Variant report

Variant	esv1005203
Chromosome Location	chr19:45675812-45684868
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:932)
CpG islands
(count:1284)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:45681488-45682369	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:45681621-45682077	K562	blood:	n/a	n/a
3	ATF1	chr19:45681004-45682199	K562	blood:	n/a	n/a
4	ATF2	chr19:45676954-45677442	GM12878	blood:	n/a	n/a
5	ATF2	chr19:45680892-45682228	GM12878	blood:	n/a	n/a
6	ATF3	chr19:45681519-45682167	H1-hESC	embryonic stem cell:	n/a	chr19:45681614-45681623 chr19:45681659-45681668
7	ATF3	chr19:45681512-45682044	H1-hESC	embryonic stem cell:	n/a	chr19:45681614-45681623 chr19:45681659-45681668
8	ATF3	chr19:45681371-45682278	K562	blood:	n/a	chr19:45681614-45681623 chr19:45681659-45681668
9	BCL3	chr19:45680260-45680594	GM12878	blood:	n/a	n/a
10	BCL3	chr19:45680734-45682586	A549	lung:	n/a	n/a
11	BCL3	chr19:45681211-45682392	A549	lung:	n/a	n/a
12	BCLAF1	chr19:45681169-45681637	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:45681127-45682679	HepG2	liver:	n/a	chr19:45682072-45682088
14	BHLHE40	chr19:45680390-45680590	K562	blood:	n/a	n/a
15	BHLHE40	chr19:45680931-45683148	K562	blood:	n/a	chr19:45682072-45682088
16	BHLHE40	chr19:45681236-45682748	GM12878	blood:	n/a	chr19:45682072-45682088
17	BHLHE40	chr19:45681463-45682616	A549	lung:	n/a	chr19:45682072-45682088
18	BRCA1	chr19:45681173-45682297	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr19:45682164-45682559	HepG2	liver:	n/a	n/a
20	BRCA1	chr19:45681523-45682223	GM12878	blood:	n/a	n/a
21	CBX3	chr19:45681243-45682890	K562	blood:	n/a	n/a
22	CBX3	chr19:45680249-45680632	K562	blood:	n/a	n/a
23	CCNT2	chr19:45682473-45683161	K562	blood:	n/a	n/a
24	CCNT2	chr19:45681299-45682206	K562	blood:	n/a	n/a
25	CEBPB	chr19:45679618-45679803	K562	blood:	n/a	n/a
26	CEBPB	chr19:45681419-45681951	A549	lung:	n/a	n/a
27	CEBPB	chr19:45681322-45682131	K562	blood:	n/a	n/a
28	CEBPB	chr19:45681144-45682214	K562	blood:	n/a	n/a
29	CEBPB	chr19:45678964-45679267	A549	lung:	n/a	n/a
30	CEBPB	chr19:45681219-45682117	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:45681025-45682247	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr19:45679115-45679244	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:45681189-45682144	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr19:45681392-45681867	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr19:45681430-45681812	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:45679004-45679261	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:45681009-45682042	A549	lung:	n/a	n/a
38	CEBPB	chr19:45681374-45681882	K562	blood:	n/a	n/a
39	CEBPB	chr19:45681010-45682133	IMR90	lung:	n/a	n/a
40	CEBPB	chr19:45681061-45682118	A549	lung:	n/a	n/a
41	CEBPB	chr19:45681048-45682141	MCF-7	breast:	n/a	n/a
42	CEBPB	chr19:45681106-45682206	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr19:45681306-45681973	MCF-7	breast:	n/a	n/a
44	CEBPB	chr19:45681148-45682188	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:45681431-45681838	HepG2	liver:	n/a	n/a
46	CEBPB	chr19:45679090-45679254	K562	blood:	n/a	n/a
47	CEBPD	chr19:45681417-45681786	HepG2	liver:	n/a	n/a
48	CEBPD	chr19:45681308-45681751	HepG2	liver:	n/a	n/a
49	CEBPD	chr19:45681310-45681900	K562	blood:	n/a	n/a
50	CEBPZ	chr19:45681689-45682009	HepG2	liver:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45681580-45681630	BE2_C	brain:	n/a
2	chr19:45681945-45681995	HRE	kidney:	n/a
3	chr19:45682841-45682891	SK-N-SH	brain:	n/a
4	chr19:45681580-45681630	BE2_C	brain:	n/a
5	chr19:45681945-45681995	HRE	kidney:	n/a
6	chr19:45682841-45682891	SK-N-SH	brain:	n/a
7	chr19:45681664-45681714	MCF-7	breast:	n/a
8	chr19:45681987-45682037	HNPCEpiC	eye:	n/a
9	chr19:45681987-45682037	PFSK-1	brain:	n/a
10	chr19:45681846-45681896	HEEpiC	esophagus:	n/a
11	chr19:45681407-45681457	BE2_C	brain:	n/a
12	chr19:45682064-45682114	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:45682354-45682404	HCPEpiC	choroid plexus:	n/a
14	chr19:45680948-45680998	GM12892	blood:	n/a
15	chr19:45681968-45682018	SK-N-MC	brain:	n/a
16	chr19:45681846-45681896	HMEC	breast:	n/a
17	chr19:45682354-45682404	HCF	heart:	n/a
18	chr19:45681503-45681553	HCM	heart:	n/a
19	chr19:45681510-45681560	BJ	skin:	n/a
20	chr19:45680948-45680998	H1-hESC	embryonic stem cell:	embryo
21	chr19:45681987-45682037	AG04449	skin:	fetal
22	chr19:45683155-45683205	A549	lung:	n/a
