Variant report

Variant	nsv1023261
Chromosome Location	chr7:111593889-111780337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1322)
CpG islands
(count:369)
Chromatin interactive
region (count:129)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1322 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111728610-111728926	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111726569-111727045	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111678508-111678604	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:111772512-111772712	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:111690725-111690739	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111700572-111701211	HepG2	liver:	n/a	n/a
7	ATF1	chr7:111594624-111594810	K562	blood:	n/a	n/a
8	ATF1	chr7:111737923-111738078	K562	blood:	n/a	n/a
9	ATF2	chr7:111720368-111721555	GM12878	blood:	n/a	n/a
10	ATF3	chr7:111720334-111721046	A549	lung:	n/a	n/a
11	BACH1	chr7:111765021-111765023	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:111724712-111724899	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:111696482-111696705	GM12878	blood:	n/a	n/a
14	BATF	chr7:111696477-111696715	GM12878	blood:	n/a	n/a
15	BATF	chr7:111720504-111720854	GM12878	blood:	n/a	n/a
16	BATF	chr7:111649269-111649566	GM12878	blood:	n/a	chr7:111649378-111649389
17	BATF	chr7:111720449-111720774	GM12878	blood:	n/a	n/a
18	BCL3	chr7:111720272-111721481	A549	lung:	n/a	chr7:111720760-111720768
19	BHLHE40	chr7:111724486-111724855	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:111696578-111696783	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:111641299-111641477	A549	lung:	n/a	n/a
22	BHLHE40	chr7:111709967-111709974	K562	blood:	n/a	n/a
23	BHLHE40	chr7:111721174-111721423	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:111640947-111641678	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:111720412-111720874	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr7:111627122-111627442	IMR90	lung:	n/a	n/a
27	CEBPB	chr7:111720401-111720996	A549	lung:	n/a	n/a
28	CEBPB	chr7:111705690-111705996	HepG2	liver:	n/a	chr7:111705853-111705864 chr7:111705853-111705866 chr7:111705854-111705865 chr7:111705853-111705866 chr7:111705853-111705864
29	CEBPB	chr7:111707136-111707256	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:111720404-111720808	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr7:111627149-111627454	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:111689686-111689918	Hela-S3	cervix:	n/a	chr7:111689818-111689829
33	CEBPB	chr7:111660096-111660264	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:111720233-111721142	A549	lung:	n/a	n/a
35	CEBPB	chr7:111696469-111696926	A549	lung:	n/a	chr7:111696646-111696657
36	CEBPB	chr7:111700631-111701117	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:111720505-111720822	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:111641231-111641571	IMR90	lung:	n/a	chr7:111641381-111641392
39	CEBPB	chr7:111700626-111701071	A549	lung:	n/a	n/a
40	CEBPB	chr7:111660008-111660341	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:111769991-111770354	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:111733250-111733294	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:111676236-111676654	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:111658768-111659101	HepG2	liver:	n/a	chr7:111658927-111658938
45	CEBPB	chr7:111752870-111753129	HepG2	liver:	n/a	chr7:111753004-111753015
46	CEBPB	chr7:111726517-111726972	HepG2	liver:	n/a	n/a
47	CEBPB	chr7:111724194-111724437	A549	lung:	n/a	chr7:111724301-111724312 chr7:111724317-111724328
48	CEBPB	chr7:111689704-111689969	K562	blood:	n/a	chr7:111689818-111689829
49	CEBPB	chr7:111761577-111761764	HepG2	liver:	n/a	chr7:111761632-111761643
50	CEBPB	chr7:111704710-111704986	HepG2	liver:	n/a	chr7:111704852-111704863

(count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111721233-111721283	HUVEC	blood vessel:	n/a
2	chr7:111731013-111731063	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:111731013-111731063	GM12891	blood:	n/a
4	chr7:111721233-111721283	HUVEC	blood vessel:	n/a
5	chr7:111731013-111731063	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:111731013-111731063	GM12891	blood:	n/a
7	chr7:111721233-111721283	Jurkat	blood:	n/a
8	chr7:111770158-111770208	HCF	heart:	n/a
9	chr7:111776496-111776546	MCF10A-Er-Src	breast:	n/a
10	chr7:111776496-111776546	AG10803	skin:	n/a
11	chr7:111776496-111776546	HCT-116	colon:	n/a
12	chr7:111770158-111770208	NT2-D1	testis:	n/a
13	chr7:111721233-111721283	BJ	skin:	n/a
14	chr7:111721233-111721283	AG10803	skin:	n/a
