Variant report

Variant	nsv878546
Chromosome Location	chr4:7285356-7376694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:7291600-7291628	K562	blood:	n/a	n/a
2	ATF3	chr4:7325347-7326029	A549	lung:	n/a	n/a
3	ATF3	chr4:7325569-7325906	A549	lung:	n/a	n/a
4	BACH1	chr4:7351001-7351177	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr4:7309436-7309751	GM12878	blood:	n/a	n/a
6	BCL3	chr4:7309477-7309799	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:7342329-7342469	K562	blood:	n/a	chr4:7342363-7342376
8	BHLHE40	chr4:7326359-7326668	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:7289378-7289811	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:7332888-7333034	K562	blood:	n/a	chr4:7332974-7332983 chr4:7332968-7332989 chr4:7332975-7332984 chr4:7332974-7332983 chr4:7332972-7332985
11	BHLHE40	chr4:7337542-7337783	K562	blood:	n/a	n/a
12	BHLHE40	chr4:7297759-7297998	K562	blood:	n/a	chr4:7297811-7297827
13	BHLHE40	chr4:7371415-7371470	K562	blood:	n/a	n/a
14	BHLHE40	chr4:7297755-7297955	GM12878	blood:	n/a	chr4:7297811-7297827
15	BRCA1	chr4:7297940-7298009	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:7297835-7297868	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:7360137-7360214	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:7337624-7337876	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:7314956-7315381	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
20	CEBPB	chr4:7350554-7351087	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
21	CEBPB	chr4:7314975-7315352	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
22	CEBPB	chr4:7324654-7324913	IMR90	lung:	n/a	chr4:7324854-7324865
23	CEBPB	chr4:7314905-7315396	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
24	CEBPB	chr4:7315008-7315270	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
25	CEBPB	chr4:7350688-7351037	K562	blood:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
26	CEBPB	chr4:7314977-7315363	H1-hESC	embryonic stem cell:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
27	CEBPB	chr4:7350681-7351058	IMR90	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
28	CEBPB	chr4:7350677-7351048	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
29	CEBPB	chr4:7314975-7315351	IMR90	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
30	CEBPB	chr4:7314974-7315334	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
31	CEBPB	chr4:7350773-7351029	MCF-7	breast:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
32	CEBPB	chr4:7350726-7351008	H1-hESC	embryonic stem cell:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
33	CEBPB	chr4:7350683-7351098	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
34	CEBPB	chr4:7314983-7315346	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
35	CEBPB	chr4:7314977-7315349	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
36	CEBPB	chr4:7360125-7360418	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:7350739-7350998	Hela-S3	cervix:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
38	CEBPB	chr4:7314937-7315345	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
39	CEBPB	chr4:7324731-7324857	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:7360151-7360464	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:7349851-7350214	A549	lung:	n/a	n/a
42	CEBPB	chr4:7314946-7315363	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
43	CEBPB	chr4:7315029-7315275	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
44	CEBPB	chr4:7350682-7351059	HepG2	liver:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
45	CEBPB	chr4:7315082-7315202	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
46	CEBPB	chr4:7315017-7315331	Hela-S3	cervix:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
47	CHD2	chr4:7337159-7337242	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:7330720-7330870	NHEK	skin:	n/a	n/a
49	CTCF	chr4:7337620-7337770	GM12870	blood:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695
50	CTCF	chr4:7335616-7335823	H1-hESC	embryonic stem cell:	n/a	chr4:7335713-7335731

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7373451-7373501	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:7287492-7287542	GM12892	blood:	n/a
3	chr4:7338792-7338842	RPTEC	kidney:	n/a
4	chr4:7304739-7304789	GM19239	blood:	n/a
