Variant report

Variant	esv1804419
Chromosome Location	chr12:11103505-11149830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:367)
Chromatin interactive
region (count:1)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:11134883-11135228	GM12878	blood:	n/a	n/a
2	BATF	chr12:11134866-11135249	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:11134926-11135203	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:11135657-11135714	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:11148042-11148079	K562	blood:	n/a	n/a
6	CEBPB	chr12:11121449-11121832	IMR90	lung:	n/a	chr12:11121638-11121649
7	CEBPB	chr12:11121545-11121715	A549	lung:	n/a	chr12:11121638-11121649
8	CEBPB	chr12:11107460-11107606	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:11121480-11121817	ECC-1	luminal epithelium:	n/a	chr12:11121638-11121649
10	CEBPB	chr12:11122383-11122390	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:11121485-11121799	Hela-S3	cervix:	n/a	chr12:11121638-11121649
12	CEBPB	chr12:11121480-11121758	HepG2	liver:	n/a	chr12:11121638-11121649
13	CTCF	chr12:11107000-11107150	GM12875	blood:	n/a	n/a
14	CTCF	chr12:11112478-11112661	HepG2	liver:	n/a	n/a
15	CTCF	chr12:11112520-11112670	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr12:11112520-11112670	HCM	heart:	n/a	n/a
17	CTCF	chr12:11112509-11112629	HepG2	liver:	n/a	n/a
18	CTCF	chr12:11119020-11119170	A549	lung:	n/a	n/a
19	CTCF	chr12:11112500-11112650	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr12:11112500-11112650	HepG2	liver:	n/a	n/a
21	CTCF	chr12:11112580-11112730	RPTEC	kidney:	n/a	n/a
22	CTCF	chr12:11112540-11112690	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr12:11112482-11112636	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr12:11112440-11112590	HMF	breast:	n/a	n/a
25	CTCF	chr12:11112387-11112746	GM12878	blood:	n/a	n/a
26	CTCF	chr12:11112480-11112630	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr12:11112447-11112778	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11112544-11112636	NHEK	skin:	n/a	n/a
29	CTCF	chr12:11147020-11147170	GM12869	blood:	n/a	n/a
30	CTCF	chr12:11112556-11112633	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr12:11112564-11112604	K562	blood:	n/a	n/a
32	CTCF	chr12:11112480-11112630	GM12873	blood:	n/a	n/a
33	CTCF	chr12:11112460-11112610	AG09319	gingival:	n/a	n/a
34	CTCF	chr12:11112480-11112630	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr12:11112420-11112570	HMF	breast:	n/a	n/a
36	CTCF	chr12:11112560-11112710	Caco-2	colon:	n/a	n/a
37	CTCF	chr12:11112561-11112637	GM19239	blood:	n/a	n/a
38	CTCF	chr12:11112420-11112570	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr12:11112470-11112662	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:11112500-11112650	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr12:11112460-11112610	HPF	lung:	n/a	n/a
42	CTCF	chr12:11112500-11112650	NHLF	lung:	n/a	n/a
43	CTCF	chr12:11112538-11112598	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr12:11112440-11112590	AG09319	gingival:	n/a	n/a
45	CTCF	chr12:11112420-11112570	BE2_C	brain:	n/a	n/a
46	CTCF	chr12:11112480-11112630	HAc	cerebellar:	n/a	n/a
