Variant report

Variant	esv2761960
Chromosome Location	chr17:46504489-46529846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:456)
CpG islands
(count:917)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:46517526-46517723	K562	blood:	n/a	n/a
2	ARID3A	chr17:46505099-46505317	K562	blood:	n/a	n/a
3	ARID3A	chr17:46520297-46520566	K562	blood:	n/a	n/a
4	ATF1	chr17:46505022-46505258	K562	blood:	n/a	n/a
5	ATF1	chr17:46518847-46519052	K562	blood:	n/a	n/a
6	ATF1	chr17:46520195-46520572	K562	blood:	n/a	n/a
7	ATF2	chr17:46518506-46519201	GM12878	blood:	n/a	n/a
8	ATF2	chr17:46504911-46505380	GM12878	blood:	n/a	n/a
9	ATF2	chr17:46518501-46519101	GM12878	blood:	n/a	n/a
10	ATF3	chr17:46520275-46520521	K562	blood:	n/a	n/a
11	ATF3	chr17:46520233-46520598	K562	blood:	n/a	n/a
12	BATF	chr17:46520245-46520580	GM12878	blood:	n/a	chr17:46520393-46520404
13	BATF	chr17:46517549-46517967	GM12878	blood:	n/a	n/a
14	BATF	chr17:46518617-46519117	GM12878	blood:	n/a	n/a
15	BCL11A	chr17:46518578-46518977	GM12878	blood:	n/a	chr17:46518890-46518899
16	BCL11A	chr17:46518490-46519044	GM12878	blood:	n/a	chr17:46518890-46518899
17	BCL3	chr17:46518564-46519010	GM12878	blood:	n/a	chr17:46518890-46518899
18	BCLAF1	chr17:46518459-46519156	GM12878	blood:	n/a	chr17:46518890-46518899
19	BCLAF1	chr17:46507174-46507906	GM12878	blood:	n/a	chr17:46507552-46507565
20	BCLAF1	chr17:46520082-46520602	K562	blood:	n/a	n/a
21	BCLAF1	chr17:46518397-46519149	GM12878	blood:	n/a	chr17:46518890-46518899
22	BHLHE40	chr17:46518501-46519144	GM12878	blood:	n/a	n/a
23	BHLHE40	chr17:46516947-46517619	GM12878	blood:	n/a	n/a
24	BHLHE40	chr17:46520265-46520603	GM12878	blood:	n/a	n/a
25	BHLHE40	chr17:46507388-46508007	GM12878	blood:	n/a	chr17:46507651-46507667
26	BHLHE40	chr17:46520242-46520514	K562	blood:	n/a	n/a
27	BHLHE40	chr17:46510412-46510888	K562	blood:	n/a	n/a
28	BHLHE40	chr17:46505144-46505182	K562	blood:	n/a	n/a
29	CBX3	chr17:46521952-46522532	K562	blood:	n/a	n/a
30	CBX3	chr17:46504943-46505376	K562	blood:	n/a	chr17:46505250-46505261
31	CBX3	chr17:46519847-46520729	K562	blood:	n/a	n/a
32	CBX3	chr17:46520211-46520597	K562	blood:	n/a	n/a
33	CEBPB	chr17:46516471-46516832	HepG2	liver:	n/a	chr17:46516656-46516667
34	CEBPB	chr17:46516483-46516916	K562	blood:	n/a	chr17:46516656-46516667
35	CEBPB	chr17:46516533-46516814	IMR90	lung:	n/a	chr17:46516656-46516667
36	CEBPB	chr17:46517536-46517897	K562	blood:	n/a	n/a
37	CEBPB	chr17:46518449-46519367	GM12878	blood:	n/a	chr17:46519285-46519298 chr17:46519046-46519054
38	CEBPB	chr17:46516483-46516804	A549	lung:	n/a	chr17:46516656-46516667
39	CEBPB	chr17:46518626-46519003	GM12878	blood:	n/a	n/a
40	CHD1	chr17:46505006-46505923	GM12878	blood:	n/a	n/a
41	CHD1	chr17:46518435-46519479	GM12878	blood:	n/a	n/a
42	CHD1	chr17:46517297-46517527	GM12878	blood:	n/a	n/a
43	CHD1	chr17:46507077-46507644	GM12878	blood:	n/a	n/a
44	CHD2	chr17:46518534-46519683	GM12878	blood:	n/a	n/a
45	CHD2	chr17:46504994-46505362	GM12878	blood:	n/a	n/a
46	CHD2	chr17:46507378-46507877	GM12878	blood:	n/a	chr17:46507681-46507691
47	CHD2	chr17:46517296-46517789	GM12878	blood:	n/a	n/a
48	CHD2	chr17:46505131-46505178	K562	blood:	n/a	n/a
49	CREB1	chr17:46518530-46519153	GM12878	blood:	n/a	n/a
50	CREB1	chr17:46518441-46519214	GM12878	blood:	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	chr17:46508097-46508147	AG04450	lung:	fetal
2	chr17:46506947-46506997	NHDF-neo	bronchial:	n/a
3	chr17:46508097-46508147	AG04450	lung:	fetal
4	chr17:46506947-46506997	NHDF-neo	bronchial:	n/a
5	chr17:46522464-46522514	HL-60	blood:	n/a
6	chr17:46522560-46522610	AG04449	skin:	fetal
7	chr17:46507705-46507755	HepG2	liver:	n/a
8	chr17:46522560-46522610	NT2-D1	testis:	n/a
9	chr17:46507690-46507740	H1-hESC	embryonic stem cell:	embryo
10	chr17:46507549-46507599	HCF	heart:	n/a
11	chr17:46506947-46506997	HIPEpiC	eye:	n/a
12	chr17:46507549-46507599	HEK293	kidney:	embryo
13	chr17:46507763-46507813	SAEC	small airway:	n/a
14	chr17:46507763-46507813	MCF10A-Er-Src	breast:	n/a
15	chr17:46507857-46507907	PrEC	prostate:	n/a
16	chr17:46510392-46510442	HCPEpiC	choroid plexus:	n/a