23	chr19:45683263-45683313	GM19239	blood:	n/a
24	chr19:45681716-45681766	HepG2	liver:	n/a
25	chr19:45683263-45683313	HCT-116	colon:	n/a
26	chr19:45681846-45681896	GM06990	blood:	n/a
27	chr19:45680948-45680998	AG10803	skin:	n/a
28	chr19:45681510-45681560	NH-A	brain:	n/a
29	chr19:45681487-45681537	U87	brain:	n/a
30	chr19:45682064-45682114	SK-N-SH	brain:	n/a
31	chr19:45681664-45681714	MCF10A-Er-Src	breast:	n/a
32	chr19:45681407-45681457	HL-60	blood:	n/a
33	chr19:45681968-45682018	Hepatocyte	liver:	n/a
34	chr19:45681828-45681878	MCF-7	breast:	n/a
35	chr19:45681828-45681878	Caco-2	colon:	n/a
36	chr19:45683155-45683205	GM12891	blood:	n/a
37	chr19:45680969-45681019	Caco-2	colon:	n/a
38	chr19:45681968-45682018	A549	lung:	n/a
39	chr19:45681945-45681995	BJ	skin:	n/a
40	chr19:45680948-45680998	ovcar-3	ovarian:	n/a
41	chr19:45682064-45682114	AG04449	skin:	fetal
42	chr19:45681503-45681553	NH-A	brain:	n/a
43	chr19:45681899-45681949	HEK293	kidney:	embryo
44	chr19:45681846-45681896	T-47D	breast:	n/a
45	chr19:45681407-45681457	HCM	heart:	n/a
46	chr19:45681664-45681714	Hela-S3	cervix:	n/a
47	chr19:45680969-45681019	HUVEC	blood vessel:	n/a
48	chr19:45681487-45681537	GM12892	blood:	n/a
49	chr19:45681828-45681878	HMEC	breast:	n/a
50	chr19:45681828-45681878	GM12878	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45644450..45646816-chr19:45679774..45683109,3	MCF-7	breast:
2	chr19:45594755..45598539-chr19:45681810..45685400,4	K562	blood:
3	chr11:69061460..69062140-chr19:45681721..45682573,2	HCT-116	colon:
4	chr19:45662986..45665751-chr19:45672149..45675841,4	MCF-7	breast:
5	chr19:45654421..45658397-chr19:45679888..45682724,3	K562	blood:
6	chr19:45680559..45684359-chr19:45688843..45692525,5	MCF-7	breast:
7	chr19:45639686..45641880-chr19:45681901..45684356,2	MCF-7	breast:
8	chr19:45578352..45580821-chr19:45679388..45681588,2	K562	blood:
9	chr19:45675726..45677672-chr19:45752421..45754832,2	MCF-7	breast:
10	chr19:45660357..45662141-chr19:45673721..45675839,2	MCF-7	breast:
11	chr19:45681420..45684587-chr19:45687242..45692393,7	MCF-7	breast:
12	chr19:45581068..45583958-chr19:45681428..45684016,2	K562	blood:
13	chr19:45675822..45679295-chr19:45679475..45683800,7	MCF-7	breast:
14	chr19:45680180..45683713-chr19:45733323..45737109,3	K562	blood:
15	chr19:45681162..45683480-chr19:45842144..45844672,3	K562	blood:
16	chr19:45652739..45654632-chr19:45677367..45679374,2	MCF-7	breast:
17	chr19:45658848..45663469-chr19:45680259..45684163,6	MCF-7	breast:
18	chr19:45594874..45597676-chr19:45681810..45683655,2	K562	blood:
19	chr17:16341750..16342479-chr19:45681510..45682384,2	Hela-S3	cervix:
20	chr19:45594892..45596535-chr19:45681783..45683354,2	MCF-7	breast:
21	chr19:45673214..45674833-chr19:45677772..45679460,2	K562	blood:
22	chr19:45662322..45668242-chr19:45680645..45684470,7	K562	blood:
23	chr19:45541123..45542652-chr19:45681977..45683668,2	MCF-7	breast:
24	chr19:45682254..45683005-chr6:26156173..26156727,2	Hela-S3	cervix:
25	chr19:45672317..45675503-chr19:45675709..45677747,4	K562	blood:
26	chr19:45663965..45672033-chr19:45672145..45675901,9	K562	blood:
27	chr19:45594586..45596499-chr19:45682181..45685187,4	MCF-7	breast:
28	chr19:45675317..45679355-chr19:45679533..45681845,4	K562	blood:
29	chr19:45674624..45677350-chr19:45825375..45827077,2	K562	blood:
30	chr19:45675481..45678583-chr19:45681504..45683285,3	K562	blood:
31	chr19:45684774..45686419-chr19:45697877..45700267,2	MCF-7	breast:
32	chr19:45655086..45657605-chr19:45680853..45682730,2	MCF-7	breast:
33	chr19:45652567..45654233-chr19:45681921..45683559,2	MCF-7	breast:
34	chr19:45667869..45670716-chr19:45675537..45677306,2	MCF-7	breast:
35	chr19:45503982..45506844-chr19:45681115..45683310,3	K562	blood:
36	chr19:45672516..45674709-chr19:45674785..45678342,3	MCF-7	breast:
37	chr19:45665456..45669944-chr19:45672662..45676859,4	MCF-7	breast:
38	chr19:45596183..45598071-chr19:45678820..45681016,3	K562	blood:
39	chr19:45662322..45663842-chr19:45681568..45683237,2	K562	blood:
40	chr19:45679504..45683518-chr19:45685241..45688488,5	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BLOC1S3	hsa-miR-378a-3p	chr19:45684405-45684426

Variant related genes	Relation type
ENSG00000267545	TF binding region
BLOC1S3	TF binding region
TRAPPC6A	TF binding region
ENSG00000267545	CpG island
BLOC1S3	CpG island
TRAPPC6A	CpG island
ENSG00000189114	chromatin interactions
ENSG00000179846	chromatin interactions
