Variant report

Variant	nsv569403
Chromosome Location	chr15:51191421-51304373
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1370)
CpG islands
(count:1344)
Chromatin interactive
region (count:129)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:51200645-51201018	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:51200644-51200980	K562	blood:	n/a	n/a
3	ARID3A	chr15:51296241-51296598	K562	blood:	n/a	n/a
4	ARID3A	chr15:51231131-51231188	K562	blood:	n/a	n/a
5	ARID3A	chr15:51199157-51199872	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:51199764-51200126	K562	blood:	n/a	n/a
7	ATF1	chr15:51200612-51200941	K562	blood:	n/a	n/a
8	ATF1	chr15:51296262-51296736	K562	blood:	n/a	n/a
9	ATF1	chr15:51199869-51200286	K562	blood:	n/a	n/a
10	ATF2	chr15:51199022-51200255	GM12878	blood:	n/a	n/a
11	ATF2	chr15:51200451-51201054	GM12878	blood:	n/a	n/a
12	ATF2	chr15:51199053-51200228	GM12878	blood:	n/a	n/a
13	ATF2	chr15:51200525-51200969	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr15:51200334-51200936	GM12878	blood:	n/a	n/a
15	ATF3	chr15:51200438-51201123	A549	lung:	n/a	chr15:51200541-51200550
16	ATF3	chr15:51200619-51200996	GM12878	blood:	n/a	n/a
17	ATF3	chr15:51200678-51200970	K562	blood:	n/a	n/a
18	ATF3	chr15:51200573-51200927	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr15:51200728-51201008	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr15:51200708-51200992	HepG2	liver:	n/a	n/a
21	ATF3	chr15:51200479-51201018	A549	lung:	n/a	chr15:51200541-51200550
22	ATF3	chr15:51296217-51296673	K562	blood:	n/a	n/a
23	ATF3	chr15:51200678-51200911	GM12878	blood:	n/a	n/a
24	BACH1	chr15:51200225-51200944	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr15:51200407-51200852	K562	blood:	n/a	n/a
26	BATF	chr15:51298834-51299059	GM12878	blood:	n/a	n/a
27	BATF	chr15:51252266-51252532	GM12878	blood:	n/a	n/a
28	BATF	chr15:51252287-51252483	GM12878	blood:	n/a	n/a
29	BATF	chr15:51199088-51199721	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:51199186-51199767	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:51199036-51199772	GM12878	blood:	n/a	n/a
32	BCL3	chr15:51200416-51200971	GM12878	blood:	n/a	chr15:51200874-51200883 chr15:51200458-51200471
33	BCL3	chr15:51199084-51199846	GM12878	blood:	n/a	n/a
34	BCL3	chr15:51200420-51201096	A549	lung:	n/a	chr15:51200874-51200883 chr15:51200458-51200471
35	BCL3	chr15:51199221-51199783	GM12878	blood:	n/a	n/a
36	BCL3	chr15:51200474-51201104	A549	lung:	n/a	chr15:51200874-51200883
37	BCLAF1	chr15:51199038-51201064	GM12878	blood:	n/a	chr15:51200874-51200883 chr15:51200101-51200109 chr15:51200458-51200471
38	BCLAF1	chr15:51199041-51201111	GM12878	blood:	n/a	chr15:51200874-51200883 chr15:51200101-51200109 chr15:51200458-51200471
39	BHLHE40	chr15:51296249-51296756	K562	blood:	n/a	n/a
40	BHLHE40	chr15:51199749-51200987	K562	blood:	n/a	n/a
41	BHLHE40	chr15:51199100-51201249	GM12878	blood:	n/a	n/a
42	BHLHE40	chr15:51199229-51199485	K562	blood:	n/a	n/a
43	BHLHE40	chr15:51200228-51201116	HepG2	liver:	n/a	n/a
44	BRCA1	chr15:51200279-51201040	HepG2	liver:	n/a	chr15:51200811-51200820
45	BRCA1	chr15:51200499-51201690	Hela-S3	cervix:	n/a	chr15:51200811-51200820
46	BRCA1	chr15:51295844-51296596	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr15:51199207-51199783	GM12878	blood:	n/a	n/a
48	BRCA1	chr15:51200406-51200995	GM12878	blood:	n/a	chr15:51200811-51200820
49	BRCA1	chr15:51200589-51200995	H1-hESC	embryonic stem cell:	n/a	chr15:51200811-51200820
50	CBX3	chr15:51200373-51201045	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51201076-51201126	SK-N-MC	brain:	n/a
2	chr15:51236304-51236354	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:51201076-51201126	SK-N-MC	brain:	n/a
4	chr15:51236304-51236354	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:51201261-51201311	HCF	heart:	n/a
6	chr15:51235727-51235777	ECC-1	luminal epithelium:	n/a
7	chr15:51236304-51236354	PFSK-1	brain:	n/a
8	chr15:51235727-51235777	AG09319	gingival:	n/a
9	chr15:51199642-51199692	ECC-1	luminal epithelium:	n/a
10	chr15:51200672-51200722	Hepatocyte	liver:	n/a
11	chr15:51235727-51235777	HPAEpiC	pulmonary alveolar:	n/a
12	chr15:51203304-51203354	RPTEC	kidney:	n/a
13	chr15:51201076-51201126	HEK293	kidney:	embryo
14	chr15:51200723-51200773	PFSK-1	brain:	n/a
15	chr15:51200825-51200875	MCF10A-Er-Src	breast:	n/a
16	chr15:51295331-51295381	HIPEpiC	eye:	n/a
17	chr15:51203304-51203354	AG04450	lung:	fetal
18	chr15:51200715-51200765	NHDF-neo	bronchial:	n/a
19	chr15:51199395-51199445	Jurkat	blood:	n/a
20	chr15:51200259-51200309	ECC-1	luminal epithelium:	n/a
21	chr15:51200847-51200897	AoSMC	blood vessel:	n/a
22	chr15:51235727-51235777	NH-A	brain:	n/a
