| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:148807827-148808227 | Common:6; Rare:143 | ||||
| chr5:148826340-148826633 | Common:4; Rare:69 | ||||
| chr5:149002118-149002326 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:149019782-149019908 | Rare:19 | ||||
| chr5:149422729-149423031 | Common:1; Rare:62 | ||||
| chr5:149442494-149442894 | Common:2; Rare:102 | ||||
| chr5:150138827-150139108 | Common:1; Rare:46 | ||||
| chr5:150458890-150459166 | Common:2; Rare:56 | ||||
| chr5:150652138-150652573 | Common:1; Rare:144 | ||||
| chr5:150656560-150656900 | Common:4; Rare:126 | ||||
| chr5:150778646-150778855 | Common:1; Rare:85 | ||||
| chr5:151150456-151150856 | Common:3; Rare:96 | ||||
| chr5:151156036-151156442 | Common:7; Rare:112 | ||||
| chr5:151699351-151699483 | Common:1; Rare:17 | ||||
| chr5:152606960-152607881 | Common:6; Rare:251 |