Variant report

Variant	nsv875548
Chromosome Location	chr2:186798249-187164657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1327)
CpG islands
(count:305)
Chromatin interactive
region (count:45)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1327 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:186973201-186973628	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186855637-186856004	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:186933182-186933390	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:187046339-187046834	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:187121356-187121642	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:186994689-186995458	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:187164433-187164716	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:187062701-187063034	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:186835223-186835544	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:186853506-186853842	HepG2	liver:	n/a	n/a
11	BACH1	chr2:186855743-186855846	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr2:186917756-186918018	H1-hESC	embryonic stem cell:	n/a	chr2:186917846-186917860
13	BHLHE40	chr2:186896017-186896505	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:186929279-186929572	GM12878	blood:	n/a	n/a
15	CBX3	chr2:186836912-186837170	K562	blood:	n/a	n/a
16	CCNT2	chr2:186798987-186799212	K562	blood:	n/a	n/a
17	CCNT2	chr2:186905250-186905377	K562	blood:	n/a	n/a
18	CCNT2	chr2:186966417-186966617	K562	blood:	n/a	n/a
19	CCNT2	chr2:186984780-186984935	K562	blood:	n/a	n/a
20	CEBPB	chr2:186994884-186995064	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:186828874-186829177	A549	lung:	n/a	chr2:186829026-186829037
22	CEBPB	chr2:187160429-187160719	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:186994808-186995412	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:187046357-187046763	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:186828867-186829198	HepG2	liver:	n/a	chr2:186829026-186829037
26	CEBPB	chr2:186918858-186919191	IMR90	lung:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
27	CEBPB	chr2:187101217-187101408	A549	lung:	n/a	n/a
28	CEBPB	chr2:186973194-186973541	IMR90	lung:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
29	CEBPB	chr2:186863446-186863745	Hela-S3	cervix:	n/a	chr2:186863590-186863601
30	CEBPB	chr2:186994645-186995518	HCT-116	colon:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
31	CEBPB	chr2:187160425-187160666	A549	lung:	n/a	n/a
32	CEBPB	chr2:187119718-187119844	HepG2	liver:	n/a	chr2:187119776-187119787
33	CEBPB	chr2:186853669-186853919	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:187046375-187046652	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:186812025-186812311	HepG2	liver:	n/a	chr2:186812055-186812066
36	CEBPB	chr2:186886854-186887053	A549	lung:	n/a	n/a
37	CEBPB	chr2:186995329-186995732	ECC-1	luminal epithelium:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
38	CEBPB	chr2:186906365-186906557	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:186918854-186919223	HepG2	liver:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
40	CEBPB	chr2:186994842-186995446	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:186888225-186888463	A549	lung:	n/a	chr2:186888282-186888293 chr2:186888300-186888311
42	CEBPB	chr2:186994724-186995491	HCT-116	colon:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
43	CEBPB	chr2:186973240-186973488	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
44	CEBPB	chr2:186886764-186886992	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:186819161-186819361	K562	blood:	n/a	chr2:186819279-186819290
46	CEBPB	chr2:186988737-186988903	A549	lung:	n/a	n/a
47	CEBPB	chr2:187101857-187102129	A549	lung:	n/a	n/a
48	CEBPB	chr2:187047299-187047519	HepG2	liver:	n/a	chr2:187047425-187047436
49	CEBPB	chr2:187139715-187140087	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:187060567-187060855	HepG2	liver:	n/a	chr2:187060674-187060685 chr2:187060674-187060687

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186988953-186989003	HEK293	kidney:	embryo
2	chr2:186988953-186989003	HRPEpiC	eye:	n/a
3	chr2:186988953-186989003	HL-60	blood:	n/a
4	chr2:187081534-187081584	GM12892	blood:	n/a
5	chr2:186924071-186924121	HCF	heart:	n/a
6	chr2:186968467-186968517	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:186988953-186989003	AG04450	lung:	fetal
8	chr2:187120710-187120760	HUVEC	blood vessel:	n/a
9	chr2:186988953-186989003	SAEC	small airway:	n/a
10	chr2:186988953-186989003	K562	blood:	n/a
11	chr2:187081534-187081584	HRE	kidney:	n/a
12	chr2:186968467-186968517	GM12892	blood:	n/a
13	chr2:187081534-187081584	IMR90	lung:	fetal
14	chr2:186968467-186968517	ProgFib	skin:	n/a
15	chr2:186968467-186968517	A549	lung:	n/a
16	chr2:186924071-186924121	SAEC	small airway:	n/a
17	chr2:186924071-186924121	Caco-2	colon:	n/a
18	chr2:187120710-187120760	HCF	heart:	n/a
19	chr2:187081534-187081584	HCM	heart:	n/a
20	chr2:186968467-186968517	HUVEC	blood vessel:	n/a
21	chr2:186968467-186968517	HNPCEpiC	eye:	n/a
