Variant report

Variant	nsv526441
Chromosome Location	chr11:3626177-3756686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1489)
CpG islands
(count:3116)
Chromatin interactive
region (count:47)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1489 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:3630802-3631209	K562	blood:	n/a	n/a
2	ARID3A	chr11:3626269-3626631	K562	blood:	n/a	n/a
3	ARID3A	chr11:3734293-3734360	K562	blood:	n/a	n/a
4	ATF1	chr11:3626172-3626398	K562	blood:	n/a	n/a
5	ATF1	chr11:3706112-3706517	K562	blood:	n/a	n/a
6	ATF2	chr11:3663209-3663719	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:3663244-3663670	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:3676805-3677048	K562	blood:	n/a	n/a
9	ATF3	chr11:3663693-3664003	K562	blood:	n/a	n/a
10	BACH1	chr11:3663791-3664352	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:3663480-3663584	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr11:3674928-3676125	GM12878	blood:	n/a	n/a
13	BATF	chr11:3674900-3676081	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:3674918-3676100	GM12878	blood:	n/a	n/a
15	BCL11A	chr11:3674934-3676015	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:3666142-3666460	K562	blood:	n/a	n/a
17	BHLHE40	chr11:3663388-3664125	HepG2	liver:	n/a	chr11:3663567-3663583 chr11:3663448-3663464
18	BHLHE40	chr11:3663320-3664175	K562	blood:	n/a	chr11:3663382-3663398 chr11:3663567-3663583 chr11:3663448-3663464
19	BHLHE40	chr11:3635894-3636214	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:3635535-3636206	K562	blood:	n/a	n/a
21	BRCA1	chr11:3663383-3663568	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr11:3663683-3664177	K562	blood:	n/a	n/a
23	CBX3	chr11:3663165-3663682	K562	blood:	n/a	n/a
24	CBX3	chr11:3647544-3647861	K562	blood:	n/a	n/a
25	CBX3	chr11:3665609-3666396	K562	blood:	n/a	n/a
26	CBX3	chr11:3664322-3664810	K562	blood:	n/a	n/a
27	CCNT2	chr11:3626204-3626406	K562	blood:	n/a	chr11:3626337-3626357
28	CCNT2	chr11:3663210-3664109	K562	blood:	n/a	chr11:3663964-3663973
29	CEBPB	chr11:3731225-3731991	ECC-1	luminal epithelium:	n/a	chr11:3731793-3731804 chr11:3731793-3731806 chr11:3731793-3731804
30	CEBPB	chr11:3710824-3710975	K562	blood:	n/a	chr11:3710926-3710937
31	CEBPB	chr11:3626133-3626406	K562	blood:	n/a	n/a
32	CEBPB	chr11:3749136-3749449	A549	lung:	n/a	n/a
33	CEBPB	chr11:3710855-3710974	HepG2	liver:	n/a	chr11:3710926-3710937
34	CEBPB	chr11:3663456-3663825	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr11:3754089-3754402	A549	lung:	n/a	chr11:3754346-3754357 chr11:3754115-3754128
36	CEBPB	chr11:3710788-3711031	Hela-S3	cervix:	n/a	chr11:3710926-3710937
37	CEBPB	chr11:3744281-3744729	A549	lung:	n/a	n/a
38	CEBPB	chr11:3710806-3711040	A549	lung:	n/a	chr11:3710926-3710937
39	CEBPB	chr11:3731189-3731574	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr11:3733518-3733812	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:3744324-3744648	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:3749110-3749455	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:3710860-3710963	H1-hESC	embryonic stem cell:	n/a	chr11:3710926-3710937
44	CEBPB	chr11:3695984-3695993	A549	lung:	n/a	n/a
45	CEBPB	chr11:3744196-3744772	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:3744204-3744817	A549	lung:	n/a	n/a
47	CEBPB	chr11:3749260-3749298	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:3749129-3749443	IMR90	lung:	n/a	n/a
49	CEBPB	chr11:3755549-3755799	HepG2	liver:	n/a	chr11:3755656-3755667
50	CEBPB	chr11:3749258-3749357	H1-hESC	embryonic stem cell:	n/a	n/a

(count:3116 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3692562-3692612	HCM	heart:	n/a
2	chr11:3706578-3706628	AoSMC	blood vessel:	n/a
3	chr11:3665525-3665575	BE2_C	brain:	n/a
4	chr11:3662967-3663017	AG09319	gingival:	n/a
5	chr11:3723921-3723971	GM12878	blood:	n/a
6	chr11:3692562-3692612	HCM	heart:	n/a
7	chr11:3706578-3706628	AoSMC	blood vessel:	n/a
8	chr11:3665525-3665575	BE2_C	brain:	n/a
9	chr11:3662967-3663017	AG09319	gingival:	n/a
10	chr11:3723921-3723971	GM12878	blood:	n/a
11	chr11:3690320-3690370	HMEC	breast:	n/a
12	chr11:3638448-3638498	K562	blood:	n/a
13	chr11:3733666-3733716	HEK293	kidney:	embryo
14	chr11:3666662-3666712	SAEC	small airway:	n/a
15	chr11:3688985-3689035	K562	blood:	n/a
16	chr11:3647419-3647469	PFSK-1	brain:	n/a
17	chr11:3637658-3637708	HCT-116	colon:	n/a
18	chr11:3689006-3689056	AG10803	skin:	n/a
19	chr11:3647695-3647745	HRPEpiC	eye:	n/a
20	chr11:3693157-3693207	GM12878	blood:	n/a
