Variant report

Variant	nsv4642
Chromosome Location	chr4:187085182-187136414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1433)
CpG islands
(count:1466)
Chromatin interactive
region (count:41)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187112517-187112766	K562	blood:	n/a	n/a
2	ARID3A	chr4:187123009-187123375	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:187124713-187124813	K562	blood:	n/a	n/a
4	ARID3A	chr4:187112910-187112928	HepG2	liver:	n/a	n/a
5	ATF1	chr4:187125220-187125793	K562	blood:	n/a	n/a
6	ATF2	chr4:187112363-187112834	GM12878	blood:	n/a	n/a
7	ATF2	chr4:187111626-187112084	GM12878	blood:	n/a	n/a
8	ATF2	chr4:187112340-187112962	GM12878	blood:	n/a	n/a
9	ATF3	chr4:187123084-187123309	K562	blood:	n/a	n/a
10	ATF3	chr4:187112294-187112519	K562	blood:	n/a	n/a
11	BACH1	chr4:187111645-187113416	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:187112705-187112885	K562	blood:	n/a	n/a
13	BCL11A	chr4:187112453-187112795	GM12878	blood:	n/a	chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
14	BCL3	chr4:187112454-187113086	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
15	BCL3	chr4:187123689-187124048	GM12878	blood:	n/a	n/a
16	BCL3	chr4:187112551-187113002	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
17	BCLAF1	chr4:187112309-187112982	K562	blood:	n/a	chr4:187112372-187112380 chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
18	BCLAF1	chr4:187112386-187113126	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
19	BCLAF1	chr4:187112371-187112924	K562	blood:	n/a	chr4:187112372-187112380 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
20	BCLAF1	chr4:187112247-187113106	GM12878	blood:	n/a	chr4:187112372-187112380 chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
21	BHLHE40	chr4:187090880-187090890	K562	blood:	n/a	n/a
22	BHLHE40	chr4:187112379-187112888	HepG2	liver:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112853-187112869
23	BHLHE40	chr4:187123027-187123351	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:187112212-187112996	GM12878	blood:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112957-187112973 chr4:187112853-187112869 chr4:187112956-187112972
25	BHLHE40	chr4:187123023-187123354	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:187112517-187112894	HepG2	liver:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112853-187112869
27	BHLHE40	chr4:187125626-187125724	K562	blood:	n/a	n/a
28	BHLHE40	chr4:187123095-187123359	K562	blood:	n/a	n/a
29	BHLHE40	chr4:187124362-187124827	K562	blood:	n/a	n/a
30	BHLHE40	chr4:187111886-187113562	K562	blood:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112957-187112973 chr4:187112853-187112869 chr4:187112956-187112972
31	BHLHE40	chr4:187113492-187113615	HepG2	liver:	n/a	n/a
32	BRCA1	chr4:187112323-187112508	HepG2	liver:	n/a	n/a
33	BRCA1	chr4:187112533-187112912	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr4:187125169-187125671	K562	blood:	n/a	n/a
35	CBX3	chr4:187112100-187113171	K562	blood:	n/a	n/a
36	CBX3	chr4:187124447-187124877	K562	blood:	n/a	n/a
37	CCNT2	chr4:187111976-187113411	K562	blood:	n/a	chr4:187111995-187112004
38	CCNT2	chr4:187124521-187124882	K562	blood:	n/a	n/a
39	CEBPB	chr4:187112308-187112819	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:187112501-187112887	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:187113324-187113839	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:187135180-187135291	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:187112281-187112777	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:187122990-187123265	Hela-S3	cervix:	n/a	chr4:187123065-187123076
45	CEBPB	chr4:187112294-187113353	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:187112139-187112943	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:187120243-187120434	K562	blood:	n/a	chr4:187120342-187120353
48	CEBPB	chr4:187112353-187112824	K562	blood:	n/a	n/a
49	CEBPB	chr4:187112591-187112784	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:187123006-187123320	MCF-7	breast:	n/a	chr4:187123065-187123076

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187113285-187113335	Jurkat	blood:	n/a
2	chr4:187112519-187112569	NHBE	bronchial:	n/a
3	chr4:187113285-187113335	Jurkat	blood:	n/a
4	chr4:187112519-187112569	NHBE	bronchial:	n/a
5	chr4:187112650-187112700	K562	blood:	n/a
6	chr4:187126139-187126189	NH-A	brain:	n/a
7	chr4:187111853-187111903	NT2-D1	testis:	n/a
8	chr4:187115308-187115358	ProgFib	skin:	n/a
9	chr4:187126073-187126123	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:187126114-187126164	ECC-1	luminal epithelium:	n/a
11	chr4:187112145-187112195	HEK293	kidney:	embryo
