Variant report

Variant	esv3367220
Chromosome Location	chr17:33699489-33701437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:228)
CpG islands
(count:858)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:228 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:33700735-33700996	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr17:33700435-33700893	GM12878	blood:	n/a	n/a
3	BHLHE40	chr17:33700507-33700933	GM12878	blood:	n/a	n/a
4	BRCA1	chr17:33700927-33700952	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr17:33701311-33701959	IMR90	lung:	n/a	n/a
6	CEBPB	chr17:33701339-33701878	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr17:33700361-33701097	GM12878	blood:	n/a	n/a
8	CEBPB	chr17:33700583-33700911	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr17:33701236-33701436	GM12878	blood:	n/a	n/a
10	CHD1	chr17:33700415-33700981	GM12878	blood:	n/a	n/a
11	CHD2	chr17:33700473-33701031	GM12878	blood:	n/a	n/a
12	CHD2	chr17:33700484-33700849	Hela-S3	cervix:	n/a	n/a
13	CREB1	chr17:33700480-33700931	A549	lung:	n/a	n/a
14	CREB1	chr17:33700509-33700895	A549	lung:	n/a	n/a
15	CREB1	chr17:33700477-33700995	GM12878	blood:	n/a	n/a
16	CTBP2	chr17:33700638-33701688	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr17:33700720-33700790	GM12878	blood:	n/a	n/a
18	CTCF	chr17:33699860-33700010	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr17:33699840-33699990	HMF	breast:	n/a	n/a
20	CTCF	chr17:33701380-33701530	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr17:33699800-33699950	GM12873	blood:	n/a	n/a
22	CTCF	chr17:33699840-33699990	BJ	skin:	n/a	n/a
23	CTCF	chr17:33699840-33699990	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr17:33699700-33699850	HMF	breast:	n/a	n/a
25	CTCF	chr17:33699980-33700130	A549	lung:	n/a	n/a
26	CTCF	chr17:33699800-33699950	HEK293	kidney:	n/a	n/a
27	CTCF	chr17:33699840-33699990	HEK293	kidney:	n/a	n/a
28	CTCF	chr17:33699860-33700010	AG09319	gingival:	n/a	n/a
29	CTCF	chr17:33699860-33700010	AG04450	lung:	n/a	n/a
30	CTCF	chr17:33699840-33699990	AG09319	gingival:	n/a	n/a
31	CTCF	chr17:33699860-33700010	AG10803	skin:	n/a	n/a
32	CTCF	chr17:33701420-33701570	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr17:33700663-33700800	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr17:33699880-33700030	AG10803	skin:	n/a	n/a
35	CTCF	chr17:33699901-33699935	Gliobla	brain:	n/a	n/a
36	CTCF	chr17:33699900-33700050	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr17:33699980-33700130	AG04449	skin:	n/a	n/a
38	E2F1	chr17:33700504-33700869	Hela-S3	cervix:	n/a	chr17:33700678-33700689
39	E2F4	chr17:33700554-33700939	Hela-S3	cervix:	n/a	n/a
40	E2F4	chr17:33700541-33700939	GM12878	blood:	n/a	n/a
41	E2F6	chr17:33700524-33701226	A549	lung:	n/a	n/a
42	EBF1	chr17:33700453-33700842	GM12878	blood:	n/a	chr17:33700638-33700649
43	EBF1	chr17:33700064-33700079	GM12878	blood:	n/a	n/a
44	EGR1	chr17:33700534-33700805	GM12878	blood:	n/a	n/a
45	EGR1	chr17:33700539-33700841	K562	blood:	n/a	n/a
46	EGR1	chr17:33700535-33700895	K562	blood:	n/a	n/a
47	EGR1	chr17:33700460-33700846	GM12878	blood:	n/a	n/a
48	ELF1	chr17:33700920-33701702	GM12878	blood:	n/a	n/a
49	ELF1	chr17:33700052-33700885	GM12878	blood:	n/a	n/a
50	ELK1	chr17:33700553-33700798	GM12878	blood:	n/a	n/a

