Variant report

Variant	esv3359712
Chromosome Location	chr8:42994795-42996943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:42995210-42995216	K562	blood:	n/a	n/a
2	ATF3	chr8:42995331-42995646	K562	blood:	n/a	n/a
3	ATF3	chr8:42995383-42995655	K562	blood:	n/a	n/a
4	BACH1	chr8:42996113-42996297	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:42995343-42995655	GM12878	blood:	n/a	n/a
6	BCL3	chr8:42995755-42996243	GM12878	blood:	n/a	chr8:42995818-42995827
7	BCLAF1	chr8:42995611-42996100	GM12878	blood:	n/a	chr8:42995818-42995827
8	BCLAF1	chr8:42995614-42996056	GM12878	blood:	n/a	chr8:42995818-42995827
9	BHLHE40	chr8:42995027-42995593	K562	blood:	n/a	chr8:42995275-42995291
10	BHLHE40	chr8:42994973-42996085	GM12878	blood:	n/a	chr8:42995275-42995291 chr8:42996016-42996032
11	BHLHE40	chr8:42995802-42996307	K562	blood:	n/a	chr8:42996016-42996032
12	BRCA1	chr8:42995249-42995263	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr8:42995709-42995776	HepG2	liver:	n/a	n/a
14	BRCA1	chr8:42995017-42995619	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr8:42995197-42995529	K562	blood:	n/a	n/a
16	CCNT2	chr8:42995265-42996603	K562	blood:	n/a	n/a
17	CEBPB	chr8:42996322-42996826	ECC-1	luminal epithelium:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
18	CEBPB	chr8:42996353-42997082	K562	blood:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
19	CEBPB	chr8:42996007-42996024	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:42996792-42997132	MCF-7	breast:	n/a	chr8:42996953-42996966
21	CEBPB	chr8:42996351-42996967	HepG2	liver:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
22	CEBPB	chr8:42996430-42996791	MCF-7	breast:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
23	CEBPB	chr8:42996431-42996669	HepG2	liver:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
24	CEBPB	chr8:42996385-42996769	HepG2	liver:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
25	CEBPB	chr8:42994856-42995118	HepG2	liver:	n/a	chr8:42994983-42994994
26	CEBPB	chr8:42996457-42996749	ECC-1	luminal epithelium:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
27	CEBPB	chr8:42996361-42997101	HepG2	liver:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
28	CEBPB	chr8:42994814-42997147	Hela-S3	cervix:	n/a	chr8:42994983-42994994 chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
29	CEBPB	chr8:42996448-42996766	A549	lung:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
30	CEBPB	chr8:42996380-42997104	A549	lung:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
31	CEBPB	chr8:42996389-42996735	MCF-7	breast:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
32	CEBPB	chr8:42996371-42997130	H1-hESC	embryonic stem cell:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
33	CEBPB	chr8:42996356-42997128	IMR90	lung:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
34	CEBPB	chr8:42996160-42997203	A549	lung:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559 chr8:42996953-42996966
35	CEBPB	chr8:42996426-42996702	K562	blood:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
36	CEBPB	chr8:42996370-42996826	K562	blood:	n/a	chr8:42996548-42996559 chr8:42996548-42996561 chr8:42996550-42996559
37	CEBPD	chr8:42995172-42995769	HepG2	liver:	n/a	n/a
38	CEBPD	chr8:42996378-42996713	HepG2	liver:	n/a	chr8:42996549-42996560
39	CEBPD	chr8:42996342-42996761	HepG2	liver:	n/a	chr8:42996549-42996560
40	CHD1	chr8:42996750-42996789	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr8:42994749-42997764	IMR90	lung:	n/a	chr8:42996201-42996211
42	CHD1	chr8:42994606-42994924	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr8:42996579-42997886	GM12878	blood:	n/a	n/a
44	CHD1	chr8:42995148-42996255	GM12878	blood:	n/a	chr8:42996201-42996211
45	CHD1	chr8:42995367-42995384	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr8:42996159-42996654	HepG2	liver:	n/a	chr8:42996201-42996211
47	CHD2	chr8:42995382-42995593	HepG2	liver:	n/a	n/a
48	CHD2	chr8:42995205-42995515	K562	blood:	n/a	n/a
49	CHD2	chr8:42996514-42996600	GM12878	blood:	n/a	n/a
50	CHD2	chr8:42995427-42995498	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:42995265-42995315	BE2_C	brain:	n/a
2	chr8:42996139-42996189	NT2-D1	testis:	n/a
3	chr8:42995265-42995315	BE2_C	brain:	n/a
4	chr8:42996139-42996189	NT2-D1	testis:	n/a
5	chr8:42996206-42996256	SK-N-SH	brain:	n/a
6	chr8:42995089-42995139	HCT-116	colon:	n/a
7	chr8:42996139-42996189	ECC-1	luminal epithelium:	n/a
8	chr8:42995089-42995139	HCF	heart:	n/a
9	chr8:42996634-42996684	GM12892	blood:	n/a
10	chr8:42996139-42996189	HepG2	liver:	n/a
11	chr8:42996206-42996256	Caco-2	colon:	n/a
12	chr8:42996512-42996562	NT2-D1	testis:	n/a
13	chr8:42995659-42995709	AG04450	lung:	fetal
14	chr8:42995659-42995709	ECC-1	luminal epithelium:	n/a
15	chr8:42995659-42995709	AG09319	gingival:	n/a
16	chr8:42995380-42995430	PrEC	prostate:	n/a
17	chr8:42996206-42996256	SK-N-SH_RA	brain:	n/a
18	chr8:42996139-42996189	A549	lung:	n/a
19	chr8:42995380-42995430	AG10803	skin:	n/a
20	chr8:42995564-42995614	IMR90	lung:	fetal
21	chr8:42995265-42995315	AG09309	skin:	n/a
22	chr8:42995564-42995614	PANC-1	pancreas:	n/a
23	chr8:42995265-42995315	A549	lung:	n/a
24	chr8:42996634-42996684	IMR90	lung:	fetal
25	chr8:42996512-42996562	Hepatocyte	liver:	n/a
26	chr8:42996206-42996256	HCPEpiC	choroid plexus:	n/a
