Variant report

Variant	nsv528556
Chromosome Location	chr12:21664879-21680363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:122)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:122 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr12:21678978-21679210	K562	blood:	n/a	n/a
2	BACH1	chr12:21674625-21674693	K562	blood:	n/a	n/a
3	CCNT2	chr12:21674469-21674678	K562	blood:	n/a	n/a
4	CEBPB	chr12:21678916-21679400	A549	lung:	n/a	chr12:21679146-21679157
5	CEBPB	chr12:21678952-21679350	A549	lung:	n/a	chr12:21679146-21679157
6	CEBPB	chr12:21679034-21679406	MCF-7	breast:	n/a	chr12:21679146-21679157
7	CEBPB	chr12:21678928-21679487	HCT-116	colon:	n/a	chr12:21679146-21679157
8	CEBPB	chr12:21678984-21679313	H1-hESC	embryonic stem cell:	n/a	chr12:21679146-21679157
9	CEBPB	chr12:21676115-21676449	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:21678873-21679461	A549	lung:	n/a	chr12:21679146-21679157
11	CEBPB	chr12:21678966-21679339	Hela-S3	cervix:	n/a	chr12:21679146-21679157
12	CEBPB	chr12:21678962-21679321	K562	blood:	n/a	chr12:21679146-21679157
13	CEBPB	chr12:21678967-21679310	IMR90	lung:	n/a	chr12:21679146-21679157
14	CEBPB	chr12:21678974-21679293	ECC-1	luminal epithelium:	n/a	chr12:21679146-21679157
15	CEBPB	chr12:21679036-21679285	K562	blood:	n/a	chr12:21679146-21679157
16	CEBPB	chr12:21679071-21679242	K562	blood:	n/a	chr12:21679146-21679157
17	CEBPB	chr12:21679058-21679180	HepG2	liver:	n/a	chr12:21679146-21679157
18	CEBPB	chr12:21678961-21679327	HepG2	liver:	n/a	chr12:21679146-21679157
19	CTBP2	chr12:21680322-21681135	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr12:21680200-21680350	HCPEpiC	choroid plexus:	n/a	n/a
21	CUX1	chr12:21678796-21679127	K562	blood:	n/a	n/a
22	E2F4	chr12:21679107-21679279	MCF10A-Er-Src	breast:	n/a	n/a
23	EP300	chr12:21679096-21679287	K562	blood:	n/a	chr12:21679143-21679157
24	EP300	chr12:21678987-21679289	HepG2	liver:	n/a	chr12:21679143-21679157
25	FOS	chr12:21668327-21668632	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr12:21668303-21668643	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr12:21679921-21680266	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:21678965-21679330	MCF10A-Er-Src	breast:	n/a	chr12:21679120-21679132
29	FOS	chr12:21678949-21679581	MCF10A-Er-Src	breast:	n/a	chr12:21679120-21679132 chr12:21679482-21679494
30	FOS	chr12:21678930-21679371	MCF10A-Er-Src	breast:	n/a	chr12:21679120-21679132
31	FOS	chr12:21678960-21679428	MCF10A-Er-Src	breast:	n/a	chr12:21679120-21679132
32	FOSL2	chr12:21678869-21679374	A549	lung:	n/a	chr12:21679120-21679132
33	FOXA1	chr12:21679744-21679939	ECC-1	luminal epithelium:	n/a	n/a
34	FOXA2	chr12:21679039-21679367	A549	lung:	n/a	n/a
35	FOXA2	chr12:21667604-21668006	A549	lung:	n/a	chr12:21667975-21667987
36	GATA3	chr12:21679043-21679272	T-47D	breast:	n/a	n/a
37	GTF2F1	chr12:21680210-21680365	H1-hESC	embryonic stem cell:	n/a	n/a
38	HNF4A	chr12:21676093-21676399	HepG2	liver:	n/a	chr12:21676265-21676280
39	HNF4A	chr12:21676093-21676376	HepG2	liver:	n/a	chr12:21676265-21676280
40	IRF1	chr12:21666973-21667001	K562	blood:	n/a	n/a
41	JUN	chr12:21678985-21679317	HepG2	liver:	n/a	chr12:21679143-21679156 chr12:21679120-21679132
42	JUND	chr12:21678983-21679307	HepG2	liver:	n/a	chr12:21679120-21679132
43	JUND	chr12:21678966-21679326	K562	blood:	n/a	chr12:21679120-21679132
44	MAFF	chr12:21667015-21667016	HepG2	liver:	n/a	n/a
45	MAFF	chr12:21678989-21679295	HepG2	liver:	n/a	chr12:21679113-21679131
46	MAFK	chr12:21668021-21668077	HepG2	liver:	n/a	n/a
47	MAFK	chr12:21666867-21667129	HepG2	liver:	n/a	n/a
48	MAFK	chr12:21676834-21676933	HepG2	liver:	n/a	n/a
49	MAFK	chr12:21676183-21676454	HepG2	liver:	n/a	n/a
50	MAFK	chr12:21679041-21679202	HepG2	liver:	n/a	chr12:21679115-21679126

