Variant report

Variant	nsv881766
Chromosome Location	chr5:68401941-68448694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:123)
Chromatin interactive
region (count:30)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:68405855-68406032	K562	blood:	n/a	n/a
2	ARID3A	chr5:68402081-68402382	K562	blood:	n/a	n/a
3	ATF1	chr5:68447672-68447684	K562	blood:	n/a	n/a
4	ATF1	chr5:68402131-68402440	K562	blood:	n/a	n/a
5	ATF2	chr5:68401979-68402425	GM12878	blood:	n/a	n/a
6	BACH1	chr5:68425609-68425613	K562	blood:	n/a	n/a
7	BATF	chr5:68402110-68402482	GM12878	blood:	n/a	n/a
8	BATF	chr5:68402148-68402413	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:68432184-68432591	GM12878	blood:	n/a	n/a
10	CBX3	chr5:68436659-68437094	HCT-116	colon:	n/a	n/a
11	CBX3	chr5:68436703-68436962	K562	blood:	n/a	n/a
12	CCNT2	chr5:68401601-68402223	K562	blood:	n/a	n/a
13	CEBPB	chr5:68425630-68425805	K562	blood:	n/a	n/a
14	CEBPB	chr5:68402200-68402387	K562	blood:	n/a	n/a
15	CEBPB	chr5:68402081-68402445	K562	blood:	n/a	n/a
16	CEBPB	chr5:68411386-68411713	A549	lung:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
17	CEBPB	chr5:68411415-68411643	H1-hESC	embryonic stem cell:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
18	CEBPB	chr5:68411376-68411712	HepG2	liver:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
19	CEBPB	chr5:68411441-68411639	Hela-S3	cervix:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
20	CEBPB	chr5:68426013-68426509	A549	lung:	n/a	n/a
21	CEBPB	chr5:68411363-68411728	IMR90	lung:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
22	CEBPB	chr5:68425257-68425766	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:68440713-68440836	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:68425208-68425740	A549	lung:	n/a	n/a
25	CEBPB	chr5:68425190-68425786	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:68411389-68411734	K562	blood:	n/a	chr5:68411549-68411558 chr5:68411547-68411558
27	CEBPB	chr5:68425255-68425691	A549	lung:	n/a	n/a
28	CEBPB	chr5:68426221-68426404	A549	lung:	n/a	n/a
29	CTCF	chr5:68417669-68417686	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:68402342-68402355	K562	blood:	n/a	n/a
31	CTCF	chr5:68416077-68416094	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:68445220-68445370	HepG2	liver:	n/a	n/a
33	CUX1	chr5:68402005-68402408	K562	blood:	n/a	n/a
34	E2F4	chr5:68425455-68425564	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr5:68432150-68432327	GM12878	blood:	n/a	chr5:68432195-68432206
36	EBF1	chr5:68432346-68432543	GM12878	blood:	n/a	n/a
37	EBF1	chr5:68432031-68432485	GM12878	blood:	n/a	chr5:68432195-68432206
38	EBF1	chr5:68432040-68432605	GM12878	blood:	n/a	chr5:68432195-68432206
39	EP300	chr5:68402129-68402492	GM12878	blood:	n/a	chr5:68402251-68402260
40	EP300	chr5:68419308-68419477	K562	blood:	n/a	n/a
41	EP300	chr5:68432089-68432529	GM12878	blood:	n/a	n/a
42	EP300	chr5:68425175-68425661	A549	lung:	n/a	n/a
43	EP300	chr5:68402229-68402355	K562	blood:	n/a	chr5:68402251-68402260
44	FOS	chr5:68425298-68425639	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr5:68425294-68425657	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:68411436-68411715	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr5:68418746-68418841	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr5:68411406-68411706	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr5:68411409-68411776	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:68425333-68425678	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68425189-68425239	MCF10A-Er-Src	breast:	n/a
2	chr5:68425189-68425239	MCF10A-Er-Src	breast:	n/a
3	chr5:68425189-68425239	SK-N-SH	brain:	n/a
4	chr5:68425189-68425239	IMR90	lung:	fetal
5	chr5:68425189-68425239	HRPEpiC	eye:	n/a
6	chr5:68431589-68431639	GM12878	blood:	n/a
7	chr5:68425189-68425239	HUVEC	blood vessel:	n/a
8	chr5:68425189-68425239	AoSMC	blood vessel:	n/a
9	chr5:68431589-68431639	AG04450	lung:	fetal
10	chr5:68425189-68425239	SK-N-MC	brain:	n/a
11	chr5:68425189-68425239	HCM	heart:	n/a
12	chr5:68431589-68431639	Caco-2	colon:	n/a
13	chr5:68431589-68431639	U87	brain:	n/a
14	chr5:68425189-68425239	SKMC	muscle:	n/a
15	chr5:68425189-68425239	ProgFib	skin:	n/a
