Variant report

Variant	nsv4918
Chromosome Location	chr5:92898426-92943359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2032)
CpG islands
(count:6290)
Chromatin interactive
region (count:23)
LncRNA
region (count:97)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2032 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:92915534-92915703	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:92917157-92919131	HepG2	liver:	n/a	chr5:92917924-92917940
3	ATF1	chr5:92918414-92918880	K562	blood:	n/a	n/a
4	ATF2	chr5:92899840-92900431	GM12878	blood:	n/a	n/a
5	ATF2	chr5:92918277-92918690	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:92899881-92900429	GM12878	blood:	n/a	n/a
7	ATF3	chr5:92917002-92917453	A549	lung:	n/a	n/a
8	BACH1	chr5:92908680-92909056	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:92923404-92923463	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:92906081-92906982	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:92932794-92933035	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:92924060-92924095	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:92916969-92917364	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:92915010-92915158	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:92915818-92916029	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr5:92930688-92930882	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:92924448-92924582	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:92939703-92939887	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:92908191-92908323	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:92921407-92921738	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr5:92927743-92927997	GM12878	blood:	n/a	n/a
22	BATF	chr5:92899943-92900191	GM12878	blood:	n/a	chr5:92900108-92900119
23	BATF	chr5:92899906-92900253	GM12878	blood:	n/a	chr5:92900108-92900119
24	BATF	chr5:92927780-92927981	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:92899900-92900197	GM12878	blood:	n/a	n/a
26	BCL3	chr5:92899943-92900323	GM12878	blood:	n/a	n/a
27	BCL3	chr5:92916986-92917506	A549	lung:	n/a	chr5:92917010-92917023 chr5:92917297-92917310
28	BCL3	chr5:92918357-92918921	A549	lung:	n/a	n/a
29	BCL3	chr5:92917102-92917994	A549	lung:	n/a	chr5:92917297-92917310
30	BHLHE40	chr5:92912841-92913054	K562	blood:	n/a	n/a
31	BHLHE40	chr5:92936118-92936440	HepG2	liver:	n/a	n/a
32	BHLHE40	chr5:92915599-92916172	HepG2	liver:	n/a	n/a
33	BHLHE40	chr5:92934492-92934783	HepG2	liver:	n/a	chr5:92934634-92934655
34	BHLHE40	chr5:92912890-92913069	GM12878	blood:	n/a	n/a
35	BHLHE40	chr5:92917063-92917475	HepG2	liver:	n/a	n/a
36	BHLHE40	chr5:92918669-92918911	K562	blood:	n/a	n/a
37	BHLHE40	chr5:92918322-92919119	HepG2	liver:	n/a	n/a
38	BHLHE40	chr5:92934638-92934649	GM12878	blood:	n/a	n/a
39	BRCA1	chr5:92933907-92934287	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr5:92932940-92933052	HepG2	liver:	n/a	n/a
41	BRCA1	chr5:92921519-92921687	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr5:92918418-92919068	HepG2	liver:	n/a	n/a
43	BRCA1	chr5:92918027-92919167	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr5:92916691-92917427	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr5:92932817-92933295	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr5:92932840-92933001	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr5:92918197-92919092	HCT-116	colon:	n/a	n/a
48	CBX3	chr5:92899601-92900427	HCT-116	colon:	n/a	n/a
49	CEBPB	chr5:92920043-92920495	A549	lung:	n/a	n/a
50	CEBPB	chr5:92920110-92920435	HepG2	liver:	n/a	n/a

