Variant report

Variant	nsv520799
Chromosome Location	chr15:55645661-55760522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1694)
CpG islands
(count:1405)
Chromatin interactive
region (count:97)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:4)

(count:1694 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:55695766-55696116	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:55693945-55694278	K562	blood:	n/a	n/a
3	ARID3A	chr15:55688544-55689215	K562	blood:	n/a	n/a
4	ARID3A	chr15:55662471-55662715	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:55654793-55654993	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:55711482-55711586	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:55700139-55701084	K562	blood:	n/a	n/a
8	ARID3A	chr15:55694987-55696143	K562	blood:	n/a	n/a
9	ARID3A	chr15:55699681-55700995	HepG2	liver:	n/a	chr15:55699936-55699952
10	ATF1	chr15:55731955-55732174	K562	blood:	n/a	n/a
11	ATF1	chr15:55700302-55701186	K562	blood:	n/a	n/a
12	ATF1	chr15:55695695-55696130	K562	blood:	n/a	n/a
13	ATF2	chr15:55700143-55700984	GM12878	blood:	n/a	n/a
14	ATF2	chr15:55700234-55700505	GM12878	blood:	n/a	n/a
15	ATF2	chr15:55700338-55700728	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr15:55697469-55697665	K562	blood:	n/a	n/a
17	ATF3	chr15:55700118-55701112	A549	lung:	n/a	n/a
18	ATF3	chr15:55700358-55700740	K562	blood:	n/a	n/a
19	ATF3	chr15:55695638-55696206	K562	blood:	n/a	n/a
20	BACH1	chr15:55700665-55700854	K562	blood:	n/a	n/a
21	BACH1	chr15:55653033-55653079	K562	blood:	n/a	n/a
22	BACH1	chr15:55659431-55659478	K562	blood:	n/a	n/a
23	BACH1	chr15:55693951-55694258	K562	blood:	n/a	n/a
24	BACH1	chr15:55695752-55696274	K562	blood:	n/a	n/a
25	BACH1	chr15:55700619-55701045	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr15:55700313-55701096	A549	lung:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
27	BCLAF1	chr15:55700112-55700929	GM12878	blood:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
28	BCLAF1	chr15:55700180-55700876	GM12878	blood:	n/a	chr15:55700652-55700665 chr15:55700787-55700795 chr15:55700649-55700662
29	BHLHE40	chr15:55689050-55689682	K562	blood:	n/a	n/a
30	BHLHE40	chr15:55700025-55701233	GM12878	blood:	n/a	chr15:55700654-55700670 chr15:55700528-55700544 chr15:55700677-55700693
31	BHLHE40	chr15:55694074-55694195	K562	blood:	n/a	n/a
32	BHLHE40	chr15:55699728-55701170	K562	blood:	n/a	chr15:55700654-55700670 chr15:55700528-55700544 chr15:55700677-55700693
33	BHLHE40	chr15:55690413-55690747	K562	blood:	n/a	chr15:55690612-55690625
34	BHLHE40	chr15:55697522-55697947	K562	blood:	n/a	n/a
35	BHLHE40	chr15:55731973-55732178	GM12878	blood:	n/a	n/a
36	BRCA1	chr15:55700467-55700697	GM12878	blood:	n/a	n/a
37	BRCA1	chr15:55700452-55700784	HepG2	liver:	n/a	n/a
38	BRCA1	chr15:55699596-55701223	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr15:55700512-55700973	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr15:55700143-55700934	K562	blood:	n/a	n/a
41	CBX3	chr15:55700369-55700677	K562	blood:	n/a	n/a
42	CBX3	chr15:55687028-55687394	K562	blood:	n/a	n/a
43	CBX3	chr15:55697420-55697995	K562	blood:	n/a	n/a
44	CCNT2	chr15:55689104-55689478	K562	blood:	n/a	n/a
45	CCNT2	chr15:55699564-55700830	K562	blood:	n/a	n/a
46	CCNT2	chr15:55695657-55696054	K562	blood:	n/a	n/a
47	CEBPB	chr15:55683766-55683772	K562	blood:	n/a	n/a
48	CEBPB	chr15:55695675-55696072	A549	lung:	n/a	chr15:55695839-55695856 chr15:55695841-55695852
49	CEBPB	chr15:55753699-55753864	A549	lung:	n/a	n/a
50	CEBPB	chr15:55712763-55712988	Hela-S3	cervix:	n/a	chr15:55712901-55712912

