Variant report

Variant	nsv878499
Chromosome Location	chr4:3602109-3714659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:865)
CpG islands
(count:4828)
Chromatin interactive
region (count:78)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:865 , 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	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
10	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
13	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
18	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
20	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
21	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
22	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
24	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
25	CEBPB	chr4:3608606-3609111	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
26	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
27	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
28	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
29	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
31	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
32	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
33	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
35	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
36	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
37	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
38	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
39	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
40	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
41	CEBPB	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
43	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
44	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
45	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
46	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
47	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
48	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
50	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839

(count:4828 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3651354-3651404	HCT-116	colon:	n/a
2	chr4:3657880-3657930	GM19239	blood:	n/a
3	chr4:3691033-3691083	HRCEpiC	kidney:	n/a
4	chr4:3640481-3640531	HCT-116	colon:	n/a
5	chr4:3681759-3681809	T-47D	breast:	n/a
6	chr4:3704824-3704874	NT2-D1	testis:	n/a
7	chr4:3616943-3616993	NT2-D1	testis:	n/a
8	chr4:3642351-3642401	SAEC	small airway:	n/a
9	chr4:3690828-3690878	ovcar-3	ovarian:	n/a
10	chr4:3651354-3651404	HCT-116	colon:	n/a
11	chr4:3657880-3657930	GM19239	blood:	n/a
12	chr4:3691033-3691083	HRCEpiC	kidney:	n/a
13	chr4:3640481-3640531	HCT-116	colon:	n/a
14	chr4:3681759-3681809	T-47D	breast:	n/a
15	chr4:3704824-3704874	NT2-D1	testis:	n/a
16	chr4:3616943-3616993	NT2-D1	testis:	n/a
17	chr4:3642351-3642401	SAEC	small airway:	n/a
18	chr4:3690828-3690878	ovcar-3	ovarian:	n/a
19	chr4:3691397-3691447	ovcar-3	ovarian:	n/a
20	chr4:3671199-3671249	NT2-D1	testis:	n/a
21	chr4:3671067-3671117	GM12892	blood:	n/a
22	chr4:3643770-3643820	HEK293	kidney:	embryo
23	chr4:3617256-3617306	HNPCEpiC	eye:	n/a
24	chr4:3660005-3660055	AG09319	gingival:	n/a
25	chr4:3643475-3643525	HUVEC	blood vessel:	n/a
26	chr4:3643959-3644009	SK-N-SH_RA	brain:	n/a
27	chr4:3652433-3652483	A549	lung:	n/a
28	chr4:3704852-3704902	GM19239	blood:	n/a
29	chr4:3651233-3651283	MCF-7	breast:	n/a
30	chr4:3691824-3691874	SK-N-MC	brain:	n/a
31	chr4:3617603-3617653	AG10803	skin:	n/a
32	chr4:3644437-3644487	AG10803	skin:	n/a
33	chr4:3677497-3677547	HRE	kidney:	n/a
34	chr4:3675363-3675413	HUVEC	blood vessel:	n/a
35	chr4:3652326-3652376	NH-A	brain:	n/a
36	chr4:3680721-3680771	CMK	blood:	n/a
37	chr4:3657880-3657930	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:3691297-3691347	SK-N-MC	brain:	n/a
39	chr4:3616829-3616879	ProgFib	skin:	n/a
40	chr4:3680721-3680771	Hepatocyte	liver:	n/a
41	chr4:3692142-3692192	K562	blood:	n/a
42	chr4:3704880-3704930	GM19239	blood:	n/a
43	chr4:3682627-3682677	BE2_C	brain:	n/a
44	chr4:3664117-3664167	NHDF-neo	bronchial:	n/a
45	chr4:3671199-3671249	HCF	heart:	n/a
46	chr4:3651354-3651404	SK-N-MC	brain:	n/a
47	chr4:3682525-3682575	U87	brain:	n/a
48	chr4:3643635-3643685	HRE	kidney:	n/a
49	chr4:3667715-3667765	GM06990	blood:	n/a
50	chr4:3677553-3677603	ECC-1	luminal epithelium:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
2	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
3	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
4	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
5	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
6	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
7	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
8	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
9	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
10	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
11	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
12	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
13	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
14	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
15	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
16	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
17	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
18	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
19	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
20	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
21	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
22	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
23	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
24	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
25	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
26	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
27	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
28	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
29	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
30	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
31	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
32	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
33	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
34	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
35	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
36	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
37	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
38	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
39	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
40	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
41	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
42	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
43	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
44	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
45	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
46	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
47	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
48	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
49	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