27	chr8:42995564-42995614	HUVEC	blood vessel:	n/a
28	chr8:42996206-42996256	NH-A	brain:	n/a
29	chr8:42996139-42996189	H1-hESC	embryonic stem cell:	embryo
30	chr8:42995564-42995614	Hela-S3	cervix:	n/a
31	chr8:42996634-42996684	NB4	blood:	n/a
32	chr8:42996206-42996256	SAEC	small airway:	n/a
33	chr8:42996512-42996562	GM12891	blood:	n/a
34	chr8:42996634-42996684	GM12891	blood:	n/a
35	chr8:42995564-42995614	HEEpiC	esophagus:	n/a
36	chr8:42995380-42995430	ECC-1	luminal epithelium:	n/a
37	chr8:42995089-42995139	HRE	kidney:	n/a
38	chr8:42996634-42996684	PANC-1	pancreas:	n/a
39	chr8:42996139-42996189	AG10803	skin:	n/a
40	chr8:42995659-42995709	Hepatocyte	liver:	n/a
41	chr8:42996634-42996684	PrEC	prostate:	n/a
42	chr8:42995265-42995315	HL-60	blood:	n/a
43	chr8:42995659-42995709	AG04449	skin:	fetal
44	chr8:42995380-42995430	SAEC	small airway:	n/a
45	chr8:42996512-42996562	CMK	blood:	n/a
46	chr8:42995089-42995139	Hela-S3	cervix:	n/a
47	chr8:42995380-42995430	HIPEpiC	eye:	n/a
48	chr8:42995564-42995614	HCM	heart:	n/a
49	chr8:42996512-42996562	AG04450	lung:	fetal
50	chr8:42995659-42995709	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:42749464..42752003-chr8:42994418..42997135,2	K562	blood:
2	chr8:42948599..42949121-chr8:42995318..42995873,2	MCF-7	breast:
3	chr8:42995838..42997656-chr8:43013709..43015481,3	K562	blood:
4	chr8:42981388..42985439-chr8:42992719..42998148,8	MCF-7	breast:
5	chr12:49658655..49659446-chr8:42995137..42996126,2	Hela-S3	cervix:
6	chr8:42946276..42950766-chr8:42994093..42997306,5	K562	blood:
7	chr8:42911213..42913248-chr8:42996874..42998972,2	MCF-7	breast:
8	chr8:42946558..42950569-chr8:42993092..42998053,7	MCF-7	breast:
9	chr8:42945466..42950308-chr8:42993029..42998171,6	K562	blood:
10	chr8:42750503..42753349-chr8:42995062..42997135,2	K562	blood:
11	chr3:128902188..128902691-chr8:42996029..42996895,2	Hela-S3	cervix:
12	chr8:42995805..42997640-chr8:43004666..43006310,2	K562	blood:
13	chr6:126101699..126102238-chr8:42996427..42997007,2	Hela-S3	cervix:
14	chr8:42996020..42997656-chr8:43013709..43015215,2	K562	blood:
15	chr8:42947374..42951238-chr8:42993087..42998137,7	MCF-7	breast:
16	chr2:15730718..15733461-chr8:42996717..42999655,2	MCF-7	breast:

Variant related genes	Relation type
HGSNAT	TF binding region
HGSNAT	CpG island
ENSG00000079785	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000185900	chromatin interactions
ENSG00000254198	chromatin interactions
ENSG00000266044	chromatin interactions
ENSG00000168522	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000167553	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550826658	chr8:42994841-42994842	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs4523300	chr8:42994883-42994884	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539333215	chr8:42994928-42994929	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs559835409	chr8:42994941-42994942	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs146367206	chr8:42994981-42994982	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs528809452	chr8:42995007-42995008	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs73629198	chr8:42995047-42995048	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs535643232	chr8:42995110-42995111	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs540398974	chr8:42995192-42995193	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs138190152	chr8:42995193-42995194	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs543961168	chr8:42995246-42995247	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs557375896	chr8:42995298-42995299	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs577322709	chr8:42995299-42995300	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs562321730	chr8:42995401-42995402	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs140692013	chr8:42995420-42995421	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs559996941	chr8:42995435-42995436	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs528639163	chr8:42995456-42995457	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs149596192	chr8:42995466-42995467	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs562194013	chr8:42995468-42995469	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs530608686	chr8:42995471-42995472	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs13256451	chr8:42995495-42995496	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs534597242	chr8:42995516-42995517	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs550296652	chr8:42995539-42995540	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs563703712	chr8:42995564-42995565	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs200867889	chr8:42995570-42995571	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs190738010	chr8:42995579-42995580	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs566748228	chr8:42995594-42995595	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs535427008	chr8:42995645-42995646	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs549139396	chr8:42995702-42995703	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs568991180	chr8:42995710-42995711	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs144225438	chr8:42995789-42995790	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs62517610	