Variant report

Variant	nsv546167
Chromosome Location	chr1:47487585-47524264
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	chr1:47489244-47489445	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:47506533-47506550	GM12878	blood:	n/a	n/a
3	BRCA1	chr1:47489311-47489598	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:47492324-47492550	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:47498926-47499218	A549	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
6	CEBPB	chr1:47498905-47499216	HepG2	liver:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
7	CEBPB	chr1:47498927-47499225	IMR90	lung:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
8	CEBPB	chr1:47498941-47499139	H1-hESC	embryonic stem cell:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
9	CEBPB	chr1:47498924-47499142	MCF-7	breast:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
10	CEBPB	chr1:47498947-47499243	K562	blood:	n/a	chr1:47499069-47499078 chr1:47499064-47499081 chr1:47499069-47499078 chr1:47499069-47499078 chr1:47499067-47499080
11	CEBPB	chr1:47496150-47496401	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr1:47489249-47489669	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr1:47516976-47517025	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:47517421-47517424	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr1:47488920-47489070	HEK293	kidney:	n/a	n/a
16	CTCF	chr1:47496049-47496142	GM13976	blood:	n/a	n/a
17	E2F4	chr1:47514515-47514687	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr1:47496815-47497060	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F6	chr1:47488602-47489632	H1-hESC	embryonic stem cell:	n/a	chr1:47489442-47489454 chr1:47489421-47489433
20	EP300	chr1:47494713-47494732	GM12878	blood:	n/a	n/a
21	EP300	chr1:47496644-47497159	MCF-7	breast:	n/a	chr1:47496970-47496979
22	EP300	chr1:47510195-47510295	GM12878	blood:	n/a	n/a
23	EP300	chr1:47509773-47509852	GM12878	blood:	n/a	n/a
24	ESR1	chr1:47496642-47497041	T-47D	breast:	n/a	n/a
25	ESR1	chr1:47496642-47497098	T-47D	breast:	n/a	n/a
26	ESR1	chr1:47496713-47497050	T-47D	breast:	n/a	n/a
27	FOS	chr1:47496042-47497616	MCF10A-Er-Src	breast:	n/a	chr1:47496302-47496311 chr1:47496302-47496312 chr1:47496304-47496311 chr1:47496303-47496312 chr1:47496301-47496313 chr1:47496303-47496311 chr1:47496301-47496312
28	FOS	chr1:47496142-47497054	MCF10A-Er-Src	breast:	n/a	chr1:47496302-47496311 chr1:47496302-47496312 chr1:47496304-47496311 chr1:47496303-47496312 chr1:47496301-47496313 chr1:47496303-47496311 chr1:47496301-47496312
29	FOS	chr1:47495268-47495468	MCF10A-Er-Src	breast:	n/a	chr1:47495452-47495464
30	FOS	chr1:47498054-47498760	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr1:47514675-47514684	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:47497336-47497536	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:47496748-47497514	HUVEC	blood vessel:	n/a	n/a
34	FOS	chr1:47496016-47497620	MCF10A-Er-Src	breast:	n/a	chr1:47496302-47496311 chr1:47496302-47496312 chr1:47496304-47496311 chr1:47496303-47496312 chr1:47496301-47496313 chr1:47496303-47496311 chr1:47496301-47496312
35	FOS	chr1:47495862-47497618	MCF10A-Er-Src	breast:	n/a	chr1:47496302-47496311 chr1:47496302-47496312 chr1:47496304-47496311 chr1:47496303-47496312 chr1:47496301-47496313 chr1:47496303-47496311 chr1:47496301-47496312
36	FOS	chr1:47497970-47498816	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:47496170-47496529	HUVEC	blood vessel:	n/a	chr1:47496302-47496311 chr1:47496302-47496312 chr1:47496304-47496311 chr1:47496303-47496312 chr1:47496301-47496313 chr1:47496303-47496311 chr1:47496301-47496312
38	FOS	chr1:47498078-47498782	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr1:47501685-47501939	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:47498087-47498668	MCF10A-Er-Src	breast:	n/a	n/a
41	FOXA1	chr1:47496647-47497013	T-47D	breast:	n/a	chr1:47496856-47496871
42	FOXA1	chr1:47496702-47497040	A549	lung:	n/a	chr1:47496856-47496871
43	FOXA1	chr1:47501059-47501450	HepG2	liver:	n/a	n/a
44	FOXA1	chr1:47496720-47496995	HepG2	liver:	n/a	chr1:47496856-47496871
45	FOXA1	chr1:47496729-47497135	T-47D	breast:	n/a	chr1:47496856-47496871
46	FOXA1	chr1:47496767-47497073	HepG2	liver:	n/a	chr1:47496856-47496871
47	FOXA1	chr1:47501186-47501419	HepG2	liver:	n/a	n/a
48	FOXA1	chr1:47496719-47497080	A549	lung:	n/a	chr1:47496856-47496871
49	FOXA1	chr1:47501171-47501475	HepG2	liver:	n/a	n/a
50	FOXA1	chr1:47501185-47501480	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:47489413-47489463	LNCaP	prostate:	n/a
2	chr1:47489776-47489826	Jurkat	blood:	n/a
3	chr1:47489776-47489826	HRE	kidney:	n/a
4	chr1:47488111-47488161	CMK	blood:	n/a
5	chr1:47514752-47514802	PANC-1	pancreas:	n/a
6	chr1:47488111-47488161	BE2_C	brain:	n/a
7	chr1:47488934-47488984	GM12891	blood:	n/a
8	chr1:47488757-47488807	T-47D	breast:	n/a
9	chr1:47514752-47514802	HCT-116	colon:	n/a
10	chr1:47488256-47488306	AG09319	gingival:	n/a
11	chr1:47489195-47489245	Caco-2	colon:	n/a
12	chr1:47489776-47489826	HAEpiC	amniotic membrane:	n/a
13	chr1:47493419-47493469	Hepatocyte	liver:	n/a
14	chr1:47488757-47488807	SAEC	small airway:	n/a
