EnhancerDB
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Enhancers that regulate AMN[ENSG00000166126.6]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr14 103279525 103296435 enh3472 103388993 92558
Skin (Keratinocyte) Prostate (PC-3) Liver (HepG2) Brain (SK-N-MC) Prostate (RWPE1) Blood (T-cell) Esophagus Astrocyte Bone (Osteoblast) Blood (GM12878) Muscle (A673) Placenta Blood (Karpas-422) Lung (PC-9) Pancreas Thymus Stomach
chr14 103297614 103301915 enh68848 103388993 87078
Neural Stem Cells (H9)
chr14 103299136 103299384 vista19184 103388993 89609
VISTA
chr14 103302532 103309662 enh68849 103388993 79331
Neural Stem Cells (H9)
chr14 103313239 103318275 enh47818 103388993 70718
Brain (SK-N-SH) Large Intestine Pancreas Spleen Uterus Thymus Stomach
chr14 103318529 103322679 enh62442 103388993 66314
Esophagus
chr14 103325265 103335615 enh15968 103388993 53378
Placenta Liver (HepG2) Epithelial (MCF-7)
chr14 103337645 103341795 enh92576 103388993 47198
Liver (HepG2)
chr14 103343196 103351935 enh15969 103388993 37058
Placenta Large Intestine Colon (HCT116)
chr14 103365045 103369521 enh3473 103388993 19472
Thyroid Blood (Karpas-422) Heart
chr14 103379205 103383355 enh3474 103388993 5638
Blood (Karpas-422)
chr14 103398868 103403052 enh60526 103388993 9875
Blood (OCI-LY7)
chr14 103454905 103462413 enh3475 103388993 65912
Skin (Keratinocyte) Prostate (PC-3) Cervix (HeLa-S3) Large Intestine Prostate (RWPE1) Esophagus Bone (Osteoblast) Stomach Blood (Karpas-422) Lung (PC-9) Pancreas (Panc1) Muscle (Myotube) Epithelial (MCF-7)
chr14 103463733 103468349 enh102511 103388993 74740
Bone (Osteoblast)
chr14 103473369 103502375 enh15970 103388993 84376
Prostate (PC-3) Cervix (HeLa-S3) Brain (SK-N-SH) Large Intestine Prostate (RWPE1) Esophagus Astrocyte Bone (Osteoblast) Stomach Muscle (A673) Placenta Uterus Embryonic Stem Cell Line (H1-hESC) Lung (PC-9) Muscle (Myoblast) Pancreas (Panc1) Muscle (Myotube) Neural Stem Cells (H9) Epithelial (MCF-7)
Transcript facotrs that regulate AMN[ENSG00000166126.6]
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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 AMN[ENSG00000166126.6], 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
chr14 104359602 rs111555389 C T 959669 Heart 0.0921054 3817755
chr14 103389003 rs2295829 G C,T 0 Pancreas 1.32053e-08 3809050
chr14 103545192 rs10147347 C T 145259 Spleen 0.0795565 3810336
chr14 103389003 rs2295829 G C,T 0 Liver 4.32159e-26 3809050
chr14 103389003 rs2295829 G C,T 0 Stomach 4.99943e-08 3809050
Details of AMN[ENSG00000166126.6]
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Genomic Location chr14:103388993-103399933[+]
TSS 103388993
Gene Name AMN
Ensembl ID ENSG00000166126.6
ENTREZID 81693
Uniprot
B3KP64
Q9BXJ7
Protein Name
Expression levels of AMN[ENSG00000166126.6]
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