Variant report

Variant	nsv870040
Chromosome Location	chr19:53291253-53375097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:1342)
Chromatin interactive
region (count:19)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53324738-53324945	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr19:53360719-53361014	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr19:53294543-53294932	GM12878	blood:	n/a	chr19:53294862-53294873 chr19:53294863-53294873 chr19:53294867-53294877
4	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
5	BATF	chr19:53294643-53295039	GM12878	blood:	n/a	chr19:53294862-53294873 chr19:53294863-53294873 chr19:53294867-53294877
6	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
7	BCL11A	chr19:53360679-53360916	GM12878	blood:	n/a	chr19:53360828-53360837
8	BCL11A	chr19:53362420-53362624	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:53324867-53324898	K562	blood:	n/a	n/a
10	BHLHE40	chr19:53360687-53361035	GM12878	blood:	n/a	chr19:53360820-53360836 chr19:53360998-53361014
11	CBX3	chr19:53324640-53325255	K562	blood:	n/a	n/a
12	CBX3	chr19:53360595-53361343	K562	blood:	n/a	n/a
13	CBX3	chr19:53303091-53303540	K562	blood:	n/a	n/a
14	CBX3	chr19:53303081-53303524	K562	blood:	n/a	n/a
15	CCNT2	chr19:53361004-53361276	K562	blood:	n/a	n/a
16	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
17	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
18	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
19	CEBPB	chr19:53300965-53301050	IMR90	lung:	n/a	n/a
20	CEBPB	chr19:53363042-53363321	K562	blood:	n/a	n/a
21	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr19:53363179-53363319	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr19:53319087-53319167	HepG2	liver:	n/a	chr19:53319119-53319130
24	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
25	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
26	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
27	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
28	CEBPB	chr19:53363838-53364091	IMR90	lung:	n/a	n/a
29	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
30	CEBPD	chr19:53360693-53360926	HepG2	liver:	n/a	n/a
31	CHD2	chr19:53360719-53360909	K562	blood:	n/a	n/a
32	CHD2	chr19:53360829-53361263	GM12878	blood:	n/a	n/a
33	CTCF	chr19:53360771-53361087	Spleen_OC	spleen:	n/a	chr19:53360990-53361003
34	CTCF	chr19:53324949-53325037	LNCaP	prostate:	n/a	chr19:53325004-53325017
35	CTCF	chr19:53361020-53361170	GM12871	blood:	n/a	n/a
36	CTCF	chr19:53333123-53333177	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr19:53361020-53361170	HCM	heart:	n/a	n/a
38	CTCF	chr19:53360920-53361070	HMEC	breast:	n/a	chr19:53360990-53361003
39	CTCF	chr19:53324779-53325090	Spleen_OC	spleen:	n/a	chr19:53325004-53325017
40	CTCF	chr19:53361020-53361170	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr19:53361040-53361190	GM12873	blood:	n/a	n/a
42	CTCF	chr19:53324980-53325130	SAEC	small airway:	n/a	chr19:53325004-53325017
43	CTCF	chr19:53360901-53361081	K562	blood:	n/a	chr19:53360990-53361003
44	CTCF	chr19:53360828-53360986	GM19239	blood:	n/a	n/a
45	CTCF	chr19:53361000-53361150	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr19:53361020-53361170	HMF	breast:	n/a	n/a
47	CTCF	chr19:53360887-53361019	GM12891	blood:	n/a	chr19:53360990-53361003
48	CTCF	chr19:53361020-53361170	K562	blood:	n/a	n/a
49	CTCF	chr19:53324904-53325077	GM19240	blood:	n/a	chr19:53325004-53325017
50	CTCF	chr19:53324960-53325110	HMEC	breast:	n/a	chr19:53325004-53325017

