Variant report

Variant	esv1821329
Chromosome Location	chr11:3616884-3801429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1778)
CpG islands
(count:3112)
Chromatin interactive
region (count:56)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:3734293-3734360	K562	blood:	n/a	n/a
2	ARID3A	chr11:3630802-3631209	K562	blood:	n/a	n/a
3	ARID3A	chr11:3626269-3626631	K562	blood:	n/a	n/a
4	ATF1	chr11:3706112-3706517	K562	blood:	n/a	n/a
5	ATF1	chr11:3626172-3626398	K562	blood:	n/a	n/a
6	ATF2	chr11:3663244-3663670	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:3663209-3663719	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	chr11:3663480-3663584	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:3663791-3664352	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr11:3674900-3676081	GM12878	blood:	n/a	n/a
13	BATF	chr11:3674928-3676125	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	chr11:3635894-3636214	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:3663320-3664175	K562	blood:	n/a	chr11:3663382-3663398 chr11:3663567-3663583 chr11:3663448-3663464
18	BHLHE40	chr11:3635535-3636206	K562	blood:	n/a	n/a
19	BHLHE40	chr11:3666142-3666460	K562	blood:	n/a	n/a
20	BHLHE40	chr11:3663388-3664125	HepG2	liver:	n/a	chr11:3663567-3663583 chr11:3663448-3663464
21	BRCA1	chr11:3663383-3663568	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr11:3664322-3664810	K562	blood:	n/a	n/a
23	CBX3	chr11:3665609-3666396	K562	blood:	n/a	n/a
24	CBX3	chr11:3663683-3664177	K562	blood:	n/a	n/a
25	CBX3	chr11:3663165-3663682	K562	blood:	n/a	n/a
26	CBX3	chr11:3647544-3647861	K562	blood:	n/a	n/a
27	CCNT2	chr11:3663210-3664109	K562	blood:	n/a	chr11:3663964-3663973
28	CCNT2	chr11:3626204-3626406	K562	blood:	n/a	chr11:3626337-3626357
29	CEBPB	chr11:3733518-3733812	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:3663456-3663825	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:3749110-3749455	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:3766361-3766735	MCF-7	breast:	n/a	n/a
33	CEBPB	chr11:3749129-3749443	IMR90	lung:	n/a	n/a
34	CEBPB	chr11:3769003-3769302	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:3749136-3749449	A549	lung:	n/a	n/a
36	CEBPB	chr11:3744324-3744648	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:3744204-3744817	A549	lung:	n/a	n/a
38	CEBPB	chr11:3710860-3710963	H1-hESC	embryonic stem cell:	n/a	chr11:3710926-3710937
39	CEBPB	chr11:3749258-3749357	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:3731271-3731962	H1-hESC	embryonic stem cell:	n/a	chr11:3731793-3731804 chr11:3731793-3731806 chr11:3731793-3731804
41	CEBPB	chr11:3766405-3766711	MCF-7	breast:	n/a	n/a
42	CEBPB	chr11:3768911-3769351	MCF-7	breast:	n/a	n/a
43	CEBPB	chr11:3749198-3749438	K562	blood:	n/a	n/a
44	CEBPB	chr11:3744196-3744772	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:3768870-3769429	MCF-7	breast:	n/a	n/a
46	CEBPB	chr11:3768955-3769348	IMR90	lung:	n/a	n/a
47	CEBPB	chr11:3710806-3711040	A549	lung:	n/a	chr11:3710926-3710937
48	CEBPB	chr11:3754089-3754402	A549	lung:	n/a	chr11:3754346-3754357 chr11:3754115-3754128
49	CEBPB	chr11:3744281-3744729	A549	lung:	n/a	n/a
50	CEBPB	chr11:3710824-3710975	K562	blood:	n/a	chr11:3710926-3710937

(count:3112 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3637427-3637477	HPAEpiC	pulmonary alveolar:	n/a
2	chr11:3637427-3637477	HPAEpiC	pulmonary alveolar:	n/a
3	chr11:3689006-3689056	BJ	skin:	n/a
4	chr11:3692697-3692747	NB4	blood:	n/a
5	chr11:3663801-3663851	GM12892	blood:	n/a
6	chr11:3663801-3663851	NHDF-neo	bronchial:	n/a
7	chr11:3647086-3647136	HUVEC	blood vessel:	n/a
8	chr11:3647419-3647469	PFSK-1	brain:	n/a
9	chr11:3692562-3692612	HMEC	breast:	n/a
10	chr11:3688722-3688772	Hela-S3	cervix:	n/a
11	chr11:3688526-3688576	LNCaP	prostate:	n/a
12	chr11:3666483-3666533	SK-N-SH	brain:	n/a
13	chr11:3666271-3666321	HCF	heart:	n/a
14	chr11:3647086-3647136	PANC-1	pancreas:	n/a
15	chr11:3665003-3665053	GM19239	blood:	n/a
16	chr11:3666271-3666321	AoSMC	blood vessel:	n/a
17	chr11:3706578-3706628	HCPEpiC	choroid plexus:	n/a
18	chr11:3663777-3663827	SKMC	muscle:	n/a
19	chr11:3663198-3663248	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:3659810-3659860	HL-60	blood:	n/a
21	chr11:3692562-3692612	SK-N-SH	brain:	n/a
22	chr11:3694018-3694068	AG09309	skin:	n/a
23	chr11:3690320-3690370	SK-N-SH_RA	brain:	n/a
24	chr11:3723921-3723971	AG09309	skin:	n/a
25	chr11:3663511-3663561	Caco-2	colon:	n/a
26	chr11:3637658-3637708	AoSMC	blood vessel:	n/a
