Variant report

Variant	nsv899217
Chromosome Location	chr12:67472631-67501987
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	BACH1	chr12:67490689-67490982	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr12:67490653-67491492	Hela-S3	cervix:	n/a	chr12:67490976-67490989
3	CEBPB	chr12:67490663-67491009	K562	blood:	n/a	chr12:67490976-67490989
4	CEBPB	chr12:67490655-67491044	MCF-7	breast:	n/a	chr12:67490976-67490989
5	CEBPB	chr12:67490806-67491066	HepG2	liver:	n/a	chr12:67490976-67490989
6	CEBPB	chr12:67490609-67491058	MCF-7	breast:	n/a	chr12:67490976-67490989
7	CEBPB	chr12:67496495-67496717	HepG2	liver:	n/a	n/a
8	CEBPB	chr12:67479539-67479955	MCF-7	breast:	n/a	n/a
9	CHD2	chr12:67474121-67474235	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr12:67485200-67485350	HMEC	breast:	n/a	n/a
11	CTCF	chr12:67485240-67485390	RPTEC	kidney:	n/a	n/a
12	CTCF	chr12:67485200-67485350	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr12:67491860-67492010	GM06990	blood:	n/a	n/a
14	CTCF	chr12:67485100-67485250	HMEC	breast:	n/a	n/a
15	CTCF	chr12:67485300-67485400	MCF-7	breast:	n/a	n/a
16	CTCF	chr12:67485160-67485310	HRE	kidney:	n/a	n/a
17	CTCF	chr12:67485020-67485170	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr12:67476748-67476819	GM10248	blood:	n/a	n/a
19	CTCF	chr12:67485120-67485270	MCF-7	breast:	n/a	n/a
20	CTCF	chr12:67485100-67485250	NHEK	skin:	n/a	n/a
21	CTCF	chr12:67485140-67485290	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr12:67501340-67501490	GM12867	blood:	n/a	n/a
23	CTCF	chr12:67485083-67485238	NHEK	skin:	n/a	n/a
24	E2F4	chr12:67490725-67491021	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr12:67490735-67491007	Hela-S3	cervix:	n/a	n/a
26	FOS	chr12:67490430-67491395	MCF10A-Er-Src	breast:	n/a	chr12:67490840-67490850 chr12:67490840-67490850 chr12:67490841-67490849 chr12:67490839-67490851 chr12:67490840-67490850
27	FOS	chr12:67490153-67491520	MCF10A-Er-Src	breast:	n/a	chr12:67490840-67490850 chr12:67490840-67490850 chr12:67490841-67490849 chr12:67490839-67490851 chr12:67490840-67490850
28	FOS	chr12:67484972-67485890	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:67485017-67485820	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr12:67485018-67485832	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr12:67475985-67476451	MCF10A-Er-Src	breast:	n/a	chr12:67476094-67476106
32	FOS	chr12:67490547-67491027	Hela-S3	cervix:	n/a	chr12:67490840-67490850 chr12:67490840-67490850 chr12:67490841-67490849 chr12:67490839-67490851 chr12:67490840-67490850
33	FOS	chr12:67485134-67485279	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr12:67476113-67476350	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:67489458-67489527	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:67490329-67491209	MCF10A-Er-Src	breast:	n/a	chr12:67490840-67490850 chr12:67490840-67490850 chr12:67490841-67490849 chr12:67490839-67490851 chr12:67490840-67490850
37	FOS	chr12:67490653-67491143	MCF10A-Er-Src	breast:	n/a	chr12:67490840-67490850 chr12:67490840-67490850 chr12:67490841-67490849 chr12:67490839-67490851 chr12:67490840-67490850
38	FOS	chr12:67486342-67486437	MCF10A-Er-Src	breast:	n/a	chr12:67486410-67486421
39	FOS	chr12:67476037-67476451	MCF10A-Er-Src	breast:	n/a	chr12:67476094-67476106
40	FOS	chr12:67485524-67485804	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr12:67476037-67476454	MCF10A-Er-Src	breast:	n/a	chr12:67476094-67476106
42	FOXA1	chr12:67479344-67479840	T-47D	breast:	n/a	chr12:67479670-67479682
43	FOXA1	chr12:67479432-67479682	ECC-1	luminal epithelium:	n/a	chr12:67479670-67479682
44	FOXA1	chr12:67479469-67479821	T-47D	breast:	n/a	chr12:67479670-67479682
45	GATA3	chr12:67477400-67478047	MCF-7	breast:	n/a	chr12:67477856-67477863
46	GATA3	chr12:67479427-67480233	MCF-7	breast:	n/a	chr12:67479969-67479990 chr12:67479972-67479988 chr12:67479976-67479983 chr12:67479843-67479850 chr12:67479839-67479855 chr12:67479976-67479983 chr12:67479976-67479983
47	GATA3	chr12:67479446-67480115	MCF-7	breast:	n/a	chr12:67479969-67479990 chr12:67479972-67479988 chr12:67479976-67479983 chr12:67479843-67479850 chr12:67479839-67479855 chr12:67479976-67479983 chr12:67479976-67479983
48	GATA3	chr12:67480010-67480188	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr12:67479514-67480138	MCF-7	breast:	n/a	chr12:67479969-67479990 chr12:67479972-67479988 chr12:67479976-67479983 chr12:67479843-67479850 chr12:67479839-67479855 chr12:67479976-67479983 chr12:67479976-67479983