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53324732-53324782	Hela-S3	cervix:	n/a
2	chr19:53326219-53326269	Jurkat	blood:	n/a
3	chr19:53360213-53360263	NH-A	brain:	n/a
4	chr19:53362925-53362975	HEK293	kidney:	embryo
5	chr19:53361066-53361116	Hepatocyte	liver:	n/a
6	chr19:53362925-53362975	HepG2	liver:	n/a
7	chr19:53342580-53342630	RPTEC	kidney:	n/a
8	chr19:53324278-53324328	GM19239	blood:	n/a
9	chr19:53325080-53325130	HCF	heart:	n/a
10	chr19:53302456-53302506	HNPCEpiC	eye:	n/a
11	chr19:53359733-53359783	NT2-D1	testis:	n/a
12	chr19:53359733-53359783	SK-N-SH	brain:	n/a
13	chr19:53324278-53324328	GM06990	blood:	n/a
14	chr19:53324732-53324782	SK-N-SH_RA	brain:	n/a
15	chr19:53360728-53360778	HNPCEpiC	eye:	n/a
16	chr19:53325104-53325154	HIPEpiC	eye:	n/a
17	chr19:53293012-53293062	AG10803	skin:	n/a
18	chr19:53360213-53360263	HRE	kidney:	n/a
19	chr19:53326091-53326141	HIPEpiC	eye:	n/a
20	chr19:53303448-53303498	Jurkat	blood:	n/a
21	chr19:53326219-53326269	CMK	blood:	n/a
22	chr19:53324198-53324248	K562	blood:	n/a
23	chr19:53325104-53325154	HAEpiC	amniotic membrane:	n/a
24	chr19:53361448-53361498	SKMC	muscle:	n/a
25	chr19:53359733-53359783	LNCaP	prostate:	n/a
26	chr19:53324732-53324782	NB4	blood:	n/a
27	chr19:53361164-53361214	GM12878	blood:	n/a
28	chr19:53342580-53342630	AG04449	skin:	fetal
29	chr19:53359733-53359783	NHDF-neo	bronchial:	n/a
30	chr19:53342580-53342630	PFSK-1	brain:	n/a
31	chr19:53326091-53326141	T-47D	breast:	n/a
32	chr19:53325913-53325963	BJ	skin:	n/a
33	chr19:53363482-53363532	A549	lung:	n/a
34	chr19:53360213-53360263	U87	brain:	n/a
35	chr19:53325913-53325963	RPTEC	kidney:	n/a
36	chr19:53325104-53325154	HL-60	blood:	n/a
37	chr19:53325913-53325963	HUVEC	blood vessel:	n/a
38	chr19:53357134-53357184	AG09309	skin:	n/a
39	chr19:53342580-53342630	SK-N-SH_RA	brain:	n/a
40	chr19:53360728-53360778	ProgFib	skin:	n/a
41	chr19:53361448-53361498	Hela-S3	cervix:	n/a
42	chr19:53326091-53326141	HRPEpiC	eye:	n/a
43	chr19:53293012-53293062	NH-A	brain:	n/a
44	chr19:53302456-53302506	ProgFib	skin:	n/a
45	chr19:53303448-53303498	BE2_C	brain:	n/a
46	chr19:53359733-53359783	HepG2	liver:	n/a
47	chr19:53326219-53326269	HPAEpiC	pulmonary alveolar:	n/a
48	chr19:53342580-53342630	H1-hESC	embryonic stem cell:	embryo
49	chr19:53326091-53326141	HUVEC	blood vessel:	n/a
50	chr19:53357134-53357184	BE2_C	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
2	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
3	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
4	chr19:53324563..53325122-chr19:53360322..53360852,2	NB4	blood:
5	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
6	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
7	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
8	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
9	chr19:53359757..53362433-chr19:53464752..53467349,2	MCF-7	breast:
10	chr19:53359564..53361265-chr19:53424872..53426783,2	MCF-7	breast:
11	chr19:53288948..53291766-chr19:53301308..53304079,2	K562	blood:
12	chr19:53324392..53324894-chr19:53934932..53935516,2	MCF-7	breast:
13	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
14	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
15	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
16	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
17	chr19:53296635..53299410-chr19:53311177..53313587,2	K562	blood:
18	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
19	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
2	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
3	lnc-ZNF468-3	chr19:53324839-53324886	NONHSAT067588
4	lnc-ZNF468-1	chr19:53360825-53360902	NR_102300
5	lnc-ZNF468-1	chr19:53360825-53360902	NR_102301
6	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
7	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
8	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
9	lnc-ZNF701-2	chr19:53300917-53301869	NONHSAT067585
10	lnc-ZNF468-1	chr19:53360825-53360902	NR_102299
11	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
12	lnc-ZNF468-3	chr19:53311129-53311386	NONHSAT067588
13	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301
14	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
15	lnc-ZNF320-3	chr19:53367175-53367412	NONHSAT067592
16	lnc-ZNF320-3	chr19:53367043-53367412	NONHSAT067591
17	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
18	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
19	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
20	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
21	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
22	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
23	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
24	lnc-ZNF468-3	chr19:53321197-53321281	NONHSAT067589
25	lnc-ZNF701-2	chr19:53301030-53301858	NONHSAT067586
26	lnc-ZNF468-3	chr19:53317537-53317679	NONHSAT067589
27	lnc-ZNF468-3	chr19:53321197-53321284	NONHSAT067588
28	lnc-ZNF468-2	chr19:53365060-53366119	NONHSAT067590

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF28	hsa-miR-155-5p	chr19:53301652-53301677
2	ZNF28	hsa-miR-155-5p	chr19:53301585-53301611

Variant related genes	Relation type
ENSG00000255875	TF binding region
ENSG00000268225	TF binding region
ZNF600	TF binding region
ZNF28	TF binding region
ZNF468	TF binding region
ENSG00000255875	CpG island
ENSG00000268225	CpG island
ZNF600	CpG island
ZNF28	CpG island
ZNF468	CpG island
ENSG00000180257	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000213793	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000189190	chromatin interactions
ENSG00000255875	chromatin interactions
ENSG00000241015	chromatin interactions
ENSG00000160336	chromatin interactions