27	chr11:3663644-3663694	AG09309	skin:	n/a
28	chr11:3663491-3663541	NT2-D1	testis:	n/a
29	chr11:3666278-3666328	AG10803	skin:	n/a
30	chr11:3647654-3647704	NHDF-neo	bronchial:	n/a
31	chr11:3692187-3692237	ECC-1	luminal epithelium:	n/a
32	chr11:3663773-3663823	AoSMC	blood vessel:	n/a
33	chr11:3663511-3663561	PANC-1	pancreas:	n/a
34	chr11:3689006-3689056	U87	brain:	n/a
35	chr11:3663372-3663422	HAEpiC	amniotic membrane:	n/a
36	chr11:3647419-3647469	GM12891	blood:	n/a
37	chr11:3665954-3666004	ProgFib	skin:	n/a
38	chr11:3648013-3648063	Hepatocyte	liver:	n/a
39	chr11:3663198-3663248	HRE	kidney:	n/a
40	chr11:3694018-3694068	AG04449	skin:	fetal
41	chr11:3662967-3663017	NB4	blood:	n/a
42	chr11:3731649-3731699	HNPCEpiC	eye:	n/a
43	chr11:3659810-3659860	H1-hESC	embryonic stem cell:	embryo
44	chr11:3663773-3663823	U87	brain:	n/a
45	chr11:3688722-3688772	PrEC	prostate:	n/a
46	chr11:3648013-3648063	IMR90	lung:	fetal
47	chr11:3693172-3693222	ovcar-3	ovarian:	n/a
48	chr11:3723921-3723971	K562	blood:	n/a
49	chr11:3744085-3744135	ovcar-3	ovarian:	n/a
50	chr11:3688722-3688772	A549	lung:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:3705048..3707585-chr11:4118303..4120939,2	K562	blood:
2	chr11:3663179..3665930-chr11:3817516..3820122,2	K562	blood:
3	chr11:3667429..3669628-chr11:3844274..3846106,2	K562	blood:
4	chr11:3661894..3664122-chr11:3664715..3667131,2	K562	blood:
5	chr11:3652693..3655624-chr11:3656023..3659226,3	K562	blood:
6	chr11:3661894..3664122-chr11:3664715..3667131,2	K562	blood:
7	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
8	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:
9	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:
10	chr11:3635648..3637182-chr11:3642262..3644691,2	K562	blood:
11	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
12	chr11:3769093..3770823-chr11:3816155..3819010,2	K562	blood:
13	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
14	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
15	chr11:3794758..3796517-chr11:3818346..3820029,2	K562	blood:
16	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
17	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:
18	chr11:3790669..3792410-chr11:3794798..3796374,2	K562	blood:
19	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
20	chr11:3680170..3682412-chr11:3684306..3686947,3	K562	blood:
21	chr11:3733596..3735433-chr11:3817089..3819371,2	K562	blood:
22	chr11:3784255..3786743-chr11:3787491..3789884,2	MCF-7	breast:
23	chr11:3727085..3729822-chr11:3743744..3745444,2	MCF-7	breast:
24	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
25	chr11:3726751..3729655-chr11:3738609..3740778,2	K562	blood:
26	chr11:3635682..3637406-chr11:3642517..3644691,2	K562	blood:
27	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
28	chr11:3696995..3699038-chr11:3705872..3708869,2	MCF-7	breast:
29	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
30	chr11:3764124..3767130-chr11:3771414..3774261,3	K562	blood:
31	chr11:3707361..3708925-chr11:3714329..3717007,2	K562	blood:
32	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
33	chr11:3792691..3794199-chr11:3815236..3817396,2	MCF-7	breast:
34	chr11:3498062..3499877-chr11:3626508..3628362,2	MCF-7	breast:
35	chr11:3704347..3707149-chr11:3712744..3714293,2	K562	blood:
36	chr11:3732732..3736237-chr11:3737365..3740314,3	K562	blood:
37	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
38	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
39	chr11:3635375..3637756-chr11:3638069..3640906,2	K562	blood:
40	chr11:3692345..3692867-chr15:44084030..44084743,2	NB4	blood:
41	chr11:3720373..3721894-chr11:3731559..3733138,2	K562	blood:
42	chr11:3790669..3792410-chr11:3794798..3796374,2	K562	blood:
43	chr11:3679748..3681336-chr11:3687439..3689154,2	K562	blood:
44	chr11:3624727..3627376-chr11:3629301..3631751,2	K562	blood:
45	chr11:3628892..3631484-chr11:3636382..3639182,2	K562	blood:
46	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
47	chr11:3784255..3786743-chr11:3787491..3789884,2	MCF-7	breast:
48	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
49	chr11:3640981..3643163-chr11:3645928..3648472,2	K562	blood:
50	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	chr11:3680813-3680842	NONHSAT017608
2	lnc-NUP98-1	chr11:3690964-3691117	NONHSAT017612
3	lnc-NUP98-1	chr11:3689730-3690580	NONHSAT017612
4	lnc-ART1-4	chr11:3666358-3666409	NONHSAT017608
5	lnc-ART1-4	chr11:3676734-3676885	NONHSAT017608
