Variant report

Variant	nsv882393
Chromosome Location	chr5:96496189-96567950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1480)
CpG islands
(count:733)
Chromatin interactive
region (count:59)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96559836-96560263	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:96517679-96517912	K562	blood:	n/a	n/a
3	ARID3A	chr5:96517984-96519784	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:96518910-96519735	K562	blood:	n/a	n/a
5	ATF1	chr5:96566806-96567076	K562	blood:	n/a	n/a
6	ATF1	chr5:96518777-96519693	K562	blood:	n/a	n/a
7	ATF2	chr5:96518562-96519502	GM12878	blood:	n/a	n/a
8	ATF2	chr5:96518742-96519762	GM12878	blood:	n/a	n/a
9	ATF2	chr5:96518622-96519567	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:96503022-96503427	GM12878	blood:	n/a	n/a
11	ATF2	chr5:96518721-96519407	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:96503064-96503603	GM12878	blood:	n/a	n/a
13	ATF3	chr5:96518715-96519226	GM12878	blood:	n/a	n/a
14	ATF3	chr5:96518727-96519094	K562	blood:	n/a	n/a
15	ATF3	chr5:96518726-96519630	A549	lung:	n/a	n/a
16	ATF3	chr5:96518699-96519160	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr5:96518763-96519118	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr5:96518734-96519068	HepG2	liver:	n/a	n/a
19	ATF3	chr5:96518825-96519741	A549	lung:	n/a	n/a
20	BACH1	chr5:96514726-96514765	K562	blood:	n/a	n/a
21	BACH1	chr5:96518703-96519565	K562	blood:	n/a	n/a
22	BATF	chr5:96503177-96503536	GM12878	blood:	n/a	chr5:96503383-96503394
23	BATF	chr5:96503162-96503595	GM12878	blood:	n/a	chr5:96503383-96503394
24	BATF	chr5:96528640-96528915	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:96528568-96528924	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:96528575-96528962	GM12878	blood:	n/a	n/a
27	BCL3	chr5:96518637-96519903	A549	lung:	n/a	n/a
28	BCLAF1	chr5:96519046-96519886	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:96503107-96503654	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:96518655-96519736	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:96518708-96519746	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:96518681-96519779	K562	blood:	n/a	n/a
33	BRCA1	chr5:96518690-96519746	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:96518773-96519425	HepG2	liver:	n/a	n/a
35	CBX3	chr5:96518760-96519934	K562	blood:	n/a	n/a
36	CBX3	chr5:96527670-96527910	K562	blood:	n/a	n/a
37	CBX3	chr5:96518715-96519982	K562	blood:	n/a	n/a
38	CCNT2	chr5:96499379-96499468	K562	blood:	n/a	n/a
39	CCNT2	chr5:96497890-96498055	K562	blood:	n/a	n/a
40	CCNT2	chr5:96498838-96498954	K562	blood:	n/a	n/a
41	CEBPB	chr5:96520914-96521225	Hela-S3	cervix:	n/a	chr5:96521087-96521098
42	CEBPB	chr5:96532129-96532389	A549	lung:	n/a	chr5:96532230-96532241
43	CEBPB	chr5:96500665-96500821	A549	lung:	n/a	n/a
44	CEBPB	chr5:96566712-96567106	ECC-1	luminal epithelium:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
45	CEBPB	chr5:96566745-96567095	HepG2	liver:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
46	CEBPB	chr5:96566703-96567118	Hela-S3	cervix:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
47	CEBPB	chr5:96520946-96521249	HepG2	liver:	n/a	chr5:96521087-96521098
48	CEBPB	chr5:96517541-96517956	K562	blood:	n/a	chr5:96517763-96517774 chr5:96517763-96517772 chr5:96517755-96517766 chr5:96517753-96517764 chr5:96517761-96517774
49	CEBPB	chr5:96517590-96517902	A549	lung:	n/a	chr5:96517763-96517774 chr5:96517763-96517772 chr5:96517755-96517766 chr5:96517753-96517764 chr5:96517761-96517774
50	CEBPB	chr5:96532078-96532303	HepG2	liver:	n/a	chr5:96532230-96532241

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96519566-96519616	AG09319	gingival:	n/a
2	chr5:96519566-96519616	AG09319	gingival:	n/a
3	chr5:96519548-96519598	NT2-D1	testis:	n/a
4	chr5:96519005-96519055	Hepatocyte	liver:	n/a
5	chr5:96519005-96519055	H1-hESC	embryonic stem cell:	embryo
6	chr5:96519010-96519060	HEK293	kidney:	embryo
7	chr5:96519566-96519616	AoSMC	blood vessel:	n/a
8	chr5:96519566-96519616	AG09309	skin:	n/a
9	chr5:96519401-96519451	BE2_C	brain:	n/a
10	chr5:96519644-96519694	IMR90	lung:	fetal
11	chr5:96517289-96517339	SK-N-SH	brain:	n/a
12	chr5:96519010-96519060	AG09319	gingival:	n/a
13	chr5:96519010-96519060	AG04450	lung:	fetal
14	chr5:96519548-96519598	SK-N-MC	brain:	n/a
15	chr5:96497888-96497938	Caco-2	colon:	n/a
16	chr5:96519644-96519694	AG09309	skin:	n/a
17	chr5:96519644-96519694	BJ	skin:	n/a
18	chr5:96522767-96522817	GM12892	blood:	n/a
19	chr5:96519465-96519515	SKMC	muscle:	n/a
20	chr5:96519003-96519053	NHDF-neo	bronchial:	n/a
21	chr5:96519010-96519060	U87	brain:	n/a
22	chr5:96522767-96522817	HepG2	liver:	n/a
