Variant report

Variant	nsv560438
Chromosome Location	chr12:121194565-121352206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2102)
CpG islands
(count:1527)
Chromatin interactive
region (count:141)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2102 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121294858-121295111	K562	blood:	n/a	n/a
2	ARID3A	chr12:121329802-121330243	K562	blood:	n/a	n/a
3	ARID3A	chr12:121285846-121285856	K562	blood:	n/a	n/a
4	ARID3A	chr12:121237337-121237617	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121332426-121332568	K562	blood:	n/a	n/a
6	ARID3A	chr12:121291748-121291907	K562	blood:	n/a	n/a
7	ARID3A	chr12:121268487-121268712	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:121342186-121342413	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:121263154-121263508	HepG2	liver:	n/a	n/a
10	ATF1	chr12:121330028-121330347	K562	blood:	n/a	n/a
11	ATF1	chr12:121302972-121303252	K562	blood:	n/a	n/a
12	ATF1	chr12:121273261-121273357	K562	blood:	n/a	n/a
13	ATF1	chr12:121291748-121291952	K562	blood:	n/a	n/a
14	ATF1	chr12:121332249-121332569	K562	blood:	n/a	n/a
15	ATF1	chr12:121285766-121285966	K562	blood:	n/a	n/a
16	ATF2	chr12:121285516-121286028	GM12878	blood:	n/a	n/a
17	ATF2	chr12:121291504-121291983	GM12878	blood:	n/a	n/a
18	ATF2	chr12:121347442-121347981	GM12878	blood:	n/a	n/a
19	ATF2	chr12:121291561-121292023	GM12878	blood:	n/a	n/a
20	ATF2	chr12:121259457-121260078	GM12878	blood:	n/a	n/a
21	ATF3	chr12:121342059-121342424	K562	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
22	ATF3	chr12:121316865-121317332	HCT-116	colon:	n/a	n/a
23	ATF3	chr12:121342008-121342405	K562	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
24	ATF3	chr12:121342014-121342413	HepG2	liver:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
25	ATF3	chr12:121342060-121342496	HepG2	liver:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
26	ATF3	chr12:121342074-121342431	H1-hESC	embryonic stem cell:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
27	ATF3	chr12:121341947-121342470	H1-hESC	embryonic stem cell:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
28	ATF3	chr12:121342086-121342301	GM12878	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
29	ATF3	chr12:121342042-121342530	GM12878	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
30	ATF3	chr12:121342012-121342661	A549	lung:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
31	BACH1	chr12:121341177-121341437	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr12:121342594-121342773	K562	blood:	n/a	n/a
33	BATF	chr12:121259644-121260059	GM12878	blood:	n/a	chr12:121259812-121259823
34	BATF	chr12:121238482-121238807	GM12878	blood:	n/a	n/a
35	BATF	chr12:121347483-121347901	GM12878	blood:	n/a	n/a
36	BATF	chr12:121259674-121260036	GM12878	blood:	n/a	chr12:121259812-121259823
37	BATF	chr12:121347506-121347788	GM12878	blood:	n/a	n/a
38	BATF	chr12:121289273-121289619	GM12878	blood:	n/a	n/a
39	BATF	chr12:121260849-121260987	GM12878	blood:	n/a	n/a
40	BCL11A	chr12:121259716-121260016	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:121260642-121260877	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCLAF1	chr12:121285453-121286104	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:121259732-121260060	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:121235590-121236252	GM12878	blood:	n/a	chr12:121235908-121235916
45	BCLAF1	chr12:121291525-121292028	GM12878	blood:	n/a	n/a
46	BCLAF1	chr12:121259511-121260152	GM12878	blood:	n/a	n/a
47	BCLAF1	chr12:121287522-121288032	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:121311196-121311343	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:121285446-121286053	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:121341176-121341570	GM12878	blood:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121197729-121197779	AG09309	skin:	n/a
2	chr12:121211555-121211605	NHBE	bronchial:	n/a
3	chr12:121197729-121197779	AG09309	skin:	n/a
4	chr12:121211555-121211605	NHBE	bronchial:	n/a
5	chr12:121203948-121203998	IMR90	lung:	fetal
6	chr12:121341326-121341376	CMK	blood:	n/a
7	chr12:121197729-121197779	AG09319	gingival:	n/a
8	chr12:121198447-121198497	RPTEC	kidney:	n/a
9	chr12:121342288-121342338	K562	blood:	n/a
10	chr12:121341616-121341666	HCM	heart:	n/a
11	chr12:121341782-121341832	HMEC	breast:	n/a
12	chr12:121197625-121197675	HepG2	liver:	n/a
13	chr12:121239400-121239450	SK-N-SH	brain:	n/a
14	chr12:121274655-121274705	SKMC	muscle:	n/a
15	chr12:121343033-121343083	HNPCEpiC	eye:	n/a
16	chr12:121197625-121197675	SK-N-SH	brain:	n/a
17	chr12:121261039-121261089	MCF10A-Er-Src	breast:	n/a
18	chr12:121345228-121345278	HepG2	liver:	n/a
19	chr12:121198406-121198456	SK-N-SH	brain:	n/a
20	chr12:121342288-121342338	GM06990	blood:	n/a
21	chr12:121345228-121345278	HCPEpiC	choroid plexus:	n/a