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:33700255-33700305	HCT-116	colon:	n/a
2	chr17:33700180-33700230	HAEpiC	amniotic membrane:	n/a
3	chr17:33700255-33700305	K562	blood:	n/a
4	chr17:33700801-33700851	Caco-2	colon:	n/a
5	chr17:33700255-33700305	HCT-116	colon:	n/a
6	chr17:33700180-33700230	HAEpiC	amniotic membrane:	n/a
7	chr17:33700255-33700305	K562	blood:	n/a
8	chr17:33700801-33700851	Caco-2	colon:	n/a
9	chr17:33700745-33700795	AG04450	lung:	fetal
10	chr17:33700255-33700305	HEK293	kidney:	embryo
11	chr17:33701350-33701400	HNPCEpiC	eye:	n/a
12	chr17:33700745-33700795	LNCaP	prostate:	n/a
13	chr17:33700230-33700280	HL-60	blood:	n/a
14	chr17:33700180-33700230	HCT-116	colon:	n/a
15	chr17:33700230-33700280	NH-A	brain:	n/a
16	chr17:33700295-33700345	HAEpiC	amniotic membrane:	n/a
17	chr17:33700513-33700563	PrEC	prostate:	n/a
18	chr17:33700180-33700230	HIPEpiC	eye:	n/a
19	chr17:33700745-33700795	NT2-D1	testis:	n/a
20	chr17:33701350-33701400	HCM	heart:	n/a
21	chr17:33700230-33700280	HRE	kidney:	n/a
22	chr17:33701350-33701400	NB4	blood:	n/a
23	chr17:33701321-33701371	AG09319	gingival:	n/a
24	chr17:33701321-33701371	MCF10A-Er-Src	breast:	n/a
25	chr17:33700801-33700851	NB4	blood:	n/a
26	chr17:33700745-33700795	NHBE	bronchial:	n/a
27	chr17:33700759-33700809	U87	brain:	n/a
28	chr17:33700255-33700305	MCF10A-Er-Src	breast:	n/a
29	chr17:33701321-33701371	NHBE	bronchial:	n/a
30	chr17:33700757-33700807	K562	blood:	n/a
31	chr17:33700757-33700807	PANC-1	pancreas:	n/a
32	chr17:33700230-33700280	HNPCEpiC	eye:	n/a
33	chr17:33700513-33700563	HIPEpiC	eye:	n/a
34	chr17:33700817-33700867	MCF10A-Er-Src	breast:	n/a
35	chr17:33700747-33700797	GM12878	blood:	n/a
36	chr17:33700801-33700851	HPAEpiC	pulmonary alveolar:	n/a
37	chr17:33700255-33700305	HRPEpiC	eye:	n/a
38	chr17:33700745-33700795	SKMC	muscle:	n/a
39	chr17:33701353-33701403	HNPCEpiC	eye:	n/a
40	chr17:33701350-33701400	T-47D	breast:	n/a
41	chr17:33700757-33700807	HRE	kidney:	n/a
42	chr17:33700255-33700305	AG09319	gingival:	n/a
43	chr17:33700747-33700797	HRCEpiC	kidney:	n/a
44	chr17:33700180-33700230	HepG2	liver:	n/a
45	chr17:33700801-33700851	GM06990	blood:	n/a
46	chr17:33700759-33700809	NT2-D1	testis:	n/a
47	chr17:33700745-33700795	HepG2	liver:	n/a
48	chr17:33700801-33700851	PrEC	prostate:	n/a
49	chr17:33700757-33700807	IMR90	lung:	fetal
50	chr17:33700513-33700563	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:33691774..33694475-chr17:33701256..33703274,2	K562	blood:
2	chr17:33700355..33701212-chr7:100026345..100027279,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLFN12-5	chr17:33700493-33700639	NONHSAT053088

No data

Variant related genes	Relation type
SLFN11	TF binding region
SLFN11	CpG island
ENSG00000146834	chromatin interactions
ENSG00000172716	chromatin interactions
ENSG00000078487	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 112 )