23	chr5:96519003-96519053	PANC-1	pancreas:	n/a
24	chr5:96519465-96519515	HRCEpiC	kidney:	n/a
25	chr5:96522767-96522817	H1-hESC	embryonic stem cell:	embryo
26	chr5:96519548-96519598	T-47D	breast:	n/a
27	chr5:96519010-96519060	PrEC	prostate:	n/a
28	chr5:96519010-96519060	ProgFib	skin:	n/a
29	chr5:96519566-96519616	H1-hESC	embryonic stem cell:	embryo
30	chr5:96518721-96518771	NT2-D1	testis:	n/a
31	chr5:96522767-96522817	HRPEpiC	eye:	n/a
32	chr5:96517289-96517339	Jurkat	blood:	n/a
33	chr5:96519644-96519694	GM12892	blood:	n/a
34	chr5:96522767-96522817	Caco-2	colon:	n/a
35	chr5:96519010-96519060	MCF10A-Er-Src	breast:	n/a
36	chr5:96519010-96519060	H1-hESC	embryonic stem cell:	embryo
37	chr5:96519465-96519515	HRPEpiC	eye:	n/a
38	chr5:96497888-96497938	HCM	heart:	n/a
39	chr5:96517289-96517339	MCF10A-Er-Src	breast:	n/a
40	chr5:96519005-96519055	BJ	skin:	n/a
41	chr5:96522767-96522817	HCPEpiC	choroid plexus:	n/a
42	chr5:96519566-96519616	PrEC	prostate:	n/a
43	chr5:96522767-96522817	HCF	heart:	n/a
44	chr5:96519401-96519451	IMR90	lung:	fetal
45	chr5:96518721-96518771	T-47D	breast:	n/a
46	chr5:96519465-96519515	HIPEpiC	eye:	n/a
47	chr5:96519010-96519060	HCM	heart:	n/a
48	chr5:96519401-96519451	AG09309	skin:	n/a
49	chr5:96519566-96519616	HEEpiC	esophagus:	n/a
50	chr5:96519003-96519053	GM19239	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:96513502..96516317-chr5:96517939..96521183,3	K562	blood:
2	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
3	chr5:96517585..96519769-chr5:96537536..96540052,2	MCF-7	breast:
4	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
5	chr5:96087835..96088823-chr5:96498655..96499598,4	MCF-7	breast:
6	chr5:96332674..96333555-chr5:96497655..96498457,3	K562	blood:
7	chr5:96379467..96380324-chr5:96497473..96498285,2	MCF-7	breast:
8	chr5:96496426..96497975-chr5:96509660..96511880,2	K562	blood:
9	chr5:96520831..96523398-chr5:96524932..96527174,2	MCF-7	breast:
10	chr5:96507787..96509709-chr5:96511038..96513163,2	K562	blood:
11	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
12	chr11:62608625..62609592-chr5:96518540..96519360,2	Hela-S3	cervix:
13	chr5:96520831..96523398-chr5:96524932..96527174,2	MCF-7	breast:
14	chr5:96087839..96088456-chr5:96497483..96498165,2	MCF-7	breast:
15	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
16	chr5:96078120..96080024-chr5:96498248..96500707,2	K562	blood:
17	chr5:96517585..96519769-chr5:96537536..96540052,2	MCF-7	breast:
18	chr5:96521334..96524159-chr5:96530024..96533344,3	K562	blood:
19	chr5:96087099..96087726-chr5:96498883..96499456,2	MCF-7	breast:
20	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
21	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
22	chr5:96517103..96519459-chr5:98107837..98111064,3	MCF-7	breast:
23	chr5:96496779..96498459-chr5:96502787..96504322,2	K562	blood:
24	chr5:96422481..96423221-chr5:96497763..96498668,2	K562	blood:
25	chr5:96519642..96521582-chr5:96527509..96529068,2	MCF-7	breast:
26	chr5:96142348..96145031-chr5:96516210..96518138,3	K562	blood:
27	chr5:96513470..96515096-chr5:96518937..96520609,2	MCF-7	breast:
28	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
29	chr5:96521334..96524159-chr5:96530024..96533344,3	K562	blood:
30	chr5:96504565..96506934-chr5:96511490..96513264,2	K562	blood:
31	chr5:96332659..96333410-chr5:96497323..96498128,4	MCF-7	breast:
32	chr5:96503041..96507630-chr5:96507953..96511468,4	K562	blood:
33	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
34	chr5:96518600..96520567-chr5:96529112..96530644,2	MCF-7	breast:
35	chr5:96268592..96270496-chr5:96515475..96517242,2	MCF-7	breast:
36	chr5:96087837..96088851-chr5:96497370..96499403,9	K562	blood:
37	chr5:96517799..96519630-chr9:91924359..91927202,2	MCF-7	breast:
38	chr5:95680165..95680955-chr5:96498665..96499236,2	K562	blood:
39	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
40	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
41	chr5:96534501..96536985-chr5:96538534..96540888,2	MCF-7	breast:
42	chr5:95949882..95950863-chr5:96497777..96498341,2	K562	blood:
43	chr5:96142588..96144739-chr5:96517628..96519299,2	MCF-7	breast:
44	chr1:21112901..21113842-chr5:96518449..96519338,2	Hela-S3	cervix:
45	chr5:96142348..96143873-chr5:96516638..96519268,2	K562	blood:
46	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
47	chr5:96087427..96088455-chr5:96497429..96498297,3	MCF-7	breast:
48	chr5:96269896..96271438-chr5:96517931..96519494,2	MCF-7	breast:
49	chr5:96089762..96090275-chr5:96497777..96498553,2	K562	blood:
50	chr5:96518678..96521273-chr5:96521348..96524678,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIOK2-2	chr5:96563572-96563661	XLOC_004934
