Variant report

Variant	nsv5916
Chromosome Location	chr7:116825221-116870570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:549)
CpG islands
(count:366)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:549 , 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	ARID3A	chr7:116826421-116826534	K562	blood:	n/a	n/a
2	ARID3A	chr7:116850976-116851228	K562	blood:	n/a	n/a
3	ARID3A	chr7:116853087-116853400	K562	blood:	n/a	n/a
4	ATF1	chr7:116848291-116848628	K562	blood:	n/a	n/a
5	ATF1	chr7:116826241-116826633	K562	blood:	n/a	n/a
6	ATF2	chr7:116870397-116871420	GM12878	blood:	n/a	n/a
7	BATF	chr7:116835524-116835719	GM12878	blood:	n/a	n/a
8	BATF	chr7:116835473-116835804	GM12878	blood:	n/a	n/a
9	BCL3	chr7:116867150-116867414	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:116859755-116859844	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:116848335-116848598	K562	blood:	n/a	n/a
12	BHLHE40	chr7:116860973-116861168	K562	blood:	n/a	chr7:116861063-116861084
13	BHLHE40	chr7:116860955-116861155	GM12878	blood:	n/a	chr7:116861063-116861084
14	BHLHE40	chr7:116850548-116850765	K562	blood:	n/a	n/a
15	BHLHE40	chr7:116851071-116851248	K562	blood:	n/a	n/a
16	BHLHE40	chr7:116870461-116871380	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:116853090-116853325	K562	blood:	n/a	n/a
18	CCNT2	chr7:116870467-116870618	K562	blood:	n/a	n/a
19	CCNT2	chr7:116835342-116835519	K562	blood:	n/a	n/a
20	CCNT2	chr7:116848341-116848531	K562	blood:	n/a	chr7:116848438-116848458
21	CEBPB	chr7:116831551-116831866	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:116853616-116853975	IMR90	lung:	n/a	chr7:116853790-116853799 chr7:116853790-116853801
23	CEBPB	chr7:116869524-116869884	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:116867190-116867441	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:116826174-116826537	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:116826201-116826539	K562	blood:	n/a	n/a
27	CEBPB	chr7:116833673-116834062	IMR90	lung:	n/a	chr7:116833849-116833862 chr7:116833849-116833860 chr7:116833849-116833862
28	CEBPB	chr7:116831585-116831840	A549	lung:	n/a	n/a
29	CEBPB	chr7:116826241-116826489	K562	blood:	n/a	n/a
30	CEBPB	chr7:116832236-116832547	HepG2	liver:	n/a	chr7:116832371-116832382
31	CEBPB	chr7:116832194-116832552	IMR90	lung:	n/a	chr7:116832371-116832382
32	CEBPB	chr7:116869700-116869702	A549	lung:	n/a	n/a
33	CEBPB	chr7:116833808-116833941	Hela-S3	cervix:	n/a	chr7:116833849-116833862 chr7:116833849-116833860 chr7:116833849-116833862
34	CEBPB	chr7:116831601-116831879	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:116831567-116831866	K562	blood:	n/a	n/a
36	CEBPB	chr7:116833723-116834004	K562	blood:	n/a	chr7:116833849-116833862 chr7:116833849-116833860 chr7:116833849-116833862
37	CEBPB	chr7:116853725-116853891	A549	lung:	n/a	chr7:116853790-116853799 chr7:116853790-116853801
38	CEBPB	chr7:116828981-116829383	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:116853641-116853941	HepG2	liver:	n/a	chr7:116853790-116853799 chr7:116853790-116853801
40	CEBPB	chr7:116832320-116832462	Hela-S3	cervix:	n/a	chr7:116832371-116832382
41	CEBPB	chr7:116832229-116832545	K562	blood:	n/a	chr7:116832371-116832382
42	CEBPB	chr7:116853673-116853898	K562	blood:	n/a	chr7:116853790-116853799 chr7:116853790-116853801
43	CEBPB	chr7:116842644-116842917	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:116831550-116831880	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:116833800-116833980	HepG2	liver:	n/a	chr7:116833849-116833862 chr7:116833849-116833860 chr7:116833849-116833862
46	CEBPB	chr7:116833681-116833881	H1-hESC	embryonic stem cell:	n/a	chr7:116833849-116833862 chr7:116833849-116833860 chr7:116833849-116833862
47	CEBPB	chr7:116828987-116829236	K562	blood:	n/a	n/a
48	CEBPB	chr7:116832259-116832545	A549	lung:	n/a	chr7:116832371-116832382
49	CHD2	chr7:116870287-116871411	GM12878	blood:	n/a	n/a
50	CTCF	chr7:116853180-116853330	GM12868	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:116859215-116859265	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:116856666-116856716	Hela-S3	cervix:	n/a
3	chr7:116842338-116842388	HUVEC	blood vessel:	n/a
4	chr7:116842338-116842388	SK-N-MC	brain:	n/a
5	chr7:116869944-116869994	Hela-S3	cervix:	n/a
6	chr7:116869944-116869994	SKMC	muscle:	n/a
7	chr7:116850153-116850203	AG04449	skin:	fetal
8	chr7:116863357-116863407	U87	brain:	n/a
9	chr7:116863357-116863407	AG04449	skin:	fetal
10	chr7:116869944-116869994	H1-hESC	embryonic stem cell:	embryo
11	chr7:116859215-116859265	HL-60	blood:	n/a
12	chr7:116863357-116863407	BJ	skin:	n/a
13	chr7:116850153-116850203	AG04450	lung:	fetal