50	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 6636 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6636 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6856283	chr4:3602109-3602110	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs35094120	chr4:3602115-3602116	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs5020895	chr4:3602131-3602132	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs5020896	chr4:3602137-3602138	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535433786	chr4:3602138-3602139	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs5020897	chr4:3602141-3602142	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5020898	chr4:3602165-3602166	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs5020899	chr4:3602168-3602169	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62273046	chr4:3602187-3602188	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs5020900	chr4:3602192-3602193	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34176470	chr4:3602201-3602202	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111619787	chr4:3602202-3602203	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558294564	chr4:3602218-3602219	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs578097550	chr4:3602228-3602229	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73077008	chr4:3602254-3602255	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73203119	chr4:3602282-3602283	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116383461	chr4:3602289-3602290	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191923343	chr4:3602295-3602296	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73203121	chr4:3602314-3602315	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73203122	chr4:3602316-3602317	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540884920	chr4:3602333-3602334	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13130523	chr4:3602334-3602335	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532978955	chr4:3602359-3602360	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73795633	chr4:3602368-3602369	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73203123	chr4:3602391-3602392	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113332001	chr4:3602414-3602415	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528895751	chr4:3602431-3602432	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67608173	chr4:3602436-3602437	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548968359	chr4:3602445-3602446	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565793557	chr4:3602506-3602507	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534747808	chr4:3602512-3602513	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78711707	chr4:3602513-3602514	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58877580	chr4:3602540-3602541	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571859849	chr4:3602541-3602542	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537241721	chr4:3602559-3602560	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34631283	chr4:3602574-3602575	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113793162	chr4:3602603-3602604	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573949514	chr4:3602617-3602618	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536269010	chr4:3602631-3602632	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs58095472	chr4:3602642-3602643	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114846798	chr4:3602653-3602654	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545530189	chr4:3602658-3602659	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59812649	chr4:3602668-3602669	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56133380	chr4:3602681-3602682	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60844026	chr4:3602693-3602694	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs58935838	chr4:3602700-3602701	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543595281	chr4:3602706-3602707	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563593747	chr4:3602761-3602762	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529165461	chr4:3602767-3602768	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs57747150	chr4:3602827-3602828	ZNF genes & repeats 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:872 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3595800-3603400	Weak transcription	Right Atrium	heart
2	chr4:3597000-3604200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:3597000-3608000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:3598600-3607600	ZNF genes & repeats	Fetal Stomach	stomach
5	chr4:3600000-3604200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:3600200-3602200	ZNF genes & repeats	Pancreas	Pancrea
7	chr4:3601600-3611600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:3602800-3603600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:3603000-3604800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:3603200-3604000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr4:3604200-3605200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:3605000-3606600	ZNF genes & repeats	Fetal Brain Female	brain
13	chr4:3605200-3605400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
14	chr4:3605200-3605600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
15	chr4:3605200-3605600	Enhancers	Spleen	Spleen
16	chr4:3605200-3611400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:3605600-3606600	Weak transcription	Spleen	Spleen
18	chr4:3606200-3606600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr4:3606200-3607800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr4:3606400-3608000	ZNF genes & repeats	Thymus	Thymus
21	chr4:3606600-3607000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
22	chr4:3606600-3607000	Active TSS	Spleen	Spleen
23	chr4:3606600-3607400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
24	chr4:3607000-3607200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr4:3607000-3607600	ZNF genes & repeats	Spleen	Spleen
26	chr4:3607000-3607800	Bivalent Enhancer	Fetal Muscle Leg	muscle
27	chr4:3607000-3610000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr4:3607600-3607800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr4:3607600-3608600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:3608000-3608600	ZNF genes & repeats	Fetal Lung	lung
31	chr4:3608000-3609000	Enhancers	K562	blood
32	chr4:3608600-3609600	Weak transcription	Fetal Lung	lung
33	chr4:3608600-3609600	Bivalent Enhancer	Placenta	Placenta
34	chr4:3608600-3611200	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr4:3608800-3609600	ZNF genes & repeats	Spleen	Spleen
36	chr4:3608800-3611400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:3609000-3609200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:3609000-3611000	ZNF genes & repeats	Fetal Stomach	stomach
39	chr4:3609400-3610000	Enhancers	Brain Germinal Matrix	brain
40	chr4:3609400-3610000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
41	chr4:3609400-3610200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr4:3609400-3610400	Enhancers	Fetal Brain Female	brain
43	chr4:3609400-3610800	Enhancers	Fetal Brain Male	brain
44	chr4:3609600-3610000	Enhancers	Adipose Nuclei	Adipose
45	chr4:3609600-3610000	Enhancers	Fetal Lung	lung
46	chr4:3609600-3610200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr4:3609600-3610200	Enhancers	HSMMtube	muscle
48	chr4:3609600-3610400	Weak transcription	Spleen	Spleen
49	chr4:3609800-3610000	Enhancers	Right Ventricle	heart
50	chr4:3610000-3614600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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