Variant report

Variant	esv1842755
Chromosome Location	chr12:11418163-11567597
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:1038)
Chromatin interactive
region (count:2)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 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	chr12:11501400-11501725	K562	blood:	n/a	n/a
2	BCL3	chr12:11501365-11501771	GM12878	blood:	n/a	n/a
3	BCL3	chr12:11501361-11501642	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
6	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
7	CEBPB	chr12:11457994-11458258	A549	lung:	n/a	chr12:11458153-11458164
8	CEBPB	chr12:11478711-11479007	HepG2	liver:	n/a	chr12:11478828-11478841 chr12:11478830-11478839 chr12:11478828-11478839 chr12:11478829-11478840
9	CEBPB	chr12:11423258-11423283	HepG2	liver:	n/a	chr12:11423268-11423279
10	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
12	CEBPB	chr12:11458075-11458297	HepG2	liver:	n/a	chr12:11458153-11458164
13	CREB1	chr12:11501322-11501785	K562	blood:	n/a	n/a
14	CREB1	chr12:11501156-11501972	K562	blood:	n/a	n/a
15	CREB1	chr12:11501439-11501709	A549	lung:	n/a	n/a
16	CREB1	chr12:11501341-11501827	HepG2	liver:	n/a	n/a
17	CREB1	chr12:11501275-11501755	HepG2	liver:	n/a	n/a
18	CTCF	chr12:11500880-11501030	HCT-116	colon:	n/a	n/a
19	CTCF	chr12:11500880-11501030	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr12:11500800-11500950	BJ	skin:	n/a	n/a
21	CTCF	chr12:11423609-11423648	GM20000	blood:	n/a	n/a
22	CTCF	chr12:11500880-11501030	GM06990	blood:	n/a	n/a
23	CTCF	chr12:11500860-11501010	BE2_C	brain:	n/a	n/a
24	CTCF	chr12:11506052-11506137	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:11501510-11501634	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:11500840-11500990	GM12878	blood:	n/a	n/a
27	CTCF	chr12:11500820-11500970	HMF	breast:	n/a	n/a
28	CTCF	chr12:11528342-11528385	LNCaP	prostate:	n/a	n/a
29	CTCF	chr12:11459054-11459110	GM20000	blood:	n/a	n/a
30	CTCF	chr12:11545671-11545700	GM10266	blood:	n/a	n/a
31	CTCF	chr12:11545750-11545873	GM13977	blood:	n/a	n/a
32	CTCF	chr12:11506036-11506126	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:11500860-11501010	GM12874	blood:	n/a	n/a
34	CTCF	chr12:11501522-11501562	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr12:11500720-11500870	BE2_C	brain:	n/a	n/a
36	CTCF	chr12:11500907-11500926	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:11500920-11501070	HMEC	breast:	n/a	n/a
38	CTCF	chr12:11500873-11500995	K562	blood:	n/a	n/a
39	CTCF	chr12:11500800-11500950	GM12871	blood:	n/a	n/a
40	CTCF	chr12:11500860-11501010	GM12866	blood:	n/a	n/a
41	CTCF	chr12:11500800-11500950	GM12868	blood:	n/a	n/a
42	CTCF	chr12:11500840-11500990	AG04450	lung:	n/a	n/a
43	CTCF	chr12:11500844-11500992	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr12:11500820-11500970	GM12801	blood:	n/a	n/a
45	CTCF	chr12:11500840-11500990	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:11500800-11500950	GM12874	blood:	n/a	n/a
47	CTCF	chr12:11500860-11501010	GM12873	blood:	n/a	n/a
48	CTCF	chr12:11501520-11501609	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:11500867-11500968	HepG2	liver:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11549192-11549242	HCPEpiC	choroid plexus:	n/a