50	GATA3	chr12:67479434-67479845	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67473004-67473054	NHDF-neo	bronchial:	n/a
2	chr12:67473004-67473054	NHDF-neo	bronchial:	n/a
3	chr12:67473004-67473054	HNPCEpiC	eye:	n/a
4	chr12:67473004-67473054	HEK293	kidney:	embryo
5	chr12:67473004-67473054	BJ	skin:	n/a
6	chr12:67473004-67473054	ECC-1	luminal epithelium:	n/a
7	chr12:67473004-67473054	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:67473004-67473054	GM06990	blood:	n/a
9	chr12:67473004-67473054	IMR90	lung:	fetal
10	chr12:67473004-67473054	SK-N-MC	brain:	n/a
11	chr12:67473004-67473054	K562	blood:	n/a
12	chr12:67473004-67473054	HCM	heart:	n/a
13	chr12:67473004-67473054	GM19239	blood:	n/a
14	chr12:67473004-67473054	PANC-1	pancreas:	n/a
15	chr12:67473004-67473054	SKMC	muscle:	n/a
16	chr12:67473004-67473054	Caco-2	colon:	n/a
17	chr12:67473004-67473054	AoSMC	blood vessel:	n/a
18	chr12:67473004-67473054	H1-hESC	embryonic stem cell:	embryo
19	chr12:67473004-67473054	AG04449	skin:	fetal
20	chr12:67473004-67473054	HCF	heart:	n/a
21	chr12:67473004-67473054	HepG2	liver:	n/a
22	chr12:67473004-67473054	HRE	kidney:	n/a
23	chr12:67473004-67473054	HEEpiC	esophagus:	n/a
24	chr12:67473004-67473054	BE2_C	brain:	n/a
25	chr12:67473004-67473054	HMEC	breast:	n/a
26	chr12:67473004-67473054	NT2-D1	testis:	n/a
27	chr12:67473004-67473054	CMK	blood:	n/a
28	chr12:67473004-67473054	GM12878	blood:	n/a
29	chr12:67473004-67473054	T-47D	breast:	n/a
30	chr12:67473004-67473054	AG09309	skin:	n/a
31	chr12:67473004-67473054	U87	brain:	n/a
32	chr12:67473004-67473054	SK-N-SH_RA	brain:	n/a
33	chr12:67473004-67473054	GM12892	blood:	n/a
34	chr12:67473004-67473054	PrEC	prostate:	n/a
35	chr12:67473004-67473054	Hela-S3	cervix:	n/a
36	chr12:67473004-67473054	HCT-116	colon:	n/a
37	chr12:67473004-67473054	HUVEC	blood vessel:	n/a
38	chr12:67473004-67473054	Jurkat	blood:	n/a
39	chr12:67473004-67473054	HAEpiC	amniotic membrane:	n/a
40	chr12:67473004-67473054	HRPEpiC	eye:	n/a
41	chr12:67473004-67473054	SAEC	small airway:	n/a
42	chr12:67473004-67473054	PFSK-1	brain:	n/a
43	chr12:67473004-67473054	MCF-7	breast:	n/a
44	chr12:67473004-67473054	RPTEC	kidney:	n/a
45	chr12:67473004-67473054	NH-A	brain:	n/a
46	chr12:67473004-67473054	AG10803	skin:	n/a
47	chr12:67473004-67473054	ovcar-3	ovarian:	n/a
48	chr12:67473004-67473054	LNCaP	prostate:	n/a
49	chr12:67473004-67473054	HRCEpiC	kidney:	n/a
50	chr12:67473004-67473054	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:67463389..67464966-chr12:67474386..67476237,2	MCF-7	breast:
2	chr12:67478228..67481093-chr12:67612107..67614735,2	MCF-7	breast:
3	chr12:67492809..67494685-chr12:67494838..67497752,2	K562	blood:
4	chr12:67475770..67479143-chr12:67480530..67483271,3	MCF-7	breast:
5	chr12:67462252..67464052-chr12:67500249..67504193,4	MCF-7	breast:
6	chr11:70056279..70056815-chr12:67501480..67502188,2	MCF-7	breast:
7	chr12:67461965..67464455-chr12:67489883..67491932,2	MCF-7	breast:
8	chr12:67481232..67483242-chr12:67484075..67485741,2	MCF-7	breast:
9	chr12:67352783..67353464-chr12:67479586..67480363,2	MCF-7	breast:
10	chr12:67500446..67502740-chr12:67502846..67505140,2	K562	blood:
11	chr12:67482974..67485741-chr12:67492870..67495012,2	K562	blood:
12	chr12:67475770..67479143-chr12:67480530..67483271,3	MCF-7	breast:
13	chr12:67462372..67464494-chr12:67477959..67482038,6	MCF-7	breast:
14	chr12:67471853..67474414-chr12:67474964..67477043,2	K562	blood:
15	chr12:67479380..67480285-chr12:67669243..67670001,2	MCF-7	breast:
16	chr12:67460367..67464425-chr12:67465973..67473216,9	MCF-7	breast:
17	chr12:67471853..67474414-chr12:67474964..67477043,2	K562	blood:
18	chr12:67492809..67494685-chr12:67494838..67497752,2	K562	blood:
19	chr12:67483277..67484822-chr12:67518176..67519782,2	MCF-7	breast:
20	chr12:67481232..67483242-chr12:67484075..67485741,2	MCF-7	breast:
21	chr12:67482974..67485741-chr12:67492870..67495012,2	K562	blood:
22	chr12:67462240..67466033-chr12:67477122..67480393,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRIP1-2	chr12:67488510-67488637	ENSG00000257083
2	lnc-GRIP1-2	chr12:67485327-67485408	ENSG00000257083
3	lnc-CAND1-3	chr12:67473335-67473923	l_674_chr12:67463829-67473923_lymphNode
4	lnc-GRIP1-2	chr12:67485327-67485408	ENSG00000257083
5	lnc-GRIP1-2	chr12:67488510-67488637	XLOC_010110
6	lnc-GRIP1-2	chr12:67485325-67485408	XLOC_010110
7	lnc-GRIP1-2	chr12:67479102-67479354	NONHSAT029239
8	lnc-GRIP1-2	chr12:67480558-67480728	ENSG00000257083
9	lnc-GRIP1-2	chr12:67488510-67488637	ENSG00000257083
