Variant report

Variant	nsv967720
Chromosome Location	chr4:3535969-3614204
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:904)
CpG islands
(count:1954)
Chromatin interactive
region (count:26)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:3591953-3592306	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:3591938-3592292	K562	blood:	n/a	n/a
3	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:3570059-3570293	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:3538736-3538904	GM12878	blood:	n/a	n/a
6	BCL3	chr4:3590653-3590888	GM12878	blood:	n/a	n/a
7	BCL3	chr4:3565347-3565556	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:3558966-3559121	K562	blood:	n/a	n/a
9	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:3561241-3561607	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:3576432-3576518	K562	blood:	n/a	n/a
12	BHLHE40	chr4:3565199-3565519	K562	blood:	n/a	n/a
13	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3558900-3559131	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3592078-3592121	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
18	BRCA1	chr4:3578147-3578290	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:3576365-3576373	HepG2	liver:	n/a	n/a
20	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
21	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
23	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
24	CEBPB	chr4:3608707-3609063	HepG2	liver:	n/a	chr4:3608890-3608901
25	CEBPB	chr4:3558947-3558991	A549	lung:	n/a	chr4:3558956-3558967
26	CEBPB	chr4:3558772-3559159	HepG2	liver:	n/a	chr4:3558956-3558967
27	CEBPB	chr4:3592195-3592197	K562	blood:	n/a	n/a
28	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
29	CEBPB	chr4:3608709-3609077	Hela-S3	cervix:	n/a	chr4:3608890-3608901
30	CEBPB	chr4:3578250-3578520	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
32	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
33	CEBPB	chr4:3558850-3559034	K562	blood:	n/a	chr4:3558956-3558967
34	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
35	CEBPB	chr4:3558770-3559163	HepG2	liver:	n/a	chr4:3558956-3558967
36	CEBPB	chr4:3558808-3559129	IMR90	lung:	n/a	chr4:3558956-3558967
37	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
38	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
39	CEBPB	chr4:3551360-3551570	HepG2	liver:	n/a	chr4:3551516-3551529
40	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
41	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
43	CEBPB	chr4:3578297-3578444	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
45	CEBPB	chr4:3551405-3551575	IMR90	lung:	n/a	chr4:3551516-3551529
46	CEBPB	chr4:3551376-3551680	K562	blood:	n/a	chr4:3551516-3551529
47	CEBPB	chr4:3576042-3576167	HepG2	liver:	n/a	chr4:3576093-3576104
48	CEBPB	chr4:3551364-3551634	K562	blood:	n/a	chr4:3551516-3551529
49	CEBPB	chr4:3608606-3609111	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
50	CEBPB	chr4:3558857-3559121	K562	blood:	n/a	chr4:3558956-3558967

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3578583-3578633	MCF-7	breast:	n/a
2	chr4:3571919-3571969	ProgFib	skin:	n/a
3	chr4:3578583-3578633	MCF-7	breast:	n/a
4	chr4:3571919-3571969	ProgFib	skin:	n/a
5	chr4:3577496-3577546	PANC-1	pancreas:	n/a
6	chr4:3568034-3568084	SKMC	muscle:	n/a
7	chr4:3567958-3568008	AG10803	skin:	n/a
8	chr4:3578583-3578633	Caco-2	colon:	n/a
9	chr4:3577650-3577700	PrEC	prostate:	n/a
10	chr4:3565893-3565943	SK-N-SH	brain:	n/a
11	chr4:3577496-3577546	HRE	kidney:	n/a
12	chr4:3571857-3571907	SK-N-SH_RA	brain:	n/a
13	chr4:3536906-3536956	Hepatocyte	liver:	n/a
14	chr4:3591216-3591266	GM06990	blood:	n/a
15	chr4:3576489-3576539	H1-hESC	embryonic stem cell:	embryo
16	chr4:3567533-3567583	HL-60	blood:	n/a
17	chr4:3569189-3569239	AG04449	skin:	fetal
18	chr4:3567958-3568008	K562	blood:	n/a
19	chr4:3568034-3568084	HEEpiC	esophagus:	n/a
20	chr4:3568034-3568084	HNPCEpiC	eye:	n/a
21	chr4:3565893-3565943	AoSMC	blood vessel:	n/a
22	chr4:3536906-3536956	BE2_C	brain:	n/a
23	chr4:3569189-3569239	AG04450	lung:	fetal
24	chr4:3565646-3565696	HCM	heart:	n/a
25	chr4:3568236-3568286	NB4	blood:	n/a
26	chr4:3577496-3577546	Caco-2	colon:	n/a
27	chr4:3591216-3591266	BJ	skin:	n/a