15	chr1:47488757-47488807	GM06990	blood:	n/a
16	chr1:47488934-47488984	T-47D	breast:	n/a
17	chr1:47514752-47514802	SKMC	muscle:	n/a
18	chr1:47489543-47489593	RPTEC	kidney:	n/a
19	chr1:47493419-47493469	MCF10A-Er-Src	breast:	n/a
20	chr1:47489413-47489463	PANC-1	pancreas:	n/a
21	chr1:47488934-47488984	GM12878	blood:	n/a
22	chr1:47489543-47489593	HAEpiC	amniotic membrane:	n/a
23	chr1:47514752-47514802	AG04450	lung:	fetal
24	chr1:47489413-47489463	GM12892	blood:	n/a
25	chr1:47488256-47488306	GM12878	blood:	n/a
26	chr1:47488256-47488306	HRE	kidney:	n/a
27	chr1:47514752-47514802	SK-N-SH	brain:	n/a
28	chr1:47489413-47489463	Hepatocyte	liver:	n/a
29	chr1:47489539-47489589	NT2-D1	testis:	n/a
30	chr1:47514752-47514802	GM12892	blood:	n/a
31	chr1:47488934-47488984	LNCaP	prostate:	n/a
32	chr1:47493419-47493469	HRCEpiC	kidney:	n/a
33	chr1:47489282-47489332	HRPEpiC	eye:	n/a
34	chr1:47488111-47488161	AG09309	skin:	n/a
35	chr1:47489539-47489589	AG04450	lung:	fetal
36	chr1:47489282-47489332	GM06990	blood:	n/a
37	chr1:47489282-47489332	HAEpiC	amniotic membrane:	n/a
38	chr1:47489543-47489593	AG09309	skin:	n/a
39	chr1:47489776-47489826	H1-hESC	embryonic stem cell:	embryo
40	chr1:47489195-47489245	GM06990	blood:	n/a
41	chr1:47488111-47488161	AoSMC	blood vessel:	n/a
42	chr1:47488757-47488807	PrEC	prostate:	n/a
43	chr1:47493419-47493469	HEEpiC	esophagus:	n/a
44	chr1:47489195-47489245	AG04449	skin:	fetal
45	chr1:47493419-47493469	HEK293	kidney:	embryo
46	chr1:47488256-47488306	AG10803	skin:	n/a
47	chr1:47488256-47488306	HCT-116	colon:	n/a
48	chr1:47489539-47489589	ovcar-3	ovarian:	n/a
49	chr1:47489282-47489332	BE2_C	brain:	n/a
50	chr1:47489539-47489589	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:47481637..47484566-chr1:47494285..47496054,2	K562	blood:
2	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
3	chr1:47497049..47498622-chr1:47515812..47517726,2	MCF-7	breast:
4	chr1:47489896..47492133-chr1:47492275..47494697,2	K562	blood:
5	chr1:47497049..47498622-chr1:47515812..47517726,2	MCF-7	breast:
6	chr1:47500877..47503360-chr1:47503581..47505847,2	K562	blood:

Variant related genes	Relation type
CYP4X1	TF binding region
CYP4X1	CpG island
ENSG00000186377	chromatin interactions

Extended variants
information (count: 1326 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1326 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1021827	chr1:47487585-47487586	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140606319	chr1:47487588-47487589	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs532224561	chr1:47487592-47487593	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs74073803	chr1:47487666-47487667	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs138218759	chr1:47487697-47487698	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs116162165	chr1:47487703-47487704	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs542131400	chr1:47487761-47487762	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs17102950	chr1:47487804-47487805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568164954	chr1:47487833-47487834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377128877	chr1:47487834-47487835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563499596	chr1:47487908-47487909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374750731	chr1:47487940-47487941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149603780	chr1:47487942-47487943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373500038	chr1:47487953-47487954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112142147	chr1:47487954-47487955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375016182	chr1:47487955-47487956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11352280	chr1:47487981-47487982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs180895295	chr1:47488023-47488024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568774847	chr1:47488050-47488051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374296045	chr1:47488053-47488054	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs564196827	chr1:47488108-47488109	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs529325658	chr1:47488112-47488113	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs538442737	chr1:47488119-47488120	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs139318767	chr1:47488120-47488121	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs575076659	chr1:47488248-47488249	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs536399998	chr1:47488351-47488352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554627990	chr1:47488455-47488456	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200761621	chr1:47488481-47488482	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373268668	chr1:47488487-47488488	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557064744	chr1:47488539-47488540	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs543072146	chr1:47488544-47488545	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs9326152	chr1:47488569-47488570	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs74730229	