23	chr15:51243589-51243639	NB4	blood:	n/a
24	chr15:51200195-51200245	HPAEpiC	pulmonary alveolar:	n/a
25	chr15:51200259-51200309	LNCaP	prostate:	n/a
26	chr15:51200847-51200897	PrEC	prostate:	n/a
27	chr15:51201076-51201126	NHDF-neo	bronchial:	n/a
28	chr15:51200825-51200875	HCF	heart:	n/a
29	chr15:51200847-51200897	GM19239	blood:	n/a
30	chr15:51197587-51197637	MCF10A-Er-Src	breast:	n/a
31	chr15:51199395-51199445	HEK293	kidney:	embryo
32	chr15:51200825-51200875	GM06990	blood:	n/a
33	chr15:51235757-51235807	RPTEC	kidney:	n/a
34	chr15:51200259-51200309	IMR90	lung:	fetal
35	chr15:51200363-51200413	AG10803	skin:	n/a
36	chr15:51200259-51200309	T-47D	breast:	n/a
37	chr15:51236304-51236354	HCF	heart:	n/a
38	chr15:51200672-51200722	SKMC	muscle:	n/a
39	chr15:51197587-51197637	GM12892	blood:	n/a
40	chr15:51200822-51200872	HIPEpiC	eye:	n/a
41	chr15:51200847-51200897	AG04450	lung:	fetal
42	chr15:51200672-51200722	NB4	blood:	n/a
43	chr15:51200195-51200245	K562	blood:	n/a
44	chr15:51235727-51235777	SK-N-SH_RA	brain:	n/a
45	chr15:51200814-51200864	Caco-2	colon:	n/a
46	chr15:51200363-51200413	PANC-1	pancreas:	n/a
47	chr15:51243589-51243639	AG10803	skin:	n/a
48	chr15:51200847-51200897	CMK	blood:	n/a
49	chr15:51235757-51235807	HCF	heart:	n/a
50	chr15:51199395-51199445	GM06990	blood:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:51291454..51293095-chr15:51294731..51296517,2	K562	blood:
2	chr15:51294396..51297961-chr15:51303486..51306032,4	MCF-7	breast:
3	chr1:180123605..180124282-chr15:51200703..51201684,2	MCF-7	breast:
4	chr15:51207605..51209547-chr15:51210912..51214832,3	K562	blood:
5	chr15:50977442..50979922-chr15:51198976..51201748,2	MCF-7	breast:
6	chr15:51198585..51200191-chr20:47687011..47688512,2	K562	blood:
7	chr15:51201141..51202699-chr15:51202955..51205782,2	K562	blood:
8	chr15:51200426..51201356-chr16:89988887..89989457,2	Hela-S3	cervix:
9	chr15:51189648..51191735-chr15:51199427..51201147,2	MCF-7	breast:
10	chr15:51199801..51202034-chr15:51214666..51217495,2	K562	blood:
11	chr15:51202456..51205148-chr15:51207377..51210449,3	MCF-7	breast:
12	chr15:51197121..51199959-chr15:51225911..51227445,2	MCF-7	breast:
13	chr15:51201141..51203041-chr15:51203150..51205782,2	K562	blood:
14	chr15:50977199..50979864-chr15:51198670..51201821,3	K562	blood:
15	chr15:51213719..51215639-chr15:51221253..51222973,2	MCF-7	breast:
16	chr15:50966474..50968190-chr15:51199130..51200749,2	K562	blood:
17	chr15:51242549..51245131-chr15:51257817..51260638,2	MCF-7	breast:
18	chr15:51055794..51057333-chr15:51198910..51200716,2	K562	blood:
19	chr15:51295054..51296990-chr15:51420438..51423061,2	K562	blood:
20	chr15:51215851..51217409-chr15:51217838..51220834,2	MCF-7	breast:
21	chr15:50977199..50981459-chr15:51198510..51202863,6	K562	blood:
22	chr15:51201141..51202699-chr15:51202955..51205782,2	K562	blood:
23	chr15:51176297..51178705-chr15:51190226..51192825,2	MCF-7	breast:
24	chr15:51208651..51211313-chr15:51228835..51231106,2	MCF-7	breast:
25	chr15:51255834..51257399-chr15:51273683..51276237,2	MCF-7	breast:
26	chr15:51248351..51249869-chr15:51253170..51254880,2	MCF-7	breast:
27	chr15:51243593..51246491-chr15:51256296..51259050,2	MCF-7	breast:
28	chr15:51275705..51277653-chr15:51278587..51281161,2	MCF-7	breast:
29	chr15:51186902..51189872-chr15:51192876..51194518,2	K562	blood:
30	chr15:51275789..51278184-chr15:51333901..51335893,2	MCF-7	breast:
31	chr15:51259926..51261571-chr15:51483708..51485228,2	MCF-7	breast:
32	chr15:51269282..51271249-chr15:51274355..51276243,2	MCF-7	breast:
33	chr15:51191099..51192622-chr15:51197592..51200160,2	K562	blood:
34	chr15:50967384..50968440-chr15:51199299..51199841,3	K562	blood:
35	chr15:51240708..51242711-chr15:51242889..51245874,2	K562	blood:
36	chr15:51174662..51176293-chr15:51192005..51193675,2	K562	blood:
37	chr15:50715057..50718112-chr15:51199966..51202837,4	MCF-7	breast:
38	chr15:51293258..51295626-chr15:51337830..51340357,2	MCF-7	breast:
39	chr15:51291454..51293095-chr15:51294731..51296517,2	K562	blood:
40	chr15:50649363..50652046-chr15:51189573..51192655,3	MCF-7	breast:
41	chr15:51234956..51237517-chr15:51240627..51243200,3	K562	blood:
42	chr15:51230290..51232178-chr15:51234294..51236150,2	MCF-7	breast:
43	chr15:51303494..51305144-chr15:51312892..51315605,2	MCF-7	breast:
44	chr15:51190200..51192622-chr15:51197284..51200160,3	K562	blood:
45	chr15:51171477..51173642-chr15:51201316..51203040,2	K562	blood:
46	chr15:51230290..51232178-chr15:51234294..51236150,2	MCF-7	breast:
47	chr15:51242549..51245131-chr15:51257817..51260638,2	MCF-7	breast:
48	chr1:121484254..121485225-chr15:51241675..51242617,2	MCF-7	breast:
49	chr15:50646809..50648452-chr15:51207818..51210363,2	MCF-7	breast:
50	chr15:51224967..51227623-chr15:51229522..51232521,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP8-5	chr15:51207753-51208169	NONHSAT042444
2	lnc-SPPL2A.1-1	chr15:51200749-51200796	ENSG00000247586
3	lnc-USP8-5	chr15:51210227-51210312	NONHSAT042444
4	lnc-GLDN-5	chr15:51236860-51238193	NONHSAT042447
5	lnc-SPPL2A.1-1	chr15:51199113-51200792	NONHSAT042443
6	lnc-GLDN-5	chr15:51236326-51238762	NONHSAT042446
7	lnc-GLDN-6	chr15:51213504-51214133	NONHSAT042445

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	AP4E1	hsa-miR-148b-3p	chr15:51297926-51297933
2	AP4E1	hsa-miR-148b-3p	chr15:51298073-51298096
3	AP4E1	hsa-miR-148b-3p	chr15:51297911-51297933

Variant related genes	Relation type
AP4E1	TF binding region
DCAF13P3	TF binding region
AP4E1	CpG island
DCAF13P3	CpG island
ENSG00000243027	chromatin interactions
ENSG00000111897	chromatin interactions
ENSG00000126215	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000100711	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000165661	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000259378	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000092439	chromatin interactions
GCFC1	miRNA target sites

Extended variants
information (count: 4165 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4165 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2663542	chr15:51191421-51191422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537864871	chr15:51191454-51191455	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531327423	chr15:51191491-51191492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183626693	chr15:51191540-51191541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147177881	chr15:51191558-51191559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545336016	chr15:51191576-51191577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554435850	chr15:51191649-51191650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572722354	chr15:51191657-51191658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs34955287	chr15:51191681-51191682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543218663	chr15:51191770-51191771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560997662	chr15:51191774-51191775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531408898	chr15:51191840-51191841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140296149	chr15:51191841-51191842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564687621	chr15:51191876-51191877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144234249	chr15:51191894-51191895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs578184860	chr15:51191907-51191908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113313710	chr15:51191991-51191992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147322108	chr15:51192046-51192047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529872866	chr15:51192056-51192057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547948646	chr15:51192080-51192081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545756561	chr15:51192086-51192087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537901604	chr15:51192103-51192104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs140007489	chr15:51192169-51192170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7170963	chr15:51192185-51192186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549875140	chr15:51192202-51192203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2663541	chr15:51192206-51192207	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554194019	chr15:51192222-51192223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1147132	chr15:51192233-51192234	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536850100	chr15:51192234-51192235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369350208	chr15:51192248-51192249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555156876	chr15:51192292-51192293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77907426	chr15:51192336-51192337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551512747	chr15:51192361-51192362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543194704	chr15:51192362-51192363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148990812	chr15:51192363-51192364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144288889	chr15:51192493-51192494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541006989	chr15:51192507-51192508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559238734	chr15:51192575-51192576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566833699	