Variant report

Variant	nsv916522
Chromosome Location	chr1:147228396-147309062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:1098)
Chromatin interactive
region (count:53)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:147287788-147287850	K562	blood:	n/a	n/a
2	ARID3A	chr1:147280155-147280630	HepG2	liver:	n/a	n/a
3	ATF1	chr1:147293156-147293271	K562	blood:	n/a	n/a
4	ATF1	chr1:147283979-147283988	K562	blood:	n/a	n/a
5	ATF3	chr1:147280132-147280418	HepG2	liver:	n/a	n/a
6	BACH1	chr1:147305765-147305846	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr1:147280178-147280382	HepG2	liver:	n/a	n/a
8	BHLHE40	chr1:147280127-147280501	HepG2	liver:	n/a	n/a
9	BRCA1	chr1:147273148-147273197	Hela-S3	cervix:	n/a	chr1:147273166-147273173
10	CEBPB	chr1:147280132-147280751	A549	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
11	CEBPB	chr1:147259630-147259998	MCF-7	breast:	n/a	n/a
12	CEBPB	chr1:147259655-147259937	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:147247214-147247439	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:147280134-147280507	H1-hESC	embryonic stem cell:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
15	CEBPB	chr1:147277511-147277661	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:147280093-147280519	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
17	CEBPB	chr1:147280112-147280723	MCF-7	breast:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
18	CEBPB	chr1:147280158-147280664	IMR90	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
19	CEBPB	chr1:147277448-147277776	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:147280141-147280538	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
21	CEBPB	chr1:147229432-147229831	ECC-1	luminal epithelium:	n/a	chr1:147229607-147229618
22	CEBPB	chr1:147279582-147279829	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:147229334-147229924	MCF-7	breast:	n/a	chr1:147229607-147229618
24	CEBPB	chr1:147278481-147278496	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:147229457-147229747	HepG2	liver:	n/a	chr1:147229607-147229618
26	CEBPB	chr1:147280153-147280499	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
27	CEBPB	chr1:147280100-147280410	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
28	CEBPB	chr1:147229451-147229745	Hela-S3	cervix:	n/a	chr1:147229607-147229618
29	CEBPB	chr1:147229299-147229827	MCF-7	breast:	n/a	chr1:147229607-147229618
30	CEBPB	chr1:147259715-147259949	A549	lung:	n/a	n/a
31	CEBPB	chr1:147253715-147253880	HepG2	liver:	n/a	chr1:147253804-147253815 chr1:147253805-147253816
32	CEBPB	chr1:147229401-147229823	ECC-1	luminal epithelium:	n/a	chr1:147229607-147229618
33	CEBPB	chr1:147280084-147280789	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
34	CEBPB	chr1:147259680-147259951	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:147280136-147280454	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
36	CEBPB	chr1:147269626-147269645	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:147280103-147280524	Hela-S3	cervix:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
38	CEBPB	chr1:147259741-147259892	K562	blood:	n/a	n/a
39	CEBPD	chr1:147280137-147280442	HepG2	liver:	n/a	n/a
40	CEBPD	chr1:147280125-147280437	HepG2	liver:	n/a	n/a
41	CTCF	chr1:147228620-147228770	HMEC	breast:	n/a	n/a
42	CTCF	chr1:147287640-147287790	BE2_C	brain:	n/a	n/a
43	CTCF	chr1:147287680-147287830	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr1:147287675-147287818	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:147285040-147285190	GM12866	blood:	n/a	n/a
46	CTCF	chr1:147287763-147287796	LNCaP	prostate:	n/a	n/a
47	CTCF	chr1:147287640-147287790	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:147287660-147287810	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:147266640-147266790	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr1:147287780-147287930	HFF-Myc	foreskin:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:147231061-147231111	Hepatocyte	liver:	n/a
2	chr1:147233110-147233160	SK-N-MC	brain:	n/a
3	chr1:147233738-147233788	PFSK-1	brain:	n/a
4	chr1:147245626-147245676	SAEC	small airway:	n/a
5	chr1:147231524-147231574	PFSK-1	brain:	n/a
6	chr1:147246329-147246379	AG09309	skin:	n/a
7	chr1:147246839-147246889	AG04450	lung:	fetal
8	chr1:147233110-147233160	U87	brain:	n/a
9	chr1:147245168-147245218	HMEC	breast:	n/a
10	chr1:147245168-147245218	PFSK-1	brain:	n/a
11	chr1:147245168-147245218	NH-A	brain:	n/a
12	chr1:147246329-147246379	HRCEpiC	kidney:	n/a
13	chr1:147232608-147232658	Hepatocyte	liver:	n/a
14	chr1:147245485-147245535	GM12892	blood:	n/a
15	chr1:147230452-147230502	NHBE	bronchial:	n/a
16	chr1:147246329-147246379	BE2_C	brain:	n/a
17	chr1:147253401-147253451	PFSK-1	brain:	n/a
18	chr1:147245485-147245535	NH-A	brain:	n/a