2	chr12:11549192-11549242	HCPEpiC	choroid plexus:	n/a
3	chr12:11548019-11548069	HMEC	breast:	n/a
4	chr12:11548019-11548069	AG09319	gingival:	n/a
5	chr12:11423120-11423170	CMK	blood:	n/a
6	chr12:11460710-11460760	HL-60	blood:	n/a
7	chr12:11548867-11548917	SK-N-SH	brain:	n/a
8	chr12:11548019-11548069	SKMC	muscle:	n/a
9	chr12:11549555-11549605	GM12892	blood:	n/a
10	chr12:11549555-11549605	T-47D	breast:	n/a
11	chr12:11461798-11461848	GM12892	blood:	n/a
12	chr12:11508049-11508099	Hepatocyte	liver:	n/a
13	chr12:11464607-11464657	HRCEpiC	kidney:	n/a
14	chr12:11422920-11422970	HPAEpiC	pulmonary alveolar:	n/a
15	chr12:11549555-11549605	GM12878	blood:	n/a
16	chr12:11549555-11549605	LNCaP	prostate:	n/a
17	chr12:11461798-11461848	LNCaP	prostate:	n/a
18	chr12:11548867-11548917	K562	blood:	n/a
19	chr12:11422920-11422970	NB4	blood:	n/a
20	chr12:11509583-11509633	Jurkat	blood:	n/a
21	chr12:11549192-11549242	GM12891	blood:	n/a
22	chr12:11423020-11423070	HL-60	blood:	n/a
23	chr12:11463937-11463987	HL-60	blood:	n/a
24	chr12:11420895-11420945	CMK	blood:	n/a
25	chr12:11549192-11549242	HNPCEpiC	eye:	n/a
26	chr12:11422897-11422947	Hela-S3	cervix:	n/a
27	chr12:11464607-11464657	BE2_C	brain:	n/a
28	chr12:11420895-11420945	ECC-1	luminal epithelium:	n/a
29	chr12:11461798-11461848	AG04450	lung:	fetal
30	chr12:11423020-11423070	PANC-1	pancreas:	n/a
31	chr12:11461798-11461848	Jurkat	blood:	n/a
32	chr12:11548019-11548069	HEK293	kidney:	embryo
33	chr12:11509583-11509633	NH-A	brain:	n/a
34	chr12:11463937-11463987	NT2-D1	testis:	n/a
35	chr12:11548867-11548917	NB4	blood:	n/a
36	chr12:11548867-11548917	CMK	blood:	n/a
37	chr12:11460710-11460760	GM06990	blood:	n/a
38	chr12:11508049-11508099	K562	blood:	n/a
39	chr12:11463844-11463894	GM12892	blood:	n/a
40	chr12:11422920-11422970	NH-A	brain:	n/a
41	chr12:11464607-11464657	HEEpiC	esophagus:	n/a
42	chr12:11549192-11549242	BJ	skin:	n/a
43	chr12:11464607-11464657	AG04450	lung:	fetal
44	chr12:11548019-11548069	AG04449	skin:	fetal
45	chr12:11463844-11463894	HCPEpiC	choroid plexus:	n/a
46	chr12:11464607-11464657	NHDF-neo	bronchial:	n/a
47	chr12:11422920-11422970	MCF10A-Er-Src	breast:	n/a
48	chr12:11423020-11423070	K562	blood:	n/a
49	chr12:11548019-11548069	SK-N-SH	brain:	n/a
50	chr12:11460710-11460760	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:
2	chr12:11494392..11497234-chr12:11500928..11503308,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB4-2	chr12:11421567-11421602	NONHSAT026934
2	lnc-PRB4-2	chr12:11422540-11422641	NONHSAT026934
3	lnc-PRB4-2	chr12:11420927-11421082	NONHSAT026934
4	lnc-PRB1-1	chr12:11559632-11559826	ENSG00000255790.1
5	lnc-PRB4-1	chr12:11461584-11461816	NONHSAT026935
6	lnc-PRB4-1	chr12:11462305-11462339	NONHSAT026935
7	lnc-PRB4-1	chr12:11461162-11461375	NONHSAT026935
8	lnc-PRB4-2	chr12:11420109-11420359	NONHSAT026934
9	lnc-PRB4-2	chr12:11418890-11418962	NONHSAT026934
10	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1
11	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
12	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1
13	lnc-PRB4-1	chr12:11463270-11463369	NONHSAT026935