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:55700768-55700818	U87	brain:	n/a
2	chr15:55700587-55700637	SKMC	muscle:	n/a
3	chr15:55700768-55700818	U87	brain:	n/a
4	chr15:55700587-55700637	SKMC	muscle:	n/a
5	chr15:55700901-55700951	Caco-2	colon:	n/a
6	chr15:55701181-55701231	HCM	heart:	n/a
7	chr15:55697065-55697115	HepG2	liver:	n/a
8	chr15:55700471-55700521	U87	brain:	n/a
9	chr15:55710020-55710070	AG09319	gingival:	n/a
10	chr15:55737718-55737768	ECC-1	luminal epithelium:	n/a
11	chr15:55737718-55737768	AG09309	skin:	n/a
12	chr15:55700549-55700599	LNCaP	prostate:	n/a
13	chr15:55700482-55700532	SAEC	small airway:	n/a
14	chr15:55700768-55700818	BE2_C	brain:	n/a
15	chr15:55737718-55737768	A549	lung:	n/a
16	chr15:55700894-55700944	AG10803	skin:	n/a
17	chr15:55700768-55700818	AG09309	skin:	n/a
18	chr15:55665236-55665286	NH-A	brain:	n/a
19	chr15:55704519-55704569	NHDF-neo	bronchial:	n/a
20	chr15:55699975-55700025	CMK	blood:	n/a
21	chr15:55666568-55666618	PrEC	prostate:	n/a
22	chr15:55699975-55700025	BE2_C	brain:	n/a
23	chr15:55700894-55700944	HepG2	liver:	n/a
24	chr15:55665153-55665203	SK-N-SH_RA	brain:	n/a
25	chr15:55700894-55700944	Caco-2	colon:	n/a
26	chr15:55700471-55700521	GM12891	blood:	n/a
27	chr15:55700780-55700830	PFSK-1	brain:	n/a
28	chr15:55666362-55666412	Hepatocyte	liver:	n/a
29	chr15:55665236-55665286	SK-N-SH_RA	brain:	n/a
30	chr15:55737718-55737768	ovcar-3	ovarian:	n/a
31	chr15:55700743-55700793	NB4	blood:	n/a
32	chr15:55710020-55710070	NH-A	brain:	n/a
33	chr15:55701181-55701231	NH-A	brain:	n/a
34	chr15:55665153-55665203	PANC-1	pancreas:	n/a
35	chr15:55700743-55700793	HCM	heart:	n/a
36	chr15:55701181-55701231	AG09319	gingival:	n/a
37	chr15:55666362-55666412	AoSMC	blood vessel:	n/a
38	chr15:55700482-55700532	HIPEpiC	eye:	n/a
39	chr15:55700780-55700830	A549	lung:	n/a
40	chr15:55700743-55700793	HEEpiC	esophagus:	n/a
41	chr15:55701181-55701231	MCF-7	breast:	n/a
42	chr15:55700471-55700521	K562	blood:	n/a
43	chr15:55700471-55700521	HIPEpiC	eye:	n/a
44	chr15:55700471-55700521	CMK	blood:	n/a
45	chr15:55700689-55700739	NB4	blood:	n/a
46	chr15:55699975-55700025	GM12878	blood:	n/a
47	chr15:55666362-55666412	HRE	kidney:	n/a
48	chr15:55700593-55700643	GM06990	blood:	n/a
49	chr15:55700768-55700818	HAEpiC	amniotic membrane:	n/a
50	chr15:55666362-55666412	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:55687284..55689317-chr15:55695984..55697982,2	MCF-7	breast:
2	chr15:55650827..55653650-chr15:55729879..55732717,2	K562	blood:
3	chr15:55698446..55701018-chr15:55709702..55712524,2	MCF-7	breast:
4	chr15:55582304..55584506-chr15:55726191..55728043,2	MCF-7	breast:
5	chr15:55609877..55611698-chr15:55698360..55701817,3	MCF-7	breast:
6	chr15:55700022..55700552-chr9:133454540..133455085,2	Hela-S3	cervix:
7	chr15:55644113..55647083-chr15:55650261..55652459,2	MCF-7	breast:
8	chr15:55623887..55626442-chr15:55671919..55674129,2	K562	blood:
9	chr15:55698992..55701610-chr15:55725082..55727679,2	K562	blood:
10	chr15:55607682..55613892-chr15:55697623..55703247,7	K562	blood:
11	chr15:55631303..55633200-chr15:55699872..55702073,2	MCF-7	breast:
12	chr15:55579894..55582757-chr15:55689915..55691723,2	K562	blood:
13	chr15:55486981..55489906-chr15:55690724..55692379,2	K562	blood:
14	chr15:55698446..55701018-chr15:55709702..55712524,2	MCF-7	breast:
15	chr15:55711236..55714133-chr15:55717728..55719591,2	K562	blood:
16	chr15:55613382..55615549-chr15:55714258..55716081,2	K562	blood:
17	chr15:55641489..55644289-chr15:55644644..55647294,3	MCF-7	breast:
18	chr15:55711236..55714133-chr15:55717728..55719591,2	K562	blood:
19	chr14:68162088..68162732-chr15:55699888..55700416,2	Hela-S3	cervix:
20	chr15:55609398..55612428-chr15:55693917..55698358,4	K562	blood:
21	chr15:55687261..55690621-chr15:55699123..55703142,5	K562	blood:
22	chr15:55646940..55648644-chr15:55651865..55653826,3	K562	blood:
23	chr15:55641538..55644525-chr15:55662930..55665274,2	MCF-7	breast:
24	chr15:55686108..55691081-chr15:55692026..55698243,11	K562	blood:
25	chr15:55659460..55661361-chr15:55668355..55670079,2	K562	blood:
26	chr15:55577567..55579089-chr15:55694528..55696394,2	K562	blood:
27	chr15:55659246..55661372-chr15:55665281..55667567,2	K562	blood:
28	chr15:55650072..55650948-chr15:55700057..55700575,2	MCF-7	breast:
29	chr15:55689930..55691529-chr15:55699148..55701673,2	MCF-7	breast:
30	chr15:55678437..55680637-chr15:55698819..55700727,3	K562	blood:
31	chr15:55687261..55690621-chr15:55699123..55703142,5	K562	blood:
32	chr15:55675144..55677484-chr15:55677756..55679408,2	K562	blood:
33	chr15:55694340..55696767-chr15:55697475..55699670,2	MCF-7	breast:
34	chr15:55696852..55699665-chr15:55712534..55714960,2	K562	blood:
35	chr15:55638918..55640677-chr15:55646160..55647680,2	K562	blood:
36	chr15:55689930..55691529-chr15:55699148..55701673,2	MCF-7	breast:
37	chr15:55580643..55583951-chr15:55698978..55701737,3	K562	blood:
38	chr15:55659246..55661372-chr15:55665281..55667567,2	K562	blood:
39	chr15:55509498..55510422-chr15:55731553..55732482,2	K562	blood:
40	chr15:55664031..55666470-chr15:55667052..55669566,2	K562	blood:
41	chr15:55610040..55612568-chr15:55696345..55698141,2	MCF-7	breast:
42	chr15:55641994..55643661-chr15:55645653..55648003,2	K562	blood:
43	chr15:55646940..55648633-chr15:55651865..55653826,2	K562	blood:
44	chr13:60970048..60970785-chr15:55700070..55700954,2	Hela-S3	cervix:
45	chr1:179943932..179944436-chr15:55649661..55650212,2	MCF-7	breast:
46	chr15:55700561..55702324-chr15:55712580..55714464,2	K562	blood:
47	chr15:55656332..55658633-chr15:55699668..55701557,2	MCF-7	breast:
48	chr15:55700044..55700555-chr15:65596754..65597469,2	Hela-S3	cervix:
49	chr15:55687039..55689361-chr15:55690418..55692819,3	K562	blood:
50	chr15:55645555..55647417-chr15:55656372..55659364,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-628-5p	chr15:55665189-55665210	MIMAT0004809
hsa-miR-628-3p	chr15:55665152-55665172	MIMAT0003297