5	chr4:7373451-7373501	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:7287492-7287542	GM12892	blood:	n/a
7	chr4:7338792-7338842	RPTEC	kidney:	n/a
8	chr4:7304739-7304789	GM19239	blood:	n/a
9	chr4:7374622-7374672	NH-A	brain:	n/a
10	chr4:7287492-7287542	HepG2	liver:	n/a
11	chr4:7373451-7373501	GM12891	blood:	n/a
12	chr4:7373451-7373501	BJ	skin:	n/a
13	chr4:7373065-7373115	HRPEpiC	eye:	n/a
14	chr4:7301491-7301541	MCF-7	breast:	n/a
15	chr4:7301529-7301579	U87	brain:	n/a
16	chr4:7289507-7289557	HMEC	breast:	n/a
17	chr4:7301491-7301541	Hepatocyte	liver:	n/a
18	chr4:7337225-7337275	H1-hESC	embryonic stem cell:	embryo
19	chr4:7373022-7373072	HAEpiC	amniotic membrane:	n/a
20	chr4:7301491-7301541	NHDF-neo	bronchial:	n/a
21	chr4:7326576-7326626	NH-A	brain:	n/a
22	chr4:7368808-7368858	HL-60	blood:	n/a
23	chr4:7368808-7368858	NHBE	bronchial:	n/a
24	chr4:7373343-7373393	SK-N-MC	brain:	n/a
25	chr4:7326576-7326626	Hela-S3	cervix:	n/a
26	chr4:7287615-7287665	GM12878	blood:	n/a
27	chr4:7289497-7289547	H1-hESC	embryonic stem cell:	embryo
28	chr4:7289723-7289773	SAEC	small airway:	n/a
29	chr4:7300999-7301049	HNPCEpiC	eye:	n/a
30	chr4:7373375-7373425	BE2_C	brain:	n/a
31	chr4:7301491-7301541	U87	brain:	n/a
32	chr4:7326576-7326626	HRCEpiC	kidney:	n/a
33	chr4:7373022-7373072	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:7374582-7374632	MCF-7	breast:	n/a
35	chr4:7301854-7301904	MCF-7	breast:	n/a
36	chr4:7338792-7338842	GM19239	blood:	n/a
37	chr4:7301176-7301226	PFSK-1	brain:	n/a
38	chr4:7301823-7301873	NB4	blood:	n/a
39	chr4:7289497-7289547	GM06990	blood:	n/a
40	chr4:7301491-7301541	GM12878	blood:	n/a
41	chr4:7289497-7289547	NB4	blood:	n/a
42	chr4:7289763-7289813	ProgFib	skin:	n/a
43	chr4:7289482-7289532	SAEC	small airway:	n/a
44	chr4:7304739-7304789	GM12892	blood:	n/a
45	chr4:7289507-7289557	HRE	kidney:	n/a
46	chr4:7301823-7301873	HUVEC	blood vessel:	n/a
47	chr4:7289763-7289813	IMR90	lung:	fetal
48	chr4:7326576-7326626	SK-N-SH	brain:	n/a
49	chr4:7289507-7289557	SK-N-SH	brain:	n/a
50	chr4:7373065-7373115	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7282916..7284476-chr4:7287220..7289745,2	K562	blood:
2	chr4:7277788..7279515-chr4:7289410..7291563,2	MCF-7	breast:
3	chr4:7282808..7284476-chr4:7287220..7289819,2	K562	blood:
4	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
5	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:
6	chr4:7335965..7337731-chr4:7346043..7348434,2	MCF-7	breast:
7	chr4:7343522..7345728-chr4:7361522..7364374,3	MCF-7	breast:
8	chr4:7193590..7194707-chr4:7297338..7298352,5	MCF-7	breast:
9	chr4:7193870..7194671-chr4:7337290..7338117,4	MCF-7	breast:
10	chr4:7355383..7357989-chr4:7359924..7361691,2	MCF-7	breast:
11	chr4:7196017..7196563-chr4:7337188..7337952,2	MCF-7	breast:
12	chr4:7375155..7379159-chr4:7380747..7383834,3	K562	blood:
13	chr4:7344494..7346063-chr4:7349701..7352195,2	MCF-7	breast:
14	chr4:7343522..7345728-chr4:7361522..7364374,3	MCF-7	breast:
15	chr4:7214030..7216634-chr4:7290499..7293149,2	MCF-7	breast:
16	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
17	chr4:7192934..7196110-chr4:7296657..7299976,3	MCF-7	breast:
18	chr4:7153324..7154166-chr4:7297397..7298037,2	MCF-7	breast:
19	chr4:7331028..7333099-chr4:7336513..7338486,2	K562	blood:
20	chr4:7344494..7346063-chr4:7349701..7352195,2	MCF-7	breast:
21	chr4:7281415..7283268-chr4:7284765..7287667,2	MCF-7	breast:
22	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
23	chr4:7288760..7290651-chr4:7292846..7295423,2	MCF-7	breast:
24	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
25	chr4:7193728..7194793-chr4:7297053..7298951,15	MCF-7	breast:
26	chr4:7190742..7191404-chr4:7337213..7337934,2	MCF-7	breast:
27	chr4:7193444..7195418-chr4:7373102..7374832,2	MCF-7	breast:
28	chr4:7355383..7357989-chr4:7359924..7361691,2	MCF-7	breast:
29	chr4:7195671..7196829-chr4:7297061..7298292,4	MCF-7	breast:
30	chr4:7195636..7196730-chr4:7297372..7298445,9	MCF-7	breast:
31	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
32	chr4:7221313..7223378-chr4:7286434..7289285,2	MCF-7	breast:
33	chr4:7194014..7196749-chr4:7291748..7294581,2	MCF-7	breast:
34	chr4:7200738..7202710-chr4:7296032..7298626,2	MCF-7	breast:
35	chr4:7196173..7199298-chr4:7297617..7300967,3	MCF-7	breast:
36	chr4:7335965..7337731-chr4:7346043..7348434,2	MCF-7	breast:
37	chr4:7288760..7290651-chr4:7292846..7295423,2	MCF-7	breast:
