Variant report

Variant	nsv1010063
Chromosome Location	chr1:47264205-47285118
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	CEBPB	chr1:47272292-47272727	HepG2	liver:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
2	CEBPB	chr1:47272508-47272610	K562	blood:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
3	CEBPB	chr1:47272373-47272770	ECC-1	luminal epithelium:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
4	CEBPB	chr1:47272398-47272736	Hela-S3	cervix:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
5	CEBPB	chr1:47272465-47272698	IMR90	lung:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
6	CEBPB	chr1:47275993-47276259	HepG2	liver:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
7	CEBPB	chr1:47275979-47276251	K562	blood:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
8	CEBPB	chr1:47272476-47272676	H1-hESC	embryonic stem cell:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
9	CEBPB	chr1:47275958-47276196	IMR90	lung:	n/a	chr1:47276116-47276125 chr1:47276116-47276125 chr1:47276114-47276125 chr1:47276116-47276125 chr1:47276114-47276127 chr1:47276116-47276127 chr1:47276116-47276125
10	CEBPB	chr1:47272175-47272836	MCF-7	breast:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
11	CEBPB	chr1:47272435-47272799	MCF-7	breast:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
12	CEBPB	chr1:47272347-47272776	ECC-1	luminal epithelium:	n/a	chr1:47272566-47272577 chr1:47272565-47272578
13	CTCF	chr1:47278520-47278670	GM12872	blood:	n/a	chr1:47278531-47278540
14	CTCF	chr1:47272919-47272921	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:47272878-47272978	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:47272840-47272990	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr1:47272820-47272970	HepG2	liver:	n/a	n/a
18	CTCF	chr1:47272840-47272990	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:47272960-47273110	NHEK	skin:	n/a	n/a
20	CTCF	chr1:47272400-47272550	NHEK	skin:	n/a	n/a
21	CTCF	chr1:47272860-47272917	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:47272077-47272151	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr1:47272820-47272970	Caco-2	colon:	n/a	n/a
24	CTCF	chr1:47272860-47273010	SAEC	small airway:	n/a	n/a
25	CTCF	chr1:47272920-47273070	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:47272920-47273070	NHEK	skin:	n/a	n/a
27	E2F4	chr1:47271897-47271911	MCF10A-Er-Src	breast:	n/a	n/a
28	EBF1	chr1:47278124-47278273	GM12878	blood:	n/a	chr1:47278159-47278170
29	ELF1	chr1:47272335-47272757	MCF-7	breast:	n/a	chr1:47272463-47272474
30	EP300	chr1:47272929-47273386	T-47D	breast:	n/a	n/a
31	EP300	chr1:47272987-47273371	T-47D	breast:	n/a	n/a
32	EP300	chr1:47272353-47272699	T-47D	breast:	n/a	chr1:47272662-47272678 chr1:47272459-47272473
33	FOS	chr1:47283999-47284062	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:47272199-47272662	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:47272313-47272600	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:47272232-47272741	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:47272171-47272710	MCF10A-Er-Src	breast:	n/a	chr1:47272180-47272187
38	FOXA1	chr1:47267838-47268136	HepG2	liver:	n/a	n/a
39	FOXA1	chr1:47267870-47268105	HepG2	liver:	n/a	n/a
40	FOXA1	chr1:47267902-47268101	HepG2	liver:	n/a	n/a
41	FOXA2	chr1:47267894-47268077	HepG2	liver:	n/a	n/a
42	GATA3	chr1:47269914-47270772	MCF-7	breast:	n/a	n/a
43	GATA3	chr1:47270099-47270516	MCF-7	breast:	n/a	n/a
44	GATA3	chr1:47272955-47273509	T-47D	breast:	n/a	chr1:47272971-47272983 chr1:47272972-47272982 chr1:47272969-47272985 chr1:47272972-47272981
45	GATA3	chr1:47272274-47272887	MCF-7	breast:	n/a	chr1:47272461-47272471
46	GATA3	chr1:47272964-47273424	T-47D	breast:	n/a	chr1:47272971-47272983 chr1:47272972-47272982 chr1:47272969-47272985 chr1:47272972-47272981
47	GATA3	chr1:47270093-47270440	T-47D	breast:	n/a	n/a
48	GATA3	chr1:47272200-47272701	T-47D	breast:	n/a	chr1:47272461-47272471
49	IRF3	chr1:47281323-47281462	GM12878	blood:	n/a	n/a
50	JUND	chr1:47283848-47284106	HepG2	liver:	n/a	chr1:47284073-47284081 chr1:47284071-47284083 chr1:47284074-47284081 chr1:47284072-47284081 chr1:47284073-47284082 chr1:47283938-47283947

