Variant report

Variant	nsv546868
Chromosome Location	chr1:98175878-98194845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:98192995-98193291	IMR90	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
2	CEBPB	chr1:98177430-98177801	IMR90	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
3	CEBPB	chr1:98177450-98177788	K562	blood:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
4	CEBPB	chr1:98193045-98193294	HepG2	liver:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
5	CEBPB	chr1:98177429-98177798	HepG2	liver:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
6	CEBPB	chr1:98177451-98177762	Hela-S3	cervix:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
7	CEBPB	chr1:98193010-98193283	A549	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
8	CEBPB	chr1:98177432-98177781	A549	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
9	CEBPB	chr1:98177451-98177785	H1-hESC	embryonic stem cell:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
10	CTCF	chr1:98189752-98189901	GM10248	blood:	n/a	n/a
11	FOS	chr1:98178576-98178863	MCF10A-Er-Src	breast:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
12	FOS	chr1:98191977-98192298	MCF10A-Er-Src	breast:	n/a	chr1:98192101-98192110 chr1:98192155-98192163 chr1:98192155-98192162
13	FOS	chr1:98191976-98192269	MCF10A-Er-Src	breast:	n/a	chr1:98192101-98192110 chr1:98192155-98192163 chr1:98192155-98192162
14	FOS	chr1:98178568-98178852	MCF10A-Er-Src	breast:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
15	FOS	chr1:98191978-98192301	MCF10A-Er-Src	breast:	n/a	chr1:98192101-98192110 chr1:98192155-98192163 chr1:98192155-98192162
16	FOS	chr1:98176596-98176852	HUVEC	blood vessel:	n/a	chr1:98176714-98176722 chr1:98176712-98176723 chr1:98176708-98176717 chr1:98176713-98176723
17	FOS	chr1:98178612-98178841	MCF10A-Er-Src	breast:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
18	FOS	chr1:98192002-98192231	MCF10A-Er-Src	breast:	n/a	chr1:98192101-98192110 chr1:98192155-98192163 chr1:98192155-98192162
19	FOS	chr1:98178610-98178891	HUVEC	blood vessel:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
20	FOS	chr1:98193141-98193142	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:98178587-98178872	MCF10A-Er-Src	breast:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
22	FOS	chr1:98190410-98190485	MCF10A-Er-Src	breast:	n/a	n/a
23	GATA3	chr1:98184524-98184552	SH-SY5Y	brain:	n/a	n/a
24	GATA3	chr1:98191327-98191348	SH-SY5Y	brain:	n/a	n/a
25	JUN	chr1:98178657-98178825	HepG2	liver:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178752-98178762 chr1:98178752-98178761
26	JUND	chr1:98178596-98178876	HepG2	liver:	n/a	chr1:98178753-98178762 chr1:98178753-98178761 chr1:98178754-98178761 chr1:98178751-98178763 chr1:98178705-98178716 chr1:98178752-98178762 chr1:98178752-98178761 chr1:98178751-98178762
27	JUND	chr1:98184551-98184696	H1-hESC	embryonic stem cell:	n/a	chr1:98184578-98184590 chr1:98184580-98184589
28	MAFK	chr1:98182741-98182875	HepG2	liver:	n/a	chr1:98182783-98182798
29	MAFK	chr1:98176457-98176646	HepG2	liver:	n/a	chr1:98176555-98176566 chr1:98176547-98176564
30	MAFK	chr1:98182777-98182831	HepG2	liver:	n/a	chr1:98182783-98182798
31	MAFK	chr1:98176436-98176666	HepG2	liver:	n/a	chr1:98176555-98176566 chr1:98176547-98176564
32	MAFK	chr1:98178617-98178833	HepG2	liver:	n/a	chr1:98178754-98178763
33	MYC	chr1:98193212-98193298	GM12878	blood:	n/a	n/a
34	MYC	chr1:98194789-98194836	K562	blood:	n/a	n/a
35	POLR2A	chr1:98178997-98179015	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr1:98190634-98190834	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr1:98194221-98194233	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr1:98178243-98178319	GM12878	blood:	n/a	n/a
39	STAT3	chr1:98193051-98193157	MCF10A-Er-Src	breast:	n/a	n/a
40	USF1	chr1:98184600-98184876	H1-hESC	embryonic stem cell:	n/a	n/a