14	chr7:116856666-116856716	T-47D	breast:	n/a
15	chr7:116869944-116869994	U87	brain:	n/a
16	chr7:116856666-116856716	AG10803	skin:	n/a
17	chr7:116850153-116850203	HMEC	breast:	n/a
18	chr7:116863357-116863407	IMR90	lung:	fetal
19	chr7:116869944-116869994	NHDF-neo	bronchial:	n/a
20	chr7:116850153-116850203	HCT-116	colon:	n/a
21	chr7:116856666-116856716	LNCaP	prostate:	n/a
22	chr7:116859215-116859265	SK-N-MC	brain:	n/a
23	chr7:116869944-116869994	SK-N-SH	brain:	n/a
24	chr7:116859215-116859265	U87	brain:	n/a
25	chr7:116863357-116863407	K562	blood:	n/a
26	chr7:116842338-116842388	HRPEpiC	eye:	n/a
27	chr7:116850153-116850203	T-47D	breast:	n/a
28	chr7:116856666-116856716	PFSK-1	brain:	n/a
29	chr7:116850153-116850203	PFSK-1	brain:	n/a
30	chr7:116859215-116859265	HCPEpiC	choroid plexus:	n/a
31	chr7:116863357-116863407	GM19239	blood:	n/a
32	chr7:116863357-116863407	PFSK-1	brain:	n/a
33	chr7:116842338-116842388	PFSK-1	brain:	n/a
34	chr7:116850153-116850203	SAEC	small airway:	n/a
35	chr7:116850153-116850203	HRE	kidney:	n/a
36	chr7:116842338-116842388	HMEC	breast:	n/a
37	chr7:116859215-116859265	HCT-116	colon:	n/a
38	chr7:116863357-116863407	SK-N-MC	brain:	n/a
39	chr7:116859215-116859265	ovcar-3	ovarian:	n/a
40	chr7:116850153-116850203	HRPEpiC	eye:	n/a
41	chr7:116850153-116850203	SK-N-SH_RA	brain:	n/a
42	chr7:116842338-116842388	AG04450	lung:	fetal
43	chr7:116856666-116856716	MCF-7	breast:	n/a
44	chr7:116850153-116850203	MCF-7	breast:	n/a
45	chr7:116856666-116856716	GM06990	blood:	n/a
46	chr7:116856666-116856716	SK-N-MC	brain:	n/a
47	chr7:116856666-116856716	GM12892	blood:	n/a
48	chr7:116856666-116856716	HEK293	kidney:	embryo
49	chr7:116842338-116842388	MCF-7	breast:	n/a
50	chr7:116842338-116842388	CMK	blood:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:116851355..116854029-chr7:116854766..116858147,3	K562	blood:
2	chr7:116764303..116765242-chr7:116842912..116843689,5	MCF-7	breast:
3	chr7:116592200..116593933-chr7:116824888..116827452,2	MCF-7	breast:
4	chr7:116851355..116854029-chr7:116854766..116858147,3	K562	blood:
5	chr7:116827597..116829249-chr7:116833009..116835845,2	K562	blood:
6	chr7:116853244..116855947-chr7:117024451..117026371,2	MCF-7	breast:
7	chr7:116847213..116849415-chr7:116853067..116855506,3	K562	blood:
8	chr7:116841164..116844098-chr7:116844507..116848579,3	MCF-7	breast:
9	chr7:116846173..116849651-chr7:116851764..116855447,4	K562	blood:
10	chr7:116784886..116786468-chr7:116836006..116837802,2	K562	blood:
11	chr7:116851892..116854644-chr7:116856765..116860823,3	MCF-7	breast:
12	7:116604327-116608063..7:116827014-116829381	GM12878	blood:
13	chr7:116841164..116844098-chr7:116844507..116848579,3	MCF-7	breast:
14	chr7:116843502..116846043-chr7:116854705..116857595,2	K562	blood:
15	chr7:116838446..116841411-chr7:116844852..116847542,2	K562	blood:
16	chr7:116823583..116828705-chr7:116829904..116832528,5	K562	blood:
17	chr7:116852752..116853731-chr7:117025763..117026736,2	MCF-7	breast:
18	chr7:116764303..116765242-chr7:116842912..116843704,8	MCF-7	breast:
19	chr7:116843502..116846948-chr7:116854705..116857880,3	K562	blood:
20	7:115847372-115857098..7:116834492-116839074	H1-hESC	embryonic stem cell:	embryo
21	chr7:116831692..116834398-chr7:116842431..116844419,2	MCF-7	breast:
22	chr7:116854051..116855661-chr7:116857296..116859779,2	K562	blood:
23	7:115861595-115870968..7:116829381-116834492	GM12878	blood:
24	chr7:116852733..116853994-chr7:117025641..117026568,8	MCF-7	breast:
25	chr7:116811007..116811834-chr7:116852794..116853748,2	MCF-7	breast:
26	chr7:116843502..116846043-chr7:116854705..116857595,2	K562	blood:
27	chr7:116852620..116855541-chr7:116858571..116861195,2	K562	blood:
28	7:116610596-116619447..7:116849860-116864942	H1-hESC	embryonic stem cell:	embryo
29	chr7:116847213..116849415-chr7:116853067..116855506,3	K562	blood:
30	chr7:116810934..116811888-chr7:116842719..116843797,5	MCF-7	breast:
31	chr7:116570148..116571132-chr7:116852812..116853758,4	K562	blood:
32	chr7:116868712..116871386-chr7:116885691..116888602,2	K562	blood:
33	chr7:116833755..116835279-chr7:116843331..116844941,2	K562	blood:
34	chr7:116810934..116811888-chr7:116842719..116843797,4	MCF-7	breast:
35	chr7:116856634..116860393-chr7:116862526..116866419,4	MCF-7	breast:
36	chr7:116821945..116824050-chr7:116827423..116829218,2	K562	blood:
37	chr7:116831692..116834398-chr7:116842431..116844419,2	MCF-7	breast:
38	chr7:116832809..116834371-chr7:116834554..116836125,2	MCF-7	breast:
39	chr7:116835045..116836833-chr7:116852463..116855168,2	K562	blood:
40	chr7:116846173..116849651-chr7:116851764..116855447,4	K562	blood:
41	chr7:116832809..116834371-chr7:116834554..116836125,2	MCF-7	breast:
42	chr7:116865370..116869396-chr7:116871341..116874775,5	K562	blood:
43	chr7:116820620..116824050-chr7:116827423..116829396,3	K562	blood:
44	chr7:116835045..116836833-chr7:116852463..116855168,2	K562	blood:
45	chr7:116838446..116841411-chr7:116844852..116847542,2	K562	blood:
46	chr7:116864347..116866979-chr7:116868628..116871312,2	K562	blood:
47	chr7:116864347..116866979-chr7:116868628..116871312,2	K562	blood:
48	chr7:116764325..116765196-chr7:116842810..116843683,3	MCF-7	breast:
49	chr7:116852820..116853712-chr7:117015574..117016124,3	MCF-7	breast:
50	chr7:116856986..116859380-chr7:116861436..116863428,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000227532	TF binding region
ST7	TF binding region
ENSG00000227532	CpG island
ST7	CpG island
ENSG00000004866	chromatin interactions
ENSG00000213050	chromatin interactions
ENSG00000226367	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000227532	chromatin interactions
ENSG00000228368	chromatin interactions

Extended variants
information (count: 1495 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546766794	chr7:116825224-116825225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559578343	chr7:116825261-116825262	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs184496859	chr7:116825266-116825267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533436940	chr7:116825291-116825292	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189164482	chr7:116825350-116825351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563517028	chr7:116825354-116825355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182568572	chr7:116825398-116825399	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559297048	chr7:116825400-116825401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186196870	chr7:116825422-116825423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548632315	chr7:116825442-116825443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201894095	chr7:116825498-116825499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576754783	chr7:116825519-116825520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567456624	chr7:116825521-116825522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534767475	chr7:116825571-116825572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189050097	chr7:116825573-116825574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571612736	chr7:116825577-116825578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111641989	chr7:116825598-116825599	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538917171	chr7:116825605-116825606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556954550	chr7:116825625-116825626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575099278	chr7:116825685-116825686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536370132	chr7:116825690-116825691	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111751603	chr7:116825701-116825702	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375078526	chr7:116825702-116825703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573906657	chr7:116825718-116825719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541267742	chr7:116825819-116825820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150311594	chr7:116825839-116825840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs38879	chr7:116825848-116825849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545342213	chr7:116825882-116825883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563722372	chr7:116825891-116825892	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530763944	chr7:116825892-116825893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181606801	chr7:116825909-116825910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs530251836	chr7:116825980-116825981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561263528	chr7:116826016-116826017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554345954	chr7:116826093-116826094	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185730015	chr7:116826115-116826116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191451073	chr7:116826149-116826150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571455179	chr7:116826230-116826231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532465752	chr7:116826235-116826236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550575757	chr7:116826253-116826254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1141227	chr7:116826263-116826264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143571699	