Variant report

Variant	nsv912475
Chromosome Location	chr19:55874986-55888598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:1222)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:55885287-55886087	A549	lung:	n/a	chr19:55885847-55885856 chr19:55885736-55885750
2	ATF3	chr19:55883880-55884469	A549	lung:	n/a	chr19:55884324-55884335 chr19:55884324-55884335 chr19:55884323-55884336 chr19:55884322-55884335
3	ATF3	chr19:55883907-55884582	A549	lung:	n/a	chr19:55884324-55884335 chr19:55884324-55884335 chr19:55884323-55884336 chr19:55884322-55884335
4	ATF3	chr19:55881068-55881527	A549	lung:	n/a	chr19:55881199-55881208
5	BACH1	chr19:55881559-55881756	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:55887886-55888195	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:55875139-55875872	A549	lung:	n/a	n/a
8	BCL3	chr19:55874913-55876452	A549	lung:	n/a	n/a
9	BCL3	chr19:55881375-55881893	A549	lung:	n/a	chr19:55881514-55881523 chr19:55881694-55881703 chr19:55881774-55881787
10	BCL3	chr19:55887893-55888448	A549	lung:	n/a	n/a
11	BCL3	chr19:55883381-55884667	A549	lung:	n/a	chr19:55884199-55884208
12	BCL3	chr19:55881146-55882765	A549	lung:	n/a	chr19:55881514-55881523 chr19:55881694-55881703 chr19:55881774-55881787
13	BCL3	chr19:55884746-55886219	A549	lung:	n/a	n/a
14	BCL3	chr19:55883861-55884932	A549	lung:	n/a	chr19:55884199-55884208
15	BCL3	chr19:55885019-55886309	A549	lung:	n/a	n/a
16	BCL3	chr19:55880142-55880947	A549	lung:	n/a	chr19:55880719-55880732
17	BRCA1	chr19:55884113-55884357	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr19:55887887-55888175	K562	blood:	n/a	n/a
19	CCNT2	chr19:55880558-55880889	K562	blood:	n/a	n/a
20	CEBPB	chr19:55885441-55886256	A549	lung:	n/a	n/a
21	CEBPB	chr19:55884027-55884240	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:55885484-55886052	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:55876101-55876394	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:55885750-55886097	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:55883911-55884647	A549	lung:	n/a	n/a
26	CEBPB	chr19:55885677-55886148	A549	lung:	n/a	n/a
27	CEBPD	chr19:55885836-55886066	HepG2	liver:	n/a	n/a
28	CHD1	chr19:55879027-55882893	IMR90	lung:	n/a	chr19:55881216-55881226 chr19:55879790-55879800
29	CHD2	chr19:55887562-55888473	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr19:55877713-55877739	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr19:55881221-55881390	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr19:55881277-55881751	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr19:55880595-55880795	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr19:55883635-55884509	Hela-S3	cervix:	n/a	chr19:55883767-55883777
35	CHD2	chr19:55886860-55887034	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr19:55887745-55887751	K562	blood:	n/a	n/a
37	CHD2	chr19:55885117-55886019	Hela-S3	cervix:	n/a	n/a
38	CREB1	chr19:55884005-55884543	HepG2	liver:	n/a	n/a
39	CREB1	chr19:55884107-55884457	A549	lung:	n/a	n/a
40	CREB1	chr19:55883964-55884518	A549	lung:	n/a	n/a
41	CREB1	chr19:55881975-55882307	A549	lung:	n/a	n/a
42	CREB1	chr19:55885763-55886097	A549	lung:	n/a	n/a
43	CREB1	chr19:55880453-55880908	A549	lung:	n/a	n/a
44	CREB1	chr19:55881045-55881833	A549	lung:	n/a	n/a
45	CREB1	chr19:55885443-55886240	A549	lung:	n/a	n/a
46	CTBP2	chr19:55881284-55881728	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:55880140-55880290	AG04449	skin:	n/a	n/a
48	CTCF	chr19:55881200-55881350	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr19:55881340-55881490	AG04449	skin:	n/a	n/a
50	CTCF	chr19:55881200-55881350	NHEK	skin:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55887905-55887955	RPTEC	kidney:	n/a
2	chr19:55880843-55880893	HRE	kidney:	n/a
3	chr19:55887905-55887955	RPTEC	kidney:	n/a
4	chr19:55880843-55880893	HRE	kidney:	n/a
5	chr19:55887704-55887754	AoSMC	blood vessel:	n/a
6	chr19:55885168-55885218	HNPCEpiC	eye:	n/a
7	chr19:55880843-55880893	NT2-D1	testis:	n/a
8	chr19:55877371-55877421	RPTEC	kidney:	n/a
9	chr19:55880843-55880893	MCF-7	breast:	n/a
10	chr19:55880984-55881034	SK-N-SH	brain:	n/a
11	chr19:55888082-55888132	ECC-1	luminal epithelium:	n/a
12	chr19:55876060-55876110	HEK293	kidney:	embryo
13	chr19:55880593-55880643	Caco-2	colon:	n/a
14	chr19:55880984-55881034	SK-N-SH_RA	brain:	n/a
15	chr19:55880843-55880893	T-47D	breast:	n/a
16	chr19:55880593-55880643	HUVEC	blood vessel:	n/a
17	chr19:55875605-55875655	LNCaP	prostate:	n/a
