| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:41870472-41870553 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:41904122-41904391 | Common:2; Rare:95 | ||||
| chr5:41925240-41925429 | Common:1; Rare:57 | ||||
| chr5:42756717-42756872 | Common:1; Rare:30 | ||||
| chr5:43043207-43043319 | Common:1; Rare:22 | ||||
| chr5:43064780-43065137 | Rare:81 | ||||
| chr5:43067127-43067517 | Rare:64 | ||||
| chr5:43120817-43121211 | Common:7; Rare:151 | ||||
| chr5:43121420-43121688 | Common:1; Rare:99 | ||||
| chr5:43313372-43313657 | Common:3; Rare:75 | ||||
| chr5:43397003-43397239 | Rare:39 | ||||
| chr5:43483816-43483974 | Common:3; Rare:53 | ||||
| chr5:43484328-43484390 | Rare:17 | ||||
| chr5:43515066-43515243 | Common:3; Rare:67 | ||||
| chr5:43556835-43557202 | Common:4; Rare:116 |