12	chr4:187113285-187113335	GM12892	blood:	n/a
13	chr4:187112537-187112587	HCPEpiC	choroid plexus:	n/a
14	chr4:187113578-187113628	HMEC	breast:	n/a
15	chr4:187112523-187112573	MCF10A-Er-Src	breast:	n/a
16	chr4:187112519-187112569	MCF-7	breast:	n/a
17	chr4:187113578-187113628	LNCaP	prostate:	n/a
18	chr4:187112145-187112195	MCF-7	breast:	n/a
19	chr4:187113285-187113335	HCM	heart:	n/a
20	chr4:187112763-187112813	GM12892	blood:	n/a
21	chr4:187113578-187113628	HCT-116	colon:	n/a
22	chr4:187090536-187090586	HepG2	liver:	n/a
23	chr4:187133287-187133337	Hela-S3	cervix:	n/a
24	chr4:187126139-187126189	IMR90	lung:	fetal
25	chr4:187112523-187112573	IMR90	lung:	fetal
26	chr4:187125413-187125463	MCF10A-Er-Src	breast:	n/a
27	chr4:187126114-187126164	LNCaP	prostate:	n/a
28	chr4:187112664-187112714	NHBE	bronchial:	n/a
29	chr4:187111853-187111903	HEK293	kidney:	embryo
30	chr4:187111841-187111891	PANC-1	pancreas:	n/a
31	chr4:187111841-187111891	AG09309	skin:	n/a
32	chr4:187112145-187112195	AoSMC	blood vessel:	n/a
33	chr4:187088169-187088219	MCF-7	breast:	n/a
34	chr4:187113285-187113335	MCF-7	breast:	n/a
35	chr4:187111841-187111891	GM12892	blood:	n/a
36	chr4:187125413-187125463	MCF-7	breast:	n/a
37	chr4:187088169-187088219	GM12878	blood:	n/a
38	chr4:187090481-187090531	Jurkat	blood:	n/a
39	chr4:187126114-187126164	AG04450	lung:	fetal
40	chr4:187133287-187133337	AG09319	gingival:	n/a
41	chr4:187112537-187112587	HRCEpiC	kidney:	n/a
42	chr4:187112664-187112714	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:187126139-187126189	Hela-S3	cervix:	n/a
44	chr4:187112523-187112573	SKMC	muscle:	n/a
45	chr4:187088191-187088241	HepG2	liver:	n/a
46	chr4:187112145-187112195	H1-hESC	embryonic stem cell:	embryo
47	chr4:187126114-187126164	U87	brain:	n/a
48	chr4:187115308-187115358	HEEpiC	esophagus:	n/a
49	chr4:187126114-187126164	SK-N-SH	brain:	n/a
50	chr4:187112537-187112587	U87	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187098304..187101860-chr4:187110284..187112773,3	K562	blood:
2	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
3	chr4:186009075..186012021-chr4:187112974..187115666,2	K562	blood:
4	chr4:187111478..187116148-chr4:187117012..187120938,6	MCF-7	breast:
5	chr4:187111874..187113781-chr4:187171263..187172793,2	MCF-7	breast:
6	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
7	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
8	chr4:187122087..187123852-chr4:187421026..187423788,3	K562	blood:
9	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
10	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
11	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
12	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
13	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
14	chr4:187122668..187125601-chr4:187127008..187128619,2	K562	blood:
15	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
16	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
17	chr4:187106383..187110529-chr4:187110531..187113610,6	K562	blood:
18	chr4:187111353..187115983-chr4:187119045..187124895,10	MCF-7	breast:
19	chr4:187131236..187132870-chr4:187133223..187136052,3	MCF-7	breast:
20	chr4:187091730..187094624-chr4:187097179..187100415,3	MCF-7	breast:
21	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
22	chr4:187131236..187132870-chr4:187133223..187136052,3	MCF-7	breast:
23	chr4:187106828..187109765-chr4:187110186..187112854,4	K562	blood:
24	chr4:187116069..187118838-chr4:187120195..187124189,4	MCF-7	breast:
25	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
26	chr15:69111702..69112637-chr4:187112678..187113182,2	Hela-S3	cervix:
27	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
28	chr4:187110911..187113910-chr4:187131548..187135864,4	K562	blood:
29	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
30	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
31	chr12:52452615..52453609-chr4:187112686..187113538,2	Hela-S3	cervix:
32	chr22:41487362..41488310-chr4:187112180..187112692,2	Hela-S3	cervix:
33	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
34	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
35	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
36	chr2:10182889..10183701-chr4:187112369..187113247,2	Hela-S3	cervix:
37	chr4:187112410..187114289-chr4:187132953..187135385,2	K562	blood:
38	chr4:187116673..187118663-chr4:187119222..187120976,2	MCF-7	breast:
39	chr4:187112006..187113547-chr4:187122764..187123712,6	MCF-7	breast:
40	chr4:187111478..187116148-chr4:187117012..187120938,6	MCF-7	breast:
41	chr4:187128886..187131532-chr4:187133645..187136600,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLKB1-1	chr4:187125389-187125458	NONHSAT099648