18	chr19:55880984-55881034	AG04450	lung:	fetal
19	chr19:55888082-55888132	AG04449	skin:	fetal
20	chr19:55875605-55875655	HepG2	liver:	n/a
21	chr19:55888156-55888206	HL-60	blood:	n/a
22	chr19:55882550-55882600	LNCaP	prostate:	n/a
23	chr19:55882550-55882600	HUVEC	blood vessel:	n/a
24	chr19:55887799-55887849	HRE	kidney:	n/a
25	chr19:55877371-55877421	A549	lung:	n/a
26	chr19:55875605-55875655	ECC-1	luminal epithelium:	n/a
27	chr19:55888082-55888132	HCPEpiC	choroid plexus:	n/a
28	chr19:55882550-55882600	U87	brain:	n/a
29	chr19:55881893-55881943	SK-N-MC	brain:	n/a
30	chr19:55887704-55887754	HMEC	breast:	n/a
31	chr19:55882550-55882600	GM19239	blood:	n/a
32	chr19:55888156-55888206	ECC-1	luminal epithelium:	n/a
33	chr19:55888150-55888200	HepG2	liver:	n/a
34	chr19:55876060-55876110	Jurkat	blood:	n/a
35	chr19:55888146-55888196	AG04450	lung:	fetal
36	chr19:55882154-55882204	NHBE	bronchial:	n/a
37	chr19:55882504-55882554	AG04450	lung:	fetal
38	chr19:55887799-55887849	AG04449	skin:	fetal
39	chr19:55877371-55877421	HepG2	liver:	n/a
40	chr19:55880286-55880336	SKMC	muscle:	n/a
41	chr19:55887799-55887849	GM06990	blood:	n/a
42	chr19:55880286-55880336	HUVEC	blood vessel:	n/a
43	chr19:55877371-55877421	SK-N-SH_RA	brain:	n/a
44	chr19:55882550-55882600	Hepatocyte	liver:	n/a
45	chr19:55881893-55881943	Hepatocyte	liver:	n/a
46	chr19:55880593-55880643	MCF-7	breast:	n/a
47	chr19:55888146-55888196	NH-A	brain:	n/a
48	chr19:55888146-55888196	NHBE	bronchial:	n/a
49	chr19:55880984-55881034	ProgFib	skin:	n/a
50	chr19:55881893-55881943	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:55789877..55791428-chr19:55876107..55878357,2	K562	blood:
2	chr19:55876201..55879946-chr19:55894605..55900149,8	K562	blood:
3	chr19:55851377..55854272-chr19:55873809..55875979,2	MCF-7	breast:
4	chr19:55880381..55884285-chr19:55886063..55890457,4	K562	blood:
5	chr19:55866844..55868519-chr19:55877122..55879184,2	K562	blood:
6	chr19:55845491..55847724-chr19:55884578..55887231,2	MCF-7	breast:
7	chr19:55880381..55884285-chr19:55886063..55890457,4	K562	blood:
8	chr19:55857308..55859712-chr19:55880679..55883398,3	MCF-7	breast:
9	chr18:68131982..68132686-chr19:55877078..55877580,2	HCT-116	colon:
10	chr19:55872147..55875417-chr19:55876123..55877733,3	K562	blood:
11	chr19:55877367..55879452-chr19:55882812..55884383,2	K562	blood:
12	chr19:55851056..55852786-chr19:55880756..55882333,2	MCF-7	breast:
13	chr19:55876167..55879423-chr19:55882046..55885127,4	K562	blood:
14	chr19:55767450..55771021-chr19:55880319..55882334,3	MCF-7	breast:
15	chr19:55865908..55868131-chr19:55880960..55883611,2	MCF-7	breast:
16	chr19:55591142..55593634-chr19:55888302..55890512,2	K562	blood:
17	chr19:55872735..55877378-chr19:55878459..55880098,5	MCF-7	breast:
18	chr19:55874602..55877064-chr19:55916927..55920725,3	K562	blood:
19	chr19:55872617..55875125-chr19:55881370..55883672,2	K562	blood:
20	chr19:55849062..55852611-chr19:55879307..55883496,5	MCF-7	breast:
21	chr19:55876167..55879423-chr19:55882046..55885127,4	K562	blood:
22	chr19:55868108..55872228-chr19:55874382..55877630,4	K562	blood:
23	chr19:55869619..55872464-chr19:55877833..55879873,3	K562	blood:
24	chr19:55886090..55886775-chr9:93886966..93887466,2	Hela-S3	cervix:
25	chr19:55865433..55867142-chr19:55875019..55877075,2	MCF-7	breast:
26	chr19:55855835..55857937-chr19:55888038..55890020,2	K562	blood:
27	chr19:55851020..55853815-chr19:55885583..55887551,2	K562	blood:
28	chr19:55861836..55864418-chr19:55872988..55875222,3	K562	blood:
29	chr19:55853165..55857260-chr19:55879821..55883048,3	MCF-7	breast:
30	chr19:55877367..55879452-chr19:55882812..55884383,2	K562	blood:
31	chr19:55868105..55871088-chr19:55873603..55877567,3	MCF-7	breast:
32	chr19:55880628..55883032-chr19:55887908..55889776,2	K562	blood:
33	chr19:55806050..55808279-chr19:55877591..55880047,2	K562	blood:
34	chr19:55856384..55859080-chr19:55879922..55882670,2	K562	blood:
35	chr19:55874299..55876098-chr19:55878780..55880715,2	K562	blood:
36	chr19:55852315..55853947-chr19:55885473..55887551,2	K562	blood:
37	chr19:55864955..55867658-chr19:55880222..55883231,3	MCF-7	breast:
38	chr19:55880628..55883032-chr19:55887908..55889776,2	K562	blood:
39	chr19:55874299..55876098-chr19:55878780..55880715,2	K562	blood:
40	chr19:55872617..55875125-chr19:55881370..55883672,2	K562	blood:

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	IL11	hsa-miR-211-5p	chr19:55877002-55877023
2	IL11	hsa-miR-124-3p	chr19:55877218-55877236
