Variant report

Variant	nsv1045088
Chromosome Location	chr11:33331237-33560445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2062)
CpG islands
(count:1281)
Chromatin interactive
region (count:137)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:2062 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33529658-33529797	K562	blood:	n/a	n/a
3	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
4	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
6	ARID3A	chr11:33364523-33364723	K562	blood:	n/a	n/a
7	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
8	ARID3A	chr11:33499524-33499864	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
11	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
12	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
13	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
14	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
15	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
16	ATF2	chr11:33547216-33547636	GM12878	blood:	n/a	n/a
17	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
18	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
19	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
20	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
21	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
22	ATF3	chr11:33382233-33382453	K562	blood:	n/a	chr11:33382358-33382372
23	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr11:33364471-33364818	K562	blood:	n/a	n/a
25	BATF	chr11:33547673-33547858	GM12878	blood:	n/a	n/a
26	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
27	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a
28	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
29	BATF	chr11:33363592-33363812	GM12878	blood:	n/a	n/a
30	BATF	chr11:33363521-33363808	GM12878	blood:	n/a	n/a
31	BATF	chr11:33547665-33547985	GM12878	blood:	n/a	n/a
32	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
33	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:33409572-33409836	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:33404557-33404945	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:33409034-33409543	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:33409556-33409888	GM12878	blood:	n/a	n/a
38	BCL3	chr11:33547150-33547634	GM12878	blood:	n/a	n/a
39	BCL3	chr11:33409282-33409904	GM12878	blood:	n/a	n/a
40	BCL3	chr11:33404619-33404913	GM12878	blood:	n/a	n/a
41	BCL3	chr11:33512690-33512977	GM12878	blood:	n/a	n/a
42	BCLAF1	chr11:33341910-33342551	GM12878	blood:	n/a	n/a
43	BCLAF1	chr11:33409061-33410037	GM12878	blood:	n/a	n/a
44	BCLAF1	chr11:33409067-33410001	GM12878	blood:	n/a	n/a
45	BCLAF1	chr11:33404519-33404990	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:33401529-33401825	GM12878	blood:	n/a	n/a
47	BHLHE40	chr11:33427892-33427983	K562	blood:	n/a	n/a
48	BHLHE40	chr11:33369101-33369338	GM12878	blood:	n/a	n/a
49	BHLHE40	chr11:33404539-33405771	GM12878	blood:	n/a	n/a
50	BHLHE40	chr11:33484666-33484886	K562	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33398173-33398223	NH-A	brain:	n/a
2	chr11:33442321-33442371	PrEC	prostate:	n/a
3	chr11:33506184-33506234	AG04450	lung:	fetal
4	chr11:33474484-33474534	NHDF-neo	bronchial:	n/a
5	chr11:33399978-33400028	A549	lung:	n/a
6	chr11:33397153-33397203	GM12891	blood:	n/a
7	chr11:33346306-33346356	HNPCEpiC	eye:	n/a
8	chr11:33397821-33397871	A549	lung:	n/a
9	chr11:33398173-33398223	HMEC	breast:	n/a
10	chr11:33453389-33453439	HAEpiC	amniotic membrane:	n/a
11	chr11:33474484-33474534	HNPCEpiC	eye:	n/a
12	chr11:33398173-33398223	PANC-1	pancreas:	n/a
13	chr11:33398173-33398223	NB4	blood:	n/a
14	chr11:33375412-33375462	Hepatocyte	liver:	n/a
15	chr11:33375412-33375462	HCM	heart:	n/a
16	chr11:33442321-33442371	HepG2	liver:	n/a
17	chr11:33474484-33474534	MCF10A-Er-Src	breast:	n/a
18	chr11:33399978-33400028	HAEpiC	amniotic membrane:	n/a
19	chr11:33397387-33397437	HCPEpiC	choroid plexus:	n/a
20	chr11:33506184-33506234	NHBE	bronchial:	n/a
21	chr11:33399978-33400028	T-47D	breast:	n/a
22	chr11:33554009-33554059	BE2_C	brain:	n/a
23	chr11:33397689-33397739	Hepatocyte	liver:	n/a
24	chr11:33554009-33554059	GM12878	blood:	n/a
25	chr11:33334443-33334493	NHBE	bronchial:	n/a
26	chr11:33453389-33453439	GM12891	blood:	n/a
27	chr11:33397153-33397203	T-47D	breast:	n/a
28	chr11:33397821-33397871	HUVEC	blood vessel:	n/a
29	chr11:33397689-33397739	HMEC	breast:	n/a
30	chr11:33346306-33346356	SKMC	muscle:	n/a
31	chr11:33396983-33397033	HMEC	breast:	n/a
32	chr11:33394273-33394323	ovcar-3	ovarian:	n/a
33	chr11:33394273-33394323	ECC-1	luminal epithelium:	n/a