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	rs566702639	chr17:33699557-33699558	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs534455467	chr17:33699586-33699587	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538444349	chr17:33699602-33699603	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558845306	chr17:33699608-33699609	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs1913544	chr17:33699635-33699636	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs4796079	chr17:33699650-33699651	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs144409051	chr17:33699661-33699662	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs557361390	chr17:33699677-33699678	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs574193367	chr17:33699705-33699706	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs8082408	chr17:33699718-33699719	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs72825961	chr17:33699736-33699737	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs8078071	chr17:33699772-33699773	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs575509666	chr17:33699792-33699793	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545257781	chr17:33699815-33699816	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371312052	chr17:33699818-33699819	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12941857	chr17:33699833-33699834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs546051196	chr17:33699840-33699841	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531075737	chr17:33699878-33699879	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550170181	chr17:33699900-33699901	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563756961	chr17:33699914-33699915	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560500983	chr17:33700044-33700045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529634785	chr17:33700055-33700056	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546326904	chr17:33700112-33700113	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs884018	chr17:33700162-33700163	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs538853433	chr17:33700179-33700180	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186359896	chr17:33700181-33700182	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114442143	chr17:33700186-33700187	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201554722	chr17:33700244-33700245	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538100325	chr17:33700303-33700304	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112268471	chr17:33700341-33700342	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557397655	chr17:33700361-33700362	Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs116430594	chr17:33700404-33700405	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536639203	chr17:33700447-33700448	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs66756976	chr17:33700470-33700471	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530909773	chr17:33700493-33700494	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs376453757	chr17:33700496-33700497	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs545597832	chr17:33700501-33700502	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs9303685	chr17:33700578-33700579	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs575896600	chr17:33700584-33700585	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs544549078	chr17:33700608-33700609	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs12944176	chr17:33700618-33700619	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189926971	chr17:33700694-33700695	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs539818681	chr17:33700696-33700697	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs560216619	chr17:33700708-33700709	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs56021229	chr17:33700731-33700732	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs144060839	chr17:33700756-33700757	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs552361003	chr17:33700772-33700773	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs12944726	chr17:33700787-33700788	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531531923	chr17:33700817-33700818	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs61358706	chr17:33700830-33700831	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Melanoma	18172304	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cancer	20164919	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
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	17603634	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
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17157792	CNVD
Bladder cancer	19088036	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
Meningioma	19431122	CNVD
Neurocytoma	17123091	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Cervical cancer	21062161	CNVD
Colorectal cancer	22860045	CNVD
Ductal carcinoma	18381933	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Renal cysts	20603712	CNVD
Epilepsy	21858020	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Autism	20587423	CNVD
Renal cysts	20587423	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Mayer-Rokitansky-Kuster-Hauser syndrome	19889212	CNVD
Endometrial cancer	23636398	CNVD
Urothelial cell carcinoma	18451213	CNVD
Gastric cancer	24379144	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	17850661	CNVD
Primary lung adenocarcinoma	16799635	CNVD
HIV/AIDS	18848619	CNVD
Rheumatoid arthritis	19220326	CNVD
Rheumatoid arthritis	18848619	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	18848619	CNVD
Type 1 diabetes	19220326	CNVD
HIV/AIDS	17330138	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	19955444	CNVD
Schizophrenia	19955444	CNVD
Acute monocytic leukemia	16498392	CNVD
Breast cancer	20409316	CNVD
Myelodysplastic syndrome	18663149	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33673800-33699800	Weak transcription	Ovary	ovary
2	chr17:33674200-33699800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr17:33675800-33699800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr17:33678400-33700000	Weak transcription	Esophagus	oesophagus
5	chr17:33688600-33700000	Weak transcription	Colon Smooth Muscle	Colon
6	chr17:33691800-33699800	Weak transcription	Aorta	Aorta
7	chr17:33693800-33700000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr17:33695600-33699600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr17:33695800-33699600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr17:33695800-33700000	Weak transcription	Placenta	Placenta
11	chr17:33696000-33699600	Weak transcription	Primary B cells from peripheral blood	blood
12	chr17:33696200-33700000	Weak transcription	Lung	lung
13	chr17:33696400-33700000	Weak transcription	Spleen	Spleen
14	chr17:33696600-33699600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr17:33696600-33699600	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr17:33696600-33699800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr17:33696600-33699800	Weak transcription	Left Ventricle	heart
18	chr17:33696600-33699800	Weak transcription	Thymus	Thymus
19	chr17:33696800-33699600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr17:33698000-33699600	Flanking Active TSS	Dnd41	blood
21	chr17:33698000-33700200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr17:33698200-33699600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr17:33698400-33700800	Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr17:33698400-33701000	Active TSS	NHLF	lung
25	chr17:33698600-33699600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr17:33698600-33699600	Active TSS	Adipose Nuclei	Adipose
27	chr17:33698600-33699800	Enhancers	Primary B cells from cord blood	blood
28	chr17:33698600-33700000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr17:33698600-33700400	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr17:33698800-33699600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr17:33698800-33699600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr17:33698800-33699800	Enhancers	Primary T cells from cord blood	blood
33	chr17:33698800-33699800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr17:33698800-33702000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr17:33699000-33699600	Enhancers	Primary hematopoietic stem cells	blood
36	chr17:33699000-33699800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr17:33699000-33699800	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr17:33699000-33699800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:33699000-33700000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr17:33699000-33700800	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr17:33699000-33701000	Active TSS	Right Atrium	heart
42	chr17:33699200-33699600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr17:33699200-33700600	Active TSS	Stomach Smooth Muscle	stomach
44	chr17:33699200-33700800	Active TSS	HUVEC	blood vessel
45	chr17:33699400-33699600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr17:33699400-33699800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr17:33699400-33699800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr17:33699400-33700400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr17:33699400-33701600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr17:33699400-33701800	Active TSS	Right Ventricle	heart

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