Extended variants
information (count: 4441 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4441 , 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	rs10405790	chr19:53291297-53291298	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs113901203	chr19:53291352-53291353	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs193047717	chr19:53291364-53291365	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs142200574	chr19:53291369-53291370	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs558584780	chr19:53291387-53291388	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs576783823	chr19:53291407-53291408	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544171144	chr19:53291408-53291409	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs144525773	chr19:53291423-53291424	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs148455991	chr19:53291436-53291437	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs185306394	chr19:53291443-53291444	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs188917773	chr19:53291463-53291464	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs527449558	chr19:53291480-53291481	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147637516	chr19:53291484-53291485	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs565358747	chr19:53291498-53291499	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs532436918	chr19:53291511-53291512	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs550942262	chr19:53291517-53291518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs569616398	chr19:53291555-53291556	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs10405247	chr19:53291572-53291573	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs548860220	chr19:53291600-53291601	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs181416644	chr19:53291645-53291646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571319893	chr19:53291691-53291692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184174796	chr19:53291695-53291696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113571890	chr19:53291760-53291761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2059177	chr19:53291766-53291767	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs188384722	chr19:53291768-53291769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs574057301	chr19:53291772-53291773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180821151	chr19:53291773-53291774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559987924	chr19:53291775-53291776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571939061	chr19:53291776-53291777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545964888	chr19:53291782-53291783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565275638	chr19:53291804-53291805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142304741	chr19:53291896-53291897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557543459	chr19:53292037-53292038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544332871	chr19:53292046-53292047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562880082	chr19:53292050-53292051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144198848	chr19:53292066-53292067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371454513	chr19:53292092-53292093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567146081	chr19:53292096-53292097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372694279	chr19:53292120-53292121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527913372	chr19:53292134-53292135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552736317	chr19:53292145-53292146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570911104	chr19:53292191-53292192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537956222	chr19:53292202-53292203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555805649	chr19:53292231-53292232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567743316	chr19:53292327-53292328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567202842	chr19:53292342-53292343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34748465	chr19:53292356-53292357	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35784937	chr19:53292417-53292418	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs527382675	chr19:53292441-53292442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572000821	chr19:53292483-53292484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2221 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53289000-53291400	Active TSS	Duodenum Smooth Muscle	Duodenum
2	chr19:53290600-53292200	Weak transcription	HepG2	liver
3	chr19:53290600-53292400	Weak transcription	Spleen	Spleen
4	chr19:53290600-53293200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:53290600-53295600	Weak transcription	Gastric	stomach
6	chr19:53290600-53300000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:53290600-53301600	Weak transcription	Ovary	ovary
8	chr19:53290800-53291400	Enhancers	Primary B cells from cord blood	blood
9	chr19:53290800-53291400	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr19:53290800-53291600	Enhancers	Primary T cells fromperipheralblood	blood
11	chr19:53290800-53291800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr19:53290800-53292600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:53290800-53294400	Weak transcription	Thymus	Thymus
14	chr19:53290800-53302400	Weak transcription	Brain Germinal Matrix	brain
15	chr19:53291000-53291400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr19:53291000-53291600	Flanking Active TSS	Dnd41	blood
17	chr19:53291200-53291400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr19:53291200-53291400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr19:53291200-53291400	Active TSS	Brain Substantia Nigra	brain
20	chr19:53291200-53291600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
21	chr19:53291200-53291600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr19:53291200-53292200	Weak transcription	Placenta	Placenta
23	chr19:53291200-53294200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr19:53291200-53297400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:53291600-53292400	Weak transcription	Brain Substantia Nigra	brain
26	chr19:53291600-53292400	Enhancers	Dnd41	blood
27	chr19:53291800-53293200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr19:53292200-53292600	Enhancers	Placenta	Placenta
29	chr19:53292200-53292800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr19:53292200-53293000	Enhancers	HepG2	liver
31	chr19:53292400-53301600	Weak transcription	Dnd41	blood
32	chr19:53292600-53293800	Weak transcription	Placenta	Placenta
33	chr19:53292600-53294400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr19:53292800-53293000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chr19:53293000-53293200	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr19:53293200-53299800	Weak transcription	Fetal Brain Female	brain
37	chr19:53293800-53294200	Enhancers	Placenta	Placenta
38	chr19:53294200-53294400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr19:53294400-53294800	ZNF genes & repeats	Thymus	Thymus
40	chr19:53294400-53294800	Enhancers	HUVEC	blood vessel
41	chr19:53294400-53295000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr19:53294600-53311400	ZNF genes & repeats	Liver	Liver
43	chr19:53296200-53324000	Weak transcription	Fetal Brain Male	brain
44	chr19:53297400-53314000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
45	chr19:53297600-53299600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
46	chr19:53298800-53299400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:53299000-53299800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr19:53299000-53299800	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr19:53299000-53300000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr19:53299200-53299800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--

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