Variant report

Variant	nsv881718
Chromosome Location	chr5:60147754-60313015
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1640)
CpG islands
(count:1164)
Chromatin interactive
region (count:76)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
2	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
5	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
6	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
7	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
8	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
9	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
10	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
11	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
12	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
13	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
15	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
16	BHLHE40	chr5:60274319-60275283	K562	blood:	n/a	n/a
17	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
18	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
19	BHLHE40	chr5:60273867-60274075	K562	blood:	n/a	n/a
20	BHLHE40	chr5:60168934-60168938	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
22	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a
23	BRCA1	chr5:60306630-60306773	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr5:60242705-60242764	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
26	CBX3	chr5:60289206-60289789	K562	blood:	n/a	n/a
27	CBX3	chr5:60289241-60289660	HCT-116	colon:	n/a	n/a
28	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
29	CBX3	chr5:60274796-60275180	K562	blood:	n/a	n/a
30	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
31	CBX3	chr5:60289190-60289610	K562	blood:	n/a	n/a
32	CBX3	chr5:60166733-60166960	K562	blood:	n/a	n/a
33	CBX3	chr5:60277815-60278245	K562	blood:	n/a	n/a
34	CBX3	chr5:60274711-60275276	K562	blood:	n/a	n/a
35	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
36	CCNT2	chr5:60274822-60275307	K562	blood:	n/a	n/a
37	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
38	CCNT2	chr5:60148817-60149120	K562	blood:	n/a	n/a
39	CCNT2	chr5:60273908-60274052	K562	blood:	n/a	n/a
40	CCNT2	chr5:60257762-60257798	K562	blood:	n/a	n/a
41	CEBPB	chr5:60257552-60257954	K562	blood:	n/a	chr5:60257738-60257749
42	CEBPB	chr5:60165087-60165233	A549	lung:	n/a	chr5:60165165-60165176 chr5:60165118-60165129
43	CEBPB	chr5:60257603-60257821	MCF-7	breast:	n/a	chr5:60257738-60257749
44	CEBPB	chr5:60257618-60257870	K562	blood:	n/a	chr5:60257738-60257749
45	CEBPB	chr5:60239556-60240203	HepG2	liver:	n/a	chr5:60239733-60239744
46	CEBPB	chr5:60257625-60257868	ECC-1	luminal epithelium:	n/a	chr5:60257738-60257749
47	CEBPB	chr5:60239532-60239892	K562	blood:	n/a	chr5:60239733-60239744
48	CEBPB	chr5:60151932-60152299	IMR90	lung:	n/a	chr5:60152122-60152133
49	CEBPB	chr5:60257710-60257892	H1-hESC	embryonic stem cell:	n/a	chr5:60257738-60257749
50	CEBPB	chr5:60168749-60169059	IMR90	lung:	n/a	chr5:60168912-60168923

(count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60240926-60240976	NT2-D1	testis:	n/a
2	chr5:60241428-60241478	HUVEC	blood vessel:	n/a
3	chr5:60240926-60240976	RPTEC	kidney:	n/a
4	chr5:60240926-60240976	NHDF-neo	bronchial:	n/a
5	chr5:60240938-60240988	PANC-1	pancreas:	n/a
6	chr5:60240926-60240976	NT2-D1	testis:	n/a
7	chr5:60241428-60241478	HUVEC	blood vessel:	n/a
8	chr5:60240926-60240976	RPTEC	kidney:	n/a
9	chr5:60240926-60240976	NHDF-neo	bronchial:	n/a
10	chr5:60240938-60240988	PANC-1	pancreas:	n/a
11	chr5:60239580-60239630	GM19239	blood:	n/a
12	chr5:60148273-60148323	LNCaP	prostate:	n/a
13	chr5:60240891-60240941	U87	brain:	n/a
14	chr5:60241003-60241053	HNPCEpiC	eye:	n/a
15	chr5:60148273-60148323	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:60187211-60187261	PANC-1	pancreas:	n/a
17	chr5:60241019-60241069	MCF10A-Er-Src	breast:	n/a
18	chr5:60241019-60241069	GM19239	blood:	n/a
19	chr5:60240870-60240920	SKMC	muscle:	n/a
20	chr5:60241019-60241069	AG10803	skin:	n/a
21	chr5:60240838-60240888	Hepatocyte	liver:	n/a
22	chr5:60241324-60241374	HAEpiC	amniotic membrane:	n/a
23	chr5:60148273-60148323	ovcar-3	ovarian:	n/a
24	chr5:60241424-60241474	K562	blood:	n/a
25	chr5:60240817-60240867	ECC-1	luminal epithelium:	n/a
26	chr5:60241324-60241374	AG09319	gingival:	n/a
27	chr5:60241428-60241478	ProgFib	skin:	n/a
28	chr5:60241324-60241374	SK-N-SH	brain:	n/a
29	chr5:60240938-60240988	SK-N-MC	brain:	n/a
30	chr5:60240870-60240920	GM12878	blood:	n/a
31	chr5:60240891-60240941	HUVEC	blood vessel:	n/a
32	chr5:60240568-60240618	MCF10A-Er-Src	breast:	n/a
33	chr5:60240926-60240976	HIPEpiC	eye:	n/a
34	chr5:60241428-60241478	ECC-1	luminal epithelium:	n/a
35	chr5:60241019-60241069	NHBE	bronchial:	n/a
36	chr5:60170058-60170108	MCF10A-Er-Src	breast:	n/a
37	chr5:60240817-60240867	ProgFib	skin:	n/a
38	chr5:60241324-60241374	HRPEpiC	eye:	n/a
39	chr5:60240938-60240988	HIPEpiC	eye:	n/a
40	chr5:60240838-60240888	BJ	skin:	n/a
41	chr5:60241424-60241474	NH-A	brain:	n/a
42	chr5:60240952-60241002	AG04449	skin:	fetal
43	chr5:60187211-60187261	AG10803	skin:	n/a
44	chr5:60241019-60241069	NH-A	brain:	n/a
45	chr5:60239580-60239630	K562	blood:	n/a
46	chr5:60187211-60187261	HRPEpiC	eye:	n/a
47	chr5:60240670-60240720	U87	brain:	n/a
48	chr5:60239580-60239630	A549	lung:	n/a
49	chr5:60170058-60170108	HL-60	blood:	n/a
50	chr5:60241428-60241478	Caco-2	colon:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
2	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
3	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
4	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
