Variant report

Variant	nsv980286
Chromosome Location	chr4:3579270-3636820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:794)
Chromatin interactive
region (count:35)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:3622207-3622400	K562	blood:	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	BACH1	chr4:3591953-3592306	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr4:3590653-3590888	GM12878	blood:	n/a	n/a
6	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:3592078-3592121	K562	blood:	n/a	n/a
8	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
9	BHLHE40	chr4:3587360-3587604	K562	blood:	n/a	n/a
10	BHLHE40	chr4:3586629-3586990	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
12	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
13	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
14	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
15	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:3608709-3609077	Hela-S3	cervix:	n/a	chr4:3608890-3608901
19	CEBPB	chr4:3592195-3592197	K562	blood:	n/a	n/a
20	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
21	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
22	CEBPB	chr4:3608707-3609063	HepG2	liver:	n/a	chr4:3608890-3608901
23	CEBPB	chr4:3608606-3609111	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
24	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
25	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
26	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
27	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
28	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
29	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
30	CEBPB	chr4:3608675-3609108	MCF-7	breast:	n/a	chr4:3608890-3608901
31	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
32	CEBPB	chr4:3608726-3609020	A549	lung:	n/a	chr4:3608890-3608901
33	CEBPB	chr4:3621234-3621287	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPD	chr4:3608662-3609107	K562	blood:	n/a	n/a
36	CEBPZ	chr4:3610104-3610260	HepG2	liver:	n/a	n/a
37	CHD2	chr4:3606516-3606589	HepG2	liver:	n/a	n/a
38	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
39	CHD2	chr4:3605527-3605779	HepG2	liver:	n/a	n/a
40	CHD2	chr4:3608550-3608560	GM12878	blood:	n/a	n/a
41	CTCF	chr4:3582500-3582650	BE2_C	brain:	n/a	n/a
42	CTCF	chr4:3621580-3621730	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr4:3615609-3615624	GM19239	blood:	n/a	n/a
44	CTCF	chr4:3597445-3597577	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr4:3592339-3592356	K562	blood:	n/a	n/a
46	CTCF	chr4:3609840-3609990	Caco-2	colon:	n/a	n/a
47	CTCF	chr4:3597640-3597790	K562	blood:	n/a	n/a
48	CTCF	chr4:3592320-3592470	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr4:3602420-3602509	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr4:3614701-3614781	NHEK	skin:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3597580-3597630	H1-hESC	embryonic stem cell:	embryo
2	chr4:3597580-3597630	H1-hESC	embryonic stem cell:	embryo
3	chr4:3597859-3597909	HCT-116	colon:	n/a
4	chr4:3616829-3616879	HRCEpiC	kidney:	n/a
5	chr4:3597859-3597909	HEK293	kidney:	embryo
6	chr4:3591216-3591266	HCPEpiC	choroid plexus:	n/a
7	chr4:3617256-3617306	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:3616829-3616879	ECC-1	luminal epithelium:	n/a
9	chr4:3617603-3617653	SAEC	small airway:	n/a
10	chr4:3630603-3630653	HAEpiC	amniotic membrane:	n/a
11	chr4:3617888-3617938	HAEpiC	amniotic membrane:	n/a
12	chr4:3591243-3591293	RPTEC	kidney:	n/a
13	chr4:3616829-3616879	AG04450	lung:	fetal
14	chr4:3616829-3616879	HEK293	kidney:	embryo
15	chr4:3616943-3616993	HEK293	kidney:	embryo
16	chr4:3597859-3597909	GM12892	blood:	n/a
17	chr4:3591253-3591303	AG09309	skin:	n/a
18	chr4:3597580-3597630	BE2_C	brain:	n/a
19	chr4:3591253-3591303	HepG2	liver:	n/a
20	chr4:3591253-3591303	ECC-1	luminal epithelium:	n/a
21	chr4:3630746-3630796	MCF-7	breast:	n/a