16	chr5:68431589-68431639	NHBE	bronchial:	n/a
17	chr5:68425189-68425239	GM19239	blood:	n/a
18	chr5:68431589-68431639	LNCaP	prostate:	n/a
19	chr5:68425189-68425239	AG09319	gingival:	n/a
20	chr5:68425189-68425239	HEEpiC	esophagus:	n/a
21	chr5:68425189-68425239	SAEC	small airway:	n/a
22	chr5:68425189-68425239	PANC-1	pancreas:	n/a
23	chr5:68431589-68431639	MCF-7	breast:	n/a
24	chr5:68431589-68431639	GM12892	blood:	n/a
25	chr5:68425189-68425239	GM12878	blood:	n/a
26	chr5:68425189-68425239	Hepatocyte	liver:	n/a
27	chr5:68431589-68431639	HepG2	liver:	n/a
28	chr5:68425189-68425239	HCT-116	colon:	n/a
29	chr5:68425189-68425239	AG09309	skin:	n/a
30	chr5:68431589-68431639	ECC-1	luminal epithelium:	n/a
31	chr5:68425189-68425239	AG10803	skin:	n/a
32	chr5:68425189-68425239	MCF-7	breast:	n/a
33	chr5:68431589-68431639	RPTEC	kidney:	n/a
34	chr5:68425189-68425239	ovcar-3	ovarian:	n/a
35	chr5:68431589-68431639	AG10803	skin:	n/a
36	chr5:68431589-68431639	NH-A	brain:	n/a
37	chr5:68431589-68431639	ProgFib	skin:	n/a
38	chr5:68431589-68431639	PrEC	prostate:	n/a
39	chr5:68431589-68431639	SAEC	small airway:	n/a
40	chr5:68425189-68425239	HL-60	blood:	n/a
41	chr5:68431589-68431639	GM19239	blood:	n/a
42	chr5:68431589-68431639	GM12891	blood:	n/a
43	chr5:68425189-68425239	NHDF-neo	bronchial:	n/a
44	chr5:68425189-68425239	BE2_C	brain:	n/a
45	chr5:68431589-68431639	HIPEpiC	eye:	n/a
46	chr5:68425189-68425239	HMEC	breast:	n/a
47	chr5:68431589-68431639	PFSK-1	brain:	n/a
48	chr5:68431589-68431639	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:68425189-68425239	GM12892	blood:	n/a
50	chr5:68431589-68431639	HEEpiC	esophagus:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68400088..68402437-chr5:68472699..68475072,2	K562	blood:
2	chr5:68389331..68393521-chr5:68397846..68403936,9	K562	blood:
3	chr5:68440313..68440824-chr8:141846436..141847092,2	MCF-7	breast:
4	chr5:68407951..68409881-chr5:68417199..68419048,3	K562	blood:
5	chr5:68407951..68409881-chr5:68417199..68419048,3	K562	blood:
6	chr5:68407951..68409711-chr5:68417199..68419048,2	K562	blood:
7	chr5:68400690..68402320-chr5:68488616..68490544,2	K562	blood:
8	chr5:68388225..68391847-chr5:68400422..68403677,3	MCF-7	breast:
9	chr5:68406324..68407918-chr5:68411033..68412631,2	K562	blood:
10	chr5:68413764..68415573-chr5:68416370..68418501,2	MCF-7	breast:
11	chr5:68416264..68417845-chr5:68422518..68425156,2	K562	blood:
12	chr5:68416264..68417845-chr5:68422518..68425156,2	K562	blood:
13	chr5:68402335..68404943-chr5:68424563..68427049,2	K562	blood:
14	chr5:68402335..68404943-chr5:68424563..68427049,2	K562	blood:
15	chr5:68446696..68449610-chr5:68457555..68460307,2	MCF-7	breast:
16	chr5:68394864..68397048-chr5:68401666..68403726,2	MCF-7	breast:
17	chr5:68410842..68413494-chr5:68417164..68418893,2	MCF-7	breast:
18	chr5:68442716..68444754-chr5:68449777..68451574,2	K562	blood:
19	chr5:68407951..68409711-chr5:68417199..68419048,2	K562	blood:
20	chr5:68431059..68433417-chr5:68453828..68456749,2	K562	blood:
21	chr5:68400479..68402854-chr5:68409637..68411171,2	MCF-7	breast:
22	chr5:68402227..68404179-chr5:68627103..68628743,2	MCF-7	breast:
23	chr5:68400479..68402854-chr5:68409637..68411171,2	MCF-7	breast:
24	chr5:68398171..68400473-chr5:68404244..68405792,2	K562	blood:
25	chr5:68424217..68426251-chr5:68431451..68433521,2	K562	blood:
26	chr5:68414032..68415957-chr5:68420239..68422360,2	K562	blood:
27	chr5:68406324..68407918-chr5:68411033..68412631,2	K562	blood:
28	chr5:68397308..68403256-chr5:68407006..68412772,7	K562	blood:
29	chr5:68392345..68395131-chr5:68404844..68408147,4	K562	blood:
30	chr5:68337237..68339052-chr5:68416019..68418711,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC125-2	chr5:68431978-68432221	ENSG00000248664.1
2	lnc-CCDC125-2	chr5:68423861-68423935	ENSG00000248664.1
3	lnc-CCDC125-2	chr5:68430344-68430429	ENSG00000248664.1
4	lnc-CCDC125-2	chr5:68408939-68409108	ENSG00000248664.1
5	lnc-CCDC125-2	chr5:68426170-68426372	ENSG00000248664.1
6	lnc-CCDC125-2	chr5:68430029-68430429	XLOC_004863
7	lnc-CCDC125-2	chr5:68411062-68411229	ENSG00000248664.1

No data

Variant related genes	Relation type
SLC30A5	TF binding region
ENSG00000248664	TF binding region
SLC30A5	CpG island
ENSG00000248664	CpG island
