Variant report

Variant	nsv1007094
Chromosome Location	chr4:3582626-3709627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1075)
CpG islands
(count:5006)
Chromatin interactive
region (count:86)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3673560-3674036	HepG2	liver:	n/a	n/a
2	ATF1	chr4:3622207-3622400	K562	blood:	n/a	n/a
3	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
6	BACH1	chr4:3591938-3592292	K562	blood:	n/a	n/a
7	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3591953-3592306	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
13	BCL3	chr4:3590653-3590888	GM12878	blood:	n/a	n/a
14	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
15	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:3592078-3592121	K562	blood:	n/a	n/a
19	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
20	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
21	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
22	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
23	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
24	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
27	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
32	CEBPB	chr4:3592195-3592197	K562	blood:	n/a	n/a
33	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
34	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
36	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
37	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
38	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
39	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
40	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
42	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
43	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
44	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
45	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
46	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
47	CEBPB	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
49	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
50	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946

(count:5006 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3652326-3652376	MCF-7	breast:	n/a
2	chr4:3685438-3685488	K562	blood:	n/a
3	chr4:3616943-3616993	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:3680970-3681020	Caco-2	colon:	n/a
5	chr4:3652326-3652376	MCF-7	breast:	n/a
6	chr4:3685438-3685488	K562	blood:	n/a
7	chr4:3616943-3616993	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:3680970-3681020	Caco-2	colon:	n/a
9	chr4:3652433-3652483	ECC-1	luminal epithelium:	n/a
10	chr4:3664471-3664521	GM06990	blood:	n/a
11	chr4:3664401-3664451	PANC-1	pancreas:	n/a
12	chr4:3692574-3692624	HRE	kidney:	n/a
13	chr4:3643404-3643454	HAEpiC	amniotic membrane:	n/a
14	chr4:3671380-3671430	NT2-D1	testis:	n/a
15	chr4:3597859-3597909	AG10803	skin:	n/a
16	chr4:3692712-3692762	NHBE	bronchial:	n/a
17	chr4:3685438-3685488	Jurkat	blood:	n/a
18	chr4:3669900-3669950	PFSK-1	brain:	n/a
19	chr4:3684756-3684806	HCF	heart:	n/a
20	chr4:3644703-3644753	SAEC	small airway:	n/a
21	chr4:3677553-3677603	HEK293	kidney:	embryo
22	chr4:3643404-3643454	ProgFib	skin:	n/a
23	chr4:3591253-3591303	BJ	skin:	n/a
24	chr4:3675363-3675413	AoSMC	blood vessel:	n/a
25	chr4:3682525-3682575	IMR90	lung:	fetal
26	chr4:3617888-3617938	HCT-116	colon:	n/a
27	chr4:3669900-3669950	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:3682525-3682575	GM06990	blood:	n/a
29	chr4:3651233-3651283	Jurkat	blood:	n/a
30	chr4:3642351-3642401	HepG2	liver:	n/a
31	chr4:3616829-3616879	HNPCEpiC	eye:	n/a
32	chr4:3630603-3630653	HepG2	liver:	n/a
33	chr4:3664401-3664451	K562	blood:	n/a
34	chr4:3643475-3643525	HNPCEpiC	eye:	n/a
35	chr4:3597859-3597909	AG09309	skin:	n/a
36	chr4:3644437-3644487	Hepatocyte	liver:	n/a
37	chr4:3675120-3675170	ECC-1	luminal epithelium:	n/a
38	chr4:3675120-3675170	AG09319	gingival:	n/a
39	chr4:3630746-3630796	AoSMC	blood vessel:	n/a
40	chr4:3677497-3677547	SK-N-MC	brain:	n/a
41	chr4:3692574-3692624	IMR90	lung:	fetal
42	chr4:3704852-3704902	BJ	skin:	n/a
43	chr4:3681759-3681809	U87	brain:	n/a
44	chr4:3677553-3677603	HCT-116	colon:	n/a
45	chr4:3650777-3650827	U87	brain:	n/a
46	chr4:3591253-3591303	HCT-116	colon:	n/a