No data

Variant related genes	Relation type
PRB4	TF binding region
PRB2	TF binding region
PRB1	TF binding region
PRB3	TF binding region
PRB4	CpG island
PRB2	CpG island
PRB1	CpG island
PRB3	CpG island

Extended variants
information (count: 5217 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:5217 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74060726	chr12:11418179-11418180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7308141	chr12:11418261-11418262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs538751636	chr12:11418284-11418285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367916988	chr12:11418347-11418348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572331777	chr12:11418374-11418375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111623572	chr12:11418377-11418378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554464139	chr12:11418402-11418403	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs549610771	chr12:11418410-11418411	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs75082046	chr12:11418436-11418437	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs374378403	chr12:11418466-11418467	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs543222210	chr12:11418519-11418520	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs563133545	chr12:11418595-11418596	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs576900432	chr12:11418614-11418615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367868115	chr12:11418648-11418649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545565437	chr12:11418713-11418714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559367470	chr12:11418757-11418758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372161978	chr12:11418798-11418799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528097070	chr12:11418801-11418802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548163186	chr12:11418855-11418856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7294995	chr12:11418867-11418868	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs1896551	chr12:11418954-11418955	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550442284	chr12:11419076-11419077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570237344	chr12:11419129-11419130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539155638	chr12:11419135-11419136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552404180	chr12:11419186-11419187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566135917	chr12:11419202-11419203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534709899	chr12:11419209-11419210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148565362	chr12:11419241-11419242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574432714	chr12:11419270-11419271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536926539	chr12:11419357-11419358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35642250	chr12:11419374-11419375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555610826	chr12:11419376-11419377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145623091	chr12:11419377-11419378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576981689	chr12:11419386-11419387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73270219	chr12:11419403-11419404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs559187942	chr12:11419570-11419571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572857300	chr12:11419598-11419599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541890825	chr12:11419627-11419628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561666650	chr12:11419673-11419674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191856770	chr12:11419678-11419679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11054200	chr12:11419757-11419758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs117399726	chr12:11419779-11419780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532617149	chr12:11419827-11419828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372445901	chr12:11419856-11419857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552691373	chr12:11419868-11419869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566048985	chr12:11419883-11419884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4763658	chr12:11419894-11419895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111996663	chr12:11419915-11419916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528555046	chr12:11419981-11419982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548223450	chr12:11420000-11420001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Mental retardation	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	20531469	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11407400-11440200	Weak transcription	Primary T cells from cord blood	blood
2	chr12:11418400-11418600	Bivalent Enhancer	HUVEC	blood vessel
3	chr12:11418600-11419200	Enhancers	HUVEC	blood vessel
4	chr12:11420200-11420400	ZNF genes & repeats	Pancreas	Pancrea
5	chr12:11420400-11423000	Weak transcription	Pancreas	Pancrea
6	chr12:11422400-11422600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:11423000-11423200	ZNF genes & repeats	Pancreas	Pancrea
8	chr12:11424400-11425000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:11425000-11432400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:11426200-11427000	Enhancers	HMEC	breast
11	chr12:11429800-11433800	Weak transcription	Liver	Liver
12	chr12:11430600-11433200	Weak transcription	Left Ventricle	heart
13	chr12:11431000-11431200	Active TSS	Adipose Nuclei	Adipose
14	chr12:11431000-11433200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr12:11431200-11433400	Weak transcription	Adipose Nuclei	Adipose
16	chr12:11432400-11433000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:11433400-11434000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr12:11433400-11434200	Strong transcription	Adipose Nuclei	Adipose
19	chr12:11433800-11434000	ZNF genes & repeats	Liver	Liver
20	chr12:11434200-11434400	ZNF genes & repeats	Adipose Nuclei	Adipose
21	chr12:11449800-11450600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
22	chr12:11450200-11450600	Enhancers	Stomach Mucosa	stomach
23	chr12:11450200-11450800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
24	chr12:11450200-11450800	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr12:11450200-11450800	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr12:11450200-11450800	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr12:11450400-11450800	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr12:11450400-11450800	Active TSS	Rectal Mucosa Donor 31	rectum
29	chr12:11460200-11460800	Enhancers	HUVEC	blood vessel
30	chr12:11461200-11462200	Enhancers	Spleen	Spleen
31	chr12:11467000-11467200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:11473600-11475800	Enhancers	Fetal Heart	heart
33	chr12:11474600-11475000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:11475400-11478200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr12:11478200-11479200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr12:11478800-11479400	Enhancers	HMEC	breast
37	chr12:11479000-11479200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:11479200-11480200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr12:11479200-11493000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:11486800-11487000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:11493000-11493200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:11493000-11493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:11493000-11494200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:11494200-11496400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:11496600-11496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:11496800-11499400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr12:11497200-11497800	Enhancers	HepG2	liver
48	chr12:11497800-11498600	Enhancers	Fetal Intestine Small	intestine
49	chr12:11498200-11498600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr12:11504000-11505000	Enhancers	HUVEC	blood vessel

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