10	lnc-GRIP1-2	chr12:67485327-67485408	ENSG00000257083
11	lnc-GRIP1-2	chr12:67489886-67490160	XLOC_010110
12	lnc-GRIP1-2	chr12:67489307-67489334	ENSG00000257083
13	lnc-GRIP1-2	chr12:67488510-67488637	ENSG00000257083
14	lnc-GRIP1-2	chr12:67489886-67490064	ENSG00000257083
15	lnc-GRIP1-2	chr12:67489886-67490186	ENSG00000257083
16	lnc-GRIP1-2	chr12:67485327-67485348	NONHSAT029239

Variant related genes	Relation type
ENSG00000257083	TF binding region
ENSG00000257083	CpG island
ENSG00000256248	chromatin interactions
STRADB	miRNA target sites
STOM	miRNA target sites

Extended variants
information (count: 1123 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11176566	chr12:67472631-67472632	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10878556	chr12:67472697-67472698	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs140686319	chr12:67472743-67472744	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4913522	chr12:67472754-67472755	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568894369	chr12:67472789-67472790	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527504610	chr12:67472827-67472828	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536367964	chr12:67472888-67472889	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201628639	chr12:67472910-67472911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573084296	chr12:67472911-67472912	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535308475	chr12:67472922-67472923	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183351408	chr12:67472926-67472927	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558937645	chr12:67472974-67472975	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375165936	chr12:67473026-67473027	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577197500	chr12:67473092-67473093	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs187845261	chr12:67473094-67473095	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191563406	chr12:67473104-67473105	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567102088	chr12:67473117-67473118	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183704903	chr12:67473165-67473166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536008517	chr12:67473358-67473359	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs542326746	chr12:67473392-67473393	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs560176401	chr12:67473396-67473397	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs369128480	chr12:67473416-67473417	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs189643017	chr12:67473448-67473449	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs150094584	chr12:67473471-67473472	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs570850322	chr12:67473480-67473481	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs7973341	chr12:67473511-67473512	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557933069	chr12:67473584-67473585	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs192492492	chr12:67473594-67473595	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs576973316	chr12:67473638-67473639	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs184761872	chr12:67473641-67473642	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs76508495	chr12:67473661-67473662	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs145472423	chr12:67473746-67473747	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs569562360	chr12:67473782-67473783	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs566566644	chr12:67473791-67473792	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs190259212	chr12:67473830-67473831	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs558767418	chr12:67473868-67473869	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs577088787	chr12:67473997-67473998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139329459	chr12:67474136-67474137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374964789	chr12:67474139-67474140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199947385	chr12:67474140-67474141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556151894	chr12:67474142-67474143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574788195	chr12:67474150-67474151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114257594	chr12:67474229-67474230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560260596	chr12:67474231-67474232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576439326	chr12:67474239-67474240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527770933	chr12:67474288-67474289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546023051	chr12:67474295-67474296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564319724	chr12:67474299-67474300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17183481	chr12:67474315-67474316	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550457838	chr12:67474350-67474351	Enhancers Weak transcription	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
