Variant report

Variant	nsv535144
Chromosome Location	chr1:147196527-147356634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:1282)
Chromatin interactive
region (count:108)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:147280155-147280630	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:147287788-147287850	K562	blood:	n/a	n/a
3	ARID3A	chr1:147323221-147323706	HepG2	liver:	n/a	n/a
4	ATF1	chr1:147323378-147323664	K562	blood:	n/a	n/a
5	ATF1	chr1:147283979-147283988	K562	blood:	n/a	n/a
6	ATF1	chr1:147293156-147293271	K562	blood:	n/a	n/a
7	ATF3	chr1:147280132-147280418	HepG2	liver:	n/a	n/a
8	ATF3	chr1:147323244-147323730	K562	blood:	n/a	n/a
9	BACH1	chr1:147305765-147305846	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:147309256-147309748	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr1:147321530-147321918	GM12878	blood:	n/a	n/a
12	BCL3	chr1:147311445-147311805	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:147314786-147315093	K562	blood:	n/a	chr1:147314922-147314931 chr1:147314921-147314930 chr1:147314922-147314931 chr1:147314916-147314937
14	BHLHE40	chr1:147280127-147280501	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:147314816-147315023	HepG2	liver:	n/a	chr1:147314922-147314931 chr1:147314921-147314930 chr1:147314922-147314931 chr1:147314916-147314937
16	BHLHE40	chr1:147280178-147280382	HepG2	liver:	n/a	n/a
17	BRCA1	chr1:147273148-147273197	Hela-S3	cervix:	n/a	chr1:147273166-147273173
18	CBX3	chr1:147323338-147323739	K562	blood:	n/a	n/a
19	CCNT2	chr1:147320063-147320309	K562	blood:	n/a	n/a
20	CEBPB	chr1:147277511-147277661	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:147280141-147280538	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
22	CEBPB	chr1:147247214-147247439	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:147278481-147278496	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:147259630-147259998	MCF-7	breast:	n/a	n/a
25	CEBPB	chr1:147229299-147229827	MCF-7	breast:	n/a	chr1:147229607-147229618
26	CEBPB	chr1:147216573-147216767	Hela-S3	cervix:	n/a	chr1:147216614-147216625
27	CEBPB	chr1:147229334-147229924	MCF-7	breast:	n/a	chr1:147229607-147229618
28	CEBPB	chr1:147280100-147280410	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
29	CEBPB	chr1:147216542-147216757	HepG2	liver:	n/a	chr1:147216614-147216625
30	CEBPB	chr1:147259680-147259951	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:147269626-147269645	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:147324913-147325090	Hela-S3	cervix:	n/a	chr1:147325017-147325028
33	CEBPB	chr1:147253715-147253880	HepG2	liver:	n/a	chr1:147253804-147253815 chr1:147253805-147253816
34	CEBPB	chr1:147229457-147229747	HepG2	liver:	n/a	chr1:147229607-147229618
35	CEBPB	chr1:147324930-147325087	HepG2	liver:	n/a	chr1:147325017-147325028
36	CEBPB	chr1:147280153-147280499	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
37	CEBPB	chr1:147280112-147280723	MCF-7	breast:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
38	CEBPB	chr1:147280134-147280507	H1-hESC	embryonic stem cell:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
39	CEBPB	chr1:147280084-147280789	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
40	CEBPB	chr1:147280093-147280519	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
41	CEBPB	chr1:147259741-147259892	K562	blood:	n/a	n/a
42	CEBPB	chr1:147279582-147279829	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:147280132-147280751	A549	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
44	CEBPB	chr1:147354442-147354528	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr1:147280103-147280524	Hela-S3	cervix:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
46	CEBPB	chr1:147259715-147259949	A549	lung:	n/a	n/a
47	CEBPB	chr1:147277448-147277776	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:147280136-147280454	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
49	CEBPB	chr1:147280158-147280664	IMR90	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
50	CEBPB	chr1:147229451-147229745	Hela-S3	cervix:	n/a	chr1:147229607-147229618

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:147309347-147309397	IMR90	lung:	fetal
2	chr1:147309347-147309397	IMR90	lung:	fetal
3	chr1:147320855-147320905	HUVEC	blood vessel:	n/a
4	chr1:147246154-147246204	AG09309	skin:	n/a
5	chr1:147233743-147233793	HMEC	breast:	n/a
6	chr1:147233110-147233160	SK-N-MC	brain:	n/a
7	chr1:147245494-147245544	NB4	blood:	n/a
8	chr1:147197536-147197586	HRCEpiC	kidney:	n/a
9	chr1:147230209-147230259	NB4	blood:	n/a
10	chr1:147245494-147245544	T-47D	breast:	n/a
11	chr1:147245168-147245218	HL-60	blood:	n/a
12	chr1:147309347-147309397	HCT-116	colon:	n/a
13	chr1:147245168-147245218	LNCaP	prostate:	n/a
14	chr1:147320855-147320905	A549	lung:	n/a
15	chr1:147232608-147232658	NB4	blood:	n/a
16	chr1:147246154-147246204	SK-N-SH	brain:	n/a
17	chr1:147246154-147246204	Jurkat	blood:	n/a
18	chr1:147233738-147233788	HL-60	blood:	n/a
19	chr1:147320855-147320905	HMEC	breast:	n/a
