Variant report

Variant	nsv878547
Chromosome Location	chr4:7289113-7376694
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	chr4:7309477-7309799	GM12878	blood:	n/a	n/a
6	BCL3	chr4:7309436-7309751	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:7371415-7371470	K562	blood:	n/a	n/a
8	BHLHE40	chr4:7289378-7289811	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:7297759-7297998	K562	blood:	n/a	chr4:7297811-7297827
10	BHLHE40	chr4:7342329-7342469	K562	blood:	n/a	chr4:7342363-7342376
11	BHLHE40	chr4:7337542-7337783	K562	blood:	n/a	n/a
12	BHLHE40	chr4:7326359-7326668	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:7332888-7333034	K562	blood:	n/a	chr4:7332974-7332983 chr4:7332968-7332989 chr4:7332975-7332984 chr4:7332974-7332983 chr4:7332972-7332985
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	chr4:7337624-7337876	H1-hESC	embryonic stem cell:	n/a	n/a
17	BRCA1	chr4:7360137-7360214	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr4:7297835-7297868	GM12878	blood:	n/a	n/a
19	CEBPB	chr4:7314946-7315363	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
20	CEBPB	chr4:7314937-7315345	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
21	CEBPB	chr4:7324654-7324913	IMR90	lung:	n/a	chr4:7324854-7324865
22	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
23	CEBPB	chr4:7314975-7315352	K562	blood:	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	chr4:7360151-7360464	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:7350739-7350998	Hela-S3	cervix:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
27	CEBPB	chr4:7350726-7351008	H1-hESC	embryonic stem cell:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
28	CEBPB	chr4:7350688-7351037	K562	blood:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
29	CEBPB	chr4:7350683-7351098	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
30	CEBPB	chr4:7350677-7351048	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
31	CEBPB	chr4:7314977-7315349	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
32	CEBPB	chr4:7360125-7360418	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:7314974-7315334	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
34	CEBPB	chr4:7350554-7351087	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
35	CEBPB	chr4:7314983-7315346	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
36	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
37	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
38	CEBPB	chr4:7324731-7324857	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:7350682-7351059	HepG2	liver:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
40	CEBPB	chr4:7314975-7315351	IMR90	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
41	CEBPB	chr4:7350681-7351058	IMR90	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
42	CEBPB	chr4:7315082-7315202	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
43	CEBPB	chr4:7315017-7315331	Hela-S3	cervix:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
44	CEBPB	chr4:7314905-7315396	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
45	CEBPB	chr4:7350773-7351029	MCF-7	breast:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
46	CEBPB	chr4:7349851-7350214	A549	lung:	n/a	n/a
47	CHD2	chr4:7337159-7337242	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:7297780-7297930	GM12871	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
49	CTCF	chr4:7297740-7297890	GM12878	blood:	n/a	chr4:7297850-7297868 chr4:7297851-7297867 chr4:7297857-7297865 chr4:7297845-7297866
50	CTCF	chr4:7337620-7337770	HPAF	blood vessel:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7330616-7330666	CMK	blood:	n/a
2	chr4:7373022-7373072	HEK293	kidney:	embryo
3	chr4:7304739-7304789	HUVEC	blood vessel:	n/a
4	chr4:7330616-7330666	CMK	blood:	n/a
5	chr4:7373022-7373072	HEK293	kidney:	embryo
6	chr4:7304739-7304789	HUVEC	blood vessel:	n/a
7	chr4:7373065-7373115	HepG2	liver:	n/a
8	chr4:7326576-7326626	NT2-D1	testis:	n/a
9	chr4:7304777-7304827	LNCaP	prostate:	n/a
10	chr4:7373022-7373072	HUVEC	blood vessel:	n/a
11	chr4:7301529-7301579	IMR90	lung:	fetal
12	chr4:7289507-7289557	HRE	kidney:	n/a
13	chr4:7304777-7304827	H1-hESC	embryonic stem cell:	embryo
14	chr4:7373022-7373072	T-47D	breast:	n/a
15	chr4:7289723-7289773	PFSK-1	brain:	n/a
16	chr4:7333381-7333431	NHDF-neo	bronchial:	n/a
17	chr4:7338730-7338780	HCT-116	colon:	n/a
18	chr4:7289858-7289908	PANC-1	pancreas:	n/a
19	chr4:7304739-7304789	NB4	blood:	n/a
20	chr4:7337225-7337275	HRPEpiC	eye:	n/a
21	chr4:7301491-7301541	SK-N-SH	brain:	n/a
22	chr4:7304777-7304827	U87	brain:	n/a
23	chr4:7337225-7337275	HCPEpiC	choroid plexus:	n/a
24	chr4:7301176-7301226	T-47D	breast:	n/a
25	chr4:7333381-7333431	Hepatocyte	liver:	n/a
26	chr4:7301491-7301541	NT2-D1	testis:	n/a
27	chr4:7373343-7373393	RPTEC	kidney:	n/a
28	chr4:7373088-7373138	HL-60	blood:	n/a
29	chr4:7289723-7289773	HL-60	blood:	n/a
30	chr4:7289763-7289813	Caco-2	colon:	n/a
31	chr4:7374622-7374672	SKMC	muscle:	n/a
32	chr4:7289507-7289557	HRPEpiC	eye:	n/a
33	chr4:7333381-7333431	HMEC	breast:	n/a
34	chr4:7338730-7338780	NT2-D1	testis:	n/a
35	chr4:7373375-7373425	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:7373375-7373425	AG09319	gingival:	n/a
37	chr4:7289482-7289532	PrEC	prostate:	n/a
38	chr4:7301529-7301579	HCPEpiC	choroid plexus:	n/a
39	chr4:7338730-7338780	SKMC	muscle:	n/a
40	chr4:7368808-7368858	HEK293	kidney:	embryo
41	chr4:7373375-7373425	Hela-S3	cervix:	n/a
42	chr4:7300999-7301049	AG04449	skin:	fetal
43	chr4:7337225-7337275	PrEC	prostate:	n/a
44	chr4:7338792-7338842	ovcar-3	ovarian:	n/a
45	chr4:7374622-7374672	AG09309	skin:	n/a
46	chr4:7373451-7373501	NHDF-neo	bronchial:	n/a
47	chr4:7368808-7368858	HCT-116	colon:	n/a
48	chr4:7368808-7368858	CMK	blood:	n/a
49	chr4:7338792-7338842	HIPEpiC	eye:	n/a
50	chr4:7301854-7301904	PFSK-1	brain:	n/a