47	CTCF	chr12:11112520-11112670	HPF	lung:	n/a	n/a
48	CTCF	chr12:11131072-11131138	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:11112480-11112630	BE2_C	brain:	n/a	n/a
50	CTCF	chr12:11112504-11112638	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11140560-11140610	CMK	blood:	n/a
2	chr12:11140560-11140610	CMK	blood:	n/a
3	chr12:11139304-11139354	GM12891	blood:	n/a
4	chr12:11139962-11140012	SK-N-MC	brain:	n/a
5	chr12:11139710-11139760	AG10803	skin:	n/a
6	chr12:11139304-11139354	LNCaP	prostate:	n/a
7	chr12:11139304-11139354	NB4	blood:	n/a
8	chr12:11127185-11127235	ProgFib	skin:	n/a
9	chr12:11139304-11139354	HAEpiC	amniotic membrane:	n/a
10	chr12:11139962-11140012	ovcar-3	ovarian:	n/a
11	chr12:11139962-11140012	RPTEC	kidney:	n/a
12	chr12:11139710-11139760	ECC-1	luminal epithelium:	n/a
13	chr12:11139962-11140012	AG04449	skin:	fetal
14	chr12:11139962-11140012	BJ	skin:	n/a
15	chr12:11139710-11139760	HMEC	breast:	n/a
16	chr12:11139304-11139354	HRE	kidney:	n/a
17	chr12:11139962-11140012	HCT-116	colon:	n/a
18	chr12:11149362-11149412	ovcar-3	ovarian:	n/a
19	chr12:11149362-11149412	H1-hESC	embryonic stem cell:	embryo
20	chr12:11139962-11140012	Hela-S3	cervix:	n/a
21	chr12:11127185-11127235	PFSK-1	brain:	n/a
22	chr12:11140560-11140610	SKMC	muscle:	n/a
23	chr12:11139962-11140012	CMK	blood:	n/a
24	chr12:11127185-11127235	NT2-D1	testis:	n/a
25	chr12:11140560-11140610	PFSK-1	brain:	n/a
26	chr12:11149362-11149412	SAEC	small airway:	n/a
27	chr12:11149362-11149412	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:11149362-11149412	SKMC	muscle:	n/a
29	chr12:11139962-11140012	GM06990	blood:	n/a
30	chr12:11139304-11139354	K562	blood:	n/a
31	chr12:11127185-11127235	HPAEpiC	pulmonary alveolar:	n/a
32	chr12:11127185-11127235	HCF	heart:	n/a
33	chr12:11140560-11140610	GM12878	blood:	n/a
34	chr12:11139962-11140012	SK-N-SH_RA	brain:	n/a
35	chr12:11139304-11139354	NT2-D1	testis:	n/a
36	chr12:11140560-11140610	SAEC	small airway:	n/a
37	chr12:11149362-11149412	PrEC	prostate:	n/a
38	chr12:11127185-11127235	MCF10A-Er-Src	breast:	n/a
39	chr12:11139710-11139760	HCM	heart:	n/a
40	chr12:11140560-11140610	HAEpiC	amniotic membrane:	n/a
41	chr12:11139962-11140012	AG09319	gingival:	n/a
42	chr12:11139710-11139760	ovcar-3	ovarian:	n/a
43	chr12:11127185-11127235	A549	lung:	n/a
44	chr12:11127185-11127235	HCT-116	colon:	n/a
45	chr12:11149362-11149412	Hela-S3	cervix:	n/a
46	chr12:11140560-11140610	HepG2	liver:	n/a
47	chr12:11149362-11149412	AG09319	gingival:	n/a
48	chr12:11139304-11139354	PANC-1	pancreas:	n/a
49	chr12:11140560-11140610	Hela-S3	cervix:	n/a
50	chr12:11139962-11140012	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11111049..11113421-chr12:11322867..11324787,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11126254-11126305	NONHSAT026910
2	lnc-PRH1-1	chr12:11126254-11126320	NR_037918
3	lnc-PRH1-1	chr12:11125883-11126320	NONHSAT026914
4	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026912
5	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026908
6	lnc-TAS2R50-1	chr12:11117024-11117951	NONHSAT026913
7	lnc-PRH1-1	chr12:11126254-11126320	NONHSAT026907