chr15:51192578-51192579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs74015228	chr15:51192610-51192611	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs547983289	chr15:51192619-51192620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187486816	chr15:51192677-51192678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530609137	chr15:51192679-51192680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146585905	chr15:51192811-51192812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199534530	chr15:51192896-51192897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571691309	chr15:51192965-51192966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34928106	chr15:51192982-51192983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538688911	chr15:51193050-51193051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141200893	chr15:51193062-51193063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145002104	chr15:51193076-51193077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Breast cancer	21785460	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3717 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51177800-51199200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr15:51177800-51199600	Weak transcription	Ovary	ovary
3	chr15:51179000-51199200	Weak transcription	Brain Angular Gyrus	brain
4	chr15:51183800-51199200	Weak transcription	Brain Substantia Nigra	brain
5	chr15:51185800-51199800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr15:51187200-51199000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:51187200-51199200	Weak transcription	Placenta	Placenta
8	chr15:51188400-51199200	Weak transcription	Fetal Lung	lung
9	chr15:51190000-51198800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr15:51191000-51191600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr15:51191200-51192000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:51191200-51195200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:51191400-51191600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr15:51191600-51192400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:51191600-51194800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:51191600-51199000	Weak transcription	Thymus	Thymus
17	chr15:51192000-51199200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:51192400-51193000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr15:51192400-51193000	Enhancers	NHDF-Ad	bronchial
20	chr15:51192400-51193200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr15:51192400-51193400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:51192600-51193200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:51193000-51194400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:51193200-51193800	Weak transcription	NHDF-Ad	bronchial
25	chr15:51193200-51199000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr15:51193400-51194800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:51194000-51194200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr15:51194000-51194200	Weak transcription	Right Ventricle	heart
29	chr15:51194200-51194400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr15:51194200-51194400	Enhancers	Right Ventricle	heart
31	chr15:51194200-51199200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr15:51194400-51195000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:51194400-51199200	Weak transcription	Right Ventricle	heart
34	chr15:51194800-51195000	Enhancers	Primary T cells from cord blood	blood
35	chr15:51194800-51195200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr15:51194800-51195200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:51194800-51195200	Enhancers	Dnd41	blood
38	chr15:51194800-51196600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:51194800-51200000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:51195000-51195200	Enhancers	A549	lung
41	chr15:51195000-51198800	Weak transcription	Primary T cells from cord blood	blood
42	chr15:51195000-51199000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr15:51195200-51197000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr15:51195200-51198800	Weak transcription	Dnd41	blood
45	chr15:51195200-51199000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:51195200-51199200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr15:51195400-51199000	Weak transcription	Fetal Intestine Small	intestine
48	chr15:51195400-51199200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr15:51195400-51199600	Weak transcription	Fetal Stomach	stomach
50	chr15:51195600-51199600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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