Variant report

Variant	esv3421024
Chromosome Location	chr12:121471004-121493702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:309)
CpG islands
(count:428)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:121480947-121481240	K562	blood:	n/a	n/a
2	ATF2	chr12:121476753-121477249	GM12878	blood:	n/a	n/a
3	ATF3	chr12:121484435-121484678	K562	blood:	n/a	n/a
4	ATF3	chr12:121488586-121488835	GM12878	blood:	n/a	n/a
5	BCL3	chr12:121470923-121471217	GM12878	blood:	n/a	n/a
6	BCL3	chr12:121471028-121471342	GM12878	blood:	n/a	n/a
7	BRCA1	chr12:121476486-121476946	GM12878	blood:	n/a	n/a
8	CEBPB	chr12:121471090-121471110	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:121474490-121474871	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:121471062-121471089	K562	blood:	n/a	chr12:121471076-121471089 chr12:121471077-121471088 chr12:121471076-121471089 chr12:121471076-121471087
11	CEBPB	chr12:121474546-121474839	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:121474495-121474842	A549	lung:	n/a	n/a
13	CHD2	chr12:121471801-121472030	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr12:121476705-121477344	GM12878	blood:	n/a	n/a
15	CREB1	chr12:121476785-121477064	A549	lung:	n/a	n/a
16	CTCF	chr12:121486220-121486370	BE2_C	brain:	n/a	n/a
17	CTCF	chr12:121490839-121490885	GM20000	blood:	n/a	n/a
18	CTCF	chr12:121473120-121473270	HEK293	kidney:	n/a	n/a
19	CTCF	chr12:121482700-121482850	NB4	blood:	n/a	n/a
20	E2F4	chr12:121471764-121471957	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr12:121475946-121475986	GM12878	blood:	n/a	n/a
22	E2F4	chr12:121474591-121474823	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr12:121476987-121477187	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F6	chr12:121484492-121484640	K562	blood:	n/a	n/a
25	E2F6	chr12:121484459-121484771	H1-hESC	embryonic stem cell:	n/a	n/a
26	EBF1	chr12:121471698-121472027	GM12878	blood:	n/a	n/a
27	EBF1	chr12:121476647-121476960	GM12878	blood:	n/a	n/a
28	EBF1	chr12:121476601-121477298	GM12878	blood:	n/a	n/a
29	EBF1	chr12:121476604-121476986	GM12878	blood:	n/a	n/a
30	EBF1	chr12:121471660-121472106	GM12878	blood:	n/a	n/a
31	EGR1	chr12:121476809-121476999	GM12878	blood:	n/a	n/a
32	EGR1	chr12:121485299-121485525	K562	blood:	n/a	n/a
33	ELF1	chr12:121487288-121487485	K562	blood:	n/a	chr12:121487383-121487396
34	EP300	chr12:121476593-121477277	GM12878	blood:	n/a	n/a
35	EP300	chr12:121485889-121486917	SK-N-SH	brain:	n/a	n/a
36	EP300	chr12:121474480-121475049	SK-N-SH	brain:	n/a	n/a
37	EP300	chr12:121480963-121481089	K562	blood:	n/a	n/a
38	ETS1	chr12:121488577-121488914	K562	blood:	n/a	n/a
39	FOS	chr12:121471034-121471233	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr12:121471072-121471088	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr12:121471606-121472084	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr12:121474438-121474862	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr12:121474505-121474847	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr12:121471675-121472119	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr12:121481068-121481151	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr12:121476914-121477114	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr12:121471076-121471258	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr12:121474474-121474863	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr12:121488715-121488779	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr12:121471670-121472133	MCF10A-Er-Src	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121476792-121476842	SK-N-MC	brain:	n/a
2	chr12:121476792-121476842	SK-N-MC	brain:	n/a
3	chr12:121476792-121476842	A549	lung:	n/a
4	chr12:121476549-121476599	HMEC	breast:	n/a
5	chr12:121476549-121476599	RPTEC	kidney:	n/a
6	chr12:121477061-121477111	Hela-S3	cervix:	n/a
7	chr12:121476720-121476770	H1-hESC	embryonic stem cell:	embryo
8	chr12:121477061-121477111	HRE	kidney:	n/a
9	chr12:121477854-121477904	MCF-7	breast:	n/a
10	chr12:121476792-121476842	SKMC	muscle:	n/a
11	chr12:121477854-121477904	SK-N-SH_RA	brain:	n/a
12	chr12:121477854-121477904	GM12892	blood:	n/a
13	chr12:121476549-121476599	H1-hESC	embryonic stem cell:	embryo
14	chr12:121477061-121477111	CMK	blood:	n/a
15	chr12:121476720-121476770	NH-A	brain:	n/a
16	chr12:121477061-121477111	ovcar-3	ovarian:	n/a
17	chr12:121477093-121477143	HepG2	liver:	n/a
18	chr12:121477061-121477111	GM06990	blood:	n/a
19	chr12:121476549-121476599	HAEpiC	amniotic membrane:	n/a
20	chr12:121477093-121477143	K562	blood:	n/a
21	chr12:121476792-121476842	Caco-2	colon:	n/a
22	chr12:121477854-121477904	ProgFib	skin:	n/a
23	chr12:121476792-121476842	AG04450	lung:	fetal
24	chr12:121477061-121477111	PANC-1	pancreas:	n/a
25	chr12:121476792-121476842	HAEpiC	amniotic membrane:	n/a
26	chr12:121476549-121476599	SK-N-SH	brain:	n/a
27	chr12:121476720-121476770	GM12892	blood:	n/a
28	chr12:121476720-121476770	AG09319	gingival:	n/a
29	chr12:121477093-121477143	HNPCEpiC	eye:	n/a
30	chr12:121476549-121476599	NT2-D1	testis:	n/a
31	chr12:121476549-121476599	AG09319	gingival:	n/a
32	chr12:121476549-121476599	Jurkat	blood:	n/a
33	chr12:121476720-121476770	GM06990	blood:	n/a
