Variant report

Variant	nsv1014504
Chromosome Location	chr1:144889465-144970212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1890)
CpG islands
(count:1528)
Chromatin interactive
region (count:121)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1890 , 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	chr1:144931414-144931602	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:144921610-144922130	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:144923974-144924494	HepG2	liver:	n/a	chr1:144924178-144924194
4	ARID3A	chr1:144893871-144894101	K562	blood:	n/a	n/a
5	ARID3A	chr1:144937109-144937725	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:144931963-144932828	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:144938243-144938360	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:144918079-144918361	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:144918090-144918310	K562	blood:	n/a	n/a
10	ARID3A	chr1:144938874-144939338	HepG2	liver:	n/a	n/a
11	ATF1	chr1:144893850-144893916	K562	blood:	n/a	n/a
12	ATF1	chr1:144918124-144918317	K562	blood:	n/a	n/a
13	ATF2	chr1:144931876-144932753	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr1:144908048-144908805	GM12878	blood:	n/a	n/a
15	ATF2	chr1:144931922-144932867	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr1:144908134-144908746	GM12878	blood:	n/a	n/a
17	ATF2	chr1:144931771-144932702	GM12878	blood:	n/a	n/a
18	BACH1	chr1:144924377-144924386	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:144931477-144932093	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr1:144908154-144908914	GM12878	blood:	n/a	n/a
21	BATF	chr1:144954925-144955119	GM12878	blood:	n/a	n/a
22	BATF	chr1:144954919-144955123	GM12878	blood:	n/a	n/a
23	BATF	chr1:144908200-144908921	GM12878	blood:	n/a	n/a
24	BATF	chr1:144965985-144966330	GM12878	blood:	n/a	n/a
25	BATF	chr1:144965596-144965880	GM12878	blood:	n/a	chr1:144965602-144965610 chr1:144965715-144965724
26	BATF	chr1:144918063-144918340	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:144963027-144963277	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:144965972-144966276	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:144908211-144908941	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:144908224-144908540	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:144965672-144966363	GM12878	blood:	n/a	n/a
32	BCL3	chr1:144931803-144933017	A549	lung:	n/a	chr1:144932014-144932027 chr1:144932069-144932082 chr1:144931862-144931875 chr1:144932058-144932071 chr1:144932171-144932179
33	BCLAF1	chr1:144931095-144932686	GM12878	blood:	n/a	chr1:144932014-144932027 chr1:144931744-144931753 chr1:144932069-144932082 chr1:144931862-144931875 chr1:144931747-144931756 chr1:144931740-144931753 chr1:144931749-144931762 chr1:144931743-144931756 chr1:144932058-144932071 chr1:144931741-144931750 chr1:144931742-144931755 chr1:144932171-144932179
34	BCLAF1	chr1:144965819-144966130	GM12878	blood:	n/a	n/a
35	BHLHE40	chr1:144918068-144918289	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:144931358-144932896	GM12878	blood:	n/a	chr1:144931851-144931867 chr1:144931740-144931756 chr1:144932069-144932085
37	BHLHE40	chr1:144935383-144935704	GM12878	blood:	n/a	n/a
38	BHLHE40	chr1:144921698-144922064	HepG2	liver:	n/a	n/a
39	BHLHE40	chr1:144966129-144966186	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:144907946-144908684	GM12878	blood:	n/a	n/a
41	BRCA1	chr1:144916619-144916671	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:144931904-144933128	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:144932110-144933073	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr1:144932346-144932836	GM12878	blood:	n/a	n/a
45	BRCA1	chr1:144938742-144938911	H1-hESC	embryonic stem cell:	n/a	n/a
46	BRCA1	chr1:144931824-144932592	HepG2	liver:	n/a	n/a
47	BRCA1	chr1:144912899-144912910	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr1:144938833-144938875	Hela-S3	cervix:	n/a	n/a
49	CBX3	chr1:144931897-144932645	K562	blood:	n/a	n/a
50	CCNT2	chr1:144931633-144932040	K562	blood:	n/a	chr1:144931905-144931914