20	chr1:147245626-147245676	HRE	kidney:	n/a
21	chr1:147231862-147231912	RPTEC	kidney:	n/a
22	chr1:147246839-147246889	NH-A	brain:	n/a
23	chr1:147197536-147197586	AG04450	lung:	fetal
24	chr1:147231862-147231912	NHBE	bronchial:	n/a
25	chr1:147246839-147246889	HNPCEpiC	eye:	n/a
26	chr1:147232608-147232658	NHDF-neo	bronchial:	n/a
27	chr1:147245626-147245676	NB4	blood:	n/a
28	chr1:147232608-147232658	NT2-D1	testis:	n/a
29	chr1:147309347-147309397	HEEpiC	esophagus:	n/a
30	chr1:147231862-147231912	SAEC	small airway:	n/a
31	chr1:147233738-147233788	H1-hESC	embryonic stem cell:	embryo
32	chr1:147197536-147197586	HCPEpiC	choroid plexus:	n/a
33	chr1:147230452-147230502	ProgFib	skin:	n/a
34	chr1:147230452-147230502	NHBE	bronchial:	n/a
35	chr1:147245168-147245218	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:147309347-147309397	Hepatocyte	liver:	n/a
37	chr1:147233738-147233788	HCM	heart:	n/a
38	chr1:147230452-147230502	HL-60	blood:	n/a
39	chr1:147233738-147233788	AoSMC	blood vessel:	n/a
40	chr1:147233110-147233160	NB4	blood:	n/a
41	chr1:147245485-147245535	PFSK-1	brain:	n/a
42	chr1:147197536-147197586	GM19239	blood:	n/a
43	chr1:147245494-147245544	AG10803	skin:	n/a
44	chr1:147246839-147246889	BE2_C	brain:	n/a
45	chr1:147320855-147320905	HepG2	liver:	n/a
46	chr1:147233738-147233788	GM12891	blood:	n/a
47	chr1:147309347-147309397	GM12892	blood:	n/a
48	chr1:147246154-147246204	HCM	heart:	n/a
49	chr1:147230452-147230502	H1-hESC	embryonic stem cell:	embryo
50	chr1:147246154-147246204	BJ	skin:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:147342644..147346148-chr1:147349020..147352796,4	MCF-7	breast:
2	chr1:147216774..147217411-chr1:147362235..147362885,2	K562	blood:
3	chr1:147258662..147261590-chr1:147270902..147273169,3	MCF-7	breast:
4	chr1:147257526..147261196-chr1:147263496..147265511,3	MCF-7	breast:
5	chr1:147315649..147317263-chr1:147320620..147323315,2	MCF-7	breast:
6	chr1:147274506..147277076-chr1:147285425..147287009,2	K562	blood:
7	chr1:147343972..147346618-chr1:147346953..147349715,3	MCF-7	breast:
8	chr1:147306497..147308637-chr1:147308840..147310925,2	MCF-7	breast:
9	chr1:147266191..147267912-chr1:147271628..147273288,2	MCF-7	breast:
10	chr1:147229847..147231847-chr1:147237550..147240548,2	MCF-7	breast:
11	chr1:147315587..147317893-chr1:147319705..147321568,2	MCF-7	breast:
12	chr1:147233480..147234335-chr7:139299862..139300589,2	MCF-7	breast:
13	chr1:147234853..147236683-chr1:147245113..147247839,2	K562	blood:
14	chr1:147190469..147193203-chr1:147339308..147341475,2	MCF-7	breast:
15	chr1:147214667..147217419-chr1:147235402..147238099,2	MCF-7	breast:
16	chr1:147268842..147272094-chr1:147272923..147275545,3	K562	blood:
17	chr1:147195860..147197594-chr1:147201052..147203782,2	K562	blood:
18	chr1:147225486..147227195-chr1:147227978..147229551,2	MCF-7	breast:
19	chr1:147276129..147278611-chr1:147279190..147281299,2	MCF-7	breast:
20	chr1:147195260..147198617-chr1:147199229..147201930,3	MCF-7	breast:
21	chr1:147224461..147227120-chr1:147242032..147244708,3	MCF-7	breast:
22	chr1:147208419..147212694-chr1:147216367..147220265,3	MCF-7	breast:
23	chr1:147315587..147317893-chr1:147319705..147321568,2	MCF-7	breast:
24	chr1:147252565..147254194-chr1:147257728..147259512,2	MCF-7	breast:
25	chr1:147194515..147197013-chr1:147361402..147365473,61	MCF-7	breast:
26	chr1:147196156..147196754-chr1:147364745..147365855,4	K562	blood:
27	chr1:147218454..147220532-chr1:147233214..147234923,2	MCF-7	breast:
28	chr1:147252565..147254194-chr1:147257728..147259512,2	MCF-7	breast:
29	chr1:147276129..147278611-chr1:147279190..147281299,2	MCF-7	breast:
30	chr1:147245849..147248322-chr1:147252642..147255104,2	MCF-7	breast:
31	chr1:147240071..147242067-chr1:147245350..147247970,2	MCF-7	breast:
32	chr1:147287314..147288194-chr1:147312838..147313452,2	MCF-7	breast:
33	chr1:147348553..147350573-chr1:147355843..147358338,2	K562	blood:
34	chr1:147209469..147211828-chr1:147222916..147225569,2	MCF-7	breast:
35	chr1:147254319..147256959-chr1:147257613..147260137,2	K562	blood:
36	chr1:147258662..147261590-chr1:147270902..147273169,3	MCF-7	breast:
37	chr1:147243473..147246240-chr1:147264648..147266460,2	MCF-7	breast:
38	chr1:147214204..147216721-chr1:147219885..147221877,2	K562	blood:
39	chr1:147348553..147350573-chr1:147355843..147358338,2	K562	blood:
40	chr1:147195860..147197594-chr1:147201052..147203782,2	K562	blood:
41	chr1:147280614..147282894-chr1:147286254..147288918,3	K562	blood:
42	chr1:147224415..147227866-chr1:147242709..147245199,3	MCF-7	breast:
43	chr1:147272185..147274968-chr1:147288763..147290507,2	K562	blood:
44	chr1:147327159..147327751-chr1:147364434..147365228,2	MCF-7	breast:
45	chr1:147274506..147277076-chr1:147285425..147287009,2	K562	blood:
46	chr1:147254319..147256959-chr1:147257613..147260137,2	K562	blood:
47	chr1:147306497..147308637-chr1:147308840..147310925,2	MCF-7	breast:
48	chr1:147248547..147250748-chr1:147270374..147272494,2	MCF-7	breast:
49	chr1:147247003..147248756-chr1:147253569..147255678,2	K562	blood:
50	chr1:147326651..147329295-chr1:147342003..147343727,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL9-4	chr1:147199410-147199544	ucscGeneNc_uc009wkw_1
2	lnc-GJA5-2	chr1:147283214-147283468	XLOC_001007
3	lnc-GJA5-1	chr1:147209596-147209751	XLOC_001006
4	lnc-GJA8-1	chr1:147249689-147249833	XLOC_000387
5	lnc-BCL9-4	chr1:147199410-147199544	NONHSAT006043
6	lnc-BCL9-4	chr1:147197029-147197201	ucscGeneNc_uc009wkw_1
7	lnc-BCL9-4	chr1:147217869-147218218	NONHSAT006041
8	lnc-GJA8-1	chr1:147264755-147267415	XLOC_000387
9	lnc-GJA5-2	chr1:147281915-147282433	XLOC_001007
10	lnc-BCL9-4	chr1:147199410-147199544	NONHSAT006041
11	lnc-BCL9-4	chr1:147199915-147200203	NONHSAT006044
12	lnc-BCL9-2	chr1:147230462-147230517	ENSG00000234482.1
13	lnc-BCL9-4	chr1:147199409-147199544	NONHSAT006044
14	lnc-GJA8-1	chr1:147249700-147249833	XLOC_000387
15	lnc-GJA8-1	chr1:147260720-147261065	XLOC_000387
16	lnc-BCL9-4	chr1:147199915-147199992	ucscGeneNc_uc009wkw_1
17	lnc-BCL9-4	chr1:147199915-147199992	NONHSAT006043
18	lnc-BCL9-4	chr1:147218961-147219678	ucscGeneNc_uc009wkw_1
19	lnc-BCL9-2	chr1:147229426-147229879	ENSG00000234482.1
20	lnc-GJA5-1	chr1:147210816-147210939	XLOC_001006

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
ENSG00000234482	chromatin interactions
ENSG00000234190	chromatin interactions
ENSG00000121634	chromatin interactions
ENSG00000223728	chromatin interactions
ENSG00000143140	chromatin interactions
ARHGAP1	miRNA target sites
SOCS4	miRNA target sites

Extended variants
information (count: 4796 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:4796 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587757071	chr1:147196537-147196538	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587647462	chr1:147196559-147196560	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4950338	chr1:147196656-147196657	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587629722	chr1:147196690-147196691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587688989	chr1:147196692-147196693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4950339	chr1:147196727-147196728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs587706438	chr1:147196774-147196775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146512704	chr1:147196778-147196779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374760247	chr1:147196779-147196780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587658651	chr1:147196789-147196790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587734411	chr1:147196790-147196791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587613906	chr1:147196816-147196817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368347009	chr1:147196886-147196887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113499793	chr1:147196932-147196933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4950340	chr1:147196934-147196935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs71584660	chr1:147196956-147196957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587630326	chr1:147196983-147196984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587685827	chr1:147196985-147196986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587767958	chr1:147197082-147197083	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs11810292	chr1:147197083-147197084	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11576209	chr1:147197093-147197094	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184756930	chr1:147197110-147197111	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs187879234	chr1:147197122-147197123	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs145894409	chr1:147197150-147197151	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs374670042	chr1:147197151-147197152	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs148319442	chr1:147197160-147197161	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs112537785	chr1:147197162-147197163	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs71083859	chr1:147197167-147197168	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs587660458	chr1:147197192-147197193	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs10604394	chr1:147197193-147197194	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs201646958	chr1:147197196-147197197	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs368135227	chr1:147197220-147197221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs57484328	chr1:147197234-147197235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79025066	chr1:147197247-147197248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375028962	chr1:147197310-147197311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587668883	chr1:147197419-147197420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140841855	chr1:147197520-147197521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587623563	