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47264866-47264916	HEEpiC	esophagus:	n/a
2	chr1:47264866-47264916	HEEpiC	esophagus:	n/a
3	chr1:47264866-47264916	Hepatocyte	liver:	n/a
4	chr1:47264866-47264916	PFSK-1	brain:	n/a
5	chr1:47279985-47280035	U87	brain:	n/a
6	chr1:47279985-47280035	Caco-2	colon:	n/a
7	chr1:47284627-47284677	HUVEC	blood vessel:	n/a
8	chr1:47284627-47284677	HRPEpiC	eye:	n/a
9	chr1:47264866-47264916	Caco-2	colon:	n/a
10	chr1:47284627-47284677	T-47D	breast:	n/a
11	chr1:47279985-47280035	NB4	blood:	n/a
12	chr1:47279985-47280035	SK-N-SH	brain:	n/a
13	chr1:47284627-47284677	HIPEpiC	eye:	n/a
14	chr1:47279985-47280035	MCF10A-Er-Src	breast:	n/a
15	chr1:47279985-47280035	HRE	kidney:	n/a
16	chr1:47284627-47284677	HEEpiC	esophagus:	n/a
17	chr1:47264866-47264916	A549	lung:	n/a
18	chr1:47264601-47264651	ECC-1	luminal epithelium:	n/a
19	chr1:47279985-47280035	ECC-1	luminal epithelium:	n/a
20	chr1:47264866-47264916	HCT-116	colon:	n/a
21	chr1:47284627-47284677	HAEpiC	amniotic membrane:	n/a
22	chr1:47284627-47284677	GM06990	blood:	n/a
23	chr1:47279985-47280035	NH-A	brain:	n/a
24	chr1:47279985-47280035	LNCaP	prostate:	n/a
25	chr1:47284627-47284677	RPTEC	kidney:	n/a
26	chr1:47264601-47264651	PFSK-1	brain:	n/a
27	chr1:47284627-47284677	LNCaP	prostate:	n/a
28	chr1:47284627-47284677	A549	lung:	n/a
29	chr1:47279985-47280035	GM12891	blood:	n/a
30	chr1:47264601-47264651	IMR90	lung:	fetal
31	chr1:47284627-47284677	AG04450	lung:	fetal
32	chr1:47284627-47284677	MCF10A-Er-Src	breast:	n/a
33	chr1:47264866-47264916	H1-hESC	embryonic stem cell:	embryo
34	chr1:47279985-47280035	SK-N-MC	brain:	n/a
35	chr1:47284627-47284677	GM12891	blood:	n/a
36	chr1:47284627-47284677	MCF-7	breast:	n/a
37	chr1:47279985-47280035	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:47279985-47280035	BE2_C	brain:	n/a
39	chr1:47284627-47284677	AG10803	skin:	n/a
40	chr1:47264866-47264916	GM12891	blood:	n/a
41	chr1:47279985-47280035	ovcar-3	ovarian:	n/a
42	chr1:47284627-47284677	AG09309	skin:	n/a
43	chr1:47284627-47284677	HNPCEpiC	eye:	n/a
44	chr1:47279985-47280035	PFSK-1	brain:	n/a
45	chr1:47264601-47264651	RPTEC	kidney:	n/a
46	chr1:47279985-47280035	NT2-D1	testis:	n/a
47	chr1:47264601-47264651	HCT-116	colon:	n/a
48	chr1:47264866-47264916	CMK	blood:	n/a
49	chr1:47264601-47264651	AG09319	gingival:	n/a
50	chr1:47264866-47264916	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:47221048..47223209-chr1:47267479..47269912,2	MCF-7	breast:
2	chr1:47263919..47266818-chr1:47267658..47269946,3	MCF-7	breast:
3	chr1:47272192..47274421-chr1:47282299..47283950,2	K562	blood:
4	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:
5	chr1:47275758..47278616-chr1:47280662..47283634,2	K562	blood:
6	chr1:47270918..47272980-chr1:47278589..47280565,2	K562	blood:
7	chr1:47272192..47274421-chr1:47282299..47283950,2	K562	blood:
8	chr1:47264251..47266259-chr1:47267707..47269923,2	K562	blood:
9	chr1:47266762..47268483-chr1:47274674..47276282,2	MCF-7	breast:
10	chr1:47274872..47277380-chr1:47277423..47279681,2	K562	blood:
11	chr1:47263957..47267463-chr1:47271063..47272982,3	MCF-7	breast:
12	chr1:47266762..47268483-chr1:47274674..47276282,2	MCF-7	breast:
13	chr1:47263957..47267463-chr1:47271063..47272982,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATPAF1-AS1-2	chr1:47276480-47276522	NONHSAT003037

Variant related genes	Relation type
CYP4B1	TF binding region
CYP4B1	CpG island
ENSG00000142973	chromatin interactions

