Variant report

Variant	esv2763335
Chromosome Location	chr4:3609390-3714185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:777)
CpG islands
(count:4830)
Chromatin interactive
region (count:70)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
6	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
10	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
13	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
17	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
21	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
22	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
24	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
25	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
26	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
27	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
28	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
29	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
30	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
31	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
35	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
36	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
37	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
38	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
39	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
40	CEBPZ	chr4:3610104-3610260	HepG2	liver:	n/a	n/a
41	CHD2	chr4:3642375-3642459	HepG2	liver:	n/a	n/a
42	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
44	CHD2	chr4:3657873-3658157	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr4:3676953-3677446	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr4:3677024-3677462	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:3703257-3703425	HepG2	liver:	n/a	chr4:3703375-3703384
48	CTCF	chr4:3677100-3677250	A549	lung:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
49	CTCF	chr4:3679505-3679566	Gliobla	brain:	n/a	n/a
50	CTCF	chr4:3609920-3610070	WERI-Rb-1	eye:	n/a	n/a

(count:4830 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3704852-3704902	AoSMC	blood vessel:	n/a
2	chr4:3644703-3644753	IMR90	lung:	fetal
3	chr4:3680721-3680771	SAEC	small airway:	n/a
4	chr4:3675363-3675413	PFSK-1	brain:	n/a
5	chr4:3677553-3677603	Caco-2	colon:	n/a
6	chr4:3704824-3704874	NT2-D1	testis:	n/a
7	chr4:3691824-3691874	GM12878	blood:	n/a
8	chr4:3704824-3704874	NHDF-neo	bronchial:	n/a
9	chr4:3692574-3692624	HCF	heart:	n/a
10	chr4:3640481-3640531	GM06990	blood:	n/a
11	chr4:3705147-3705197	HRE	kidney:	n/a
12	chr4:3704852-3704902	AoSMC	blood vessel:	n/a
13	chr4:3644703-3644753	IMR90	lung:	fetal
14	chr4:3680721-3680771	SAEC	small airway:	n/a
15	chr4:3675363-3675413	PFSK-1	brain:	n/a
16	chr4:3677553-3677603	Caco-2	colon:	n/a
17	chr4:3704824-3704874	NT2-D1	testis:	n/a
18	chr4:3691824-3691874	GM12878	blood:	n/a
19	chr4:3704824-3704874	NHDF-neo	bronchial:	n/a
20	chr4:3692574-3692624	HCF	heart:	n/a
21	chr4:3640481-3640531	GM06990	blood:	n/a
22	chr4:3705147-3705197	HRE	kidney:	n/a
23	chr4:3664401-3664451	SK-N-SH	brain:	n/a
24	chr4:3643475-3643525	AG09319	gingival:	n/a
25	chr4:3651471-3651521	HAEpiC	amniotic membrane:	n/a
26	chr4:3692712-3692762	SKMC	muscle:	n/a
27	chr4:3647047-3647097	GM19239	blood:	n/a
28	chr4:3685875-3685925	HAEpiC	amniotic membrane:	n/a
29	chr4:3683268-3683318	HNPCEpiC	eye:	n/a
30	chr4:3681759-3681809	HRPEpiC	eye:	n/a
31	chr4:3685875-3685925	LNCaP	prostate:	n/a
32	chr4:3685309-3685359	HAEpiC	amniotic membrane:	n/a
33	chr4:3643475-3643525	U87	brain:	n/a
34	chr4:3644703-3644753	HIPEpiC	eye:	n/a
35	chr4:3671697-3671747	NB4	blood:	n/a
36	chr4:3673098-3673148	T-47D	breast:	n/a
37	chr4:3685875-3685925	NHBE	bronchial:	n/a
38	chr4:3685438-3685488	NB4	blood:	n/a
39	chr4:3713209-3713259	HRE	kidney:	n/a
40	chr4:3642351-3642401	HMEC	breast:	n/a
41	chr4:3644703-3644753	H1-hESC	embryonic stem cell:	embryo
42	chr4:3617256-3617306	ovcar-3	ovarian:	n/a
43	chr4:3646912-3646962	SK-N-MC	brain:	n/a
44	chr4:3646912-3646962	PANC-1	pancreas:	n/a
45	chr4:3682627-3682677	GM12878	blood:	n/a
46	chr4:3630603-3630653	HL-60	blood:	n/a
47	chr4:3664471-3664521	AG04450	lung:	fetal
48	chr4:3682525-3682575	Caco-2	colon:	n/a
49	chr4:3630603-3630653	U87	brain:	n/a
50	chr4:3680970-3681020	AG04449	skin:	fetal