34	chr11:33397821-33397871	GM19239	blood:	n/a
35	chr11:33397821-33397871	T-47D	breast:	n/a
36	chr11:33334443-33334493	HEEpiC	esophagus:	n/a
37	chr11:33398245-33398295	NHDF-neo	bronchial:	n/a
38	chr11:33398366-33398416	PFSK-1	brain:	n/a
39	chr11:33397387-33397437	GM19239	blood:	n/a
40	chr11:33396983-33397033	Hepatocyte	liver:	n/a
41	chr11:33398173-33398223	HCF	heart:	n/a
42	chr11:33442321-33442371	Jurkat	blood:	n/a
43	chr11:33399978-33400028	Jurkat	blood:	n/a
44	chr11:33397689-33397739	T-47D	breast:	n/a
45	chr11:33554009-33554059	HCM	heart:	n/a
46	chr11:33397387-33397437	NB4	blood:	n/a
47	chr11:33453389-33453439	Jurkat	blood:	n/a
48	chr11:33397153-33397203	HCM	heart:	n/a
49	chr11:33399978-33400028	HNPCEpiC	eye:	n/a
50	chr11:33397153-33397203	U87	brain:	n/a

(count:137 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:33450480..33453431-chr11:33470843..33473158,2	MCF-7	breast:
2	chr11:33278421..33280319-chr11:33347854..33349569,2	K562	blood:
3	chr11:33412811..33414591-chr11:33744029..33746622,2	K562	blood:
4	chr11:33353025..33355412-chr11:33355874..33357955,2	MCF-7	breast:
5	chr11:33277681..33279194-chr11:33330254..33333182,2	MCF-7	breast:
6	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
7	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
8	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
9	chr11:33392077..33394205-chr11:33397342..33400084,3	K562	blood:
10	chr11:33464022..33465573-chr11:33469227..33471332,2	K562	blood:
11	chr11:33403805..33405903-chr11:33414463..33417062,2	MCF-7	breast:
12	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:
13	chr11:33474719..33477394-chr11:33482084..33484055,2	K562	blood:
14	chr11:33366273..33368343-chr11:33370196..33371959,2	K562	blood:
15	chr11:33360581..33362754-chr11:33365388..33367285,2	K562	blood:
16	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:
17	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
18	chr11:33343171..33345414-chr11:33349512..33351209,2	K562	blood:
19	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
20	chr11:33432981..33435559-chr11:33436354..33439310,2	K562	blood:
21	chr11:33492401..33495030-chr11:33579028..33581044,2	K562	blood:
22	chr11:33382588..33385319-chr11:33707872..33709435,2	MCF-7	breast:
23	chr11:33323694..33328844-chr11:33341332..33344470,4	K562	blood:
24	chr11:33187260..33188477-chr11:33350825..33351973,13	MCF-7	breast:
25	chr11:33278606..33279290-chr11:33341646..33342645,2	MCF-7	breast:
26	chr11:33383578..33384538-chr11:33708929..33709708,5	K562	blood:
27	chr11:33351340..33351943-chr11:33383658..33384527,2	K562	blood:
28	chr11:33347406..33349145-chr11:33350262..33352793,2	MCF-7	breast:
29	chr11:33495157..33498013-chr11:33505516..33507926,2	K562	blood:
30	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
31	chr11:33429478..33432664-chr11:33434233..33436615,3	K562	blood:
32	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
33	chr11:33513897..33516124-chr11:33565308..33567092,2	K562	blood:
34	chr11:33330031..33332498-chr11:33332591..33335075,2	MCF-7	breast:
35	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
36	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
37	chr11:33183085..33184714-chr11:33357286..33359018,2	K562	blood:
38	chr11:33347406..33349145-chr11:33350262..33352793,2	MCF-7	breast:
39	chr11:33396319..33398155-chr11:33401081..33403706,2	MCF-7	breast:
40	chr11:33365715..33367217-chr11:33368914..33370934,2	K562	blood:
41	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
42	chr11:33278431..33280994-chr11:33343148..33345280,2	MCF-7	breast:
43	chr11:33278004..33279582-chr11:33355016..33356972,2	MCF-7	breast:
44	chr11:33366360..33368007-chr11:33376347..33377878,2	K562	blood:
45	chr11:33380757..33382861-chr11:33395684..33398398,2	MCF-7	breast:
46	chr11:33360349..33362095-chr11:33370787..33373728,2	MCF-7	breast:
47	chr11:33366360..33368007-chr11:33376347..33377878,2	K562	blood:
48	chr11:33375467..33377991-chr11:33379064..33381208,2	MCF-7	breast:
49	chr11:33384382..33386417-chr11:33393888..33396516,2	K562	blood:
50	chr11:33517532..33520480-chr11:33524551..33527358,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
2	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
3	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700
4	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIPK3	hsa-miR-124-3p	chr11:33375376-33375395
2	HIPK3	hsa-miR-92a-3p	chr11:33375228-33375234
3	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704
4	HIPK3	hsa-miR-106a-5p	chr11:33375709-33375730
5	HIPK3	hsa-miR-19b-3p	chr11:33375275-33375282