2	lnc-KLKB1-1	chr4:187125555-187125762	NONHSAT099648
3	lnc-KLKB1-1	chr4:187125266-187125400	NONHSAT099647
4	lnc-SORBS2-4	chr4:187110186-187112644	NONHSAT099644
5	lnc-KLKB1-1	chr4:187125257-187125426	NONHSAT099646
6	lnc-KLKB1-1	chr4:187125593-187125738	NONHSAT099647
7	lnc-KLKB1-1	chr4:187125555-187125774	NONHSAT099646

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CYP4V2	hsa-miR-192-5p	chr4:187130411-187130426
2	CYP4V2	hsa-miR-192-5p	chr4:187131623-187131627

Variant related genes	Relation type
FAM149A	TF binding region
CYP4V2	TF binding region
ENSG00000269302	TF binding region
KLKB1	TF binding region
ORAOV1P1	TF binding region
FAM149A	CpG island
CYP4V2	CpG island
ENSG00000269302	CpG island
KLKB1	CpG island
ORAOV1P1	CpG island
ENSG00000100393	chromatin interactions
ENSG00000164344	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000259884	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000251008	chromatin interactions
ENSG00000145476	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000212387	chromatin interactions
DOK3	miRNA target sites
EIF3J	miRNA target sites

Extended variants
information (count: 2201 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529289659	chr4:187085206-187085207	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539152684	chr4:187085214-187085215	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574491339	chr4:187085232-187085233	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540191382	chr4:187085234-187085235	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373370804	chr4:187085244-187085245	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs62350492	chr4:187085250-187085251	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577492932	chr4:187085259-187085260	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546162854	chr4:187085260-187085261	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7688336	chr4:187085429-187085430	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs531745074	chr4:187085461-187085462	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369488801	chr4:187085493-187085494	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373984717	chr4:187085494-187085495	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561813089	chr4:187085512-187085513	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116498352	chr4:187085536-187085537	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547801502	chr4:187085538-187085539	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570743585	chr4:187085559-187085560	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377701287	chr4:187085569-187085570	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375498325	chr4:187085584-187085585	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538966809	chr4:187085593-187085594	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs28611387	chr4:187085604-187085605	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533499783	chr4:187085605-187085606	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138037768	chr4:187085609-187085610	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554718837	chr4:187085632-187085633	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568133928	chr4:187085665-187085666	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533629588	chr4:187085666-187085667	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs553763922	chr4:187085704-187085705	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs114103514	chr4:187085712-187085713	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182214786	chr4:187085773-187085774	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs186860298	chr4:187085775-187085776	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551982511	chr4:187085776-187085777	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369786688	chr4:187085779-187085780	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372638852	chr4:187085783-187085784	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541991943	chr4:187085785-187085786	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534108713	chr4:187085788-187085789	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78973737	chr4:187085804-187085805	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527823060	chr4:187085805-187085806	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7669101	chr4:187085888-187085889	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs191853991	chr4:187085892-187085893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564550114	chr4:187085940-187085941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2241818	