Variant report

Variant	nsv1047675
Chromosome Location	chr12:68303674-68337325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:68337071-68337457	HepG2	liver:	n/a	chr12:68337247-68337263
2	ARID3A	chr12:68337100-68337433	K562	blood:	n/a	chr12:68337247-68337263
3	ARID3A	chr12:68309138-68309370	HepG2	liver:	n/a	n/a
4	BCL3	chr12:68304060-68304535	A549	lung:	n/a	n/a
5	BCLAF1	chr12:68337085-68337471	GM12878	blood:	n/a	n/a
6	CEBPB	chr12:68304147-68304918	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:68312294-68312520	K562	blood:	n/a	chr12:68312404-68312415 chr12:68312403-68312416
8	CEBPB	chr12:68312286-68312548	IMR90	lung:	n/a	chr12:68312404-68312415 chr12:68312403-68312416
9	CEBPB	chr12:68304053-68304985	A549	lung:	n/a	n/a
10	CEBPB	chr12:68312272-68312561	K562	blood:	n/a	chr12:68312404-68312415 chr12:68312403-68312416
11	CEBPB	chr12:68304339-68304878	A549	lung:	n/a	n/a
12	CEBPB	chr12:68334443-68334959	IMR90	lung:	n/a	chr12:68334847-68334860
13	CEBPB	chr12:68334452-68334843	A549	lung:	n/a	n/a
14	CEBPB	chr12:68318941-68319671	MCF-7	breast:	n/a	n/a
15	CEBPB	chr12:68304465-68304834	A549	lung:	n/a	n/a
16	CEBPB	chr12:68312299-68312598	A549	lung:	n/a	chr12:68312404-68312415 chr12:68312403-68312416
17	CEBPB	chr12:68328139-68328191	HepG2	liver:	n/a	chr12:68328167-68328178 chr12:68328150-68328161
18	CEBPB	chr12:68312298-68312550	HepG2	liver:	n/a	chr12:68312404-68312415 chr12:68312403-68312416
19	CHD2	chr12:68310214-68310417	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr12:68337160-68337310	HepG2	liver:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
21	CTCF	chr12:68331720-68331870	GM12864	blood:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
22	CTCF	chr12:68331751-68331921	GM19238	blood:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
23	CTCF	chr12:68337161-68337369	SK-N-SH_RA	brain:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
24	CTCF	chr12:68331744-68331943	GM12878	blood:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
25	CTCF	chr12:68337207-68337400	NHEK	skin:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
26	CTCF	chr12:68337160-68337310	GM12875	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
27	CTCF	chr12:68331880-68332030	RPTEC	kidney:	n/a	n/a
28	CTCF	chr12:68337180-68337330	GM12878	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
29	CTCF	chr12:68323398-68323509	MCF-7	breast:	n/a	chr12:68323461-68323469 chr12:68323457-68323473 chr12:68323451-68323472 chr12:68323456-68323474
30	CTCF	chr12:68331720-68331870	HMEC	breast:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
31	CTCF	chr12:68337151-68337421	GM10266	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
32	CTCF	chr12:68331700-68331850	Caco-2	colon:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
33	CTCF	chr12:68337173-68337395	GM10248	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
34	CTCF	chr12:68337066-68337459	H1-hESC	embryonic stem cell:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
35	CTCF	chr12:68337155-68337363	HepG2	liver:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
36	CTCF	chr12:68331756-68331916	NHEK	skin:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
37	CTCF	chr12:68337180-68337330	AG09309	skin:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
38	CTCF	chr12:68337180-68337330	NHDF-neo	bronchial:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
39	CTCF	chr12:68337240-68337390	HFF	foreskin:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
40	CTCF	chr12:68337000-68337150	K562	blood:	n/a	n/a
41	CTCF	chr12:68321160-68321310	BE2_C	brain:	n/a	n/a
42	CTCF	chr12:68337189-68337394	HepG2	liver:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
43	CTCF	chr12:68337240-68337390	GM12868	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
44	CTCF	chr12:68331780-68331930	GM12869	blood:	n/a	chr12:68331833-68331843 chr12:68331831-68331847 chr12:68331830-68331848 chr12:68331825-68331846
45	CTCF	chr12:68337126-68337465	K562	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
46	CTCF	chr12:68323360-68323510	Caco-2	colon:	n/a	chr12:68323461-68323469 chr12:68323393-68323401 chr12:68323457-68323473 chr12:68323451-68323472 chr12:68323456-68323474
47	CTCF	chr12:68337240-68337390	GM12864	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
48	CTCF	chr12:68337261-68337353	GM19240	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282