3	IL11	hsa-miR-204-5p	chr19:55877002-55877023
4	IL11	hsa-miR-211-5p	chr19:55875919-55875940
5	IL11	hsa-miR-204-5p	chr19:55875919-55875940
6	IL11	hsa-miR-124-3p	chr19:55877224-55877217

Variant related genes	Relation type
ENSG00000267706	TF binding region
IL11	TF binding region
TMEM190	TF binding region
FAM71E2	TF binding region
ENSG00000267706	CpG island
IL11	CpG island
TMEM190	CpG island
FAM71E2	CpG island
ENSG00000108107	chromatin interactions
ENSG00000267706	chromatin interactions
ENSG00000180043	chromatin interactions
ENSG00000133247	chromatin interactions
ENSG00000267531	chromatin interactions
ENSG00000160471	chromatin interactions
ENSG00000269275	chromatin interactions
ENSG00000131037	chromatin interactions
ENSG00000233493	chromatin interactions
ENSG00000105063	chromatin interactions
ENSG00000133265	chromatin interactions
ENSG00000095752	chromatin interactions
ENSG00000160472	chromatin interactions
ENSG00000108106	chromatin interactions

Extended variants
information (count: 593 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4252567	chr19:55874986-55874987	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570200927	chr19:55874998-55874999	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs529414179	chr19:55875019-55875020	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs374049358	chr19:55875026-55875027	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs549453932	chr19:55875027-55875028	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs4252566	chr19:55875035-55875036	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534677161	chr19:55875049-55875050	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs544124990	chr19:55875198-55875199	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs571826506	chr19:55875206-55875207	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs4252565	chr19:55875212-55875213	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs138669230	chr19:55875282-55875283	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs573856864	chr19:55875342-55875343	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs372778607	chr19:55875353-55875354	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs4252564	chr19:55875419-55875420	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs555009570	chr19:55875436-55875437	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs572040053	chr19:55875451-55875452	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs540646751	chr19:55875465-55875466	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs564450492	chr19:55875518-55875519	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs577849761	chr19:55875519-55875520	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs543658834	chr19:55875522-55875523	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs143577315	chr19:55875570-55875571	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs529074807	chr19:55875605-55875606	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs147986301	chr19:55875696-55875697	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs530989757	chr19:55875703-55875704	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs184375712	chr19:55875743-55875744	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs189230995	chr19:55875744-55875745	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs61613895	chr19:55875760-55875761	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs551482506	chr19:55875915-55875916	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs571948130	chr19:55875935-55875936	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region miRNA target site	7 gene(s)	Overlapped CNVs	n/a
30	rs543176750	chr19:55875997-55875998	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs537353871	chr19:55876012-55876013	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs3181994	chr19:55876062-55876063	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs142337805	chr19:55876068-55876069	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs1126760	chr19:55876074-55876075	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs4252562	chr19:55876162-55876163	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572040598	chr19:55876226-55876227	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs546592797	chr19:55876229-55876230	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs534651788	chr19:55876230-55876231	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs2298885	