Enhancers that regulate NOTUM[ENSG00000185269.7]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr17 79823005 79827155 enh4643 79919716 92561
chr17 79840269 79844916 enh32381 79919716 74800
chr17 79886802 79887109 vista26429 79919716 32607
chr17 79925685 79926075 vista26430 79919716 5969
chr17 79942701 79942868 vista26431 79919716 22985
chr17 79946865 79952395 enh17448 79919716 27149
chr17 79949658 79950000 vista26432 79919716 29942
chr17 79950743 79950987 vista26433 79919716 31027
chr17 79955085 79966579 enh17449 79919716 35369
chr17 79958827 79959194 vista26434 79919716 39111
chr17 79968705 79972855 enh92760 79919716 48989
chr17 79975885 79980035 enh4644 79919716 56169
chr17 79979263 79979824 vista26435 79919716 59547

Transcript facotrs that regulate NOTUM[ENSG00000185269.7]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
chr17 79923857 79925718 ZBTB33 GTRD no Lung (A549) 79919716 4141 108310376
chr17 79923931 79926198 ZBTB33 GTRD no Lung (A549) 79919716 4215 108310377
chr17 79923973 79926205 ZBTB33 GTRD no Lung (A549) 79919716 4257 108310378
chr17 79923998 79926235 ZNF274 GTRD no Cervix (HeLa-S3) 79919716 4282 108310379
chr17 79924002 79925960 ZNF143 GTRD no Epithelial (MCF-7) 79919716 4286 108310380
chr17 79924003 79926164 ZBTB33 GTRD no Lung (A549) 79919716 4287 108310381
chr17 79924008 79932381 TCF7L2 GTRD no Colon (HCT116) 79919716 4292 108310382
chr17 79924011 79925873 ZNF143 GTRD no Epithelial (MCF-7) 79919716 4295 108310383
chr17 79924013 79925813 ZNF274 GTRD no Cervix (HeLa-S3) 79919716 4297 108310384
chr17 79924015 79929938 ZNF274 GTRD no Liver (HepG2) 79919716 4299 108310385
chr17 79924026 79926109 ZNF143 GTRD no Epithelial (MCF-7) 79919716 4310 108310386
chr17 79924064 79925803 ZBTB33 GTRD no Lung (A549) 79919716 4348 108310387
chr17 79924113 79925950 ZNF143 GTRD no Epithelial (MCF-7) 79919716 4397 108310388
chr17 79924204 79925772 ZBTB33 GTRD no Lung (A549) 79919716 4488 108310389

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr17 80023991 rs4606789 C A 104275 Esophagus 0.0148476 5118234
chr17 79696321 rs193030143 G T 214067 Breast 0.0903564 5116141
chr17 79373791 rs150648447 C T 536597 Spleen 0.351855 5113324
chr17 80702510 rs2635417 A C 782794 Uterus 0.332053 5124434
chr17 79338376 rs140680263 G A 572012 Thyroid 0.100201 5112827
chr17 79338144 rs2004797 G A 572244 Liver 0.0771317 5112818
chr17 80269484 rs58962763 A G 349768 Lung 0.19405 5120903
chr17 80751140 rs74000100 T G 831424 Stomach 0.0917853 5124815

Genomic Location chr17:79910388-79919716[-]
TSS 79919716
Gene Name NOTUM
Ensembl ID ENSG00000185269.7
ENTREZID 147111
Uniprot
Q6P988
Protein Name
Palmitoleoyl-protein carboxylesterase NOTUM