6	HIPK3	hsa-miR-92a-3p	chr11:33375214-33375235
7	HIPK3	hsa-miR-92a-3p	chr11:33375388-33375409
8	HIPK3	hsa-miR-335-5p	chr11:33375589-33375614
9	HIPK3	hsa-miR-124-3p	chr11:33375651-33375670
10	HIPK3	hsa-miR-124-3p	chr11:33375663-33375670
11	HIPK3	hsa-miR-106a-5p	chr11:33375245-33375267
12	HIPK3	hsa-miR-20b-5p	chr11:33375709-33375730
13	HIPK3	hsa-miR-19b-3p	chr11:33375260-33375282
14	HIPK3	hsa-miR-20b-5p	chr11:33375245-33375267

Variant related genes	Relation type
HIPK3	TF binding region
ENSG00000255207	TF binding region
KIAA1549L	TF binding region
ENSG00000254537	TF binding region
ENSG00000223134	TF binding region
HIPK3	CpG island
ENSG00000255207	CpG island
KIAA1549L	CpG island
ENSG00000254537	CpG island
ENSG00000223134	CpG island
ENSG00000247151	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000254537	chromatin interactions
ENSG00000255207	chromatin interactions
ENSG00000206808	chromatin interactions
ENSG00000223134	chromatin interactions

Extended variants
information (count: 8233 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:8233 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534027862	chr11:33331243-33331244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs59282125	chr11:33331262-33331263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574059972	chr11:33331277-33331278	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12805743	chr11:33331282-33331283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs556305459	chr11:33331336-33331337	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185624043	chr11:33331388-33331389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545273319	chr11:33331552-33331553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574160180	chr11:33331553-33331554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188814686	chr11:33331566-33331567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs180746280	chr11:33331590-33331591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563095329	chr11:33331646-33331647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541235711	chr11:33331731-33331732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147544737	chr11:33331763-33331764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375704874	chr11:33331775-33331776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs71034669	chr11:33331799-33331800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78061974	chr11:33331808-33331809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371072801	chr11:33331812-33331813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs55847120	chr11:33331820-33331821	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs67856762	chr11:33331823-33331824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111327983	chr11:33331827-33331828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs71034670	chr11:33331847-33331848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558512426	chr11:33331849-33331850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs71455501	chr11:33331852-33331853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79845928	chr11:33331853-33331854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201462426	chr11:33331854-33331855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199986990	chr11:33331855-33331856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs200750282	chr11:33331856-33331857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs202044269	chr11:33331857-33331858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs58618595	chr11:33331862-33331863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs266455	chr11:33331902-33331903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185405184	chr11:33331912-33331913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554946871	chr11:33331927-33331928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531363529	chr11:33331943-33331944	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551699789	chr11:33331973-33331974	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571612525	chr11:33332010-33332011	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192109322	chr11:33332012-33332013	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571216865	chr11:33332055-33332056	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544200106	chr11:33332105-33332106	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs266454	chr11:33332120-33332121	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567721821	chr11:33332145-33332146	