| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72375944-72376124 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474195-72474333 | Rare:50 | ||||
| chr15:72686157-72686220 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633193-73633293 | Rare:44 | ||||
| chr15:73633354-73633405 | Rare:16 | ||||
| chr15:73926313-73926466 | Rare:42 | ||||
| chr15:73994606-73994716 | Rare:17 | ||||
| chr15:74173601-74173876 | Common:2; Rare:68 | ||||
| chr15:74461107-74461307 | Rare:62 | ||||
| chr15:74540966-74541270 | Common:3; Rare:108 | ||||
| chr15:74615567-74615884 | Common:4; Rare:101 | ||||
| chr15:74843113-74843318 | Common:1; Rare:62 | ||||
| chr15:75347533-75347910 | Common:2; Rare:95 | ||||
| chr15:75368585-75368644 | Rare:26 | ||||
| chr15:75451677-75451989 | Common:1; Rare:84 |