15	chr7:111662594-111662644	AG10803	skin:	n/a
16	chr7:111662594-111662644	ovcar-3	ovarian:	n/a
17	chr7:111731013-111731063	RPTEC	kidney:	n/a
18	chr7:111770158-111770208	GM12892	blood:	n/a
19	chr7:111776496-111776546	Jurkat	blood:	n/a
20	chr7:111731013-111731063	ovcar-3	ovarian:	n/a
21	chr7:111693032-111693082	HIPEpiC	eye:	n/a
22	chr7:111662594-111662644	HEEpiC	esophagus:	n/a
23	chr7:111693032-111693082	HepG2	liver:	n/a
24	chr7:111770158-111770208	ovcar-3	ovarian:	n/a
25	chr7:111770158-111770208	LNCaP	prostate:	n/a
26	chr7:111731013-111731063	BJ	skin:	n/a
27	chr7:111662594-111662644	HNPCEpiC	eye:	n/a
28	chr7:111776496-111776546	HIPEpiC	eye:	n/a
29	chr7:111693032-111693082	SK-N-MC	brain:	n/a
30	chr7:111770158-111770208	HRCEpiC	kidney:	n/a
31	chr7:111693032-111693082	BE2_C	brain:	n/a
32	chr7:111693032-111693082	NH-A	brain:	n/a
33	chr7:111776496-111776546	ovcar-3	ovarian:	n/a
34	chr7:111662594-111662644	HepG2	liver:	n/a
35	chr7:111721233-111721283	HRCEpiC	kidney:	n/a
36	chr7:111731013-111731063	AG04449	skin:	fetal
37	chr7:111693032-111693082	GM19239	blood:	n/a
38	chr7:111662594-111662644	AG09319	gingival:	n/a
39	chr7:111731013-111731063	HL-60	blood:	n/a
40	chr7:111770158-111770208	GM12878	blood:	n/a
41	chr7:111662594-111662644	HUVEC	blood vessel:	n/a
42	chr7:111662594-111662644	RPTEC	kidney:	n/a
43	chr7:111731013-111731063	Hela-S3	cervix:	n/a
44	chr7:111731013-111731063	AG10803	skin:	n/a
45	chr7:111776496-111776546	K562	blood:	n/a
46	chr7:111776496-111776546	GM06990	blood:	n/a
47	chr7:111770158-111770208	HIPEpiC	eye:	n/a
48	chr7:111776496-111776546	PrEC	prostate:	n/a
49	chr7:111721233-111721283	GM12891	blood:	n/a
50	chr7:111731013-111731063	AG09309	skin:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111724914..111725707-chr7:111777452..111778442,2	MCF-7	breast:
2	chr7:111719751..111721639-chr7:111721753..111724570,2	K562	blood:
3	chr7:111622597..111625048-chr7:111627500..111629873,3	MCF-7	breast:
4	chr7:111669068..111671369-chr7:111671874..111673697,2	K562	blood:
5	chr7:111739006..111741614-chr7:111745042..111747741,2	K562	blood:
6	chr7:111634123..111636309-chr7:111638803..111641214,2	K562	blood:
7	chr7:111712128..111713955-chr7:111714116..111716651,2	MCF-7	breast:
8	chr7:111638349..111643869-chr7:111644026..111648526,5	MCF-7	breast:
9	chr7:111658895..111662375-chr7:111662426..111664044,3	MCF-7	breast:
10	chr7:111637130..111639282-chr7:111640957..111644072,3	K562	blood:
11	chr7:111683205..111686070-chr7:111696191..111697758,2	K562	blood:
12	chr7:111722754..111725358-chr7:111846243..111848256,2	MCF-7	breast:
13	chr10:115901849..115902419-chr7:111775863..111776650,2	MCF-7	breast:
14	chr7:111724807..111725873-chr7:111784185..111785009,6	MCF-7	breast:
15	chr7:111591201..111593587-chr7:111596427..111598075,3	K562	blood:
16	chr7:111727653..111730337-chr7:111737903..111739641,2	K562	blood:
17	chr7:111673451..111677355-chr7:111678241..111682927,4	MCF-7	breast:
18	chr7:111696985..111699973-chr7:111702426..111704136,2	K562	blood:
19	chr7:111739006..111741614-chr7:111745042..111747741,2	K562	blood:
20	chr7:111635442..111637426-chr7:111724707..111726732,2	MCF-7	breast:
21	chr20:52529863..52532284-chr7:111681323..111683323,2	MCF-7	breast:
22	chr7:111596682..111600443-chr7:111601469..111604653,3	MCF-7	breast:
23	chr7:111679099..111681078-chr7:111697466..111700106,2	MCF-7	breast:
24	chr7:111711136..111713687-chr7:111723265..111726073,2	MCF-7	breast:
25	chr7:111597718..111599970-chr7:111623023..111624546,2	MCF-7	breast:
26	chr7:111667061..111669402-chr7:111698388..111701090,2	K562	blood:
27	chr7:111648094..111649963-chr7:111652794..111654673,2	K562	blood:
28	chr7:111711136..111713687-chr7:111723265..111726073,2	MCF-7	breast:
29	chr7:111780038..111783030-chr7:111786825..111789464,2	MCF-7	breast:
30	chr7:111673451..111677355-chr7:111678241..111682927,4	MCF-7	breast:
31	chr7:111719879..111722087-chr7:111722721..111725922,3	MCF-7	breast:
32	chr7:111727544..111730183-chr7:111730698..111732624,2	MCF-7	breast:
33	chr7:111654679..111656709-chr7:111671878..111674292,2	MCF-7	breast:
34	chr7:111623241..111625570-chr7:111627494..111630034,2	K562	blood:
35	chr7:111592856..111595719-chr7:112049563..112051825,3	MCF-7	breast:
36	chr7:111718019..111719728-chr7:111726986..111728960,2	MCF-7	breast:
37	chr7:111705385..111707110-chr7:111712714..111715574,2	MCF-7	breast:
38	chr7:111639696..111641501-chr7:111645130..111646643,2	K562	blood:
39	chr7:111603025..111604726-chr7:112089502..112091092,2	MCF-7	breast:
40	chr7:111730398..111731930-chr7:111732566..111734324,2	MCF-7	breast:
41	chr7:111733344..111737264-chr7:111740377..111743669,3	MCF-7	breast:
42	chr7:111648763..111650835-chr7:111713942..111716550,2	K562	blood:
43	chr7:111725319..111725839-chr7:111784610..111785137,2	MCF-7	breast:
44	chr7:111777527..111779593-chr7:111780314..111781926,2	K562	blood:
45	chr7:111381576..111382122-chr7:111719685..111720408,2	MCF-7	breast:
46	chr7:111779086..111784915-chr7:111786394..111790128,6	K562	blood:
47	chr7:111744902..111746458-chr7:111746527..111748789,2	MCF-7	breast:
48	chr7:111719561..111720111-chr7:112051016..112051524,2	MCF-7	breast:
49	chr7:111596682..111600443-chr7:111601469..111604653,3	MCF-7	breast:
50	chr7:111597718..111599970-chr7:111623023..111624546,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP237	TF binding region
ENSG00000234358	TF binding region
DOCK4	TF binding region
RNA5SP237	CpG island
ENSG00000234358	CpG island
DOCK4	CpG island
ENSG00000198839	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000128512	chromatin interactions
ENSG00000226851	chromatin interactions
ENSG00000234358	chromatin interactions

Extended variants
information (count: 6878 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:6878 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188207701	chr7:111593970-111593971	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs180780284	chr7:111594023-111594024	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs545059379	chr7:111594068-111594069	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs115922836	chr7:111594072-111594073	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs186398142	chr7:111594104-111594105	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs563346299	chr7:111594113-111594114	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569575921	chr7:111594124-111594125	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs546986013	chr7:111594154-111594155	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs537089410	chr7:111594213-111594214	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377338451	chr7:111594214-111594215	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548962907	chr7:111594220-111594221	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs567449619	chr7:111594248-111594249	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs534778819	chr7:111594284-111594285	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs111850195	chr7:111594295-111594296	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs145624042	chr7:111594351-111594352	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539180323	chr7:111594359-111594360	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs557408904	chr7:111594399-111594400	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs112258247	chr7:111594409-111594410	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575583084	chr7:111594410-111594411	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs543469157	chr7:111594430-111594431	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs575207318	chr7:111594460-111594461	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532306670	chr7:111594461-111594462	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs372027124	chr7:111594468-111594469	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs540792874	chr7:111594472-111594473	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs189683656	chr7:111594529-111594530	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs561187033	chr7:111594533-111594534	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs542530602	chr7:111594540-111594541	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs532993343	chr7:111594541-111594542	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs551546367	chr7:111594558-111594559	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs181723325	chr7:111594615-111594616	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528305579	chr7:111594629-111594630	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs148483309	chr7:111594630-111594631	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs549001313	chr7:111594632-111594633	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs546773155	chr7:111594633-111594634	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs564867664	chr7:111594634-111594635	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs567339173	chr7:111594679-111594680	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs142593647	chr7:111594680-111594681	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs10458290	chr7:111594719-111594720	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs571703705	chr7:111594757-111594758	