Variant report

Variant	nsv878502
Chromosome Location	chr4:3627237-3729652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:704)
CpG islands
(count:4829)
Chromatin interactive
region (count:76)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
5	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	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	BCL3	chr4:3715787-3716400	GM12878	blood:	n/a	chr4:3715840-3715849
9	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
10	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3715793-3716328	GM12878	blood:	n/a	chr4:3715840-3715849
13	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
17	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
19	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
20	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
21	CEBPB	chr4:3726548-3726682	HepG2	liver:	n/a	chr4:3726602-3726613
22	CEBPB	chr4:3726430-3726784	H1-hESC	embryonic stem cell:	n/a	chr4:3726602-3726613
23	CEBPB	chr4:3726439-3726733	K562	blood:	n/a	chr4:3726602-3726613
24	CEBPB	chr4:3726438-3726775	HepG2	liver:	n/a	chr4:3726602-3726613
25	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
27	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
28	CEBPB	chr4:3726407-3726677	A549	lung:	n/a	chr4:3726602-3726613
29	CEBPB	chr4:3726453-3726738	Hela-S3	cervix:	n/a	chr4:3726602-3726613
30	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
31	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
32	CEBPB	chr4:3726331-3726812	ECC-1	luminal epithelium:	n/a	chr4:3726602-3726613
33	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
34	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
35	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
36	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:3726444-3726759	A549	lung:	n/a	chr4:3726602-3726613
38	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
39	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
40	CEBPB	chr4:3726435-3726790	IMR90	lung:	n/a	chr4:3726602-3726613
41	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
42	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
43	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
44	CEBPB	chr4:3726397-3726886	A549	lung:	n/a	chr4:3726602-3726613
45	CEBPB	chr4:3726434-3726839	MCF-7	breast:	n/a	chr4:3726602-3726613
46	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
47	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:3726376-3726789	ECC-1	luminal epithelium:	n/a	chr4:3726602-3726613
49	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
50	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a

(count:4829 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3646912-3646962	BJ	skin:	n/a
2	chr4:3691238-3691288	GM06990	blood:	n/a
3	chr4:3647047-3647097	HCPEpiC	choroid plexus:	n/a
4	chr4:3651354-3651404	ovcar-3	ovarian:	n/a
5	chr4:3690828-3690878	HCT-116	colon:	n/a
6	chr4:3675120-3675170	HCM	heart:	n/a
7	chr4:3677497-3677547	MCF-7	breast:	n/a
8	chr4:3691238-3691288	IMR90	lung:	fetal
9	chr4:3691297-3691347	GM19239	blood:	n/a
10	chr4:3705147-3705197	A549	lung:	n/a
11	chr4:3646912-3646962	BJ	skin:	n/a
12	chr4:3691238-3691288	GM06990	blood:	n/a
13	chr4:3647047-3647097	HCPEpiC	choroid plexus:	n/a
14	chr4:3651354-3651404	ovcar-3	ovarian:	n/a
15	chr4:3690828-3690878	HCT-116	colon:	n/a
16	chr4:3675120-3675170	HCM	heart:	n/a
17	chr4:3677497-3677547	MCF-7	breast:	n/a
18	chr4:3691238-3691288	IMR90	lung:	fetal
19	chr4:3691297-3691347	GM19239	blood:	n/a
20	chr4:3705147-3705197	A549	lung:	n/a
21	chr4:3630603-3630653	HCM	heart:	n/a
22	chr4:3652326-3652376	U87	brain:	n/a
23	chr4:3692574-3692624	HCT-116	colon:	n/a
24	chr4:3685438-3685488	HCM	heart:	n/a
25	chr4:3691397-3691447	SKMC	muscle:	n/a
26	chr4:3691033-3691083	SK-N-SH_RA	brain:	n/a
27	chr4:3685438-3685488	ECC-1	luminal epithelium:	n/a
28	chr4:3651471-3651521	HUVEC	blood vessel:	n/a
29	chr4:3643404-3643454	SAEC	small airway:	n/a
30	chr4:3713224-3713274	H1-hESC	embryonic stem cell:	embryo
31	chr4:3685875-3685925	GM19239	blood:	n/a
32	chr4:3643770-3643820	PrEC	prostate:	n/a
33	chr4:3644187-3644237	HepG2	liver:	n/a
34	chr4:3726701-3726751	SK-N-SH_RA	brain:	n/a
35	chr4:3643770-3643820	Hepatocyte	liver:	n/a
36	chr4:3664117-3664167	ProgFib	skin:	n/a
37	chr4:3691824-3691874	HNPCEpiC	eye:	n/a
38	chr4:3692375-3692425	NHDF-neo	bronchial:	n/a
39	chr4:3726450-3726500	HepG2	liver:	n/a
40	chr4:3726255-3726305	K562	blood:	n/a
41	chr4:3657880-3657930	A549	lung:	n/a
42	chr4:3650474-3650524	HRCEpiC	kidney:	n/a
43	chr4:3682627-3682677	ProgFib	skin:	n/a
44	chr4:3680721-3680771	RPTEC	kidney:	n/a
45	chr4:3680970-3681020	HRE	kidney:	n/a
46	chr4:3651233-3651283	HCM	heart:	n/a
47	chr4:3713287-3713337	U87	brain:	n/a
48	chr4:3704824-3704874	HCPEpiC	choroid plexus:	n/a
49	chr4:3671199-3671249	RPTEC	kidney:	n/a
50	chr4:3640481-3640531	HL-60	blood:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
2	chr4:3715270..3718190-chr4:3721526..3723393,2	K562	blood:
3	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
4	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
5	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
6	chr4:3719651..3722174-chr4:3722524..3724517,2	K562	blood:
7	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
8	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
9	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
10	chr4:3720840..3724300-chr4:3724381..3726602,3	MCF-7	breast:
11	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