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144913803-144913853	ovcar-3	ovarian:	n/a
2	chr1:144942354-144942404	K562	blood:	n/a
3	chr1:144932227-144932277	BJ	skin:	n/a
4	chr1:144913803-144913853	ovcar-3	ovarian:	n/a
5	chr1:144942354-144942404	K562	blood:	n/a
6	chr1:144932227-144932277	BJ	skin:	n/a
7	chr1:144928806-144928856	HUVEC	blood vessel:	n/a
8	chr1:144931980-144932030	PFSK-1	brain:	n/a
9	chr1:144932311-144932361	AG10803	skin:	n/a
10	chr1:144931966-144932016	HIPEpiC	eye:	n/a
11	chr1:144931862-144931912	PFSK-1	brain:	n/a
12	chr1:144930572-144930622	NH-A	brain:	n/a
13	chr1:144892566-144892616	K562	blood:	n/a
14	chr1:144931476-144931526	PFSK-1	brain:	n/a
15	chr1:144932473-144932523	HUVEC	blood vessel:	n/a
16	chr1:144932311-144932361	U87	brain:	n/a
17	chr1:144930572-144930622	K562	blood:	n/a
18	chr1:144892566-144892616	AG04450	lung:	fetal
19	chr1:144952173-144952223	MCF10A-Er-Src	breast:	n/a
20	chr1:144932473-144932523	HMEC	breast:	n/a
21	chr1:144931975-144932025	T-47D	breast:	n/a
22	chr1:144931379-144931429	HCPEpiC	choroid plexus:	n/a
23	chr1:144931862-144931912	SKMC	muscle:	n/a
24	chr1:144892566-144892616	MCF10A-Er-Src	breast:	n/a
25	chr1:144931980-144932030	HNPCEpiC	eye:	n/a
26	chr1:144932625-144932675	HRCEpiC	kidney:	n/a
27	chr1:144935409-144935459	HRCEpiC	kidney:	n/a
28	chr1:144942354-144942404	SK-N-SH	brain:	n/a
29	chr1:144932914-144932964	NB4	blood:	n/a
30	chr1:144931476-144931526	HEK293	kidney:	embryo
31	chr1:144932207-144932257	ovcar-3	ovarian:	n/a
32	chr1:144928806-144928856	AG09319	gingival:	n/a
33	chr1:144932476-144932526	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:144931980-144932030	IMR90	lung:	fetal
35	chr1:144892566-144892616	LNCaP	prostate:	n/a
36	chr1:144930964-144931014	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:144913803-144913853	NHBE	bronchial:	n/a
38	chr1:144892111-144892161	Hela-S3	cervix:	n/a
39	chr1:144932625-144932675	GM06990	blood:	n/a
40	chr1:144931980-144932030	GM12892	blood:	n/a
41	chr1:144913803-144913853	SK-N-SH	brain:	n/a
42	chr1:144932625-144932675	SK-N-SH	brain:	n/a
43	chr1:144926986-144927036	Hepatocyte	liver:	n/a
44	chr1:144932914-144932964	AoSMC	blood vessel:	n/a
45	chr1:144937317-144937367	GM06990	blood:	n/a
46	chr1:144926986-144927036	PANC-1	pancreas:	n/a
47	chr1:144913803-144913853	HCT-116	colon:	n/a
48	chr1:144931966-144932016	ProgFib	skin:	n/a
49	chr1:144892566-144892616	PrEC	prostate:	n/a
50	chr1:144932914-144932964	H1-hESC	embryonic stem cell:	embryo