chr1:147197524-147197525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587630955	chr1:147197532-147197533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372604947	chr1:147197533-147197534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191535970	chr1:147197552-147197553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374839809	chr1:147197571-147197572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144603818	chr1:147197619-147197620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587609836	chr1:147197657-147197658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35101318	chr1:147197676-147197677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373297872	chr1:147197687-147197688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587618451	chr1:147197698-147197699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587665275	chr1:147197720-147197721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587747078	chr1:147197772-147197773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17160582	chr1:147197837-147197838	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:152)

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
Lung squamous cell carcinoma	20842114	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
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Melanoma	21430779	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Neuroblastoma	19536264	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147190200-147198800	Weak transcription	Right Atrium	heart
2	chr1:147194200-147198200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:147194600-147197400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:147194600-147197600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:147194600-147198200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:147195800-147196600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr1:147196000-147196600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
8	chr1:147196000-147196600	Enhancers	Hela-S3	cervix
9	chr1:147196200-147197000	Enhancers	HMEC	breast
10	chr1:147196400-147196600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr1:147196400-147196600	Enhancers	Placenta	Placenta
12	chr1:147196400-147197200	Enhancers	Fetal Heart	heart
13	chr1:147196600-147197800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:147196600-147198200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr1:147197200-147197600	Weak transcription	Fetal Heart	heart
16	chr1:147197600-147197800	Enhancers	Fetal Heart	heart
17	chr1:147197600-147199000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:147197800-147199000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:147197800-147205600	Weak transcription	Fetal Heart	heart
20	chr1:147198000-147198200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr1:147198000-147199000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:147198000-147199000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:147198200-147198600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:147198200-147198800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr1:147198200-147198800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
26	chr1:147198200-147199000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:147198200-147199000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:147198200-147199000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:147198200-147199000	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:147198200-147199000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr1:147198200-147199200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:147198400-147199000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr1:147198400-147199000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr1:147198400-147199000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:147198400-147199000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:147198600-147199000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:147198600-147199000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr1:147198600-147199000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:147198600-147199000	Enhancers	Primary hematopoietic stem cells	blood
40	chr1:147198800-147199000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr1:147198800-147199000	Enhancers	Right Atrium	heart
42	chr1:147199000-147200200	Weak transcription	Right Atrium	heart
43	chr1:147200200-147200600	Bivalent Enhancer	Fetal Lung	lung
44	chr1:147200200-147200800	Enhancers	Fetal Intestine Large	intestine
45	chr1:147200400-147200600	Enhancers	Right Atrium	heart
46	chr1:147205600-147209400	Enhancers	Fetal Heart	heart
47	chr1:147206400-147206600	Enhancers	Pancreas	Pancrea
48	chr1:147206600-147207600	Weak transcription	Pancreas	Pancrea
49	chr1:147206800-147208000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr1:147207000-147207600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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