Variant report

Variant	nsv462200
Chromosome Location	chr5:60135985-60266875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1827)
CpG islands
(count:2017)
Chromatin interactive
region (count:68)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1827 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
2	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
3	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
5	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
6	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
7	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
8	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
9	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
10	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
11	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
12	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
13	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
14	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
15	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:60168934-60168938	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:60139760-60140304	HepG2	liver:	n/a	chr5:60139813-60139829
21	BHLHE40	chr5:60139908-60140548	K562	blood:	n/a	n/a
22	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a
23	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
24	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
25	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
26	BHLHE40	chr5:60139857-60140324	GM12878	blood:	n/a	n/a
27	BRCA1	chr5:60242705-60242764	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr5:60139999-60140699	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
30	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
31	CBX3	chr5:60166733-60166960	K562	blood:	n/a	n/a
32	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
33	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
34	CCNT2	chr5:60148817-60149120	K562	blood:	n/a	n/a
35	CCNT2	chr5:60257762-60257798	K562	blood:	n/a	n/a
36	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
37	CCNT2	chr5:60139486-60140436	K562	blood:	n/a	n/a
38	CEBPB	chr5:60257603-60257821	MCF-7	breast:	n/a	chr5:60257738-60257749
39	CEBPB	chr5:60135974-60136156	A549	lung:	n/a	n/a
40	CEBPB	chr5:60257618-60257870	K562	blood:	n/a	chr5:60257738-60257749
41	CEBPB	chr5:60257590-60257926	HepG2	liver:	n/a	chr5:60257738-60257749
42	CEBPB	chr5:60239556-60240203	HepG2	liver:	n/a	chr5:60239733-60239744
43	CEBPB	chr5:60164990-60165291	HepG2	liver:	n/a	chr5:60165165-60165176 chr5:60165118-60165129
44	CEBPB	chr5:60168796-60169050	A549	lung:	n/a	chr5:60168912-60168923
45	CEBPB	chr5:60165087-60165233	A549	lung:	n/a	chr5:60165165-60165176 chr5:60165118-60165129
46	CEBPB	chr5:60257587-60257962	A549	lung:	n/a	chr5:60257738-60257749
47	CEBPB	chr5:60239532-60239892	K562	blood:	n/a	chr5:60239733-60239744
48	CEBPB	chr5:60151908-60152292	HepG2	liver:	n/a	chr5:60152122-60152133
49	CEBPB	chr5:60146445-60146704	HepG2	liver:	n/a	chr5:60146565-60146576
50	CEBPB	chr5:60257710-60257892	H1-hESC	embryonic stem cell:	n/a	chr5:60257738-60257749