ENSG00000267545	chromatin interactions
ENSG00000267044	chromatin interactions
ENSG00000130201	chromatin interactions
ENSG00000104866	chromatin interactions
ENSG00000007047	chromatin interactions
ENSG00000104879	chromatin interactions
ENSG00000104892	chromatin interactions
ENSG00000268341	chromatin interactions
ENSG00000266958	chromatin interactions
ENSG00000104856	chromatin interactions
ENSG00000172927	chromatin interactions
ENSG00000142252	chromatin interactions
ENSG00000267037	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000104859	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000007255	chromatin interactions
ENSG00000170684	chromatin interactions
ENSG00000225157	chromatin interactions

Extended variants
information (count: 435 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531629120	chr19:45675844-45675845	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs555669193	chr19:45675847-45675848	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs543487485	chr19:45675849-45675850	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs550661533	chr19:45675852-45675853	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs569036497	chr19:45675858-45675859	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs7247764	chr19:45675873-45675874	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs147570048	chr19:45675911-45675912	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs529429856	chr19:45675965-45675966	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs577379866	chr19:45675977-45675978	Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs192278798	chr19:45676027-45676028	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs553561420	chr19:45676108-45676109	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs184665023	chr19:45676126-45676127	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs114758345	chr19:45676141-45676142	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs563226493	chr19:45676158-45676159	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs532040071	chr19:45676178-45676179	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs56796781	chr19:45676195-45676196	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565482560	chr19:45676218-45676219	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs142062812	chr19:45676240-45676241	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs114181998	chr19:45676241-45676242	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs114783480	chr19:45676245-45676246	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs60460304	chr19:45676250-45676251	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs549901574	chr19:45676267-45676268	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs377267227	chr19:45676276-45676277	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs375691363	chr19:45676293-45676294	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs12975698	chr19:45676294-45676295	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs57627123	chr19:45676318-45676319	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs117908989	chr19:45676326-45676327	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs28555639	chr19:45676364-45676365	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553868281	chr19:45676465-45676466	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs573634716	chr19:45676467-45676468	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs371943799	chr19:45676474-45676475	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs58504789	chr19:45676492-45676493	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190467979	chr19:45676493-45676494	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs140277552	chr19:45676697-45676698	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs140897289	chr19:45676708-45676709	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs4012975	chr19:45676721-45676722	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs565543945	chr19:45676833-45676834	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs572711694	chr19:45676835-45676836	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs541242578	chr19:45676836-45676837	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs556989826	chr19:45676840-45676841	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs367738034	chr19:45676891-45676892	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs193099921	