17	chr17:46506947-46506997	Caco-2	colon:	n/a
18	chr17:46522560-46522610	NB4	blood:	n/a
19	chr17:46507830-46507880	Caco-2	colon:	n/a
20	chr17:46507895-46507945	HEEpiC	esophagus:	n/a
21	chr17:46522513-46522563	Jurkat	blood:	n/a
22	chr17:46504791-46504841	GM06990	blood:	n/a
23	chr17:46507857-46507907	NB4	blood:	n/a
24	chr17:46507857-46507907	ovcar-3	ovarian:	n/a
25	chr17:46507777-46507827	Hela-S3	cervix:	n/a
26	chr17:46522560-46522610	GM12891	blood:	n/a
27	chr17:46508097-46508147	HEK293	kidney:	embryo
28	chr17:46507549-46507599	IMR90	lung:	fetal
29	chr17:46507830-46507880	SAEC	small airway:	n/a
30	chr17:46507857-46507907	K562	blood:	n/a
31	chr17:46522464-46522514	HRCEpiC	kidney:	n/a
32	chr17:46504791-46504841	HIPEpiC	eye:	n/a
33	chr17:46522560-46522610	MCF-7	breast:	n/a
34	chr17:46522464-46522514	HMEC	breast:	n/a
35	chr17:46507690-46507740	HRE	kidney:	n/a
36	chr17:46506947-46506997	RPTEC	kidney:	n/a
37	chr17:46507763-46507813	ECC-1	luminal epithelium:	n/a
38	chr17:46510392-46510442	NB4	blood:	n/a
39	chr17:46507690-46507740	HCF	heart:	n/a
40	chr17:46507549-46507599	GM12892	blood:	n/a
41	chr17:46507895-46507945	BE2_C	brain:	n/a
42	chr17:46507763-46507813	HIPEpiC	eye:	n/a
43	chr17:46507690-46507740	MCF-7	breast:	n/a
44	chr17:46507895-46507945	Caco-2	colon:	n/a
45	chr17:46506947-46506997	MCF-7	breast:	n/a
46	chr17:46507705-46507755	SAEC	small airway:	n/a
47	chr17:46507705-46507755	NHBE	bronchial:	n/a
48	chr17:46507857-46507907	AG10803	skin:	n/a
49	chr17:46507763-46507813	U87	brain:	n/a
50	chr17:46507763-46507813	PFSK-1	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46505182..46508070-chr17:46508849..46511744,2	K562	blood:
2	chr17:46517956..46520413-chr17:46654283..46656139,2	K562	blood:
3	chr17:46509583..46511402-chr17:46522704..46524795,2	K562	blood:
4	chr17:46519351..46522263-chr17:46657755..46660569,3	K562	blood:
5	chr17:46514248..46517781-chr17:46547190..46550869,3	K562	blood:
6	chr17:46340880..46343379-chr17:46515799..46517839,2	K562	blood:
7	chr17:46505363..46507156-chr17:46658355..46659859,2	K562	blood:
8	chr17:46523875..46525523-chr17:46528781..46531393,2	K562	blood:
9	chr17:46518879..46521874-chr17:46522695..46525277,2	K562	blood:
10	chr17:46515918..46518045-chr17:46519847..46521809,2	K562	blood:
11	chr17:46503026..46505286-chr17:46512719..46514914,2	K562	blood:
12	chr17:46523875..46525523-chr17:46528781..46531393,2	K562	blood:
13	chr17:46524023..46526457-chr17:46528439..46531393,2	K562	blood:
14	chr17:46529747..46531538-chr17:46533200..46534780,2	K562	blood:
15	chr17:46519655..46521952-chr17:46522773..46525043,2	K562	blood:
16	chr17:46519655..46521952-chr17:46522773..46525043,2	K562	blood:
17	chr17:46511985..46515396-chr17:46515822..46520337,5	K562	blood:
18	chr17:46503026..46505286-chr17:46512719..46514914,2	K562	blood:
19	chr17:46511985..46515396-chr17:46515822..46520337,5	K562	blood:
20	chr17:46519089..46520799-chr17:46536940..46538843,2	K562	blood:
21	chr17:46516289..46518100-chr17:46524558..46526108,2	K562	blood:
22	chr17:46516289..46518100-chr17:46524558..46526108,2	K562	blood:
23	chr17:46505182..46508631-chr17:46508849..46512538,4	K562	blood:
24	chr17:46525263..46527446-chr17:46657806..46659592,2	K562	blood:
25	chr17:46524023..46526457-chr17:46528439..46531393,2	K562	blood:
26	chr17:46519351..46522056-chr17:46657755..46660727,3	K562	blood:
27	chr17:46518879..46521874-chr17:46522695..46525277,2	K562	blood:
28	chr17:46432035..46433984-chr17:46508339..46510187,2	K562	blood:
29	chr17:46466673..46468665-chr17:46514612..46517414,2	K562	blood:
30	chr17:46503757..46506567-chr17:46674757..46677231,2	K562	blood:
31	chr17:46529355..46532196-chr17:46660157..46661823,2	K562	blood:
32	chr17:46516365..46518843-chr17:46533348..46535328,2	K562	blood:
33	chr17:46515918..46518045-chr17:46519847..46521809,2	K562	blood:
34	chr17:46509583..46511402-chr17:46522704..46524795,2	K562	blood:
35	chr17:46523948..46525611-chr17:46533793..46535794,2	K562	blood:

No data

Variant related genes	Relation type
SKAP1	TF binding region
SKAP1	CpG island
ENSG00000120093	chromatin interactions
ENSG00000257178	chromatin interactions
