Variant report

Variant	nsv1050385
Chromosome Location	chr15:50843495-50949798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:650)
CpG islands
(count:122)
Chromatin interactive
region (count:87)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:50888476-50888556	K562	blood:	n/a	n/a
2	ARID3A	chr15:50914579-50914778	K562	blood:	n/a	n/a
3	ARID3A	chr15:50885990-50886949	K562	blood:	n/a	n/a
4	ATF1	chr15:50916939-50917053	K562	blood:	n/a	n/a
5	ATF1	chr15:50886574-50886849	K562	blood:	n/a	n/a
6	ATF2	chr15:50946651-50947033	GM12878	blood:	n/a	n/a
7	ATF2	chr15:50844379-50844831	GM12878	blood:	n/a	n/a
8	BACH1	chr15:50869845-50869896	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:50869823-50869907	K562	blood:	n/a	n/a
10	BATF	chr15:50946619-50946969	GM12878	blood:	n/a	n/a
11	BATF	chr15:50946645-50947003	GM12878	blood:	n/a	n/a
12	CCNT2	chr15:50886474-50886898	K562	blood:	n/a	n/a
13	CCNT2	chr15:50933565-50933899	K562	blood:	n/a	n/a
14	CEBPB	chr15:50905809-50906222	A549	lung:	n/a	n/a
15	CEBPB	chr15:50931692-50932047	A549	lung:	n/a	n/a
16	CEBPB	chr15:50931794-50931833	K562	blood:	n/a	n/a
17	CEBPB	chr15:50889075-50889077	K562	blood:	n/a	n/a
18	CEBPB	chr15:50929902-50930087	IMR90	lung:	n/a	chr15:50930024-50930035
19	CEBPB	chr15:50929899-50930169	HepG2	liver:	n/a	chr15:50930024-50930035
20	CEBPB	chr15:50874149-50874329	HepG2	liver:	n/a	chr15:50874215-50874226
21	CEBPB	chr15:50905849-50906159	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:50879839-50880023	HepG2	liver:	n/a	chr15:50879905-50879916
23	CEBPB	chr15:50916902-50917200	IMR90	lung:	n/a	n/a
24	CEBPB	chr15:50861954-50862152	A549	lung:	n/a	n/a
25	CEBPB	chr15:50905830-50906159	K562	blood:	n/a	n/a
26	CEBPB	chr15:50879756-50879976	A549	lung:	n/a	chr15:50879905-50879916
27	CEBPB	chr15:50880400-50880451	A549	lung:	n/a	n/a
28	CEBPB	chr15:50880374-50880513	K562	blood:	n/a	chr15:50880463-50880474
29	CEBPB	chr15:50881475-50881754	K562	blood:	n/a	chr15:50881581-50881594 chr15:50881581-50881594
30	CEBPB	chr15:50929889-50930144	A549	lung:	n/a	chr15:50930024-50930035
31	CEBPB	chr15:50905825-50906178	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:50894818-50895097	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:50889065-50889265	IMR90	lung:	n/a	n/a
34	CEBPB	chr15:50886533-50886784	K562	blood:	n/a	n/a
35	CEBPB	chr15:50916897-50917199	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr15:50916905-50917183	A549	lung:	n/a	n/a
37	CEBPB	chr15:50905719-50906245	MCF-7	breast:	n/a	n/a
38	CEBPB	chr15:50916859-50917181	K562	blood:	n/a	n/a
39	CEBPB	chr15:50905894-50906111	A549	lung:	n/a	n/a
40	CEBPB	chr15:50905827-50906151	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:50894829-50895045	A549	lung:	n/a	n/a
42	CEBPB	chr15:50905848-50906147	A549	lung:	n/a	n/a
43	CEBPB	chr15:50858006-50858029	K562	blood:	n/a	n/a
44	CEBPB	chr15:50881597-50881743	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:50905892-50906190	MCF-7	breast:	n/a	n/a
46	CEBPB	chr15:50881732-50881885	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPD	chr15:50886481-50887012	K562	blood:	n/a	n/a
48	CEBPD	chr15:50933672-50934006	K562	blood:	n/a	n/a
49	CEBPD	chr15:50886419-50886927	K562	blood:	n/a	n/a
50	CTCF	chr15:50914456-50914878	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50920452-50920502	HCM	heart:	n/a
2	chr15:50853806-50853856	NB4	blood:	n/a
3	chr15:50920452-50920502	AoSMC	blood vessel:	n/a
4	chr15:50920452-50920502	K562	blood:	n/a
5	chr15:50920452-50920502	HAEpiC	amniotic membrane:	n/a
6	chr15:50920452-50920502	MCF10A-Er-Src	breast:	n/a
7	chr15:50853806-50853856	HNPCEpiC	eye:	n/a
8	chr15:50853806-50853856	LNCaP	prostate:	n/a
9	chr15:50853806-50853856	Hepatocyte	liver:	n/a
10	chr15:50853806-50853856	SK-N-SH_RA	brain:	n/a
11	chr15:50853806-50853856	GM12892	blood:	n/a
12	chr15:50920452-50920502	H1-hESC	embryonic stem cell:	embryo
13	chr15:50920452-50920502	U87	brain:	n/a
14	chr15:50920452-50920502	AG04449	skin:	fetal
15	chr15:50920452-50920502	SAEC	small airway:	n/a
16	chr15:50853806-50853856	SAEC	small airway:	n/a
17	chr15:50853806-50853856	AG10803	skin:	n/a
18	chr15:50920452-50920502	Caco-2	colon:	n/a
19	chr15:50853806-50853856	SKMC	muscle:	n/a
20	chr15:50853806-50853856	MCF-7	breast:	n/a
21	chr15:50853806-50853856	SK-N-SH	brain:	n/a
22	chr15:50853806-50853856	AG04450	lung:	fetal
23	chr15:50920452-50920502	GM19239	blood:	n/a
24	chr15:50920452-50920502	HEEpiC	esophagus:	n/a
25	chr15:50853806-50853856	Hela-S3	cervix:	n/a
26	chr15:50920452-50920502	SK-N-SH_RA	brain:	n/a
27	chr15:50920452-50920502	PANC-1	pancreas:	n/a
28	chr15:50853806-50853856	RPTEC	kidney:	n/a
29	chr15:50920452-50920502	HMEC	breast:	n/a
30	chr15:50920452-50920502	GM12892	blood:	n/a
