Variant report

Variant	esv3325636
Chromosome Location	chr11:33294437-33360064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:587)
CpG islands
(count:428)
Chromatin interactive
region (count:89)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
2	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
3	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
4	ATF1	chr11:33329665-33330069	K562	blood:	n/a	n/a
5	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
6	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
7	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
8	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
9	BCLAF1	chr11:33341910-33342551	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:33313026-33313370	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:33308243-33308452	K562	blood:	n/a	n/a
12	BHLHE40	chr11:33345920-33346220	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:33342530-33342916	K562	blood:	n/a	n/a
14	BRCA1	chr11:33295193-33295271	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr11:33337746-33337909	HepG2	liver:	n/a	n/a
16	CCNT2	chr11:33306514-33306664	K562	blood:	n/a	n/a
17	CEBPB	chr11:33351032-33351033	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr11:33338242-33338385	H1-hESC	embryonic stem cell:	n/a	chr11:33338319-33338330
19	CEBPB	chr11:33298377-33298553	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:33342449-33342823	K562	blood:	n/a	n/a
21	CEBPB	chr11:33338152-33338466	IMR90	lung:	n/a	chr11:33338319-33338330
22	CEBPB	chr11:33342400-33342909	K562	blood:	n/a	n/a
23	CEBPB	chr11:33332237-33332437	K562	blood:	n/a	n/a
24	CEBPB	chr11:33332158-33332527	MCF-7	breast:	n/a	n/a
25	CEBPB	chr11:33342462-33342728	K562	blood:	n/a	n/a
26	CEBPB	chr11:33345871-33346122	A549	lung:	n/a	chr11:33346014-33346027
27	CEBPB	chr11:33338268-33338364	K562	blood:	n/a	chr11:33338319-33338330
28	CEBPB	chr11:33338182-33338375	HepG2	liver:	n/a	chr11:33338319-33338330
29	CEBPD	chr11:33342455-33343048	K562	blood:	n/a	n/a
30	CEBPD	chr11:33342441-33342930	K562	blood:	n/a	n/a
31	CEBPD	chr11:33331503-33332110	K562	blood:	n/a	n/a
32	CHD1	chr11:33312856-33313287	GM12878	blood:	n/a	n/a
33	CHD2	chr11:33312979-33313342	GM12878	blood:	n/a	n/a
34	CHD2	chr11:33346058-33346074	GM12878	blood:	n/a	n/a
35	CTCF	chr11:33351357-33351565	ProgFib	skin:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
36	CTCF	chr11:33330980-33331130	GM12873	blood:	n/a	n/a
37	CTCF	chr11:33345060-33345210	AG04449	skin:	n/a	n/a
38	CTCF	chr11:33351264-33351627	HCT-116	colon:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
39	CTCF	chr11:33351340-33351490	HepG2	liver:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
40	CTCF	chr11:33351420-33351570	GM12872	blood:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
41	CTCF	chr11:33341655-33341777	GM12878	blood:	n/a	n/a
42	CTCF	chr11:33351400-33351550	HMF	breast:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
43	CTCF	chr11:33341660-33341772	GM13977	blood:	n/a	n/a
44	CTCF	chr11:33312935-33312937	GM12878	blood:	n/a	n/a
45	CTCF	chr11:33351330-33351615	K562	blood:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
46	CTCF	chr11:33345200-33345350	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr11:33351259-33351658	IMR90	lung:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
48	CTCF	chr11:33351400-33351550	GM12874	blood:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
49	CTCF	chr11:33351400-33351550	HCT-116	colon:	n/a	chr11:33351462-33351483 chr11:33351467-33351485 chr11:33351472-33351480 chr11:33351468-33351484
50	CTCF	chr11:33345860-33346010	Caco-2	colon:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33308345-33308395	Jurkat	blood:	n/a
2	chr11:33308345-33308395	Jurkat	blood:	n/a
3	chr11:33317093-33317143	MCF10A-Er-Src	breast:	n/a
4	chr11:33308345-33308395	HepG2	liver:	n/a
5	chr11:33346306-33346356	Hela-S3	cervix:	n/a
6	chr11:33308345-33308395	HCPEpiC	choroid plexus:	n/a
7	chr11:33317093-33317143	HNPCEpiC	eye:	n/a
8	chr11:33334443-33334493	ovcar-3	ovarian:	n/a
9	chr11:33317093-33317143	SK-N-MC	brain:	n/a
10	chr11:33308269-33308319	AG04449	skin:	fetal
11	chr11:33317015-33317065	ovcar-3	ovarian:	n/a
12	chr11:33346306-33346356	A549	lung:	n/a
13	chr11:33308269-33308319	MCF-7	breast:	n/a
14	chr11:33317015-33317065	HRE	kidney:	n/a
15	chr11:33308345-33308395	NHDF-neo	bronchial:	n/a
16	chr11:33317015-33317065	GM12878	blood:	n/a
17	chr11:33334443-33334493	AG04449	skin:	fetal