ENSG00000141293	chromatin interactions
ENSG00000264451	chromatin interactions

Extended variants
information (count: 793 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553398415	chr17:46504490-46504491	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs9900511	chr17:46504524-46504525	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs150849910	chr17:46504530-46504531	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs570879603	chr17:46504551-46504552	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs79496389	chr17:46504581-46504582	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs574834409	chr17:46504590-46504591	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs111380436	chr17:46504615-46504616	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs534969545	chr17:46504616-46504617	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs553635322	chr17:46504651-46504652	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs138710979	chr17:46504703-46504704	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs180989146	chr17:46504775-46504776	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs149557871	chr17:46504791-46504792	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs552011545	chr17:46504805-46504806	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs559355270	chr17:46504819-46504820	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs574886368	chr17:46504843-46504844	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs536042906	chr17:46504851-46504852	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs548803522	chr17:46504854-46504855	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs556590464	chr17:46504856-46504857	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs537372907	chr17:46504874-46504875	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs185755925	chr17:46504897-46504898	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs550843372	chr17:46504936-46504937	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs570527008	chr17:46504952-46504953	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs373771017	chr17:46504971-46504972	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs539791808	chr17:46504977-46504978	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs553193367	chr17:46505001-46505002	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs112984686	chr17:46505018-46505019	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs559144009	chr17:46505021-46505022	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs114239124	chr17:46505053-46505054	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs554833523	chr17:46505056-46505057	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs80112766	chr17:46505105-46505106	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs144156399	chr17:46505191-46505192	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs557267467	chr17:46505325-46505326	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs372183263	chr17:46505370-46505371	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576913787	chr17:46505371-46505372	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545744937	chr17:46505384-46505385	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368772392	chr17:46505389-46505390	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373845380	chr17:46505396-46505397	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs528234530	chr17:46505464-46505465	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs140580572	chr17:46505561-46505562	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs561975893	chr17:46505645-46505646	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77463459	chr17:46505687-46505688	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs7211712	chr17:46505696-46505697	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs371975219	chr17:46505709-46505710	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142806741	chr17:46505714-46505715	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182291502	chr17:46505716-46505717	