| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72474161-72474349 | Rare:70 | ||||
| chr15:72686104-72686449 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72783697-72783840 | Common:2; Rare:60 | ||||
| chr15:73633184-73633573 | Common:2; Rare:148 | ||||
| chr15:73684203-73684414 | Rare:60 | ||||
| chr15:73992245-73992425 | Rare:59 | ||||
| chr15:73994587-73994795 | Rare:45 | ||||
| chr15:74100189-74100315 | Rare:16 | ||||
| chr15:74461107-74461440 | Rare:90 | ||||
| chr15:74540909-74541271 | Common:4; Rare:127 | ||||
| chr15:74598335-74598511 | Common:1; Rare:78 | ||||
| chr15:74615622-74615898 | Common:3; Rare:92 | ||||
| chr15:74695974-74696138 | Rare:48 | ||||
| chr15:74781941-74782111 | Common:3; Rare:55 | ||||
| chr15:74843110-74843334 | Common:1; Rare:66 |