28	chr4:3563357-3563407	SK-N-SH_RA	brain:	n/a
29	chr4:3577496-3577546	SK-N-MC	brain:	n/a
30	chr4:3577496-3577546	BE2_C	brain:	n/a
31	chr4:3571527-3571577	PrEC	prostate:	n/a
32	chr4:3578432-3578482	AG10803	skin:	n/a
33	chr4:3567670-3567720	AG09319	gingival:	n/a
34	chr4:3591243-3591293	GM12891	blood:	n/a
35	chr4:3566660-3566710	ovcar-3	ovarian:	n/a
36	chr4:3567958-3568008	AG04449	skin:	fetal
37	chr4:3567670-3567720	AG04450	lung:	fetal
38	chr4:3567533-3567583	NHBE	bronchial:	n/a
39	chr4:3597859-3597909	BJ	skin:	n/a
40	chr4:3567533-3567583	SK-N-SH_RA	brain:	n/a
41	chr4:3576273-3576323	BE2_C	brain:	n/a
42	chr4:3566794-3566844	GM19239	blood:	n/a
43	chr4:3568236-3568286	BJ	skin:	n/a
44	chr4:3566660-3566710	H1-hESC	embryonic stem cell:	embryo
45	chr4:3567670-3567720	Hela-S3	cervix:	n/a
46	chr4:3571919-3571969	AG09319	gingival:	n/a
47	chr4:3536906-3536956	ECC-1	luminal epithelium:	n/a
48	chr4:3578583-3578633	AG04449	skin:	fetal
49	chr4:3567445-3567495	PANC-1	pancreas:	n/a
50	chr4:3576336-3576386	HPAEpiC	pulmonary alveolar:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
2	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
3	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
4	chr4:3532686..3534345-chr4:3544776..3546772,2	MCF-7	breast:
5	chr12:94805847..94806347-chr4:3589447..3589978,2	K562	blood:
6	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
7	chr4:3576753..3579179-chr4:3579407..3585070,6	K562	blood:
8	chr4:3573176..3575691-chr4:3650301..3652396,2	MCF-7	breast:
9	chr4:3532775..3535041-chr4:3574379..3576145,2	K562	blood:
10	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
11	chr4:3485927..3488368-chr4:3533732..3536345,3	MCF-7	breast:
12	chr4:3557568..3561232-chr4:3567417..3570129,3	K562	blood:
13	chr4:3574894..3577613-chr4:3578076..3580368,2	K562	blood:
14	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
15	chr4:3596211..3598668-chr4:3781245..3783965,2	K562	blood:
16	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
17	chr4:3557568..3561232-chr4:3567417..3570129,3	K562	blood:
18	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
19	chr4:3532636..3535397-chr4:3592609..3595369,2	K562	blood:
20	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
21	chr4:3533888..3535501-chr4:3581402..3583969,2	MCF-7	breast:
22	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
23	chr4:3577226..3578815-chr4:3583775..3586576,2	K562	blood:
24	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
25	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
26	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-2	chr4:3546615-3546650	XLOC_003427
2	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428
3	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	XLOC_003427
4	lnc-RP3-368B9.1.1-2	chr4:3546282-3546650	ENSG00000270090.1
5	lnc-RP3-368B9.1.1-2	chr4:3547241-3547393	XLOC_003427
6	lnc-RP3-368B9.1.1-6	chr4:3559576-3559712	ucscGeneNc_uc003ghk_1
7	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	ENSG00000270090.1
8	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890
9	lnc-RP3-368B9.1.1-2	chr4:3546822-3546956	XLOC_003427
10	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
11	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	NR_040045
12	lnc-RP3-368B9.1.1-1	chr4:3590661-3592712	NR_040045
13	lnc-RP3-368B9.1.1-2	chr4:3547897-3548075	XLOC_003427
14	lnc-RP3-368B9.1.1-2	chr4:3546453-3546650	XLOC_003427
15	lnc-RP3-368B9.1.1-6	chr4:3561789-3562236	ucscGeneNc_uc003ghk_1
16	lnc-RP3-368B9.1.1-2	chr4:3547896-3548077	NONHSAT094884
17	lnc-RP3-368B9.1.1-2	chr4:3546433-3547467	NONHSAT094884
18	lnc-RP3-368B9.1.1-6	chr4:3560459-3560539	ucscGeneNc_uc003ghk_1
19	lnc-RP3-368B9.1.1-2	chr4:3550187-3550309	NONHSAT094884
20	lnc-RP3-368B9.1.1-1	chr4:3590661-3590741	XLOC_003428
21	lnc-RP3-368B9.1.1-2	chr4:3546666-3547063	XLOC_003427
22	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	NR_040045
23	lnc-RP3-368B9.1.1-2	chr4:3550402-3550523	XLOC_003427
24	lnc-RP3-368B9.1.1-2	chr4:3550188-3550315	ENSG00000270090.1
25	lnc-RP3-368B9.1.1-2	chr4:3547897-3548077	XLOC_003427
26	lnc-RP3-368B9.1.1-6	chr4:3548394-3548648	ucscGeneNc_uc003ghk_1
27	lnc-RP3-368B9.1.1-2	chr4:3550401-3550523	NONHSAT094884
28	lnc-RP3-368B9.1.1-1	chr4:3578596-3578850	XLOC_003428
