Variant report

Variant	nsv1064207
Chromosome Location	chr19:51474525-51497278
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr19:51475980-51476815	HCT-116	colon:	n/a	n/a
2	CEBPB	chr19:51474450-51474685	K562	blood:	n/a	chr19:51474553-51474566 chr19:51474555-51474564 chr19:51474553-51474564
3	CEBPB	chr19:51474410-51474638	H1-hESC	embryonic stem cell:	n/a	chr19:51474553-51474566 chr19:51474555-51474564 chr19:51474553-51474564
4	CEBPB	chr19:51480253-51480376	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr19:51474427-51474673	HepG2	liver:	n/a	chr19:51474553-51474566 chr19:51474555-51474564 chr19:51474553-51474564
6	CEBPB	chr19:51480248-51480292	K562	blood:	n/a	n/a
7	EGR1	chr19:51484902-51485125	K562	blood:	n/a	n/a
8	EGR1	chr19:51487065-51487637	HCT-116	colon:	n/a	chr19:51487378-51487391 chr19:51487264-51487274 chr19:51487373-51487395 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487377-51487392 chr19:51487261-51487270
9	EGR1	chr19:51484908-51485157	K562	blood:	n/a	n/a
10	EGR1	chr19:51486963-51487635	HCT-116	colon:	n/a	chr19:51487378-51487391 chr19:51487373-51487395 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487264-51487274 chr19:51487377-51487392 chr19:51487261-51487270
11	EGR1	chr19:51487232-51487507	K562	blood:	n/a	chr19:51487378-51487391 chr19:51487264-51487274 chr19:51487373-51487395 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487377-51487392 chr19:51487261-51487270
12	EGR1	chr19:51487250-51487445	K562	blood:	n/a	chr19:51487378-51487391 chr19:51487264-51487274 chr19:51487373-51487395 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487377-51487392 chr19:51487261-51487270
13	EGR1	chr19:51487130-51487484	H1-hESC	embryonic stem cell:	n/a	chr19:51487378-51487391 chr19:51487264-51487274 chr19:51487373-51487395 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487378-51487391 chr19:51487377-51487392 chr19:51487261-51487270
14	ELF1	chr19:51478988-51479507	MCF-7	breast:	n/a	chr19:51479159-51479170
15	ELF1	chr19:51478984-51479505	MCF-7	breast:	n/a	chr19:51479159-51479170
16	EP300	chr19:51478920-51479337	MCF-7	breast:	n/a	n/a
17	FOS	chr19:51476195-51476469	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr19:51476179-51476464	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr19:51482281-51482690	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr19:51482281-51482620	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr19:51482285-51482650	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr19:51479130-51479340	MCF10A-Er-Src	breast:	n/a	chr19:51479281-51479289
23	FOS	chr19:51495178-51495481	MCF10A-Er-Src	breast:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495429-51495440 chr19:51495324-51495331 chr19:51495324-51495333
24	FOS	chr19:51482281-51482603	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr19:51495196-51495459	MCF10A-Er-Src	breast:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495429-51495440 chr19:51495324-51495331 chr19:51495324-51495333
26	FOSL1	chr19:51495054-51495731	HCT-116	colon:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495429-51495440 chr19:51495324-51495331 chr19:51495324-51495333
27	FOSL1	chr19:51475910-51476674	HCT-116	colon:	n/a	n/a
28	FOSL2	chr19:51495073-51495533	MCF-7	breast:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495429-51495440 chr19:51495324-51495331 chr19:51495324-51495333
29	FOSL2	chr19:51482148-51482571	A549	lung:	n/a	n/a
30	FOSL2	chr19:51479021-51479531	MCF-7	breast:	n/a	chr19:51479281-51479289
31	FOSL2	chr19:51482184-51482707	MCF-7	breast:	n/a	n/a
32	GATA3	chr19:51495074-51495508	MCF-7	breast:	n/a	chr19:51495365-51495372
33	GATA3	chr19:51495196-51495487	MCF-7	breast:	n/a	chr19:51495365-51495372
34	GATA3	chr19:51478906-51479582	MCF-7	breast:	n/a	chr19:51479102-51479114 chr19:51479103-51479113 chr19:51479105-51479112
35	GATA3	chr19:51478977-51479476	MCF-7	breast:	n/a	chr19:51479102-51479114 chr19:51479103-51479113 chr19:51479105-51479112
36	GATA3	chr19:51478930-51479709	MCF-7	breast:	n/a	chr19:51479102-51479114 chr19:51479103-51479113 chr19:51479105-51479112
37	HDAC2	chr19:51478973-51479440	MCF-7	breast:	n/a	chr19:51479104-51479113 chr19:51479377-51479386
38	HDAC2	chr19:51476389-51476641	K562	blood:	n/a	n/a
39	JUND	chr19:51482319-51482622	HepG2	liver:	n/a	chr19:51482440-51482451
40	JUND	chr19:51495030-51495512	HCT-116	colon:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495322-51495333 chr19:51495429-51495440 chr19:51495324-51495331 chr19:51495324-51495333