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60187211-60187261	AoSMC	blood vessel:	n/a
2	chr5:60137757-60137807	LNCaP	prostate:	n/a
3	chr5:60139293-60139343	Hela-S3	cervix:	n/a
4	chr5:60241424-60241474	HRCEpiC	kidney:	n/a
5	chr5:60187211-60187261	AoSMC	blood vessel:	n/a
6	chr5:60137757-60137807	LNCaP	prostate:	n/a
7	chr5:60139293-60139343	Hela-S3	cervix:	n/a
8	chr5:60241424-60241474	HRCEpiC	kidney:	n/a
9	chr5:60187211-60187261	ovcar-3	ovarian:	n/a
10	chr5:60241003-60241053	HRE	kidney:	n/a
11	chr5:60240938-60240988	Hepatocyte	liver:	n/a
12	chr5:60170058-60170108	PrEC	prostate:	n/a
13	chr5:60142446-60142496	PrEC	prostate:	n/a
14	chr5:60138761-60138811	AoSMC	blood vessel:	n/a
15	chr5:60241636-60241686	GM12891	blood:	n/a
16	chr5:60240926-60240976	GM12891	blood:	n/a
17	chr5:60139938-60139988	RPTEC	kidney:	n/a
18	chr5:60240938-60240988	GM19239	blood:	n/a
19	chr5:60239580-60239630	AG09319	gingival:	n/a
20	chr5:60240568-60240618	LNCaP	prostate:	n/a
21	chr5:60241324-60241374	HAEpiC	amniotic membrane:	n/a
22	chr5:60138883-60138933	CMK	blood:	n/a
23	chr5:60141082-60141132	HNPCEpiC	eye:	n/a
24	chr5:60138761-60138811	Hepatocyte	liver:	n/a
25	chr5:60139938-60139988	HCF	heart:	n/a
26	chr5:60241428-60241478	HCF	heart:	n/a
27	chr5:60137757-60137807	Hepatocyte	liver:	n/a
28	chr5:60139420-60139470	Caco-2	colon:	n/a
29	chr5:60241428-60241478	T-47D	breast:	n/a
30	chr5:60241428-60241478	AoSMC	blood vessel:	n/a
31	chr5:60187211-60187261	HL-60	blood:	n/a
32	chr5:60240838-60240888	HRCEpiC	kidney:	n/a
33	chr5:60142446-60142496	T-47D	breast:	n/a
34	chr5:60241636-60241686	SKMC	muscle:	n/a
35	chr5:60240568-60240618	Caco-2	colon:	n/a
36	chr5:60139293-60139343	GM06990	blood:	n/a
37	chr5:60240670-60240720	IMR90	lung:	fetal
38	chr5:60240838-60240888	NB4	blood:	n/a
39	chr5:60170058-60170108	PFSK-1	brain:	n/a
40	chr5:60139938-60139988	HRE	kidney:	n/a
41	chr5:60240870-60240920	NHBE	bronchial:	n/a
42	chr5:60240926-60240976	BJ	skin:	n/a
43	chr5:60142446-60142496	NHBE	bronchial:	n/a
44	chr5:60138883-60138933	ECC-1	luminal epithelium:	n/a
45	chr5:60170058-60170108	SAEC	small airway:	n/a
46	chr5:60141082-60141132	A549	lung:	n/a
47	chr5:60241324-60241374	HUVEC	blood vessel:	n/a
48	chr5:60241019-60241069	PANC-1	pancreas:	n/a
49	chr5:60139516-60139566	SK-N-MC	brain:	n/a
50	chr5:60241324-60241374	MCF10A-Er-Src	breast:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
2	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
3	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
4	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
5	chr5:59995721..59997582-chr5:60231998..60233519,2	K562	blood:
6	chr5:60261942..60265146-chr5:60457137..60459002,3	MCF-7	breast:
7	chr5:60150200..60152775-chr5:60153410..60154990,2	MCF-7	breast:
8	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
9	chr5:60139874..60141783-chr5:60145611..60148462,2	K562	blood:
10	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
11	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
12	chr5:60138882..60141126-chr5:60148557..60150953,2	MCF-7	breast:
13	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
14	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
15	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
16	chr5:60138677..60141411-chr5:60155273..60157219,2	MCF-7	breast:
17	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
18	chr5:59973507..59975333-chr5:60177921..60180223,2	MCF-7	breast:
19	chr5:10761355..10761920-chr5:60240758..60241387,2	NB4	blood:
20	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
21	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
22	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
23	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
24	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
25	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
26	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
27	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
28	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
29	chr5:60141307..60144527-chr5:60240837..60243388,3	K562	blood:
30	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
31	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
32	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
33	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
34	chr19:10314099..10314599-chr5:60155075..60155644,2	Hela-S3	cervix:
35	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
36	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
37	chr5:60234534..60237256-chr5:60239004..60241956,3	K562	blood:
38	chr5:60231929..60237280-chr5:60239098..60242865,6	MCF-7	breast:
39	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
40	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
41	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
42	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
43	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
44	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
45	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
46	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
47	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
48	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
49	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
50	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
2	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
3	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
4	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
5	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1

No data

Variant related genes	Relation type
ELOVL7	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
ELOVL7	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
NDUFAF2	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
ENSG00000143319	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000112977	chromatin interactions