18	chr11:33317015-33317065	HCM	heart:	n/a
19	chr11:33317093-33317143	PANC-1	pancreas:	n/a
20	chr11:33308345-33308395	CMK	blood:	n/a
21	chr11:33317093-33317143	GM06990	blood:	n/a
22	chr11:33334443-33334493	NB4	blood:	n/a
23	chr11:33308345-33308395	GM19239	blood:	n/a
24	chr11:33317093-33317143	HCM	heart:	n/a
25	chr11:33308269-33308319	HCPEpiC	choroid plexus:	n/a
26	chr11:33317015-33317065	ProgFib	skin:	n/a
27	chr11:33308269-33308319	HIPEpiC	eye:	n/a
28	chr11:33317015-33317065	HepG2	liver:	n/a
29	chr11:33346306-33346356	SKMC	muscle:	n/a
30	chr11:33317039-33317089	GM12892	blood:	n/a
31	chr11:33317015-33317065	GM19239	blood:	n/a
32	chr11:33317039-33317089	Hepatocyte	liver:	n/a
33	chr11:33308269-33308319	PrEC	prostate:	n/a
34	chr11:33317015-33317065	GM12892	blood:	n/a
35	chr11:33317039-33317089	HCM	heart:	n/a
36	chr11:33334443-33334493	HMEC	breast:	n/a
37	chr11:33317015-33317065	T-47D	breast:	n/a
38	chr11:33308269-33308319	SKMC	muscle:	n/a
39	chr11:33317093-33317143	K562	blood:	n/a
40	chr11:33308269-33308319	Jurkat	blood:	n/a
41	chr11:33317093-33317143	GM12892	blood:	n/a
42	chr11:33334443-33334493	PrEC	prostate:	n/a
43	chr11:33308269-33308319	RPTEC	kidney:	n/a
44	chr11:33317015-33317065	HEEpiC	esophagus:	n/a
45	chr11:33317039-33317089	Jurkat	blood:	n/a
46	chr11:33317015-33317065	HAEpiC	amniotic membrane:	n/a
47	chr11:33308269-33308319	PFSK-1	brain:	n/a
48	chr11:33346306-33346356	GM12891	blood:	n/a
49	chr11:33308269-33308319	PANC-1	pancreas:	n/a
50	chr11:33308269-33308319	SAEC	small airway:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:33278421..33280319-chr11:33347854..33349569,2	K562	blood:
2	chr11:33340003..33342699-chr11:33347574..33349225,2	K562	blood:
3	chr11:33277703..33279288-chr11:33314208..33316687,2	K562	blood:
4	chr11:33277785..33280697-chr11:33298696..33301567,3	K562	blood:
5	chr11:33353025..33355412-chr11:33355874..33357955,2	MCF-7	breast:
6	chr11:33192932..33194844-chr11:33338349..33340157,2	K562	blood:
7	chr11:33278126..33279710-chr11:33347501..33349004,2	MCF-7	breast:
8	chr11:33294153..33295925-chr11:33303597..33306470,2	MCF-7	breast:
9	chr11:33313913..33316207-chr11:33316446..33318411,2	MCF-7	breast:
10	chr11:33302394..33304355-chr11:33304871..33306410,2	MCF-7	breast:
11	chr11:33352566..33355131-chr11:33757100..33758985,2	MCF-7	breast:
12	chr11:33278813..33281447-chr11:33356120..33358697,4	MCF-7	breast:
13	chr11:33278606..33279290-chr11:33341646..33342645,2	MCF-7	breast:
14	chr11:33323694..33328844-chr11:33341332..33344470,4	K562	blood:
15	chr11:33303628..33306131-chr11:33323858..33326842,2	MCF-7	breast:
16	chr11:33187604..33188364-chr11:33351039..33351579,2	MCF-7	breast:
17	chr11:33300069..33303546-chr11:33304515..33307878,3	K562	blood:
18	chr11:33330031..33332498-chr11:33332591..33335075,2	MCF-7	breast:
19	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
20	chr11:33301670..33304585-chr11:33308750..33310555,2	MCF-7	breast:
21	chr11:33330605..33333745-chr11:33333939..33336380,3	K562	blood:
22	chr11:33345699..33348337-chr11:33348377..33350579,2	K562	blood:
23	chr11:33294153..33295925-chr11:33303597..33306470,2	MCF-7	breast:
24	chr11:33315778..33318693-chr11:33329241..33331442,2	K562	blood:
25	chr11:33326071..33328703-chr11:33331126..33332666,2	K562	blood:
26	chr11:33290160..33295323-chr11:33296264..33299611,6	K562	blood:
27	chr11:33187513..33188468-chr11:33351019..33351906,6	K562	blood:
28	chr11:33287096..33288603-chr11:33295589..33298178,2	K562	blood:
29	chr11:33330031..33332498-chr11:33332591..33335075,2	MCF-7	breast:
30	chr11:33278004..33279582-chr11:33355016..33356972,2	MCF-7	breast:
31	chr11:33275628..33278249-chr11:33296623..33299579,2	MCF-7	breast:
32	chr11:33295510..33298168-chr11:33350276..33353237,2	K562	blood:
33	chr11:33278431..33280994-chr11:33343148..33345280,2	MCF-7	breast:
34	chr11:33327923..33330739-chr11:33334207..33336221,2	K562	blood:
35	chr11:33300069..33303546-chr11:33304515..33307878,3	K562	blood:
36	chr11:33323694..33328844-chr11:33341332..33344470,4	K562	blood:
37	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
38	chr11:33183085..33184714-chr11:33357286..33359018,2	K562	blood:
39	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
40	chr11:33300641..33303261-chr11:33311159..33314863,3	K562	blood:
41	chr11:33350757..33353405-chr11:33354429..33357042,2	K562	blood:
42	chr11:33277050..33279115-chr11:33307731..33309675,2	K562	blood:
43	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:
44	chr11:33278050..33279877-chr11:33311339..33315045,4	MCF-7	breast:
45	chr11:33277710..33282201-chr11:33292143..33296310,6	K562	blood:
46	chr11:33292487..33295323-chr11:33297832..33299611,2	K562	blood:
47	chr11:33327923..33330739-chr11:33334207..33336221,2	K562	blood:
48	chr11:33326071..33328703-chr11:33331126..33332666,2	K562	blood:
49	chr11:33277681..33279194-chr11:33330254..33333182,2	MCF-7	breast:
50	chr11:33330605..33333745-chr11:33333939..33336380,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
2	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704

Variant related genes	Relation type
HIPK3	TF binding region
HIPK3	CpG island
ENSG00000110422	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000206808	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000085063	chromatin interactions

Extended variants
information (count: 2326 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569959653	chr11:33294466-33294467	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539272481	chr11:33294469-33294470	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534951545	chr11:33294474-33294475	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374324358	chr11:33294508-33294509	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553260259	chr11:33294535-33294536	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs832794	chr11:33294559-33294560	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192160343	chr11:33294776-33294777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs183890431	chr11:33294783-33294784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186811974	chr11:33294786-33294787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376123883	chr11:33294789-33294790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563740745	chr11:33294866-33294867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573394757	chr11:33294877-33294878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs116916728	chr11:33294900-33294901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568445	chr11:33294928-33294929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113422817	chr11:33294981-33294982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556079473	chr11:33294987-33294988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374115500	chr11:33295007-33295008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567545	chr11:33295015-33295016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112222811	chr11:33295019-33295020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377564788	chr11:33295021-33295022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs71034666	chr11:33295022-33295023	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs645341	chr11:33295034-33295035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551596839	chr11:33295048-33295049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs645318	chr11:33295057-33295058	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377504900	chr11:33295058-33295059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376665214	chr11:33295059-33295060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs398015727	chr11:33295078-33295079	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs61511546	chr11:33295084-33295085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373329391	chr11:33295085-33295086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545254561	chr11:33295131-33295132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558558444	chr11:33295133-33295134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146402654	chr11:33295145-33295146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190459372	chr11:33295146-33295147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs183046844	chr11:33295205-33295206	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139080918	chr11:33295213-33295214	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543553856	chr11:33295216-33295217	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186956116	chr11:33295223-33295224	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370114158	chr11:33295317-33295318	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191751449	chr11:33295351-33295352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs530912575	chr11:33295358-33295359	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552573886	