Variant report

Variant	nsv508340
Chromosome Location	chr4:187059173-187136958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1864)
CpG islands
(count:2688)
Chromatin interactive
region (count:51)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1864 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187112910-187112928	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187124713-187124813	K562	blood:	n/a	n/a
3	ARID3A	chr4:187123009-187123375	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:187112517-187112766	K562	blood:	n/a	n/a
5	ATF1	chr4:187125220-187125793	K562	blood:	n/a	n/a
6	ATF2	chr4:187112340-187112962	GM12878	blood:	n/a	n/a
7	ATF2	chr4:187112363-187112834	GM12878	blood:	n/a	n/a
8	ATF2	chr4:187071057-187071421	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:187111626-187112084	GM12878	blood:	n/a	n/a
10	ATF3	chr4:187112294-187112519	K562	blood:	n/a	n/a
11	ATF3	chr4:187123084-187123309	K562	blood:	n/a	n/a
12	BACH1	chr4:187082521-187082663	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:187066156-187066584	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:187111645-187113416	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:187112705-187112885	K562	blood:	n/a	n/a
16	BCL11A	chr4:187112453-187112795	GM12878	blood:	n/a	chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
17	BCL3	chr4:187059720-187060074	GM12878	blood:	n/a	n/a
18	BCL3	chr4:187112551-187113002	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
19	BCL3	chr4:187123689-187124048	GM12878	blood:	n/a	n/a
20	BCL3	chr4:187112454-187113086	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
21	BCLAF1	chr4:187112371-187112924	K562	blood:	n/a	chr4:187112372-187112380 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
22	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
23	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
24	BCLAF1	chr4:187112386-187113126	GM12878	blood:	n/a	chr4:187112925-187112938 chr4:187112961-187112974 chr4:187112583-187112596 chr4:187112636-187112645 chr4:187112569-187112582
25	BHLHE40	chr4:187123023-187123354	GM12878	blood:	n/a	n/a
26	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
27	BHLHE40	chr4:187125626-187125724	K562	blood:	n/a	n/a
28	BHLHE40	chr4:187059455-187059456	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:187123027-187123351	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:187112517-187112894	HepG2	liver:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112853-187112869
31	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
32	BHLHE40	chr4:187090880-187090890	K562	blood:	n/a	n/a
33	BHLHE40	chr4:187113492-187113615	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:187123095-187123359	K562	blood:	n/a	n/a
35	BHLHE40	chr4:187124362-187124827	K562	blood:	n/a	n/a
36	BHLHE40	chr4:187112379-187112888	HepG2	liver:	n/a	chr4:187112845-187112861 chr4:187112767-187112783 chr4:187112578-187112594 chr4:187112853-187112869
37	BRCA1	chr4:187082411-187082510	GM12878	blood:	n/a	n/a
38	BRCA1	chr4:187112533-187112912	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr4:187112323-187112508	HepG2	liver:	n/a	n/a
40	CBX3	chr4:187124447-187124877	K562	blood:	n/a	n/a
41	CBX3	chr4:187125169-187125671	K562	blood:	n/a	n/a
42	CBX3	chr4:187112100-187113171	K562	blood:	n/a	n/a
43	CCNT2	chr4:187124521-187124882	K562	blood:	n/a	n/a
44	CCNT2	chr4:187111976-187113411	K562	blood:	n/a	chr4:187111995-187112004
45	CEBPB	chr4:187113239-187113835	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:187136509-187136687	K562	blood:	n/a	chr4:187136650-187136663
47	CEBPB	chr4:187123006-187123320	MCF-7	breast:	n/a	chr4:187123065-187123076
48	CEBPB	chr4:187125299-187125736	K562	blood:	n/a	n/a
49	CEBPB	chr4:187135180-187135291	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:187120221-187120489	IMR90	lung:	n/a	chr4:187120342-187120353