31	chr15:50853806-50853856	HCPEpiC	choroid plexus:	n/a
32	chr15:50920452-50920502	NH-A	brain:	n/a
33	chr15:50920452-50920502	NHDF-neo	bronchial:	n/a
34	chr15:50920452-50920502	BE2_C	brain:	n/a
35	chr15:50920452-50920502	HL-60	blood:	n/a
36	chr15:50920452-50920502	ProgFib	skin:	n/a
37	chr15:50920452-50920502	MCF-7	breast:	n/a
38	chr15:50920452-50920502	SK-N-MC	brain:	n/a
39	chr15:50920452-50920502	HCF	heart:	n/a
40	chr15:50853806-50853856	GM06990	blood:	n/a
41	chr15:50853806-50853856	HL-60	blood:	n/a
42	chr15:50920452-50920502	RPTEC	kidney:	n/a
43	chr15:50853806-50853856	HCM	heart:	n/a
44	chr15:50920452-50920502	SK-N-SH	brain:	n/a
45	chr15:50853806-50853856	HRE	kidney:	n/a
46	chr15:50920452-50920502	HNPCEpiC	eye:	n/a
47	chr15:50853806-50853856	HEK293	kidney:	embryo
48	chr15:50920452-50920502	BJ	skin:	n/a
49	chr15:50853806-50853856	ovcar-3	ovarian:	n/a
50	chr15:50853806-50853856	HCT-116	colon:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:50890587..50894134-chr15:50900500..50903052,3	MCF-7	breast:
2	chr15:50864188..50868322-chr15:50872346..50875460,4	MCF-7	breast:
3	chr15:50842951..50845112-chr15:50852235..50854464,2	MCF-7	breast:
4	chr15:50850389..50851956-chr15:50856015..50858567,2	MCF-7	breast:
5	chr15:50871076..50873819-chr15:50876627..50878202,2	MCF-7	breast:
6	chr15:50885914..50887497-chr15:50920391..50922756,2	K562	blood:
7	chr15:50917148..50919923-chr15:50927346..50929750,2	MCF-7	breast:
8	chr15:50867388..50869846-chr15:50878063..50879633,2	MCF-7	breast:
9	chr15:50891850..50893589-chr15:50903220..50904870,2	MCF-7	breast:
10	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
11	chr15:50939543..50942459-chr15:50946221..50948158,2	K562	blood:
12	chr15:50646568..50648510-chr15:50882199..50884053,2	MCF-7	breast:
13	chr15:50871076..50873819-chr15:50876627..50878202,2	MCF-7	breast:
14	chr15:50840672..50844284-chr15:50844552..50846855,4	K562	blood:
15	chr15:50925249..50927102-chr15:51201168..51202804,2	MCF-7	breast:
16	chr15:50647415..50649249-chr15:50862816..50866408,3	MCF-7	breast:
17	chr15:50850389..50851956-chr15:50856015..50858567,2	MCF-7	breast:
18	chr15:50900703..50903174-chr15:51177027..51179659,2	K562	blood:
19	chr15:50889745..50892079-chr19:13048030..13049882,2	MCF-7	breast:
20	chr15:50847628..50850307-chr15:50851191..50853232,2	MCF-7	breast:
21	chr15:50909782..50912270-chr15:50977423..50980353,2	MCF-7	breast:
22	chr15:50878762..50881023-chr15:50884773..50886938,2	K562	blood:
23	chr15:50869586..50872138-chr15:50874488..50876598,3	K562	blood:
24	chr15:50838341..50841082-chr15:50844328..50846854,3	MCF-7	breast:
25	chr15:50854287..50856205-chr15:51176623..51178248,2	MCF-7	breast:
26	chr15:50881070..50883291-chr15:50976406..50979005,2	MCF-7	breast:
27	chr15:50855242..50858331-chr15:50858835..50863040,3	MCF-7	breast:
28	chr15:50842296..50845000-chr15:50847608..50850215,3	MCF-7	breast:
29	chr15:50856695..50857215-chr19:16191667..16192187,2	MCF-7	breast:
30	chr15:50865776..50869008-chr15:50882396..50886787,3	K562	blood:
31	chr15:50647510..50649094-chr15:50844767..50846494,2	MCF-7	breast:
32	chr15:50646500..50650701-chr15:50853140..50859875,5	MCF-7	breast:
33	chr15:50853846..50855593-chr15:50859811..50861403,2	MCF-7	breast:
34	chr15:50861509..50865180-chr15:50865318..50870216,6	K562	blood:
35	chr15:50859308..50861522-chr15:50879370..50881097,2	K562	blood:
36	chr15:50839132..50840777-chr15:50843129..50844721,2	K562	blood:
37	chr15:50916413..50918620-chr15:50919827..50924015,3	K562	blood:
38	chr15:50646822..50648460-chr15:50870305..50871829,2	MCF-7	breast:
39	chr15:50889435..50893254-chr15:50893944..50897716,3	K562	blood:
40	chr15:50644948..50647496-chr15:50903184..50905724,2	MCF-7	breast:
41	chr15:50933534..50935259-chr15:51198839..51201144,2	MCF-7	breast:
42	chr15:50932446..50935258-chr15:50953275..50954778,2	K562	blood:
43	chr15:50918354..50921026-chr15:51021586..51024072,2	MCF-7	breast:
44	chr15:50914714..50916559-chr15:50917058..50919826,2	K562	blood:
45	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
46	chr15:50646216..50648190-chr15:50918382..50920055,2	MCF-7	breast:
47	chr15:50840672..50844284-chr15:50844552..50846855,4	K562	blood:
48	chr15:50914267..50915255-chr15:51177811..51178741,3	MCF-7	breast:
49	chr15:50645350..50647759-chr15:50913615..50916284,2	K562	blood:
50	chr15:50872498..50875116-chr15:50878753..50881368,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP8-3	chr15:50873840-50874894	l_1155_chr15:50872073-50874894_testes
2	lnc-USP50-5	chr15:50883698-50883786	l_1156_chr15:50879698-50884434_liver
3	lnc-USP8-1	chr15:50850820-50850825	ENSG00000259684.1
4	lnc-USP8-3	chr15:50872074-50872178	l_1155_chr15:50872073-50874894_testes
5	lnc-USP8-1	chr15:50852196-50852697	ENSG00000259684.1