22	chr2:186988953-186989003	NH-A	brain:	n/a
23	chr2:186968467-186968517	U87	brain:	n/a
24	chr2:186968467-186968517	RPTEC	kidney:	n/a
25	chr2:187081534-187081584	HCT-116	colon:	n/a
26	chr2:186968467-186968517	HRPEpiC	eye:	n/a
27	chr2:187120710-187120760	AoSMC	blood vessel:	n/a
28	chr2:186988953-186989003	SK-N-MC	brain:	n/a
29	chr2:186988953-186989003	PANC-1	pancreas:	n/a
30	chr2:187120710-187120760	AG10803	skin:	n/a
31	chr2:187120710-187120760	HCM	heart:	n/a
32	chr2:186924071-186924121	HRCEpiC	kidney:	n/a
33	chr2:186924071-186924121	SKMC	muscle:	n/a
34	chr2:186988953-186989003	HCF	heart:	n/a
35	chr2:187120710-187120760	MCF10A-Er-Src	breast:	n/a
36	chr2:187081534-187081584	BE2_C	brain:	n/a
37	chr2:187081534-187081584	SK-N-SH	brain:	n/a
38	chr2:187120710-187120760	HRCEpiC	kidney:	n/a
39	chr2:187081534-187081584	K562	blood:	n/a
40	chr2:187120710-187120760	SK-N-MC	brain:	n/a
41	chr2:187081534-187081584	PFSK-1	brain:	n/a
42	chr2:186988953-186989003	PFSK-1	brain:	n/a
43	chr2:187120710-187120760	BJ	skin:	n/a
44	chr2:186988953-186989003	Caco-2	colon:	n/a
45	chr2:186988953-186989003	HAEpiC	amniotic membrane:	n/a
46	chr2:186924071-186924121	HAEpiC	amniotic membrane:	n/a
47	chr2:187120710-187120760	Hela-S3	cervix:	n/a
48	chr2:186924071-186924121	AG09309	skin:	n/a
49	chr2:187120710-187120760	PFSK-1	brain:	n/a
50	chr2:186924071-186924121	NH-A	brain:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186966503..186967236-chr4:21954917..21955427,2	MCF-7	breast:
2	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
3	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
4	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
5	chr2:187121005..187121910-chr2:187323354..187324097,2	MCF-7	breast:
6	chr2:187027645..187029211-chr2:187033628..187036309,2	MCF-7	breast:
7	chr10:23092682..23094839-chr2:187127661..187130019,2	MCF-7	breast:
8	chr2:186898326..186901023-chr2:187349730..187351831,2	K562	blood:
9	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
10	chr2:186819232..186820505-chr2:187121247..187122132,3	MCF-7	breast:
11	chr2:186983605..186985165-chr2:186986733..186988771,2	MCF-7	breast:
12	chr2:186983605..186985165-chr2:186986733..186988771,2	MCF-7	breast:
13	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
14	chr2:187144221..187146013-chr2:187148146..187151029,2	K562	blood:
15	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
16	chr2:187111432..187114258-chr2:187118686..187120723,2	MCF-7	breast:
17	chr2:43453747..43454591-chr2:186974749..186975692,2	HCT-116	colon:
18	chr2:186603423..186604198-chr2:187120988..187121931,3	MCF-7	breast:
19	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
20	chr2:187020003..187021879-chr2:187026559..187028779,2	MCF-7	breast:
21	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
22	chr2:186603700..186604546-chr2:187121410..187122246,2	MCF-7	breast:
23	chr2:187111432..187114258-chr2:187118686..187120723,2	MCF-7	breast:
24	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
25	chr17:57913762..57915412-chr2:186861621..186864023,2	MCF-7	breast:
26	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
27	chr2:186861297..186864828-chr2:186866334..186869154,3	K562	blood:
28	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
29	chr2:186493563..186494107-chr2:187121512..187122407,2	MCF-7	breast:
30	chr2:186882755..186884529-chr2:186886544..186888768,2	K562	blood:
31	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
32	chr2:187046232..187048383-chr2:187048758..187051703,2	MCF-7	breast:
33	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:
34	chr2:186791324..186793332-chr2:186796322..186798371,2	K562	blood:
35	chr2:187077199..187079062-chr2:187349198..187350991,2	K562	blood:
36	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
37	chr2:186844422..186846233-chr2:187042627..187045441,2	K562	blood:
38	chr2:186943617..186946004-chr2:186946269..186949362,3	K562	blood:
39	chr2:186851763..186854059-chr2:186854208..186855953,2	MCF-7	breast:
40	chr2:187080091..187081693-chr2:187086828..187089165,2	K562	blood:
41	chr2:187144221..187146013-chr2:187148146..187151029,2	K562	blood:
42	chr2:186807275..186808106-chr7:110453455..110454048,2	HCT-116	colon:
43	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
44	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
45	chr2:186819232..186820505-chr2:187121247..187122132,3	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-3	chr2:186903058-186903162	NR_110218
2	lnc-ZSWIM2-3	chr2:186898261-186898529	NR_110218
3	lnc-FSIP2-3	chr2:186963163-186964146	NONHSAT075986
4	lnc-ZSWIM2-3	chr2:186897618-186898529	ENSG00000237877.2
5	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
6	lnc-ZSWIM2-10	chr2:187027676-187027972	NONHSAT075988
7	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877
8	lnc-ZSWIM2-4	chr2:186815194-186815488	XLOC_002427
9	lnc-ZSWIM2-3	chr2:187006495-187007373	NONHSAT075981
10	lnc-FSIP2-4	chr2:186964372-186965726	NONHSAT075984
11	lnc-ZSWIM2-13	chr2:186799635-186800049	NONHSAT075976
12	lnc-ZSWIM2-3	chr2:187035921-187036575	NONHSAT075981
13	lnc-FSIP2-4	chr2:186947780-186951158	NONHSAT075984
