Variant report

Variant	nsv899159
Chromosome Location	chr12:62783967-62945245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1740)
CpG islands
(count:1161)
Chromatin interactive
region (count:141)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:1740 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:62859923-62860652	K562	blood:	n/a	n/a
2	ARID3A	chr12:62807642-62807755	K562	blood:	n/a	n/a
3	ARID3A	chr12:62862638-62862682	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:62860011-62860685	HepG2	liver:	n/a	n/a
5	ATF1	chr12:62819909-62820109	K562	blood:	n/a	n/a
6	ATF1	chr12:62787812-62787902	K562	blood:	n/a	n/a
7	ATF1	chr12:62860385-62860754	K562	blood:	n/a	chr12:62860569-62860583
8	ATF2	chr12:62860389-62860824	GM12878	blood:	n/a	chr12:62860569-62860583
9	ATF2	chr12:62860314-62861131	GM12878	blood:	n/a	chr12:62861109-62861120 chr12:62860569-62860583
10	ATF3	chr12:62819892-62820179	K562	blood:	n/a	n/a
11	ATF3	chr12:62860426-62860772	K562	blood:	n/a	chr12:62860572-62860592 chr12:62860499-62860508
12	BACH1	chr12:62792830-62792831	K562	blood:	n/a	n/a
13	BACH1	chr12:62860110-62860709	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr12:62877993-62878340	GM12878	blood:	n/a	n/a
15	BATF	chr12:62860405-62860768	GM12878	blood:	n/a	n/a
16	BATF	chr12:62877988-62878259	GM12878	blood:	n/a	n/a
17	BCL3	chr12:62807639-62808318	K562	blood:	n/a	n/a
18	BCL3	chr12:62809633-62810295	K562	blood:	n/a	n/a
19	BCL3	chr12:62811352-62811976	K562	blood:	n/a	n/a
20	BCL3	chr12:62860088-62861198	A549	lung:	n/a	chr12:62860700-62860713 chr12:62860514-62860527 chr12:62860559-62860568 chr12:62860707-62860716 chr12:62860532-62860541
21	BCLAF1	chr12:62860290-62860918	GM12878	blood:	n/a	chr12:62860700-62860713 chr12:62860514-62860527 chr12:62860559-62860568 chr12:62860707-62860716 chr12:62860532-62860541
22	BHLHE40	chr12:62829561-62829779	K562	blood:	n/a	n/a
23	BHLHE40	chr12:62860200-62861028	K562	blood:	n/a	chr12:62860697-62860713
24	BHLHE40	chr12:62878236-62878284	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:62860334-62860768	GM12878	blood:	n/a	chr12:62860697-62860713
26	BRCA1	chr12:62860666-62860929	GM12878	blood:	n/a	n/a
27	BRCA1	chr12:62936941-62936943	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr12:62859904-62860742	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr12:62860291-62860446	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:62829383-62829523	GM12878	blood:	n/a	n/a
31	CBX3	chr12:62907942-62908234	K562	blood:	n/a	n/a
32	CBX3	chr12:62838507-62838755	K562	blood:	n/a	n/a
33	CBX3	chr12:62838444-62838742	K562	blood:	n/a	n/a
34	CBX3	chr12:62860187-62860785	K562	blood:	n/a	n/a
35	CBX3	chr12:62857065-62857409	K562	blood:	n/a	n/a
36	CBX3	chr12:62857041-62857386	K562	blood:	n/a	n/a
37	CBX3	chr12:62907886-62908248	K562	blood:	n/a	n/a
38	CCNT2	chr12:62804111-62804311	K562	blood:	n/a	n/a
39	CCNT2	chr12:62804946-62805509	K562	blood:	n/a	n/a
40	CCNT2	chr12:62860309-62860880	K562	blood:	n/a	chr12:62860431-62860440 chr12:62860493-62860502
41	CEBPB	chr12:62859242-62859645	K562	blood:	n/a	chr12:62859390-62859401 chr12:62859391-62859402 chr12:62859327-62859338
42	CEBPB	chr12:62935055-62935244	A549	lung:	n/a	n/a
43	CEBPB	chr12:62860563-62860791	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:62859254-62859585	IMR90	lung:	n/a	chr12:62859390-62859401 chr12:62859391-62859402 chr12:62859327-62859338
45	CEBPB	chr12:62804676-62804876	K562	blood:	n/a	n/a
46	CEBPB	chr12:62890163-62890324	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:62859269-62859588	A549	lung:	n/a	chr12:62859390-62859401 chr12:62859391-62859402 chr12:62859327-62859338
48	CEBPB	chr12:62859243-62859737	Hela-S3	cervix:	n/a	chr12:62859390-62859401 chr12:62859391-62859402 chr12:62859327-62859338
49	CEBPB	chr12:62802886-62803160	HepG2	liver:	n/a	chr12:62803005-62803016 chr12:62803004-62803017
