Variant report

Variant	nsv887637
Chromosome Location	chr7:12424405-12508894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1523)
CpG islands
(count:917)
Chromatin interactive
region (count:52)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12445132-12445205	K562	blood:	n/a	n/a
2	ARID3A	chr7:12424775-12425636	K562	blood:	n/a	n/a
3	ARID3A	chr7:12442512-12442624	K562	blood:	n/a	n/a
4	ARID3A	chr7:12425885-12425929	K562	blood:	n/a	n/a
5	ARID3A	chr7:12473668-12473988	K562	blood:	n/a	n/a
6	ARID3A	chr7:12498199-12498492	K562	blood:	n/a	n/a
7	ARID3A	chr7:12473648-12473985	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:12428736-12429092	K562	blood:	n/a	n/a
9	ARID3A	chr7:12443002-12443779	K562	blood:	n/a	n/a
10	ARID3A	chr7:12441428-12441976	K562	blood:	n/a	n/a
11	ARID3A	chr7:12498256-12498470	HepG2	liver:	n/a	n/a
12	ATF1	chr7:12442940-12444036	K562	blood:	n/a	n/a
13	ATF1	chr7:12484873-12485016	K562	blood:	n/a	n/a
14	ATF1	chr7:12424857-12425489	K562	blood:	n/a	n/a
15	ATF1	chr7:12441677-12441884	K562	blood:	n/a	n/a
16	ATF1	chr7:12437894-12438340	K562	blood:	n/a	n/a
17	ATF2	chr7:12463437-12464243	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr7:12463290-12464092	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr7:12443361-12443704	K562	blood:	n/a	n/a
20	BACH1	chr7:12443045-12443428	K562	blood:	n/a	n/a
21	BACH1	chr7:12443123-12443675	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr7:12463807-12464153	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr7:12463938-12464115	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCLAF1	chr7:12442724-12444060	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
25	BCLAF1	chr7:12424838-12425482	K562	blood:	n/a	n/a
26	BCLAF1	chr7:12443085-12443960	K562	blood:	n/a	chr7:12443627-12443636 chr7:12443692-12443705
27	BHLHE40	chr7:12441675-12441916	K562	blood:	n/a	n/a
28	BHLHE40	chr7:12431674-12431880	K562	blood:	n/a	n/a
29	BHLHE40	chr7:12442950-12443807	K562	blood:	n/a	n/a
30	BHLHE40	chr7:12444086-12444098	K562	blood:	n/a	n/a
31	BRCA1	chr7:12443076-12443269	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr7:12437595-12438594	K562	blood:	n/a	n/a
33	CBX3	chr7:12424861-12425408	K562	blood:	n/a	n/a
34	CBX3	chr7:12437315-12438267	K562	blood:	n/a	n/a
35	CBX3	chr7:12442888-12444084	K562	blood:	n/a	n/a
36	CBX3	chr7:12442863-12443396	K562	blood:	n/a	n/a
37	CCNT2	chr7:12430237-12430378	K562	blood:	n/a	n/a
38	CCNT2	chr7:12442982-12443788	K562	blood:	n/a	n/a
39	CCNT2	chr7:12432707-12432774	K562	blood:	n/a	n/a
40	CCNT2	chr7:12424779-12425447	K562	blood:	n/a	n/a
41	CEBPB	chr7:12428718-12429069	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:12427225-12427566	K562	blood:	n/a	chr7:12427390-12427401
43	CEBPB	chr7:12428774-12429020	K562	blood:	n/a	n/a
44	CEBPB	chr7:12463236-12464248	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr7:12443418-12444101	K562	blood:	n/a	n/a
46	CEBPB	chr7:12484968-12485143	K562	blood:	n/a	chr7:12485017-12485034 chr7:12485020-12485033 chr7:12485020-12485033 chr7:12485022-12485033 chr7:12485022-12485033
47	CEBPB	chr7:12435084-12435284	HepG2	liver:	n/a	chr7:12435202-12435215 chr7:12435203-12435214 chr7:12435204-12435213 chr7:12435202-12435215 chr7:12435202-12435213
48	CEBPB	chr7:12475774-12475947	A549	lung:	n/a	chr7:12475916-12475927 chr7:12475916-12475927 chr7:12475914-12475927
49	CEBPB	chr7:12427269-12427479	HepG2	liver:	n/a	chr7:12427390-12427401
50	CEBPB	chr7:12428720-12429075	H1-hESC	embryonic stem cell:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12443146-12443196	SK-N-SH_RA	brain:	n/a
2	chr7:12443926-12443976	AG04450	lung:	fetal
3	chr7:12443146-12443196	SK-N-SH_RA	brain:	n/a
4	chr7:12443926-12443976	AG04450	lung:	fetal
5	chr7:12443704-12443754	HRPEpiC	eye:	n/a
6	chr7:12443146-12443196	AG09319	gingival:	n/a
7	chr7:12443880-12443930	HIPEpiC	eye:	n/a
8	chr7:12444115-12444165	NHDF-neo	bronchial:	n/a
9	chr7:12443704-12443754	CMK	blood:	n/a
10	chr7:12443926-12443976	AG04449	skin:	fetal
11	chr7:12444290-12444340	PrEC	prostate:	n/a
12	chr7:12443191-12443241	MCF10A-Er-Src	breast:	n/a
13	chr7:12462597-12462647	Hela-S3	cervix:	n/a
14	chr7:12443542-12443592	HUVEC	blood vessel:	n/a
15	chr7:12444290-12444340	HRE	kidney:	n/a
16	chr7:12443880-12443930	IMR90	lung:	fetal
17	chr7:12444115-12444165	AoSMC	blood vessel:	n/a
18	chr7:12443542-12443592	MCF10A-Er-Src	breast:	n/a
19	chr7:12443704-12443754	HCF	heart:	n/a
20	chr7:12443191-12443241	ECC-1	luminal epithelium:	n/a