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs538909077	chr7:111594779-111594780	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs185845196	chr7:111594815-111594816	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs35618334	chr7:111594833-111594834	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs71147499	chr7:111594834-111594835	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs576040070	chr7:111594845-111594846	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs536958733	chr7:111594852-111594853	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113878380	chr7:111594887-111594888	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs573684892	chr7:111594900-111594901	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs540982479	chr7:111594904-111594905	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373806183	chr7:111594909-111594910	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559225483	chr7:111594916-111594917	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Glioblastoma multiforme	20824129	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:3021 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111557200-111594800	Weak transcription	Fetal Heart	heart
2	chr7:111580400-111599200	Weak transcription	Fetal Brain Female	brain
3	chr7:111583000-111610800	Weak transcription	Fetal Stomach	stomach
4	chr7:111583600-111594200	Weak transcription	Esophagus	oesophagus
5	chr7:111583600-111596400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:111583600-111598800	Weak transcription	Aorta	Aorta
7	chr7:111583600-111599000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:111583600-111630800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:111584200-111594600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr7:111584200-111631800	Weak transcription	A549	lung
11	chr7:111585200-111630600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr7:111585600-111594200	Weak transcription	Left Ventricle	heart
13	chr7:111592200-111595200	Enhancers	Dnd41	blood
14	chr7:111592200-111599200	Enhancers	Fetal Lung	lung
15	chr7:111592600-111594400	Enhancers	NHEK	skin
16	chr7:111592800-111594400	Enhancers	HMEC	breast
17	chr7:111592800-111595200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr7:111593000-111594200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:111593000-111594400	Enhancers	Liver	Liver
20	chr7:111593000-111595200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:111593000-111595200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:111593000-111595200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr7:111593000-111595600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr7:111593000-111600000	Enhancers	Brain Anterior Caudate	brain
25	chr7:111593200-111594000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr7:111593200-111594400	Enhancers	HepG2	liver
27	chr7:111593200-111594600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:111593200-111595200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:111593200-111595200	Enhancers	Brain Angular Gyrus	brain
30	chr7:111593200-111596400	Enhancers	Fetal Kidney	kidney
31	chr7:111593200-111596800	Enhancers	Brain Substantia Nigra	brain
32	chr7:111593400-111594000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:111593400-111594400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:111593400-111594600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:111593400-111594800	Enhancers	Adipose Nuclei	Adipose
36	chr7:111593400-111594800	Weak transcription	HUVEC	blood vessel
37	chr7:111593400-111595600	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:111593400-111597000	Enhancers	Brain Hippocampus Middle	brain
39	chr7:111593600-111594000	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr7:111593600-111594200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:111593600-111595000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr7:111593600-111595000	Enhancers	Lung	lung
43	chr7:111593600-111595400	Enhancers	Brain Cingulate Gyrus	brain
44	chr7:111593600-111598200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr7:111593600-111638200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr7:111593800-111594000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr7:111593800-111594200	Weak transcription	Ovary	ovary
48	chr7:111593800-111594600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:111593800-111594600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:111593800-111594800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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