47	chr4:3690945-3690995	HepG2	liver:	n/a
48	chr4:3616829-3616879	HRE	kidney:	n/a
49	chr4:3597739-3597789	GM12892	blood:	n/a
50	chr4:3680721-3680771	T-47D	breast:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
2	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
3	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
4	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
5	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
6	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
7	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
8	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
9	chr4:3577226..3578815-chr4:3583775..3586576,2	K562	blood:
10	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
11	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
12	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
13	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
14	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
15	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
16	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
17	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
18	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
19	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
20	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
21	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
22	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
23	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
24	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
25	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
26	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
27	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
28	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
29	chr4:3533888..3535501-chr4:3581402..3583969,2	MCF-7	breast:
30	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
31	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
32	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
33	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
34	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
35	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
36	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
37	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
38	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
39	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
40	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
41	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
42	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
43	chr4:3532636..3535397-chr4:3592609..3595369,2	K562	blood:
44	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
45	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
46	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
47	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
48	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
49	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
50	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
2	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
3	lnc-RP3-368B9.1.1-1	chr4:3589778-3589914	XLOC_003428
4	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	NR_040045
5	lnc-LRPAP1-6	chr4:3645119-3645386	ucscGeneNc_uc003ghl_2
6	lnc-RP3-368B9.1.1-1	chr4:3590661-3592712	NR_040045
7	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
8	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890
9	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	XLOC_003428
10	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
11	lnc-RP3-368B9.1.1-1	chr4:3591991-3592438	XLOC_003428
12	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
13	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
14	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632
15	lnc-RP3-368B9.1.1-1	chr4:3590661-3590741	XLOC_003428
16	lnc-RP3-368B9.1.1-5	chr4:3650108-3650607	XLOC_003431
17	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
18	lnc-RP3-368B9.1.1-1	chr4:3590661-3592166	XLOC_003428
19	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
20	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
21	lnc-LRPAP1-6	chr4:3648128-3648206	ucscGeneNc_uc003ghl_2
22	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2