14	lnc-ZSWIM2-3	chr2:186946057-186946143	NONHSAT075981
15	lnc-FSIP2-1	chr2:186999554-187000911	XLOC_001781
16	lnc-ZSWIM2-3	chr2:186904227-186904282	ENSG00000237877
17	lnc-FSIP2-1	chr2:187001824-187002215	XLOC_001781
18	lnc-ZSWIM2-3	chr2:186947881-186947951	NONHSAT075981
19	lnc-ZSWIM2-3	chr2:186897872-186898529	ENSG00000237877
20	lnc-ZSWIM2-3	chr2:186904227-186904282	NONHSAT075981
21	lnc-ZSWIM2-3	chr2:186897623-186897908	NONHSAT075981
22	lnc-ZSWIM2-3	chr2:187079525-187079817	NONHSAT075981
23	lnc-ZSWIM2-3	chr2:186903058-186903162	NONHSAT075981
24	lnc-FSIP2-2	chr2:186953806-186955337	NONHSAT075985
25	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
26	lnc-FSIP2-4	chr2:186932840-186933840	NONHSAT075984
27	lnc-ZSWIM2-11	chr2:186821314-186821790	NONHSAT075979
28	lnc-ZSWIM2-3	chr2:187002952-187003542	NONHSAT075981
29	lnc-ZSWIM2-3	chr2:186898258-186898529	ENSG00000237877
30	lnc-ZSWIM2-3	chr2:186903058-186903159	ENSG00000237877
31	lnc-ZSWIM2-3	chr2:186947881-186947948	NR_110218
32	lnc-ZSWIM2-3	chr2:186898222-186898531	NONHSAT075981
33	lnc-ZSWIM2-3	chr2:186946057-186946143	NR_110218
34	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877.2
35	lnc-ZSWIM2-3	chr2:186951028-186951044	NR_110218
36	lnc-ZSWIM2-3	chr2:186904227-186904282	NR_110218
37	lnc-ZSWIM2-12	chr2:186800286-186800551	NONHSAT075977
38	lnc-ZSWIM2-4	chr2:186817485-186817647	XLOC_002427
39	lnc-FSIP2-4	chr2:186923254-186923714	NONHSAT075984
40	lnc-FSIP2-4	chr2:186946053-186946143	NONHSAT075984
41	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877.2
42	lnc-ZSWIM2-3	chr2:186947881-186947950	ENSG00000237877
43	lnc-ZSWIM2-3	chr2:187126284-187126336	NONHSAT075981

No data

Variant related genes	Relation type
RPL23AP35	TF binding region
ENSG00000237877	TF binding region
RPL21P32	TF binding region
ENSG00000226410	TF binding region
RPL23AP35	CpG island
ENSG00000237877	CpG island
RPL21P32	CpG island
ENSG00000226410	CpG island
ENSG00000226747	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000237877	chromatin interactions
ENSG00000152518	chromatin interactions
ENSG00000188738	chromatin interactions
ENSG00000226410	chromatin interactions
SNAI2	miRNA target sites

Extended variants
information (count: 11212 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:11212 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6745509	chr2:186798249-186798250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192825468	chr2:186798288-186798289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572429701	chr2:186798378-186798379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140451355	chr2:186798438-186798439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554883114	chr2:186798455-186798456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184372720	chr2:186798521-186798522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540220730	chr2:186798648-186798649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543660651	chr2:186798652-186798653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370277813	chr2:186798666-186798667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565148392	chr2:186798678-186798679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532564705	chr2:186798689-186798690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142674806	chr2:186798735-186798736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117780369	chr2:186798772-186798773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34721978	chr2:186798773-186798774	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs35810743	chr2:186798806-186798807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188810537	chr2:186798902-186798903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13015006	chr2:186798933-186798934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs531643595	chr2:186799026-186799027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550063437	chr2:186799027-186799028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577740287	chr2:186799059-186799060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147352855	chr2:186799160-186799161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112557936	chr2:186799161-186799162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372507395	chr2:186799163-186799164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139736379	chr2:186799192-186799193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369139197	chr2:186799201-186799202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10202092	chr2:186799293-186799294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114135798	chr2:186799333-186799334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575988590	chr2:186799337-186799338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537364659	chr2:186799377-186799378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558797437	chr2:186799378-186799379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577396197	chr2:186799395-186799396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541252242	chr2:186799404-186799405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557180626	