Extended variants
information (count: 978 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs632233	chr1:47264205-47264206	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536110900	chr1:47264281-47264282	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145084805	chr1:47264295-47264296	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572669450	chr1:47264305-47264306	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147172929	chr1:47264324-47264325	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540087945	chr1:47264333-47264334	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558667027	chr1:47264357-47264358	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4646476	chr1:47264409-47264410	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs140472026	chr1:47264423-47264424	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs186167427	chr1:47264480-47264481	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574351718	chr1:47264484-47264485	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541679752	chr1:47264489-47264490	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554195570	chr1:47264491-47264492	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs632133	chr1:47264495-47264496	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs527479974	chr1:47264546-47264547	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs551981961	chr1:47264557-47264558	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564407373	chr1:47264562-47264563	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531805116	chr1:47264585-47264586	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550009861	chr1:47264602-47264603	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs113772992	chr1:47264660-47264661	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568403985	chr1:47264663-47264664	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546482796	chr1:47264688-47264689	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190883747	chr1:47264720-47264721	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2297813	chr1:47264724-47264725	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs558294422	chr1:47264735-47264736	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576580507	chr1:47264740-47264741	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113351559	chr1:47264765-47264766	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs111476033	chr1:47264766-47264767	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs555992529	chr1:47264820-47264821	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183371507	chr1:47264826-47264827	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200131677	chr1:47264829-47264830	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs367935135	chr1:47264833-47264834	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs55672106	chr1:47264856-47264857	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553628563	chr1:47264857-47264858	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576666017	chr1:47264892-47264893	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs45522235	chr1:47264900-47264901	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs55642000	chr1:47264930-47264931	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377260959	chr1:47264946-47264947	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs45518538	chr1:47264947-47264948	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs34257324	chr1:47264959-47264960	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200775315	chr1:47264977-47264978	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs367641755	chr1:47264978-47264979	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56181920	chr1:47264991-47264992	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562089850	chr1:47265017-47265018	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs45628233	chr1:47265024-47265025	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527721711	chr1:47265087-47265088	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566097590	chr1:47265193-47265194	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs151216427	chr1:47265217-47265218	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs3766210	chr1:47265268-47265269	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs3766209	chr1:47265273-47265274	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:93)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47263600-47264600	Enhancers	Esophagus	oesophagus
2	chr1:47263600-47264600	Weak transcription	Gastric	stomach
3	chr1:47263600-47264600	Weak transcription	Lung	lung
4	chr1:47263600-47264800	Enhancers	Duodenum Mucosa	Duodenum
5	chr1:47263600-47264800	Enhancers	NHEK	skin
6	chr1:47263600-47265400	Enhancers	Fetal Intestine Small	intestine
7	chr1:47263800-47264400	Enhancers	Adipose Nuclei	Adipose
8	chr1:47263800-47264600	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr1:47264000-47265200	Enhancers	Stomach Mucosa	stomach
10	chr1:47264200-47264400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:47264200-47265200	Enhancers	Right Atrium	heart
12	chr1:47264400-47265200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:47264400-47265800	Flanking Active TSS	Adipose Nuclei	Adipose
14	chr1:47264600-47264800	Flanking Active TSS	Esophagus	oesophagus
15	chr1:47264600-47264800	Enhancers	Fetal Muscle Leg	muscle
16	chr1:47264600-47264800	Enhancers	Lung	lung
17	chr1:47264600-47264800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
18	chr1:47264600-47265000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
19	chr1:47264600-47265600	Enhancers	Gastric	stomach
20	chr1:47264600-47265600	Bivalent/Poised TSS	Psoas Muscle	Psoas
21	chr1:47264600-47269200	Active TSS	Left Ventricle	heart
22	chr1:47264800-47265000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:47264800-47265000	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr1:47264800-47265200	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr1:47264800-47265200	Flanking Active TSS	Lung	lung
26	chr1:47264800-47265600	Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr1:47264800-47265800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
28	chr1:47264800-47266800	Active TSS	Esophagus	oesophagus
29	chr1:47265000-47265400	Active TSS	Duodenum Mucosa	Duodenum
30	chr1:47265000-47265600	Active TSS	Colon Smooth Muscle	Colon
31	chr1:47265000-47265600	Enhancers	Pancreas	Pancrea
32	chr1:47265000-47265600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
33	chr1:47265000-47265600	Active TSS	Spleen	Spleen
34	chr1:47265200-47265600	Flanking Active TSS	Right Atrium	heart
35	chr1:47265200-47265800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:47265200-47267200	Active TSS	Lung	lung
37	chr1:47265200-47267400	Weak transcription	Stomach Mucosa	stomach
38	chr1:47265400-47268600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr1:47265400-47271400	Weak transcription	Fetal Intestine Small	intestine
40	chr1:47265600-47265800	Active TSS	Right Atrium	heart
41	chr1:47265600-47266400	Weak transcription	Colon Smooth Muscle	Colon
42	chr1:47265600-47268800	Active TSS	Psoas Muscle	Psoas
43	chr1:47265600-47271800	Weak transcription	Spleen	Spleen
44	chr1:47265600-47279200	Weak transcription	Gastric	stomach
45	chr1:47265800-47266400	Active TSS	Adipose Nuclei	Adipose
46	chr1:47265800-47269800	Weak transcription	Right Atrium	heart
47	chr1:47266400-47266800	Enhancers	Colon Smooth Muscle	Colon
48	chr1:47266400-47269200	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr1:47266400-47273800	Enhancers	Placenta	Placenta
50	chr1:47266800-47267200	Flanking Active TSS	Esophagus	oesophagus

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