chr8:42995811-42995812	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs577261388	chr8:42995826-42995827	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs539848664	chr8:42995850-42995851	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs553135875	chr8:42995956-42995957	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs183247583	chr8:42995978-42995979	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs542190194	chr8:42995994-42995995	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs562295141	chr8:42996001-42996002	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs575449316	chr8:42996019-42996020	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs62517626	chr8:42996090-42996091	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs563843834	chr8:42996091-42996092	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs532726881	chr8:42996139-42996140	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs144515124	chr8:42996153-42996154	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs559919623	chr8:42996155-42996156	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs529171328	chr8:42996178-42996179	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs549022870	chr8:42996286-42996287	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs569003111	chr8:42996291-42996292	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs147419445	chr8:42996351-42996352	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs551052079	chr8:42996356-42996357	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs370782374	chr8:42996383-42996384	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Medulloblastoma	19270706	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21045282	CNVD
Lung cancer	17925434	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:42982000-42994800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr8:42982200-42994800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:42983800-42994800	Weak transcription	Gastric	stomach
4	chr8:42984000-42994800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:42984000-42994800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr8:42984000-42994800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr8:42984000-42994800	Weak transcription	Thymus	Thymus
8	chr8:42985200-42994800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr8:42994200-42994800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:42994200-42994800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:42994200-42994800	Enhancers	Primary B cells from peripheral blood	blood
12	chr8:42994200-42994800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr8:42994200-42994800	Enhancers	Fetal Brain Male	brain
14	chr8:42994200-42994800	Enhancers	Lung	lung
15	chr8:42994200-42994800	Enhancers	Placenta Amnion	Placenta Amnion
16	chr8:42994200-42994800	Enhancers	HMEC	breast
17	chr8:42994200-42995200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:42994200-42995200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:42994200-42995200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:42994200-42995400	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr8:42994200-42997000	Active TSS	Colon Smooth Muscle	Colon
22	chr8:42994400-42994800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:42994400-42994800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr8:42994400-42994800	Enhancers	Primary T cells from cord blood	blood
25	chr8:42994400-42994800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr8:42994400-42994800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr8:42994400-42994800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr8:42994400-42994800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr8:42994400-42994800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr8:42994400-42994800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr8:42994400-42994800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr8:42994400-42994800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:42994400-42994800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr8:42994400-42994800	Flanking Active TSS	Brain Substantia Nigra	brain
35	chr8:42994400-42994800	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr8:42994400-42994800	Enhancers	Fetal Thymus	thymus
37	chr8:42994400-42994800	Flanking Active TSS	HepG2	liver
38	chr8:42994400-42995000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr8:42994400-42995000	Flanking Active TSS	Brain Anterior Caudate	brain
40	chr8:42994400-42995000	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr8:42994400-42995000	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr8:42994400-42995000	Flanking Active TSS	Fetal Brain Female	brain
43	chr8:42994400-42995000	Flanking Active TSS	Fetal Heart	heart
44	chr8:42994400-42995000	Flanking Active TSS	Fetal Kidney	kidney
45	chr8:42994400-42995000	Flanking Active TSS	Fetal Lung	lung
46	chr8:42994400-42995000	Enhancers	Spleen	Spleen
47	chr8:42994400-42995000	Flanking Active TSS	A549	lung
48	chr8:42994400-42995000	Flanking Active TSS	Hela-S3	cervix
49	chr8:42994400-42995000	Flanking Active TSS	NHDF-Ad	bronchial
50	chr8:42994400-42995200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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