12	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
13	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
14	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
15	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
16	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
17	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
18	chr4:3717339..3719373-chr4:3721279..3722918,2	MCF-7	breast:
19	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
20	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
21	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
22	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
23	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
24	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
25	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
26	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
27	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
28	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
29	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
30	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
31	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
32	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
33	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
34	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
35	chr4:3717857..3720056-chr4:3723644..3725873,2	MCF-7	breast:
36	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
37	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
38	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
39	chr4:3720745..3724824-chr4:3727644..3730429,3	K562	blood:
40	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
41	chr4:3728407..3730608-chr4:3954837..3956442,2	K562	blood:
42	chr4:3717339..3719373-chr4:3721279..3722918,2	MCF-7	breast:
43	chr4:3720840..3724300-chr4:3724381..3726602,3	MCF-7	breast:
44	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
45	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
46	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
47	chr4:3717857..3720056-chr4:3723644..3725873,2	MCF-7	breast:
48	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
49	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
50	chr4:3631211..3633906-chr4:3645708..3648279,2	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	chr4:3650108-3650607	XLOC_003431
3	lnc-LRPAP1-6	chr4:3648128-3648206	ucscGeneNc_uc003ghl_2
4	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
5	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
6	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
7	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
8	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
9	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
10	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2
11	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
12	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
13	lnc-LRPAP1-2	chr4:3675320-3675588	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
ENSG00000250681	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000250632	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000163956	chromatin interactions

Extended variants
information (count: 5808 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5808 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73205000	chr4:3627266-3627267	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs73205001	chr4:3627267-3627268	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs73081170	chr4:3627292-3627293	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs193007034	chr4:3627304-3627305	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs574882326	chr4:3627347-3627348	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs75706034	chr4:3627354-3627355	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs79039544	chr4:3627356-3627357	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs76778801	chr4:3627359-3627360	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs73205002	chr4:3627371-3627372	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs386670750	chr4:3627415-3627416	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77780779	chr4:3627416-3627417	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75206228	chr4:3627417-3627418	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150980043	chr4:3627431-3627432	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559294586	chr4:3627432-3627433	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572669113	chr4:3627438-3627439	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112409604	chr4:3627445-3627446	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs66704131	chr4:3627448-3627449	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530702172	chr4:3627458-3627459	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79659915	chr4:3627479-3627480	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111788373	chr4:3627485-3627486	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556073020	chr4:3627486-3627487	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550343026	chr4:3627487-3627488	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560932955	chr4:3627501-3627502	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529753397	chr4:3627524-3627525	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373776139	chr4:3627558-3627559	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73206704	chr4:3627559-3627560	