Variant report

Variant	esv3410983
Chromosome Location	chr1:85461789-85464337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:794)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:85461001-85462170	GM12878	blood:	n/a	n/a
2	ATF2	chr1:85460975-85462328	GM12878	blood:	n/a	n/a
3	BACH1	chr1:85463795-85463995	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:85462556-85462963	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:85463401-85463435	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:85461158-85462031	GM12878	blood:	n/a	chr1:85461561-85461572
7	BATF	chr1:85461580-85461958	GM12878	blood:	n/a	n/a
8	BCL3	chr1:85461098-85462125	GM12878	blood:	n/a	chr1:85461391-85461400
9	BCLAF1	chr1:85460942-85462854	GM12878	blood:	n/a	chr1:85461391-85461400
10	BCLAF1	chr1:85461500-85462338	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:85462352-85462829	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:85462315-85463615	GM12878	blood:	n/a	chr1:85463418-85463434 chr1:85463404-85463420
13	BHLHE40	chr1:85461025-85462056	GM12878	blood:	n/a	n/a
14	BRCA1	chr1:85463618-85463875	GM12878	blood:	n/a	n/a
15	CEBPB	chr1:85460992-85462110	GM12878	blood:	n/a	n/a
16	CHD1	chr1:85459740-85463594	GM12878	blood:	n/a	chr1:85462833-85462843 chr1:85462244-85462251
17	CHD1	chr1:85462604-85462804	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:85463247-85463250	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:85462572-85462787	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:85461067-85464026	GM12878	blood:	n/a	chr1:85462833-85462843 chr1:85462244-85462251
21	CTBP2	chr1:85462997-85464123	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:85463209-85463240	GM10266	blood:	n/a	n/a
23	CTCF	chr1:85463320-85463470	GM12865	blood:	n/a	n/a
24	CTCF	chr1:85463440-85463590	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr1:85462860-85463010	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr1:85462737-85462822	GM12892	blood:	n/a	n/a
27	CTCF	chr1:85462880-85463030	GM12875	blood:	n/a	n/a
28	CTCF	chr1:85462760-85462910	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr1:85463160-85463310	GM12873	blood:	n/a	n/a
30	CTCF	chr1:85462880-85463030	GM12878	blood:	n/a	n/a
31	CTCF	chr1:85463000-85463150	GM12866	blood:	n/a	n/a
32	CTCF	chr1:85462742-85463425	GM12878	blood:	n/a	n/a
33	CTCF	chr1:85462820-85462970	HMEC	breast:	n/a	n/a
34	CTCF	chr1:85462780-85462930	HPF	lung:	n/a	n/a
35	CTCF	chr1:85462900-85463050	BJ	skin:	n/a	n/a
36	CTCF	chr1:85463200-85463350	GM06990	blood:	n/a	n/a
37	CTCF	chr1:85463300-85463450	GM12864	blood:	n/a	n/a
38	CTCF	chr1:85462733-85462841	GM19239	blood:	n/a	n/a
39	CTCF	chr1:85463220-85463370	GM12867	blood:	n/a	n/a
40	CTCF	chr1:85463040-85463190	GM12865	blood:	n/a	n/a
41	CTCF	chr1:85462760-85462910	GM12868	blood:	n/a	n/a
42	CTCF	chr1:85463200-85463350	GM12872	blood:	n/a	n/a