50	CEBPB	chr12:62863756-62864081	K562	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:62862960-62863010	GM06990	blood:	n/a
2	chr12:62862960-62863010	U87	brain:	n/a
3	chr12:62862960-62863010	GM06990	blood:	n/a
4	chr12:62862960-62863010	U87	brain:	n/a
5	chr12:62829123-62829173	U87	brain:	n/a
6	chr12:62857919-62857969	GM19239	blood:	n/a
7	chr12:62860029-62860079	NHBE	bronchial:	n/a
8	chr12:62857919-62857969	NB4	blood:	n/a
9	chr12:62860351-62860401	GM12891	blood:	n/a
10	chr12:62829582-62829632	HEEpiC	esophagus:	n/a
11	chr12:62857919-62857969	A549	lung:	n/a
12	chr12:62860029-62860079	BJ	skin:	n/a
13	chr12:62857919-62857969	GM12878	blood:	n/a
14	chr12:62861114-62861164	Jurkat	blood:	n/a
15	chr12:62855292-62855342	SK-N-SH	brain:	n/a
16	chr12:62860780-62860830	AG09319	gingival:	n/a
17	chr12:62861053-62861103	GM19239	blood:	n/a
18	chr12:62857919-62857969	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:62862960-62863010	Jurkat	blood:	n/a
20	chr12:62860780-62860830	AG10803	skin:	n/a
21	chr12:62860451-62860501	HEK293	kidney:	embryo
22	chr12:62798679-62798729	HEK293	kidney:	embryo
23	chr12:62860172-62860222	HRPEpiC	eye:	n/a
24	chr12:62855292-62855342	IMR90	lung:	fetal
25	chr12:62860430-62860480	HMEC	breast:	n/a
26	chr12:62861053-62861103	PFSK-1	brain:	n/a
27	chr12:62860687-62860737	Hepatocyte	liver:	n/a
28	chr12:62861053-62861103	HCF	heart:	n/a
29	chr12:62860430-62860480	HCT-116	colon:	n/a
30	chr12:62861053-62861103	U87	brain:	n/a
31	chr12:62798679-62798729	MCF-7	breast:	n/a
32	chr12:62860399-62860449	HepG2	liver:	n/a
33	chr12:62860029-62860079	HEK293	kidney:	embryo
34	chr12:62829123-62829173	HEEpiC	esophagus:	n/a
35	chr12:62857919-62857969	HCM	heart:	n/a
36	chr12:62857919-62857969	SKMC	muscle:	n/a
37	chr12:62855292-62855342	HEK293	kidney:	embryo
38	chr12:62861114-62861164	RPTEC	kidney:	n/a
39	chr12:62860780-62860830	GM12891	blood:	n/a
40	chr12:62860451-62860501	U87	brain:	n/a
41	chr12:62860451-62860501	RPTEC	kidney:	n/a
42	chr12:62918364-62918414	HAEpiC	amniotic membrane:	n/a
43	chr12:62860462-62860512	NB4	blood:	n/a
44	chr12:62861114-62861164	NT2-D1	testis:	n/a
45	chr12:62860687-62860737	GM12891	blood:	n/a
46	chr12:62860451-62860501	HNPCEpiC	eye:	n/a
47	chr12:62860780-62860830	MCF10A-Er-Src	breast:	n/a
48	chr12:62860780-62860830	HAEpiC	amniotic membrane:	n/a
49	chr12:62860351-62860401	HRE	kidney:	n/a
50	chr12:62860470-62860520	GM12878	blood:	n/a

(count:141 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:62892704..62894662-chr12:62995139..62997140,2	K562	blood:
2	chr12:62859513..62862110-chr12:62869380..62871676,3	K562	blood:
3	chr12:62880525..62882340-chr12:62885368..62887187,2	MCF-7	breast:
4	chr12:62915089..62916755-chr12:62920315..62922629,2	MCF-7	breast:
5	chr12:62858973..62862705-chr12:62864289..62872208,17	MCF-7	breast:
6	chr12:62802223..62804398-chr12:62996125..62998801,2	K562	blood:
7	chr12:62653651..62654206-chr12:62829373..62830105,3	MCF-7	breast:
8	chr12:62868642..62871581-chr12:62880565..62882888,3	K562	blood:
9	chr12:62828524..62830092-chr12:62859054..62860968,2	MCF-7	breast:
10	chr12:62872291..62875006-chr12:62876565..62879431,3	K562	blood:
11	chr12:62914778..62916591-chr12:62918347..62920592,2	K562	blood:
12	chr12:62809064..62811353-chr12:62812515..62814478,2	K562	blood:
13	chr12:62859326..62863326-chr12:62876630..62881311,5	K562	blood:
14	chr12:62936384..62938344-chr12:62940152..62942077,2	MCF-7	breast:
15	chr12:62931071..62933138-chr12:62938483..62940782,2	MCF-7	breast:
16	chr12:62828778..62831303-chr12:62995867..62998066,3	MCF-7	breast:
17	chr12:62866735..62869361-chr12:62869978..62871567,2	K562	blood:
18	chr12:62831822..62832575-chr12:63207029..63207544,2	MCF-7	breast:
19	chr12:62828192..62830358-chr12:62897908..62900786,2	MCF-7	breast:
20	chr12:62863411..62864986-chr12:62871030..62872716,2	MCF-7	breast:
21	chr12:62940703..62942604-chr12:62944482..62947077,2	MCF-7	breast:
22	chr12:62887479..62889929-chr12:62903301..62905417,2	MCF-7	breast:
23	chr12:62859503..62861171-chr12:62910614..62912246,2	MCF-7	breast:
24	chr12:62828192..62830358-chr12:62897908..62900786,2	MCF-7	breast:
25	chr12:62828172..62830488-chr12:62995280..62997278,2	MCF-7	breast:
26	chr12:62870116..62872263-chr12:62874889..62877782,3	K562	blood:
27	chr12:62936384..62938344-chr12:62940152..62942077,2	MCF-7	breast:
28	chr12:62793306..62795703-chr12:62795951..62798733,2	MCF-7	breast:
29	chr12:62874210..62877124-chr12:62898589..62900755,2	K562	blood:
30	chr12:62920513..62925358-chr12:62927927..62931461,4	K562	blood:
31	chr12:62859286..62861275-chr12:62995759..62997449,2	MCF-7	breast:
32	chr12:62821295..62823425-chr12:62823538..62826041,2	MCF-7	breast:
33	chr12:62790233..62792343-chr12:62793733..62795768,2	MCF-7	breast:
34	chr12:62821295..62823425-chr12:62823538..62826041,2	MCF-7	breast:
35	chr12:62800166..62802965-chr12:62803094..62805711,2	K562	blood:
36	chr12:62887087..62888673-chr12:62894503..62897008,2	K562	blood:
37	chr12:62802154..62805925-chr12:62805959..62810469,4	K562	blood:
38	chr12:62848675..62850421-chr12:62858765..62861480,2	MCF-7	breast:
39	chr12:62829632..62831889-chr12:62864077..62865718,2	MCF-7	breast:
40	chr12:62887087..62888673-chr12:62894503..62897008,2	K562	blood:
41	chr12:62897832..62899888-chr12:62900613..62903392,2	K562	blood:
42	chr12:62874817..62876919-chr12:62877529..62879256,2	MCF-7	breast:
43	chr12:62863210..62865017-chr12:62887916..62890399,2	K562	blood:
44	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
45	chr12:62915089..62916755-chr12:62920315..62922629,2	MCF-7	breast:
46	chr12:62901029..62903305-chr12:62910983..62913530,2	MCF-7	breast:
47	chr12:62860603..62862408-chr12:62877064..62881508,4	MCF-7	breast:
48	chr12:62800166..62802965-chr12:62803094..62805711,2	K562	blood:
49	chr12:62831609..62832559-chr12:63187320..63188381,5	K562	blood:
50	chr12:62874210..62877124-chr12:62898589..62900755,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf61-1	chr12:62878549-62878722	ENSG00000246324
2	lnc-C12orf61-1	chr12:62878549-62878712	ENSG00000257568.1
3	lnc-C12orf61-1	chr12:62876129-62876812	ENSG00000257568.1
4	lnc-C12orf61-1	chr12:62876131-62876812	ENSG00000246324

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	USP15	hsa-miR-103a-3p	chr12:62798406-62798428
2	USP15	hsa-miR-16-5p	chr12:62798406-62798429
3	USP15	hsa-miR-103a-3p	chr12:62799349-62799371
4	USP15	hsa-miR-16-5p	chr12:62799351-62799372
5	USP15	hsa-miR-16-5p	chr12:62799365-62799371
6	USP15	hsa-miR-16-5p	chr12:62798422-62798428
7	USP15	hsa-let-7b-5p	chr12:62799457-62799477

Variant related genes	Relation type
USP15	TF binding region
RNU6-399P	TF binding region
MON2	TF binding region
ENSG00000257568	TF binding region
USP15	CpG island
RNU6-399P	CpG island
MON2	CpG island
ENSG00000257568	CpG island
ENSG00000257354	chromatin interactions
ENSG00000203865	chromatin interactions
ENSG00000198673	chromatin interactions
ENSG00000202034	chromatin interactions
ENSG00000221949	chromatin interactions
ENSG00000061987	chromatin interactions
ENSG00000199179	chromatin interactions
ENSG00000257568	chromatin interactions
ENSG00000135655	chromatin interactions
SPRYD4	miRNA target sites
WDR25	miRNA target sites

Extended variants