chr7:116826340-116826341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182780869	chr7:116826352-116826353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554540404	chr7:116826414-116826415	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566278230	chr7:116826451-116826452	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531473276	chr7:116826476-116826477	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs73211939	chr7:116826489-116826490	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186264114	chr7:116826533-116826534	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190737626	chr7:116826636-116826637	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577786633	chr7:116826729-116826730	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545685581	chr7:116826736-116826737	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	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
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	21569311	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116776400-116830200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:116785200-116856600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:116787200-116830200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr7:116787400-116834000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:116793400-116830600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:116795600-116830200	Weak transcription	Fetal Intestine Small	intestine
7	chr7:116796800-116829400	Weak transcription	Fetal Brain Male	brain
8	chr7:116798000-116829800	Weak transcription	Gastric	stomach
9	chr7:116798000-116850000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:116798200-116866600	Weak transcription	HMEC	breast
11	chr7:116798400-116849800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:116798600-116830000	Weak transcription	Brain Angular Gyrus	brain
13	chr7:116800200-116830000	Weak transcription	Colon Smooth Muscle	Colon
14	chr7:116805200-116830000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:116805200-116850000	Weak transcription	Psoas Muscle	Psoas
16	chr7:116805400-116826200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:116807600-116857800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr7:116808400-116871800	Weak transcription	Rectal Smooth Muscle	rectum
19	chr7:116809800-116829600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr7:116810200-116829400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:116810200-116830200	Weak transcription	Spleen	Spleen
22	chr7:116810200-116832400	Weak transcription	A549	lung
23	chr7:116810200-116850000	Weak transcription	Brain Hippocampus Middle	brain
24	chr7:116810400-116826200	Weak transcription	NH-A	brain
25	chr7:116811400-116829600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:116811400-116830200	Weak transcription	Right Ventricle	heart
27	chr7:116811600-116829600	Weak transcription	Ovary	ovary
28	chr7:116811600-116838400	Weak transcription	Pancreas	Pancrea
29	chr7:116811800-116828200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr7:116811800-116830200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:116811800-116833200	Weak transcription	NHDF-Ad	bronchial
32	chr7:116812000-116829400	Weak transcription	Placenta	Placenta
33	chr7:116812200-116829400	Weak transcription	Brain Substantia Nigra	brain
34	chr7:116812200-116830000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:116812200-116850000	Weak transcription	Hela-S3	cervix
36	chr7:116812400-116830000	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr7:116812400-116830800	Weak transcription	HSMM	muscle
38	chr7:116812800-116829200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr7:116813000-116826200	Weak transcription	Osteobl	bone
40	chr7:116813400-116829200	Weak transcription	Fetal Heart	heart
41	chr7:116813400-116829800	Weak transcription	Lung	lung
42	chr7:116813600-116829400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:116813600-116829600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr7:116813800-116826400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:116813800-116829200	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr7:116813800-116829400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr7:116813800-116829400	Weak transcription	Aorta	Aorta
48	chr7:116813800-116829400	Weak transcription	HepG2	liver
49	chr7:116813800-116829800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr7:116813800-116830000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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