EnhancerDB
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Enhancers that regulate BSN[ENSG00000164061.4]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr3 49479245 49501124 enh7204 49591922 90798
Bone Marrow (K562) Brain (SK-N-MC) Colon (HCT116) Blood (Karpas-422) Pancreas Blood (T-cell) Epithelial (MCF-7) Stomach Ovary Bone (Osteoblast) Peripheral Blood (MM.1S) Neural Stem Cells (H9) Thymus Cervix (HeLa-S3) Esophagus Placenta Lung (PC-9) Muscle (Myoblast) Spleen Muscle (Myotube) Liver (HepG2) Prostate (RWPE1) Heart
chr3 49503154 49503264 vista40880 49591922 88658
VISTA
chr3 49518245 49524115 enh20586 49591922 67807
Liver (HepG2) Colon (HCT116) Placenta Neural Stem Cells (H9) Heart
chr3 49529405 49541046 enh20587 49591922 50876
Bone Marrow (K562) Prostate (PC-3) Liver (HepG2) Cervix (HeLa-S3) Large Intestine Prostate (RWPE1) Esophagus Astrocyte Bone (Osteoblast) Stomach Placenta Colon (HCT116) Breast Thyroid Pancreas Spleen Muscle (Myotube) Uterus Thymus Heart
chr3 49545745 49553515 enh20588 49591922 38407
Stomach Placenta Lung (PC-9) Epithelial (MCF-7)
chr3 49553545 49563819 enh20589 49591922 28103
Skin (Keratinocyte) Liver (HepG2) Prostate (RWPE1) Esophagus Liver Placenta Breast Pancreas Muscle (Myotube) Thymus Stomach
chr3 49572785 49580115 enh7205 49591922 11807
Bone Marrow (K562) Pancreas (Panc1) Uterus Blood (Karpas-422)
chr3 49605526 49610055 enh70570 49591922 13604
Liver (HepG2) Neural Stem Cells (H9)
chr3 49628645 49632795 enh82530 49591922 36723
Prostate (PC-3)
chr3 49635125 49649714 enh63138 49591922 43203
Prostate (PC-3) Cervix (HeLa-S3) Brain (SK-N-SH) Brain (SK-N-MC) Prostate (RWPE1) Esophagus Colon (HCT116) Lung (PC-9) Blood (T-cell) Stomach
chr3 49651964 49658119 enh70571 49591922 60042
Muscle (A673) Neural Stem Cells (H9) Bone (Osteoblast)
chr3 49672246 49678327 enh45407 49591922 80324
Bone Marrow (K562) Skin (Keratinocyte) Cervix (HeLa-S3) Prostate (RWPE1) Lung (PC-9) Spleen Muscle (Myotube)
chr3 49683283 49687495 enh65653 49591922 91361
Pancreas Liver (HepG2) Stomach Heart
Transcript facotrs that regulate BSN[ENSG00000164061.4]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
SNPs associated with BSN[ENSG00000164061.4], confirmed by eQTL
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Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr3 50562913 rs115160149 G A 853935 Esophagus 0.394486 6729538
chr3 49792029 rs71278637 G GT 83051 Ovary 0.438084 6726887
chr3 50217234 rs9831967 C A,T 508256 Thyroid 0.142814 6728002
chr3 50201924 rs2188151 G T 492946 Liver 0.0581151 6727875
chr3 50486057 rs2236977 A G 777079 Adrenal 0.417272 6729126
Details of BSN[ENSG00000164061.4]
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Genomic Location chr3:49591922-49708978[+]
TSS 49591922
Gene Name BSN
Ensembl ID ENSG00000164061.4
ENTREZID 8927
Uniprot
Q9UPA5
Protein Name
Bassoon
Protein bassoon
Expression levels of BSN[ENSG00000164061.4]
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