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CCPG1	hsa-miR-30a-5p	chr15:55647691-55647712
2	CCPG1	hsa-miR-30a-5p	chr15:55648622-55648616
3	CCPG1	hsa-miR-30a-5p	chr15:55647461-55647482
4	CCPG1	hsa-miR-30a-5p	chr15:55648616-55648637

Variant related genes	Relation type
C15orf65	TF binding region
CCPG1	TF binding region
ENSG00000260036	TF binding region
MIR628	TF binding region
PIGB	TF binding region
C15orf65	CpG island
CCPG1	CpG island
ENSG00000260036	CpG island
MIR628	CpG island
PIGB	CpG island
ENSG00000270141	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000072042	chromatin interactions
ENSG00000207964	chromatin interactions
ENSG00000225973	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000260916	chromatin interactions
ENSG00000261652	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000083544	chromatin interactions
ENSG00000069943	chromatin interactions
ENSG00000069974	chromatin interactions
ENSG00000137876	chromatin interactions
ENSG00000107164	chromatin interactions
ENSG00000202077	chromatin interactions
NELFE	Mature miRNA region
TGFBRAP1	Mature miRNA region
LRP6	Mature miRNA region
CDC14A	Mature miRNA region
AGO1	Mature miRNA region

Extended variants
information (count: 5027 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:5027 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4774766	chr15:55645661-55645662	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs56810972	chr15:55645688-55645689	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs138916755	chr15:55645713-55645714	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs553120442	chr15:55645772-55645773	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs185359094	chr15:55645789-55645790	Enhancers Weak transcription Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs541645471	chr15:55645818-55645819	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs189813587	chr15:55645828-55645829	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs12909448	chr15:55645857-55645858	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs2444040	chr15:55645862-55645863	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs146612345	chr15:55645882-55645883	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553055237	chr15:55645889-55645890	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs563952504	chr15:55645964-55645965	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs141398500	chr15:55646048-55646049	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs181128795	chr15:55646078-55646079	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs185717402	chr15:55646080-55646081	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs117308486	chr15:55646149-55646150	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs112479438	chr15:55646196-55646197	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs568739073	chr15:55646197-55646198	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs200366187	chr15:55646201-55646202	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs370984298	chr15:55646202-55646203	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs188184680	chr15:55646249-55646250	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs569362826	chr15:55646271-55646272	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs180938480	chr15:55646315-55646316	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs186394219	chr15:55646329-55646330	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs34045125	chr15:55646330-55646331	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs534221819	chr15:55646346-55646347	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs143904281	chr15:55646354-55646355	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs146410932	chr15:55646370-55646371	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs534217035	chr15:55646385-55646386	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs552964418	chr15:55646434-55646435	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs566761907	chr15:55646462-55646463	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs535233573	chr15:55646463-55646464	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs555184156	chr15:55646467-55646468	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs111863140	chr15:55646508-55646509	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs80018167	chr15:55646509-55646510	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs28653717	chr15:55646596-55646597	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs543935886	chr15:55646610-55646611	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs557830254	chr15:55646678-55646679	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs74015572	chr15:55646688-55646689	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577537681	chr15:55646697-55646698	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs192059430	chr15:55646749-55646750	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs183613653	chr15:55646782-55646783	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs529652187	chr15:55646828-55646829	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs543238723	chr15:55646872-55646873	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs186572807	chr15:55646961-55646962	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs368022268	chr15:55646965-55646966	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs191860992	chr15:55646985-55646986	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs372719891	chr15:55646993-55646994	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs377161481	chr15:55647037-55647038	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs182425933	chr15:55647038-55647039	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1672 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55611800-55699400	Weak transcription	Colonic Mucosa	Colon
2	chr15:55612000-55665000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr15:55612000-55671000	Weak transcription	Right Ventricle	heart
4	chr15:55612000-55671000	Weak transcription	Small Intestine	intestine
5	chr15:55612600-55650200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:55612600-55663600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:55612600-55675600	Weak transcription	Aorta	Aorta
8	chr15:55612800-55649600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:55612800-55677600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:55614800-55649000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr15:55620400-55658000	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr15:55623000-55652600	Weak transcription	Psoas Muscle	Psoas
13	chr15:55623800-55660200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr15:55626000-55649600	Weak transcription	HUVEC	blood vessel
15	chr15:55628600-55647800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr15:55630000-55695000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr15:55630200-55649000	Weak transcription	Osteobl	bone
18	chr15:55630400-55654600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr15:55630400-55675600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr15:55630600-55648000	Weak transcription	HepG2	liver
21	chr15:55630600-55655800	Weak transcription	Brain Angular Gyrus	brain
22	chr15:55630600-55660200	Weak transcription	Brain Cingulate Gyrus	brain
23	chr15:55630600-55663200	Weak transcription	Fetal Lung	lung
24	chr15:55630600-55667800	Weak transcription	Colon Smooth Muscle	Colon
25	chr15:55630600-55668400	Weak transcription	Brain Substantia Nigra	brain
26	chr15:55630800-55647000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr15:55630800-55652400	Weak transcription	Fetal Muscle Leg	muscle
28	chr15:55630800-55683600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr15:55631000-55667800	Weak transcription	Brain Hippocampus Middle	brain
30	chr15:55631200-55646600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr15:55631200-55663200	Weak transcription	Pancreas	Pancrea
32	chr15:55631200-55674000	Weak transcription	Placenta	Placenta
33	chr15:55631800-55649600	Weak transcription	NH-A	brain
34	chr15:55632000-55646800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr15:55633400-55646400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr15:55633600-55667200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr15:55635800-55675200	Weak transcription	Fetal Brain Male	brain
38	chr15:55636200-55647000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr15:55636400-55646600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr15:55636600-55649000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr15:55636600-55657000	Weak transcription	Fetal Brain Female	brain
42	chr15:55636600-55678200	Weak transcription	Fetal Thymus	thymus
43	chr15:55636800-55646000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr15:55636800-55646600	Weak transcription	Adipose Nuclei	Adipose
45	chr15:55636800-55647800	Weak transcription	HSMM	muscle
46	chr15:55636800-55649600	Weak transcription	HMEC	breast
47	chr15:55636800-55651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:55636800-55652000	Weak transcription	Left Ventricle	heart
49	chr15:55636800-55666200	Weak transcription	Brain Germinal Matrix	brain
50	chr15:55637000-55645800	Weak transcription	Fetal Heart	heart

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