49	CTCF	chr12:68337037-68337490	MCF-7	breast:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281
50	CTCF	chr12:68337200-68337350	GM12872	blood:	n/a	chr12:68337272-68337279 chr12:68337265-68337283 chr12:68337266-68337282 chr12:68337260-68337281

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:68304774-68304824	GM12891	blood:	n/a
2	chr12:68304774-68304824	Hela-S3	cervix:	n/a
3	chr12:68337288-68337338	AG09309	skin:	n/a
4	chr12:68337288-68337338	HNPCEpiC	eye:	n/a
5	chr12:68337288-68337338	HCT-116	colon:	n/a
6	chr12:68304774-68304824	HCPEpiC	choroid plexus:	n/a
7	chr12:68304774-68304824	PrEC	prostate:	n/a
8	chr12:68304774-68304824	NHBE	bronchial:	n/a
9	chr12:68337288-68337338	AG09319	gingival:	n/a
10	chr12:68337288-68337338	PrEC	prostate:	n/a
11	chr12:68304774-68304824	NT2-D1	testis:	n/a
12	chr12:68337288-68337338	GM12878	blood:	n/a
13	chr12:68304774-68304824	PFSK-1	brain:	n/a
14	chr12:68304774-68304824	RPTEC	kidney:	n/a
15	chr12:68304774-68304824	HRPEpiC	eye:	n/a
16	chr12:68337288-68337338	HIPEpiC	eye:	n/a
17	chr12:68304774-68304824	SK-N-SH	brain:	n/a
18	chr12:68304774-68304824	K562	blood:	n/a
19	chr12:68337288-68337338	SK-N-SH	brain:	n/a
20	chr12:68304774-68304824	ECC-1	luminal epithelium:	n/a
21	chr12:68304774-68304824	HCM	heart:	n/a
22	chr12:68337288-68337338	AG04449	skin:	fetal
23	chr12:68304774-68304824	T-47D	breast:	n/a
24	chr12:68304774-68304824	BJ	skin:	n/a
25	chr12:68304774-68304824	HepG2	liver:	n/a
26	chr12:68304774-68304824	ProgFib	skin:	n/a
27	chr12:68304774-68304824	NHDF-neo	bronchial:	n/a
28	chr12:68304774-68304824	HCF	heart:	n/a
29	chr12:68337288-68337338	HRPEpiC	eye:	n/a
30	chr12:68337288-68337338	HEEpiC	esophagus:	n/a
31	chr12:68337288-68337338	SK-N-MC	brain:	n/a
32	chr12:68337288-68337338	HCF	heart:	n/a
33	chr12:68337288-68337338	LNCaP	prostate:	n/a
34	chr12:68337288-68337338	NHDF-neo	bronchial:	n/a
35	chr12:68304774-68304824	Caco-2	colon:	n/a
36	chr12:68304774-68304824	HEEpiC	esophagus:	n/a
37	chr12:68337288-68337338	HCPEpiC	choroid plexus:	n/a
38	chr12:68337288-68337338	HPAEpiC	pulmonary alveolar:	n/a
39	chr12:68304774-68304824	LNCaP	prostate:	n/a
40	chr12:68304774-68304824	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:68337288-68337338	AG10803	skin:	n/a
42	chr12:68304774-68304824	U87	brain:	n/a
43	chr12:68337288-68337338	HMEC	breast:	n/a
44	chr12:68337288-68337338	NHBE	bronchial:	n/a
45	chr12:68304774-68304824	GM19239	blood:	n/a
46	chr12:68337288-68337338	HEK293	kidney:	embryo
47	chr12:68337288-68337338	ECC-1	luminal epithelium:	n/a
48	chr12:68337288-68337338	GM12892	blood:	n/a
49	chr12:68337288-68337338	NH-A	brain:	n/a
50	chr12:68337288-68337338	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:68330507..68333392-chr12:68338678..68341151,2	K562	blood:
2	chr12:68307323..68311643-chr12:68312148..68315840,4	K562	blood:
3	chr12:68326933..68329428-chr12:68332676..68334378,2	MCF-7	breast:
4	chr12:68321249..68323681-chr12:68328311..68330339,3	MCF-7	breast:
5	chr12:68325726..68328495-chr12:68330999..68332774,2	MCF-7	breast:
6	chr12:68329675..68332537-chr12:68336237..68339598,3	MCF-7	breast:
7	chr12:67824150..67825044-chr12:68331354..68332021,2	MCF-7	breast:
8	chr12:67835312..67836119-chr12:68336837..68337738,4	MCF-7	breast:
9	chr12:68302716..68305733-chr12:68312803..68316283,4	MCF-7	breast:
10	chr12:68329675..68332537-chr12:68336237..68339598,3	MCF-7	breast:
11	chr12:68306230..68308010-chr12:68310665..68313391,3	MCF-7	breast:
12	chr12:68275094..68278065-chr12:68327324..68329137,2	MCF-7	breast:
13	chr12:68044625..68045772-chr12:68336973..68337703,4	MCF-7	breast:
14	chr12:68302716..68305733-chr12:68312803..68316283,4	MCF-7	breast:
15	chr12:67749654..67750348-chr12:68336874..68337753,3	MCF-7	breast:
16	chr12:68304416..68306533-chr12:68307789..68310636,2	MCF-7	breast:
17	chr12:68325726..68328495-chr12:68330999..68332774,2	MCF-7	breast:
18	chr12:67807149..67807779-chr12:68336675..68337459,2	MCF-7	breast:
19	chr12:68306230..68308010-chr12:68310665..68313391,3	MCF-7	breast:
20	chr12:68307323..68311643-chr12:68312148..68315840,4	K562	blood:
21	chr12:68042733..68044799-chr12:68333613..68335676,2	MCF-7	breast:
22	chr12:68304416..68306533-chr12:68307789..68310636,2	MCF-7	breast:
23	chr12:68326933..68329428-chr12:68332676..68334378,2	MCF-7	breast:
24	chr12:68041413..68045340-chr12:68327964..68331582,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DYRK2-2	chr12:68323053-68323167	NONHSAT029271
