Variant report

Variant	esv13824
Chromosome Location	chr7:6123263-6144717
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:975)
CpG islands
(count:734)
Chromatin interactive
region (count:70)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6142661-6142946	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6132523-6132819	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6144020-6144574	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6144216-6144499	K562	blood:	n/a	n/a
5	ATF1	chr7:6144054-6144615	K562	blood:	n/a	n/a
6	ATF2	chr7:6143973-6144554	GM12878	blood:	n/a	n/a
7	ATF2	chr7:6143963-6144389	GM12878	blood:	n/a	n/a
8	ATF2	chr7:6143969-6144475	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr7:6144063-6144497	H1-hESC	embryonic stem cell:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
10	ATF3	chr7:6144175-6144636	H1-hESC	embryonic stem cell:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
11	ATF3	chr7:6144173-6144629	HepG2	liver:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
12	ATF3	chr7:6143916-6144364	A549	lung:	n/a	chr7:6144238-6144247
13	ATF3	chr7:6144119-6144750	K562	blood:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
14	ATF3	chr7:6143966-6144624	GM12878	blood:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
15	ATF3	chr7:6144239-6144555	GM12878	blood:	n/a	chr7:6144358-6144369
16	ATF3	chr7:6144003-6144589	A549	lung:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
17	BACH1	chr7:6144078-6144449	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr7:6143876-6144448	A549	lung:	n/a	chr7:6144233-6144246
19	BCLAF1	chr7:6143958-6144586	GM12878	blood:	n/a	chr7:6144233-6144246
20	BCLAF1	chr7:6143976-6144609	GM12878	blood:	n/a	chr7:6144233-6144246
21	BHLHE40	chr7:6144032-6144593	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:6144020-6144538	K562	blood:	n/a	n/a
23	BHLHE40	chr7:6144159-6144652	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:6144167-6144503	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr7:6144073-6144492	HepG2	liver:	n/a	n/a
26	BRCA1	chr7:6142378-6142578	HepG2	liver:	n/a	n/a
27	BRCA1	chr7:6144086-6144519	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:6143567-6143579	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr7:6143832-6144479	K562	blood:	n/a	n/a
30	CCNT2	chr7:6144077-6145397	K562	blood:	n/a	chr7:6145165-6145174
31	CEBPB	chr7:6144055-6144537	Hela-S3	cervix:	n/a	chr7:6144318-6144326
32	CEBPB	chr7:6136224-6136319	HepG2	liver:	n/a	chr7:6136278-6136289
33	CEBPB	chr7:6144198-6144352	HepG2	liver:	n/a	chr7:6144318-6144326
34	CEBPB	chr7:6144216-6144477	H1-hESC	embryonic stem cell:	n/a	chr7:6144318-6144326
35	CEBPB	chr7:6134330-6134597	H1-hESC	embryonic stem cell:	n/a	chr7:6134474-6134485
36	CEBPB	chr7:6136175-6136408	K562	blood:	n/a	chr7:6136278-6136289
37	CEBPB	chr7:6134395-6134626	HepG2	liver:	n/a	chr7:6134474-6134485
38	CEBPB	chr7:6134417-6134609	A549	lung:	n/a	chr7:6134474-6134485
39	CEBPB	chr7:6134326-6134634	K562	blood:	n/a	chr7:6134474-6134485
40	CEBPB	chr7:6134421-6134596	Hela-S3	cervix:	n/a	chr7:6134474-6134485
41	CEBPB	chr7:6134397-6134550	IMR90	lung:	n/a	chr7:6134474-6134485
42	CEBPB	chr7:6134269-6134562	K562	blood:	n/a	chr7:6134474-6134485
43	CEBPD	chr7:6143958-6144528	HepG2	liver:	n/a	n/a
44	CEBPD	chr7:6144048-6144445	HepG2	liver:	n/a	n/a
45	CEBPZ	chr7:6142437-6142902	HepG2	liver:	n/a	n/a
46	CHD1	chr7:6144040-6144331	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr7:6144040-6144289	GM12878	blood:	n/a	n/a
48	CHD2	chr7:6144081-6144509	K562	blood:	n/a	n/a
49	CHD2	chr7:6144023-6144696	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr7:6144018-6144501	H1-hESC	embryonic stem cell:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6140990-6141040	A549	lung:	n/a
2	chr7:6144372-6144422	IMR90	lung:	fetal
3	chr7:6140990-6141040	A549	lung:	n/a
4	chr7:6144372-6144422	IMR90	lung:	fetal
5	chr7:6140693-6140743	PrEC	prostate:	n/a
6	chr7:6144372-6144422	ovcar-3	ovarian:	n/a
7	chr7:6143736-6143786	PrEC	prostate:	n/a
8	chr7:6144369-6144419	HCM	heart:	n/a
9	chr7:6144127-6144177	PANC-1	pancreas:	n/a
10	chr7:6140990-6141040	SK-N-SH	brain:	n/a
11	chr7:6144367-6144417	NB4	blood:	n/a
12	chr7:6140990-6141040	AG09319	gingival:	n/a
13	chr7:6143736-6143786	AG04450	lung:	fetal
14	chr7:6144308-6144358	PrEC	prostate:	n/a
15	chr7:6144372-6144422	SAEC	small airway:	n/a
16	chr7:6144308-6144358	HRPEpiC	eye:	n/a
17	chr7:6144298-6144348	ECC-1	luminal epithelium:	n/a
18	chr7:6144127-6144177	AoSMC	blood vessel:	n/a
19	chr7:6144127-6144177	BJ	skin:	n/a
20	chr7:6140693-6140743	HCPEpiC	choroid plexus:	n/a