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

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

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

Extended variants
information (count: 4710 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4710 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4689682	chr4:7289113-7289114	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568887845	chr4:7289145-7289146	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs539504041	chr4:7289157-7289158	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs4689683	chr4:7289165-7289166	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs183182423	chr4:7289166-7289167	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs573045648	chr4:7289178-7289179	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs540533869	chr4:7289179-7289180	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs113527932	chr4:7289190-7289191	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs538089678	chr4:7289217-7289218	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs573970931	chr4:7289254-7289255	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs544324744	chr4:7289315-7289316	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs191357360	chr4:7289316-7289317	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs151269528	chr4:7289335-7289336	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs545451299	chr4:7289339-7289340	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs77505820	chr4:7289366-7289367	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs372113836	chr4:7289384-7289385	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs184160663	chr4:7289396-7289397	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs527833900	chr4:7289399-7289400	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs549277298	chr4:7289419-7289420	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs567659685	chr4:7289484-7289485	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs189874537	chr4:7289507-7289508	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs192543263	chr4:7289537-7289538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs568801539	chr4:7289618-7289619	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs140511503	chr4:7289646-7289647	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs73083741	chr4:7289656-7289657	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs377170210	chr4:7289657-7289658	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs185482463	chr4:7289674-7289675	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs571602086	chr4:7289703-7289704	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs376509716	chr4:7289724-7289725	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs149982472	chr4:7289744-7289745	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs73796603	chr4:7289745-7289746	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145216621	chr4:7289751-7289752	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs113748352	chr4:7289763-7289764	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs544482669	chr4:7289776-7289777	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs556300904	chr4:7289789-7289790	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs577944351	chr4:7289810-7289811	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs573283711	chr4:7289816-7289817	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs189045139	chr4:7289822-7289823	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs182041229	chr4:7289831-7289832	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs73796604	chr4:7289867-7289868	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542860427	chr4:7289927-7289928	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs141384109	chr4:7289948-7289949	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs36048565	chr4:7290005-7290006	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs550420837	chr4:7290007-7290008	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs186369019	chr4:7290019-7290020	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs189357816	chr4:7290030-7290031	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs551079536	chr4:7290031-7290032	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs566615153	chr4:7290046-7290047	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs6846468	chr4:7290049-7290050	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs73208407	chr4:7290050-7290051	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	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:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

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	chr4:7283400-7297000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:7284400-7289600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:7287000-7289200	Enhancers	Brain Cingulate Gyrus	brain
8	chr4:7287000-7289200	Enhancers	Fetal Brain Male	brain
9	chr4:7287000-7289400	Enhancers	Brain Anterior Caudate	brain
10	chr4:7287000-7289600	Bivalent Enhancer	Fetal Stomach	stomach
11	chr4:7287000-7290000	Enhancers	Brain Substantia Nigra	brain
12	chr4:7287000-7290000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr4:7287000-7290200	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr4:7287200-7290000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:7287200-7294400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:7287400-7289200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr4:7287600-7290000	Enhancers	Brain Hippocampus Middle	brain
18	chr4:7287600-7293400	Weak transcription	Fetal Brain Female	brain
19	chr4:7287800-7289200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr4:7287800-7290000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:7288000-7289600	Enhancers	Colon Smooth Muscle	Colon
22	chr4:7288000-7293400	Weak transcription	Brain Angular Gyrus	brain
23	chr4:7288200-7289400	Weak transcription	Brain Germinal Matrix	brain
24	chr4:7288200-7293200	Weak transcription	Fetal Lung	lung
25	chr4:7288800-7294000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:7289000-7289200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:7289000-7290200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr4:7289200-7290800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:7289200-7291200	Weak transcription	Brain Cingulate Gyrus	brain
30	chr4:7289200-7293000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr4:7289200-7296800	Weak transcription	Fetal Brain Male	brain
32	chr4:7289400-7289800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr4:7289400-7290000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:7289400-7290200	Enhancers	Brain Germinal Matrix	brain
35	chr4:7289400-7291000	Weak transcription	Brain Anterior Caudate	brain
36	chr4:7289600-7289800	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:7289600-7290000	Enhancers	Fetal Stomach	stomach
38	chr4:7289600-7290200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:7289600-7290400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:7289600-7290800	Weak transcription	Colon Smooth Muscle	Colon
41	chr4:7289800-7290000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr4:7289800-7291200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:7290000-7290200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:7290000-7291000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr4:7290000-7291000	Weak transcription	Brain Hippocampus Middle	brain
46	chr4:7290000-7291400	Weak transcription	Fetal Stomach	stomach
47	chr4:7290000-7293000	Weak transcription	Brain Substantia Nigra	brain
48	chr4:7290200-7290600	Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr4:7290200-7291400	Weak transcription	Brain Germinal Matrix	brain
50	chr4:7290400-7296400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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