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DPYD	hsa-miR-124-3p	chr1:98185550-98185569

Variant related genes	Relation type
DPYD	TF binding region

Extended variants
information (count: 656 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34455783	chr1:98175878-98175879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532802628	chr1:98175891-98175892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149745492	chr1:98175900-98175901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373846441	chr1:98175971-98175972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538729288	chr1:98175984-98175985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147838785	chr1:98176009-98176010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141347757	chr1:98176017-98176018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534900478	chr1:98176019-98176020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552658196	chr1:98176057-98176058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191810515	chr1:98176181-98176182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145648107	chr1:98176228-98176229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182055337	chr1:98176267-98176268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186592762	chr1:98176269-98176270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146722577	chr1:98176276-98176277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557814789	chr1:98176306-98176307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542386862	chr1:98176311-98176312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545911563	chr1:98176383-98176384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74568113	chr1:98176399-98176400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77627802	chr1:98176401-98176402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541251600	chr1:98176488-98176489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371172164	chr1:98176620-98176621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs11588242	chr1:98176656-98176657	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs113706676	chr1:98176659-98176660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561805451	chr1:98176687-98176688	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376333359	chr1:98176730-98176731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369129358	chr1:98176742-98176743	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372891442	chr1:98176762-98176763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12565248	chr1:98176814-98176815	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370811997	chr1:98176816-98176817	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563330046	chr1:98176825-98176826	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111639194	chr1:98176844-98176845	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532415271	chr1:98176857-98176858	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552214905	chr1:98176931-98176932	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143705846	chr1:98176965-98176966	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148100155	chr1:98176976-98176977	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78409791	chr1:98176979-98176980	Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568597191	chr1:98177004-98177005	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537741524	chr1:98177012-98177013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140911074	chr1:98177170-98177171	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377232664	chr1:98177208-98177209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191552359	chr1:98177229-98177230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539449483	chr1:98177236-98177237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553069127	chr1:98177239-98177240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201522099	chr1:98177273-98177274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200650303	chr1:98177310-98177311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572994594	chr1:98177328-98177329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145167877	chr1:98177337-98177338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561903212	chr1:98177367-98177368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374184810	chr1:98177369-98177370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575386979	chr1:98177532-98177533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98136200-98188800	Weak transcription	Left Ventricle	heart
2	chr1:98141800-98185400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:98144000-98176600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:98153400-98187800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr1:98160200-98183200	Weak transcription	Primary T cells from cord blood	blood
7	chr1:98160400-98182800	Weak transcription	Primary B cells from cord blood	blood
8	chr1:98163200-98185400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:98165800-98180200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:98166000-98183200	Weak transcription	Liver	Liver
11	chr1:98166200-98186800	Weak transcription	HSMM	muscle
12	chr1:98167400-98183000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:98167400-98185000	Weak transcription	NHDF-Ad	bronchial
14	chr1:98171600-98185400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr1:98172200-98182600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:98172600-98185400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr1:98173400-98182600	Weak transcription	Dnd41	blood
18	chr1:98173400-98185200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:98175400-98176600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr1:98175400-98176800	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr1:98175400-98185200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr1:98176400-98188200	Weak transcription	Right Ventricle	heart
23	chr1:98176600-98177200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:98176600-98177200	Enhancers	HUVEC	blood vessel
25	chr1:98176600-98179800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:98176800-98177000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
27	chr1:98176800-98179600	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr1:98177000-98188200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr1:98177200-98185800	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr1:98177200-98254600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:98177600-98185400	Weak transcription	Adipose Nuclei	Adipose
32	chr1:98177800-98183200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:98178200-98184200	Weak transcription	Esophagus	oesophagus
34	chr1:98179000-98182000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:98179000-98188000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr1:98179000-98220800	Weak transcription	Psoas Muscle	Psoas
37	chr1:98179400-98183200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:98179400-98185400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:98179600-98187400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr1:98179800-98185200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr1:98179800-98187400	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr1:98180200-98187200	Strong transcription	Primary hematopoietic stem cells	blood
43	chr1:98181200-98183000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr1:98181200-98188600	Weak transcription	Lung	lung
45	chr1:98181400-98204400	Weak transcription	Osteobl	bone
46	chr1:98181600-98188600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr1:98181800-98183200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:98181800-98187400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr1:98182000-98183200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:98182000-98183400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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