Extended variants
information (count: 4550 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4550 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4700398	chr5:60135985-60135986	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573077331	chr5:60135988-60135989	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140226803	chr5:60136060-60136061	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150293069	chr5:60136113-60136114	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555534285	chr5:60136130-60136131	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575372362	chr5:60136133-60136134	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544307343	chr5:60136213-60136214	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564192152	chr5:60136250-60136251	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147573267	chr5:60136310-60136311	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540584288	chr5:60136316-60136317	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142636663	chr5:60136317-60136318	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370356218	chr5:60136364-60136365	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529590776	chr5:60136397-60136398	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549353706	chr5:60136421-60136422	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4700399	chr5:60136454-60136455	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs146879596	chr5:60136495-60136496	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550719277	chr5:60136516-60136517	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116493872	chr5:60136527-60136528	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186195010	chr5:60136528-60136529	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9291697	chr5:60136568-60136569	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs17332419	chr5:60136626-60136627	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs190559065	chr5:60136679-60136680	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552326173	chr5:60136737-60136738	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367782697	chr5:60136799-60136800	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71630083	chr5:60136824-60136825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs199897622	chr5:60136833-60136834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534932388	chr5:60136851-60136852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397997937	chr5:60136871-60136872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542961114	chr5:60136896-60136897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182724486	chr5:60136902-60136903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188301274	chr5:60137043-60137044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546876072	chr5:60137052-60137053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191352208	chr5:60137093-60137094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183270408	chr5:60137102-60137103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537054629	chr5:60137135-60137136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116265107	chr5:60137136-60137137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577698600	chr5:60137153-60137154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114836799	chr5:60137154-60137155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7731760	chr5:60137168-60137169	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs368350110	chr5:60137176-60137177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7717909	chr5:60137270-60137271	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs543311820	chr5:60137380-60137381	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563148581	chr5:60137381-60137382	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139357177	chr5:60137388-60137389	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187699172	chr5:60137406-60137407	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564198541	chr5:60137461-60137462	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533043432	chr5:60137481-60137482	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546319687	chr5:60137484-60137485	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191373292	chr5:60137485-60137486	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74925644	chr5:60137501-60137502	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	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
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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	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
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2156 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60102200-60137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:60129400-60137200	Weak transcription	Fetal Intestine Small	intestine
3	chr5:60132000-60138600	Weak transcription	HMEC	breast
4	chr5:60132400-60138600	Weak transcription	A549	lung
5	chr5:60134200-60137200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr5:60134200-60137400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr5:60134400-60138000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:60134400-60138400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr5:60134400-60138400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:60134400-60138400	Weak transcription	Gastric	stomach
11	chr5:60134400-60138400	Weak transcription	Pancreas	Pancrea
12	chr5:60134400-60138400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr5:60134400-60139000	Weak transcription	Lung	lung
14	chr5:60134400-60139000	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr5:60134600-60137000	Weak transcription	Fetal Intestine Large	intestine
16	chr5:60135400-60136200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:60135400-60136400	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr5:60135600-60136400	Active TSS	Brain Anterior Caudate	brain
19	chr5:60135600-60136600	Enhancers	Brain Hippocampus Middle	brain
20	chr5:60136000-60136200	Flanking Active TSS	Brain Angular Gyrus	brain
21	chr5:60136200-60136600	Enhancers	Brain Cingulate Gyrus	brain
22	chr5:60136200-60136800	Active TSS	Brain Angular Gyrus	brain
23	chr5:60136200-60137600	Enhancers	Brain Substantia Nigra	brain
24	chr5:60136200-60138800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr5:60136400-60137400	Weak transcription	Brain Anterior Caudate	brain
26	chr5:60136400-60137800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr5:60136600-60137000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr5:60136600-60137000	Weak transcription	Brain Hippocampus Middle	brain
29	chr5:60136800-60137000	Weak transcription	Brain Angular Gyrus	brain
30	chr5:60137000-60137200	Enhancers	Brain Angular Gyrus	brain
31	chr5:60137000-60137400	Enhancers	Brain Hippocampus Middle	brain
32	chr5:60137000-60137600	Enhancers	Brain Cingulate Gyrus	brain
33	chr5:60137000-60137600	Enhancers	Fetal Intestine Large	intestine
34	chr5:60137200-60137400	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr5:60137200-60138200	Enhancers	Fetal Intestine Small	intestine
36	chr5:60137400-60137800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr5:60137400-60138400	Active TSS	Brain Angular Gyrus	brain
38	chr5:60137400-60138400	Active TSS	Brain Anterior Caudate	brain
39	chr5:60137400-60138400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr5:60137400-60140600	Active TSS	Brain Hippocampus Middle	brain
41	chr5:60137600-60137800	Active TSS	Fetal Intestine Large	intestine
42	chr5:60137600-60138200	Flanking Active TSS	Brain Cingulate Gyrus	brain
43	chr5:60137600-60138200	Flanking Active TSS	Brain Substantia Nigra	brain
44	chr5:60137600-60138600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:60137800-60138000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr5:60137800-60138000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
47	chr5:60137800-60138000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr5:60137800-60138000	Flanking Active TSS	Fetal Intestine Large	intestine
49	chr5:60137800-60138000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr5:60137800-60138200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell

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