Variant report

Variant	nsv1000830
Chromosome Location	chr4:3613907-3706509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:4642)
Chromatin interactive
region (count:68)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
10	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
13	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
15	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
16	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
19	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
20	CEBPB	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
23	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
24	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
25	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
26	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
27	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
28	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
29	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
30	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
31	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
32	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
33	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
35	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
37	CHD2	chr4:3657873-3658157	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:3642375-3642459	HepG2	liver:	n/a	n/a
40	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
41	CREB1	chr4:3677024-3677462	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr4:3676953-3677446	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:3646151-3646188	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:3659600-3659750	AG04449	skin:	n/a	n/a
45	CTCF	chr4:3659660-3659810	NHEK	skin:	n/a	chr4:3659774-3659787
46	CTCF	chr4:3677180-3677330	HEK293	kidney:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
47	CTCF	chr4:3614701-3614781	NHEK	skin:	n/a	n/a
48	CTCF	chr4:3703301-3703427	MCF-7	breast:	n/a	chr4:3703375-3703384
49	CTCF	chr4:3655916-3655976	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr4:3703220-3703370	HBMEC	blood vessel:	n/a	n/a

(count:4642 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3685875-3685925	Caco-2	colon:	n/a
2	chr4:3669900-3669950	GM12892	blood:	n/a
3	chr4:3704824-3704874	HCT-116	colon:	n/a
4	chr4:3643635-3643685	PFSK-1	brain:	n/a
5	chr4:3675363-3675413	HL-60	blood:	n/a
6	chr4:3675363-3675413	SK-N-SH_RA	brain:	n/a
7	chr4:3685875-3685925	Caco-2	colon:	n/a
8	chr4:3669900-3669950	GM12892	blood:	n/a
9	chr4:3704824-3704874	HCT-116	colon:	n/a
10	chr4:3643635-3643685	PFSK-1	brain:	n/a
11	chr4:3675363-3675413	HL-60	blood:	n/a
12	chr4:3675363-3675413	SK-N-SH_RA	brain:	n/a
13	chr4:3704824-3704874	GM06990	blood:	n/a
14	chr4:3691238-3691288	PrEC	prostate:	n/a
15	chr4:3642351-3642401	AG04450	lung:	fetal
16	chr4:3691238-3691288	SK-N-SH	brain:	n/a
17	chr4:3617256-3617306	HEEpiC	esophagus:	n/a
18	chr4:3657880-3657930	Hepatocyte	liver:	n/a
19	chr4:3673098-3673148	GM12878	blood:	n/a
20	chr4:3664401-3664451	U87	brain:	n/a
21	chr4:3650474-3650524	NH-A	brain:	n/a
22	chr4:3675363-3675413	GM12891	blood:	n/a
23	chr4:3685309-3685359	SK-N-SH	brain:	n/a
24	chr4:3685309-3685359	HRE	kidney:	n/a
25	chr4:3704824-3704874	HUVEC	blood vessel:	n/a
26	chr4:3691297-3691347	U87	brain:	n/a
27	chr4:3671697-3671747	HAEpiC	amniotic membrane:	n/a
28	chr4:3689478-3689528	ProgFib	skin:	n/a
29	chr4:3677497-3677547	HUVEC	blood vessel:	n/a
30	chr4:3643404-3643454	BJ	skin:	n/a
31	chr4:3690945-3690995	Hela-S3	cervix:	n/a
32	chr4:3646912-3646962	HMEC	breast:	n/a
33	chr4:3646912-3646962	SK-N-SH	brain:	n/a
34	chr4:3685875-3685925	HRE	kidney:	n/a
35	chr4:3671503-3671553	ProgFib	skin:	n/a
36	chr4:3692712-3692762	AoSMC	blood vessel:	n/a
37	chr4:3671697-3671747	NHBE	bronchial:	n/a
38	chr4:3692712-3692762	AG10803	skin:	n/a
39	chr4:3617603-3617653	NT2-D1	testis:	n/a
40	chr4:3651471-3651521	NT2-D1	testis:	n/a
41	chr4:3644187-3644237	HRE	kidney:	n/a
42	chr4:3677497-3677547	HCF	heart:	n/a
43	chr4:3643959-3644009	SK-N-SH	brain:	n/a
44	chr4:3704824-3704874	SK-N-SH_RA	brain:	n/a
45	chr4:3675363-3675413	HRPEpiC	eye:	n/a
46	chr4:3692712-3692762	HL-60	blood:	n/a
47	chr4:3685357-3685407	HCT-116	colon:	n/a
48	chr4:3685357-3685407	SAEC	small airway:	n/a
49	chr4:3692142-3692192	NT2-D1	testis:	n/a
50	chr4:3660005-3660055	CMK	blood:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
2	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
3	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
4	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
5	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
6	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
7	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
8	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
9	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
10	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
11	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
12	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
13	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
14	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
15	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
16	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
17	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
18	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
19	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
20	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
21	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
22	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
23	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
24	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
25	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
26	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
27	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
28	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
29	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
30	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
31	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
32	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
33	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
34	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
35	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
36	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
37	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
38	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
39	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
40	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
41	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
42	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
43	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
44	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
45	chr4:3531986..3534650-chr4:3657102..3659521,2	MCF-7	breast:
46	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
47	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
48	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
49	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
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-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
2	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
3	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
4	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
5	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
6	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
7	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
8	lnc-RP3-368B9.1.1-5	chr4:3650108-3650607	XLOC_003431
9	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632
10	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2
11	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
12	lnc-LRPAP1-6	chr4:3645119-3645386	ucscGeneNc_uc003ghl_2
13	lnc-LRPAP1-6	chr4:3648128-3648206	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
ENSG00000184160	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000250632	chromatin interactions

