Variant report

Variant	esv1805438
Chromosome Location	chr12:11213879-11257793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:246)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
2	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
3	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
4	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
5	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
6	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
7	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
8	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
9	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
10	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
14	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
18	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
19	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
20	CTCF	chr12:11257042-11257094	GM20000	blood:	n/a	n/a
21	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
22	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
23	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
24	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
25	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
26	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
27	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
28	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
29	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
30	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
31	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
32	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
33	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
34	FOXA2	chr12:11223617-11224724	HepG2	liver:	n/a	n/a
35	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
36	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a
37	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a
38	GATA3	chr12:11221936-11222225	MCF-7	breast:	n/a	n/a
39	HDAC2	chr12:11223990-11224345	HepG2	liver:	n/a	n/a
40	IKZF1	chr12:11238336-11238561	GM12878	blood:	n/a	n/a
41	IRF4	chr12:11247559-11247865	GM12878	blood:	n/a	n/a
42	IRF4	chr12:11247411-11247911	GM12878	blood:	n/a	n/a
43	JUND	chr12:11224111-11224296	HepG2	liver:	n/a	n/a
44	KAP1	chr12:11233595-11233844	HEK293	kidney:	n/a	n/a
45	MAFF	chr12:11234615-11234942	HepG2	liver:	n/a	n/a
46	MAFK	chr12:11254181-11254247	HepG2	liver:	n/a	n/a
47	MAFK	chr12:11234630-11234922	HepG2	liver:	n/a	chr12:11234789-11234806
48	MAFK	chr12:11234616-11234980	HepG2	liver:	n/a	chr12:11234789-11234806
49	MAFK	chr12:11230418-11230581	HepG2	liver:	n/a	chr12:11230570-11230581 chr12:11230528-11230539 chr12:11230527-11230538 chr12:11230527-11230538 chr12:11230570-11230581
50	MAFK	chr12:11234617-11234968	IMR90	lung:	n/a	chr12:11234789-11234806

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244939-11244989	NH-A	brain:	n/a
2	chr12:11215083-11215133	MCF-7	breast:	n/a
3	chr12:11244939-11244989	NH-A	brain:	n/a
4	chr12:11215083-11215133	MCF-7	breast:	n/a
5	chr12:11244899-11244949	HEEpiC	esophagus:	n/a
6	chr12:11215083-11215133	GM12878	blood:	n/a
7	chr12:11215083-11215133	PrEC	prostate:	n/a
8	chr12:11216351-11216401	NT2-D1	testis:	n/a
9	chr12:11244939-11244989	SK-N-MC	brain:	n/a
10	chr12:11244899-11244949	HL-60	blood:	n/a
11	chr12:11215083-11215133	GM19239	blood:	n/a
12	chr12:11244899-11244949	NHDF-neo	bronchial:	n/a
13	chr12:11244899-11244949	NH-A	brain:	n/a
14	chr12:11244939-11244989	AG09319	gingival:	n/a
15	chr12:11244899-11244949	K562	blood:	n/a
16	chr12:11244899-11244949	IMR90	lung:	fetal
17	chr12:11244939-11244989	HRCEpiC	kidney:	n/a
18	chr12:11215083-11215133	SK-N-MC	brain:	n/a
19	chr12:11215083-11215133	BJ	skin:	n/a
20	chr12:11244939-11244989	NHBE	bronchial:	n/a
21	chr12:11244899-11244949	BJ	skin:	n/a
22	chr12:11244899-11244949	HRPEpiC	eye:	n/a
23	chr12:11215083-11215133	AG04449	skin:	fetal
24	chr12:11215083-11215133	K562	blood:	n/a
25	chr12:11216351-11216401	HCM	heart:	n/a
26	chr12:11244899-11244949	HIPEpiC	eye:	n/a
27	chr12:11244899-11244949	Jurkat	blood:	n/a
28	chr12:11215083-11215133	T-47D	breast:	n/a
29	chr12:11244899-11244949	MCF10A-Er-Src	breast:	n/a
30	chr12:11244939-11244989	U87	brain:	n/a
31	chr12:11244899-11244949	HepG2	liver:	n/a
32	chr12:11215083-11215133	BE2_C	brain:	n/a
33	chr12:11244939-11244989	GM19239	blood:	n/a
34	chr12:11215083-11215133	Hepatocyte	liver:	n/a
35	chr12:11244899-11244949	HAEpiC	amniotic membrane:	n/a
36	chr12:11215083-11215133	HCPEpiC	choroid plexus:	n/a
37	chr12:11244899-11244949	HRE	kidney:	n/a
38	chr12:11216351-11216401	AG09309	skin:	n/a
39	chr12:11215083-11215133	SK-N-SH	brain:	n/a
40	chr12:11216351-11216401	PrEC	prostate:	n/a
41	chr12:11216351-11216401	Hepatocyte	liver:	n/a
42	chr12:11244939-11244989	RPTEC	kidney:	n/a
43	chr12:11244899-11244949	GM12892	blood:	n/a
44	chr12:11215083-11215133	GM06990	blood:	n/a
45	chr12:11216351-11216401	AG09319	gingival:	n/a
46	chr12:11215083-11215133	PFSK-1	brain:	n/a
47	chr12:11244899-11244949	Hela-S3	cervix:	n/a
48	chr12:11244939-11244989	MCF10A-Er-Src	breast:	n/a
49	chr12:11244939-11244989	SAEC	small airway:	n/a
50	chr12:11216351-11216401	HPAEpiC	pulmonary alveolar:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
2	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
3	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918
2	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056