chr4:187085945-187085946	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs372755063	chr4:187085982-187085983	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377367117	chr4:187085994-187085995	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370721846	chr4:187086026-187086027	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7669366	chr4:187086053-187086054	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531558456	chr4:187086073-187086074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548432198	chr4:187086104-187086105	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568245104	chr4:187086133-187086134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79791579	chr4:187086144-187086145	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73027974	chr4:187086150-187086151	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs570437949	chr4:187086188-187086189	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187067200-187091800	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:187067400-187088000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:187067600-187085800	Weak transcription	Colonic Mucosa	Colon
4	chr4:187070600-187091200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr4:187071400-187088800	Weak transcription	Right Atrium	heart
6	chr4:187071400-187090000	Weak transcription	Stomach Mucosa	stomach
7	chr4:187071600-187089400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr4:187071600-187089600	Weak transcription	Placenta	Placenta
9	chr4:187071600-187091200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:187073600-187087200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr4:187074600-187088400	Strong transcription	Fetal Intestine Small	intestine
12	chr4:187074800-187085200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr4:187078800-187086600	Strong transcription	Fetal Brain Female	brain
14	chr4:187080000-187087600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:187080000-187087600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr4:187080000-187088000	Weak transcription	Aorta	Aorta
17	chr4:187080000-187089000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:187080000-187090000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr4:187080000-187091400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:187080000-187091600	Strong transcription	Fetal Stomach	stomach
21	chr4:187080000-187092200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr4:187080000-187092200	Weak transcription	Spleen	Spleen
23	chr4:187080000-187094000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr4:187080200-187094000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr4:187080600-187090400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr4:187081000-187099200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:187081400-187087600	Weak transcription	Esophagus	oesophagus
28	chr4:187081600-187087400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:187081600-187089800	Weak transcription	Brain Hippocampus Middle	brain
30	chr4:187082000-187087400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:187082000-187089200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:187082000-187090000	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:187082000-187090800	Weak transcription	Fetal Kidney	kidney
34	chr4:187082000-187091400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr4:187082000-187095000	Weak transcription	Fetal Brain Male	brain
36	chr4:187082200-187085600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:187082200-187092000	Weak transcription	Fetal Lung	lung
38	chr4:187083400-187086600	Strong transcription	Pancreas	Pancrea
39	chr4:187083400-187087400	Strong transcription	Adipose Nuclei	Adipose
40	chr4:187083600-187086000	Strong transcription	Fetal Intestine Large	intestine
41	chr4:187083600-187087000	Strong transcription	Ovary	ovary
42	chr4:187083600-187090400	Strong transcription	Stomach Smooth Muscle	stomach
43	chr4:187083800-187090000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:187084200-187085600	Strong transcription	Liver	Liver
45	chr4:187084400-187085400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:187084600-187085600	Weak transcription	Brain Anterior Caudate	brain
47	chr4:187084600-187086400	Weak transcription	Gastric	stomach
48	chr4:187084800-187085200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:187084800-187085600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr4:187084800-187087200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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