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
2	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
3	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
4	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
5	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
6	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
7	chr4:3531986..3534650-chr4:3657102..3659521,2	MCF-7	breast:
8	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
9	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
10	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
11	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
12	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
13	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
14	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
15	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
16	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
17	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
18	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
19	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
20	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
21	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
22	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
23	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
24	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
25	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
26	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
27	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
28	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
29	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
30	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
31	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
32	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
33	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
34	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
35	chr4:3532356..3534055-chr4:3658252..3659865,2	K562	blood:
36	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
37	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
38	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
39	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
40	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
41	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
42	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
43	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
44	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
45	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
46	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
47	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
48	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
49	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
50	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5960 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5960 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1810606	chr4:3609390-3609391	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs73204940	chr4:3609403-3609404	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1810605	chr4:3609408-3609409	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539993624	chr4:3609413-3609414	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556918636	chr4:3609414-3609415	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190998774	chr4:3609431-3609432	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73204943	chr4:3609433-3609434	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73204944	chr4:3609438-3609439	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73204945	chr4:3609452-3609453	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375619003	chr4:3609481-3609482	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150122304	chr4:3609485-3609486	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572348275	chr4:3609487-3609488	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142703363	chr4:3609490-3609491	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs80234298	chr4:3609498-3609499	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79943857	chr4:3609499-3609500	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76308394	chr4:3609500-3609501	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78044682	chr4:3609505-3609506	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78733867	chr4:3609509-3609510	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551916779	chr4:3609511-3609512	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562326885	chr4:3609522-3609523	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs66667292	chr4:3609524-3609525	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147092100	chr4:3609535-3609536	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73204946	chr4:3609540-3609541	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73204947	chr4:3609555-3609556	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548184847	chr4:3609557-3609558	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs67484815	chr4:3609571-3609572	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568088258	chr4:3609582-3609583	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533513287	chr4:3609594-3609595	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs67911990	chr4:3609601-3609602	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547520362	chr4:3609622-3609623	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570534709	chr4:3609627-3609628	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540056702	chr4:3609635-3609636	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200460602	chr4:3609657-3609658	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73204950	chr4:3609683-3609684	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73204951	chr4:3609687-3609688	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556832416	chr4:3609688-3609689	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79820358	chr4:3609690-3609691	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536194394	chr4:3609703-3609704	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115486659	chr4:3609719-3609720	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73204952	chr4:3609724-3609725	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs180727007	chr4:3609737-3609738	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572405604	chr4:3609739-3609740	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35322891	chr4:3609740-3609741	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1806677	chr4:3609751-3609752	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557843491	chr4:3609776-3609777	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577747500	chr4:3609778-3609779	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73204954	chr4:3609784-3609785	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74932380	chr4:3609789-3609790	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77159087	chr4:3609796-3609797	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs67423032	chr4:3609800-3609801	ZNF genes & repeats Enhancers Bivalent Enhancer 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
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3601600-3611600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:3605200-3611400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:3607000-3610000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:3608600-3609600	Weak transcription	Fetal Lung	lung
5	chr4:3608600-3609600	Bivalent Enhancer	Placenta	Placenta
6	chr4:3608600-3611200	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:3608800-3609600	ZNF genes & repeats	Spleen	Spleen
8	chr4:3608800-3611400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr4:3609000-3611000	ZNF genes & repeats	Fetal Stomach	stomach
10	chr4:3609400-3610000	Enhancers	Brain Germinal Matrix	brain
11	chr4:3609400-3610000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
12	chr4:3609400-3610200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr4:3609400-3610400	Enhancers	Fetal Brain Female	brain
14	chr4:3609400-3610800	Enhancers	Fetal Brain Male	brain
15	chr4:3609600-3610000	Enhancers	Adipose Nuclei	Adipose
16	chr4:3609600-3610000	Enhancers	Fetal Lung	lung
17	chr4:3609600-3610200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr4:3609600-3610200	Enhancers	HSMMtube	muscle
19	chr4:3609600-3610400	Weak transcription	Spleen	Spleen
20	chr4:3609800-3610000	Enhancers	Right Ventricle	heart
21	chr4:3610000-3614600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr4:3610400-3611400	ZNF genes & repeats	Fetal Brain Female	brain
23	chr4:3610400-3612200	ZNF genes & repeats	Spleen	Spleen
24	chr4:3610800-3611400	ZNF genes & repeats	Fetal Brain Male	brain
25	chr4:3611000-3611400	Enhancers	Esophagus	oesophagus
26	chr4:3611200-3611600	Enhancers	Fetal Muscle Leg	muscle
27	chr4:3611400-3612800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:3611600-3612600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:3611600-3614400	Weak transcription	Fetal Muscle Leg	muscle
30	chr4:3612600-3613200	ZNF genes & repeats	Spleen	Spleen
31	chr4:3612600-3615000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:3612800-3613200	ZNF genes & repeats	Pancreas	Pancrea
33	chr4:3612800-3613400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:3612800-3613400	ZNF genes & repeats	Gastric	stomach
35	chr4:3613200-3613400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:3613200-3613800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:3613200-3614600	Weak transcription	Pancreas	Pancrea
38	chr4:3613200-3614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr4:3613200-3615600	Weak transcription	Adipose Nuclei	Adipose
40	chr4:3613400-3613600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:3613400-3614600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3613400-3614600	Weak transcription	Gastric	stomach
43	chr4:3613600-3614400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:3614400-3614600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:3614400-3614600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:3614400-3614600	Weak transcription	Spleen	Spleen
47	chr4:3614400-3615000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr4:3614400-3616400	Enhancers	Fetal Muscle Leg	muscle
49	chr4:3614600-3614800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr4:3614600-3614800	Enhancers	Cortex derived primary cultured neurospheres	brain

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