41	JUND	chr19:51478881-51479746	HCT-116	colon:	n/a	chr19:51479281-51479289
42	JUND	chr19:51482271-51482627	Hela-S3	cervix:	n/a	chr19:51482440-51482451
43	JUND	chr19:51482150-51482799	HCT-116	colon:	n/a	chr19:51482440-51482451
44	JUND	chr19:51483571-51483695	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr19:51495176-51495421	HepG2	liver:	n/a	chr19:51495323-51495332 chr19:51495324-51495332 chr19:51495322-51495333 chr19:51495324-51495331 chr19:51495324-51495333
46	JUND	chr19:51482411-51482458	K562	blood:	n/a	chr19:51482440-51482451
47	MAFF	chr19:51489394-51489554	HepG2	liver:	n/a	n/a
48	MAFK	chr19:51489416-51489602	HepG2	liver:	n/a	chr19:51489525-51489540
49	MAFK	chr19:51489415-51489668	HepG2	liver:	n/a	chr19:51489525-51489540
50	MAFK	chr19:51485370-51485550	IMR90	lung:	n/a	chr19:51485424-51485433 chr19:51485495-51485510 chr19:51485417-51485437 chr19:51485420-51485434

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51480730-51480780	SKMC	muscle:	n/a
2	chr19:51487136-51487186	HRPEpiC	eye:	n/a
3	chr19:51480730-51480780	MCF-7	breast:	n/a
4	chr19:51480730-51480780	SKMC	muscle:	n/a
5	chr19:51487136-51487186	HRPEpiC	eye:	n/a
6	chr19:51480730-51480780	MCF-7	breast:	n/a
7	chr19:51481472-51481522	Jurkat	blood:	n/a
8	chr19:51487280-51487330	BJ	skin:	n/a
9	chr19:51487478-51487528	NB4	blood:	n/a
10	chr19:51487109-51487159	NH-A	brain:	n/a
11	chr19:51487968-51488018	HEK293	kidney:	embryo
12	chr19:51487305-51487355	SK-N-SH	brain:	n/a
13	chr19:51487478-51487528	HL-60	blood:	n/a
14	chr19:51487245-51487295	SAEC	small airway:	n/a
15	chr19:51487109-51487159	Hela-S3	cervix:	n/a
16	chr19:51487109-51487159	SK-N-MC	brain:	n/a
17	chr19:51487594-51487644	CMK	blood:	n/a
18	chr19:51481472-51481522	HCT-116	colon:	n/a
19	chr19:51487478-51487528	A549	lung:	n/a
20	chr19:51487245-51487295	ovcar-3	ovarian:	n/a
21	chr19:51487594-51487644	PFSK-1	brain:	n/a
22	chr19:51487136-51487186	SAEC	small airway:	n/a
23	chr19:51487280-51487330	HCT-116	colon:	n/a
24	chr19:51487305-51487355	HL-60	blood:	n/a
25	chr19:51487360-51487410	HEEpiC	esophagus:	n/a
26	chr19:51487305-51487355	HIPEpiC	eye:	n/a
27	chr19:51480730-51480780	PANC-1	pancreas:	n/a
28	chr19:51487478-51487528	AG04449	skin:	fetal
29	chr19:51480730-51480780	HCM	heart:	n/a
30	chr19:51487136-51487186	CMK	blood:	n/a
31	chr19:51487594-51487644	IMR90	lung:	fetal
32	chr19:51481472-51481522	AG04449	skin:	fetal
33	chr19:51481472-51481522	HepG2	liver:	n/a
34	chr19:51487136-51487186	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:51487968-51488018	HAEpiC	amniotic membrane:	n/a
36	chr19:51487968-51488018	HCPEpiC	choroid plexus:	n/a
37	chr19:51487360-51487410	HNPCEpiC	eye:	n/a
38	chr19:51487245-51487295	Hela-S3	cervix:	n/a
39	chr19:51487305-51487355	HCM	heart:	n/a
40	chr19:51480730-51480780	HPAEpiC	pulmonary alveolar:	n/a
41	chr19:51487478-51487528	SK-N-MC	brain:	n/a
42	chr19:51487136-51487186	NH-A	brain:	n/a
43	chr19:51487968-51488018	ECC-1	luminal epithelium:	n/a
44	chr19:51487109-51487159	HRE	kidney:	n/a
45	chr19:51487109-51487159	IMR90	lung:	fetal
46	chr19:51486901-51486951	SAEC	small airway:	n/a
47	chr19:51487245-51487295	HNPCEpiC	eye:	n/a
48	chr19:51487968-51488018	PANC-1	pancreas:	n/a
49	chr19:51487229-51487279	RPTEC	kidney:	n/a
50	chr19:51487478-51487528	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:51306475..51309071-chr19:51474363..51476587,2	MCF-7	breast:
2	chr19:51480144..51482461-chr19:51505463..51507645,2	MCF-7	breast:
3	chr19:51473357..51476193-chr19:51479340..51481047,2	K562	blood:
4	chr19:51473357..51476193-chr19:51479340..51481047,2	K562	blood:
5	chr19:51465141..51466716-chr19:51492896..51495060,2	K562	blood:
6	chr19:51487899..51489635-chr19:51493828..51496214,2	MCF-7	breast:
7	chr19:51474799..51477178-chr19:51477869..51480485,2	MCF-7	breast:
8	chr19:51478311..51481235-chr19:51486537..51488716,3	MCF-7	breast:
9	chr19:51480632..51483251-chr19:51496429..51498251,2	K562	blood:
10	chr19:51474799..51477178-chr19:51477869..51480485,2	MCF-7	breast:
11	chr19:51474380..51475999-chr19:51476075..51479052,2	MCF-7	breast:
12	chr19:51482020..51484953-chr19:51487883..51489631,2	MCF-7	breast:
13	chr19:51496140..51499135-chr19:51503262..51506454,3	MCF-7	breast:
14	chr19:51480632..51483251-chr19:51496429..51498251,2	K562	blood:
15	chr19:51487899..51489635-chr19:51493828..51496214,2	MCF-7	breast:
16	chr19:51470577..51472254-chr19:51478017..51480801,2	K562	blood:
17	chr19:51432732..51437222-chr19:51477627..51480793,4	MCF-7	breast:
18	chr19:51474380..51475999-chr19:51476075..51479052,2	MCF-7	breast:
19	chr19:51470577..51473158-chr19:51478017..51482058,3	K562	blood:
20	chr19:51466266..51466970-chr19:51493872..51494430,2	MCF-7	breast:
21	chr19:51465646..51468437-chr19:51495218..51498068,3	MCF-7	breast:
22	chr19:51482020..51484953-chr19:51487883..51489631,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLK7-1	chr19:51485351-51485713	NONHSAT067402
2	lnc-KLK7-1	chr19:51487107-51487320	NONHSAT067402
3	lnc-KLK2-5	chr19:51476437-51476589	ENSG00000267879.1
4	lnc-KLK2-5	chr19:51494205-51494336	ENSG00000267879.1

Variant related genes	Relation type
KLK6	TF binding region
KLK7	TF binding region
KLK6	CpG island
KLK7	CpG island
ENSG00000129455	chromatin interactions
ENSG00000169035	chromatin interactions
ENSG00000167747	chromatin interactions
ENSG00000167755	chromatin interactions
ENSG00000267879	chromatin interactions
ENSG00000269741	chromatin interactions

Extended variants
information (count: 1063 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1063 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1701952	chr19:51474525-51474526	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs59473545	chr19:51474531-51474532	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs386810293	chr19:51474542-51474543	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs1701951	chr19:51474543-51474544	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs1722542	chr19:51474585-51474586	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs543405415	chr19:51474631-51474632	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556074587	chr19:51474641-51474642	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574370118	chr19:51474662-51474663	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139901656	chr19:51474665-51474666	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs268890	chr19:51474674-51474675	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527404147	chr19:51474677-51474678	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs113478222	chr19:51474683-51474684	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs189631352	chr19:51474715-51474716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533724609	chr19:51474792-51474793	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs11376678	chr19:51474896-51474897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs397959096	chr19:51474906-51474907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192602522	chr19:51474923-51474924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1722541	chr19:51474937-51474938	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112305563	chr19:51474975-51474976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549785776	chr19:51475043-51475044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs80209459	chr19:51475045-51475046	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs565050996	chr19:51475048-51475049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529580979	chr19:51475049-51475050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532468556	chr19:51475076-51475077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547684874	chr19:51475088-51475089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566219889	chr19:51475151-51475152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557030251	chr19:51475152-51475153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113184998	chr19:51475231-51475232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539643907	chr19:51475245-51475246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370880220	chr19:51475255-51475256	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558274073	chr19:51475256-51475257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570037201	chr19:51475268-51475269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs118047624	chr19:51475285-51475286	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374760466	chr19:51475310-51475311	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs111968309	chr19:51475343-51475344	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs555313512	chr19:51475362-51475363	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143720877	chr19:51475398-51475399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184443639	chr19:51475415-51475416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530459980	chr19:51475416-51475417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112633459	