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183931001	chr11:33332153-33332154	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528401082	chr11:33332157-33332158	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs556654126	chr11:33332210-33332211	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs143339272	chr11:33332211-33332212	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538686545	chr11:33332237-33332238	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558785031	chr11:33332246-33332247	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs75750261	chr11:33332271-33332272	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541195523	chr11:33332275-33332276	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187631460	chr11:33332306-33332307	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541476193	chr11:33332312-33332313	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2930 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33290000-33336800	Weak transcription	Lung	lung
2	chr11:33296400-33332200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:33298800-33339000	Weak transcription	NHEK	skin
4	chr11:33302200-33333400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:33308600-33331400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:33309000-33331800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:33309000-33332200	Weak transcription	Fetal Thymus	thymus
8	chr11:33309000-33339000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:33309600-33332200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:33310800-33334400	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr11:33313200-33332600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr11:33313400-33333200	Weak transcription	Aorta	Aorta
13	chr11:33316600-33335400	Weak transcription	Esophagus	oesophagus
14	chr11:33317200-33340600	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr11:33317400-33332800	Weak transcription	Pancreas	Pancrea
16	chr11:33317400-33336800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr11:33317400-33337200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:33317400-33345800	Weak transcription	Gastric	stomach
19	chr11:33318000-33360200	Weak transcription	Primary T cells from cord blood	blood
20	chr11:33318400-33333000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:33318400-33335400	Weak transcription	Ovary	ovary
22	chr11:33318600-33338200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr11:33319200-33335000	Weak transcription	Fetal Lung	lung
24	chr11:33319200-33348800	Weak transcription	Hela-S3	cervix
25	chr11:33319600-33332000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr11:33319800-33332400	Weak transcription	Fetal Intestine Small	intestine
27	chr11:33319800-33342800	Weak transcription	Fetal Intestine Large	intestine
28	chr11:33319800-33352600	Weak transcription	Dnd41	blood
29	chr11:33320000-33332200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr11:33320200-33331800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:33320200-33332400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr11:33320400-33332200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:33320400-33338800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:33320400-33340400	Weak transcription	Primary hematopoietic stem cells	blood
35	chr11:33320400-33341600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:33320400-33341800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:33320600-33369400	Weak transcription	Fetal Brain Male	brain
38	chr11:33321600-33338000	Weak transcription	Fetal Stomach	stomach
39	chr11:33322400-33332200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:33323200-33332200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr11:33323200-33332400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:33323400-33331800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr11:33323600-33332000	Weak transcription	Fetal Muscle Leg	muscle
44	chr11:33323600-33341600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr11:33325000-33333800	Weak transcription	Rectal Smooth Muscle	rectum
46	chr11:33325200-33332400	Weak transcription	Brain Cingulate Gyrus	brain
47	chr11:33325200-33337000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr11:33325400-33332200	Weak transcription	HSMMtube	muscle
49	chr11:33325400-33334200	Weak transcription	Brain Germinal Matrix	brain
50	chr11:33326800-33341600	Weak transcription	Spleen	Spleen

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