Variant report

Variant	nsv428524
Chromosome Location	chr8:130731660-130894467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2219)
CpG islands
(count:918)
Chromatin interactive
region (count:56)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:2219 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130738533-130738902	K562	blood:	n/a	n/a
2	ARID3A	chr8:130734277-130734292	K562	blood:	n/a	n/a
3	ARID3A	chr8:130740929-130741022	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:130848514-130848551	K562	blood:	n/a	n/a
5	ARID3A	chr8:130838550-130838860	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:130738547-130738921	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:130740874-130741037	K562	blood:	n/a	n/a
8	ATF1	chr8:130852963-130852975	K562	blood:	n/a	n/a
9	ATF1	chr8:130837611-130837969	K562	blood:	n/a	n/a
10	ATF2	chr8:130838376-130838826	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr8:130838408-130838788	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:130764218-130764642	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:130765606-130766143	K562	blood:	n/a	n/a
14	BACH1	chr8:130764273-130764563	K562	blood:	n/a	n/a
15	BACH1	chr8:130765562-130766043	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:130830587-130830844	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:130738640-130738754	K562	blood:	n/a	n/a
18	BACH1	chr8:130765247-130765348	K562	blood:	n/a	n/a
19	BATF	chr8:130869600-130869857	GM12878	blood:	n/a	chr8:130869749-130869760
20	BCL3	chr8:130850326-130851676	A549	lung:	n/a	n/a
21	BCLAF1	chr8:130838456-130838808	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:130738532-130738794	K562	blood:	n/a	n/a
23	BHLHE40	chr8:130832512-130832647	K562	blood:	n/a	n/a
24	BHLHE40	chr8:130838466-130838746	GM12878	blood:	n/a	n/a
25	BRCA1	chr8:130799219-130799663	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr8:130894457-130895096	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr8:130810532-130811031	K562	blood:	n/a	n/a
28	CBX3	chr8:130832074-130832738	K562	blood:	n/a	n/a
29	CBX3	chr8:130838282-130838834	K562	blood:	n/a	n/a
30	CBX3	chr8:130810676-130810995	K562	blood:	n/a	n/a
31	CBX3	chr8:130795919-130796248	HCT-116	colon:	n/a	n/a
32	CBX3	chr8:130807970-130808279	K562	blood:	n/a	n/a
33	CBX3	chr8:130807988-130808275	K562	blood:	n/a	n/a
34	CBX3	chr8:130843864-130844189	K562	blood:	n/a	n/a
35	CCNT2	chr8:130847562-130847775	K562	blood:	n/a	n/a
36	CEBPB	chr8:130878464-130878686	K562	blood:	n/a	chr8:130878567-130878576 chr8:130878567-130878576 chr8:130878565-130878578 chr8:130878567-130878576 chr8:130878567-130878578 chr8:130878565-130878578 chr8:130878565-130878576 chr8:130878567-130878578 chr8:130878567-130878576
37	CEBPB	chr8:130741910-130742100	K562	blood:	n/a	n/a
38	CEBPB	chr8:130860999-130861512	Hela-S3	cervix:	n/a	chr8:130861232-130861243 chr8:130861230-130861243
39	CEBPB	chr8:130799829-130800094	HepG2	liver:	n/a	chr8:130799923-130799934
40	CEBPB	chr8:130878384-130878717	IMR90	lung:	n/a	chr8:130878567-130878576 chr8:130878567-130878576 chr8:130878565-130878578 chr8:130878567-130878576 chr8:130878567-130878578 chr8:130878565-130878578 chr8:130878565-130878576 chr8:130878567-130878578 chr8:130878567-130878576
41	CEBPB	chr8:130838452-130838802	A549	lung:	n/a	n/a
42	CEBPB	chr8:130756313-130756661	HepG2	liver:	n/a	chr8:130756486-130756497
43	CEBPB	chr8:130765137-130765947	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr8:130889841-130889868	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:130741824-130742759	IMR90	lung:	n/a	n/a
46	CEBPB	chr8:130741823-130742196	A549	lung:	n/a	n/a
47	CEBPB	chr8:130799198-130799649	MCF-7	breast:	n/a	chr8:130799436-130799447
48	CEBPB	chr8:130878357-130878726	HepG2	liver:	n/a	chr8:130878567-130878576 chr8:130878567-130878576 chr8:130878565-130878578 chr8:130878567-130878576 chr8:130878567-130878578 chr8:130878565-130878578 chr8:130878565-130878576 chr8:130878567-130878578 chr8:130878567-130878576