chr19:51475458-51475459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553687562	chr19:51475491-51475492	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1654532	chr19:51475535-51475536	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545669727	chr19:51475570-51475571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189247126	chr19:51475596-51475597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531410919	chr19:51475638-51475639	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200026333	chr19:51475648-51475649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1654531	chr19:51475649-51475650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs112113362	chr19:51475650-51475651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs552770436	chr19:51475674-51475675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146341749	chr19:51475700-51475701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51471200-51474800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51471600-51474800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:51472800-51482200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr19:51473000-51477400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr19:51473000-51480600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:51473200-51474800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr19:51473200-51474800	Enhancers	Brain Substantia Nigra	brain
8	chr19:51473200-51476200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr19:51473200-51477600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:51473200-51479000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr19:51473200-51479000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:51473200-51480800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr19:51473200-51482400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:51473800-51479000	Weak transcription	NHEK	skin
15	chr19:51474000-51475600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:51474000-51475600	Weak transcription	Esophagus	oesophagus
17	chr19:51474000-51475600	Weak transcription	HMEC	breast
18	chr19:51474400-51474800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr19:51474800-51476000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:51474800-51479000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:51474800-51479000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr19:51474800-51482200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr19:51475600-51476200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr19:51475600-51476400	Enhancers	HMEC	breast
25	chr19:51475600-51476600	Enhancers	Esophagus	oesophagus
26	chr19:51476000-51477400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:51476200-51477800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr19:51476200-51479000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr19:51476400-51479000	Weak transcription	HMEC	breast
30	chr19:51476600-51479000	Weak transcription	Esophagus	oesophagus
31	chr19:51477400-51478000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr19:51477400-51479200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:51477600-51477800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr19:51477600-51478000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr19:51477800-51479200	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr19:51478000-51479000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr19:51478000-51479000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:51479000-51479400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr19:51479000-51479400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr19:51479000-51479400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr19:51479000-51479400	Bivalent Enhancer	A549	lung
42	chr19:51479000-51479600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr19:51479000-51479600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr19:51479000-51479600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr19:51479000-51479600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr19:51479000-51479600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:51479000-51479600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:51479000-51479600	Enhancers	Esophagus	oesophagus
49	chr19:51479000-51479600	Enhancers	NHEK	skin
50	chr19:51479000-51479800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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