(count:6290 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:92930813-92930863	A549	lung:	n/a
2	chr5:92918072-92918122	Jurkat	blood:	n/a
3	chr5:92904377-92904427	AG09319	gingival:	n/a
4	chr5:92908771-92908821	HEEpiC	esophagus:	n/a
5	chr5:92931401-92931451	HRE	kidney:	n/a
6	chr5:92918072-92918122	NH-A	brain:	n/a
7	chr5:92907553-92907603	GM12891	blood:	n/a
8	chr5:92930813-92930863	A549	lung:	n/a
9	chr5:92918072-92918122	Jurkat	blood:	n/a
10	chr5:92904377-92904427	AG09319	gingival:	n/a
11	chr5:92908771-92908821	HEEpiC	esophagus:	n/a
12	chr5:92931401-92931451	HRE	kidney:	n/a
13	chr5:92918072-92918122	NH-A	brain:	n/a
14	chr5:92907553-92907603	GM12891	blood:	n/a
15	chr5:92936528-92936578	HCM	heart:	n/a
16	chr5:92908771-92908821	AG10803	skin:	n/a
17	chr5:92918517-92918567	MCF-7	breast:	n/a
18	chr5:92904377-92904427	GM12891	blood:	n/a
19	chr5:92907151-92907201	AG09319	gingival:	n/a
20	chr5:92916474-92916524	HRPEpiC	eye:	n/a
21	chr5:92931173-92931223	SK-N-SH_RA	brain:	n/a
22	chr5:92929573-92929623	HIPEpiC	eye:	n/a
23	chr5:92918560-92918610	SK-N-MC	brain:	n/a
24	chr5:92925524-92925574	ovcar-3	ovarian:	n/a
25	chr5:92930530-92930580	NB4	blood:	n/a
26	chr5:92920256-92920306	HAEpiC	amniotic membrane:	n/a
27	chr5:92920498-92920548	PrEC	prostate:	n/a
28	chr5:92920496-92920546	SK-N-MC	brain:	n/a
29	chr5:92904875-92904925	Hepatocyte	liver:	n/a
30	chr5:92930813-92930863	Caco-2	colon:	n/a
31	chr5:92907553-92907603	ProgFib	skin:	n/a
32	chr5:92919647-92919697	NH-A	brain:	n/a
33	chr5:92929372-92929422	A549	lung:	n/a
34	chr5:92937739-92937789	ECC-1	luminal epithelium:	n/a
35	chr5:92909434-92909484	HL-60	blood:	n/a
36	chr5:92928615-92928665	IMR90	lung:	fetal
37	chr5:92928458-92928508	NH-A	brain:	n/a
38	chr5:92931173-92931223	NB4	blood:	n/a
39	chr5:92918068-92918118	T-47D	breast:	n/a
40	chr5:92931817-92931867	HAEpiC	amniotic membrane:	n/a
41	chr5:92914290-92914340	PrEC	prostate:	n/a
42	chr5:92935283-92935333	K562	blood:	n/a
43	chr5:92939842-92939892	HRE	kidney:	n/a
44	chr5:92931994-92932044	AG04450	lung:	fetal
45	chr5:92930634-92930684	T-47D	breast:	n/a
46	chr5:92937739-92937789	PANC-1	pancreas:	n/a
47	chr5:92930813-92930863	HEEpiC	esophagus:	n/a
48	chr5:92920256-92920306	HUVEC	blood vessel:	n/a
49	chr5:92928615-92928665	PFSK-1	brain:	n/a
50	chr5:92904875-92904925	HPAEpiC	pulmonary alveolar:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:92917150..92917848-chr5:93250486..93251539,3	MCF-7	breast:
2	chr5:92925322..92926942-chr5:92936051..92937789,2	MCF-7	breast:
3	chr5:92925322..92926942-chr5:92936051..92937789,2	MCF-7	breast:
4	chr5:92933083..92935901-chr5:92946824..92949229,2	MCF-7	breast:
5	chr5:92914959..92917781-chr5:92918156..92922060,3	MCF-7	breast:
6	chr5:92932499..92933302-chr5:93136722..93137235,2	MCF-7	breast:
7	chr5:92918392..92920422-chr5:92954459..92956574,2	MCF-7	breast:
8	chr5:92899115..92901267-chr5:92906370..92908951,2	MCF-7	breast:
9	chr5:92914959..92917781-chr5:92918156..92922060,3	MCF-7	breast:
10	chr5:77590309..77590978-chr5:92932828..92933802,2	Hela-S3	cervix:
11	chr5:92910337..92912494-chr5:92915588..92917901,2	MCF-7	breast:
12	chr5:92919342..92920132-chr9:33025119..33025739,2	HCT-116	colon:
13	chr5:92940969..92942896-chr5:92944582..92947117,2	MCF-7	breast:
14	chr5:92931819..92934085-chr5:92938375..92940060,2	MCF-7	breast:
15	chr20:30192477..30192989-chr5:92915117..92915645,2	NB4	blood:
16	chr5:92933301..92936219-chr5:93128052..93129645,2	MCF-7	breast:
17	chr5:92934725..92936472-chr5:92938554..92940357,2	MCF-7	breast:
18	chr5:92918931..92920737-chr5:92932516..92934451,3	MCF-7	breast:
19	chr5:92931819..92934085-chr5:92938375..92940060,2	MCF-7	breast:
20	chr5:92934725..92936472-chr5:92938554..92940357,2	MCF-7	breast:
21	chr5:92943322..92944183-chr5:93136863..93137431,3	MCF-7	breast:
22	chr5:92932535..92933391-chr5:93137058..93137717,3	MCF-7	breast:
23	chr5:92932477..92933445-chr5:93135854..93136694,2	MCF-7	breast:

(count:97 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102809
2	lnc-FAM172A-2	chr5:92905596-92906499	ENSG00000237187.4
3	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102803
4	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187
5	lnc-FAM172A-2	chr5:92916848-92917026	NR_021490
6	lnc-FAM172A-2	chr5:92916848-92917003	ENSG00000237187
7	lnc-FAM172A-2	chr5:92916173-92916713	ENSG00000237187
8	lnc-FAM172A-2	chr5:92899070-92899166	NONHSAT102806
9	lnc-FAM172A-2	chr5:92899070-92899169	NR_021490
10	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187
11	lnc-NR2F1-1	chr5:92909152-92909896	NONHSAT102810
12	lnc-FAM172A-2	chr5:92916848-92917026	NR_109818
13	lnc-FAM172A-2	chr5:92924826-92924925	ucscGeneNc_uc003kkg_2
14	lnc-FAM172A-2	chr5:92906204-92906525	NONHSAT102787
15	lnc-NR2F1-1	chr5:92908567-92908913	NONHSAT102810
16	lnc-NR2F1-1	chr5:92906676-92907480	NONHSAT102813
17	lnc-FAM172A-2	chr5:92916848-92916925	ENSG00000237187.4
18	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187.4
19	lnc-NR2F1-5	chr5:92932191-92933236	l_2975_chr5:92932190-92934697_testes
20	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187.4
21	lnc-FAM172A-2	chr5:92942604-92942759	ucscGeneNc_uc003kkg_2
22	lnc-FAM172A-2	chr5:92905596-92905708	ENSG00000237187
23	lnc-FAM172A-2	chr5:92899070-92899169	NR_021491
24	lnc-FAM172A-2	chr5:92916173-92916805	NONHSAT102796
25	lnc-FAM172A-2	chr5:92905596-92905708	NR_109818
26	lnc-FAM172A-2	chr5:92916173-92916419	NONHSAT102806
27	lnc-FAM172A-2	chr5:92916848-92916994	ENSG00000237187.4
28	lnc-FAM172A-2	chr5:92916848-92917003	NONHSAT102803
29	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187.4
30	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102793
31	lnc-FAM172A-2	chr5:92916848-92917026	NR_109823
32	lnc-FAM172A-2	chr5:92899070-92899166	NONHSAT102796
33	lnc-FAM172A-2	chr5:92906204-92907049	NR_109825
34	lnc-FAM172A-2	chr5:92916336-92916457	ucscGeneNc_uc003kkg_2
35	lnc-FAM172A-2	chr5:92906204-92907441	NONHSAT102809
36	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102791
37	lnc-FAM172A-2	chr5:92916173-92916970	NONHSAT102792
38	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187
39	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT147347
40	lnc-FAM172A-2	chr5:92905596-92907049	ENSG00000237187.4
41	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102789
42	lnc-FAM172A-2	chr5:92915223-92915325	ucscGeneNc_uc003kkg_2
43	lnc-NR2F1-1	chr5:92907588-92907718	XLOC_004475
44	lnc-FAM172A-2	chr5:92916173-92916738	NONHSAT102791
45	lnc-FAM172A-2	chr5:92905596-92905708	NR_109825
46	lnc-FAM172A-2	chr5:92899070-92899169	ENSG00000237187.4
47	lnc-FAM172A-2	chr5:92916848-92917026	NR_021491
48	lnc-FAM172A-2	chr5:92899070-92899169	NONHSAT102792
49	lnc-NR2F1-1	chr5:92906435-92907480	XLOC_004475
50	lnc-FAM172A-2	chr5:92916848-92917026	NR_109824

No data

Variant related genes	Relation type
NR2F1	TF binding region
NR2F1-AS1	TF binding region
NR2F1	CpG island
NR2F1-AS1	CpG island
ENSG00000137074	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000237187	chromatin interactions
ENSG00000175745	chromatin interactions
ENSG00000251725	chromatin interactions
ENSG00000132842	chromatin interactions
WEE1	miRNA target sites
C14orf45	miRNA target sites
PTPN9	miRNA target sites
APPL1	miRNA target sites
HMGA2	miRNA target sites
C5orf34	miRNA target sites
MSH2	miRNA target sites
GRIA2	miRNA target sites
MRPS23	miRNA target sites
KIF5C	miRNA target sites