ENSG00000183323	chromatin interactions
ENSG00000220986	chromatin interactions
ENSG00000145740	chromatin interactions
ENSG00000248664	chromatin interactions
ENSG00000265968	chromatin interactions
ENSG00000134057	chromatin interactions
DNAJC1	miRNA target sites

Extended variants
information (count: 1791 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1791 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4976217	chr5:68401941-68401942	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533148903	chr5:68401955-68401956	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs74740247	chr5:68401979-68401980	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs181613379	chr5:68402029-68402030	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185985520	chr5:68402071-68402072	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554902070	chr5:68402078-68402079	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190054413	chr5:68402084-68402085	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs116368379	chr5:68402094-68402095	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs183203632	chr5:68402120-68402121	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs115085142	chr5:68402153-68402154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565802606	chr5:68402170-68402171	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs143657930	chr5:68402214-68402215	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557782445	chr5:68402221-68402222	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs75177629	chr5:68402239-68402240	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs10434546	chr5:68402266-68402267	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs449607	chr5:68402269-68402270	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574256673	chr5:68402326-68402327	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs552342176	chr5:68402329-68402330	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs541674069	chr5:68402378-68402379	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs139658266	chr5:68402382-68402383	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs533505136	chr5:68402397-68402398	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs540912731	chr5:68402401-68402402	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs545069147	chr5:68402481-68402482	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375594725	chr5:68402498-68402499	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs10434547	chr5:68402500-68402501	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530830860	chr5:68402502-68402503	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549638825	chr5:68402527-68402528	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs35884229	chr5:68402578-68402579	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576920273	chr5:68402659-68402660	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs187676788	chr5:68402744-68402745	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149746457	chr5:68402750-68402751	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs34695098	chr5:68402757-68402758	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539473927	chr5:68402832-68402833	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551196134	chr5:68402842-68402843	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569634676	chr5:68402845-68402846	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190807981	chr5:68402932-68402933	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs34332682	chr5:68402949-68402950	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs556073764	chr5:68402972-68402973	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537526429	chr5:68403025-68403026	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs574417941	chr5:68403105-68403106	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs144579921	chr5:68403184-68403185	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556138488	chr5:68403192-68403193	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574063541	chr5:68403205-68403206	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs578111328	chr5:68403220-68403221	