21	chr7:6144298-6144348	GM12891	blood:	n/a
22	chr7:6144127-6144177	NH-A	brain:	n/a
23	chr7:6143736-6143786	AG04449	skin:	fetal
24	chr7:6144127-6144177	GM12878	blood:	n/a
25	chr7:6144399-6144449	SKMC	muscle:	n/a
26	chr7:6143736-6143786	HIPEpiC	eye:	n/a
27	chr7:6124631-6124681	HL-60	blood:	n/a
28	chr7:6142285-6142335	AG09309	skin:	n/a
29	chr7:6140693-6140743	HRCEpiC	kidney:	n/a
30	chr7:6144399-6144449	SAEC	small airway:	n/a
31	chr7:6142285-6142335	H1-hESC	embryonic stem cell:	embryo
32	chr7:6140990-6141040	ECC-1	luminal epithelium:	n/a
33	chr7:6143736-6143786	A549	lung:	n/a
34	chr7:6144127-6144177	HEEpiC	esophagus:	n/a
35	chr7:6144399-6144449	H1-hESC	embryonic stem cell:	embryo
36	chr7:6124631-6124681	HCF	heart:	n/a
37	chr7:6144127-6144177	HMEC	breast:	n/a
38	chr7:6144369-6144419	SAEC	small airway:	n/a
39	chr7:6144367-6144417	PrEC	prostate:	n/a
40	chr7:6140990-6141040	HCT-116	colon:	n/a
41	chr7:6144372-6144422	AG04449	skin:	fetal
42	chr7:6144127-6144177	HRE	kidney:	n/a
43	chr7:6144399-6144449	NHBE	bronchial:	n/a
44	chr7:6144367-6144417	ECC-1	luminal epithelium:	n/a
45	chr7:6144399-6144449	NH-A	brain:	n/a
46	chr7:6143736-6143786	GM12892	blood:	n/a
47	chr7:6144372-6144422	HL-60	blood:	n/a
48	chr7:6142285-6142335	Caco-2	colon:	n/a
49	chr7:6144369-6144419	GM19239	blood:	n/a
50	chr7:6144127-6144177	Hepatocyte	liver:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:6065831..6068709-chr7:6141820..6144838,4	MCF-7	breast:
2	chr7:6120819..6122928-chr7:6131075..6133699,2	K562	blood:
3	chr7:6138615..6140730-chr7:6142793..6145640,3	K562	blood:
4	chr11:537982..538482-chr7:6143933..6144434,2	HCT-116	colon:
5	chr7:6140966..6142574-chr7:6434049..6436038,2	K562	blood:
6	chr7:6094946..6099638-chr7:6140891..6146239,12	K562	blood:
7	chr7:6118962..6122557-chr7:6124155..6128114,4	MCF-7	breast:
8	chr19:17516059..17516719-chr7:6143769..6144365,2	NB4	blood:
9	chr7:6118878..6122850-chr7:6140823..6146720,14	MCF-7	breast:
10	chr7:6127500..6130529-chr7:6140681..6143799,3	MCF-7	breast:
11	chr10:17243122..17243935-chr7:6143879..6144532,2	HCT-116	colon:
12	chr7:6119410..6124898-chr7:6141396..6145150,7	MCF-7	breast:
13	chr7:6048826..6049627-chr7:6143766..6144544,2	HCT-116	colon:
14	chr7:6118471..6120891-chr7:6135399..6137782,2	K562	blood:
15	chr7:6090422..6101465-chr7:6116449..6124326,16	K562	blood:
16	chr7:6133404..6135856-chr7:6136642..6138588,2	MCF-7	breast:
17	chr7:6139809..6142435-chr7:6386007..6388709,2	K562	blood:
18	chr7:6064661..6068184-chr7:6142795..6145849,5	MCF-7	breast:
19	chr7:6143900..6146202-chr7:6155214..6157141,2	MCF-7	breast:
20	chr7:6054308..6057610-chr7:6144384..6145966,3	K562	blood:
21	chr7:6055602..6058271-chr7:6142750..6144893,2	MCF-7	breast:
22	chr7:6118710..6122632-chr7:6142742..6146844,10	K562	blood:
23	chr7:6062330..6064601-chr7:6141391..6143688,2	MCF-7	breast:
24	chr7:6143877..6144677-chr9:134000320..134001058,2	Hela-S3	cervix:
25	chr7:6129689..6132230-chr7:6141187..6143186,2	K562	blood:
26	chr7:6132461..6134616-chr7:6143450..6145084,2	K562	blood:
27	chr7:6130749..6132668-chr7:6140261..6142428,2	MCF-7	breast:
28	chr7:6097502..6099818-chr7:6138149..6139969,2	K562	blood:
29	chr7:6047026..6051403-chr7:6141746..6146462,7	K562	blood:
30	chr7:6134399..6135940-chr7:6137950..6139940,2	K562	blood:
31	chr13:103248649..103249379-chr7:6143733..6144282,2	NB4	blood:
32	chr7:6049211..6051236-chr7:6138312..6140816,2	MCF-7	breast:
33	chr7:6136281..6138801-chr7:6142810..6145571,2	MCF-7	breast:
34	chr7:6096872..6099965-chr7:6142845..6147736,5	MCF-7	breast:
35	chr7:6110355..6112451-chr7:6141705..6143583,2	K562	blood:
36	chr7:6138619..6141275-chr7:6177878..6179542,2	K562	blood:
37	chr7:6118943..6121901-chr7:6135468..6137928,2	MCF-7	breast:
38	chr5:176830787..176831503-chr7:6143819..6144569,2	Hela-S3	cervix:
39	chr1:38061256..38061780-chr7:6143823..6144821,2	NB4	blood:
40	chr7:6143403..6145262-chr7:6310829..6313708,2	MCF-7	breast:
41	chr7:6134295..6136999-chr7:6143069..6146027,4	MCF-7	breast:
42	chr7:6140101..6142777-chr7:6142839..6145208,2	MCF-7	breast:
43	chr7:6047404..6049912-chr7:6142714..6146343,4	MCF-7	breast:
44	chr17:56708604..56709142-chr7:6143631..6144302,2	Hela-S3	cervix:
45	chr7:6143696..6144293-chr7:73153152..73153874,2	Hela-S3	cervix:
46	chr7:6138803..6142532-chr7:6142595..6145839,5	MCF-7	breast:
47	chr3:73160101..73161088-chr7:6143657..6144592,2	Hela-S3	cervix:
48	chr7:6119521..6122293-chr7:6142698..6146719,8	K562	blood:
49	chr7:6133404..6135856-chr7:6136642..6138588,2	MCF-7	breast:
50	chr7:6100114..6101811-chr7:6141887..6144361,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP42-1	chr7:6132660-6132683	XLOC_005979