29	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	XLOC_003428
30	lnc-RP3-368B9.1.1-1	chr4:3590661-3592166	XLOC_003428
31	lnc-RP3-368B9.1.1-1	chr4:3591991-3592438	XLOC_003428
32	lnc-RP3-368B9.1.1-2	chr4:3550188-3550309	XLOC_003427
33	lnc-RP3-368B9.1.1-1	chr4:3589778-3589914	XLOC_003428

No data

Variant related genes	Relation type
LRPAP1	TF binding region
ENSG00000270090	TF binding region
LINC00955	TF binding region
LRPAP1	CpG island
ENSG00000270090	CpG island
LINC00955	CpG island
ENSG00000175920	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000173588	chromatin interactions
TMEM2	miRNA target sites
TGFBI	miRNA target sites
TGFB2	miRNA target sites
TGFA	miRNA target sites

Extended variants
information (count: 5203 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5203 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189133058	chr4:3535994-3535995	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs193299792	chr4:3535997-3535998	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs7672287	chr4:3536002-3536003	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs558964897	chr4:3536029-3536030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528071656	chr4:3536034-3536035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368838714	chr4:3536070-3536071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563931147	chr4:3536095-3536096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2073502	chr4:3536112-3536113	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs544263291	chr4:3536118-3536119	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151134666	chr4:3536146-3536147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531024789	chr4:3536161-3536162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185471753	chr4:3536162-3536163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2073503	chr4:3536176-3536177	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs536906747	chr4:3536180-3536181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200994626	chr4:3536193-3536194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566902014	chr4:3536240-3536241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539022969	chr4:3536253-3536254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs367708522	chr4:3536265-3536266	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1794431	chr4:3536329-3536330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs10937932	chr4:3536505-3536506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189209774	chr4:3536506-3536507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374980323	chr4:3536514-3536515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369180359	chr4:3536531-3536532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573746539	chr4:3536538-3536539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181654264	chr4:3536564-3536565	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559199685	chr4:3536573-3536574	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs572539456	chr4:3536574-3536575	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs62272719	chr4:3536575-3536576	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs564658160	chr4:3536576-3536577	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs3108671	chr4:3536588-3536589	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs530579413	chr4:3536629-3536630	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550901662	chr4:3536635-3536636	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs561567910	chr4:3536637-3536638	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs530213909	chr4:3536693-3536694	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185990343	chr4:3536707-3536708	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs149890013	chr4:3536723-3536724	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs59393260	chr4:3536732-3536733	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201400261	chr4:3536823-3536824	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs375154543	chr4:3536829-3536830	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs199610860	chr4:3536830-3536831	