| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72118167-72118434 | Common:2; Rare:88 | ||||
| chr15:72231120-72231447 | Common:3; Rare:105 | ||||
| chr15:72375944-72376118 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:73994595-73994806 | Rare:45 | ||||
| chr15:74461107-74461298 | Rare:61 | ||||
| chr15:74540954-74541262 | Common:3; Rare:106 | ||||
| chr15:75625617-75625821 | Common:1; Rare:49 | ||||
| chr15:77420088-77420461 | Common:2; Rare:109 | ||||
| chr15:77420882-77420937 | Rare:22 | ||||
| chr15:77421116-77421363 | Common:1; Rare:58 | ||||
| chr15:78149177-78149406 | Common:1; Rare:75 | ||||
| chr15:78299562-78299670 | Rare:45 | ||||
| chr15:78438002-78438334 | Common:3; Rare:136 | ||||
| chr15:78944934-78945307 | Common:11; Rare:145 | ||||
| chr15:78998129-78998423 | Common:1; Rare:54 |