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21678044-21678094	PANC-1	pancreas:	n/a
2	chr12:21679634-21679684	Hepatocyte	liver:	n/a
3	chr12:21678044-21678094	HCM	heart:	n/a
4	chr12:21678386-21678436	HNPCEpiC	eye:	n/a
5	chr12:21670234-21670284	HRCEpiC	kidney:	n/a
6	chr12:21670234-21670284	Hepatocyte	liver:	n/a
7	chr12:21680220-21680270	SAEC	small airway:	n/a
8	chr12:21670234-21670284	IMR90	lung:	fetal
9	chr12:21680220-21680270	GM12892	blood:	n/a
10	chr12:21680220-21680270	CMK	blood:	n/a
11	chr12:21678386-21678436	GM12878	blood:	n/a
12	chr12:21670234-21670284	NB4	blood:	n/a
13	chr12:21678386-21678436	HIPEpiC	eye:	n/a
14	chr12:21678044-21678094	AG09319	gingival:	n/a
15	chr12:21680220-21680270	HCT-116	colon:	n/a
16	chr12:21678386-21678436	AG04449	skin:	fetal
17	chr12:21670234-21670284	K562	blood:	n/a
18	chr12:21680220-21680270	H1-hESC	embryonic stem cell:	embryo
19	chr12:21670234-21670284	MCF-7	breast:	n/a
20	chr12:21679634-21679684	ECC-1	luminal epithelium:	n/a
21	chr12:21670234-21670284	RPTEC	kidney:	n/a
22	chr12:21679634-21679684	ovcar-3	ovarian:	n/a
23	chr12:21670234-21670284	HCT-116	colon:	n/a
24	chr12:21678044-21678094	HepG2	liver:	n/a
25	chr12:21670234-21670284	HNPCEpiC	eye:	n/a
26	chr12:21670234-21670284	A549	lung:	n/a
27	chr12:21678044-21678094	GM06990	blood:	n/a
28	chr12:21678044-21678094	PrEC	prostate:	n/a
29	chr12:21678386-21678436	IMR90	lung:	fetal
30	chr12:21680220-21680270	AG10803	skin:	n/a
31	chr12:21670234-21670284	AG04449	skin:	fetal
32	chr12:21670234-21670284	U87	brain:	n/a
33	chr12:21679634-21679684	PFSK-1	brain:	n/a
34	chr12:21680220-21680270	HCPEpiC	choroid plexus:	n/a
35	chr12:21679634-21679684	Hela-S3	cervix:	n/a
36	chr12:21679634-21679684	BJ	skin:	n/a
37	chr12:21678386-21678436	AG04450	lung:	fetal
38	chr12:21678044-21678094	HMEC	breast:	n/a
39	chr12:21678044-21678094	SK-N-SH	brain:	n/a
40	chr12:21678044-21678094	SK-N-SH_RA	brain:	n/a
41	chr12:21678386-21678436	CMK	blood:	n/a
42	chr12:21670234-21670284	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:21679634-21679684	RPTEC	kidney:	n/a
44	chr12:21679634-21679684	HMEC	breast:	n/a
45	chr12:21679634-21679684	IMR90	lung:	fetal
46	chr12:21678386-21678436	AG09319	gingival:	n/a
47	chr12:21670234-21670284	NHDF-neo	bronchial:	n/a
48	chr12:21678044-21678094	LNCaP	prostate:	n/a
49	chr12:21670234-21670284	NT2-D1	testis:	n/a
50	chr12:21678386-21678436	HEK293	kidney:	embryo

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21666099..21668505-chr12:21668536..21671439,2	K562	blood:
2	chr12:21667585..21669254-chr12:21672387..21674128,2	K562	blood:
3	chr12:21659539..21661221-chr12:21663545..21665442,3	K562	blood:
4	chr12:21655984..21659478-chr12:21666041..21668591,3	K562	blood:
5	chr12:21667585..21669254-chr12:21672387..21674128,2	K562	blood:
6	chr12:21653310..21655607-chr12:21663313..21666443,3	K562	blood:
7	chr12:21666099..21668505-chr12:21668536..21671439,2	K562	blood:
8	chr12:21659626..21662190-chr12:21669299..21671528,2	K562	blood:
9	chr12:21654128..21656631-chr12:21667062..21669279,3	MCF-7	breast:
10	chr12:21671832..21674785-chr12:21687913..21690095,2	K562	blood:
11	chr12:21652497..21655022-chr12:21664755..21666261,2	K562	blood:
12	chr12:21654473..21659052-chr12:21670057..21674835,6	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	GOLT1B	hsa-miR-155-5p	chr12:21669700-21669724
2	GOLT1B	hsa-miR-16-5p	chr12:21670993-21670999
3	GOLT1B	hsa-miR-103a-3p	chr12:21670976-21670999
4	GOLT1B	hsa-let-7d-5p	chr12:21670278-21670285
5	GOLT1B	hsa-miR-16-5p	chr12:21670982-21671000
6	GOLT1B	hsa-miR-155-5p	chr12:21670582-21670603
7	GOLT1B	hsa-let-7d-5p	chr12:21670264-21670285

