Variant report

Variant	esv1807901
Chromosome Location	chr12:11214927-11246351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:244)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 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	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
5	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
6	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
7	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
8	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
11	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
12	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
15	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
16	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
17	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
18	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
19	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
20	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
21	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
22	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
23	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
24	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
25	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
26	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
27	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
28	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a
29	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
30	FOXA2	chr12:11223617-11224724	HepG2	liver:	n/a	n/a
31	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a
32	GATA3	chr12:11221936-11222225	MCF-7	breast:	n/a	n/a
33	HDAC2	chr12:11223990-11224345	HepG2	liver:	n/a	n/a
34	IKZF1	chr12:11238336-11238561	GM12878	blood:	n/a	n/a
35	JUND	chr12:11224111-11224296	HepG2	liver:	n/a	n/a
36	KAP1	chr12:11233595-11233844	HEK293	kidney:	n/a	n/a
37	MAFF	chr12:11234615-11234942	HepG2	liver:	n/a	n/a
38	MAFK	chr12:11234630-11234922	HepG2	liver:	n/a	chr12:11234789-11234806
39	MAFK	chr12:11234655-11234917	H1-hESC	embryonic stem cell:	n/a	chr12:11234789-11234806
40	MAFK	chr12:11234617-11234968	IMR90	lung:	n/a	chr12:11234789-11234806
41	MAFK	chr12:11234616-11234980	HepG2	liver:	n/a	chr12:11234789-11234806
42	MAFK	chr12:11220562-11220586	HepG2	liver:	n/a	n/a
43	MAFK	chr12:11230418-11230581	HepG2	liver:	n/a	chr12:11230570-11230581 chr12:11230528-11230539 chr12:11230527-11230538 chr12:11230527-11230538 chr12:11230570-11230581
44	MXI1	chr12:11238156-11238251	GM12878	blood:	n/a	n/a
45	MYC	chr12:11226626-11226646	H1-hESC	embryonic stem cell:	n/a	n/a
46	NANOG	chr12:11224022-11224335	H1-hESC	embryonic stem cell:	n/a	n/a
47	NFATC1	chr12:11237942-11238414	GM12878	blood:	n/a	n/a
48	NFATC1	chr12:11238014-11238349	GM12878	blood:	n/a	n/a
49	NFIC	chr12:11220110-11220596	ECC-1	luminal epithelium:	n/a	n/a
50	NFIC	chr12:11228182-11228652	GM12878	blood:	n/a	chr12:11228325-11228341

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244899-11244949	Hela-S3	cervix:	n/a
2	chr12:11244939-11244989	HCT-116	colon:	n/a
3	chr12:11215083-11215133	ProgFib	skin:	n/a
4	chr12:11244939-11244989	GM12891	blood:	n/a
5	chr12:11244899-11244949	RPTEC	kidney:	n/a
6	chr12:11244899-11244949	GM06990	blood:	n/a
7	chr12:11244939-11244989	GM12878	blood:	n/a
8	chr12:11244939-11244989	HRPEpiC	eye:	n/a
9	chr12:11215083-11215133	RPTEC	kidney:	n/a
10	chr12:11244939-11244989	AoSMC	blood vessel:	n/a
11	chr12:11244899-11244949	K562	blood:	n/a
12	chr12:11216351-11216401	SKMC	muscle:	n/a
13	chr12:11215083-11215133	GM12891	blood:	n/a
14	chr12:11244899-11244949	PANC-1	pancreas:	n/a
15	chr12:11215083-11215133	BJ	skin:	n/a
16	chr12:11216351-11216401	SK-N-SH	brain:	n/a
17	chr12:11244899-11244949	BE2_C	brain:	n/a
18	chr12:11244939-11244989	HCM	heart:	n/a
19	chr12:11244939-11244989	AG09309	skin:	n/a
20	chr12:11216351-11216401	HIPEpiC	eye:	n/a
21	chr12:11244899-11244949	AG09309	skin:	n/a
22	chr12:11244939-11244989	SK-N-SH_RA	brain:	n/a
23	chr12:11244899-11244949	HepG2	liver:	n/a
24	chr12:11216351-11216401	RPTEC	kidney:	n/a
25	chr12:11215083-11215133	AG04450	lung:	fetal
26	chr12:11216351-11216401	BJ	skin:	n/a
27	chr12:11215083-11215133	NH-A	brain:	n/a
28	chr12:11216351-11216401	HCPEpiC	choroid plexus:	n/a
29	chr12:11216351-11216401	Jurkat	blood:	n/a
30	chr12:11216351-11216401	A549	lung:	n/a
31	chr12:11244939-11244989	AG04450	lung:	fetal
32	chr12:11244899-11244949	SK-N-SH_RA	brain:	n/a
33	chr12:11244899-11244949	MCF-7	breast:	n/a
34	chr12:11244899-11244949	HCM	heart:	n/a
35	chr12:11215083-11215133	GM12878	blood:	n/a
36	chr12:11244939-11244989	IMR90	lung:	fetal
37	chr12:11215083-11215133	HCPEpiC	choroid plexus:	n/a
38	chr12:11244939-11244989	Hepatocyte	liver:	n/a
39	chr12:11215083-11215133	HRE	kidney:	n/a
40	chr12:11215083-11215133	NHDF-neo	bronchial:	n/a
41	chr12:11215083-11215133	AG09309	skin:	n/a
42	chr12:11216351-11216401	NB4	blood:	n/a
43	chr12:11244939-11244989	NHDF-neo	bronchial:	n/a
44	chr12:11244899-11244949	Caco-2	colon:	n/a
45	chr12:11215083-11215133	HEEpiC	esophagus:	n/a
46	chr12:11216351-11216401	HCT-116	colon:	n/a
47	chr12:11244899-11244949	LNCaP	prostate:	n/a
48	chr12:11244899-11244949	ECC-1	luminal epithelium:	n/a
49	chr12:11216351-11216401	HEEpiC	esophagus:	n/a
50	chr12:11244939-11244989	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:

(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
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 2071 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2071 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562139680	chr12:11214935-11214936	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs531135797	chr12:11214950-11214951	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs550844931	chr12:11214978-11214979	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571038261	chr12:11215028-11215029	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs2708379	chr12:11215029-11215030	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547076441	chr12:11215032-11215033	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs61912070	chr12:11215033-11215034	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs2708378	chr12:11215038-11215039	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs555844914	chr12:11215046-11215047	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575687873	chr12:11215049-11215050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538178368	chr12:11215054-11215055	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112424719	chr12:11215095-11215096	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs376279027	chr12:11215106-11215107	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs557734193	chr12:11215120-11215121	Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs113332226	chr12:11215221-11215222	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs544303122	chr12:11215233-11215234	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs546920270	chr12:11215252-11215253	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs566298532	chr12:11215280-11215281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545691607	chr12:11215497-11215498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540012326	chr12:11215506-11215507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368964857	chr12:11215513-11215514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560285720	chr12:11215514-11215515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573447839	chr12:11215537-11215538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542291302	chr12:11215568-11215569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111922081	chr12:11215569-11215570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189199057	chr12:11215616-11215617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371890701	chr12:11215638-11215639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551276437	chr12:11215688-11215689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1817043	chr12:11215852-11215853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs549066598	chr12:11215934-11215935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568996137	chr12:11215983-11215984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533584415	chr12:11215994-11215995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532994669	chr12:11216004-11216005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546920851	chr12:11216010-11216011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144798488	chr12:11216089-11216090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183284198	chr12:11216119-11216120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187580936	chr12:11216136-11216137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199881531	chr12:11216148-11216149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569290779	chr12:11216241-11216242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538195240	chr12:11216255-11216256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2708377	chr12:11216315-11216316	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
42	rs571491251	chr12:11216341-11216342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534091284	chr12:11216357-11216358	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs374749624	chr12:11216359-11216360	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs111319462	chr12:11216369-11216370	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs117327261	chr12:11216437-11216438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542328304	chr12:11216440-11216441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555809722	chr12:11216452-11216453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575637856	chr12:11216456-11216457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192004413	chr12:11216506-11216507	Weak transcription	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:197 , 50 per page) page: 1 2 3 4

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	chr12:11199800-11222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr12:11201600-11227800	Weak transcription	HSMM	muscle
13	chr12:11203600-11216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:11203600-11240000	Weak transcription	Ovary	ovary
15	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:11204600-11224000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:11204600-11227600	Weak transcription	Fetal Lung	lung
18	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr12:11205800-11218200	Weak transcription	Primary B cells from cord blood	blood
20	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:11206000-11221600	Weak transcription	Fetal Muscle Leg	muscle
22	chr12:11207000-11223000	Weak transcription	HepG2	liver
23	chr12:11207000-11224200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:11208600-11218400	Weak transcription	Primary T cells from cord blood	blood
25	chr12:11208600-11228000	Weak transcription	Dnd41	blood
26	chr12:11208600-11232400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:11211600-11227800	Weak transcription	Aorta	Aorta
29	chr12:11211800-11223000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr12:11211800-11225000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr12:11212000-11217400	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr12:11212000-11225600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:11212600-11224200	Weak transcription	Brain Angular Gyrus	brain
34	chr12:11212600-11224200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr12:11212600-11234400	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr12:11214200-11220200	Weak transcription	Small Intestine	intestine
37	chr12:11214600-11215000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:11214600-11222200	Weak transcription	Brain Substantia Nigra	brain
39	chr12:11214600-11225400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:11215000-11215400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr12:11216400-11228000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:11217200-11218200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:11217400-11217600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr12:11217600-11226400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr12:11218200-11256800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:11218400-11222200	Weak transcription	Primary B cells from peripheral blood	blood
47	chr12:11218600-11226600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:11219200-11225400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:11220000-11220200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr12:11220200-11220400	Enhancers	Gastric	stomach

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