-31394238	A549	lung:	n/a
28	chr15:31395221-31395271	BE2_C	brain:	n/a
29	chr15:31395221-31395271	HPAEpiC	pulmonary alveolar:	n/a
30	chr15:31420951-31421001	HIPEpiC	eye:	n/a
31	chr15:31395221-31395271	PrEC	prostate:	n/a
32	chr15:31395221-31395271	NH-A	brain:	n/a
33	chr15:31393845-31393895	A549	lung:	n/a
34	chr15:31391491-31391541	BE2_C	brain:	n/a
35	chr15:31394021-31394071	AG04450	lung:	fetal
36	chr15:31393845-31393895	LNCaP	prostate:	n/a
37	chr15:31391491-31391541	RPTEC	kidney:	n/a
38	chr15:31393845-31393895	H1-hESC	embryonic stem cell:	embryo
39	chr15:31420951-31421001	CMK	blood:	n/a
40	chr15:31394021-31394071	NT2-D1	testis:	n/a
41	chr15:31395221-31395271	CMK	blood:	n/a
42	chr15:31394021-31394071	HRPEpiC	eye:	n/a
43	chr15:31420951-31421001	Hepatocyte	liver:	n/a
44	chr15:31391491-31391541	U87	brain:	n/a
45	chr15:31394021-31394071	IMR90	lung:	fetal
46	chr15:31394188-31394238	PrEC	prostate:	n/a
47	chr15:31393845-31393895	Jurkat	blood:	n/a
48	chr15:31394285-31394335	MCF10A-Er-Src	breast:	n/a
49	chr15:31420951-31421001	IMR90	lung:	fetal
50	chr15:31394285-31394335	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:31197911..31198672-chr15:31421206..31422134,2	K562	blood:
2	chr15:31196058..31198354-chr15:31402829..31405030,2	MCF-7	breast:
3	chr15:31197732..31198235-chr15:31391287..31392163,2	MCF-7	breast:
4	chr15:31197767..31198496-chr15:31421210..31421757,2	MCF-7	breast:
5	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
6	chr15:31197730..31198708-chr15:31390791..31392081,3	MCF-7	breast:
7	chr15:31196230..31197982-chr15:31421412..31424156,2	MCF-7	breast:
8	chr15:31186419..31186925-chr15:31421231..31422125,2	MCF-7	breast:
9	chr15:31197918..31198657-chr15:31420885..31421796,3	MCF-7	breast:

Variant related genes	Relation type
TRPM1	TF binding region
TRPM1	CpG island
ENSG00000198690	chromatin interactions

Extended variants
information (count: 845 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535427885	chr15:31391227-31391228	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs181740793	chr15:31391261-31391262	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs550842728	chr15:31391268-31391269	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs139443330	chr15:31391279-31391280	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs149671533	chr15:31391282-31391283	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553112500	chr15:31391283-31391284	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs573198101	chr15:31391285-31391286	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs146864074	chr15:31391344-31391345	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs555410322	chr15:31391449-31391450	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs575262143	chr15:31391467-31391468	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs544189569	chr15:31391471-31391472	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs186820111	chr15:31391491-31391492	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs577651714	chr15:31391513-31391514	Enhancers Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs543728203	chr15:31391606-31391607	Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs546107670	chr15:31391613-31391614	Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs559492190	chr15:31391684-31391685	Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs34449068	chr15:31391692-31391693	Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs528770431	chr15:31391748-31391749	Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs550430968	chr15:31391886-31391887	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs571629265	chr15:31391944-31391945	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs548429436	chr15:31391953-31391954	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs562041321	chr15:31391962-31391963	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530855212	chr15:31392069-31392070	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs192024645	chr15:31392140-31392141	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs11070810	chr15:31392141-31392142	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs539895933	chr15:31392160-31392161	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs75995060	chr15:31392164-31392165	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs529465675	chr15:31392203-31392204	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs183153495	chr15:31392228-31392229	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs74349507	chr15:31392301-31392302	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs535749415	chr15:31392321-31392322	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs555742691	chr15:31392331-31392332	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs575598125	chr15:31392347-31392348	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs537477409	chr15:31392359-31392360	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs10851488	chr15:31392375-31392376	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs577685421	chr15:31392376-31392377	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs112033309	chr15:31392405-31392406	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs111483758	chr15:31392425-31392426	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375802051	chr15:31392426-31392427	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs10851489	chr15:31392436-31392437	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562081825	chr15:31392466-31392467	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs531217090	chr15:31392480-31392481	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544303808	chr15:31392525-31392526	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs146605543	chr15:31392568-31392569	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs533273866	chr15:31392677-31392678	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs547066913	chr15:31392703-31392704	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566964790	chr15:31392705-31392706	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs529140302	chr15:31392707-31392708	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs117836080	chr15:31392723-31392724	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs569203374	chr15:31392791-31392792	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:156)

Disease	PMID	Source
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
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	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
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31386000-31392400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:31388800-31391400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr15:31389200-31391600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:31389200-31393000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:31389600-31393200	Enhancers	Liver	Liver
6	chr15:31389800-31392200	Enhancers	HepG2	liver
7	chr15:31390600-31391800	Enhancers	Pancreas	Pancrea
8	chr15:31390800-31391400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:31390800-31391600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:31390800-31391600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr15:31390800-31391600	Flanking Active TSS	Fetal Kidney	kidney
12	chr15:31390800-31391600	Enhancers	Placenta	Placenta
13	chr15:31390800-31391800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr15:31390800-31391800	Enhancers	Stomach Mucosa	stomach
15	chr15:31390800-31392000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr15:31390800-31392200	Enhancers	Brain Substantia Nigra	brain
17	chr15:31390800-31392200	Enhancers	A549	lung
18	chr15:31390800-31393800	Enhancers	Primary B cells from peripheral blood	blood
19	chr15:31391000-31391600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr15:31391000-31391800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr15:31391000-31392000	Enhancers	Fetal Brain Female	brain
22	chr15:31391000-31392200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr15:31391000-31393800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr15:31391000-31395600	Enhancers	Brain Hippocampus Middle	brain
25	chr15:31391200-31391400	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr15:31391200-31391600	Enhancers	H1 Cell Line	embryonic stem cell
27	chr15:31391200-31391800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr15:31391200-31392000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr15:31391200-31392200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr15:31391200-31392200	Enhancers	Brain Cingulate Gyrus	brain
31	chr15:31391200-31392800	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr15:31391400-31391600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr15:31391400-31391600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr15:31391400-31391600	Enhancers	Brain Angular Gyrus	brain
35	chr15:31391400-31391600	Enhancers	Brain Anterior Caudate	brain
36	chr15:31391400-31391800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:31391400-31392400	Enhancers	GM12878-XiMat	blood
38	chr15:31391400-31393200	Enhancers	Primary B cells from cord blood	blood
39	chr15:31391400-31393800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:31391400-31394600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:31391600-31392000	Enhancers	Brain Germinal Matrix	brain
42	chr15:31391600-31392400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:31391600-31392600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr15:31391600-31392800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr15:31391600-31393200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:31391600-31393200	Weak transcription	Brain Angular Gyrus	brain
47	chr15:31391600-31393400	Weak transcription	Brain Anterior Caudate	brain
48	chr15:31391600-31393400	Enhancers	Fetal Kidney	kidney
49	chr15:31391600-31396200	Weak transcription	Placenta	Placenta
50	chr15:31391800-31392200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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