43	CTCF	chr1:85463080-85463230	HRE	kidney:	n/a	n/a
44	CTCF	chr1:85463922-85464033	GM12892	blood:	n/a	n/a
45	CTCF	chr1:85462640-85462790	SAEC	small airway:	n/a	n/a
46	CTCF	chr1:85462740-85462890	GM12871	blood:	n/a	n/a
47	CTCF	chr1:85463115-85463357	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:85462880-85463030	NHEK	skin:	n/a	n/a
49	CTCF	chr1:85463945-85463980	GM12891	blood:	n/a	n/a
50	CTCF	chr1:85463320-85463470	GM12866	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85462700-85462750	ovcar-3	ovarian:	n/a
2	chr1:85462700-85462750	ovcar-3	ovarian:	n/a
3	chr1:85462812-85462862	HEEpiC	esophagus:	n/a
4	chr1:85462939-85462989	AG10803	skin:	n/a
5	chr1:85462953-85463003	GM12891	blood:	n/a
6	chr1:85464261-85464311	SK-N-MC	brain:	n/a
7	chr1:85462812-85462862	NHDF-neo	bronchial:	n/a
8	chr1:85464166-85464216	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:85462857-85462907	AG04450	lung:	fetal
10	chr1:85462885-85462935	HAEpiC	amniotic membrane:	n/a
11	chr1:85462885-85462935	A549	lung:	n/a
12	chr1:85462885-85462935	CMK	blood:	n/a
13	chr1:85463364-85463414	BE2_C	brain:	n/a
14	chr1:85462857-85462907	PFSK-1	brain:	n/a
15	chr1:85462857-85462907	GM06990	blood:	n/a
16	chr1:85462812-85462862	HCF	heart:	n/a
17	chr1:85464166-85464216	AG04449	skin:	fetal
18	chr1:85464261-85464311	GM12891	blood:	n/a
19	chr1:85462483-85462533	BJ	skin:	n/a
20	chr1:85462953-85463003	HepG2	liver:	n/a
21	chr1:85462885-85462935	U87	brain:	n/a
22	chr1:85464110-85464160	K562	blood:	n/a
23	chr1:85464166-85464216	ECC-1	luminal epithelium:	n/a
24	chr1:85464166-85464216	RPTEC	kidney:	n/a
25	chr1:85462939-85462989	GM19239	blood:	n/a
26	chr1:85462483-85462533	PrEC	prostate:	n/a
27	chr1:85464000-85464050	GM12892	blood:	n/a
28	chr1:85462812-85462862	LNCaP	prostate:	n/a
29	chr1:85464166-85464216	NH-A	brain:	n/a
30	chr1:85464166-85464216	MCF10A-Er-Src	breast:	n/a
31	chr1:85462885-85462935	AG10803	skin:	n/a
32	chr1:85462812-85462862	HRE	kidney:	n/a
33	chr1:85462700-85462750	AG09309	skin:	n/a
34	chr1:85462812-85462862	AG10803	skin:	n/a
35	chr1:85464000-85464050	GM12891	blood:	n/a
36	chr1:85464000-85464050	U87	brain:	n/a
37	chr1:85462885-85462935	SK-N-SH	brain:	n/a
38	chr1:85464110-85464160	HepG2	liver:	n/a
39	chr1:85462939-85462989	Caco-2	colon:	n/a
40	chr1:85462939-85462989	IMR90	lung:	fetal
41	chr1:85462700-85462750	GM19239	blood:	n/a
42	chr1:85462857-85462907	Jurkat	blood:	n/a
43	chr1:85464166-85464216	K562	blood:	n/a
44	chr1:85462892-85462942	GM12878	blood:	n/a
45	chr1:85462812-85462862	Hela-S3	cervix:	n/a
46	chr1:85464110-85464160	GM12878	blood:	n/a
47	chr1:85462483-85462533	NB4	blood:	n/a
48	chr1:85464110-85464160	AG09309	skin:	n/a
49	chr1:85462483-85462533	H1-hESC	embryonic stem cell:	embryo
50	chr1:85462812-85462862	Hepatocyte	liver:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR63-1	chr1:85463140-85463597	XLOC_000274
2	lnc-WDR63-1	chr1:85463022-85463042	XLOC_000274