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	chr11:3733411-3733432
2	NUP98	hsa-miR-98-5p	chr11:3733173-3733167
3	NUP98	hsa-miR-98-5p	chr11:3733167-3733187
4	NUP98	hsa-miR-16-5p	chr11:3733110-3733130

Variant related genes	Relation type
ART5	TF binding region
RNU7-50P	TF binding region
ENSG00000230851	TF binding region
ENSG00000201279	TF binding region
ENSG00000200201	TF binding region
OR7E117P	TF binding region
CHRNA10	TF binding region
NUP98	TF binding region
ENSG00000238686	TF binding region
RNU6-1143P	TF binding region
ART1	TF binding region
TRPC2	TF binding region
ART5	CpG island
RNU7-50P	CpG island
ENSG00000230851	CpG island
ENSG00000201279	CpG island
ENSG00000200201	CpG island
OR7E117P	CpG island
CHRNA10	CpG island
NUP98	CpG island
ENSG00000238686	CpG island
RNU6-1143P	CpG island
ART1	CpG island
TRPC2	CpG island
ENSG00000201279	chromatin interactions
ENSG00000200201	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000110713	chromatin interactions
ENSG00000251934	chromatin interactions
ENSG00000148985	chromatin interactions
ENSG00000182048	chromatin interactions
ENSG00000129744	chromatin interactions
ENSG00000167311	chromatin interactions
ENSG00000129749	chromatin interactions
ENSG00000238686	chromatin interactions

Extended variants
information (count: 8915 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8915 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181598523	chr11:3616888-3616889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567170951	chr11:3616946-3616947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185719777	chr11:3616958-3616959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199694066	chr11:3616965-3616966	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs199846401	chr11:3617000-3617001	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs12575319	chr11:3617010-3617011	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs201558362	chr11:3617011-3617012	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs571340772	chr11:3617012-3617013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs190087182	chr11:3617015-3617016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79144648	chr11:3617034-3617035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553811329	chr11:3617037-3617038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572059246	chr11:3617038-3617039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75665349	chr11:3617053-3617054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543385838	chr11:3617064-3617065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147587855	chr11:3617067-3617068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74211156	chr11:3617079-3617080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369815784	chr11:3617083-3617084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35963588	chr11:3617091-3617092	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200838034	chr11:3617119-3617120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146969841	chr11:3617134-3617135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565310512	chr11:3617140-3617141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181652057	chr11:3617184-3617185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199536639	chr11:3617186-3617187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142914722	chr11:3617237-3617238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs74700059	chr11:3617241-3617242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546725669	chr11:3617246-3617247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185984342	chr11:3617247-3617248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151120188	chr11:3617248-3617249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560863811	chr11:3617255-3617256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531476906	chr11:3617259-3617260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192414549	chr11:3617294-3617295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571312273	chr11:3617297-3617298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201220380	chr11:3617298-3617299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111649443	chr11:3617329-3617330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538765000	chr11:3617350-3617351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71478539	chr11:3617377-3617378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183805180	