21	chr7:12446327-12446377	Caco-2	colon:	n/a
22	chr7:12443146-12443196	LNCaP	prostate:	n/a
23	chr7:12443886-12443936	ovcar-3	ovarian:	n/a
24	chr7:12443704-12443754	AG04450	lung:	fetal
25	chr7:12444095-12444145	HCM	heart:	n/a
26	chr7:12443704-12443754	U87	brain:	n/a
27	chr7:12443191-12443241	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:12443542-12443592	NB4	blood:	n/a
29	chr7:12443886-12443936	BE2_C	brain:	n/a
30	chr7:12443886-12443936	T-47D	breast:	n/a
31	chr7:12443886-12443936	SKMC	muscle:	n/a
32	chr7:12443926-12443976	LNCaP	prostate:	n/a
33	chr7:12443542-12443592	Jurkat	blood:	n/a
34	chr7:12444095-12444145	PANC-1	pancreas:	n/a
35	chr7:12444013-12444063	IMR90	lung:	fetal
36	chr7:12443478-12443528	T-47D	breast:	n/a
37	chr7:12443146-12443196	PANC-1	pancreas:	n/a
38	chr7:12443478-12443528	U87	brain:	n/a
39	chr7:12443478-12443528	A549	lung:	n/a
40	chr7:12443146-12443196	HL-60	blood:	n/a
41	chr7:12444095-12444145	HL-60	blood:	n/a
42	chr7:12443542-12443592	HCT-116	colon:	n/a
43	chr7:12462597-12462647	NB4	blood:	n/a
44	chr7:12462597-12462647	AG04449	skin:	fetal
45	chr7:12443926-12443976	MCF10A-Er-Src	breast:	n/a
46	chr7:12446327-12446377	SKMC	muscle:	n/a
47	chr7:12443542-12443592	HCF	heart:	n/a
48	chr7:12462597-12462647	HUVEC	blood vessel:	n/a
49	chr7:12443191-12443241	Hela-S3	cervix:	n/a
50	chr7:12443880-12443930	NH-A	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
2	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
3	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
4	chr7:12441796..12443703-chr7:12463390..12465045,2	MCF-7	breast:
5	chr7:12423183..12428504-chr7:12441656..12445145,7	K562	blood:
6	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
7	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
8	chr7:12488598..12490554-chr7:12506071..12508415,2	K562	blood:
9	chr7:12476531..12477332-chr7:12536046..12536815,3	MCF-7	breast:
10	chr7:12382799..12385098-chr7:12438700..12441052,2	K562	blood:
11	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
12	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
13	chr7:12421246..12422799-chr7:12438154..12440817,2	K562	blood:
14	chr7:12497629..12498696-chr7:12535919..12536815,4	MCF-7	breast:
15	chr7:12408674..12410212-chr7:12426957..12428907,2	K562	blood:
16	chr7:12488598..12490554-chr7:12506071..12508415,2	K562	blood:
17	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
18	chr7:12426277..12428963-chr7:12530535..12533181,2	K562	blood:
19	chr20:40278409..40280542-chr7:12478341..12480011,2	MCF-7	breast:
20	chr7:12497885..12498702-chr7:12558562..12559343,2	MCF-7	breast:
21	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:
22	chr7:12428351..12429175-chr7:12529458..12530800,4	MCF-7	breast:
23	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
24	chr7:12497632..12498790-chr7:12662958..12664405,3	K562	blood:
25	chr7:12443122..12444791-chr7:12465079..12466887,2	K562	blood:
26	chr7:12480338..12484247-chr7:12487058..12490542,4	K562	blood:
27	chr7:11466869..11467685-chr7:12498254..12498786,2	MCF-7	breast:
28	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
29	chr7:12442216..12444802-chr7:12483847..12486014,2	K562	blood:
30	chr7:12476440..12478383-chr7:12478787..12481785,3	K562	blood:
31	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
32	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
33	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
34	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
35	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
36	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
37	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
38	chr7:12428677..12429434-chr7:12476625..12477415,2	K562	blood:
39	chr7:12496465..12498567-chr7:12529648..12531435,2	K562	blood:
40	chr7:12474073..12478383-chr7:12480165..12482739,4	K562	blood:
41	chr7:12451807..12454928-chr7:12455660..12459229,3	K562	blood:
42	chr7:12479476..12481083-chr7:12493598..12496034,2	K562	blood:
43	chr7:12414352..12417133-chr7:12443944..12445537,2	K562	blood:
44	chr7:12422294..12424938-chr7:12449157..12451879,2	K562	blood:
45	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
46	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
47	chr20:47537945..47538638-chr7:12442691..12443569,2	Hela-S3	cervix:
48	chr7:12446921..12449137-chr7:12452426..12454685,2	K562	blood:
49	chr7:12448538..12450314-chr7:12450779..12453453,2	K562	blood:
50	chr7:12441983..12444239-chr7:12724759..12726454,2	K562	blood:

