Variant report

Variant	esv3423838
Chromosome Location	chr1:151344778-151347276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:176)
CpG islands
(count:550)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:176 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151345015-151345215	HepG2	liver:	n/a	n/a
2	BCL3	chr1:151345733-151346070	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:151345650-151345906	HepG2	liver:	n/a	n/a
4	BHLHE40	chr1:151344946-151345289	K562	blood:	n/a	n/a
5	BRCA1	chr1:151345169-151345211	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:151345110-151345191	HepG2	liver:	n/a	n/a
7	CEBPD	chr1:151344908-151345336	HepG2	liver:	n/a	n/a
8	CHD2	chr1:151344802-151345336	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr1:151344788-151345205	K562	blood:	n/a	n/a
10	CHD2	chr1:151344940-151345279	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr1:151344895-151345278	HepG2	liver:	n/a	n/a
12	CTCF	chr1:151345102-151345128	K562	blood:	n/a	n/a
13	E2F4	chr1:151345107-151345366	MCF10A-Er-Src	breast:	n/a	n/a
14	ELF1	chr1:151344949-151345359	HepG2	liver:	n/a	n/a
15	ELF1	chr1:151344616-151345497	MCF-7	breast:	n/a	n/a
16	ELF1	chr1:151344958-151345310	K562	blood:	n/a	n/a
17	ELF1	chr1:151344794-151345574	MCF-7	breast:	n/a	n/a
18	ELF1	chr1:151345003-151345295	HepG2	liver:	n/a	n/a
19	ELK1	chr1:151344998-151345267	Hela-S3	cervix:	n/a	n/a
20	EP300	chr1:151345000-151345292	K562	blood:	n/a	n/a
21	EP300	chr1:151344820-151345451	T-47D	breast:	n/a	n/a
22	EP300	chr1:151344923-151345476	T-47D	breast:	n/a	n/a
23	EP300	chr1:151344943-151345359	HepG2	liver:	n/a	n/a
24	EP300	chr1:151345094-151345290	HepG2	liver:	n/a	n/a
25	FOS	chr1:151345166-151345328	MCF10A-Er-Src	breast:	n/a	n/a
26	FOXA1	chr1:151344997-151345453	T-47D	breast:	n/a	n/a
27	FOXA1	chr1:151345074-151345454	HepG2	liver:	n/a	n/a
28	FOXA1	chr1:151345019-151345382	HepG2	liver:	n/a	n/a
29	FOXA1	chr1:151345011-151345466	HepG2	liver:	n/a	n/a
30	FOXA1	chr1:151344992-151345500	HepG2	liver:	n/a	n/a
31	FOXA1	chr1:151345064-151345439	ECC-1	luminal epithelium:	n/a	n/a
32	FOXA1	chr1:151345136-151345397	ECC-1	luminal epithelium:	n/a	n/a
33	FOXA1	chr1:151345028-151345420	T-47D	breast:	n/a	n/a
34	FOXA2	chr1:151344963-151345556	A549	lung:	n/a	n/a
35	FOXA2	chr1:151344992-151345418	HepG2	liver:	n/a	n/a
36	FOXA2	chr1:151344886-151345599	A549	lung:	n/a	n/a
37	FOXP2	chr1:151345049-151345339	PFSK-1	brain:	n/a	n/a
38	GATA3	chr1:151344850-151345396	T-47D	breast:	n/a	n/a
39	GTF2B	chr1:151345003-151345246	K562	blood:	n/a	n/a
40	GTF2F1	chr1:151344976-151345301	Hela-S3	cervix:	n/a	n/a
41	GTF2F1	chr1:151345127-151345269	H1-hESC	embryonic stem cell:	n/a	n/a
42	HCFC1	chr1:151345055-151345186	K562	blood:	n/a	n/a
43	HDAC2	chr1:151343764-151345417	MCF-7	breast:	n/a	n/a
44	HDAC2	chr1:151344937-151345359	HepG2	liver:	n/a	n/a
45	HEY1	chr1:151344949-151345342	K562	blood:	n/a	n/a
46	HEY1	chr1:151344846-151345367	HepG2	liver:	n/a	n/a
47	HEY1	chr1:151344896-151345296	HepG2	liver:	n/a	n/a
48	HEY1	chr1:151344426-151344801	HepG2	liver:	n/a	n/a
49	HNF4A	chr1:151344980-151345318	HepG2	liver:	n/a	chr1:151345128-151345143
50	HNF4A	chr1:151344883-151345324	HepG2	liver:	n/a	chr1:151345128-151345143

