Variant report

Variant	nsv898809
Chromosome Location	chr12:12488067-12509314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:668)
CpG islands
(count:673)
Chromatin interactive
region (count:38)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:12489051-12489331	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:12501261-12501512	K562	blood:	n/a	n/a
3	ARID3A	chr12:12503398-12504581	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:12506748-12507137	K562	blood:	n/a	n/a
5	ATF1	chr12:12506808-12507158	K562	blood:	n/a	n/a
6	ATF1	chr12:12501331-12501592	K562	blood:	n/a	n/a
7	BACH1	chr12:12503062-12503140	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:12488948-12489314	GM12878	blood:	n/a	chr12:12489173-12489184
9	BATF	chr12:12509293-12509509	GM12878	blood:	n/a	n/a
10	BATF	chr12:12488984-12489341	GM12878	blood:	n/a	chr12:12489173-12489184
11	BHLHE40	chr12:12506759-12507279	K562	blood:	n/a	n/a
12	BHLHE40	chr12:12503086-12503570	HepG2	liver:	n/a	chr12:12503142-12503158
13	BHLHE40	chr12:12503123-12503489	GM12878	blood:	n/a	chr12:12503142-12503158
14	BHLHE40	chr12:12502837-12503637	K562	blood:	n/a	chr12:12503027-12503043 chr12:12503142-12503158
15	CBX3	chr12:12502999-12503438	K562	blood:	n/a	n/a
16	CBX3	chr12:12506807-12507195	K562	blood:	n/a	n/a
17	CBX3	chr12:12501319-12501585	K562	blood:	n/a	n/a
18	CCNT2	chr12:12506817-12507046	K562	blood:	n/a	n/a
19	CCNT2	chr12:12502919-12503510	K562	blood:	n/a	n/a
20	CEBPB	chr12:12503124-12503263	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:12503987-12504451	HepG2	liver:	n/a	chr12:12504280-12504292
22	CEBPB	chr12:12504019-12504367	HepG2	liver:	n/a	chr12:12504280-12504292
23	CEBPB	chr12:12489034-12489312	IMR90	lung:	n/a	chr12:12489167-12489178
24	CEBPB	chr12:12488989-12489363	HepG2	liver:	n/a	chr12:12489167-12489178
25	CEBPB	chr12:12489006-12489330	Hela-S3	cervix:	n/a	chr12:12489167-12489178
26	CEBPB	chr12:12503894-12504461	HepG2	liver:	n/a	chr12:12504280-12504292
27	CEBPB	chr12:12503857-12504515	HepG2	liver:	n/a	chr12:12504280-12504292
28	CEBPB	chr12:12488980-12489370	HepG2	liver:	n/a	chr12:12489167-12489178
29	CEBPB	chr12:12488995-12489280	K562	blood:	n/a	chr12:12489167-12489178
30	CEBPB	chr12:12489065-12489258	A549	lung:	n/a	chr12:12489167-12489178
31	CEBPB	chr12:12488985-12489351	HepG2	liver:	n/a	chr12:12489167-12489178
32	CEBPB	chr12:12489081-12489270	HepG2	liver:	n/a	chr12:12489167-12489178
33	CEBPB	chr12:12489015-12489358	K562	blood:	n/a	chr12:12489167-12489178
34	CEBPD	chr12:12489080-12489273	HepG2	liver:	n/a	n/a
35	CHD1	chr12:12503495-12503558	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr12:12502652-12502717	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr12:12503026-12503225	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr12:12503138-12503364	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr12:12502848-12503271	HepG2	liver:	n/a	n/a
40	CHD2	chr12:12503051-12503321	K562	blood:	n/a	n/a
41	CHD2	chr12:12503178-12503434	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr12:12502971-12503449	A549	lung:	n/a	n/a
43	CTCF	chr12:12503340-12503490	GM12875	blood:	n/a	n/a
44	CTCF	chr12:12502720-12502870	AG09309	skin:	n/a	n/a
45	CTCF	chr12:12503255-12503600	K562	blood:	n/a	chr12:12503316-12503329
46	CTCF	chr12:12503320-12503470	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr12:12503362-12503483	MCF-7	breast:	n/a	n/a
48	CTCF	chr12:12502740-12502890	NHEK	skin:	n/a	n/a
49	CTCF	chr12:12503120-12503270	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr12:12502767-12502844	LNCaP	prostate:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12503224-12503274	K562	blood:	n/a
2	chr12:12503455-12503505	BJ	skin:	n/a
3	chr12:12503224-12503274	K562	blood:	n/a
4	chr12:12503455-12503505	BJ	skin:	n/a
5	chr12:12502846-12502896	Hela-S3	cervix:	n/a
6	chr12:12503307-12503357	RPTEC	kidney:	n/a
7	chr12:12507213-12507263	A549	lung:	n/a
8	chr12:12503224-12503274	HCM	heart:	n/a
9	chr12:12503030-12503080	LNCaP	prostate:	n/a
10	chr12:12503224-12503274	ovcar-3	ovarian:	n/a
11	chr12:12503307-12503357	Hela-S3	cervix:	n/a
12	chr12:12503189-12503239	Hela-S3	cervix:	n/a
13	chr12:12502846-12502896	HUVEC	blood vessel:	n/a
14	chr12:12503194-12503244	PrEC	prostate:	n/a
15	chr12:12507213-12507263	AoSMC	blood vessel:	n/a
16	chr12:12503457-12503507	HRCEpiC	kidney:	n/a
