| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44662753-44663902 | Common:12; Rare:1224; Clinvar:61; Clinvar (benign):37; Clinvar (pathogenic):3 | ||||
| chr15:44710532-44711720 | Common:8; Rare:786; Clinvar:6; Clinvar (pathogenic):4 | ||||
| chr15:44711722-44712130 | Common:1; Rare:281 | ||||
| chr15:44712560-44712900 | Rare:130 | ||||
| chr15:44728630-44729528 | Common:5; Rare:405 | ||||
| chr15:44729536-44729936 | Common:1; Rare:71 | ||||
| chr15:44735615-44736192 | Common:13; Rare:248 | ||||
| chr15:45022891-45023291 | Common:29; Rare:445 | ||||
| chr15:45023625-45024025 | Common:5; Rare:83 | ||||
| chr15:45187826-45188226 | Common:10; Rare:275 | ||||
| chr15:45200185-45200703 | Common:7; Rare:413 | ||||
| chr15:45200983-45201383 | Common:10; Rare:315 | ||||
| chr15:45401558-45401958 | Common:2; Rare:89 | ||||
| chr15:45402039-45402720 | Common:57; Rare:996; Clinvar:5 | ||||
| chr15:45402688-45403127 | Common:2; Rare:330 |