34	chr12:121476596-121476646	HepG2	liver:	n/a
35	chr12:121476792-121476842	AG10803	skin:	n/a
36	chr12:121477854-121477904	Hepatocyte	liver:	n/a
37	chr12:121476792-121476842	IMR90	lung:	fetal
38	chr12:121476596-121476646	Hela-S3	cervix:	n/a
39	chr12:121477093-121477143	HL-60	blood:	n/a
40	chr12:121476549-121476599	AG10803	skin:	n/a
41	chr12:121477093-121477143	ProgFib	skin:	n/a
42	chr12:121477093-121477143	HCF	heart:	n/a
43	chr12:121476596-121476646	NH-A	brain:	n/a
44	chr12:121476720-121476770	ECC-1	luminal epithelium:	n/a
45	chr12:121476792-121476842	K562	blood:	n/a
46	chr12:121476596-121476646	HCF	heart:	n/a
47	chr12:121476549-121476599	GM12891	blood:	n/a
48	chr12:121477854-121477904	AoSMC	blood vessel:	n/a
49	chr12:121476720-121476770	GM12891	blood:	n/a
50	chr12:121476549-121476599	MCF-7	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:120729256..120731429-chr12:121471533..121473045,2	MCF-7	breast:
2	chr12:121483901..121486142-chr12:121487218..121490045,2	K562	blood:
3	chr12:121473524..121476101-chr12:121524769..121527497,2	K562	blood:
4	chr12:121463340..121465773-chr12:121472717..121474961,3	MCF-7	breast:
5	chr12:121488470..121488989-chr3:111085239..111085759,2	MCF-7	breast:
6	chr12:121472155..121474661-chr12:121478426..121481122,2	K562	blood:
7	chr12:121481372..121483233-chr12:121486748..121488250,2	K562	blood:
8	chr12:121490675..121493658-chr12:121495456..121497011,2	K562	blood:
9	chr12:121472155..121474661-chr12:121478426..121481122,2	K562	blood:
10	chr12:121488415..121490899-chr12:121492548..121494191,2	K562	blood:
11	chr12:121481372..121483233-chr12:121486748..121488250,2	K562	blood:
12	chr12:121488415..121490899-chr12:121492548..121494191,2	K562	blood:
13	chr12:121483901..121486142-chr12:121487218..121490045,2	K562	blood:
14	chr12:121471397..121473334-chr12:121474789..121478157,3	MCF-7	breast:
15	chr12:121459441..121461737-chr12:121477927..121480607,2	K562	blood:

No data

Variant related genes	Relation type
OASL	TF binding region
OASL	CpG island
ENSG00000200795	chromatin interactions
ENSG00000135114	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 999 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377439239	chr12:121471018-121471019	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144836150	chr12:121471019-121471020	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556480526	chr12:121471031-121471032	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568668927	chr12:121471068-121471069	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145790240	chr12:121471083-121471084	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568909284	chr12:121471087-121471088	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576362534	chr12:121471110-121471111	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190450121	chr12:121471133-121471134	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577373940	chr12:121471153-121471154	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546198328	chr12:121471154-121471155	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553068473	chr12:121471195-121471196	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201476777	chr12:121471215-121471216	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3213546	chr12:121471216-121471217	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181628128	chr12:121471240-121471241	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369520507	chr12:121471241-121471242	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371593303	chr12:121471263-121471264	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61733227	chr12:121471283-121471284	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184510019	chr12:121471285-121471286	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148528798	chr12:121471296-121471297	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143705680	chr12:121471307-121471308	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150665123	chr12:121471313-121471314	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140970607	chr12:121471314-121471315	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs61733224	chr12:121471325-121471326	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3213545	chr12:121471337-121471338	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
25	rs140204273	chr12:121471341-121471342	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149658390	chr12:121471363-121471364	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143025848	chr12:121471364-121471365	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553252644	chr12:121471366-121471367	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145474725	chr12:121471382-121471383	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374804957	chr12:121471388-121471389	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568732289	chr12:121471411-121471412	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148845781	chr12:121471459-121471460	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368869842	chr12:121471512-121471513	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373574251	chr12:121471523-121471524	