2	lnc-RIOK2-1	chr5:96537546-96537584	ENSG00000248758.1
3	lnc-LIX1-2	chr5:96518830-96518864	NONHSAT102923
4	lnc-RIOK2-1	chr5:96523794-96523947	ENSG00000248758.1
5	lnc-RIOK2-2	chr5:96559075-96559398	XLOC_004934
6	lnc-CTD-2215E18.1.1-1	chr5:96519303-96519373	ENSG00000251513.1
7	lnc-LIX1-2	chr5:96514534-96514897	NONHSAT102923

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RIOK2	hsa-miR-101-3p	chr5:96498716-96498737
2	RIOK2	hsa-miR-155-5p	chr5:96498413-96498438

Variant related genes	Relation type
ENSG00000251054	TF binding region
ENSG00000251513	TF binding region
ENSG00000248758	TF binding region
RNU1-73P	TF binding region
RIOK2	TF binding region
ENSG00000251054	CpG island
ENSG00000251513	CpG island
ENSG00000248758	CpG island
RNU1-73P	CpG island
RIOK2	CpG island
ENSG00000123975	chromatin interactions
ENSG00000164307	chromatin interactions
ENSG00000249180	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000246763	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000113441	chromatin interactions
ENSG00000265112	chromatin interactions
ENSG00000206698	chromatin interactions
ENSG00000248758	chromatin interactions
ENSG00000127483	chromatin interactions
ENSG00000058729	chromatin interactions
ENSG00000174136	chromatin interactions
ENSG00000251054	chromatin interactions

Extended variants
information (count: 2507 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2507 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs30998	chr5:96496189-96496190	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371364097	chr5:96496229-96496230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185760306	chr5:96496231-96496232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576598291	chr5:96496247-96496248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147659872	chr5:96496250-96496251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542387050	chr5:96496259-96496260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529815383	chr5:96496345-96496346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115244283	chr5:96496362-96496363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs30997	chr5:96496389-96496390	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs144955121	chr5:96496421-96496422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527343595	chr5:96496426-96496427	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs17629822	chr5:96496437-96496438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs112189843	chr5:96496471-96496472	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10053369	chr5:96496476-96496477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191107591	chr5:96496479-96496480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549569345	chr5:96496490-96496491	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs316185	chr5:96496491-96496492	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs116694740	chr5:96496510-96496511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554021702	chr5:96496552-96496553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572385906	chr5:96496555-96496556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538869280	chr5:96496556-96496557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555713226	chr5:96496567-96496568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114389623	chr5:96496610-96496611	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75344648	chr5:96496639-96496640	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79346077	chr5:96496657-96496658	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562274646	chr5:96496658-96496659	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78365495	chr5:96496663-96496664	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541904692	chr5:96496672-96496673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528952654	chr5:96496691-96496692	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs73778017	chr5:96496706-96496707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs113126140	chr5:96496713-96496714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182820691	chr5:96496770-96496771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs551909341	chr5:96496787-96496788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143743417	chr5:96496830-96496831	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201557698	chr5:96496840-96496841	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs200627248	chr5:96496841-96496842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201080822	chr5:96496842-96496843	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77440668	chr5:96496843-96496844	