19	chr1:147233887-147233937	BJ	skin:	n/a
20	chr1:147232608-147232658	NT2-D1	testis:	n/a
21	chr1:147233887-147233937	HRPEpiC	eye:	n/a
22	chr1:147245626-147245676	HAEpiC	amniotic membrane:	n/a
23	chr1:147233110-147233160	PFSK-1	brain:	n/a
24	chr1:147230209-147230259	AG04449	skin:	fetal
25	chr1:147230209-147230259	SK-N-SH_RA	brain:	n/a
26	chr1:147230452-147230502	HNPCEpiC	eye:	n/a
27	chr1:147231524-147231574	U87	brain:	n/a
28	chr1:147232608-147232658	HUVEC	blood vessel:	n/a
29	chr1:147232608-147232658	U87	brain:	n/a
30	chr1:147233743-147233793	SK-N-SH_RA	brain:	n/a
31	chr1:147231862-147231912	GM12891	blood:	n/a
32	chr1:147245485-147245535	HRCEpiC	kidney:	n/a
33	chr1:147230209-147230259	HRPEpiC	eye:	n/a
34	chr1:147246154-147246204	Hepatocyte	liver:	n/a
35	chr1:147245494-147245544	SAEC	small airway:	n/a
36	chr1:147253401-147253451	MCF-7	breast:	n/a
37	chr1:147231862-147231912	NHBE	bronchial:	n/a
38	chr1:147245168-147245218	BE2_C	brain:	n/a
39	chr1:147246154-147246204	LNCaP	prostate:	n/a
40	chr1:147232608-147232658	CMK	blood:	n/a
41	chr1:147232608-147232658	BJ	skin:	n/a
42	chr1:147231524-147231574	HCF	heart:	n/a
43	chr1:147233738-147233788	SKMC	muscle:	n/a
44	chr1:147245485-147245535	HCF	heart:	n/a
45	chr1:147245485-147245535	SK-N-SH	brain:	n/a
46	chr1:147233887-147233937	AG04449	skin:	fetal
47	chr1:147231061-147231111	HUVEC	blood vessel:	n/a
48	chr1:147245494-147245544	AG04450	lung:	fetal
49	chr1:147253401-147253451	AG04450	lung:	fetal
50	chr1:147245485-147245535	PFSK-1	brain:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:147290796..147294633-chr1:147295711..147299117,4	K562	blood:
2	chr1:147240071..147242067-chr1:147245350..147247970,2	MCF-7	breast:
3	chr1:147252565..147254194-chr1:147257728..147259512,2	MCF-7	breast:
4	chr1:147224461..147227120-chr1:147242032..147244708,3	MCF-7	breast:
5	chr1:147280614..147282894-chr1:147286254..147288918,3	K562	blood:
6	chr1:147275715..147278808-chr1:147281982..147285305,3	K562	blood:
7	chr1:147306497..147308637-chr1:147308840..147310925,2	MCF-7	breast:
8	chr1:147234853..147236683-chr1:147245113..147247839,2	K562	blood:
9	chr1:147287314..147288194-chr1:147312838..147313452,2	MCF-7	breast:
10	chr1:147247003..147248756-chr1:147253569..147255678,2	K562	blood:
11	chr1:147257526..147261196-chr1:147263496..147265511,3	MCF-7	breast:
12	chr1:147276129..147278611-chr1:147279190..147281299,2	MCF-7	breast:
13	chr1:147266191..147267912-chr1:147271628..147273288,2	MCF-7	breast:
14	chr1:147214667..147217419-chr1:147235402..147238099,2	MCF-7	breast:
15	chr1:147272185..147274968-chr1:147288763..147290507,2	K562	blood:
16	chr1:147229847..147231847-chr1:147237550..147240548,2	MCF-7	breast:
17	chr1:147268842..147272094-chr1:147272923..147275545,3	K562	blood:
18	chr1:147232773..147235381-chr1:147235921..147238475,2	K562	blood:
19	chr1:147257526..147261196-chr1:147263496..147265511,3	MCF-7	breast:
20	chr1:147229847..147231847-chr1:147237550..147240548,2	MCF-7	breast:
21	chr1:147259078..147261479-chr1:147266280..147268485,2	MCF-7	breast:
22	chr1:147245849..147248322-chr1:147252642..147255104,2	MCF-7	breast:
23	chr1:147245849..147248322-chr1:147252642..147255104,2	MCF-7	breast:
24	chr1:147290796..147294633-chr1:147295711..147299117,4	K562	blood:
25	chr1:147258662..147261590-chr1:147270902..147273169,3	MCF-7	breast:
26	chr1:147247003..147248756-chr1:147253569..147255678,2	K562	blood:
27	chr1:147280614..147282894-chr1:147286254..147288918,3	K562	blood:
28	chr1:147218454..147220532-chr1:147233214..147234923,2	MCF-7	breast:
29	chr1:147259078..147261479-chr1:147266280..147268485,2	MCF-7	breast:
30	chr1:147276129..147278611-chr1:147279190..147281299,2	MCF-7	breast:
31	chr1:147253982..147256046-chr1:147260183..147262374,2	K562	blood:
32	chr1:147306497..147308637-chr1:147308840..147310925,2	MCF-7	breast:
33	chr1:147266191..147267912-chr1:147271628..147273288,2	MCF-7	breast:
34	chr1:147252565..147254194-chr1:147257728..147259512,2	MCF-7	breast:
35	chr1:147234187..147237058-chr1:147240099..147241730,2	MCF-7	breast:
36	chr1:147274506..147277076-chr1:147285425..147287009,2	K562	blood:
37	chr1:147272185..147274968-chr1:147288763..147290507,2	K562	blood:
38	chr1:147243473..147246240-chr1:147264648..147266460,2	MCF-7	breast:
39	chr1:147274506..147277076-chr1:147285425..147287009,2	K562	blood:
40	chr1:147234187..147237058-chr1:147240099..147241730,2	MCF-7	breast:
41	chr1:147253982..147256046-chr1:147260183..147262374,2	K562	blood:
42	chr1:147235840..147238345-chr1:147247832..147250076,2	MCF-7	breast:
43	chr1:147306922..147308460-chr1:147311767..147313691,2	K562	blood:
44	chr1:147254319..147256959-chr1:147257613..147260137,2	K562	blood:
45	chr1:147232773..147235381-chr1:147235921..147238475,2	K562	blood:
46	chr1:147248547..147250748-chr1:147270374..147272494,2	MCF-7	breast:
47	chr1:147243719..147246413-chr1:147246599..147248961,2	MCF-7	breast:
48	chr1:147254319..147256959-chr1:147257613..147260137,2	K562	blood:
49	chr1:147233480..147234335-chr7:139299862..139300589,2	MCF-7	breast:
50	chr1:147224415..147227866-chr1:147242709..147245199,3	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL9-2	chr1:147229426-147229879	ENSG00000234482.1
2	lnc-GJA8-1	chr1:147264755-147267415	XLOC_000387
3	lnc-BCL9-2	chr1:147230462-147230517	ENSG00000234482.1
4	lnc-GJA5-2	chr1:147281915-147282433	XLOC_001007
5	lnc-GJA5-2	chr1:147283214-147283468	XLOC_001007
6	lnc-GJA8-1	chr1:147249700-147249833	XLOC_000387
7	lnc-GJA8-1	chr1:147260720-147261065	XLOC_000387
8	lnc-GJA8-1	chr1:147249689-147249833	XLOC_000387

No data

Variant related genes	Relation type
GJA5	TF binding region
ENSG00000234482	TF binding region
ENSG00000223728	TF binding region
ENSG00000234190	TF binding region
GJA5	CpG island
ENSG00000234482	CpG island
ENSG00000223728	CpG island
ENSG00000234190	CpG island
ENSG00000143140	chromatin interactions
ENSG00000234190	chromatin interactions
ENSG00000223728	chromatin interactions

Extended variants
information (count: 2713 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:2713 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587676638	chr1:147228404-147228405	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs587763167	chr1:147228454-147228455	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs587632843	chr1:147228478-147228479	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185168088	chr1:147228514-147228515	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs587771829	chr1:147228528-147228529	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs587673022	chr1:147228533-147228534	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs587742014	chr1:147228660-147228661	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs587598301	chr1:147228664-147228665	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs188772110	chr1:147228688-147228689	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs587705904	chr1:147228692-147228693	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs78252771	chr1:147228743-147228744	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs587669284	chr1:147228752-147228753	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114300383	chr1:147228764-147228765	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs138622477	chr1:147228835-147228836	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181096214	chr1:147228839-147228840	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370916542	chr1:147228853-147228854	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587727245	chr1:147228864-147228865	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11240121	chr1:147228874-147228875	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs72702309	chr1:147228907-147228908	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs587736364	chr1:147228997-147228998	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs587624199	chr1:147229090-147229091	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369554360	chr1:147229091-147229092	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146147548	chr1:147229121-147229122	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587719205	chr1:147229163-147229164	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113910552	chr1:147229164-147229165	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186143033	chr1:147229173-147229174	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587662296	chr1:147229226-147229227	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs111583502	chr1:147229292-147229293	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs1043806	chr1:147229299-147229300	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs587757056	chr1:147229329-147229330	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs10900395	chr1:147229382-147229383	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs191751867	chr1:147229503-147229504	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
33	rs370924807	chr1:147229504-147229505	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
34	rs112410877	chr1:147229514-147229515	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
35	rs1043802	chr1:147229563-147229564	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs587647000	chr1:147229565-147229566	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
37	rs587716397	chr1:147229595-147229596	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
38	rs587595278	chr1:147229604-147229605	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
