Variant report

Variant	nsv1009842
Chromosome Location	chr4:3595033-3709627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:4825)
Chromatin interactive
region (count:81)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
18	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
20	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
23	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
24	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
25	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
26	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
28	CEBPB	chr4:3608606-3609111	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
29	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
30	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
31	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
32	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
35	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
36	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
37	CEBPB	chr4:3608709-3609077	Hela-S3	cervix:	n/a	chr4:3608890-3608901
38	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
39	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
40	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
41	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:3608707-3609063	HepG2	liver:	n/a	chr4:3608890-3608901
43	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
44	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
45	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
46	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
47	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
48	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
49	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
50	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839

(count:4825 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3664401-3664451	HMEC	breast:	n/a
2	chr4:3671199-3671249	PrEC	prostate:	n/a
3	chr4:3650777-3650827	IMR90	lung:	fetal
4	chr4:3704824-3704874	MCF10A-Er-Src	breast:	n/a
5	chr4:3671380-3671430	HAEpiC	amniotic membrane:	n/a
6	chr4:3657880-3657930	SKMC	muscle:	n/a
7	chr4:3664401-3664451	HMEC	breast:	n/a
8	chr4:3671199-3671249	PrEC	prostate:	n/a
9	chr4:3650777-3650827	IMR90	lung:	fetal
10	chr4:3704824-3704874	MCF10A-Er-Src	breast:	n/a
11	chr4:3671380-3671430	HAEpiC	amniotic membrane:	n/a
12	chr4:3657880-3657930	SKMC	muscle:	n/a
13	chr4:3647047-3647097	HCM	heart:	n/a
14	chr4:3643635-3643685	HL-60	blood:	n/a
15	chr4:3664117-3664167	AoSMC	blood vessel:	n/a
16	chr4:3644703-3644753	GM12892	blood:	n/a
17	chr4:3651471-3651521	GM06990	blood:	n/a
18	chr4:3675120-3675170	AG04450	lung:	fetal
19	chr4:3685875-3685925	LNCaP	prostate:	n/a
20	chr4:3650777-3650827	HCF	heart:	n/a
21	chr4:3643770-3643820	H1-hESC	embryonic stem cell:	embryo
22	chr4:3652326-3652376	A549	lung:	n/a
23	chr4:3691397-3691447	T-47D	breast:	n/a
24	chr4:3689478-3689528	SK-N-SH	brain:	n/a
25	chr4:3671199-3671249	HepG2	liver:	n/a
26	chr4:3651354-3651404	SK-N-SH	brain:	n/a
27	chr4:3685309-3685359	Hepatocyte	liver:	n/a
28	chr4:3644187-3644237	PrEC	prostate:	n/a
29	chr4:3664117-3664167	Jurkat	blood:	n/a
30	chr4:3685875-3685925	AG04450	lung:	fetal
31	chr4:3650777-3650827	LNCaP	prostate:	n/a
32	chr4:3630603-3630653	RPTEC	kidney:	n/a
33	chr4:3671199-3671249	MCF-7	breast:	n/a
34	chr4:3675363-3675413	HCF	heart:	n/a
35	chr4:3597739-3597789	BE2_C	brain:	n/a
36	chr4:3671380-3671430	HRPEpiC	eye:	n/a
37	chr4:3690945-3690995	BJ	skin:	n/a
38	chr4:3617603-3617653	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:3643404-3643454	NT2-D1	testis:	n/a
40	chr4:3664117-3664167	A549	lung:	n/a
41	chr4:3705147-3705197	SAEC	small airway:	n/a
42	chr4:3643770-3643820	HAEpiC	amniotic membrane:	n/a
43	chr4:3667715-3667765	HCM	heart:	n/a
44	chr4:3685695-3685745	NB4	blood:	n/a
45	chr4:3646912-3646962	HRPEpiC	eye:	n/a
46	chr4:3680721-3680771	PANC-1	pancreas:	n/a
47	chr4:3685875-3685925	HCM	heart:	n/a
48	chr4:3671199-3671249	K562	blood:	n/a
49	chr4:3650474-3650524	HMEC	breast:	n/a
50	chr4:3642351-3642401	BE2_C	brain:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
2	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
3	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
4	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
5	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
6	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
7	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
8	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
9	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
10	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
11	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
12	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
13	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
14	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
15	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
16	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
17	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
18	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
19	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
20	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
21	chr4:3532636..3535397-chr4:3592609..3595369,2	K562	blood:
22	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
23	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
24	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
25	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
26	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
27	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
28	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
29	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
30	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
31	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
32	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
33	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
34	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
35	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
36	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
37	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
38	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
39	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
40	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
41	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
42	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
43	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
44	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
45	chr4:3531986..3534650-chr4:3657102..3659521,2	MCF-7	breast:
46	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
47	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
48	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
49	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
50	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
2	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632
3	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
4	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
5	lnc-LRPAP1-6	chr4:3648128-3648206	ucscGeneNc_uc003ghl_2
6	lnc-LRPAP1-6	chr4:3645119-3645386	ucscGeneNc_uc003ghl_2
7	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
8	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
9	lnc-RP3-368B9.1.1-5	chr4:3650108-3650607	XLOC_003431
10	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
11	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
12	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
13	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2
14	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
15	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890