6	lnc-USP8-1	chr15:50849798-50849895	ENSG00000259684.1
7	lnc-USP50-5	chr15:50879699-50880406	l_1156_chr15:50879698-50884434_liver
8	lnc-USP50-5	chr15:50883983-50884434	l_1156_chr15:50879698-50884434_liver
9	lnc-USP50-5	chr15:50882478-50883336	l_1156_chr15:50879698-50884434_liver

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TRPM7	hsa-miR-10a-5p	chr15:50896593-50896615
2	TRPM7	hsa-miR-9-5p	chr15:50853543-50853537
3	TRPM7	hsa-miR-21-5p	chr15:50852622-50852616
4	TRPM7	hsa-miR-9-5p	chr15:50853537-50853560
5	TRPM7	hsa-miR-9-5p	chr15:50853009-50853003
6	TRPM7	hsa-miR-9-5p	chr15:50853004-50853026
7	TRPM7	hsa-miR-10a-5p	chr15:50853328-50853352
8	TRPM7	hsa-miR-10a-5p	chr15:50896505-50896530
9	TRPM7	hsa-miR-21-5p	chr15:50852616-50852636

Variant related genes	Relation type
USP50	TF binding region
TRPM7	TF binding region
ENSG00000259684	TF binding region
USP50	CpG island
TRPM7	CpG island
ENSG00000259684	CpG island
ENSG00000244879	chromatin interactions
ENSG00000170236	chromatin interactions
ENSG00000259684	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000179218	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000092439	chromatin interactions

Extended variants
information (count: 4442 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4442 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574021858	chr15:50843577-50843578	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs538429347	chr15:50843586-50843587	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs72740412	chr15:50843596-50843597	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562642529	chr15:50843621-50843622	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577624947	chr15:50843634-50843635	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544777994	chr15:50843690-50843691	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577871625	chr15:50843752-50843753	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369392247	chr15:50843808-50843809	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190137546	chr15:50843875-50843876	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138037980	chr15:50843930-50843931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114208375	chr15:50843983-50843984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182369820	chr15:50843989-50843990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147317077	chr15:50844004-50844005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75919483	chr15:50844027-50844028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35834131	chr15:50844075-50844076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373163537	chr15:50844081-50844082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564942982	chr15:50844084-50844085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35517805	chr15:50844096-50844097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs139997661	chr15:50844120-50844121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527341800	chr15:50844136-50844137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542195972	chr15:50844140-50844141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs117903954	chr15:50844155-50844156	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566658918	chr15:50844168-50844169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78432176	chr15:50844180-50844181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549011714	chr15:50844213-50844214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs112857198	chr15:50844307-50844308	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs3101850	chr15:50844314-50844315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs184876797	chr15:50844327-50844328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79787541	chr15:50844366-50844367	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs189342232	chr15:50844416-50844417	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200178188	chr15:50844419-50844420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs181354915	chr15:50844441-50844442	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531271997	chr15:50844448-50844449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs372461877	chr15:50844475-50844476	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs547037387	chr15:50844497-50844498	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538696051	chr15:50844502-50844503	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs180706579	chr15:50844528-50844529	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs34368659	chr15:50844543-50844544	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531021748	chr15:50844553-50844554	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73407291	