Extended variants
information (count: 5125 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5125 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368030529	chr4:3613951-3613952	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs114319442	chr4:3613998-3613999	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs540171153	chr4:3614045-3614046	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs544375242	chr4:3614053-3614054	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs576392129	chr4:3614061-3614062	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs541821932	chr4:3614069-3614070	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs555460987	chr4:3614090-3614091	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs184659486	chr4:3614101-3614102	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs541120426	chr4:3614194-3614195	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs372601875	chr4:3614196-3614197	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs189069406	chr4:3614200-3614201	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs559545296	chr4:3614216-3614217	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs546089793	chr4:3614241-3614242	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs562608001	chr4:3614248-3614249	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs35208860	chr4:3614254-3614255	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs547906329	chr4:3614264-3614265	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs568047906	chr4:3614285-3614286	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs527423945	chr4:3614288-3614289	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs547512248	chr4:3614301-3614302	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs181414092	chr4:3614344-3614345	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs78666976	chr4:3614402-3614403	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556829854	chr4:3614513-3614514	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570224170	chr4:3614540-3614541	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533415786	chr4:3614550-3614551	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150786845	chr4:3614566-3614567	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572108386	chr4:3614577-3614578	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139207644	chr4:3614581-3614582	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557792125	chr4:3614632-3614633	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576983596	chr4:3614639-3614640	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201025730	chr4:3614667-3614668	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558305332	chr4:3614671-3614672	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377499090	chr4:3614675-3614676	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184219804	chr4:3614677-3614678	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200613928	chr4:3614703-3614704	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562681845	chr4:3614733-3614734	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553995159	chr4:3614805-3614806	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs369554587	chr4:3614808-3614809	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189394329	chr4:3614837-3614838	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs12501421	chr4:3614848-3614849	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs576293524	chr4:3614894-3614895	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs532854247	chr4:3614913-3614914	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs542096991	chr4:3614928-3614929	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs561713066	chr4:3614951-3614952	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs527237195	chr4:3614963-3614964	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs547523943	chr4:3614964-3614965	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs10674236	chr4:3614976-3614977	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs36210182	chr4:3614983-3614984	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs200812852	chr4:3614984-3614985	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs201794846	chr4:3614985-3614986	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs200330998	chr4:3614986-3614987	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	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:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3610000-3614600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:3611600-3614400	Weak transcription	Fetal Muscle Leg	muscle
3	chr4:3612600-3615000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:3613200-3614600	Weak transcription	Pancreas	Pancrea
5	chr4:3613200-3614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:3613200-3615600	Weak transcription	Adipose Nuclei	Adipose
7	chr4:3613400-3614600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3613400-3614600	Weak transcription	Gastric	stomach
9	chr4:3613600-3614400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:3614400-3614600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:3614400-3614600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:3614400-3614600	Weak transcription	Spleen	Spleen
13	chr4:3614400-3615000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:3614400-3616400	Enhancers	Fetal Muscle Leg	muscle
15	chr4:3614600-3614800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr4:3614600-3614800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr4:3614600-3614800	Enhancers	Fetal Brain Female	brain
18	chr4:3614600-3615000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:3614600-3615000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:3614600-3615000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
21	chr4:3614600-3615000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3614600-3615000	ZNF genes & repeats	Fetal Brain Male	brain
23	chr4:3614600-3615000	ZNF genes & repeats	Fetal Kidney	kidney
24	chr4:3614600-3615600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:3614600-3616000	Enhancers	Gastric	stomach
26	chr4:3614600-3616400	Enhancers	Spleen	Spleen
27	chr4:3614600-3616400	Enhancers	HSMMtube	muscle
28	chr4:3614600-3616600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr4:3614600-3616600	Enhancers	Pancreas	Pancrea
30	chr4:3614800-3615000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr4:3614800-3615400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr4:3614800-3615800	Weak transcription	Fetal Brain Female	brain
33	chr4:3614800-3616200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
34	chr4:3614800-3616400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:3614800-3616400	Enhancers	Ovary	ovary
36	chr4:3614800-3616600	Enhancers	HSMM	muscle
37	chr4:3615000-3615600	Weak transcription	Fetal Brain Male	brain
38	chr4:3615000-3616000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:3615000-3616000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:3615000-3617200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:3615000-3617600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:3615400-3616800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr4:3615600-3616000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:3615600-3616200	Enhancers	Right Ventricle	heart
45	chr4:3615600-3616400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:3615600-3616400	Enhancers	Adipose Nuclei	Adipose
47	chr4:3615600-3616400	Enhancers	Fetal Heart	heart
48	chr4:3615600-3616600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:3615600-3616600	Enhancers	HepG2	liver
50	chr4:3615600-3616600	Enhancers	Osteobl	bone

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