Variant report

Variant	esv3408226
Chromosome Location	chr1:151343628-151348026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:226)
CpG islands
(count:611)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:226 , 50 per page) page: 1 2 3 4 5

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	chr1:151343717-151344423	MCF-7	breast:	n/a	n/a
7	CEBPB	chr1:151343727-151344343	A549	lung:	n/a	n/a
8	CEBPB	chr1:151343930-151344227	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr1:151343887-151344177	A549	lung:	n/a	n/a
10	CEBPB	chr1:151344013-151344228	HepG2	liver:	n/a	n/a
11	CEBPB	chr1:151343900-151344212	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:151345110-151345191	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:151343830-151344269	A549	lung:	n/a	n/a
14	CEBPB	chr1:151343870-151344239	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:151343801-151344575	MCF-7	breast:	n/a	n/a
16	CEBPB	chr1:151343916-151344209	K562	blood:	n/a	n/a
17	CEBPB	chr1:151343793-151344161	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPD	chr1:151344908-151345336	HepG2	liver:	n/a	n/a
19	CHD2	chr1:151344940-151345279	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:151344788-151345205	K562	blood:	n/a	n/a
21	CHD2	chr1:151343912-151344137	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr1:151344895-151345278	HepG2	liver:	n/a	n/a
23	CHD2	chr1:151344802-151345336	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr1:151345102-151345128	K562	blood:	n/a	n/a
25	E2F4	chr1:151345107-151345366	MCF10A-Er-Src	breast:	n/a	n/a
26	ELF1	chr1:151344958-151345310	K562	blood:	n/a	n/a
27	ELF1	chr1:151344616-151345497	MCF-7	breast:	n/a	n/a
28	ELF1	chr1:151344794-151345574	MCF-7	breast:	n/a	n/a
29	ELF1	chr1:151344949-151345359	HepG2	liver:	n/a	n/a
30	ELF1	chr1:151345003-151345295	HepG2	liver:	n/a	n/a
31	ELK1	chr1:151344998-151345267	Hela-S3	cervix:	n/a	n/a
32	EP300	chr1:151345000-151345292	K562	blood:	n/a	n/a
33	EP300	chr1:151344943-151345359	HepG2	liver:	n/a	n/a
34	EP300	chr1:151344311-151344555	SK-N-SH_RA	brain:	n/a	chr1:151344515-151344529
35	EP300	chr1:151344254-151344706	T-47D	breast:	n/a	chr1:151344515-151344529
36	EP300	chr1:151344820-151345451	T-47D	breast:	n/a	n/a
37	EP300	chr1:151345094-151345290	HepG2	liver:	n/a	n/a
38	EP300	chr1:151344923-151345476	T-47D	breast:	n/a	n/a
39	EP300	chr1:151344328-151344546	SK-N-SH_RA	brain:	n/a	chr1:151344515-151344529
40	FOS	chr1:151343882-151344117	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:151345166-151345328	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:151343863-151344114	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:151344023-151344086	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL2	chr1:151343811-151344172	A549	lung:	n/a	n/a
45	FOXA1	chr1:151344997-151345453	T-47D	breast:	n/a	n/a
46	FOXA1	chr1:151344992-151345500	HepG2	liver:	n/a	n/a
47	FOXA1	chr1:151345136-151345397	ECC-1	luminal epithelium:	n/a	n/a
48	FOXA1	chr1:151343810-151344003	ECC-1	luminal epithelium:	n/a	chr1:151343912-151343927
49	FOXA1	chr1:151345011-151345466	HepG2	liver:	n/a	n/a
50	FOXA1	chr1:151345019-151345382	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151346122-151346172	Caco-2	colon:	n/a
2	chr1:151346122-151346172	Caco-2	colon:	n/a
3	chr1:151343840-151343890	GM12892	blood:	n/a
4	chr1:151343840-151343890	CMK	blood:	n/a
5	chr1:151345123-151345173	HEK293	kidney:	embryo
6	chr1:151345173-151345223	AG09309	skin:	n/a
7	chr1:151344806-151344856	SK-N-SH_RA	brain:	n/a
8	chr1:151345248-151345298	BJ	skin:	n/a
9	chr1:151344806-151344856	MCF-7	breast:	n/a
