Variant report

Variant	esv3328460
Chromosome Location	chr11:66884901-66888249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:755)
CpG islands
(count:733)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:66886519-66886690	HepG2	liver:	n/a	n/a
2	ATF1	chr11:66886428-66886747	K562	blood:	n/a	n/a
3	ATF2	chr11:66888245-66888872	GM12878	blood:	n/a	n/a
4	ATF3	chr11:66886451-66886642	K562	blood:	n/a	chr11:66886558-66886567
5	BACH1	chr11:66885141-66886766	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr11:66888223-66888754	GM12878	blood:	n/a	chr11:66888475-66888484
7	BCLAF1	chr11:66886432-66886808	GM12878	blood:	n/a	chr11:66886721-66886729
8	BCLAF1	chr11:66886934-66887719	GM12878	blood:	n/a	chr11:66887150-66887163
9	BHLHE40	chr11:66886076-66886938	GM12878	blood:	n/a	chr11:66886386-66886402
10	BHLHE40	chr11:66887188-66887203	K562	blood:	n/a	n/a
11	BHLHE40	chr11:66887753-66887754	K562	blood:	n/a	n/a
12	BHLHE40	chr11:66887770-66888841	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:66886327-66886773	K562	blood:	n/a	chr11:66886386-66886402
14	BRCA1	chr11:66887723-66888091	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr11:66886482-66886740	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr11:66886279-66887780	K562	blood:	n/a	chr11:66886684-66886693 chr11:66886310-66886319 chr11:66886652-66886661 chr11:66887530-66887539
17	CEBPB	chr11:66886534-66886800	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:66884737-66884941	HepG2	liver:	n/a	chr11:66884840-66884851
19	CEBPD	chr11:66886341-66886751	HepG2	liver:	n/a	n/a
20	CHD1	chr11:66886861-66886931	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr11:66888131-66889212	GM12878	blood:	n/a	n/a
22	CHD1	chr11:66885996-66886157	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr11:66887244-66888120	H1-hESC	embryonic stem cell:	n/a	chr11:66887530-66887540
24	CHD1	chr11:66886091-66886187	GM12878	blood:	n/a	n/a
25	CHD1	chr11:66886631-66887341	GM12878	blood:	n/a	n/a
26	CHD2	chr11:66886330-66886849	K562	blood:	n/a	chr11:66886392-66886402
27	CHD2	chr11:66886031-66886946	GM12878	blood:	n/a	chr11:66886392-66886402
28	CHD2	chr11:66886367-66886494	HepG2	liver:	n/a	chr11:66886392-66886402
29	CHD2	chr11:66886752-66886919	HepG2	liver:	n/a	n/a
30	CHD2	chr11:66886544-66886639	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:66886093-66886960	Hela-S3	cervix:	n/a	chr11:66886392-66886402
32	CHD2	chr11:66886040-66886288	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:66887253-66887728	Hela-S3	cervix:	n/a	chr11:66887530-66887540
34	CREB1	chr11:66886224-66886943	A549	lung:	n/a	n/a
35	CREB1	chr11:66886172-66886870	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr11:66886161-66886988	GM12878	blood:	n/a	n/a
37	CREB1	chr11:66886173-66886971	K562	blood:	n/a	n/a
38	CREB1	chr11:66886131-66886806	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr11:66886436-66886688	A549	lung:	n/a	n/a
40	CREB1	chr11:66886441-66886727	ECC-1	luminal epithelium:	n/a	n/a
41	CREB1	chr11:66886144-66887060	HepG2	liver:	n/a	n/a
42	CTCF	chr11:66887100-66887250	A549	lung:	n/a	chr11:66887164-66887182 chr11:66887170-66887179
43	CTCF	chr11:66887141-66887245	GM12892	blood:	n/a	chr11:66887164-66887182 chr11:66887170-66887179
44	CTCF	chr11:66886407-66886672	IMR90	lung:	n/a	n/a
45	CTCF	chr11:66887060-66887210	SAEC	small airway:	n/a	chr11:66887164-66887182 chr11:66887170-66887179
46	CTCF	chr11:66886420-66886570	GM12864	blood:	n/a	n/a
47	CTCF	chr11:66887128-66887251	A549	lung:	n/a	chr11:66887164-66887182 chr11:66887170-66887179
48	CTCF	chr11:66886900-66887050	GM12871	blood:	n/a	n/a
49	CTCF	chr11:66886449-66886681	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:66887129-66887242	Hela-S3	cervix:	n/a	chr11:66887164-66887182 chr11:66887170-66887179