49	CEBPB	chr8:130799213-130799623	ECC-1	luminal epithelium:	n/a	chr8:130799436-130799447
50	CEBPB	chr8:130799128-130799604	ECC-1	luminal epithelium:	n/a	chr8:130799436-130799447

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130869842-130869892	HEK293	kidney:	embryo
2	chr8:130799007-130799057	IMR90	lung:	fetal
3	chr8:130838513-130838563	ovcar-3	ovarian:	n/a
4	chr8:130869842-130869892	HEK293	kidney:	embryo
5	chr8:130799007-130799057	IMR90	lung:	fetal
6	chr8:130838513-130838563	ovcar-3	ovarian:	n/a
7	chr8:130845536-130845586	NHDF-neo	bronchial:	n/a
8	chr8:130877076-130877126	A549	lung:	n/a
9	chr8:130799851-130799901	PANC-1	pancreas:	n/a
10	chr8:130845536-130845586	K562	blood:	n/a
11	chr8:130832237-130832287	ECC-1	luminal epithelium:	n/a
12	chr8:130877076-130877126	PFSK-1	brain:	n/a
13	chr8:130799851-130799901	AG04450	lung:	fetal
14	chr8:130845536-130845586	HCT-116	colon:	n/a
15	chr8:130738823-130738873	Jurkat	blood:	n/a
16	chr8:130869842-130869892	HMEC	breast:	n/a
17	chr8:130832237-130832287	HEEpiC	esophagus:	n/a
18	chr8:130738823-130738873	BE2_C	brain:	n/a
19	chr8:130869842-130869892	PFSK-1	brain:	n/a
20	chr8:130869842-130869892	NHDF-neo	bronchial:	n/a
21	chr8:130838629-130838679	HAEpiC	amniotic membrane:	n/a
22	chr8:130799007-130799057	AG04450	lung:	fetal
23	chr8:130869842-130869892	SK-N-SH_RA	brain:	n/a
24	chr8:130838629-130838679	AG04449	skin:	fetal
25	chr8:130869842-130869892	GM12891	blood:	n/a
26	chr8:130838432-130838482	HEK293	kidney:	embryo
27	chr8:130838883-130838933	Hepatocyte	liver:	n/a
28	chr8:130799093-130799143	AoSMC	blood vessel:	n/a
29	chr8:130838432-130838482	AG04450	lung:	fetal
30	chr8:130869842-130869892	U87	brain:	n/a
31	chr8:130760646-130760696	AG09309	skin:	n/a
32	chr8:130861109-130861159	HNPCEpiC	eye:	n/a
33	chr8:130861109-130861159	GM19239	blood:	n/a
34	chr8:130832237-130832287	MCF-7	breast:	n/a
35	chr8:130861109-130861159	MCF-7	breast:	n/a
36	chr8:130845536-130845586	PrEC	prostate:	n/a
37	chr8:130799007-130799057	HCF	heart:	n/a
38	chr8:130799093-130799143	U87	brain:	n/a
39	chr8:130838513-130838563	T-47D	breast:	n/a
40	chr8:130760646-130760696	SK-N-MC	brain:	n/a
41	chr8:130799093-130799143	HepG2	liver:	n/a
42	chr8:130838883-130838933	BJ	skin:	n/a
43	chr8:130832237-130832287	GM06990	blood:	n/a
44	chr8:130832237-130832287	SK-N-MC	brain:	n/a
45	chr8:130838432-130838482	HCM	heart:	n/a
46	chr8:130838432-130838482	HNPCEpiC	eye:	n/a
47	chr8:130845536-130845586	AG04450	lung:	fetal
48	chr8:130838513-130838563	U87	brain:	n/a
49	chr8:130832237-130832287	LNCaP	prostate:	n/a
50	chr8:130838513-130838563	HNPCEpiC	eye:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:130685068..130686753-chr8:130736730..130739405,2	K562	blood:
2	chr8:130889604..130891485-chr8:130894789..130897188,2	K562	blood:
3	chr8:130884702..130887738-chr8:130891037..130893861,3	K562	blood:
4	chr8:130732259..130735444-chr8:130737069..130741081,4	K562	blood:
5	chr8:130830092..130833014-chr8:130837793..130842091,3	K562	blood:
6	chr8:130593091..130595640-chr8:130733142..130736387,3	K562	blood:
7	chr8:130850096..130852746-chr8:130854534..130856077,2	K562	blood:
8	chr8:130847403..130850109-chr8:130853585..130856096,3	K562	blood:
9	chr8:130852731..130855092-chr8:130855258..130857778,2	MCF-7	breast:
10	chr7:132179184..132180204-chr8:130838562..130839258,3	MCF-7	breast:
11	chr8:130777382..130781561-chr8:130783248..130785671,3	K562	blood:
12	chr8:130830602..130833613-chr8:131027054..131030013,3	K562	blood:
13	chr8:130847403..130850109-chr8:130853585..130856096,3	K562	blood:
14	chr8:130838576..130840911-chr8:130898985..130901514,2	K562	blood:
15	chr8:130854054..130855784-chr8:130863665..130866483,2	MCF-7	breast:
16	chr8:130760414..130761002-chr8:130838183..130839066,2	MCF-7	breast:
17	chr8:130724777..130726937-chr8:130738994..130740773,2	K562	blood:
18	chr8:130777382..130781561-chr8:130783248..130785671,3	K562	blood:
19	chr8:130854054..130855784-chr8:130863665..130866483,2	MCF-7	breast:
20	chr8:130884702..130887738-chr8:130891037..130893861,3	K562	blood:
21	chr8:130870152..130872253-chr8:130876163..130877875,2	K562	blood:
22	chr8:130812388..130815875-chr8:130817210..130819491,3	MCF-7	breast:
23	chr8:128747171..128749323-chr8:130738753..130740305,2	MCF-7	breast:
24	chr8:130850282..130852746-chr8:130853910..130856034,2	K562	blood:
25	chr8:130870326..130872535-chr8:130878958..130881566,2	K562	blood:
26	chr8:130850096..130852746-chr8:130854534..130856077,2	K562	blood:
27	chr8:130868089..130870715-chr8:130884298..130886456,2	K562	blood:
28	chr8:130830092..130833014-chr8:130837793..130842091,3	K562	blood:
29	chr8:130760414..130761002-chr8:130838183..130839066,2	MCF-7	breast:
30	chr8:130778949..130780935-chr8:130781435..130782937,2	K562	blood:
31	chr8:130685068..130688410-chr8:130735715..130739405,3	K562	blood:
32	chr8:130778949..130780935-chr8:130781435..130782937,2	K562	blood:
33	chr8:130831390..130833613-chr8:131027128..131030013,2	K562	blood:
34	chr8:130699541..130700041-chr8:130738268..130738843,2	K562	blood:
35	chr8:130738688..130740229-chr8:130741129..130743486,2	K562	blood:
36	chr8:130832873..130834634-chr8:130872875..130874898,2	K562	blood:
37	chr8:130761153..130763630-chr8:130764649..130766910,2	K562	blood:
38	chr8:130694163..130694944-chr8:130737903..130739156,3	MCF-7	breast:
39	chr8:128747251..128749651-chr8:130737243..130738948,2	K562	blood:
40	chr8:130699941..130700716-chr8:130738329..130738842,2	MCF-7	breast:
41	chr8:130876185..130878507-chr8:130883790..130886588,3	K562	blood:
42	chr8:130709093..130710072-chr8:130738277..130738889,2	MCF-7	breast:
43	chr8:128748018..128748536-chr8:130738676..130739207,2	K562	blood:
44	chr8:130838362..130839036-chr8:130903623..130904767,5	MCF-7	breast:
45	chr8:130838375..130838938-chr8:130903507..130904182,2	MCF-7	breast:
46	chr8:130868089..130870715-chr8:130884298..130886456,2	K562	blood:
47	chr8:130844452..130847212-chr8:130849205..130851282,2	K562	blood:
48	chr8:130850282..130852746-chr8:130853910..130856034,2	K562	blood:
49	chr8:130888893..130890759-chr8:130891255..130893461,2	K562	blood:
50	chr8:130852434..130855409-chr8:130857919..130860602,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM49B-3	chr8:130764944-130765003	NONHSAT129132
2	lnc-MYC-16	chr8:130740990-130741553	NONHSAT129131
3	lnc-EFR3A-6	chr8:130852146-130852313	ENSG00000254317.1
4	lnc-EFR3A-6	chr8:130844547-130844675	ENSG00000254317.1
5	lnc-EFR3A-6	chr8:130856131-130856750	ENSG00000254317.1
6	lnc-MYC-16	chr8:130742355-130742691	NONHSAT129131
7	lnc-MYC-16	chr8:130742037-130742257	NONHSAT129131
8	lnc-EFR3A-11	chr8:130876724-130877298	NONHSAT129136
9	lnc-FAM49B-3	chr8:130764352-130764393	NONHSAT129132
10	lnc-FAM49B-3	chr8:130763954-130764137	NONHSAT129132

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM49B	hsa-miR-590-3p	chr8:130853738-130853757
2	FAM49B	hsa-miR-590-3p	chr8:130854095-130854115
3	FAM49B	hsa-miR-27a-3p	chr8:130853801-130853822
4	FAM49B	hsa-miR-590-3p	chr8:130854116-130854136
5	FAM49B	hsa-miR-26b-5p	chr8:130854105-130854123
6	FAM49B	hsa-miR-27a-3p	chr8:130854110-130854130
7	FAM49B	hsa-let-7b-5p	chr8:130854297-130854317
8	FAM49B	hsa-miR-128-3p	chr8:130853940-130853960
9	FAM49B	hsa-miR-27a-3p	chr8:130853939-130853956
10	FAM49B	hsa-miR-26b-5p	chr8:130854110-130854104

Variant related genes	Relation type
ENSG00000243402	TF binding region
ENSG00000200075	TF binding region
FAM49B	TF binding region
GSDMC	TF binding region
ENSG00000224110	TF binding region
ENSG00000254317	TF binding region
ENSG00000243402	CpG island
ENSG00000200075	CpG island
FAM49B	CpG island
GSDMC	CpG island
ENSG00000224110	CpG island
ENSG00000254317	CpG island
ENSG00000243402	chromatin interactions
ENSG00000254317	chromatin interactions
ENSG00000200075	chromatin interactions
ENSG00000153310	chromatin interactions
ENSG00000147697	chromatin interactions
ENSG00000224110	chromatin interactions