information (count: 4771 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4771 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11174456	chr12:62783967-62783968	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576078492	chr12:62783984-62783985	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147599911	chr12:62784017-62784018	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs367927457	chr12:62784062-62784063	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558624952	chr12:62784063-62784064	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571681640	chr12:62784071-62784072	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568960846	chr12:62784073-62784074	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190268162	chr12:62784081-62784082	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117609626	chr12:62784097-62784098	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs11613353	chr12:62784104-62784105	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs543597619	chr12:62784143-62784144	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577699249	chr12:62784171-62784172	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533801751	chr12:62784229-62784230	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs180707693	chr12:62784270-62784271	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532740610	chr12:62784290-62784291	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11613389	chr12:62784297-62784298	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs74095744	chr12:62784306-62784307	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185285043	chr12:62784318-62784319	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528477389	chr12:62784350-62784351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147829169	chr12:62784360-62784361	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567563530	chr12:62784373-62784374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536591143	chr12:62784411-62784412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550058438	chr12:62784524-62784525	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79045331	chr12:62784537-62784538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538851248	chr12:62784546-62784547	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190038030	chr12:62784553-62784554	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573741791	chr12:62784576-62784577	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559472698	chr12:62784591-62784592	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368226918	chr12:62784600-62784601	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372332594	chr12:62784609-62784610	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs367892742	chr12:62784612-62784613	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs183789286	chr12:62784631-62784632	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs75305174	chr12:62784650-62784651	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369203333	chr12:62784671-62784672	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554181894	chr12:62784693-62784694	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145954904	chr12:62784696-62784697	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs202037541	chr12:62784700-62784701	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs139869747	chr12:62784705-62784706	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143311626	chr12:62784710-62784711	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs146724831	chr12:62784758-62784759	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373274905	chr12:62784777-62784778	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200234818	chr12:62784781-62784782	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148893401	chr12:62784789-62784790	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373126215	chr12:62784800-62784801	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577331316	chr12:62785027-62785028	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139161856	chr12:62785037-62785038	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559569739	chr12:62785081-62785082	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376173861	chr12:62785090-62785091	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs149953550	chr12:62785104-62785105	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189194846	chr12:62785118-62785119	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Man infertility	21397064	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3449 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62717000-62784600	Weak transcription	Colon Smooth Muscle	Colon