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151346122-151346172	GM19239	blood:	n/a
2	chr1:151346122-151346172	GM19239	blood:	n/a
3	chr1:151345248-151345298	U87	brain:	n/a
4	chr1:151345771-151345821	GM12878	blood:	n/a
5	chr1:151346400-151346450	ovcar-3	ovarian:	n/a
6	chr1:151345181-151345231	MCF10A-Er-Src	breast:	n/a
7	chr1:151346400-151346450	HIPEpiC	eye:	n/a
8	chr1:151345771-151345821	SK-N-SH_RA	brain:	n/a
9	chr1:151346122-151346172	HMEC	breast:	n/a
10	chr1:151345248-151345298	GM19239	blood:	n/a
11	chr1:151346048-151346098	SK-N-SH_RA	brain:	n/a
12	chr1:151344806-151344856	PFSK-1	brain:	n/a
13	chr1:151345123-151345173	HCM	heart:	n/a
14	chr1:151345771-151345821	HRPEpiC	eye:	n/a
15	chr1:151346400-151346450	AoSMC	blood vessel:	n/a
16	chr1:151345771-151345821	H1-hESC	embryonic stem cell:	embryo
17	chr1:151345248-151345298	LNCaP	prostate:	n/a
18	chr1:151345123-151345173	ProgFib	skin:	n/a
19	chr1:151345771-151345821	HCT-116	colon:	n/a
20	chr1:151345248-151345298	HepG2	liver:	n/a
21	chr1:151346122-151346172	GM12878	blood:	n/a
22	chr1:151344806-151344856	HL-60	blood:	n/a
23	chr1:151345123-151345173	PFSK-1	brain:	n/a
24	chr1:151346048-151346098	RPTEC	kidney:	n/a
25	chr1:151345248-151345298	GM12892	blood:	n/a
26	chr1:151345123-151345173	GM06990	blood:	n/a
27	chr1:151346122-151346172	AG09309	skin:	n/a
28	chr1:151345181-151345231	HRE	kidney:	n/a
29	chr1:151346400-151346450	LNCaP	prostate:	n/a
30	chr1:151345181-151345231	PANC-1	pancreas:	n/a
31	chr1:151345248-151345298	NH-A	brain:	n/a
32	chr1:151344806-151344856	PANC-1	pancreas:	n/a
33	chr1:151345771-151345821	NHDF-neo	bronchial:	n/a
34	chr1:151346400-151346450	HL-60	blood:	n/a
35	chr1:151346048-151346098	AG09309	skin:	n/a
36	chr1:151345771-151345821	Jurkat	blood:	n/a
37	chr1:151346048-151346098	MCF10A-Er-Src	breast:	n/a
38	chr1:151345248-151345298	H1-hESC	embryonic stem cell:	embryo
39	chr1:151345771-151345821	HNPCEpiC	eye:	n/a
40	chr1:151345181-151345231	PFSK-1	brain:	n/a
41	chr1:151346400-151346450	GM19239	blood:	n/a
42	chr1:151346048-151346098	HNPCEpiC	eye:	n/a
43	chr1:151345248-151345298	RPTEC	kidney:	n/a
44	chr1:151346122-151346172	HCM	heart:	n/a
45	chr1:151345173-151345223	HEK293	kidney:	embryo
46	chr1:151345173-151345223	AG04450	lung:	fetal
47	chr1:151345181-151345231	U87	brain:	n/a
48	chr1:151345248-151345298	A549	lung:	n/a
49	chr1:151345771-151345821	RPTEC	kidney:	n/a
50	chr1:151344806-151344856	HIPEpiC	eye:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151298918..151301246-chr1:151343671..151345334,3	MCF-7	breast:
2	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
3	chr1:151342317..151344601-chr1:151346109..151347990,3	MCF-7	breast:
4	chr1:151312776..151315996-chr1:151344524..151347605,3	MCF-7	breast:
5	chr1:151161951..151163611-chr1:151344546..151346783,2	MCF-7	breast:
6	chr1:151340911..151342650-chr1:151344414..151346132,2	K562	blood:
7	chr1:151319574..151321193-chr1:151343801..151346115,3	MCF-7	breast:
8	chr1:151319321..151320903-chr1:151345990..151347846,2	MCF-7	breast:
9	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
10	chr1:151343373..151350462-chr1:151369795..151376328,11	MCF-7	breast:
11	chr1:151340503..151343136-chr1:151343197..151345914,3	K562	blood:
12	chr1:151253287..151255470-chr1:151344558..151346132,2	MCF-7	breast:
13	1:151171193-151178589..1:151333184-151350267	GM12878	blood:
14	chr1:151298391..151300174-chr1:151343656..151346785,4	MCF-7	breast:
15	chr1:151340916..151343487-chr1:151343853..151346001,2	MCF-7	breast:
16	1:151333184-151350267..1:151592347-151603110	K562	blood:

No data

Variant related genes	Relation type
SELENBP1	TF binding region
SELENBP1	CpG island
ENSG00000273481	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000143393	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564390477	chr1:151344821-151344822	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs12118866	chr1:151344824-151344825	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs141702929	chr1:151344912-151344913	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs560760993	chr1:151344949-151344950	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs528959572	chr1:151344959-151344960	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs549098705	chr1:151344979-151344980	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs562338383	chr1:151344996-151344997	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs189706623	chr1:151345014-151345015	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs551401945	chr1:151345026-151345027	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs115507791	chr1:151345119-151345120	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs369142667	chr1:151345124-151345125	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs534100112	chr1:151345133-151345134	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs373378022	chr1:151345134-151345135	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs377599512	chr1:151345143-151345144	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs370957781	chr1:151345146-151345147	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs375756111	chr1:151345147-151345148	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs567484849	chr1:151345158-151345159	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs535568732	chr1:151345170-151345171	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs370549770	chr1:151345173-151345174	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs533568866	chr1:151345182-151345183	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs575651684	chr1:151345188-151345189	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
22	rs541497096	chr1:151345226-151345227	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
23	rs142051862	chr1:151345233-151345234	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs557747214	chr1:151345235-151345236	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs577889841	chr1:151345247-151345248	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs540552864	chr1:151345248-151345249	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs79368523	chr1:151345273-151345274	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs112023460	chr1:151345317-151345318	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs574219262	chr1:151345324-151345325	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs147155214	chr1:151345339-151345340	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs367673803	chr1:151345340-151345341	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs370352786	chr1:151345345-151345346	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs375953718	chr1:151345377-151345378	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs573100549	chr1:151345378-151345379	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs542127869	chr1:151345381-151345382	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs3976736	chr1:151345398-151345399	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs200745274	chr1:151345399-151345400	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs140298034	chr1:151345423-151345424	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs551365442	chr1:151345424-151345425	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs564899857	chr1:151345445-151345446	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs527565151	chr1:151345521-151345522	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs185120851	chr1:151345667-151345668	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs567345730	chr1:151345756-151345757	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs562500008	chr1:151345765-151345766	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs536398907	chr1:151345799-151345800	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs146372586	chr1:151345858-151345859	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs549717117	chr1:151345872-151345873	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs112820469	chr1:151345874-151345875	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs537971615	chr1:151345903-151345904	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs557710358	chr1:151345904-151345905	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151337200-151344800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:151341600-151344800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:151341800-151344800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:151341800-151345200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:151342000-151344800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:151342200-151344800	Enhancers	Fetal Heart	heart
7	chr1:151342200-151345400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr1:151342400-151345000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:151342400-151345800	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr1:151342400-151346400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:151342400-151346600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:151343000-151345200	Flanking Active TSS	Liver	Liver
13	chr1:151343200-151346600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr1:151343400-151345200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:151343600-151345200	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr1:151343600-151345400	Active TSS	Colonic Mucosa	Colon
17	chr1:151343600-151346400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr1:151343800-151344800	Flanking Active TSS	Duodenum Mucosa	Duodenum
19	chr1:151343800-151344800	Enhancers	HSMM	muscle
20	chr1:151343800-151345000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:151343800-151345200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:151343800-151345200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr1:151343800-151345400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:151343800-151345400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:151343800-151345400	Flanking Active TSS	Hela-S3	cervix
26	chr1:151343800-151345400	Flanking Active TSS	Osteobl	bone
27	chr1:151344000-151345200	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr1:151344000-151345200	Flanking Active TSS	Fetal Intestine Small	intestine
29	chr1:151344000-151345200	Flanking Active TSS	Fetal Stomach	stomach
30	chr1:151344000-151345200	Active TSS	Gastric	stomach
31	chr1:151344000-151345200	Active TSS	Sigmoid Colon	Sigmoid Colon
32	chr1:151344000-151345400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:151344000-151345400	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr1:151344000-151345400	Flanking Active TSS	Ovary	ovary
35	chr1:151344000-151345400	Flanking Active TSS	A549	lung
36	chr1:151344000-151346200	Enhancers	Fetal Brain Male	brain
37	chr1:151344200-151344800	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr1:151344200-151344800	Weak transcription	Spleen	Spleen
39	chr1:151344200-151344800	Enhancers	NH-A	brain
40	chr1:151344200-151345000	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr1:151344200-151345000	Active TSS	Small Intestine	intestine
42	chr1:151344200-151345000	Flanking Active TSS	NHLF	lung
43	chr1:151344200-151345200	Active TSS	Aorta	Aorta
44	chr1:151344200-151345200	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr1:151344200-151345400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:151344200-151345400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:151344200-151345400	Flanking Active TSS	Fetal Muscle Trunk	muscle
48	chr1:151344200-151345400	Flanking Active TSS	Right Ventricle	heart
49	chr1:151344200-151345400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr1:151344200-151345400	Flanking Active TSS	K562	blood

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