chr2:186799414-186799415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10931208	chr2:186799423-186799424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs543094624	chr2:186799458-186799459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181952470	chr2:186799481-186799482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149961312	chr2:186799526-186799527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371760414	chr2:186799534-186799535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534502995	chr2:186799542-186799543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115191527	chr2:186799562-186799563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531302683	chr2:186799566-186799567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186173212	chr2:186799578-186799579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144177319	chr2:186799604-186799605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542628450	chr2:186799647-186799648	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs370888303	chr2:186799702-186799703	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs528633948	chr2:186799706-186799707	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs565159751	chr2:186799731-186799732	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs115784007	chr2:186799742-186799743	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs540699039	chr2:186799750-186799751	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs114402402	chr2:186799780-186799781	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186784200-186809400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr2:186791600-186810000	Weak transcription	Pancreas	Pancrea
3	chr2:186806600-186807600	Weak transcription	Left Ventricle	heart
4	chr2:186806800-186809400	Weak transcription	Fetal Intestine Large	intestine
5	chr2:186807200-186810400	ZNF genes & repeats	Liver	Liver
6	chr2:186807600-186809000	ZNF genes & repeats	Left Ventricle	heart
7	chr2:186808200-186808400	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr2:186808600-186809000	Weak transcription	Adipose Nuclei	Adipose
9	chr2:186808800-186809200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
10	chr2:186808800-186809600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr2:186809000-186815200	Weak transcription	Left Ventricle	heart
12	chr2:186809200-186813200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr2:186809400-186809800	ZNF genes & repeats	Fetal Intestine Large	intestine
14	chr2:186809400-186810200	Strong transcription	Duodenum Smooth Muscle	Duodenum
15	chr2:186809600-186810400	Weak transcription	Adipose Nuclei	Adipose
16	chr2:186809800-186816800	Weak transcription	Fetal Intestine Large	intestine
17	chr2:186810000-186810200	ZNF genes & repeats	Ovary	ovary
18	chr2:186810000-186810200	ZNF genes & repeats	Pancreas	Pancrea
19	chr2:186810200-186813000	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr2:186810200-186828000	Weak transcription	Ovary	ovary
21	chr2:186810400-186814400	Weak transcription	Liver	Liver
22	chr2:186815000-186827800	Weak transcription	Aorta	Aorta
23	chr2:186815200-186815600	Strong transcription	Left Ventricle	heart
24	chr2:186815600-186833800	Weak transcription	Left Ventricle	heart
25	chr2:186816600-186817000	Enhancers	Hela-S3	cervix
26	chr2:186821000-186821800	Enhancers	Fetal Brain Male	brain
27	chr2:186827800-186828400	ZNF genes & repeats	Aorta	Aorta
28	chr2:186828000-186828200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
29	chr2:186828000-186828800	Strong transcription	Ovary	ovary
30	chr2:186828200-186836800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr2:186828400-186857400	Weak transcription	Aorta	Aorta
32	chr2:186828800-186867400	Weak transcription	Ovary	ovary
33	chr2:186830600-186831400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:186831400-186834800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:186832400-186834000	Weak transcription	Fetal Intestine Small	intestine
36	chr2:186833000-186834000	Weak transcription	Fetal Intestine Large	intestine
37	chr2:186834000-186834400	Enhancers	Fetal Intestine Small	intestine
38	chr2:186834000-186836000	Enhancers	Fetal Intestine Large	intestine
39	chr2:186834400-186834600	Weak transcription	Fetal Intestine Small	intestine
40	chr2:186834600-186836200	Enhancers	Fetal Intestine Small	intestine
41	chr2:186834800-186835000	Enhancers	Duodenum Mucosa	Duodenum
42	chr2:186834800-186835600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:186834800-186835600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:186834800-186835800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:186834800-186835800	Enhancers	NHEK	skin
46	chr2:186835000-186835600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:186835000-186835600	Enhancers	Pancreas	Pancrea
48	chr2:186835000-186835800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:186835000-186835800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:186835000-186835800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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