chr15:50844572-50844573	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185142128	chr15:50844576-50844577	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs62019157	chr15:50844624-50844625	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs569308243	chr15:50844631-50844632	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs116969136	chr15:50844651-50844652	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs191313791	chr15:50844674-50844675	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377064937	chr15:50844681-50844682	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs17598264	chr15:50844711-50844712	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs560209124	chr15:50844740-50844741	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs148568830	chr15:50844750-50844751	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs57794495	chr15:50844768-50844769	Weak transcription Enhancers Active TSS	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
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
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2682 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50834600-50853200	Weak transcription	HSMMtube	muscle
2	chr15:50835600-50844000	Weak transcription	GM12878-XiMat	blood
3	chr15:50836200-50848400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:50836200-50848600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr15:50836200-50850000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:50837000-50850600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:50837000-50851600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr15:50837000-50852800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr15:50837000-50862200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr15:50837000-50882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:50839600-50848800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr15:50839800-50848800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:50840200-50848800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr15:50841200-50849800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr15:50841800-50849800	Weak transcription	Fetal Stomach	stomach
16	chr15:50841800-50852800	Weak transcription	Placenta	Placenta
17	chr15:50843400-50843600	Enhancers	H9 Cell Line	embryonic stem cell
18	chr15:50843400-50850400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:50843600-50843800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr15:50843600-50860800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:50843800-50844000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:50843800-50851600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr15:50844000-50844200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:50844000-50844600	Enhancers	GM12878-XiMat	blood
25	chr15:50844000-50845800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr15:50844000-50855200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr15:50844200-50862200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr15:50844600-50844800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr15:50844600-50845000	Active TSS	GM12878-XiMat	blood
30	chr15:50845000-50845600	Enhancers	GM12878-XiMat	blood
31	chr15:50845000-50849000	Weak transcription	HSMM	muscle
32	chr15:50845200-50849000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:50845200-50851800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr15:50845600-50848000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr15:50845600-50848800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:50845600-50851600	Weak transcription	GM12878-XiMat	blood
37	chr15:50845800-50846800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:50845800-50849600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:50846000-50849000	Weak transcription	A549	lung
40	chr15:50846000-50850400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr15:50846000-50950800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:50846200-50867000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr15:50846400-50849000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr15:50846600-50858600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr15:50846800-50848400	Weak transcription	Left Ventricle	heart
46	chr15:50846800-50848800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:50846800-50849000	Weak transcription	Osteobl	bone
48	chr15:50846800-50850400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr15:50846800-50860800	Weak transcription	NHLF	lung
50	chr15:50847000-50848800	Weak transcription	Liver	Liver

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