No data

Variant related genes	Relation type
TAS2R15	TF binding region
TAS2R50	TF binding region
PRR4	TF binding region
TAS2R15	CpG island
TAS2R50	CpG island
PRR4	CpG island
ENSG00000111215	chromatin interactions
ENSG00000256712	chromatin interactions
ENSG00000212127	chromatin interactions
ENSG00000256537	chromatin interactions

Extended variants
information (count: 1746 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2418224	chr12:11103588-11103589	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140447337	chr12:11103622-11103623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565821470	chr12:11103646-11103647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188645020	chr12:11103662-11103663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116833044	chr12:11103680-11103681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568319710	chr12:11103742-11103743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7486983	chr12:11103774-11103775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs116950552	chr12:11103785-11103786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143190125	chr12:11103796-11103797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116605292	chr12:11103852-11103853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193165162	chr12:11103853-11103854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572964234	chr12:11103884-11103885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147520072	chr12:11103928-11103929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561768466	chr12:11103943-11103944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548567806	chr12:11103953-11103954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566545538	chr12:11104025-11104026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117717030	chr12:11104033-11104034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534347128	chr12:11104071-11104072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115516855	chr12:11104087-11104088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563808155	chr12:11104088-11104089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532876280	chr12:11104089-11104090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552345496	chr12:11104093-11104094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369998676	chr12:11104105-11104106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184988305	chr12:11104109-11104110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117334312	chr12:11104207-11104208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548239040	chr12:11104224-11104225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114999666	chr12:11104328-11104329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537019624	chr12:11104330-11104331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558402245	chr12:11104356-11104357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140155360	chr12:11104404-11104405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114033618	chr12:11104469-11104470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372064213	chr12:11104499-11104500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539784375	chr12:11104537-11104538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553199915	chr12:11104571-11104572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188453675	chr12:11104585-11104586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79474658	chr12:11104605-11104606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560977992	chr12:11104690-11104691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115714890	chr12:11104723-11104724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116206007	chr12:11104776-11104777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543849686	chr12:11104796-11104797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11054082	chr12:11104810-11104811	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs546043515	chr12:11104841-11104842	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs80316384	chr12:11104853-11104854	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs528624593	chr12:11104884-11104885	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532719052	chr12:11104900-11104901	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs150067964	chr12:11104945-11104946	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs376890681	chr12:11104946-11104947	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs562018079	chr12:11104956-11104957	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs191616205	chr12:11104990-11104991	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs112568456	chr12:11105006-11105007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
small cell lung cancer	20016488	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
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Incontinentia Pigmenti	22033527	CNVD
Recurrent pregnancy loss	19789632	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioma	20126413	CNVD

Chromatin state (count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11095200-11148800	Weak transcription	HepG2	liver
2	chr12:11095600-11114000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:11095600-11121600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:11096000-11113600	Weak transcription	Hela-S3	cervix
5	chr12:11099800-11112000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:11100000-11112600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr12:11100800-11134200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr12:11101400-11104600	Weak transcription	Brain Angular Gyrus	brain
9	chr12:11101800-11105600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:11101800-11110400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:11102000-11105200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:11102000-11105200	Weak transcription	Left Ventricle	heart
13	chr12:11102000-11105200	Weak transcription	Psoas Muscle	Psoas
14	chr12:11102000-11105400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:11102000-11105400	Weak transcription	Primary T cells from cord blood	blood
16	chr12:11102000-11106000	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr12:11102000-11111200	Weak transcription	HMEC	breast
18	chr12:11102000-11114000	Weak transcription	Ovary	ovary
19	chr12:11102000-11114200	Weak transcription	Pancreas	Pancrea
20	chr12:11102000-11121200	Weak transcription	Gastric	stomach
21	chr12:11102000-11122600	Weak transcription	Spleen	Spleen
22	chr12:11102000-11127600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:11102000-11135600	Weak transcription	Aorta	Aorta
24	chr12:11102200-11111200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:11103400-11103800	Enhancers	Brain Substantia Nigra	brain
26	chr12:11103800-11104800	Weak transcription	Brain Substantia Nigra	brain
27	chr12:11104600-11105000	Enhancers	Brain Angular Gyrus	brain
28	chr12:11104600-11105000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr12:11104800-11105000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr12:11104800-11105000	Flanking Active TSS	Brain Substantia Nigra	brain
31	chr12:11104800-11106000	Enhancers	Brain Cingulate Gyrus	brain
32	chr12:11105000-11105400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr12:11105000-11106200	Enhancers	Brain Substantia Nigra	brain
34	chr12:11105200-11105400	Enhancers	Left Ventricle	heart
35	chr12:11105200-11105600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
36	chr12:11105200-11105600	Enhancers	Psoas Muscle	Psoas
37	chr12:11105400-11105600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr12:11105400-11105600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr12:11105400-11105600	Genic enhancers	Left Ventricle	heart
40	chr12:11105400-11105800	Weak transcription	Placenta	Placenta
41	chr12:11105400-11106000	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr12:11105400-11106000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr12:11105600-11105800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr12:11105600-11106000	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr12:11105600-11106400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:11105600-11112600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr12:11105600-11121200	Weak transcription	Left Ventricle	heart
48	chr12:11105600-11121200	Weak transcription	Psoas Muscle	Psoas
49	chr12:11105800-11106200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr12:11106000-11121400	Weak transcription	Skeletal Muscle Male	skeletal muscle

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