2	chr12:62737600-62784600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr12:62737600-62786600	Weak transcription	NHLF	lung
4	chr12:62738200-62787400	Weak transcription	Spleen	Spleen
5	chr12:62738200-62790600	Weak transcription	Esophagus	oesophagus
6	chr12:62738800-62784000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr12:62738800-62789600	Weak transcription	Ovary	ovary
8	chr12:62738800-62792800	Weak transcription	Lung	lung
9	chr12:62742000-62786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:62758200-62787400	Weak transcription	Fetal Muscle Leg	muscle
11	chr12:62762400-62796600	Weak transcription	Fetal Brain Male	brain
12	chr12:62763000-62805400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr12:62763800-62787600	Weak transcription	Brain Anterior Caudate	brain
14	chr12:62764200-62792000	Weak transcription	HepG2	liver
15	chr12:62764400-62786800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr12:62765800-62795000	Weak transcription	Small Intestine	intestine
17	chr12:62766200-62789200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr12:62767400-62807600	Weak transcription	HSMMtube	muscle
19	chr12:62768400-62787600	Weak transcription	Brain Hippocampus Middle	brain
20	chr12:62769200-62805000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:62769400-62797400	Weak transcription	Right Ventricle	heart
22	chr12:62769400-62809600	Weak transcription	Stomach Mucosa	stomach
23	chr12:62769600-62786600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:62769600-62787400	Weak transcription	Fetal Kidney	kidney
25	chr12:62772600-62800800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:62773000-62792800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr12:62773200-62799400	Weak transcription	Brain Substantia Nigra	brain
28	chr12:62773400-62787400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr12:62773600-62802400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr12:62773800-62786400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:62774200-62786800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr12:62774200-62800000	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr12:62774200-62802200	Strong transcription	Dnd41	blood
34	chr12:62774400-62799400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr12:62774400-62802200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:62774600-62802000	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr12:62774800-62791000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr12:62774800-62801600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr12:62774800-62802200	Strong transcription	Fetal Thymus	thymus
40	chr12:62774800-62803200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr12:62775200-62802000	Strong transcription	Primary B cells from cord blood	blood
42	chr12:62775200-62802600	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:62775600-62807800	Weak transcription	Aorta	Aorta
44	chr12:62776200-62795200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr12:62776800-62787800	Strong transcription	K562	blood
46	chr12:62777000-62799400	Strong transcription	Liver	Liver
47	chr12:62777000-62801200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:62777200-62799600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr12:62777600-62792000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:62778600-62789400	Weak transcription	Brain Germinal Matrix	brain

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