5	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
6	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
7	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
8	chr5:60138677..60141411-chr5:60155273..60157219,2	MCF-7	breast:
9	chr5:60238903..60241711-chr5:60255745..60258195,2	K562	blood:
10	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
11	chr5:60261942..60265146-chr5:60457137..60459002,3	MCF-7	breast:
12	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
13	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
14	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
15	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
16	chr5:60231929..60237280-chr5:60239098..60242865,6	MCF-7	breast:
17	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
18	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
19	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
20	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
21	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
22	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
23	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
24	chr5:60139874..60141783-chr5:60145611..60148462,2	K562	blood:
25	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
26	chr5:60239789..60242454-chr5:60245834..60249187,6	MCF-7	breast:
27	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
28	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
29	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
30	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
31	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
32	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
33	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
34	chr5:60238110..60240722-chr5:60956482..60958434,2	MCF-7	breast:
35	chr5:60234534..60237256-chr5:60239004..60241956,3	K562	blood:
36	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
37	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
38	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
39	chr5:60150200..60152775-chr5:60153410..60154990,2	MCF-7	breast:
40	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
41	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
42	chr19:10314099..10314599-chr5:60155075..60155644,2	Hela-S3	cervix:
43	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
44	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
45	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
46	chr5:60268329..60270384-chr5:60275561..60277405,2	K562	blood:
47	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
48	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
49	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
50	chr5:60274623..60276264-chr5:60290570..60293305,2	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
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
GNL3LP1	CpG island
ENSG00000233847	CpG island
NDUFAF2	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
ENSG00000112977	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000035499	chromatin interactions

Extended variants
information (count: 5857 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5857 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7723999	chr5:60147754-60147755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371488374	chr5:60147788-60147789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562490850	chr5:60147870-60147871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531499074	chr5:60147886-60147887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551612559	chr5:60147892-60147893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564938903	chr5:60147965-60147966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574781326	chr5:60148007-60148008	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116482106	chr5:60148009-60148010	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs547929896	chr5:60148062-60148063	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs184835620	chr5:60148091-60148092	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs78563232	chr5:60148097-60148098	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550193742	chr5:60148103-60148104	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112188251	chr5:60148104-60148105	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538969768	chr5:60148119-60148120	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559158938	chr5:60148124-60148125	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs554532687	chr5:60148147-60148148	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572573080	chr5:60148197-60148198	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs151117118	chr5:60148198-60148199	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188434357	chr5:60148209-60148210	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375795498	chr5:60148274-60148275	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75325499	chr5:60148292-60148293	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546433855	chr5:60148317-60148318	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542256823	chr5:60148350-60148351	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562354836	chr5:60148359-60148360	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76406721	chr5:60148392-60148393	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567215978	chr5:60148401-60148402	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565154424	chr5:60148434-60148435	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191318653	