21	chr11:3647419-3647469	HRPEpiC	eye:	n/a
22	chr11:3663198-3663248	NHBE	bronchial:	n/a
23	chr11:3706578-3706628	AG10803	skin:	n/a
24	chr11:3690320-3690370	NT2-D1	testis:	n/a
25	chr11:3706578-3706628	HMEC	breast:	n/a
26	chr11:3663198-3663248	Jurkat	blood:	n/a
27	chr11:3693172-3693222	H1-hESC	embryonic stem cell:	embryo
28	chr11:3693157-3693207	HepG2	liver:	n/a
29	chr11:3692562-3692612	NHDF-neo	bronchial:	n/a
30	chr11:3694018-3694068	HUVEC	blood vessel:	n/a
31	chr11:3663532-3663582	HCM	heart:	n/a
32	chr11:3665003-3665053	LNCaP	prostate:	n/a
33	chr11:3663511-3663561	HepG2	liver:	n/a
34	chr11:3688722-3688772	U87	brain:	n/a
35	chr11:3648013-3648063	HUVEC	blood vessel:	n/a
36	chr11:3692187-3692237	Hela-S3	cervix:	n/a
37	chr11:3637427-3637477	U87	brain:	n/a
38	chr11:3666662-3666712	SKMC	muscle:	n/a
39	chr11:3663491-3663541	GM12878	blood:	n/a
40	chr11:3692187-3692237	MCF-7	breast:	n/a
41	chr11:3638352-3638402	AG04449	skin:	fetal
42	chr11:3638448-3638498	HepG2	liver:	n/a
43	chr11:3666483-3666533	HMEC	breast:	n/a
44	chr11:3744085-3744135	CMK	blood:	n/a
45	chr11:3663511-3663561	MCF10A-Er-Src	breast:	n/a
46	chr11:3665525-3665575	IMR90	lung:	fetal
47	chr11:3688722-3688772	HRPEpiC	eye:	n/a
48	chr11:3662967-3663017	HCPEpiC	choroid plexus:	n/a
49	chr11:3666271-3666321	H1-hESC	embryonic stem cell:	embryo
50	chr11:3666278-3666328	BJ	skin:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3704347..3707149-chr11:3712744..3714293,2	K562	blood:
2	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
3	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
4	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
5	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
6	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
7	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
8	chr11:3652693..3655624-chr11:3656023..3659226,3	K562	blood:
9	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
10	chr11:3726751..3729655-chr11:3738609..3740778,2	K562	blood:
11	chr11:3663179..3665930-chr11:3817516..3820122,2	K562	blood:
12	chr11:3661894..3664122-chr11:3664715..3667131,2	K562	blood:
13	chr11:3667429..3669628-chr11:3844274..3846106,2	K562	blood:
14	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
15	chr11:3661894..3664122-chr11:3664715..3667131,2	K562	blood:
16	chr11:3635682..3637406-chr11:3642517..3644691,2	K562	blood:
17	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
18	chr11:3720373..3721894-chr11:3731559..3733138,2	K562	blood:
19	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:
20	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:
21	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
22	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:
23	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
24	chr11:3635375..3637756-chr11:3638069..3640906,2	K562	blood:
25	chr11:3720373..3721894-chr11:3731559..3733138,2	K562	blood:
26	chr11:3635682..3637406-chr11:3642517..3644691,2	K562	blood:
27	chr11:3680170..3682412-chr11:3684306..3686947,3	K562	blood:
28	chr11:3727085..3729822-chr11:3743744..3745444,2	MCF-7	breast:
29	chr11:3679748..3681336-chr11:3687439..3689154,2	K562	blood:
30	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:
31	chr11:3624727..3627376-chr11:3629301..3631751,2	K562	blood:
32	chr11:3705048..3707585-chr11:4118303..4120939,2	K562	blood:
33	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
34	chr11:3707361..3708925-chr11:3714329..3717007,2	K562	blood:
35	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
36	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
37	chr11:3640981..3643163-chr11:3645928..3648472,2	K562	blood:
38	chr11:3652693..3655624-chr11:3656023..3659226,3	K562	blood:
39	chr11:3732732..3736237-chr11:3737365..3740314,3	K562	blood:
40	chr11:3733596..3735433-chr11:3817089..3819371,2	K562	blood:
41	chr11:3498062..3499877-chr11:3626508..3628362,2	MCF-7	breast:
42	chr11:3696995..3699038-chr11:3705872..3708869,2	MCF-7	breast:
43	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
44	chr11:3679748..3681336-chr11:3687439..3689154,2	K562	blood:
45	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
46	chr11:3692345..3692867-chr15:44084030..44084743,2	NB4	blood:
47	chr11:3662844..3665441-chr11:3667397..3669023,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ART1-4	chr11:3676734-3676885	NONHSAT017608
2	lnc-ART1-4	chr11:3666358-3666409	NONHSAT017608
3	lnc-NUP98-1	chr11:3690964-3691117	NONHSAT017612
4	lnc-ART1-4	chr11:3680813-3680842	NONHSAT017608