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547011659	chr17:46505721-46505722	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375562690	chr17:46505724-46505725	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566732501	chr17:46505867-46505868	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs147393881	chr17:46505996-46505997	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369777089	chr17:46506013-46506014	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46489800-46505000	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr17:46502200-46505200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr17:46502200-46505200	Enhancers	Fetal Thymus	thymus
4	chr17:46502800-46505000	Flanking Active TSS	GM12878-XiMat	blood
5	chr17:46503200-46507000	Enhancers	Primary hematopoietic stem cells	blood
6	chr17:46503400-46505400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr17:46503400-46505600	Enhancers	Primary B cells from cord blood	blood
8	chr17:46503400-46506400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr17:46503600-46504600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr17:46503600-46505200	Bivalent Enhancer	Fetal Lung	lung
11	chr17:46503600-46505400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr17:46503600-46505400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr17:46503600-46505400	Enhancers	A549	lung
14	chr17:46503600-46505600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr17:46503600-46506000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:46503600-46506600	Enhancers	Primary B cells from peripheral blood	blood
17	chr17:46503600-46506600	Flanking Active TSS	Primary T cells from cord blood	blood
18	chr17:46503600-46506600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr17:46503800-46506400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr17:46503800-46507600	Active TSS	Primary T cells fromperipheralblood	blood
21	chr17:46504000-46504600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
22	chr17:46504000-46505000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr17:46504000-46505000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr17:46504000-46506000	Enhancers	K562	blood
25	chr17:46504200-46504600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr17:46504200-46504600	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr17:46504200-46505600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr17:46504400-46504600	Enhancers	Fetal Brain Male	brain
29	chr17:46504400-46505000	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr17:46504400-46505000	Weak transcription	Thymus	Thymus
31	chr17:46504600-46504800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr17:46504600-46505400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr17:46504600-46505600	Bivalent Enhancer	Fetal Brain Male	brain
34	chr17:46504600-46505800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr17:46504600-46506000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
36	chr17:46504800-46505600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr17:46505000-46505200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr17:46505000-46505400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr17:46505000-46505400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr17:46505000-46506600	Active TSS	GM12878-XiMat	blood
41	chr17:46505000-46507200	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr17:46505000-46507600	Active TSS	Thymus	Thymus
43	chr17:46505000-46508000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr17:46505200-46505400	Flanking Active TSS	Fetal Thymus	thymus
45	chr17:46505200-46506000	Enhancers	Fetal Kidney	kidney
46	chr17:46505200-46506200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr17:46505200-46506400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr17:46505200-46506600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr17:46505400-46505600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr17:46505400-46506400	Active TSS	Primary T regulatory cells fromperipheralblood	blood

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