ENSG00000136997	chromatin interactions

Extended variants
information (count: 6362 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:6362 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527487180	chr8:130731846-130731847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147253990	chr8:130731849-130731850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75059698	chr8:130731850-130731851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531484823	chr8:130731862-130731863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550019621	chr8:130731890-130731891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567977937	chr8:130731900-130731901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530733483	chr8:130731909-130731910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535386949	chr8:130731930-130731931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142939500	chr8:130731942-130731943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185155551	chr8:130731980-130731981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13251654	chr8:130732017-130732018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs557918879	chr8:130732019-130732020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376239646	chr8:130732023-130732024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35730494	chr8:130732029-130732030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148460159	chr8:130732034-130732035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189910679	chr8:130732041-130732042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181179786	chr8:130732075-130732076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541370274	chr8:130732086-130732087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34901866	chr8:130732163-130732164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78558794	chr8:130732230-130732231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559934283	chr8:130732262-130732263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs4733729	chr8:130732295-130732296	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs4733730	chr8:130732353-130732354	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564294740	chr8:130732410-130732411	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531498169	chr8:130732421-130732422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549815320	chr8:130732427-130732428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs57931547	chr8:130732447-130732448	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528925506	chr8:130732476-130732477	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546976516	chr8:130732517-130732518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565475475	chr8:130732526-130732527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs539127856	chr8:130732588-130732589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115271498	chr8:130732607-130732608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142549681	chr8:130732635-130732636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4733731	chr8:130732672-130732673	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571436022	chr8:130732689-130732690	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116356367	chr8:130732708-130732709	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541477723	chr8:130732717-130732718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553381237	chr8:130732725-130732726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs386729975	chr8:130732729-130732730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs186705626	chr8:130732735-130732736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs386729976	chr8:130732739-130732740	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs7831774	chr8:130732740-130732741	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs564323840	chr8:130732751-130732752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561872027	