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:144924927..144926596-chr1:145062250..145064152,2	MCF-7	breast:
2	chr1:144928885..144930474-chr1:144935425..144937244,2	K562	blood:
3	chr1:144929695..144933397-chr1:145381616..145384279,4	MCF-7	breast:
4	chr1:144917927..144918738-chr1:145057991..145059601,5	K562	blood:
5	chr1:144916627..144918753-chr1:144920547..144922373,2	K562	blood:
6	chr1:144930877..144933652-chr1:144988569..144991245,4	MCF-7	breast:
7	chr1:144917990..144918581-chr1:145061611..145062219,2	MCF-7	breast:
8	chr1:144914245..144917269-chr1:144938650..144941626,3	K562	blood:
9	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
10	chr1:144933246..144935275-chr11:64863413..64865438,2	MCF-7	breast:
11	chr1:144932003..144934560-chr1:145095329..145097401,2	MCF-7	breast:
12	chr1:144930770..144933506-chr20:52490207..52493077,2	MCF-7	breast:
13	chr1:144932022..144932702-chr7:1569907..1570774,2	Hela-S3	cervix:
14	chr1:144912685..144914252-chr1:144947438..144950034,2	K562	blood:
15	chr1:144925057..144927728-chr1:145381929..145384283,2	MCF-7	breast:
16	chr1:144932935..144935038-chr1:144937428..144939924,3	K562	blood:
17	chr1:144929958..144931521-chr17:48748229..48750387,2	MCF-7	breast:
18	chr1:144895341..144897404-chr1:144905462..144906982,2	MCF-7	breast:
19	chr1:144929981..144935077-chr1:145095230..145100493,10	MCF-7	breast:
20	chr1:144911399..144913167-chr1:144914593..144916227,2	MCF-7	breast:
21	chr1:144938723..144940543-chr1:144954443..144955999,2	K562	blood:
22	chr1:144922144..144925989-chr1:144935346..144938648,3	K562	blood:
23	chr1:144932935..144935038-chr1:144937428..144939924,3	K562	blood:
24	chr1:144931832..144934351-chr1:145043528..145045220,3	K562	blood:
25	chr1:144928885..144930474-chr1:144935425..144937244,2	K562	blood:
26	chr1:144906087..144908086-chr1:144911253..144912912,2	K562	blood:
27	chr1:144941413..144943372-chr1:144947098..144949301,2	MCF-7	breast:
28	chr1:144928277..144930324-chr1:145037550..145040548,2	MCF-7	breast:
29	chr1:144911399..144913167-chr1:144914593..144916227,2	MCF-7	breast:
30	chr1:144890884..144894068-chr1:146500995..146504405,3	K562	blood:
31	chr1:144930600..144932534-chr1:145038038..145040681,2	MCF-7	breast:
32	chr1:144932519..144933068-chr1:144989004..144989890,2	MCF-7	breast:
33	chr1:144913721..144916057-chr1:144919209..144920985,3	K562	blood:
34	chr1:144932649..144934258-chr15:98503922..98505541,2	MCF-7	breast:
35	chr1:144931917..144932538-chr1:144989172..144989676,2	MCF-7	breast:
36	chr1:144930907..144932689-chr1:144940117..144941761,2	K562	blood:
37	chr1:144929876..144935601-chr1:144987785..144996108,12	MCF-7	breast:
38	chr1:144893446..144895237-chr1:144930953..144933183,2	MCF-7	breast:
39	chr1:144892597..144895392-chr11:118795022..118797131,2	MCF-7	breast:
40	chr1:144935354..144938295-chr1:144938460..144940081,2	K562	blood:
41	chr1:144895504..144897115-chr1:144905432..144907751,3	K562	blood:
42	chr1:144935150..144939379-chr1:144940271..144942978,9	K562	blood:
43	chr1:144932256..144932802-chr2:8821849..8822771,2	HCT-116	colon:
44	chr1:144934397..144936617-chr1:145058068..145059656,2	MCF-7	breast:
45	chr1:144920944..144925051-chr1:144925584..144929146,5	K562	blood:
46	chr1:144891214..144893695-chr1:144896100..144898968,2	MCF-7	breast:
47	chr1:144923562..144926497-chr1:145006728..145009314,2	MCF-7	breast:
48	chr1:144887488..144889062-chr1:144895977..144898603,2	MCF-7	breast:
49	chr1:144912771..144915909-chr1:144922533..144924963,5	MCF-7	breast:
50	chr1:144937739..144940161-chr1:145039312..145041037,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-8	chr1:144940359-144940515	NONHSAT005866
2	lnc-POLR3GL-8	chr1:144941080-144941367	NONHSAT005866
3	lnc-POLR3GL-8	chr1:144940123-144940515	NONHSAT005865
4	lnc-POLR3GL-8	chr1:144941080-144941374	NONHSAT005865
5	lnc-POLR3GL-8	chr1:144940612-144940760	NONHSAT005866
6	lnc-POLR3GL-8	chr1:144941764-144941802	NONHSAT005865

No data

Variant related genes	Relation type
PDE4DIP	TF binding region
RNU2-38P	TF binding region
PDE4DIP	CpG island
RNU2-38P	CpG island
ENSG00000272755	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000110375	chromatin interactions
ENSG00000140450	chromatin interactions
ENSG00000269900	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000241721	chromatin interactions
ENSG00000159884	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000222788	chromatin interactions
ENSG00000186174	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000198517	chromatin interactions
ENSG00000235092	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000115738	chromatin interactions
ENSG00000117289	chromatin interactions
ENSG00000108846	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 3302 )
Associated
traits (count: 168 )