chr19:55876240-55876241	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577516789	chr19:55876241-55876242	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs543764633	chr19:55876242-55876243	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs115941539	chr19:55876249-55876250	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs532313679	chr19:55876303-55876304	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs573917377	chr19:55876358-55876359	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs542824831	chr19:55876362-55876363	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs181915571	chr19:55876455-55876456	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs528569171	chr19:55876505-55876506	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs551811635	chr19:55876510-55876511	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs565139321	chr19:55876536-55876537	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs570056352	chr19:55876584-55876585	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55866200-55880600	Weak transcription	Right Atrium	heart
2	chr19:55871400-55877000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr19:55871400-55880200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:55873400-55879800	Weak transcription	HSMM	muscle
5	chr19:55873600-55875200	Enhancers	Placenta	Placenta
6	chr19:55873600-55876200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr19:55874200-55875000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:55874200-55875200	Enhancers	A549	lung
9	chr19:55874400-55875800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:55874600-55875200	Enhancers	HepG2	liver
11	chr19:55874600-55876000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:55874600-55879600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr19:55874800-55875800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:55874800-55875800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr19:55874800-55876600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr19:55874800-55877000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:55874800-55877400	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr19:55874800-55877600	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr19:55874800-55879800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr19:55875200-55876600	Weak transcription	A549	lung
21	chr19:55875400-55875600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr19:55875400-55876000	Enhancers	HSMMtube	muscle
23	chr19:55875400-55876000	Enhancers	NH-A	brain
24	chr19:55875400-55876200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr19:55875400-55876400	Enhancers	Osteobl	bone
26	chr19:55875600-55876200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr19:55875800-55876000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr19:55875800-55876000	Enhancers	NHLF	lung
29	chr19:55875800-55876800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr19:55875800-55879800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:55876000-55876200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr19:55876000-55876200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr19:55876000-55876400	Genic enhancers	NH-A	brain
34	chr19:55876000-55879600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr19:55876000-55879600	Weak transcription	HSMMtube	muscle
36	chr19:55876000-55880200	Weak transcription	NHLF	lung
37	chr19:55876200-55878000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr19:55876200-55879400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr19:55876200-55879800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:55876200-55880000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr19:55876200-55880000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr19:55876400-55878200	Weak transcription	Osteobl	bone
43	chr19:55876400-55878400	Strong transcription	NH-A	brain
44	chr19:55876600-55877200	Strong transcription	A549	lung
45	chr19:55876800-55877800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:55876800-55879600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:55877000-55877200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr19:55877000-55877800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr19:55877000-55879800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:55877000-55880000	Weak transcription	NHEK	skin

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