39	rs587671620	chr1:147229616-147229617	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
40	rs11267274	chr1:147229628-147229629	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
41	rs35666193	chr1:147229629-147229630	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
42	rs587724016	chr1:147229631-147229632	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
43	rs371724095	chr1:147229653-147229654	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
44	rs202133825	chr1:147229654-147229655	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
45	rs375787029	chr1:147229661-147229662	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
46	rs369150521	chr1:147229662-147229663	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
47	rs587655590	chr1:147229693-147229694	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
48	rs587741640	chr1:147229762-147229763	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
49	rs587637864	chr1:147229771-147229772	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
50	rs142269930	chr1:147229775-147229776	Weak transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:149)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20369283	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Obesity	21131291	CNVD
Melanoma	21430779	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Neuroblastoma	19536264	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147220800-147228400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:147221200-147228600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:147221400-147229000	Weak transcription	Lung	lung
4	chr1:147221600-147229600	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:147223200-147229800	Weak transcription	Spleen	Spleen
6	chr1:147223400-147228600	Weak transcription	Right Ventricle	heart
7	chr1:147223600-147228600	Enhancers	Fetal Lung	lung
8	chr1:147224200-147228600	Weak transcription	Aorta	Aorta
9	chr1:147225200-147232200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:147225400-147228600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:147225400-147229200	Weak transcription	Adipose Nuclei	Adipose
12	chr1:147225400-147229200	Weak transcription	Pancreas	Pancrea
13	chr1:147225600-147228600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:147225600-147228600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:147225600-147228600	Weak transcription	Left Ventricle	heart
16	chr1:147225600-147228600	Weak transcription	Right Atrium	heart
17	chr1:147225600-147228600	Weak transcription	NHEK	skin
18	chr1:147225800-147228400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:147226400-147229000	Weak transcription	Fetal Muscle Leg	muscle
20	chr1:147226400-147230000	Weak transcription	Esophagus	oesophagus
21	chr1:147227200-147228600	Enhancers	Placenta	Placenta
22	chr1:147227800-147229600	Flanking Active TSS	Fetal Heart	heart
23	chr1:147228000-147228400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:147228200-147229200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:147228200-147232000	Enhancers	HMEC	breast
26	chr1:147228400-147228600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:147228400-147229200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:147228400-147230000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:147228400-147232400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:147228600-147228800	Enhancers	Psoas Muscle	Psoas
31	chr1:147228600-147229000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:147228600-147229000	Enhancers	Primary hematopoietic stem cells	blood
33	chr1:147228600-147229200	Flanking Active TSS	Placenta	Placenta
34	chr1:147228600-147229400	Genic enhancers	Fetal Lung	lung
35	chr1:147228600-147229800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:147228600-147229800	Enhancers	Gastric	stomach
37	chr1:147228600-147229800	Enhancers	Left Ventricle	heart
38	chr1:147228600-147230000	Enhancers	Aorta	Aorta
39	chr1:147228600-147230400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:147228600-147230800	Enhancers	NHEK	skin
41	chr1:147228600-147231000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:147228600-147231200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:147228600-147231400	Enhancers	Right Ventricle	heart
44	chr1:147228600-147232000	Weak transcription	Fetal Brain Male	brain
45	chr1:147228600-147232200	Enhancers	Placenta Amnion	Placenta Amnion
46	chr1:147228600-147232400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr1:147228600-147235200	Enhancers	Right Atrium	heart
48	chr1:147228800-147230200	Enhancers	HepG2	liver
49	chr1:147228800-147231000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr1:147228800-147232800	Weak transcription	Psoas Muscle	Psoas

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