chr11:33295386-33295387	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549417355	chr11:33295490-33295491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12417656	chr11:33295500-33295501	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566008097	chr11:33295554-33295555	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116186039	chr11:33295591-33295592	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs10836047	chr11:33295641-33295642	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs116592676	chr11:33295653-33295654	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182706628	chr11:33295707-33295708	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117745505	chr11:33295715-33295716	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556002730	chr11:33295734-33295735	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2153 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33280600-33308200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:33281400-33295200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr11:33281800-33295200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:33284200-33313000	Weak transcription	Fetal Kidney	kidney
5	chr11:33284200-33318200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr11:33285000-33297400	Weak transcription	Fetal Muscle Leg	muscle
7	chr11:33285000-33307400	Weak transcription	Gastric	stomach
8	chr11:33285000-33326200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:33285200-33306000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr11:33285200-33308000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr11:33285200-33308200	Weak transcription	Spleen	Spleen
12	chr11:33285800-33295400	Weak transcription	Brain Hippocampus Middle	brain
13	chr11:33285800-33312800	Weak transcription	Fetal Stomach	stomach
14	chr11:33286000-33296000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:33286000-33308200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:33286600-33295400	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr11:33286600-33296400	Weak transcription	Brain Angular Gyrus	brain
18	chr11:33286800-33299000	Weak transcription	Brain Anterior Caudate	brain
19	chr11:33288200-33295200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr11:33288600-33296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:33288600-33308000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:33288800-33298400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:33288800-33298800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:33288800-33308000	Weak transcription	Dnd41	blood
25	chr11:33289000-33308000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr11:33289000-33312600	Weak transcription	Aorta	Aorta
27	chr11:33289200-33298400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr11:33289600-33300600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr11:33289800-33295200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr11:33290000-33336800	Weak transcription	Lung	lung
31	chr11:33290800-33297800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:33290800-33298400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:33290800-33307400	Weak transcription	Right Atrium	heart
34	chr11:33291000-33295200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr11:33291000-33295400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:33291000-33295400	Weak transcription	Fetal Heart	heart
37	chr11:33291000-33295400	Weak transcription	HepG2	liver
38	chr11:33291000-33295600	Weak transcription	NHEK	skin
39	chr11:33291000-33295600	Weak transcription	Osteobl	bone
40	chr11:33291000-33308200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:33291000-33308200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr11:33291400-33295400	Weak transcription	Brain Substantia Nigra	brain
43	chr11:33291400-33308000	Weak transcription	NHDF-Ad	bronchial
44	chr11:33291600-33295000	Enhancers	Left Ventricle	heart
45	chr11:33291600-33295400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:33291600-33308000	Weak transcription	HSMM	muscle
47	chr11:33291800-33295400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:33291800-33295400	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:33291800-33295400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr11:33291800-33295600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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