10	chr1:151346048-151346098	NHDF-neo	bronchial:	n/a
11	chr1:151346400-151346450	BJ	skin:	n/a
12	chr1:151343840-151343890	HIPEpiC	eye:	n/a
13	chr1:151344806-151344856	Caco-2	colon:	n/a
14	chr1:151345181-151345231	AG04449	skin:	fetal
15	chr1:151346048-151346098	MCF-7	breast:	n/a
16	chr1:151345173-151345223	HRE	kidney:	n/a
17	chr1:151345248-151345298	K562	blood:	n/a
18	chr1:151345173-151345223	T-47D	breast:	n/a
19	chr1:151346122-151346172	BJ	skin:	n/a
20	chr1:151345173-151345223	ovcar-3	ovarian:	n/a
21	chr1:151345181-151345231	Caco-2	colon:	n/a
22	chr1:151345771-151345821	PrEC	prostate:	n/a
23	chr1:151344806-151344856	NB4	blood:	n/a
24	chr1:151346122-151346172	BE2_C	brain:	n/a
25	chr1:151345248-151345298	HEEpiC	esophagus:	n/a
26	chr1:151345123-151345173	SK-N-MC	brain:	n/a
27	chr1:151346048-151346098	A549	lung:	n/a
28	chr1:151345181-151345231	Hela-S3	cervix:	n/a
29	chr1:151345173-151345223	ECC-1	luminal epithelium:	n/a
30	chr1:151346400-151346450	NH-A	brain:	n/a
31	chr1:151346048-151346098	SK-N-SH_RA	brain:	n/a
32	chr1:151345181-151345231	T-47D	breast:	n/a
33	chr1:151345771-151345821	AG04450	lung:	fetal
34	chr1:151346122-151346172	GM12892	blood:	n/a
35	chr1:151345248-151345298	Hela-S3	cervix:	n/a
36	chr1:151345123-151345173	HRPEpiC	eye:	n/a
37	chr1:151346122-151346172	HRE	kidney:	n/a
38	chr1:151346400-151346450	SK-N-SH_RA	brain:	n/a
39	chr1:151345173-151345223	HAEpiC	amniotic membrane:	n/a
40	chr1:151345181-151345231	RPTEC	kidney:	n/a
41	chr1:151345123-151345173	NHBE	bronchial:	n/a
42	chr1:151345123-151345173	SK-N-SH_RA	brain:	n/a
43	chr1:151345181-151345231	NHBE	bronchial:	n/a
44	chr1:151344806-151344856	HMEC	breast:	n/a
45	chr1:151345173-151345223	H1-hESC	embryonic stem cell:	embryo
46	chr1:151344806-151344856	SK-N-MC	brain:	n/a
47	chr1:151343840-151343890	Caco-2	colon:	n/a
48	chr1:151346122-151346172	HAEpiC	amniotic membrane:	n/a
49	chr1:151345248-151345298	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:151343840-151343890	NHDF-neo	bronchial:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:151312776..151315996-chr1:151344524..151347605,3	MCF-7	breast:
2	chr1:151342317..151344601-chr1:151346109..151347990,3	MCF-7	breast:
3	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
4	chr1:151253287..151255470-chr1:151344558..151346132,2	MCF-7	breast:
5	chr1:151298626..151300231-chr1:151342802..151344473,2	K562	blood:
6	chr1:151265006..151266786-chr1:151342988..151344589,2	MCF-7	breast:
7	chr1:151317585..151319121-chr1:151341611..151344384,2	MCF-7	breast:
8	chr1:151319321..151320903-chr1:151345990..151347846,2	MCF-7	breast:
9	chr1:151298918..151301246-chr1:151343671..151345334,3	MCF-7	breast:
10	chr1:151340911..151342650-chr1:151344414..151346132,2	K562	blood:
11	chr1:151319574..151321193-chr1:151343801..151346115,3	MCF-7	breast:
12	chr1:151334136..151338213-chr1:151347669..151350682,3	MCF-7	breast:
13	1:151333184-151350267..1:151592347-151603110	K562	blood:
14	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
15	chr1:151316826..151319751-chr1:151342092..151344070,3	MCF-7	breast:
16	chr1:151340916..151343487-chr1:151343853..151346001,2	MCF-7	breast:
17	chr1:151311947..151315930-chr1:151341715..151344576,4	K562	blood:
18	chr1:151298391..151300174-chr1:151343656..151346785,4	MCF-7	breast:
19	chr1:151343373..151350462-chr1:151369795..151376328,11	MCF-7	breast:
20	1:151171193-151178589..1:151333184-151350267	GM12878	blood:
21	chr1:151340503..151343136-chr1:151343197..151345914,3	K562	blood:
22	chr1:151161951..151163611-chr1:151344546..151346783,2	MCF-7	breast:

No data

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

Extended variants
information (count: 177 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:177 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532848585	chr1:151343631-151343632	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs546329058	chr1:151343733-151343734	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs61818028	chr1:151343758-151343759	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs201943696	chr1:151343764-151343765	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs535058930	chr1:151343810-151343811	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs567372268	chr1:151343840-151343841	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs555352770	chr1:151343871-151343872	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs569023880	chr1:151343880-151343881	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs375797467	chr1:151343886-151343887	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs553659478	chr1:151343888-151343889	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs112048640	chr1:151343900-151343901	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs144905663	chr1:151343913-151343914	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs116271000	chr1:151343914-151343915	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs557908967	chr1:151343994-151343995	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs553553026	chr1:151344091-151344092	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs2769265	chr1:151344150-151344151	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs373896823	chr1:151344224-151344225	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs541821920	chr1:151344240-151344241	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs552827532	chr1:151344252-151344253	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs116765491	chr1:151344281-151344282	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs531086031	chr1:151344319-151344320	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs544538782	chr1:151344344-151344345	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs377727302	chr1:151344352-151344353	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs564329950	chr1:151344368-151344369	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs116299544	chr1:151344373-151344374	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs377655064	chr1:151344439-151344440	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs538292199	chr1:151344443-151344444	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs562245595	chr1:151344459-151344460	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs140824562	chr1:151344460-151344461	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs78635692	chr1:151344475-151344476	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs190549948	chr1:151344488-151344489	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs529001271	chr1:151344489-151344490	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs149319693	chr1:151344527-151344528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs72710114	chr1:151344539-151344540	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538125006	chr1:151344571-151344572	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs377510931	chr1:151344596-151344597	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs80025007	chr1:151344616-151344617	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs369542318	chr1:151344627-151344628	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs571466856	chr1:151344690-151344691	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs4970950	chr1:151344703-151344704	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs554023941	chr1:151344715-151344716	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs573227279	chr1:151344718-151344719	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs186854289	chr1:151344719-151344720	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs2769264	chr1:151344741-151344742	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
45	rs575634506	chr1:151344768-151344769	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs148032969	chr1:151344771-151344772	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	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
48	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
49	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
50	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

Variant related diseases (count:117)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151335000-151344600	Weak transcription	Fetal Kidney	kidney
2	chr1:151335400-151344400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:151335600-151344400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:151336200-151344600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:151336200-151344600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:151336800-151344600	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:151337000-151344400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:151337000-151344400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr1:151337000-151344600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr1:151337200-151344800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr1:151338200-151344200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:151338400-151344400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr1:151338600-151344600	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr1:151338800-151344400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:151339200-151344200	Weak transcription	Aorta	Aorta
16	chr1:151339200-151344400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:151339400-151344400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:151339400-151344400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:151339800-151344000	Enhancers	Ovary	ovary
20	chr1:151339800-151344400	Enhancers	Placenta	Placenta
21	chr1:151340000-151344000	Weak transcription	Fetal Brain Male	brain
22	chr1:151340000-151344200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:151340200-151343800	Enhancers	Brain Anterior Caudate	brain
24	chr1:151340200-151344400	Enhancers	Left Ventricle	heart
25	chr1:151340600-151344200	Enhancers	Brain Hippocampus Middle	brain
26	chr1:151340600-151344600	Enhancers	Pancreas	Pancrea
27	chr1:151341600-151344800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:151341800-151344200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr1:151341800-151344800	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr1:151341800-151345200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:151342000-151344000	Enhancers	Right Atrium	heart
32	chr1:151342000-151344200	Enhancers	Fetal Intestine Large	intestine
33	chr1:151342000-151344400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr1:151342000-151344400	Enhancers	Fetal Muscle Leg	muscle
35	chr1:151342000-151344800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr1:151342200-151343800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:151342200-151344000	Enhancers	Fetal Lung	lung
38	chr1:151342200-151344200	Enhancers	Brain Cingulate Gyrus	brain
39	chr1:151342200-151344400	Enhancers	Psoas Muscle	Psoas
40	chr1:151342200-151344400	Enhancers	NHDF-Ad	bronchial
41	chr1:151342200-151344800	Enhancers	Fetal Heart	heart
42	chr1:151342200-151345400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr1:151342400-151344000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:151342400-151344000	Enhancers	Brain Germinal Matrix	brain
45	chr1:151342400-151344000	Enhancers	A549	lung
46	chr1:151342400-151344200	Enhancers	Fetal Muscle Trunk	muscle
47	chr1:151342400-151345000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:151342400-151345800	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr1:151342400-151346400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:151342400-151346600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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