No data

Variant related genes	Relation type
MCOLN2	TF binding region
WDR63	TF binding region
MCOLN2	CpG island
WDR63	CpG island

Extended variants
information (count: 105 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371558245	chr1:85461862-85461863	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs545366097	chr1:85461914-85461915	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369955419	chr1:85461933-85461934	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10873677	chr1:85461946-85461947	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs187514871	chr1:85461953-85461954	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs111708666	chr1:85461975-85461976	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201537499	chr1:85462077-85462078	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200659040	chr1:85462089-85462090	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs201403803	chr1:85462101-85462102	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199778552	chr1:85462102-85462103	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs75518024	chr1:85462105-85462106	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs57506831	chr1:85462114-85462115	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145260540	chr1:85462132-85462133	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs538363702	chr1:85462137-85462138	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192033573	chr1:85462173-85462174	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs4907119	chr1:85462194-85462195	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
17	rs543820546	chr1:85462236-85462237	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs114977652	chr1:85462246-85462247	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs145392536	chr1:85462262-85462263	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs199880726	chr1:85462494-85462495	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs77452813	chr1:85462498-85462499	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs202107934	chr1:85462507-85462508	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs138052421	chr1:85462511-85462512	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs545503592	chr1:85462528-85462529	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs149504313	chr1:85462557-85462558	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs11161503	chr1:85462582-85462583	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs550689767	chr1:85462609-85462610	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs567663887	chr1:85462612-85462613	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs530316101	chr1:85462618-85462619	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546856011	chr1:85462627-85462628	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs149226662	chr1:85462644-85462645	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs11161504	chr1:85462652-85462653	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs11161505	chr1:85462665-85462666	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs532664263	chr1:85462674-85462675	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs568853211	chr1:85462684-85462685	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs11804811	chr1:85462692-85462693	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs554247093	chr1:85462722-85462723	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
38	rs574818216	chr1:85462729-85462730	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
39	rs540546215	chr1:85462748-85462749	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
40	rs920340	chr1:85462750-85462751	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114037164	chr1:85462772-85462773	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs545639110	chr1:85462777-85462778	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs112297575	chr1:85462799-85462800	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs371534810	chr1:85462802-85462803	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs369012332	chr1:85462812-85462813	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs530905003	chr1:85462822-85462823	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs554605802	chr1:85462852-85462853	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
48	rs72066647	chr1:85462853-85462854	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs544621524	chr1:85462862-85462863	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
50	rs57248654	chr1:85462875-85462876	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85454800-85462000	Weak transcription	Spleen	Spleen
2	chr1:85454800-85462200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:85457200-85461800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:85459800-85462000	Active TSS	Primary T helper cells PMA-I stimulated	--
5	chr1:85460400-85461800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr1:85460400-85463800	Active TSS	GM12878-XiMat	blood
7	chr1:85460600-85462200	Active TSS	Primary T killer memory cells from peripheral blood	blood
8	chr1:85460800-85462200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:85461200-85463400	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr1:85461400-85462200	Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr1:85461400-85462200	Active TSS	Rectal Mucosa Donor 31	rectum
12	chr1:85461600-85461800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
13	chr1:85461600-85461800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:85461600-85461800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
15	chr1:85461600-85462000	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
16	chr1:85461600-85462000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
17	chr1:85461600-85462000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
18	chr1:85461600-85462200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr1:85461600-85462200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:85461600-85462200	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:85461600-85462200	Active TSS	Duodenum Mucosa	Duodenum
22	chr1:85461600-85462200	Bivalent Enhancer	Fetal Intestine Large	intestine
23	chr1:85461600-85462200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
24	chr1:85461600-85462600	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr1:85461600-85464400	Active TSS	Primary T helper naive cells from peripheral blood	blood
26	chr1:85461800-85462000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr1:85461800-85462000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
28	chr1:85461800-85462000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:85461800-85462000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr1:85461800-85462200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:85461800-85462200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:85461800-85462200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:85461800-85462200	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr1:85461800-85462200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:85461800-85462200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:85461800-85462200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:85461800-85462200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
38	chr1:85461800-85462400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
39	chr1:85461800-85462800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr1:85461800-85463200	Active TSS	Rectal Smooth Muscle	rectum
41	chr1:85461800-85463200	Active TSS	A549	lung
42	chr1:85461800-85463600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr1:85461800-85464400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr1:85461800-85464600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr1:85462000-85462200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:85462000-85462200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:85462000-85462200	Enhancers	Adipose Nuclei	Adipose
48	chr1:85462000-85462200	Enhancers	Esophagus	oesophagus
49	chr1:85462000-85462200	Enhancers	Pancreas	Pancrea
50	chr1:85462000-85462200	Enhancers	Spleen	Spleen

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