Variant related genes	Relation type
C12orf39	TF binding region
C12orf39	CpG island
ENSG00000004700	chromatin interactions
ENSG00000111711	chromatin interactions

Extended variants
information (count: 579 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4762836	chr12:21664879-21664880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138996858	chr12:21664900-21664901	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs79323558	chr12:21664903-21664904	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373635776	chr12:21664947-21664948	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553115753	chr12:21664949-21664950	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531926201	chr12:21664976-21664977	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143007141	chr12:21665008-21665009	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs147470526	chr12:21665012-21665013	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140026680	chr12:21665061-21665062	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530332709	chr12:21665070-21665071	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547318702	chr12:21665080-21665081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs73079372	chr12:21665099-21665100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs532171011	chr12:21665122-21665123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187208127	chr12:21665149-21665150	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191723773	chr12:21665160-21665161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537906877	chr12:21665164-21665165	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs367645524	chr12:21665195-21665196	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371357146	chr12:21665200-21665201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs61926342	chr12:21665207-21665208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560873124	chr12:21665221-21665222	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144443367	chr12:21665244-21665245	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs34378602	chr12:21665245-21665246	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148439968	chr12:21665247-21665248	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372300868	chr12:21665256-21665257	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs199629012	chr12:21665286-21665287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs74067037	chr12:21665309-21665310	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs367921697	chr12:21665339-21665340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201364607	chr12:21665347-21665348	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs540854991	chr12:21665364-21665365	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs575342498	chr12:21665417-21665418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544249886	chr12:21665418-21665419	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561224710	chr12:21665488-21665489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530361547	chr12:21665507-21665508	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs374616136	chr12:21665528-21665529	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs139088027	chr12:21665572-21665573	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547639520	chr12:21665574-21665575	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373992836	chr12:21665576-21665577	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540457641	chr12:21665588-21665589	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560871483	chr12:21665637-21665638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187771833	chr12:21665669-21665670	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs552217823	chr12:21665676-21665677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs59102994	chr12:21665681-21665682	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113679773	chr12:21665756-21665757	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531437642	chr12:21665783-21665784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs570595077	chr12:21665804-21665805	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs568046354	chr12:21665808-21665809	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs7135694	chr12:21665877-21665878	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs547246367	chr12:21665893-21665894	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs565216989	chr12:21665917-21665918	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539305401	chr12:21665931-21665932	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21655400-21674800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:21655600-21666000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr12:21656000-21671800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:21656000-21672800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr12:21656000-21674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:21656000-21674600	Weak transcription	Fetal Kidney	kidney
7	chr12:21656200-21665000	Weak transcription	HSMMtube	muscle
8	chr12:21656200-21665200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr12:21656200-21665600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr12:21656200-21666200	Weak transcription	Colonic Mucosa	Colon
11	chr12:21656200-21669800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:21656200-21671800	Weak transcription	Thymus	Thymus
13	chr12:21656200-21680000	Weak transcription	Right Ventricle	heart
14	chr12:21656400-21668000	Weak transcription	Fetal Lung	lung
15	chr12:21656400-21680200	Weak transcription	Aorta	Aorta
16	chr12:21656600-21665200	Weak transcription	NHEK	skin
17	chr12:21656600-21665400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:21656600-21665800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr12:21656600-21669200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:21656800-21665800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr12:21656800-21666000	Weak transcription	Colon Smooth Muscle	Colon
22	chr12:21656800-21666600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr12:21656800-21671400	Weak transcription	Fetal Heart	heart
24	chr12:21656800-21680000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:21657400-21665800	Weak transcription	Brain Hippocampus Middle	brain
26	chr12:21657400-21669800	Weak transcription	Brain Substantia Nigra	brain
27	chr12:21657400-21680000	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr12:21657600-21665600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:21657600-21665800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr12:21657600-21665800	Weak transcription	Esophagus	oesophagus
31	chr12:21657600-21665800	Weak transcription	Lung	lung
32	chr12:21657600-21665800	Weak transcription	Ovary	ovary
33	chr12:21657600-21666400	Weak transcription	Psoas Muscle	Psoas
34	chr12:21657600-21666400	Weak transcription	Spleen	Spleen
35	chr12:21657600-21669600	Weak transcription	Brain Angular Gyrus	brain
36	chr12:21657600-21675000	Weak transcription	Small Intestine	intestine
37	chr12:21657600-21675400	Weak transcription	Fetal Brain Male	brain
38	chr12:21657600-21679800	Weak transcription	Pancreas	Pancrea
39	chr12:21657600-21680000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:21657600-21680400	Weak transcription	Gastric	stomach
41	chr12:21658000-21665600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr12:21658600-21666400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr12:21660000-21669400	Strong transcription	Placenta	Placenta
44	chr12:21660000-21670400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr12:21660000-21671600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:21660000-21672000	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr12:21660200-21671600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:21660200-21672600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:21660400-21671600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr12:21660400-21672200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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