2	lnc-USP42-3	chr7:6130515-6131250	NONHSAT118980
3	lnc-USP42-1	chr7:6128421-6128531	XLOC_005979
4	lnc-USP42-1	chr7:6128421-6128531	XLOC_005979
5	lnc-USP42-1	chr7:6124776-6124887	XLOC_005979
6	lnc-USP42-1	chr7:6123963-6124367	NONHSAT118977
7	lnc-USP42-1	chr7:6124060-6124243	XLOC_005979
8	lnc-USP42-4	chr7:6128922-6129206	NONHSAT118979
9	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979
10	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979
11	lnc-EIF2AK1-1	chr7:6144054-6144254	NONHSAT118982
12	lnc-USP42-2	chr7:6131319-6131626	NONHSAT118981
13	lnc-USP42-5	chr7:6124455-6124733	NONHSAT118978
14	lnc-USP42-1	chr7:6132660-6132716	XLOC_005979
15	lnc-USP42-1	chr7:6124060-6124303	XLOC_005979

No data

Variant related genes	Relation type
USP42	TF binding region
USP42	CpG island
ENSG00000134697	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000269640	chromatin interactions
ENSG00000264605	chromatin interactions
ENSG00000126883	chromatin interactions
ENSG00000172660	chromatin interactions
ENSG00000207217	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000178397	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000224043	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000141971	chromatin interactions
ENSG00000130303	chromatin interactions
ENSG00000252929	chromatin interactions
ENSG00000107614	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000106077	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000131187	chromatin interactions
ENSG00000082258	chromatin interactions
ENSG00000134900	chromatin interactions
LIN28B	miRNA target sites
IPPK	miRNA target sites
BCL2L11	miRNA target sites
NIN	miRNA target sites

Extended variants
information (count: 825 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568222646	chr7:6123308-6123309	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs377309106	chr7:6123309-6123310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs535651187	chr7:6123310-6123311	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs554107407	chr7:6123383-6123384	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs370929112	chr7:6123395-6123396	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs539400448	chr7:6123400-6123401	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs138202685	chr7:6123403-6123404	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs576008744	chr7:6123410-6123411	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs34199446	chr7:6123432-6123433	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs543114872	chr7:6123434-6123435	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs118035543	chr7:6123443-6123444	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573848924	chr7:6123520-6123521	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs541273823	chr7:6123550-6123551	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs149171993	chr7:6123559-6123560	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs564671815	chr7:6123594-6123595	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs533485471	chr7:6123619-6123620	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs186281214	chr7:6123683-6123684	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs531683072	chr7:6123709-6123710	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs563501674	chr7:6123713-6123714	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs189194151	chr7:6123714-6123715	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549913764	chr7:6123795-6123796	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs180721073	chr7:6123815-6123816	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs567809075	chr7:6123849-6123850	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374573042	chr7:6123852-6123853	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs529093930	chr7:6123882-6123883	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs547644141	chr7:6123893-6123894	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568504690	chr7:6123894-6123895	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539324140	chr7:6123902-6123903	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113343987	chr7:6123966-6123967	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs575570328	chr7:6123988-6123989	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs569509244	chr7:6124034-6124035	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs112871157	chr7:6124035-6124036	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs555040180	chr7:6124092-6124093	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs573441749	chr7:6124093-6124094	Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs547939455	chr7:6124184-6124185	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs141755211	chr7:6124200-6124201	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs186496647	chr7:6124207-6124208	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs146258927	chr7:6124218-6124219	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs545338055	chr7:6124229-6124230	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs564014045	chr7:6124279-6124280	Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs575549252	chr7:6124341-6124342	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs113059326	chr7:6124371-6124372	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543086831	chr7:6124384-6124385	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs561356232	chr7:6124418-6124419	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190908392	chr7:6124438-6124439	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368187647	chr7:6124447-6124448	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547136103	chr7:6124520-6124521	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs559246555	chr7:6124529-6124530	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs370776217	chr7:6124533-6124534	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs533159968	chr7:6124577-6124578	Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6121600-6123400	Weak transcription	Placenta	Placenta
2	chr7:6123400-6125000	Enhancers	Placenta	Placenta
3	chr7:6131400-6131600	Enhancers	K562	blood
4	chr7:6131600-6132600	Weak transcription	K562	blood
5	chr7:6132000-6133200	Enhancers	HepG2	liver
6	chr7:6132200-6132400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
7	chr7:6132400-6132600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:6132400-6132600	Enhancers	A549	lung
9	chr7:6132400-6132800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:6132400-6133000	Enhancers	Hela-S3	cervix
11	chr7:6132600-6132800	Flanking Active TSS	A549	lung
12	chr7:6132600-6132800	Enhancers	K562	blood
13	chr7:6132600-6133200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr7:6132600-6133200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:6133000-6142400	Weak transcription	Hela-S3	cervix
16	chr7:6137600-6142000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr7:6138000-6138800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:6138400-6142400	Weak transcription	Fetal Intestine Small	intestine
19	chr7:6138600-6138800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:6138800-6143400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr7:6139000-6143000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:6139200-6143200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:6139200-6144000	Weak transcription	Spleen	Spleen
24	chr7:6139800-6142800	Weak transcription	Brain Cingulate Gyrus	brain
25	chr7:6139800-6143400	Weak transcription	Right Ventricle	heart
26	chr7:6140600-6140800	Enhancers	Ovary	ovary
27	chr7:6140600-6141600	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:6140800-6141000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr7:6140800-6141000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr7:6140800-6141400	Enhancers	K562	blood
31	chr7:6141000-6141200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:6141000-6141200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr7:6141000-6143400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr7:6141200-6143000	Weak transcription	Liver	Liver
35	chr7:6141200-6143200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:6141200-6143400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr7:6141400-6142600	Weak transcription	K562	blood
38	chr7:6141600-6143200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr7:6141600-6143200	Weak transcription	Fetal Heart	heart
40	chr7:6142000-6143000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:6142200-6143000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:6142200-6143400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr7:6142400-6142600	Enhancers	Hela-S3	cervix
44	chr7:6142400-6143200	Enhancers	HepG2	liver
45	chr7:6142400-6143400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:6142400-6143400	Strong transcription	Fetal Intestine Small	intestine
47	chr7:6142600-6142800	Enhancers	Gastric	stomach
48	chr7:6142600-6142800	Enhancers	Placenta Amnion	Placenta Amnion
49	chr7:6142600-6143000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:6142600-6143000	Enhancers	Skeletal Muscle Male	skeletal muscle

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