2	lnc-DYRK2-2	chr12:68326057-68326169	ENSG00000255772
3	lnc-DYRK2-2	chr12:68326057-68326169	ENSG00000255772
4	lnc-DYRK2-2	chr12:68326056-68326147	NONHSAT029271
5	lnc-DYRK2-2	chr12:68326485-68327145	NONHSAT029271
6	lnc-DYRK2-2	chr12:68323043-68323167	ENSG00000255772
7	lnc-DYRK2-2	chr12:68326486-68327145	XLOC_009792
8	lnc-DYRK2-2	chr12:68326057-68326147	XLOC_009792
9	lnc-DYRK2-2	chr12:68323054-68323167	XLOC_009792
10	lnc-DYRK2-2	chr12:68323015-68323167	ENSG00000255772
11	lnc-DYRK2-2	chr12:68326486-68326728	ENSG00000255772

Variant related genes	Relation type
ENSG00000255772	TF binding region
ENSG00000255772	CpG island
ENSG00000255772	chromatin interactions
ENSG00000127334	chromatin interactions

Extended variants
information (count: 1204 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537625524	chr12:68303681-68303682	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs556055702	chr12:68303694-68303695	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs568553984	chr12:68303718-68303719	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs186115590	chr12:68303817-68303818	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs35796454	chr12:68303826-68303827	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs12319335	chr12:68303853-68303854	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs554186773	chr12:68303860-68303861	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs564016866	chr12:68303888-68303889	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192313391	chr12:68303891-68303892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs114989686	chr12:68303912-68303913	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs7488068	chr12:68303918-68303919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs7488069	chr12:68303921-68303922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs182400904	chr12:68303924-68303925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs187839835	chr12:68303934-68303935	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs544011598	chr12:68303968-68303969	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs145939250	chr12:68303980-68303981	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs71088301	chr12:68304020-68304021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574477353	chr12:68304026-68304027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs4454800	chr12:68304027-68304028	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs10539246	chr12:68304028-68304029	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs116977944	chr12:68304029-68304030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs76369524	chr12:68304043-68304044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs560134647	chr12:68304086-68304087	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs141540709	chr12:68304087-68304088	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552079564	chr12:68304100-68304101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144582918	chr12:68304128-68304129	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533707903	chr12:68304146-68304147	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs386763924	chr12:68304148-68304149	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs2904502	chr12:68304149-68304150	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs549955182	chr12:68304160-68304161	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs3850591	chr12:68304169-68304170	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs190978606	chr12:68304205-68304206	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs547560508	chr12:68304243-68304244	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs182596807	chr12:68304304-68304305	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs148488326	chr12:68304327-68304328	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs558149914	chr12:68304335-68304336	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7488180	chr12:68304370-68304371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141724911	chr12:68304402-68304403	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556320337	chr12:68304436-68304437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs530362021	chr12:68304440-68304441	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs537300257	chr12:68304448-68304449	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs68144547	chr12:68304458-68304459	