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66886748-66886798	CMK	blood:	n/a
2	chr11:66886748-66886798	CMK	blood:	n/a
3	chr11:66886748-66886798	GM12891	blood:	n/a
4	chr11:66887657-66887707	NHDF-neo	bronchial:	n/a
5	chr11:66885240-66885290	SK-N-MC	brain:	n/a
6	chr11:66887657-66887707	HRE	kidney:	n/a
7	chr11:66887736-66887786	RPTEC	kidney:	n/a
8	chr11:66885240-66885290	AG09309	skin:	n/a
9	chr11:66887329-66887379	A549	lung:	n/a
10	chr11:66887657-66887707	Hela-S3	cervix:	n/a
11	chr11:66886765-66886815	Hepatocyte	liver:	n/a
12	chr11:66886748-66886798	NHBE	bronchial:	n/a
13	chr11:66886118-66886168	HEK293	kidney:	embryo
14	chr11:66887657-66887707	HMEC	breast:	n/a
15	chr11:66887329-66887379	IMR90	lung:	fetal
16	chr11:66886253-66886303	Hepatocyte	liver:	n/a
17	chr11:66885276-66885326	NHDF-neo	bronchial:	n/a
18	chr11:66886141-66886191	HRE	kidney:	n/a
19	chr11:66886141-66886191	HAEpiC	amniotic membrane:	n/a
20	chr11:66885276-66885326	BJ	skin:	n/a
21	chr11:66886141-66886191	HL-60	blood:	n/a
22	chr11:66886765-66886815	CMK	blood:	n/a
23	chr11:66885276-66885326	HCT-116	colon:	n/a
24	chr11:66885281-66885331	HRE	kidney:	n/a
25	chr11:66887736-66887786	HEK293	kidney:	embryo
26	chr11:66887736-66887786	BJ	skin:	n/a
27	chr11:66886765-66886815	PrEC	prostate:	n/a
28	chr11:66886253-66886303	ovcar-3	ovarian:	n/a
29	chr11:66886765-66886815	PANC-1	pancreas:	n/a
30	chr11:66886141-66886191	CMK	blood:	n/a
31	chr11:66885240-66885290	HCPEpiC	choroid plexus:	n/a
32	chr11:66887329-66887379	SK-N-MC	brain:	n/a
33	chr11:66885276-66885326	HIPEpiC	eye:	n/a
34	chr11:66885281-66885331	HMEC	breast:	n/a
35	chr11:66887329-66887379	HRCEpiC	kidney:	n/a
36	chr11:66886918-66886968	Jurkat	blood:	n/a
37	chr11:66887736-66887786	HCF	heart:	n/a
38	chr11:66887657-66887707	AG09309	skin:	n/a
39	chr11:66887657-66887707	ProgFib	skin:	n/a
40	chr11:66887329-66887379	HUVEC	blood vessel:	n/a
41	chr11:66885276-66885326	SKMC	muscle:	n/a
42	chr11:66886141-66886191	SKMC	muscle:	n/a
43	chr11:66885276-66885326	GM12891	blood:	n/a
44	chr11:66886765-66886815	HCM	heart:	n/a
45	chr11:66886765-66886815	AG04450	lung:	fetal
46	chr11:66886765-66886815	HMEC	breast:	n/a
47	chr11:66886253-66886303	SK-N-SH_RA	brain:	n/a
48	chr11:66885281-66885331	GM12891	blood:	n/a
49	chr11:66886141-66886191	HCPEpiC	choroid plexus:	n/a
50	chr11:66886748-66886798	Hepatocyte	liver:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66885437..66888305-chr11:67055921..67058495,2	MCF-7	breast:
2	chr11:66884756..66886465-chr11:66946415..66948664,2	MCF-7	breast:
3	chr11:66821404..66826403-chr11:66884710..66889541,16	MCF-7	breast:
4	chr11:66884916..66890908-chr11:67005112..67010354,8	MCF-7	breast:
5	chr11:66845358..66847387-chr11:66887681..66889198,2	MCF-7	breast:
6	chr11:66883623..66889678-chr11:67005085..67009894,16	K562	blood:
7	chr11:66847793..66850553-chr11:66883657..66886437,2	MCF-7	breast:
8	chr1:46712974..46713939-chr11:66887574..66888204,2	Hela-S3	cervix:
9	chr11:66885158..66886682-chr11:67030764..67032501,2	K562	blood:
10	chr11:66821625..66825972-chr11:66885437..66888104,7	MCF-7	breast:
11	chr11:66886660..66888352-chr11:67075399..67077454,2	K562	blood:
12	chr11:66812155..66813969-chr11:66888125..66890651,2	K562	blood:
13	chr11:66887881..66889769-chr11:66929494..66931769,2	MCF-7	breast:
14	chr11:66886805..66888356-chr20:52209357..52211197,2	MCF-7	breast:
15	chr11:66885940..66887950-chr11:67395860..67397869,2	K562	blood:
16	chr11:66884866..66886450-chr11:67007040..67008886,2	MCF-7	breast:
17	chr11:66886604..66887153-chr17:19551576..19552186,2	NB4	blood:
18	chr11:66885002..66889173-chr11:67005085..67009324,11	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RHOD-4	chr11:66887362-66887520	NONHSAT022378