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140032605	chr5:68403271-68403272	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568737921	chr5:68403290-68403291	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs183909004	chr5:68403329-68403330	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143544250	chr5:68403343-68403344	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575214811	chr5:68403349-68403350	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs542649754	chr5:68403368-68403369	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:1022 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68390600-68405600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:68390800-68405200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:68391000-68402800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr5:68391000-68403000	Weak transcription	HSMMtube	muscle
5	chr5:68391000-68415200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr5:68391200-68402600	Weak transcription	Brain Hippocampus Middle	brain
7	chr5:68391200-68405600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:68391200-68405600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr5:68391200-68405600	Weak transcription	Psoas Muscle	Psoas
10	chr5:68391400-68402000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:68391400-68402600	Weak transcription	Brain Substantia Nigra	brain
12	chr5:68391400-68415800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:68391400-68428800	Weak transcription	Stomach Mucosa	stomach
14	chr5:68391400-68431200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr5:68392000-68402800	Weak transcription	NHLF	lung
16	chr5:68392200-68427000	Weak transcription	Fetal Heart	heart
17	chr5:68394200-68405200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:68395000-68419400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:68395000-68428400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:68395200-68403800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:68395200-68405800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:68395400-68402800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:68395400-68413200	Strong transcription	Duodenum Mucosa	Duodenum
24	chr5:68395600-68406400	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr5:68396200-68406200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:68396400-68405600	Weak transcription	Aorta	Aorta
27	chr5:68397400-68406400	Strong transcription	Fetal Intestine Large	intestine
28	chr5:68397400-68425000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr5:68397400-68426400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:68397600-68425000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:68397800-68406800	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr5:68398000-68404800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:68398600-68427400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr5:68398800-68403200	Strong transcription	Placenta Amnion	Placenta Amnion
35	chr5:68398800-68403800	Strong transcription	Dnd41	blood
36	chr5:68398800-68404200	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr5:68398800-68404600	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr5:68398800-68404800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:68398800-68413400	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr5:68398800-68426000	Strong transcription	Adipose Nuclei	Adipose
41	chr5:68399000-68403400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:68399000-68405600	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:68399000-68405600	Strong transcription	Liver	Liver
44	chr5:68399000-68406000	Strong transcription	Brain Germinal Matrix	brain
45	chr5:68399000-68406200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr5:68399000-68406200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr5:68399000-68406200	Strong transcription	HSMM	muscle
48	chr5:68399000-68406400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr5:68399000-68406600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:68399000-68406800	Strong transcription	Primary T helper cells PMA-I stimulated	--

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