Extended variants
information (count: 1341 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55751466	chr5:92898478-92898479	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552888402	chr5:92898558-92898559	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572695126	chr5:92898584-92898585	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188367459	chr5:92898643-92898644	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74870606	chr5:92898645-92898646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56111638	chr5:92898661-92898662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543774288	chr5:92898711-92898712	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147466311	chr5:92898713-92898714	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180966253	chr5:92898723-92898724	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185280973	chr5:92898733-92898734	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552897457	chr5:92898864-92898865	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115787231	chr5:92899018-92899019	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540452808	chr5:92899025-92899026	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140161571	chr5:92899032-92899033	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572333945	chr5:92899043-92899044	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541467359	chr5:92899052-92899053	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548811372	chr5:92899125-92899126	Strong transcription Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs568114841	chr5:92899194-92899195	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536723909	chr5:92899243-92899244	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573737909	chr5:92899288-92899289	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191219767	chr5:92899309-92899310	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142982957	chr5:92899329-92899330	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12657324	chr5:92899389-92899390	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539092742	chr5:92899449-92899450	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs147676008	chr5:92899453-92899454	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552799680	chr5:92899500-92899501	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116142459	chr5:92899515-92899516	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535237479	chr5:92899550-92899551	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182209567	chr5:92899583-92899584	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562738856	chr5:92899590-92899591	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs10476581	chr5:92899622-92899623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373503273	chr5:92899663-92899664	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574809208	chr5:92899690-92899691	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs557472868	chr5:92899691-92899692	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191707657	chr5:92899725-92899726	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577166266	chr5:92899759-92899760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs546223052	chr5:92899803-92899804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs528505533	chr5:92899828-92899829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs60114975	chr5:92899844-92899845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9764909	chr5:92899855-92899856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75638482	chr5:92899857-92899858	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs71639285	chr5:92899858-92899859	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71639286	chr5:92899860-92899861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560048742	chr5:92899865-92899866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540824863	chr5:92899867-92899868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs72786625	chr5:92899879-92899880	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543940698	chr5:92899910-92899911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575463193	chr5:92899923-92899924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115500157	chr5:92899975-92899976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531175345	chr5:92900050-92900051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2680 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92859200-92905000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr5:92859400-92905000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:92859400-92905600	Weak transcription	Placenta	Placenta
4	chr5:92859600-92900400	Weak transcription	Fetal Intestine Small	intestine
5	chr5:92860000-92908000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:92868600-92900200	Weak transcription	Hela-S3	cervix
7	chr5:92883200-92900800	Weak transcription	Fetal Brain Male	brain
8	chr5:92885600-92899800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr5:92886600-92899800	Weak transcription	HMEC	breast
10	chr5:92888200-92899800	Weak transcription	HUVEC	blood vessel
11	chr5:92888600-92899800	Weak transcription	NHDF-Ad	bronchial
12	chr5:92889400-92905400	Weak transcription	Fetal Brain Female	brain
13	chr5:92889600-92898800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:92889600-92900200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:92889600-92905800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr5:92889600-92909800	Weak transcription	Ovary	ovary
17	chr5:92889800-92900200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:92890000-92898600	Weak transcription	Fetal Kidney	kidney
19	chr5:92890000-92899800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr5:92890000-92904600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr5:92890600-92903200	Weak transcription	Brain Germinal Matrix	brain
22	chr5:92894800-92899000	Strong transcription	NH-A	brain
23	chr5:92894800-92899200	Strong transcription	Muscle Satellite Cultured Cells	--
24	chr5:92895400-92901400	Weak transcription	Brain Angular Gyrus	brain
25	chr5:92895800-92898800	Weak transcription	HSMM	muscle
26	chr5:92895800-92899400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:92896000-92899800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:92896600-92899600	Strong transcription	Fetal Lung	lung
29	chr5:92897000-92898600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr5:92897400-92899600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:92897800-92899200	Strong transcription	Osteobl	bone
32	chr5:92898200-92899000	Strong transcription	NHLF	lung
33	chr5:92898400-92899200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:92898400-92904400	Weak transcription	Fetal Stomach	stomach
35	chr5:92898600-92899000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr5:92898600-92899400	Strong transcription	Fetal Kidney	kidney
37	chr5:92898600-92906000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:92898800-92899000	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:92898800-92899200	Strong transcription	HSMM	muscle
40	chr5:92898800-92900200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:92899000-92899800	Weak transcription	NH-A	brain
42	chr5:92899000-92899800	Weak transcription	NHLF	lung
43	chr5:92899200-92899800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr5:92899200-92899800	Weak transcription	Osteobl	bone
45	chr5:92899200-92900200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:92899200-92906400	Weak transcription	HSMM	muscle
47	chr5:92899400-92899600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:92899400-92900200	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr5:92899400-92900600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:92899400-92902000	Weak transcription	Fetal Kidney	kidney

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