17	chr12:12503544-12503594	BE2_C	brain:	n/a
18	chr12:12503307-12503357	HRPEpiC	eye:	n/a
19	chr12:12503457-12503507	MCF10A-Er-Src	breast:	n/a
20	chr12:12503194-12503244	HPAEpiC	pulmonary alveolar:	n/a
21	chr12:12507213-12507263	SK-N-SH	brain:	n/a
22	chr12:12503189-12503239	HCT-116	colon:	n/a
23	chr12:12503186-12503236	HCPEpiC	choroid plexus:	n/a
24	chr12:12503224-12503274	GM19239	blood:	n/a
25	chr12:12503030-12503080	BE2_C	brain:	n/a
26	chr12:12503457-12503507	HRE	kidney:	n/a
27	chr12:12503189-12503239	ProgFib	skin:	n/a
28	chr12:12503544-12503594	PrEC	prostate:	n/a
29	chr12:12503455-12503505	SK-N-MC	brain:	n/a
30	chr12:12503186-12503236	A549	lung:	n/a
31	chr12:12507213-12507263	ECC-1	luminal epithelium:	n/a
32	chr12:12502846-12502896	CMK	blood:	n/a
33	chr12:12503544-12503594	SK-N-SH_RA	brain:	n/a
34	chr12:12503186-12503236	SK-N-SH_RA	brain:	n/a
35	chr12:12503457-12503507	H1-hESC	embryonic stem cell:	embryo
36	chr12:12503189-12503239	Caco-2	colon:	n/a
37	chr12:12507213-12507263	HEK293	kidney:	embryo
38	chr12:12507213-12507263	HL-60	blood:	n/a
39	chr12:12503455-12503505	HRCEpiC	kidney:	n/a
40	chr12:12502846-12502896	HepG2	liver:	n/a
41	chr12:12503455-12503505	NHDF-neo	bronchial:	n/a
42	chr12:12507213-12507263	HNPCEpiC	eye:	n/a
43	chr12:12503457-12503507	MCF-7	breast:	n/a
44	chr12:12503457-12503507	SK-N-SH_RA	brain:	n/a
45	chr12:12503224-12503274	PANC-1	pancreas:	n/a
46	chr12:12503030-12503080	NT2-D1	testis:	n/a
47	chr12:12503457-12503507	NT2-D1	testis:	n/a
48	chr12:12503224-12503274	GM12892	blood:	n/a
49	chr12:12503455-12503505	LNCaP	prostate:	n/a
50	chr12:12503189-12503239	HRE	kidney:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:12502870..12505613-chr12:12507814..12511200,4	K562	blood:
2	chr12:12507773..12511633-chr12:12848137..12852132,5	K562	blood:
3	chr12:12505451..12508886-chr12:12510975..12514166,3	K562	blood:
4	chr12:12493698..12498336-chr12:12499976..12504386,5	MCF-7	breast:
5	chr12:12501597..12504303-chr12:12848029..12850251,2	K562	blood:
6	chr12:12489787..12492519-chr12:12503031..12504558,2	MCF-7	breast:
7	chr12:12508678..12514314-chr12:12868637..12874427,7	K562	blood:
8	chr12:12492591..12498034-chr12:12508387..12511659,4	K562	blood:
9	chr12:12419645..12421343-chr12:12493271..12495911,2	MCF-7	breast:
10	chr12:12493055..12495438-chr12:12763586..12765777,2	MCF-7	breast:
11	chr12:12491237..12492051-chr12:12502345..12503099,2	MCF-7	breast:
12	chr12:12494246..12497461-chr12:12509029..12511759,3	MCF-7	breast:
13	chr12:12508799..12512106-chr12:12876417..12880418,4	MCF-7	breast:
14	chr12:12500672..12504766-chr12:12505204..12507584,5	K562	blood:
15	chr12:12501083..12504981-chr12:12508403..12511914,10	MCF-7	breast:
16	chr12:12509167..12512867-chr12:12713185..12715471,5	MCF-7	breast:
17	chr12:12502870..12504833-chr12:12508269..12511200,3	K562	blood:
18	chr12:12507988..12510235-chr12:12714031..12716523,2	MCF-7	breast:
19	chr12:12508122..12513324-chr12:12871018..12878415,8	MCF-7	breast:
20	chr12:12501083..12504981-chr12:12508403..12511914,10	MCF-7	breast:
21	chr12:12502870..12505613-chr12:12507814..12511200,4	K562	blood:
22	chr12:12492591..12496628-chr12:12508387..12511489,3	K562	blood:
23	chr12:12489787..12492519-chr12:12503031..12504558,2	MCF-7	breast:
24	chr12:12507394..12509953-chr12:12633944..12635631,2	MCF-7	breast:
25	chr12:12501756..12503820-chr12:12509545..12511706,2	MCF-7	breast:
26	chr12:12502870..12504833-chr12:12508269..12511200,3	K562	blood:
27	chr12:12419774..12421330-chr12:12508637..12511348,2	MCF-7	breast:
28	chr12:12509229..12511438-chr12:12866532..12868285,2	MCF-7	breast:
29	chr12:12493042..12496407-chr12:12508406..12511511,3	MCF-7	breast:
30	chr12:12505582..12507087-chr12:12510779..12513309,2	MCF-7	breast:
31	chr12:12496602..12498278-chr12:12498388..12501729,3	K562	blood:
32	chr12:12487375..12490317-chr12:12509840..12512376,2	MCF-7	breast:
33	chr12:12502650..12504579-chr12:12713839..12715957,2	MCF-7	breast:
34	chr12:12419232..12421863-chr12:12485161..12488276,6	MCF-7	breast:
35	chr12:12222045..12224389-chr12:12502260..12504688,2	K562	blood:
36	chr12:12497428..12499912-chr12:12500992..12503884,2	MCF-7	breast:
37	chr12:12502767..12504788-chr12:12506780..12508303,2	MCF-7	breast:
38	chr12:12496602..12498278-chr12:12498388..12501729,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007621.1-1	chr12:12508342-12509739	NR_024061