22	chr12:121274655-121274705	GM12892	blood:	n/a
23	chr12:121202554-121202604	HMEC	breast:	n/a
24	chr12:121203948-121203998	U87	brain:	n/a
25	chr12:121341782-121341832	H1-hESC	embryonic stem cell:	embryo
26	chr12:121343033-121343083	PANC-1	pancreas:	n/a
27	chr12:121274655-121274705	PANC-1	pancreas:	n/a
28	chr12:121342433-121342483	NB4	blood:	n/a
29	chr12:121273323-121273373	HNPCEpiC	eye:	n/a
30	chr12:121300455-121300505	NH-A	brain:	n/a
31	chr12:121341326-121341376	GM12892	blood:	n/a
32	chr12:121341326-121341376	Caco-2	colon:	n/a
33	chr12:121198447-121198497	SKMC	muscle:	n/a
34	chr12:121274655-121274705	HMEC	breast:	n/a
35	chr12:121261039-121261089	NT2-D1	testis:	n/a
36	chr12:121341782-121341832	AG09309	skin:	n/a
37	chr12:121282930-121282980	HCPEpiC	choroid plexus:	n/a
38	chr12:121343033-121343083	AG10803	skin:	n/a
39	chr12:121342288-121342338	Jurkat	blood:	n/a
40	chr12:121197729-121197779	HCF	heart:	n/a
41	chr12:121342433-121342483	AG04450	lung:	fetal
42	chr12:121341616-121341666	MCF10A-Er-Src	breast:	n/a
43	chr12:121198406-121198456	AG04449	skin:	fetal
44	chr12:121239400-121239450	NB4	blood:	n/a
45	chr12:121273323-121273373	SK-N-SH	brain:	n/a
46	chr12:121239400-121239450	ovcar-3	ovarian:	n/a
47	chr12:121342433-121342483	BE2_C	brain:	n/a
48	chr12:121341326-121341376	IMR90	lung:	fetal
49	chr12:121261039-121261089	Hepatocyte	liver:	n/a
50	chr12:121341782-121341832	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:121239385..121241045-chr12:121266410..121269390,2	K562	blood:
2	chr12:121198595..121200409-chr12:121209397..121212163,2	MCF-7	breast:
3	chr12:121017642..121019153-chr12:121263056..121265187,2	MCF-7	breast:
4	chr12:121251970..121254055-chr12:121269166..121270703,2	K562	blood:
5	chr12:121326911..121329389-chr12:121341221..121344102,2	MCF-7	breast:
6	chr12:121326076..121329274-chr12:121333779..121337730,3	MCF-7	breast:
7	chr12:121191123..121193615-chr12:121194473..121197241,2	K562	blood:
8	chr12:121243655..121245803-chr12:121292539..121295448,2	MCF-7	breast:
9	chr12:121291111..121293734-chr12:121317316..121319397,2	K562	blood:
10	chr12:121312962..121314720-chr12:121324076..121325928,2	K562	blood:
11	chr12:121280705..121284627-chr12:121285918..121289462,3	K562	blood:
12	chr12:121254206..121257153-chr12:121257780..121260885,3	MCF-7	breast:
13	chr12:121212492..121214058-chr12:121280617..121282475,2	MCF-7	breast:
14	chr12:121291153..121292656-chr12:121442284..121444744,2	MCF-7	breast:
15	chr12:121322045..121323969-chr12:121325111..121327661,2	K562	blood:
16	chr12:121199470..121201795-chr12:121202855..121205373,2	MCF-7	breast:
17	chr12:121294043..121295007-chr12:121441383..121442308,2	MCF-7	breast:
18	chr12:121226286..121228196-chr12:121235174..121237034,2	K562	blood:
19	chr12:120727503..120731222-chr12:121282952..121285914,3	MCF-7	breast:
20	chr12:121338472..121340356-chr12:121340571..121343275,2	MCF-7	breast:
21	chr12:121293275..121295846-chr12:121302395..121304368,2	MCF-7	breast:
22	chr12:121210691..121212247-chr12:121214029..121215560,2	K562	blood:
23	chr12:121336041..121337901-chr12:121343531..121346196,2	MCF-7	breast:
24	chr12:121331922..121335800-chr12:121336708..121340188,4	K562	blood:
25	chr12:121293275..121295846-chr12:121302395..121304368,2	MCF-7	breast:
26	chr12:121336041..121337901-chr12:121343531..121346196,2	MCF-7	breast:
27	chr12:121336528..121338127-chr12:121339319..121342244,3	K562	blood:
28	chr12:121316464..121318952-chr12:121321277..121324869,5	K562	blood:
29	chr12:121252485..121255170-chr12:121340536..121342669,2	MCF-7	breast:
30	chr12:121199470..121201795-chr12:121202855..121205373,2	MCF-7	breast:
31	chr12:121317828..121319796-chr12:121340381..121343038,3	MCF-7	breast:
32	chr12:121293123..121296169-chr12:121296958..121300717,3	MCF-7	breast:
33	chr12:121317330..121318863-chr12:121327465..121328985,2	MCF-7	breast:
34	chr12:121259584..121261305-chr12:121284288..121286336,2	K562	blood:
35	chr12:121317330..121318863-chr12:121327465..121328985,2	MCF-7	breast:
36	chr12:121227665..121229362-chr12:121229925..121232592,2	MCF-7	breast:
37	chr12:121203090..121205836-chr12:121209356..121211928,2	MCF-7	breast:
38	chr12:121239385..121241045-chr12:121266410..121269390,2	K562	blood:
39	chr12:121227665..121229362-chr12:121229925..121232592,2	MCF-7	breast:
40	chr12:121304739..121306957-chr12:121328981..121330571,2	MCF-7	breast:
41	chr12:121262055..121264947-chr12:121269553..121271661,2	K562	blood:
42	chr12:121253695..121256191-chr12:121282485..121284244,2	MCF-7	breast:
43	chr12:121319672..121322642-chr12:121322756..121324594,2	K562	blood:
44	chr12:121273900..121276013-chr12:121279474..121281086,2	MCF-7	breast:
45	chr12:121276148..121279076-chr12:121280762..121283669,2	K562	blood:
46	chr12:121297853..121300744-chr12:121301370..121304769,3	K562	blood:
47	chr12:121341147..121344429-chr12:121344566..121350516,5	K562	blood:
48	chr12:121284720..121286332-chr12:121290544..121292082,2	K562	blood:
49	chr12:121294543..121295256-chr12:121447280..121447830,2	MCF-7	breast:
50	chr12:121330698..121332432-chr12:121341997..121343765,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNF1A-1	chr12:121345458-121345803	XLOC_009911
2	lnc-HNF1A-1	chr12:121345458-121345743	XLOC_009911
3	lnc-C12orf43-4	chr12:121280273-121280537	expReg_chr12_10996_-
4	lnc-HNF1A-1	chr12:121342728-121342811	XLOC_009911
5	lnc-HNF1A-1	chr12:121342501-121342575	XLOC_009911
6	lnc-HNF1A-1	chr12:121345458-121345743	XLOC_009911
7	lnc-HNF1A-1	chr12:121342520-121342549	XLOC_009911
8	lnc-ACADS-1	chr12:121197146-121197844	expReg_chr12_11530_+
9	lnc-SPPL3.1-1	chr12:121199194-121199395	ENSG00000255946.1

No data

Variant related genes	Relation type
RPL12P33	TF binding region
CLIC1P1	TF binding region
SPPL3	TF binding region
ENSG00000255946	TF binding region
ARF1P2	TF binding region
RPL12P33	CpG island
CLIC1P1	CpG island
SPPL3	CpG island
ENSG00000255946	CpG island
ARF1P2	CpG island
ENSG00000200795	chromatin interactions
ENSG00000255946	chromatin interactions
ENSG00000157782	chromatin interactions
ENSG00000231313	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000213137	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000110917	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000122971	chromatin interactions
UBE2E2	miRNA target sites
RNF6	miRNA target sites

Extended variants
information (count: 6330 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6330 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs610578	chr12:121194565-121194566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539585877	chr12:121194567-121194568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189127393	chr12:121194568-121194569	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565822924	chr12:121194584-121194585	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139671897	chr12:121194612-121194613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs11065253	chr12:121194627-121194628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78050967	chr12:121194632-121194633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75976893	chr12:121194634-121194635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs367632060	chr12:121194652-121194653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192066760	chr12:121194708-121194709	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535415514	chr12:121194777-121194778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552168681	chr12:121194792-121194793	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373528193	chr12:121194805-121194806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372216760	chr12:121194843-121194844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555260844	chr12:121194855-121194856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs575065698	chr12:121194861-121194862	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs482522	chr12:121194862-121194863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs571232440	chr12:121194925-121194926	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536980128	chr12:121194935-121194936	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12582519	chr12:121195006-121195007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7133413	chr12:121195007-121195008	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs577013125	chr12:121195082-121195083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545901825	chr12:121195087-121195088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10849785	chr12:121195112-121195113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs116635159	chr12:121195143-121195144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185031440	chr12:121195262-121195263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs151326479	chr12:121195327-121195328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535939651	chr12:121195405-121195406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117097811	chr12:121195407-121195408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200690741	chr12:121195441-121195442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535629537	chr12:121195472-121195473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189658594	chr12:121195486-121195487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140699997	chr12:121195501-121195502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181139302	chr12:121195581-121195582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73227026	chr12:121195590-121195591	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs4767932	chr12:121195601-121195602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114194240	chr12:121195602-121195603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs525425	