38	chr4:7320638..7322307-chr4:7344162..7346358,2	K562	blood:
39	chr4:7193774..7194640-chr4:7337221..7338106,5	K562	blood:
40	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
41	chr4:7331028..7333099-chr4:7336513..7338486,2	K562	blood:
42	chr4:7207636..7209824-chr4:7302272..7304285,2	MCF-7	breast:
43	chr4:7278740..7281042-chr4:7284986..7286499,2	K562	blood:
44	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
45	chr4:7193764..7194622-chr4:7297791..7298316,3	K562	blood:
46	chr4:7320638..7322307-chr4:7344162..7346358,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4798-5p	chr4:7312186-7312207	MIMAT0019974
hsa-miR-4798-3p	chr4:7312223-7312244	MIMAT0019975

Variant related genes	Relation type
MIR4798	TF binding region
MIR4798	CpG island
ENSG00000184985	chromatin interactions

Extended variants
information (count: 4904 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4904 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3846421	chr4:7285356-7285357	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192305445	chr4:7285383-7285384	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs79873075	chr4:7285391-7285392	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs10937798	chr4:7285445-7285446	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs183791326	chr4:7285562-7285563	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs3913447	chr4:7285629-7285630	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs372067712	chr4:7285634-7285635	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs571649179	chr4:7285644-7285645	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs188114065	chr4:7285646-7285647	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs144389247	chr4:7285649-7285650	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs147836783	chr4:7285673-7285674	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs111351106	chr4:7285707-7285708	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs191825735	chr4:7285713-7285714	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs142424760	chr4:7285750-7285751	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs184794272	chr4:7285755-7285756	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs10004527	chr4:7285769-7285770	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs189448571	chr4:7285800-7285801	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs577905164	chr4:7285809-7285810	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs545266354	chr4:7285820-7285821	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs553912979	chr4:7285827-7285828	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs114724533	chr4:7285828-7285829	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs368263536	chr4:7285830-7285831	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs3913448	chr4:7285848-7285849	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs561007416	chr4:7285849-7285850	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs144721533	chr4:7285889-7285890	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs543656639	chr4:7285902-7285903	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs147868728	chr4:7285917-7285918	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs374573127	chr4:7285951-7285952	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs532726152	chr4:7285958-7285959	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs548033435	chr4:7286006-7286007	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs182028146	chr4:7286015-7286016	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs527240722	chr4:7286031-7286032	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs549111293	chr4:7286042-7286043	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs567412096	chr4:7286047-7286048	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs3913449	chr4:7286055-7286056	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550030479	chr4:7286080-7286081	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs370134764	chr4:7286103-7286104	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs550955647	chr4:7286162-7286163	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs536027760	chr4:7286169-7286170	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs186572790	chr4:7286212-7286213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538572935	