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73206706	chr4:3627570-3627571	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73206707	chr4:3627576-3627577	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58012424	chr4:3627600-3627601	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184707081	chr4:3627605-3627606	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs539206950	chr4:3627666-3627667	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs552782739	chr4:3627668-3627669	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs569604138	chr4:3627671-3627672	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs538527746	chr4:3627672-3627673	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs554669471	chr4:3627681-3627682	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs373341912	chr4:3627682-3627683	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs534050254	chr4:3627689-3627690	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs73794004	chr4:3627698-3627699	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs189684076	chr4:3627718-3627719	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs76125657	chr4:3627729-3627730	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs28670407	chr4:3627736-3627737	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576907139	chr4:3627739-3627740	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs544841353	chr4:3627759-3627760	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs35392261	chr4:3627763-3627764	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73206708	chr4:3627783-3627784	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs62274327	chr4:3627805-3627806	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113393963	chr4:3627837-3627838	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62274328	chr4:3627843-3627844	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62274329	chr4:3627880-3627881	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58404209	chr4:3627891-3627892	ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3625000-3628000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chr4:3625200-3629400	ZNF genes & repeats	Fetal Brain Female	brain
3	chr4:3625400-3627800	Enhancers	Fetal Brain Male	brain
4	chr4:3626000-3627400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:3626000-3628000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:3627000-3632000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:3627400-3627600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
8	chr4:3627400-3627800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:3627600-3627800	Weak transcription	Spleen	Spleen
10	chr4:3627600-3628000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:3627800-3628400	Weak transcription	Fetal Brain Male	brain
12	chr4:3627800-3629600	ZNF genes & repeats	Spleen	Spleen
13	chr4:3628400-3629400	ZNF genes & repeats	Fetal Brain Male	brain
14	chr4:3629200-3629400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
15	chr4:3629200-3629400	Bivalent/Poised TSS	Fetal Heart	heart
16	chr4:3629400-3629600	Weak transcription	Fetal Brain Male	brain
17	chr4:3629400-3635800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:3629600-3630400	Enhancers	Fetal Brain Male	brain
19	chr4:3629800-3630200	Enhancers	Brain Anterior Caudate	brain
20	chr4:3630000-3631800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr4:3630200-3631800	Weak transcription	Brain Anterior Caudate	brain
22	chr4:3630600-3631600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:3631200-3634800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:3631800-3633800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:3632000-3632200	Enhancers	Brain Anterior Caudate	brain
26	chr4:3632000-3632800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:3632200-3632400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:3632200-3632400	Bivalent Enhancer	Placenta	Placenta
29	chr4:3632200-3635800	ZNF genes & repeats	Fetal Intestine Small	intestine
30	chr4:3632400-3632600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:3632400-3632600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
32	chr4:3632400-3632600	Bivalent Enhancer	HepG2	liver
33	chr4:3632400-3633200	Enhancers	Fetal Intestine Large	intestine
34	chr4:3632600-3633000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:3632600-3633200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:3632600-3635800	ZNF genes & repeats	Fetal Stomach	stomach
37	chr4:3632800-3633000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:3633000-3633800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr4:3633000-3633800	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr4:3633000-3633800	Bivalent Enhancer	Placenta	Placenta
41	chr4:3633000-3633800	Bivalent Enhancer	HepG2	liver
42	chr4:3633000-3634200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:3633000-3634200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr4:3633000-3636400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:3633200-3634000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:3633200-3634200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:3633200-3634800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr4:3633400-3633600	Bivalent Enhancer	Osteobl	bone
49	chr4:3633400-3633800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:3633400-3634000	Enhancers	Fetal Kidney	kidney

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