5	lnc-NUP98-1	chr11:3689730-3690580	NONHSAT017612
6	lnc-ART1-4	chr11:3680392-3680506	NONHSAT017608

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NUP98	hsa-miR-98-5p	chr11:3733173-3733167
2	NUP98	hsa-miR-98-5p	chr11:3733411-3733432
3	NUP98	hsa-miR-98-5p	chr11:3733167-3733187
4	NUP98	hsa-miR-16-5p	chr11:3733110-3733130

Variant related genes	Relation type
ENSG00000201279	TF binding region
CHRNA10	TF binding region
NUP98	TF binding region
ENSG00000238686	TF binding region
RNU6-1143P	TF binding region
TRPC2	TF binding region
ART5	TF binding region
ENSG00000200201	TF binding region
OR7E117P	TF binding region
ART1	TF binding region
ENSG00000201279	CpG island
CHRNA10	CpG island
NUP98	CpG island
ENSG00000238686	CpG island
RNU6-1143P	CpG island
TRPC2	CpG island
ART5	CpG island
ENSG00000200201	CpG island
OR7E117P	CpG island
ART1	CpG island
ENSG00000238686	chromatin interactions
ENSG00000201279	chromatin interactions
ENSG00000167311	chromatin interactions
ENSG00000148985	chromatin interactions
ENSG00000129749	chromatin interactions
ENSG00000182048	chromatin interactions
ENSG00000251934	chromatin interactions
ENSG00000200201	chromatin interactions
ENSG00000129744	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000110713	chromatin interactions

Extended variants
information (count: 6371 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6371 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10834605	chr11:3626177-3626178	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547341088	chr11:3626193-3626194	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148267762	chr11:3626212-3626213	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs140129707	chr11:3626216-3626217	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs112051015	chr11:3626220-3626221	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs77322814	chr11:3626224-3626225	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112155005	chr11:3626232-3626233	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs112279784	chr11:3626251-3626252	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576894979	chr11:3626256-3626257	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs534732466	chr11:3626274-3626275	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs183660958	chr11:3626467-3626468	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs574886017	chr11:3626487-3626488	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs369988096	chr11:3626501-3626502	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs188753942	chr11:3626613-3626614	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs547381865	chr11:3626619-3626620	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs150288851	chr11:3626655-3626656	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs560952016	chr11:3626662-3626663	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs137947902	chr11:3626669-3626670	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs142408403	chr11:3626679-3626680	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146367555	chr11:3626690-3626691	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs375097240	chr11:3626693-3626694	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532742282	chr11:3626810-3626811	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs138446748	chr11:3626814-3626815	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs114127317	chr11:3626815-3626816	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs181178650	chr11:3626833-3626834	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs142932628	chr11:3626869-3626870	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112941454	chr11:3626930-3626931	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs12418667	chr11:3626947-3626948	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186214875	chr11:3626952-3626953	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115215350	chr11:3626966-3626967	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376104314	chr11:3627050-3627051	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553137798	chr11:3627052-3627053	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs386749910	chr11:3627079-3627080	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189024635	chr11:3627086-3627087	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370968820	chr11:3627088-3627089	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554918361	chr11:3627090-3627091	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576377215	