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs12319784	chr12:68304486-68304487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555972613	chr12:68304498-68304499	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs535874739	chr12:68304553-68304554	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12319848	chr12:68304565-68304566	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs187304304	chr12:68304585-68304586	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs192023531	chr12:68304640-68304641	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs559792622	chr12:68304676-68304677	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs12321302	chr12:68304719-68304720	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Lung cancer	18438408	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
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	21569311	CNVD
Bone cancer	16732325	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	17850661	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	21569311	CNVD
Cancer	20164920	CNVD
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:68299800-68304600	Weak transcription	Brain Substantia Nigra	brain
2	chr12:68302200-68304600	Enhancers	HSMMtube	muscle
3	chr12:68302400-68304200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:68302400-68304600	Enhancers	HSMM	muscle
5	chr12:68302400-68304600	Enhancers	NHEK	skin
6	chr12:68302400-68305200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:68302400-68305200	Enhancers	Osteobl	bone
8	chr12:68302400-68305800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:68302400-68307800	Enhancers	Fetal Muscle Leg	muscle
10	chr12:68302600-68305400	Enhancers	NHLF	lung
11	chr12:68302600-68305600	Enhancers	HMEC	breast
12	chr12:68302600-68310000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:68302800-68304000	Enhancers	A549	lung
14	chr12:68302800-68304600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:68302800-68305200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:68302800-68305400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:68302800-68305400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:68302800-68305600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:68303000-68304200	Enhancers	Fetal Heart	heart
20	chr12:68303000-68304600	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr12:68303000-68305800	Enhancers	NHDF-Ad	bronchial
22	chr12:68303200-68304000	Enhancers	Colon Smooth Muscle	Colon
23	chr12:68303400-68303800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr12:68303600-68303800	Flanking Active TSS	NH-A	brain
25	chr12:68303600-68304600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr12:68303600-68304800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr12:68303600-68305400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:68303800-68304000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
29	chr12:68303800-68304400	Weak transcription	Aorta	Aorta
30	chr12:68303800-68304600	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr12:68303800-68304800	Enhancers	NH-A	brain
32	chr12:68304000-68304400	Weak transcription	Colon Smooth Muscle	Colon
33	chr12:68304000-68304600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr12:68304000-68304800	Flanking Active TSS	A549	lung
35	chr12:68304200-68304600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:68304200-68305000	Flanking Active TSS	Fetal Heart	heart
37	chr12:68304400-68304800	Enhancers	Colon Smooth Muscle	Colon
38	chr12:68304400-68304800	Enhancers	Hela-S3	cervix
39	chr12:68304400-68305800	Enhancers	Fetal Brain Male	brain
40	chr12:68304600-68304800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr12:68304600-68304800	Enhancers	Brain Anterior Caudate	brain
42	chr12:68304600-68305000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:68304600-68305000	Enhancers	Brain Substantia Nigra	brain
44	chr12:68304600-68305000	Active TSS	Right Ventricle	heart
45	chr12:68304600-68305000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr12:68304600-68305000	Flanking Active TSS	NHEK	skin
47	chr12:68304600-68305200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr12:68304600-68305200	Active TSS	Stomach Smooth Muscle	stomach
49	chr12:68304600-68305200	Flanking Active TSS	HSMM	muscle
50	chr12:68304600-68305200	Flanking Active TSS	HSMMtube	muscle

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