chr12:121195625-121195626	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs555098573	chr12:121195699-121195700	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575175184	chr12:121195723-121195724	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372167421	chr12:121195732-121195733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76654023	chr12:121195747-121195748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185985018	chr12:121195763-121195764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532795537	chr12:121195780-121195781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188095057	chr12:121195801-121195802	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371322433	chr12:121195828-121195829	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12829816	chr12:121195838-121195839	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138439869	chr12:121195849-121195850	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544169738	chr12:121195929-121195930	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573033731	chr12:121195930-121195931	Active TSS Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:5339 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121168600-121196400	Weak transcription	Fetal Brain Female	brain
2	chr12:121177800-121197800	Weak transcription	Gastric	stomach
3	chr12:121179800-121197400	Weak transcription	Spleen	Spleen
4	chr12:121180200-121197400	Weak transcription	Pancreas	Pancrea
5	chr12:121183200-121197600	Weak transcription	Esophagus	oesophagus
6	chr12:121186400-121198400	Weak transcription	Right Ventricle	heart
7	chr12:121189600-121197000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr12:121190400-121197800	Weak transcription	Right Atrium	heart
9	chr12:121193000-121195600	Weak transcription	Fetal Stomach	stomach
10	chr12:121193000-121198400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr12:121193400-121195600	Weak transcription	Brain Germinal Matrix	brain
12	chr12:121193400-121197400	Weak transcription	Brain Hippocampus Middle	brain
13	chr12:121193600-121197000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr12:121193800-121197600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:121193800-121198200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr12:121194000-121196800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr12:121194000-121197000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:121194000-121197600	Weak transcription	GM12878-XiMat	blood
19	chr12:121194000-121200800	Weak transcription	HepG2	liver
20	chr12:121194200-121195600	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:121194200-121197200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:121194200-121197600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:121194200-121197600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:121194200-121197800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr12:121194200-121197800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr12:121194200-121202200	Weak transcription	K562	blood
27	chr12:121194400-121194600	Enhancers	Placenta	Placenta
28	chr12:121194400-121195200	Enhancers	Fetal Intestine Small	intestine
29	chr12:121194400-121195800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr12:121194400-121196800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:121194400-121197000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr12:121194600-121194800	Enhancers	Fetal Intestine Large	intestine
33	chr12:121194600-121197000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr12:121194600-121197000	Weak transcription	Placenta	Placenta
35	chr12:121194600-121197400	Weak transcription	Primary T cells from cord blood	blood
36	chr12:121194800-121195000	Enhancers	Small Intestine	intestine
37	chr12:121194800-121195200	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr12:121194800-121195400	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr12:121194800-121196600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr12:121194800-121196800	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr12:121194800-121196800	Weak transcription	Fetal Intestine Large	intestine
42	chr12:121194800-121197400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:121194800-121197400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr12:121194800-121197600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr12:121194800-121198200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:121194800-121198800	Weak transcription	A549	lung
47	chr12:121195000-121195200	Enhancers	Duodenum Mucosa	Duodenum
48	chr12:121195000-121195600	Enhancers	Colonic Mucosa	Colon
49	chr12:121195000-121195600	Enhancers	NHDF-Ad	bronchial
50	chr12:121195000-121197600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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