2	lnc-LOH12CR1-5	chr12:12491710-12492188	NONHSAT026968
3	lnc-AC007621.1-1	chr12:12508344-12509739	XLOC_010020

No data

Variant related genes	Relation type
MANSC1	TF binding region
LOH12CR1	TF binding region
ENSG00000243141	TF binding region
MANSC1	CpG island
LOH12CR1	CpG island
ENSG00000243141	CpG island
ENSG00000205791	chromatin interactions
ENSG00000178878	chromatin interactions
ENSG00000121380	chromatin interactions
ENSG00000111276	chromatin interactions
ENSG00000070018	chromatin interactions
ENSG00000111269	chromatin interactions
ENSG00000111266	chromatin interactions
ENSG00000256658	chromatin interactions
ENSG00000183150	chromatin interactions
ENSG00000111261	chromatin interactions
ENSG00000165714	chromatin interactions
ENSG00000243141	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7976154	chr12:12488067-12488068	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144439352	chr12:12488110-12488111	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs558251231	chr12:12488142-12488143	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs191170183	chr12:12488145-12488146	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs576799568	chr12:12488146-12488147	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs543880695	chr12:12488196-12488197	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs558197633	chr12:12488225-12488226	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs183380511	chr12:12488236-12488237	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs541620890	chr12:12488249-12488250	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs188312004	chr12:12488251-12488252	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs375086349	chr12:12488253-12488254	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552664987	chr12:12488270-12488271	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs145683206	chr12:12488273-12488274	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs537895458	chr12:12488274-12488275	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs370899713	chr12:12488277-12488278	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs60014261	chr12:12488283-12488284	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs11054818	chr12:12488292-12488293	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs550210203	chr12:12488313-12488314	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs112608511	chr12:12488314-12488315	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs562087530	chr12:12488316-12488317	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs112399022	chr12:12488323-12488324	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs554399531	chr12:12488331-12488332	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs11054819	chr12:12488350-12488351	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs192154841	chr12:12488415-12488416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575072122	chr12:12488422-12488423	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs61922040	chr12:12488459-12488460	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs183138843	chr12:12488470-12488471	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576873700	chr12:12488483-12488484	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs187762067	chr12:12488495-12488496	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs555785264	chr12:12488520-12488521	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs574380194	chr12:12488599-12488600	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs541754889	chr12:12488625-12488626	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs559892221	chr12:12488655-12488656	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149039190	chr12:12488664-12488665	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs4237939	chr12:12488669-12488670	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373149420	chr12:12488719-12488720	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs202106732	chr12:12488776-12488777	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs202098709	chr12:12488787-12488788	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531717817	chr12:12488788-12488789	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs199625200	chr12:12488789-12488790	