No data

Variant related genes	Relation type
VWDE	TF binding region
ENSG00000236048	TF binding region
VWDE	CpG island
ENSG00000236048	CpG island
ENSG00000122644	chromatin interactions
ENSG00000226690	chromatin interactions
ENSG00000124198	chromatin interactions
ENSG00000271253	chromatin interactions
ENSG00000203523	chromatin interactions
ENSG00000146530	chromatin interactions

Extended variants
information (count: 3342 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3342 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1036666	chr7:12424405-12424406	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569227223	chr7:12424499-12424500	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552839554	chr7:12424530-12424531	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566231049	chr7:12424540-12424541	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1036667	chr7:12424583-12424584	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs145076129	chr7:12424597-12424598	Weak transcription Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10273416	chr7:12424614-12424615	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs17547818	chr7:12424627-12424628	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs370531155	chr7:12424660-12424661	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151024880	chr7:12424669-12424670	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141064082	chr7:12424697-12424698	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555440637	chr7:12424698-12424699	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78835728	chr7:12424771-12424772	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10550728	chr7:12424786-12424787	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1659987	chr7:12424787-12424788	Weak transcription Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554830579	chr7:12424805-12424806	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538373700	chr7:12424828-12424829	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2159207	chr7:12424861-12424862	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs189814551	chr7:12424863-12424864	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112786375	chr7:12424951-12424952	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs118033296	chr7:12424955-12424956	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs17165968	chr7:12424976-12424977	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs151314419	chr7:12425038-12425039	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540916223	chr7:12425039-12425040	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181865668	chr7:12425053-12425054	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139371087	chr7:12425068-12425069	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560479148	chr7:12425122-12425123	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184938654	chr7:12425123-12425124	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531662358	chr7:12425131-12425132	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs189787850	chr7:12425174-12425175	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548611157	chr7:12425188-12425189	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs376338140	chr7:12425195-12425196	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs370253925	chr7:12425218-12425219	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577888412	chr7:12425230-12425231	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529971641	chr7:12425238-12425239	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546467717	chr7:12425250-12425251	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375307000	chr7:12425269-12425270	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540568533	chr7:12425271-12425272	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566400448	chr7:12425274-12425275	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542338618	chr7:12425284-12425285	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560154987	chr7:12425315-12425316	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs118050237	chr7:12425339-12425340	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180978925	chr7:12425346-12425347	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs954660	chr7:12425352-12425353	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563098950	chr7:12425358-12425359	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554587186	chr7:12425375-12425376	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185199613	chr7:12425388-12425389	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs5882358	chr7:12425430-12425431	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533744329	chr7:12425435-12425436	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs398094834	chr7:12425436-12425437	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12368200-12433200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:12381800-12429000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:12418800-12428600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:12418800-12428600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:12419200-12432800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:12420400-12428200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr7:12420400-12437600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:12422000-12428600	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr7:12422600-12428600	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr7:12422600-12428600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr7:12422800-12425200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr7:12423200-12426800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:12423400-12424600	Strong transcription	Primary hematopoietic stem cells	blood
14	chr7:12424000-12424600	Transcr. at gene 5' and 3'	K562	blood
15	chr7:12424000-12424800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr7:12424200-12425200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:12424200-12434800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:12424400-12426000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr7:12424600-12424800	Active TSS	K562	blood
20	chr7:12424600-12436200	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:12424800-12425000	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr7:12424800-12425200	Flanking Active TSS	K562	blood
23	chr7:12424800-12425400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:12424800-12426200	Enhancers	Fetal Heart	heart
25	chr7:12425000-12425200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:12425000-12426200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:12425000-12426400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:12425200-12425800	Active TSS	K562	blood
29	chr7:12425200-12426000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr7:12425200-12426000	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:12425200-12426200	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr7:12425200-12426800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:12425400-12431000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:12425800-12426000	Transcr. at gene 5' and 3'	K562	blood
35	chr7:12426000-12426400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:12426000-12427600	Genic enhancers	K562	blood
37	chr7:12426000-12428600	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr7:12426000-12428600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
39	chr7:12426000-12430800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr7:12426800-12427600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:12426800-12431200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:12427600-12428800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:12427600-12431400	Strong transcription	K562	blood
44	chr7:12428600-12428800	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:12428600-12428800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr7:12428600-12428800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:12428600-12428800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
48	chr7:12428600-12428800	Genic enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:12428600-12428800	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:12428600-12429000	Genic enhancers	HUES48 Cell Line	embryonic stem cell

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