22	chr4:3591216-3591266	U87	brain:	n/a
23	chr4:3630603-3630653	MCF10A-Er-Src	breast:	n/a
24	chr4:3591243-3591293	ECC-1	luminal epithelium:	n/a
25	chr4:3630746-3630796	NHDF-neo	bronchial:	n/a
26	chr4:3591243-3591293	AG10803	skin:	n/a
27	chr4:3617888-3617938	NT2-D1	testis:	n/a
28	chr4:3630603-3630653	PFSK-1	brain:	n/a
29	chr4:3597580-3597630	AG10803	skin:	n/a
30	chr4:3617603-3617653	GM19239	blood:	n/a
31	chr4:3617888-3617938	CMK	blood:	n/a
32	chr4:3617888-3617938	PANC-1	pancreas:	n/a
33	chr4:3616943-3616993	SKMC	muscle:	n/a
34	chr4:3591253-3591303	NHBE	bronchial:	n/a
35	chr4:3616943-3616993	H1-hESC	embryonic stem cell:	embryo
36	chr4:3591216-3591266	HCM	heart:	n/a
37	chr4:3591253-3591303	U87	brain:	n/a
38	chr4:3591243-3591293	SK-N-MC	brain:	n/a
39	chr4:3617256-3617306	BJ	skin:	n/a
40	chr4:3597739-3597789	IMR90	lung:	fetal
41	chr4:3616943-3616993	MCF10A-Er-Src	breast:	n/a
42	chr4:3617256-3617306	AoSMC	blood vessel:	n/a
43	chr4:3630746-3630796	NB4	blood:	n/a
44	chr4:3616829-3616879	A549	lung:	n/a
45	chr4:3617888-3617938	ovcar-3	ovarian:	n/a
46	chr4:3617603-3617653	Jurkat	blood:	n/a
47	chr4:3597580-3597630	T-47D	breast:	n/a
48	chr4:3616829-3616879	HCPEpiC	choroid plexus:	n/a
49	chr4:3630603-3630653	U87	brain:	n/a
50	chr4:3617256-3617306	Hela-S3	cervix:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
2	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
3	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
4	chr4:3533888..3535501-chr4:3581402..3583969,2	MCF-7	breast:
5	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
6	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
7	chr4:3576753..3579179-chr4:3579407..3585070,6	K562	blood:
8	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
9	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
10	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
11	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
12	chr4:3577226..3578815-chr4:3583775..3586576,2	K562	blood:
13	chr12:94805847..94806347-chr4:3589447..3589978,2	K562	blood:
14	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
15	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
16	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
17	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
18	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
19	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
20	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
21	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
22	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
23	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
24	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
25	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
26	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
27	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
28	chr4:3597398..3599572-chr4:3602811..3604906,3	K562	blood:
29	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
30	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
31	chr4:3532636..3535397-chr4:3592609..3595369,2	K562	blood:
32	chr4:3596211..3598668-chr4:3781245..3783965,2	K562	blood:
33	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
34	chr4:3589181..3591433-chr4:3604474..3606067,2	MCF-7	breast:
35	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP3-368B9.1.1-1	chr4:3589778-3589914	XLOC_003428
2	lnc-RP3-368B9.1.1-1	chr4:3590661-3590741	XLOC_003428
3	lnc-RP3-368B9.1.1-1	chr4:3590661-3592166	XLOC_003428
4	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
5	lnc-RP3-368B9.1.1-1	chr4:3591991-3592438	XLOC_003428
6	lnc-RP3-368B9.1.1-1	chr4:3590661-3592712	NR_040045
7	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	NR_040045
8	lnc-RP3-368B9.1.1-1	chr4:3589602-3589777	XLOC_003428
9	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890
10	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
11	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429