No data

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250632	TF binding region
ENSG00000250681	CpG island
ENSG00000250632	CpG island
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000250681	chromatin interactions
ENSG00000250632	chromatin interactions

Extended variants
information (count: 7019 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:7019 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561237115	chr4:3595034-3595035	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs62272997	chr4:3595072-3595073	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530165465	chr4:3595089-3595090	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs62272998	chr4:3595092-3595093	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11942075	chr4:3595097-3595098	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs542476413	chr4:3595105-3595106	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs113130463	chr4:3595111-3595112	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528278262	chr4:3595157-3595158	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370510791	chr4:3595174-3595175	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73072471	chr4:3595196-3595197	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73072472	chr4:3595237-3595238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571561279	chr4:3595252-3595253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73072473	chr4:3595283-3595284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73072476	chr4:3595330-3595331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530463021	chr4:3595333-3595334	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550509461	chr4:3595369-3595370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs73793668	chr4:3595371-3595372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73793669	chr4:3595393-3595394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386670728	chr4:3595403-3595404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62272999	chr4:3595405-3595406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566753924	chr4:3595409-3595410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73199393	chr4:3595416-3595417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538846272	chr4:3595417-3595418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73072479	chr4:3595434-3595435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558866094	chr4:3595463-3595464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575495231	chr4:3595488-3595489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537857259	chr4:3595536-3595537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369079416	chr4:3595586-3595587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373817518	chr4:3595617-3595618	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372574046	chr4:3595635-3595636	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377226609	chr4:3595636-3595637	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369215311	chr4:3595646-3595647	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373669051	chr4:3595648-3595649	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111293935	chr4:3595652-3595653	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377613275	chr4:3595663-3595664	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371263081	chr4:3595679-3595680	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200389213	chr4:3595680-3595681	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374649809	chr4:3595685-3595686	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142227112	chr4:3595687-3595688	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143697047	chr4:3595689-3595690	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377719205	chr4:3595691-3595692	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370517341	chr4:3595696-3595697	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373632218	chr4:3595697-3595698	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199738783	chr4:3595707-3595708	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201300804	chr4:3595715-3595716	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372105228	chr4:3595716-3595717	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138965353	chr4:3595719-3595720	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368077017	chr4:3595723-3595724	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141479942	chr4:3595725-3595726	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192290730	chr4:3595734-3595735	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3592000-3595400	Weak transcription	Fetal Intestine Large	intestine
2	chr4:3594600-3595200	ZNF genes & repeats	Fetal Intestine Small	intestine
3	chr4:3595200-3598000	Weak transcription	Fetal Intestine Small	intestine
4	chr4:3595600-3595800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:3595600-3595800	ZNF genes & repeats	Right Atrium	heart
6	chr4:3595600-3596000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:3595600-3600200	Weak transcription	Fetal Heart	heart
8	chr4:3595800-3599400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:3595800-3603400	Weak transcription	Right Atrium	heart
10	chr4:3597000-3597800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
11	chr4:3597000-3598000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr4:3597000-3598000	Enhancers	Spleen	Spleen
13	chr4:3597000-3598200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:3597000-3598200	ZNF genes & repeats	Fetal Brain Female	brain
15	chr4:3597000-3604200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:3597000-3608000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:3597200-3597400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr4:3597200-3599400	Enhancers	Fetal Brain Male	brain
19	chr4:3597400-3601200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
20	chr4:3598000-3598800	Weak transcription	Spleen	Spleen
21	chr4:3598400-3598600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr4:3598600-3599200	Enhancers	HepG2	liver
23	chr4:3598600-3607600	ZNF genes & repeats	Fetal Stomach	stomach
24	chr4:3598800-3601000	ZNF genes & repeats	Spleen	Spleen
25	chr4:3599200-3599600	Flanking Active TSS	HepG2	liver
26	chr4:3599400-3599800	Weak transcription	Fetal Brain Male	brain
27	chr4:3599400-3599800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr4:3599400-3601000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:3599600-3599800	Enhancers	HepG2	liver
30	chr4:3599600-3600400	Enhancers	Brain Anterior Caudate	brain
31	chr4:3599600-3601000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr4:3599800-3600600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr4:3599800-3600600	Enhancers	Fetal Brain Female	brain
34	chr4:3599800-3601800	ZNF genes & repeats	Fetal Brain Male	brain
35	chr4:3600000-3600400	Enhancers	Brain Cingulate Gyrus	brain
36	chr4:3600000-3600400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr4:3600000-3600800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
38	chr4:3600000-3601600	ZNF genes & repeats	Fetal Lung	lung
39	chr4:3600000-3604200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:3600200-3600600	ZNF genes & repeats	Fetal Heart	heart
41	chr4:3600200-3600800	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr4:3600200-3601000	ZNF genes & repeats	Gastric	stomach
43	chr4:3600200-3601400	ZNF genes & repeats	Esophagus	oesophagus
44	chr4:3600200-3601600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:3600200-3601600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:3600200-3602200	ZNF genes & repeats	Pancreas	Pancrea
47	chr4:3600400-3601000	ZNF genes & repeats	Fetal Kidney	kidney
48	chr4:3600400-3601600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
49	chr4:3600600-3601400	Weak transcription	Fetal Brain Female	brain
50	chr4:3600800-3601000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum

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