chr11:3617388-3617389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536242160	chr11:3617389-3617390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554573477	chr11:3617394-3617395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576697375	chr11:3617399-3617400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112703710	chr11:3617408-3617409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186242323	chr11:3617420-3617421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190764120	chr11:3617424-3617425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182608244	chr11:3617437-3617438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559400193	chr11:3617469-3617470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574558121	chr11:3617477-3617478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146773852	chr11:3617478-3617479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531643183	chr11:3617483-3617484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549796972	chr11:3617520-3617521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187039452	chr11:3617536-3617537	Weak transcription	n/a	n/a	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:3568 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3606400-3635800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:3621400-3621800	Enhancers	Esophagus	oesophagus
3	chr11:3625400-3625600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:3625400-3625600	Enhancers	Right Atrium	heart
5	chr11:3625400-3625800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:3625400-3625800	Enhancers	K562	blood
7	chr11:3625400-3626000	Enhancers	Fetal Intestine Small	intestine
8	chr11:3625400-3627400	Enhancers	Fetal Intestine Large	intestine
9	chr11:3625600-3626200	Enhancers	Duodenum Mucosa	Duodenum
10	chr11:3625600-3626200	Enhancers	Fetal Lung	lung
11	chr11:3625600-3627000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:3625600-3627000	Weak transcription	Right Atrium	heart
13	chr11:3625800-3626400	Flanking Active TSS	K562	blood
14	chr11:3626000-3626400	Weak transcription	Fetal Intestine Small	intestine
15	chr11:3626000-3629000	Enhancers	Placenta	Placenta
16	chr11:3626200-3627000	Active TSS	Duodenum Mucosa	Duodenum
17	chr11:3626400-3627200	Enhancers	K562	blood
18	chr11:3626400-3627400	Enhancers	Fetal Intestine Small	intestine
19	chr11:3627000-3627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr11:3627000-3627200	Enhancers	Right Atrium	heart
21	chr11:3627000-3627400	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr11:3627400-3627800	Weak transcription	Fetal Intestine Large	intestine
23	chr11:3627400-3627800	Weak transcription	Fetal Intestine Small	intestine
24	chr11:3627800-3628200	Enhancers	Fetal Intestine Large	intestine
25	chr11:3627800-3628200	Enhancers	Fetal Intestine Small	intestine
26	chr11:3628800-3629000	Enhancers	NHDF-Ad	bronchial
27	chr11:3628800-3629400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:3632000-3632800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:3634000-3634200	Enhancers	Lung	lung
30	chr11:3634200-3635800	Weak transcription	Lung	lung
31	chr11:3634800-3635200	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr11:3634800-3635400	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr11:3634800-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:3634800-3636800	Enhancers	Primary hematopoietic stem cells	blood
35	chr11:3635000-3635200	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:3635000-3635200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr11:3635000-3635400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:3635000-3635400	Enhancers	Colon Smooth Muscle	Colon
40	chr11:3635000-3635400	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr11:3635000-3636200	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr11:3635000-3636400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:3635000-3636400	Enhancers	Right Ventricle	heart
44	chr11:3635000-3639200	Enhancers	Fetal Muscle Leg	muscle
45	chr11:3635200-3635600	Enhancers	Primary T cells from cord blood	blood
46	chr11:3635200-3635600	Enhancers	Adipose Nuclei	Adipose
47	chr11:3635200-3636000	Enhancers	Right Atrium	heart
48	chr11:3635200-3636000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr11:3635200-3636000	Enhancers	Thymus	Thymus
50	chr11:3635200-3636200	Enhancers	Primary T cells fromperipheralblood	blood

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