No data

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250681	CpG island
ENSG00000173588	chromatin interactions
ENSG00000250681	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000184160	chromatin interactions
TMEM2	miRNA target sites

Extended variants
information (count: 4276 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4276 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573829744	chr4:3579318-3579319	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs113313979	chr4:3579323-3579324	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371382653	chr4:3579326-3579327	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11727990	chr4:3579335-3579336	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542689893	chr4:3579366-3579367	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186300718	chr4:3579372-3579373	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552966821	chr4:3579374-3579375	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572980297	chr4:3579399-3579400	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs10805020	chr4:3579415-3579416	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs114918772	chr4:3579416-3579417	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs10805021	chr4:3579443-3579444	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376150207	chr4:3579450-3579451	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576373780	chr4:3579451-3579452	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548066199	chr4:3579454-3579455	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs202128885	chr4:3579517-3579518	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs113745273	chr4:3579518-3579519	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112856204	chr4:3579519-3579520	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs189151671	chr4:3579529-3579530	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367955290	chr4:3579534-3579535	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10755160	chr4:3579543-3579544	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs10805022	chr4:3579557-3579558	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565353718	chr4:3579597-3579598	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142395957	chr4:3579604-3579605	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs531170606	chr4:3579619-3579620	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544457640	chr4:3579643-3579644	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs72271135	chr4:3579657-3579658	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79392818	chr4:3579659-3579660	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs398106929	chr4:3579660-3579661	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35608583	chr4:3579666-3579667	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561673169	chr4:3579687-3579688	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs7377658	chr4:3579753-3579754	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7377227	chr4:3579757-3579758	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7377228	chr4:3579773-3579774	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530319647	chr4:3579792-3579793	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs374245544	chr4:3579823-3579824	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546598740	chr4:3579830-3579831	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566481540	chr4:3579839-3579840	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181492060	chr4:3579853-3579854	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs74541279	chr4:3579854-3579855	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1188593	chr4:3579881-3579882	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111758626	chr4:3579891-3579892	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35319876	chr4:3579929-3579930	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569235122	chr4:3579932-3579933	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs537276535	chr4:3579939-3579940	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs77551522	chr4:3579944-3579945	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556871906	chr4:3579956-3579957	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567563167	chr4:3579967-3579968	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536506997	chr4:3579975-3579976	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs73086964	chr4:3579979-3579980	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553028097	chr4:3579984-3579985	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3550600-3580400	Weak transcription	Right Atrium	heart
2	chr4:3573000-3580200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:3576000-3579600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:3576600-3580200	Weak transcription	Gastric	stomach
5	chr4:3578600-3579400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:3578600-3579400	Enhancers	HepG2	liver
7	chr4:3578600-3579600	Flanking Active TSS	Fetal Intestine Small	intestine
8	chr4:3578800-3579400	Active TSS	Duodenum Mucosa	Duodenum
9	chr4:3578800-3579400	Bivalent Enhancer	Right Ventricle	heart
10	chr4:3579000-3579600	Active TSS	Fetal Intestine Large	intestine
11	chr4:3579400-3580000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:3579400-3582200	Weak transcription	HepG2	liver
13	chr4:3579600-3580400	ZNF genes & repeats	Fetal Intestine Large	intestine
14	chr4:3579600-3580600	Enhancers	Fetal Intestine Small	intestine
15	chr4:3579600-3580800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:3580000-3580600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
17	chr4:3580200-3580600	ZNF genes & repeats	Gastric	stomach
18	chr4:3580400-3582600	Weak transcription	Fetal Intestine Large	intestine
19	chr4:3580600-3582400	Weak transcription	Fetal Intestine Small	intestine
20	chr4:3580800-3581000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:3580800-3581000	Bivalent Enhancer	HSMMtube	muscle
22	chr4:3581000-3582600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:3582200-3582800	Enhancers	HepG2	liver
24	chr4:3582400-3583200	ZNF genes & repeats	Brain Germinal Matrix	brain
25	chr4:3582400-3583400	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr4:3582600-3583000	ZNF genes & repeats	Pancreas	Pancrea
27	chr4:3582600-3583200	Enhancers	Fetal Brain Male	brain
28	chr4:3582600-3583200	ZNF genes & repeats	Fetal Intestine Large	intestine
29	chr4:3582600-3584200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:3582800-3583400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
31	chr4:3582800-3583600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr4:3582800-3583600	Flanking Active TSS	HepG2	liver
33	chr4:3583000-3583200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
34	chr4:3583600-3584000	Enhancers	HepG2	liver
35	chr4:3584000-3585800	Weak transcription	HepG2	liver
36	chr4:3584200-3586200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:3584400-3584800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
38	chr4:3584600-3584800	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr4:3584800-3586000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr4:3585800-3588400	Enhancers	HepG2	liver
41	chr4:3586000-3586200	Enhancers	Duodenum Mucosa	Duodenum
42	chr4:3586000-3587000	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr4:3586200-3586400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:3586200-3586400	Enhancers	Gastric	stomach
45	chr4:3586200-3586400	ZNF genes & repeats	Pancreas	Pancrea
46	chr4:3586200-3586400	Enhancers	Small Intestine	intestine
47	chr4:3586200-3586600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr4:3586200-3586600	Enhancers	Stomach Mucosa	stomach
49	chr4:3586200-3587000	Enhancers	Liver	Liver
50	chr4:3586400-3587400	Weak transcription	Gastric	stomach

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