chr1:47488592-47488593	Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs540193226	chr1:47488668-47488669	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs565057452	chr1:47488695-47488696	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs375702412	chr1:47488726-47488727	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143342117	chr1:47488745-47488746	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs147347575	chr1:47488765-47488766	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs139495089	chr1:47488781-47488782	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs74073804	chr1:47488791-47488792	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs548309404	chr1:47488798-47488799	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs114992673	chr1:47488877-47488878	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs142560466	chr1:47488992-47488993	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs78030163	chr1:47488996-47488997	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs2055498	chr1:47489001-47489002	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185545195	chr1:47489037-47489038	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538579453	chr1:47489072-47489073	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs150525877	chr1:47489233-47489234	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs191352151	chr1:47489259-47489260	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536043584	chr1:47489268-47489269	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Squamous cell cancer	19001599	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47484400-47489000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:47484800-47487600	Enhancers	Aorta	Aorta
3	chr1:47487000-47487800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
4	chr1:47487200-47487800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:47487200-47487800	Enhancers	Adipose Nuclei	Adipose
6	chr1:47487200-47487800	Enhancers	Right Atrium	heart
7	chr1:47487400-47487600	Enhancers	Liver	Liver
8	chr1:47487400-47487600	Enhancers	Fetal Muscle Trunk	muscle
9	chr1:47487400-47487800	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr1:47487400-47487800	Enhancers	Lung	lung
11	chr1:47487400-47487800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr1:47487400-47488600	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr1:47487600-47487800	Enhancers	Left Ventricle	heart
14	chr1:47487600-47488800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:47487600-47489000	Weak transcription	Aorta	Aorta
16	chr1:47487800-47488600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:47487800-47488800	Weak transcription	Adipose Nuclei	Adipose
18	chr1:47487800-47489000	Weak transcription	Liver	Liver
19	chr1:47487800-47489200	Weak transcription	Lung	lung
20	chr1:47487800-47489200	Weak transcription	Right Atrium	heart
21	chr1:47488400-47488600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
22	chr1:47488600-47488800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr1:47488600-47488800	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr1:47488600-47489000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr1:47488600-47489200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
26	chr1:47488600-47489600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
27	chr1:47488800-47489000	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
28	chr1:47488800-47489000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr1:47488800-47489000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
30	chr1:47488800-47489000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
31	chr1:47488800-47489000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
32	chr1:47488800-47489000	Flanking Bivalent TSS/Enh	Brain Angular Gyrus	brain
33	chr1:47488800-47489000	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr1:47488800-47489000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr1:47488800-47489000	Bivalent/Poised TSS	Fetal Brain Male	brain
36	chr1:47488800-47489000	Bivalent Enhancer	Fetal Brain Female	brain
37	chr1:47488800-47489000	Bivalent Enhancer	Fetal Kidney	kidney
38	chr1:47488800-47489000	Enhancers	Psoas Muscle	Psoas
39	chr1:47488800-47489000	Bivalent Enhancer	Stomach Mucosa	stomach
40	chr1:47488800-47489000	Bivalent Enhancer	HUVEC	blood vessel
41	chr1:47488800-47489200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:47488800-47489200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
43	chr1:47488800-47489200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
44	chr1:47488800-47489200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
45	chr1:47488800-47489200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:47488800-47489200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
47	chr1:47488800-47489200	Bivalent Enhancer	Left Ventricle	heart
48	chr1:47488800-47489200	Enhancers	Pancreas	Pancrea
49	chr1:47488800-47489200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr1:47488800-47489400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach

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