No data

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250632	TF binding region
ENSG00000250681	CpG island
ENSG00000250632	CpG island
ENSG00000250681	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000173588	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000250632	chromatin interactions
TMEM2	miRNA target sites

Extended variants
information (count: 7889 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7889 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10805024	chr4:3582626-3582627	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570263322	chr4:3582632-3582633	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138502224	chr4:3582640-3582641	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs555818388	chr4:3582650-3582651	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs6817919	chr4:3582651-3582652	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs572434479	chr4:3582660-3582661	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs10755161	chr4:3582676-3582677	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541422094	chr4:3582714-3582715	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs68015973	chr4:3582716-3582717	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs386670714	chr4:3582721-3582722	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6850824	chr4:3582722-3582723	ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs578044624	chr4:3582817-3582818	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs10937943	chr4:3582838-3582839	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6851224	chr4:3582849-3582850	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545716861	chr4:3582875-3582876	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs562661343	chr4:3582884-3582885	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531507624	chr4:3582964-3582965	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs541689412	chr4:3582969-3582970	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs181809659	chr4:3582970-3582971	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs35362765	chr4:3582998-3582999	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs527319768	chr4:3583025-3583026	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs546988687	chr4:3583029-3583030	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2880806	chr4:3583053-3583054	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369883896	chr4:3583063-3583064	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186839086	chr4:3583130-3583131	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs73792298	chr4:3583140-3583141	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs142347709	chr4:3583169-3583170	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs2344221	chr4:3583176-3583177	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs386670715	chr4:3583182-3583183	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549731133	chr4:3583183-3583184	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs386670716	chr4:3583199-3583200	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs3083024	chr4:3583200-3583201	ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs2880807	chr4:3583204-3583205	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535066305	chr4:3583229-3583230	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2344224	chr4:3583261-3583262	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs558120819	chr4:3583278-3583279	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12508663	chr4:3583320-3583321	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs4543064	chr4:3583352-3583353	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537504444	chr4:3583372-3583373	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556104971	chr4:3583426-3583427	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs111436565	chr4:3583459-3583460	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575868968	chr4:3583479-3583480	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs2880808	chr4:3583491-3583492	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs541604751	chr4:3583514-3583515	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561696368	chr4:3583519-3583520	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572002620	chr4:3583521-3583522	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs67250289	chr4:3583548-3583549	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs62275451	chr4:3583553-3583554	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs11728396	chr4:3583565-3583566	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs73199363	chr4:3583586-3583587	ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3582200-3582800	Enhancers	HepG2	liver
2	chr4:3582400-3583200	ZNF genes & repeats	Brain Germinal Matrix	brain
3	chr4:3582400-3583400	ZNF genes & repeats	Fetal Intestine Small	intestine
4	chr4:3582600-3583000	ZNF genes & repeats	Pancreas	Pancrea
5	chr4:3582600-3583200	Enhancers	Fetal Brain Male	brain
6	chr4:3582600-3583200	ZNF genes & repeats	Fetal Intestine Large	intestine
7	chr4:3582600-3584200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3582800-3583400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
9	chr4:3582800-3583600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr4:3582800-3583600	Flanking Active TSS	HepG2	liver
11	chr4:3583000-3583200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
12	chr4:3583600-3584000	Enhancers	HepG2	liver
13	chr4:3584000-3585800	Weak transcription	HepG2	liver
14	chr4:3584200-3586200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:3584400-3584800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
16	chr4:3584600-3584800	ZNF genes & repeats	Fetal Intestine Small	intestine
17	chr4:3584800-3586000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr4:3585800-3588400	Enhancers	HepG2	liver
19	chr4:3586000-3586200	Enhancers	Duodenum Mucosa	Duodenum
20	chr4:3586000-3587000	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr4:3586200-3586400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3586200-3586400	Enhancers	Gastric	stomach
23	chr4:3586200-3586400	ZNF genes & repeats	Pancreas	Pancrea
24	chr4:3586200-3586400	Enhancers	Small Intestine	intestine
25	chr4:3586200-3586600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr4:3586200-3586600	Enhancers	Stomach Mucosa	stomach
27	chr4:3586200-3587000	Enhancers	Liver	Liver
28	chr4:3586400-3587400	Weak transcription	Gastric	stomach
29	chr4:3586400-3588400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:3586600-3587000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr4:3586600-3587000	Weak transcription	Stomach Mucosa	stomach
32	chr4:3586600-3589400	Enhancers	Duodenum Mucosa	Duodenum
33	chr4:3586800-3587400	Enhancers	Brain Germinal Matrix	brain
34	chr4:3587000-3587600	Enhancers	Fetal Muscle Leg	muscle
35	chr4:3587000-3587600	Enhancers	Small Intestine	intestine
36	chr4:3587000-3587600	Enhancers	Stomach Mucosa	stomach
37	chr4:3587000-3588200	Weak transcription	Fetal Intestine Small	intestine
38	chr4:3587200-3587400	Active TSS	Monocytes-CD14+_RO01746	blood
39	chr4:3587200-3587600	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr4:3587200-3587600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:3587200-3587600	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr4:3587200-3587600	Enhancers	Fetal Intestine Large	intestine
43	chr4:3587200-3587600	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr4:3587200-3593000	ZNF genes & repeats	Fetal Brain Female	brain
45	chr4:3587400-3587600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:3587400-3587600	Enhancers	Adipose Nuclei	Adipose
47	chr4:3587400-3587600	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr4:3587400-3587600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr4:3587400-3587600	Enhancers	Gastric	stomach
50	chr4:3587400-3587600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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