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188390430	chr5:96496917-96496918	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549706155	chr5:96496941-96496942	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs567913698	chr5:96496955-96496956	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs34671120	chr5:96496956-96496957	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111757929	chr5:96497086-96497087	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368145599	chr5:96497090-96497091	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs79621157	chr5:96497095-96497096	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528045537	chr5:96497099-96497100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539789711	chr5:96497113-96497114	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs67400269	chr5:96497122-96497123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557868775	chr5:96497127-96497128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs570320822	chr5:96497182-96497183	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96478400-96507800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr5:96492200-96498000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr5:96492200-96510200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:96493600-96498200	Strong transcription	Primary B cells from cord blood	blood
5	chr5:96493600-96501600	Weak transcription	NHLF	lung
6	chr5:96493800-96497800	Weak transcription	HUVEC	blood vessel
7	chr5:96494000-96496200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr5:96494000-96496600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:96494000-96496600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr5:96494000-96496600	Weak transcription	NHDF-Ad	bronchial
11	chr5:96494000-96502800	Weak transcription	Psoas Muscle	Psoas
12	chr5:96494200-96496200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr5:96494200-96496400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr5:96494200-96496400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr5:96494200-96496400	Weak transcription	Fetal Lung	lung
16	chr5:96494200-96496600	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr5:96494200-96497400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:96494200-96497800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr5:96494200-96498000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:96494200-96498000	Weak transcription	Fetal Kidney	kidney
21	chr5:96494200-96499200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:96494200-96499600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:96494200-96501000	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr5:96494200-96501400	Weak transcription	Brain Anterior Caudate	brain
25	chr5:96494200-96503000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr5:96494200-96506600	Weak transcription	Ovary	ovary
27	chr5:96494400-96496200	Weak transcription	Colon Smooth Muscle	Colon
28	chr5:96494400-96496200	Weak transcription	NH-A	brain
29	chr5:96494400-96496200	Weak transcription	NHEK	skin
30	chr5:96494400-96496600	Weak transcription	K562	blood
31	chr5:96494400-96496800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:96494400-96496800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr5:96494400-96496800	Strong transcription	Skeletal Muscle Male	skeletal muscle
34	chr5:96494400-96497400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:96494400-96497800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr5:96494400-96498000	Weak transcription	Adipose Nuclei	Adipose
37	chr5:96494400-96499600	Weak transcription	Esophagus	oesophagus
38	chr5:96494400-96501400	Strong transcription	Liver	Liver
39	chr5:96494400-96501800	Strong transcription	Primary B cells from peripheral blood	blood
40	chr5:96494400-96502800	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr5:96494400-96503200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:96494400-96505200	Weak transcription	Fetal Brain Male	brain
43	chr5:96494400-96510600	Weak transcription	Gastric	stomach
44	chr5:96494400-96515200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr5:96494400-96518000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:96494600-96496600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr5:96494600-96497000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:96494600-96497000	Strong transcription	Brain Hippocampus Middle	brain
49	chr5:96494600-96497000	Strong transcription	Brain Inferior Temporal Lobe	brain
50	chr5:96494600-96497800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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