No data

Variant related genes	Relation type
KDM2A	TF binding region
KDM2A	CpG island
ENSG00000072210	chromatin interactions
ENSG00000172932	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000085999	chromatin interactions
ENSG00000173156	chromatin interactions
ENSG00000173120	chromatin interactions
ENSG00000172830	chromatin interactions

Extended variants
information (count: 68 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368620489	chr11:66884948-66884949	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs575373982	chr11:66884958-66884959	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs75081047	chr11:66885054-66885055	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs541652387	chr11:66885055-66885056	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs559793769	chr11:66885101-66885102	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs191331286	chr11:66885129-66885130	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372880436	chr11:66885133-66885134	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs551868931	chr11:66885179-66885180	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs117266031	chr11:66885182-66885183	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs117538255	chr11:66885213-66885214	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs567564483	chr11:66885384-66885385	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549473350	chr11:66885395-66885396	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs568187797	chr11:66885475-66885476	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs7109019	chr11:66885479-66885480	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs535286795	chr11:66885533-66885534	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs553959111	chr11:66885558-66885559	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs565818514	chr11:66885613-66885614	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs4072610	chr11:66885659-66885660	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs150722876	chr11:66885730-66885731	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113643152	chr11:66885897-66885898	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs558158260	chr11:66885959-66885960	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs376237870	chr11:66886024-66886025	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs537503648	chr11:66886034-66886035	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs139077511	chr11:66886067-66886068	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs12284546	chr11:66886145-66886146	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541244650	chr11:66886610-66886611	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs528690290	chr11:66886659-66886660	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs577881403	chr11:66886734-66886735	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs545299614	chr11:66886772-66886773	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs563697375	chr11:66886782-66886783	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs531197131	chr11:66886784-66886785	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs549793548	chr11:66886815-66886816	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs561604401	chr11:66887067-66887068	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs529015990	chr11:66887068-66887069	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs547878162	chr11:66887169-66887170	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs547238122	chr11:66887224-66887225	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs370928737	chr11:66887275-66887276	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs547225440	chr11:66887281-66887282	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs565900476	chr11:66887342-66887343	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs539699491	chr11:66887363-66887364	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs568862860	chr11:66887379-66887380	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs551712101	chr11:66887383-66887384	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs570899139	chr11:66887390-66887391	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs532039802	chr11:66887403-66887404	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs374579802	chr11:66887463-66887464	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
46	rs528593391	chr11:66887486-66887487	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
47	rs140960382	chr11:66887488-66887489	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs547107231	chr11:66887495-66887496	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs568292835	chr11:66887496-66887497	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs144920685	chr11:66887531-66887532	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
Schizophrenia	21346763	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66879000-66885200	Weak transcription	Right Ventricle	heart
2	chr11:66879200-66885000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:66879200-66885000	Weak transcription	Right Atrium	heart
4	chr11:66879200-66885200	Weak transcription	Left Ventricle	heart
5	chr11:66879400-66885000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr11:66879600-66885000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:66880400-66885000	Enhancers	Fetal Intestine Small	intestine
8	chr11:66880600-66885000	Enhancers	Fetal Intestine Large	intestine
9	chr11:66881000-66886800	Weak transcription	K562	blood
10	chr11:66881200-66885000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:66881200-66885000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:66881200-66885000	Weak transcription	Esophagus	oesophagus
13	chr11:66881200-66885200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:66881200-66885200	Weak transcription	Dnd41	blood
15	chr11:66881400-66885000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:66881800-66885000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr11:66882000-66885000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:66882200-66885000	Weak transcription	Colonic Mucosa	Colon
19	chr11:66882600-66885200	Enhancers	A549	lung
20	chr11:66882800-66885000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:66882800-66885000	Enhancers	Stomach Mucosa	stomach
22	chr11:66883200-66885000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr11:66883400-66885000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr11:66883600-66885000	Enhancers	Brain Hippocampus Middle	brain
25	chr11:66883600-66885000	Enhancers	Fetal Lung	lung
26	chr11:66883600-66885000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr11:66883600-66885000	Weak transcription	GM12878-XiMat	blood
28	chr11:66883600-66885200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr11:66883600-66886000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:66883800-66885000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:66884000-66885200	Enhancers	Fetal Stomach	stomach
32	chr11:66884200-66885000	Bivalent Enhancer	Fetal Thymus	thymus
33	chr11:66884200-66885200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr11:66884200-66885400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:66884400-66885000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:66884400-66885000	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr11:66884400-66885000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr11:66884400-66885000	Enhancers	Colon Smooth Muscle	Colon
39	chr11:66884400-66885000	Weak transcription	Gastric	stomach
40	chr11:66884400-66885000	Enhancers	Rectal Smooth Muscle	rectum
41	chr11:66884400-66885400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:66884600-66885000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr11:66884600-66885000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr11:66884600-66885000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr11:66884600-66885000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:66884600-66885000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:66884600-66885000	Enhancers	Fetal Brain Male	brain
48	chr11:66884600-66885000	Flanking Active TSS	HepG2	liver
49	chr11:66884600-66885200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr11:66884600-66885200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell

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