Variant overlapped rSNPs/rCNVs (count:3302 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2653711	chr1:144889465-144889466	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587753499	chr1:144889532-144889533	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587626629	chr1:144889560-144889561	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587681880	chr1:144889782-144889783	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1698716	chr1:144889822-144889823	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587626809	chr1:144889865-144889866	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs202231845	chr1:144889866-144889867	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs67693649	chr1:144889868-144889869	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77068851	chr1:144889869-144889870	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141467176	chr1:144889873-144889874	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs67708546	chr1:144889874-144889875	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149038323	chr1:144889875-144889876	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs74226797	chr1:144889877-144889878	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587756761	chr1:144889931-144889932	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587640348	chr1:144889972-144889973	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200970584	chr1:144889974-144889975	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587751287	chr1:144889992-144889993	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587671143	chr1:144890107-144890108	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587745128	chr1:144890133-144890134	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377525523	chr1:144890173-144890174	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587731881	chr1:144890197-144890198	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1698715	chr1:144890211-144890212	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2762879	chr1:144890258-144890259	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs587629609	chr1:144890262-144890263	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587662063	chr1:144890264-144890265	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587742087	chr1:144890277-144890278	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78000995	chr1:144890279-144890280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2762880	chr1:144890347-144890348	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587599560	chr1:144890424-144890425	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587679979	chr1:144890432-144890433	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587730144	chr1:144890471-144890472	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587612019	chr1:144890478-144890479	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587671520	chr1:144890529-144890530	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs587730443	chr1:144890541-144890542	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376567043	chr1:144890655-144890656	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587683471	chr1:144890716-144890717	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587741565	chr1:144890725-144890726	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587611765	chr1:144890755-144890756	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587694482	chr1:144890765-144890766	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371479159	chr1:144890793-144890794	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587675088	chr1:144890811-144890812	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11447	chr1:144890833-144890834	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587709394	chr1:144890844-144890845	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370664186	chr1:144890970-144890971	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587666271	chr1:144890975-144890976	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587720178	chr1:144890998-144890999	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587602350	chr1:144891003-144891004	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587649497	chr1:144891061-144891062	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76879485	chr1:144891147-144891148	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190187032	chr1:144891216-144891217	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:168)

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
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	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
Breast cancer	17142309	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
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Autism	20858243	CNVD

Chromatin state (count:3449 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144850000-144894000	Strong transcription	Stomach Smooth Muscle	stomach
2	chr1:144850400-144894200	Strong transcription	Brain Germinal Matrix	brain
3	chr1:144852200-144913200	Weak transcription	Stomach Mucosa	stomach
4	chr1:144868600-144892400	Weak transcription	Fetal Thymus	thymus
5	chr1:144869400-144905000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:144874600-144901600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:144874800-144906600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:144875000-144891400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:144875000-144893600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:144875000-144911000	Weak transcription	Thymus	Thymus
11	chr1:144876800-144892400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:144877000-144890200	Weak transcription	Small Intestine	intestine
13	chr1:144877400-144902200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:144881000-144891800	Weak transcription	Colon Smooth Muscle	Colon
15	chr1:144881200-144890800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:144881400-144890600	Weak transcription	Fetal Lung	lung
17	chr1:144881400-144891000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr1:144881400-144904800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:144882000-144892600	Weak transcription	HepG2	liver
20	chr1:144882600-144891800	Weak transcription	Pancreas	Pancrea
21	chr1:144883000-144890000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr1:144883000-144890200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:144883000-144890200	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr1:144883000-144890400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr1:144883000-144891800	Weak transcription	Spleen	Spleen
26	chr1:144883000-144892400	Weak transcription	Esophagus	oesophagus
27	chr1:144883000-144893200	Weak transcription	Fetal Intestine Small	intestine
28	chr1:144883000-144902600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr1:144883000-144902800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:144883000-144911600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:144883200-144890000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:144883200-144890200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:144883200-144890200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:144883200-144890800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr1:144883200-144891000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:144883200-144891800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr1:144883200-144902600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:144883600-144890400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:144883600-144892200	Weak transcription	Primary B cells from peripheral blood	blood
40	chr1:144883600-144893200	Weak transcription	Fetal Kidney	kidney
41	chr1:144884200-144892200	Weak transcription	Ovary	ovary
42	chr1:144885400-144890400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:144885800-144890400	Weak transcription	Fetal Brain Male	brain
44	chr1:144885800-144891400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
45	chr1:144886400-144890200	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr1:144886400-144890400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr1:144886400-144891200	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr1:144886600-144892400	Weak transcription	Colonic Mucosa	Colon
49	chr1:144886800-144891000	Weak transcription	Fetal Intestine Large	intestine
50	chr1:144887000-144890000	Weak transcription	Fetal Stomach	stomach

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