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs28360476	chr12:121471532-121471533	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs146484691	chr12:121471534-121471535	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs202221662	chr12:121471535-121471536	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs543574290	chr12:121471563-121471564	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs539533463	chr12:121471564-121471565	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs199990181	chr12:121471565-121471566	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376421045	chr12:121471577-121471578	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs151045800	chr12:121471584-121471585	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201365258	chr12:121471589-121471590	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs373651836	chr12:121471593-121471594	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs542160188	chr12:121471607-121471608	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs540524237	chr12:121471631-121471632	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs181192949	chr12:121471644-121471645	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575167954	chr12:121471679-121471680	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs372956916	chr12:121471699-121471700	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371596917	chr12:121471773-121471774	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121454400-121471600	Weak transcription	GM12878-XiMat	blood
2	chr12:121454400-121472200	Weak transcription	Primary T cells from cord blood	blood
3	chr12:121454400-121475800	Weak transcription	Adipose Nuclei	Adipose
4	chr12:121454400-121476000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr12:121454400-121476400	Weak transcription	Right Atrium	heart
6	chr12:121454600-121471200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr12:121454600-121471600	Weak transcription	Fetal Thymus	thymus
8	chr12:121454600-121476200	Weak transcription	Brain Hippocampus Middle	brain
9	chr12:121454600-121476200	Weak transcription	Gastric	stomach
10	chr12:121460000-121471400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:121464800-121471200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr12:121465000-121472000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr12:121465600-121471200	Weak transcription	Lung	lung
14	chr12:121465800-121471200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr12:121465800-121471400	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr12:121465800-121471600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr12:121466200-121471400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr12:121466400-121471200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:121467800-121471800	Strong transcription	Liver	Liver
20	chr12:121468000-121471200	Weak transcription	Esophagus	oesophagus
21	chr12:121468200-121471200	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr12:121468800-121471200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr12:121469200-121471400	Genic enhancers	Stomach Mucosa	stomach
24	chr12:121469400-121471400	Weak transcription	Spleen	Spleen
25	chr12:121469400-121472200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr12:121469600-121472000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:121470200-121471400	Genic enhancers	Primary T cells fromperipheralblood	blood
28	chr12:121470200-121476200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr12:121470400-121471400	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:121470400-121476200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:121470600-121472200	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr12:121471000-121471200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr12:121471000-121471400	Enhancers	Hela-S3	cervix
34	chr12:121471000-121471600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr12:121471000-121471600	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr12:121471000-121471600	Enhancers	Colonic Mucosa	Colon
37	chr12:121471000-121471600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr12:121471000-121471600	Enhancers	Small Intestine	intestine
39	chr12:121471000-121473000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:121471000-121474200	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr12:121471000-121476000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr12:121471200-121471600	Genic enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:121471200-121471800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr12:121471200-121472200	Enhancers	Esophagus	oesophagus
45	chr12:121471200-121472400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:121471200-121472400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:121471200-121472400	Enhancers	Duodenum Mucosa	Duodenum
48	chr12:121471200-121472600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:121471200-121472600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr12:121471200-121473000	Enhancers	HMEC	breast

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