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	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
Neuroticism	17667963	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
Glioblastoma multiforme	19115005	CNVD
Cancer	20164920	CNVD
Osteosarcoma	21215367	CNVD
Lung adenocarcinoma	17982442	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	16946073	CNVD
Liposarcoma	21253554	CNVD
Cancer	23904455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67469000-67473000	Enhancers	HMEC	breast
2	chr12:67471400-67475400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:67471800-67474400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:67472200-67475400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:67472600-67474800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:67472600-67475400	Weak transcription	NHEK	skin
7	chr12:67472800-67474200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr12:67472800-67474400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:67472800-67474400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr12:67472800-67474800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr12:67473000-67473200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr12:67473000-67474400	Enhancers	H9 Cell Line	embryonic stem cell
13	chr12:67473000-67475200	Weak transcription	HMEC	breast
14	chr12:67473200-67474200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr12:67473200-67474600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:67474200-67474400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr12:67474200-67479200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:67474400-67475200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr12:67474400-67475400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:67474400-67479200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr12:67475200-67475400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr12:67475200-67476800	Enhancers	HMEC	breast
23	chr12:67475400-67476800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:67475400-67476800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:67475400-67477800	Enhancers	NHEK	skin
26	chr12:67475400-67478000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:67476800-67482200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:67478000-67482200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:67479000-67480000	Enhancers	Fetal Kidney	kidney
30	chr12:67479200-67479400	Enhancers	Gastric	stomach
31	chr12:67479200-67479400	Enhancers	Pancreas	Pancrea
32	chr12:67479200-67479600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr12:67479200-67480000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:67479400-67479600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr12:67482000-67482600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr12:67482200-67482600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:67482200-67482600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr12:67482400-67482600	Enhancers	Pancreas	Pancrea
39	chr12:67482600-67482800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr12:67482600-67482800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:67482600-67484400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:67482600-67484400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:67482600-67485000	Weak transcription	Pancreas	Pancrea
44	chr12:67484400-67485000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:67484400-67485000	Enhancers	NHEK	skin
46	chr12:67484400-67485200	Enhancers	Esophagus	oesophagus
47	chr12:67484400-67485200	Enhancers	HMEC	breast
48	chr12:67484400-67486200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:67484800-67485200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:67484800-67485600	Enhancers	Cortex derived primary cultured neurospheres	brain

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