chr19:45676904-45676905	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs116465483	chr19:45676905-45676906	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs34331532	chr19:45676990-45676991	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563348340	chr19:45676991-45676992	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs116172159	chr19:45677000-45677001	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs113722475	chr19:45677032-45677033	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs79665626	chr19:45677040-45677041	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs76049126	chr19:45677055-45677056	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs12610524	chr19:45677133-45677134	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Adrenocortical carcinoma	18281524	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:968 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45665400-45680400	Weak transcription	Brain Substantia Nigra	brain
2	chr19:45665400-45680600	Weak transcription	Fetal Lung	lung
3	chr19:45665600-45680400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr19:45665800-45680200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr19:45665800-45680400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:45667400-45681000	Weak transcription	Aorta	Aorta
7	chr19:45668000-45680600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr19:45668200-45676000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr19:45668400-45676800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr19:45668400-45680400	Weak transcription	Fetal Intestine Large	intestine
11	chr19:45668400-45680600	Weak transcription	Colon Smooth Muscle	Colon
12	chr19:45668400-45680600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr19:45668600-45679000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr19:45668800-45680400	Weak transcription	Brain Anterior Caudate	brain
15	chr19:45668800-45680400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr19:45669000-45680200	Weak transcription	Fetal Brain Female	brain
17	chr19:45670200-45680200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr19:45670200-45680400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr19:45670600-45680400	Weak transcription	Brain Angular Gyrus	brain
20	chr19:45670600-45680400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr19:45670800-45680400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr19:45671600-45677600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr19:45672400-45677000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr19:45672400-45680800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr19:45672600-45677800	Enhancers	Primary hematopoietic stem cells	blood
26	chr19:45673600-45676200	Enhancers	Placenta	Placenta
27	chr19:45673600-45678000	Enhancers	Fetal Thymus	thymus
28	chr19:45673800-45676000	Enhancers	Adipose Nuclei	Adipose
29	chr19:45673800-45676200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr19:45673800-45676400	Enhancers	Stomach Mucosa	stomach
31	chr19:45673800-45680400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:45674000-45677600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr19:45674000-45677800	Enhancers	Primary B cells from cord blood	blood
34	chr19:45674000-45678000	Enhancers	GM12878-XiMat	blood
35	chr19:45674200-45676600	Weak transcription	A549	lung
36	chr19:45674200-45677800	Enhancers	Primary B cells from peripheral blood	blood
37	chr19:45674200-45678800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr19:45674200-45680400	Weak transcription	Ovary	ovary
39	chr19:45674600-45677800	Enhancers	Thymus	Thymus
40	chr19:45674800-45676000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr19:45674800-45676000	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr19:45674800-45676800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr19:45674800-45678000	Enhancers	HepG2	liver
44	chr19:45675000-45676400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr19:45675000-45676600	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr19:45675000-45677400	Enhancers	Spleen	Spleen
47	chr19:45675000-45677800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr19:45675000-45680200	Weak transcription	Dnd41	blood
49	chr19:45675200-45676000	Enhancers	Hela-S3	cervix
50	chr19:45675200-45676000	Enhancers	K562	blood

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