chr5:60148650-60148651	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547593936	chr5:60148651-60148652	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561412975	chr5:60148698-60148699	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530205978	chr5:60148701-60148702	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183764226	chr5:60148702-60148703	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141021671	chr5:60148709-60148710	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs145121277	chr5:60148794-60148795	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138855665	chr5:60148798-60148799	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566346799	chr5:60148815-60148816	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545177810	chr5:60148848-60148849	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534914350	chr5:60148865-60148866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114225983	chr5:60148893-60148894	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574652271	chr5:60148911-60148912	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188147278	chr5:60148914-60148915	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116450047	chr5:60148965-60148966	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs374292275	chr5:60148969-60148970	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556119736	chr5:60149054-60149055	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs575966482	chr5:60149058-60149059	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543008329	chr5:60149087-60149088	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373119388	chr5:60149135-60149136	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs371694618	chr5:60149140-60149141	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs544975468	chr5:60149157-60149158	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111360331	chr5:60149172-60149173	Enhancers	Chromatin interactive region	1 gene(s)	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:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60141200-60148000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:60146800-60147800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:60147600-60149200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:60147800-60148000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:60147800-60149000	Enhancers	Fetal Intestine Small	intestine
6	chr5:60147800-60149000	Enhancers	Placenta	Placenta
7	chr5:60147800-60149200	Enhancers	Fetal Intestine Large	intestine
8	chr5:60147800-60149600	Enhancers	K562	blood
9	chr5:60148000-60148200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:60148000-60148800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:60148000-60149000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:60148000-60149200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:60148000-60149400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr5:60148200-60148800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:60148200-60149000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr5:60148200-60149200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:60148400-60148800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:60148400-60149000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr5:60148400-60149000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr5:60148400-60149600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:60149000-60149200	Enhancers	HMEC	breast
22	chr5:60149000-60149600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:60149200-60150400	Weak transcription	Fetal Intestine Large	intestine
24	chr5:60149200-60151400	Weak transcription	HMEC	breast
25	chr5:60149400-60152000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:60149600-60150600	Weak transcription	K562	blood
27	chr5:60149600-60151600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:60150600-60150800	Enhancers	Fetal Intestine Large	intestine
29	chr5:60150600-60150800	Enhancers	K562	blood
30	chr5:60151400-60152600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:60151400-60152600	Enhancers	HMEC	breast
32	chr5:60151600-60152000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:60151600-60152000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:60151600-60152400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:60151800-60152200	Enhancers	Hela-S3	cervix
36	chr5:60151800-60152200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr5:60151800-60152400	Enhancers	NHEK	skin
38	chr5:60152000-60152200	Enhancers	NHDF-Ad	bronchial
39	chr5:60152000-60152400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:60152200-60152400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr5:60162600-60166800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:60165400-60166600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:60165600-60166600	Weak transcription	Primary B cells from cord blood	blood
44	chr5:60165800-60167400	Weak transcription	Primary T cells from cord blood	blood
45	chr5:60165800-60167800	Weak transcription	Esophagus	oesophagus
46	chr5:60166600-60166800	ZNF genes & repeats	Primary B cells from cord blood	blood
47	chr5:60166600-60167200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:60166600-60177000	Weak transcription	Ovary	ovary
49	chr5:60166800-60167400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:60167000-60167200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum

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