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs61922041	chr12:12488822-12488823	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs529597358	chr12:12488838-12488839	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548137604	chr12:12488839-12488840	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566265307	chr12:12488845-12488846	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539982750	chr12:12488883-12488884	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551684908	chr12:12488892-12488893	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs117004767	chr12:12488901-12488902	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs191115395	chr12:12488909-12488910	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376220188	chr12:12488942-12488943	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs61922042	chr12:12488946-12488947	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12473200-12501600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:12473600-12493200	Weak transcription	Fetal Brain Female	brain
3	chr12:12473600-12502000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:12473800-12491800	Weak transcription	Left Ventricle	heart
5	chr12:12473800-12502400	Weak transcription	NHLF	lung
6	chr12:12474000-12489200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr12:12477200-12491800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:12480400-12490800	Weak transcription	Right Atrium	heart
9	chr12:12480400-12502400	Weak transcription	Right Ventricle	heart
10	chr12:12481200-12491000	Weak transcription	Hela-S3	cervix
11	chr12:12481200-12495400	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:12481200-12502200	Weak transcription	Fetal Heart	heart
13	chr12:12481800-12502400	Weak transcription	Psoas Muscle	Psoas
14	chr12:12482400-12502200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:12483600-12488400	Enhancers	Stomach Mucosa	stomach
16	chr12:12483600-12502800	Weak transcription	Spleen	Spleen
17	chr12:12484200-12488200	Enhancers	Fetal Intestine Large	intestine
18	chr12:12484200-12488200	Enhancers	Fetal Lung	lung
19	chr12:12484600-12488200	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr12:12484800-12491800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:12485200-12489200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr12:12485400-12489000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr12:12485400-12489200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr12:12485400-12489200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr12:12485400-12500200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:12485400-12502400	Weak transcription	Esophagus	oesophagus
27	chr12:12485400-12502800	Weak transcription	Gastric	stomach
28	chr12:12485400-12502800	Weak transcription	Small Intestine	intestine
29	chr12:12486200-12488200	Genic enhancers	HUVEC	blood vessel
30	chr12:12486400-12488200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:12486400-12488200	Enhancers	Lung	lung
32	chr12:12486400-12488200	Enhancers	HMEC	breast
33	chr12:12486400-12488200	Enhancers	Osteobl	bone
34	chr12:12486400-12488600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr12:12486400-12489800	Enhancers	Pancreas	Pancrea
36	chr12:12486600-12489800	Enhancers	HepG2	liver
37	chr12:12486800-12488200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr12:12486800-12491400	Weak transcription	Primary T cells from cord blood	blood
39	chr12:12486800-12491800	Weak transcription	Brain Angular Gyrus	brain
40	chr12:12487000-12488200	Enhancers	GM12878-XiMat	blood
41	chr12:12487000-12489200	Weak transcription	HSMMtube	muscle
42	chr12:12487000-12489800	Enhancers	Liver	Liver
43	chr12:12487000-12491000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr12:12487200-12491400	Weak transcription	Aorta	Aorta
45	chr12:12487200-12491800	Weak transcription	Ovary	ovary
46	chr12:12487200-12502600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr12:12487400-12488200	Enhancers	Primary B cells from cord blood	blood
48	chr12:12487400-12491000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:12487400-12502200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr12:12487400-12502200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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