(count:2688 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187074031-187074081	SKMC	muscle:	n/a
2	chr4:187112763-187112813	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:187069057-187069107	ProgFib	skin:	n/a
4	chr4:187071162-187071212	GM19239	blood:	n/a
5	chr4:187074031-187074081	SKMC	muscle:	n/a
6	chr4:187112763-187112813	HPAEpiC	pulmonary alveolar:	n/a
7	chr4:187069057-187069107	ProgFib	skin:	n/a
8	chr4:187071162-187071212	GM19239	blood:	n/a
9	chr4:187070357-187070407	BJ	skin:	n/a
10	chr4:187066505-187066555	HepG2	liver:	n/a
11	chr4:187069057-187069107	CMK	blood:	n/a
12	chr4:187112519-187112569	ProgFib	skin:	n/a
13	chr4:187065950-187066000	AG10803	skin:	n/a
14	chr4:187066279-187066329	ovcar-3	ovarian:	n/a
15	chr4:187112041-187112091	U87	brain:	n/a
16	chr4:187065846-187065896	HRE	kidney:	n/a
17	chr4:187113285-187113335	HIPEpiC	eye:	n/a
18	chr4:187112664-187112714	AG04449	skin:	fetal
19	chr4:187070357-187070407	GM12891	blood:	n/a
20	chr4:187126114-187126164	HRE	kidney:	n/a
21	chr4:187078771-187078821	HUVEC	blood vessel:	n/a
22	chr4:187112664-187112714	Caco-2	colon:	n/a
23	chr4:187112664-187112714	RPTEC	kidney:	n/a
24	chr4:187112523-187112573	NH-A	brain:	n/a
25	chr4:187115308-187115358	HUVEC	blood vessel:	n/a
26	chr4:187109237-187109287	GM06990	blood:	n/a
27	chr4:187065940-187065990	HRE	kidney:	n/a
28	chr4:187065944-187065994	HCM	heart:	n/a
29	chr4:187112041-187112091	NH-A	brain:	n/a
30	chr4:187112664-187112714	GM19239	blood:	n/a
31	chr4:187113285-187113335	AoSMC	blood vessel:	n/a
32	chr4:187063756-187063806	RPTEC	kidney:	n/a
33	chr4:187126073-187126123	HRE	kidney:	n/a
34	chr4:187071162-187071212	GM06990	blood:	n/a
35	chr4:187090536-187090586	HNPCEpiC	eye:	n/a
36	chr4:187133287-187133337	GM19239	blood:	n/a
37	chr4:187090536-187090586	PFSK-1	brain:	n/a
38	chr4:187112664-187112714	HRCEpiC	kidney:	n/a
39	chr4:187090536-187090586	AG09319	gingival:	n/a
40	chr4:187112519-187112569	A549	lung:	n/a
41	chr4:187071162-187071212	GM12892	blood:	n/a
42	chr4:187078828-187078878	AG04450	lung:	fetal
43	chr4:187112519-187112569	HAEpiC	amniotic membrane:	n/a
44	chr4:187070303-187070353	AoSMC	blood vessel:	n/a
45	chr4:187063756-187063806	HCPEpiC	choroid plexus:	n/a
46	chr4:187066279-187066329	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:187078828-187078878	Hepatocyte	liver:	n/a
48	chr4:187133287-187133337	RPTEC	kidney:	n/a
49	chr4:187063756-187063806	AG09319	gingival:	n/a
50	chr4:187065950-187066000	RPTEC	kidney:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:187112410..187114289-chr4:187132953..187135385,2	K562	blood:
2	chr4:187053833..187057505-chr4:187060435..187064133,3	K562	blood:
3	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
4	chr4:187110911..187113910-chr4:187131548..187135864,4	K562	blood:
5	chr22:41487362..41488310-chr4:187112180..187112692,2	Hela-S3	cervix:
6	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
7	chr4:187122087..187123852-chr4:187421026..187423788,3	K562	blood:
8	chr4:187116673..187118663-chr4:187119222..187120976,2	MCF-7	breast:
9	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
10	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:
11	chr4:187131236..187132870-chr4:187133223..187136052,3	MCF-7	breast:
12	chr4:187131236..187132870-chr4:187133223..187136052,3	MCF-7	breast:
13	chr4:187065362..187066941-chr4:187069127..187071220,2	K562	blood:
14	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
15	chr4:187112006..187113547-chr4:187122764..187123712,6	MCF-7	breast:
16	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
17	chr4:187118539..187120138-chr4:187121607..187123644,3	MCF-7	breast:
18	chr4:186988859..186989716-chr4:187058329..187059203,5	MCF-7	breast:
19	chr2:10182889..10183701-chr4:187112369..187113247,2	Hela-S3	cervix:
20	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
21	chr4:187106383..187110529-chr4:187110531..187113610,6	K562	blood:
22	chr4:187111478..187116148-chr4:187117012..187120938,6	MCF-7	breast:
23	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
24	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
25	chr4:187116069..187118838-chr4:187120195..187124189,4	MCF-7	breast:
26	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
27	chr4:187083351..187085783-chr4:187086821..187088983,2	K562	blood:
28	chr4:187109253..187118277-chr4:187122555..187126883,14	K562	blood:
29	chr4:187062784..187065890-chr4:187111242..187113420,3	MCF-7	breast:
30	chr4:186009075..186012021-chr4:187112974..187115666,2	K562	blood:
31	chr4:187111353..187115983-chr4:187119045..187124895,10	MCF-7	breast:
32	chr4:187117801..187120230-chr4:187120810..187122503,2	K562	blood:
33	chr4:187111478..187116148-chr4:187117012..187120938,6	MCF-7	breast:
34	chr4:187121686..187123375-chr4:187456206..187458817,2	K562	blood:
35	chr4:187091730..187094624-chr4:187097179..187100415,3	MCF-7	breast:
36	chr4:187080678..187082912-chr4:187084577..187086317,2	K562	blood:
37	chr4:186988972..186989928-chr4:187122701..187123491,2	MCF-7	breast:
38	chr4:187092687..187094578-chr4:187097251..187099352,2	MCF-7	breast:
39	chr12:52452615..52453609-chr4:187112686..187113538,2	Hela-S3	cervix:
40	chr4:187128886..187131532-chr4:187133645..187136600,2	K562	blood:
41	chr4:187098304..187101860-chr4:187110284..187112773,3	K562	blood:
42	chr4:187111874..187113781-chr4:187171263..187172793,2	MCF-7	breast:
43	chr4:187092198..187094078-chr4:187111646..187113279,2	MCF-7	breast:
44	chr4:187061612..187063617-chr4:187065011..187066705,2	K562	blood:
45	chr4:187122668..187125601-chr4:187127008..187128619,2	K562	blood:
46	chr4:187106828..187109765-chr4:187110186..187112854,4	K562	blood:
47	chr4:187125089..187127684-chr4:187129515..187131962,3	K562	blood:
48	chr4:187053677..187057505-chr4:187060435..187064236,4	K562	blood:
49	chr4:187058298..187058901-chr4:187122712..187123588,2	MCF-7	breast:
50	chr4:187077276..187078819-chr4:187080715..187083352,2	K562	blood:

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

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

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	chr4:187131623-187131627
2	CYP4V2	hsa-miR-192-5p	chr4:187130411-187130426

Variant related genes	Relation type
FAM149A	TF binding region
CYP4V2	TF binding region
ENSG00000250327	TF binding region
ENSG00000269302	TF binding region
KLKB1	TF binding region
ORAOV1P1	TF binding region
FAM149A	CpG island
CYP4V2	CpG island
ENSG00000250327	CpG island
ENSG00000269302	CpG island
KLKB1	CpG island
ORAOV1P1	CpG island
ENSG00000172059	chromatin interactions
ENSG00000145476	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000100393	chromatin interactions
ENSG00000269302	chromatin interactions
ENSG00000109794	chromatin interactions
ENSG00000164344	chromatin interactions
ENSG00000259884	chromatin interactions
ENSG00000251008	chromatin interactions
DOK3	miRNA target sites
EIF3J	miRNA target sites

Extended variants
information (count: 3508 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3508 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527322964	chr4:187059206-187059207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375576991	chr4:187059229-187059230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140357679	chr4:187059250-187059251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11942766	chr4:187059254-187059255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540100891	chr4:187059256-187059257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369594122	chr4:187059292-187059293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145425836	chr4:187059301-187059302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570468230	chr4:187059318-187059319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75016465	chr4:187059372-187059373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71593676	chr4:187059398-187059399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377722634	chr4:187059399-187059400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555489488	chr4:187059400-187059401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549996098	chr4:187059401-187059402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35301733	chr4:187059415-187059416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60403100	chr4:187059416-187059417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75940420	chr4:187059417-187059418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541028564	chr4:187059442-187059443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557700468	chr4:187059461-187059462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371225281	chr4:187059462-187059463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577078418	chr4:187059523-187059524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534697075	chr4:187059543-187059544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13105400	chr4:187059563-187059564	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs562615746	chr4:187059624-187059625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185911370	chr4:187059641-187059642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140890913	chr4:187059675-187059676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574578693	chr4:187059677-187059678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115881799	chr4:187059696-187059697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7660462	chr4:187059719-187059720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs150156703	chr4:187059725-187059726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570395724	chr4:187059772-187059773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138384266	chr4:187059780-187059781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13106058	chr4:187059786-187059787	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs558830575	chr4:187059812-187059813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7660977	chr4:187059822-187059823	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs546434947	chr4:187059826-187059827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536088873	chr4:187059827-187059828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372016116	chr4:187059833-187059834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149244831	chr4:187059878-187059879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147389879	chr4:187059879-187059880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557814679	chr4:187059880-187059881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190862252	chr4:187059925-187059926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181964852	chr4:187059926-187059927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185010450	chr4:187059929-187059930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113035536	chr4:187059960-187059961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556459874	chr4:187059992-187059993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576216110	chr4:187059994-187059995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542046503	chr4:187060037-187060038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7660915	chr4:187060065-187060066	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs73873732	chr4:187060066-187060067	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs541165626	chr4:187060091-187060092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:2220 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187039200-187065000	Weak transcription	Fetal Brain Female	brain
2	chr4:187047200-187063200	Weak transcription	Fetal Stomach	stomach
3	chr4:187050600-187065000	Weak transcription	Gastric	stomach
4	chr4:187054200-187065000	Weak transcription	Fetal Kidney	kidney
5	chr4:187054400-187065000	Weak transcription	Fetal Intestine Small	intestine
6	chr4:187055000-187065000	Weak transcription	Fetal Intestine Large	intestine
7	chr4:187055800-187059800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:187055800-187059800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:187058600-187065200	Weak transcription	Pancreas	Pancrea
10	chr4:187058800-187064800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:187058800-187064800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr4:187058800-187065000	Weak transcription	Adipose Nuclei	Adipose
13	chr4:187058800-187065000	Weak transcription	Liver	Liver
14	chr4:187058800-187065200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:187058800-187065200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr4:187059000-187059200	Weak transcription	NHDF-Ad	bronchial
17	chr4:187059200-187059400	Enhancers	Fetal Brain Male	brain
18	chr4:187059800-187060000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:187059800-187060200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:187060000-187063200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:187060200-187065200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:187061600-187065000	Weak transcription	NHDF-Ad	bronchial
23	chr4:187063200-187063400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:187063200-187063400	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
25	chr4:187063200-187063600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:187063200-187064000	Strong transcription	Fetal Stomach	stomach
27	chr4:187063400-187063600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:187063600-187064800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:187063600-187065000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:187063600-187065000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr4:187064000-187065200	Weak transcription	Fetal Stomach	stomach
32	chr4:187064400-187065200	Enhancers	Fetal Brain Male	brain
33	chr4:187064800-187065000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr4:187064800-187065000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr4:187064800-187065000	Enhancers	Stomach Smooth Muscle	stomach
36	chr4:187064800-187065000	Enhancers	NH-A	brain
37	chr4:187064800-187065200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:187065000-187065200	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
39	chr4:187065000-187065200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:187065000-187065200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
41	chr4:187065000-187065200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:187065000-187065200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
43	chr4:187065000-187065200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
44	chr4:187065000-187065200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:187065000-187065200	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr4:187065000-187065200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:187065000-187065200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:187065000-187065200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:187065000-187065200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:187065000-187065200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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