No data

Variant related genes	Relation type
TAS2R46	TF binding region
ENSG00000256400	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
ENSG00000256400	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 2649 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2649 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532799811	chr12:11213884-11213885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78022839	chr12:11213890-11213891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369943612	chr12:11213895-11213896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546616630	chr12:11213906-11213907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372108541	chr12:11213908-11213909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs137920081	chr12:11213909-11213910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371366678	chr12:11213915-11213916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374109594	chr12:11213921-11213922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554807484	chr12:11213939-11213940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377680929	chr12:11213947-11213948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370643592	chr12:11213949-11213950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185280425	chr12:11213980-11213981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557044065	chr12:11213997-11213998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553647348	chr12:11214009-11214010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368038360	chr12:11214019-11214020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372278369	chr12:11214025-11214026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150894148	chr12:11214032-11214033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139412224	chr12:11214060-11214061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553708509	chr12:11214063-11214064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553357638	chr12:11214073-11214074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200528237	chr12:11214074-11214075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370408044	chr12:11214092-11214093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542162895	chr12:11214095-11214096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561938546	chr12:11214102-11214103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76020872	chr12:11214133-11214134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76147157	chr12:11214137-11214138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376068759	chr12:11214144-11214145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2708381	chr12:11214145-11214146	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs377226761	chr12:11214182-11214183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370059980	chr12:11214191-11214192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371099707	chr12:11214192-11214193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375025784	chr12:11214196-11214197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200812670	chr12:11214199-11214200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2708380	chr12:11214212-11214213	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs200461484	chr12:11214214-11214215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374074547	chr12:11214215-11214216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371448520	chr12:11214228-11214229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375412933	chr12:11214238-11214239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374212046	chr12:11214264-11214265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372334609	chr12:11214269-11214270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377505981	chr12:11214273-11214274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376359978	chr12:11214274-11214275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376020270	chr12:11214299-11214300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369672636	chr12:11214300-11214301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367944505	chr12:11214323-11214324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs371367179	chr12:11214336-11214337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73260771	chr12:11214360-11214361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs377597598	chr12:11214380-11214381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115475128	chr12:11214383-11214384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377411404	chr12:11214384-11214385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel
2	chr12:11171000-11225600	Weak transcription	HSMMtube	muscle
3	chr12:11179000-11223800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:11179400-11222000	Weak transcription	Fetal Kidney	kidney
5	chr12:11181000-11217400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:11181000-11220000	Weak transcription	Gastric	stomach
7	chr12:11181000-11224800	Weak transcription	Fetal Stomach	stomach
8	chr12:11193200-11224200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr12:11196600-11215000	Weak transcription	NHLF	lung
10	chr12:11198000-11230200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr12:11199600-11214200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:11199800-11222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr12:11201600-11227800	Weak transcription	HSMM	muscle
14	chr12:11203600-11216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:11203600-11240000	Weak transcription	Ovary	ovary
16	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:11204600-11224000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:11204600-11227600	Weak transcription	Fetal Lung	lung
19	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr12:11205800-11218200	Weak transcription	Primary B cells from cord blood	blood
21	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:11206000-11221600	Weak transcription	Fetal Muscle Leg	muscle
23	chr12:11207000-11223000	Weak transcription	HepG2	liver
24	chr12:11207000-11224200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:11208400-11214400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr12:11208600-11218400	Weak transcription	Primary T cells from cord blood	blood
27	chr12:11208600-11228000	Weak transcription	Dnd41	blood
28	chr12:11208600-11232400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:11209600-11214200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:11210200-11214000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:11211600-11227800	Weak transcription	Aorta	Aorta
33	chr12:11211800-11223000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr12:11211800-11225000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr12:11212000-11217400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr12:11212000-11225600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:11212400-11214000	Weak transcription	Fetal Heart	heart
38	chr12:11212600-11224200	Weak transcription	Brain Angular Gyrus	brain
39	chr12:11212600-11224200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr12:11212600-11234400	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr12:11212800-11214000	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr12:11213800-11214000	Weak transcription	Small Intestine	intestine
43	chr12:11214000-11214200	Enhancers	Small Intestine	intestine
44	chr12:11214000-11214400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr12:11214000-11214400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr12:11214000-11214400	Enhancers	Fetal Heart	heart
47	chr12:11214000-11214600	Enhancers	Brain Substantia Nigra	brain
48	chr12:11214200-11214400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:11214200-11214600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr12:11214200-11220200	Weak transcription	Small Intestine	intestine

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