chr8:130732759-130732760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529168564	chr8:130732812-130732813	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34667627	chr8:130732813-130732814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7815332	chr8:130732820-130732821	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs558948502	chr8:130732846-130732847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532734781	chr8:130732855-130732856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191541360	chr8:130732856-130732857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Gastric cancer	22014070	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130723200-130734600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:130723400-130740400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:130733800-130734800	Enhancers	K562	blood
4	chr8:130734000-130735000	Enhancers	HSMMtube	muscle
5	chr8:130734600-130735400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:130734600-130735400	Enhancers	Osteobl	bone
7	chr8:130734800-130735600	Enhancers	A549	lung
8	chr8:130734800-130737200	Weak transcription	K562	blood
9	chr8:130735400-130738400	Weak transcription	Osteobl	bone
10	chr8:130735400-130742600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr8:130735600-130737200	Weak transcription	A549	lung
12	chr8:130737200-130739200	Enhancers	A549	lung
13	chr8:130737200-130740800	Enhancers	K562	blood
14	chr8:130737800-130738600	Enhancers	Fetal Heart	heart
15	chr8:130738000-130739200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:130738200-130738400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:130738200-130739000	Enhancers	Dnd41	blood
18	chr8:130738200-130739000	Enhancers	HUVEC	blood vessel
19	chr8:130738200-130739400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr8:130738200-130744200	Weak transcription	Esophagus	oesophagus
21	chr8:130738400-130738600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr8:130738400-130738600	Enhancers	Brain Angular Gyrus	brain
23	chr8:130738400-130738800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:130738400-130738800	Enhancers	Fetal Muscle Leg	muscle
25	chr8:130738400-130739000	Enhancers	Fetal Lung	lung
26	chr8:130738400-130739200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:130738400-130739200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:130738400-130739200	Enhancers	Osteobl	bone
29	chr8:130738400-130739400	Enhancers	NHEK	skin
30	chr8:130738600-130739400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:130738800-130739400	Enhancers	NHLF	lung
32	chr8:130739200-130739400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr8:130739200-130742200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr8:130739200-130742600	Weak transcription	Osteobl	bone
35	chr8:130739200-130742800	Weak transcription	A549	lung
36	chr8:130739400-130742000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:130739400-130742000	Weak transcription	NHEK	skin
38	chr8:130739400-130742000	Weak transcription	NHLF	lung
39	chr8:130739800-130740000	Active TSS	Spleen	Spleen
40	chr8:130740000-130745000	Weak transcription	Spleen	Spleen
41	chr8:130740400-130741200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:130740800-130741200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:130741200-130742000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:130742000-130742200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr8:130742000-130743000	Flanking Active TSS	NHEK	skin
46	chr8:130742000-130743200	Enhancers	NHLF	lung
47	chr8:130742000-130743400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr8:130742000-130743800	Enhancers	HMEC	breast
49	chr8:130742000-130744200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr8:130742200-130742600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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