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs552559078	chr4:3536844-3536845	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs11736573	chr4:3536882-3536883	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs76961379	chr4:3536889-3536890	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs149593055	chr4:3536895-3536896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181126540	chr4:3536942-3536943	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs373940515	chr4:3536962-3536963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144876544	chr4:3537000-3537001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186261495	chr4:3537040-3537041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376896377	chr4:3537053-3537054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190685700	chr4:3537054-3537055	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3535000-3536000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
2	chr4:3535000-3536800	Weak transcription	Lung	lung
3	chr4:3535400-3536000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:3535400-3537000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3537000-3537200	Enhancers	Lung	lung
6	chr4:3537000-3537400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:3546000-3546200	Bivalent/Poised TSS	HepG2	liver
8	chr4:3546000-3546600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr4:3546000-3546600	Enhancers	HUVEC	blood vessel
10	chr4:3546000-3546800	Enhancers	Lung	lung
11	chr4:3548400-3549200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:3548400-3549200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:3548400-3549200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr4:3548400-3550000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:3548600-3549000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:3548800-3549200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:3548800-3549400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr4:3548800-3549600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:3550600-3580400	Weak transcription	Right Atrium	heart
20	chr4:3554800-3557200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr4:3555000-3560600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr4:3555200-3555400	Enhancers	HepG2	liver
23	chr4:3555200-3558000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr4:3555600-3558200	Weak transcription	HepG2	liver
25	chr4:3555800-3556200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:3556000-3560800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr4:3556400-3556800	Enhancers	Primary B cells from cord blood	blood
28	chr4:3556800-3557000	Weak transcription	Primary B cells from cord blood	blood
29	chr4:3557000-3557400	Enhancers	Primary B cells from cord blood	blood
30	chr4:3557200-3557400	Enhancers	Spleen	Spleen
31	chr4:3557200-3557800	Bivalent Enhancer	K562	blood
32	chr4:3557200-3558400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:3557200-3559400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr4:3557400-3558000	Bivalent Enhancer	Placenta	Placenta
35	chr4:3557400-3558200	Weak transcription	Primary B cells from cord blood	blood
36	chr4:3557400-3562000	Weak transcription	Spleen	Spleen
37	chr4:3557800-3558400	Enhancers	K562	blood
38	chr4:3558000-3558400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:3558000-3559000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr4:3558200-3558600	Enhancers	Primary B cells from cord blood	blood
41	chr4:3558200-3559000	Enhancers	HepG2	liver
42	chr4:3558200-3559200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:3558400-3559000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr4:3558400-3565200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:3558600-3559400	Weak transcription	Primary B cells from cord blood	blood
46	chr4:3558800-3574600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:3559000-3560000	Flanking Active TSS	HepG2	liver
48	chr4:3559000-3560600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr4:3559000-3561400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr4:3559400-3559600	Enhancers	Primary B cells from cord blood	blood

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