chr11:3627113-3627114	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543643773	chr11:3627115-3627116	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7951724	chr11:3627164-3627165	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11028440	chr11:3627183-3627184	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs541119351	chr11:3627185-3627186	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs76041742	chr11:3627198-3627199	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181488611	chr11:3627215-3627216	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs78868641	chr11:3627221-3627222	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs60899201	chr11:3627242-3627243	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531064111	chr11:3627343-3627344	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201538217	chr11:3627363-3627364	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs552365731	chr11:3627366-3627367	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570705370	chr11:3627386-3627387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528605187	chr11:3627401-3627402	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	17440070	CNVD

Chromatin state (count:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3606400-3635800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:3625400-3627400	Enhancers	Fetal Intestine Large	intestine
3	chr11:3625600-3626200	Enhancers	Duodenum Mucosa	Duodenum
4	chr11:3625600-3626200	Enhancers	Fetal Lung	lung
5	chr11:3625600-3627000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:3625600-3627000	Weak transcription	Right Atrium	heart
7	chr11:3625800-3626400	Flanking Active TSS	K562	blood
8	chr11:3626000-3626400	Weak transcription	Fetal Intestine Small	intestine
9	chr11:3626000-3629000	Enhancers	Placenta	Placenta
10	chr11:3626200-3627000	Active TSS	Duodenum Mucosa	Duodenum
11	chr11:3626400-3627200	Enhancers	K562	blood
12	chr11:3626400-3627400	Enhancers	Fetal Intestine Small	intestine
13	chr11:3627000-3627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr11:3627000-3627200	Enhancers	Right Atrium	heart
15	chr11:3627000-3627400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr11:3627400-3627800	Weak transcription	Fetal Intestine Large	intestine
17	chr11:3627400-3627800	Weak transcription	Fetal Intestine Small	intestine
18	chr11:3627800-3628200	Enhancers	Fetal Intestine Large	intestine
19	chr11:3627800-3628200	Enhancers	Fetal Intestine Small	intestine
20	chr11:3628800-3629000	Enhancers	NHDF-Ad	bronchial
21	chr11:3628800-3629400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:3632000-3632800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr11:3634000-3634200	Enhancers	Lung	lung
24	chr11:3634200-3635800	Weak transcription	Lung	lung
25	chr11:3634800-3635200	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr11:3634800-3635400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr11:3634800-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:3634800-3636800	Enhancers	Primary hematopoietic stem cells	blood
29	chr11:3635000-3635200	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr11:3635000-3635200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:3635000-3635400	Enhancers	Colon Smooth Muscle	Colon
34	chr11:3635000-3635400	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr11:3635000-3636200	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr11:3635000-3636400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:3635000-3636400	Enhancers	Right Ventricle	heart
38	chr11:3635000-3639200	Enhancers	Fetal Muscle Leg	muscle
39	chr11:3635200-3635600	Enhancers	Primary T cells from cord blood	blood
40	chr11:3635200-3635600	Enhancers	Adipose Nuclei	Adipose
41	chr11:3635200-3636000	Enhancers	Right Atrium	heart
42	chr11:3635200-3636000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr11:3635200-3636000	Enhancers	Thymus	Thymus
44	chr11:3635200-3636200	Enhancers	Primary T cells fromperipheralblood	blood
45	chr11:3635200-3636200	Enhancers	Left Ventricle	heart
46	chr11:3635200-3636400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr11:3635200-3636400	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr11:3635200-3636400	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr11:3635200-3636400	Enhancers	Primary B cells from peripheral blood	blood
50	chr11:3635200-3636400	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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