chr4:7286218-7286219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111461351	chr4:7286223-7286224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572358209	chr4:7286245-7286246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377300615	chr4:7286292-7286293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536287101	chr4:7286295-7286296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554539525	chr4:7286316-7286317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73083732	chr4:7286377-7286378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543493439	chr4:7286411-7286412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566266293	chr4:7286437-7286438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4689680	chr4:7286441-7286442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
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
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1388 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7278800-7292800	Weak transcription	Right Atrium	heart
2	chr4:7279200-7289400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr4:7281400-7293200	Weak transcription	Ovary	ovary
4	chr4:7282000-7289800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:7283400-7287200	Weak transcription	Brain Germinal Matrix	brain
6	chr4:7283400-7287200	Weak transcription	HSMMtube	muscle
7	chr4:7283400-7297000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:7283800-7286400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:7284000-7286600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr4:7284000-7287000	Weak transcription	Brain Angular Gyrus	brain
11	chr4:7284000-7287000	Weak transcription	Brain Anterior Caudate	brain
12	chr4:7284000-7287600	Weak transcription	Brain Hippocampus Middle	brain
13	chr4:7284400-7287000	Weak transcription	NH-A	brain
14	chr4:7284400-7289600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:7284600-7287000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr4:7284600-7287000	Weak transcription	Brain Substantia Nigra	brain
17	chr4:7284600-7287400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr4:7284800-7287200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr4:7285000-7285400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr4:7285000-7285600	Enhancers	Fetal Lung	lung
21	chr4:7285000-7287000	Weak transcription	Fetal Brain Male	brain
22	chr4:7285200-7286200	Bivalent Enhancer	Fetal Stomach	stomach
23	chr4:7285200-7287200	Weak transcription	Fetal Brain Female	brain
24	chr4:7285200-7287800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr4:7285400-7285600	Enhancers	Brain Cingulate Gyrus	brain
26	chr4:7285600-7287000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr4:7285600-7287400	Weak transcription	Fetal Lung	lung
28	chr4:7286000-7287400	Weak transcription	HSMM	muscle
29	chr4:7286400-7288800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr4:7286600-7287200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr4:7287000-7287400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr4:7287000-7287400	Enhancers	Colon Smooth Muscle	Colon
33	chr4:7287000-7288000	Enhancers	Brain Angular Gyrus	brain
34	chr4:7287000-7288600	Enhancers	Rectal Smooth Muscle	rectum
35	chr4:7287000-7289200	Enhancers	Brain Cingulate Gyrus	brain
36	chr4:7287000-7289200	Enhancers	Fetal Brain Male	brain
37	chr4:7287000-7289400	Enhancers	Brain Anterior Caudate	brain
38	chr4:7287000-7289600	Bivalent Enhancer	Fetal Stomach	stomach
39	chr4:7287000-7290000	Enhancers	Brain Substantia Nigra	brain
40	chr4:7287000-7290000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr4:7287000-7290200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr4:7287200-7287400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
43	chr4:7287200-7287400	Enhancers	Stomach Smooth Muscle	stomach
44	chr4:7287200-7287400	Enhancers	NH-A	brain
45	chr4:7287200-7287600	Enhancers	Fetal Brain Female	brain
46	chr4:7287200-7287600	Enhancers	HSMMtube	muscle
47	chr4:7287200-7288200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:7287200-7288200	Enhancers	Brain Germinal Matrix	brain
49	chr4:7287200-7288400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:7287200-7288400	Enhancers	Esophagus	oesophagus

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