| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45023035-45023239 | Common:3; Rare:51 | ||||
| chr15:45187946-45188148 | Common:3; Rare:77 | ||||
| chr15:45200490-45200657 | Common:1; Rare:47 | ||||
| chr15:45378010-45378420 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):4 | ||||
| chr15:45378440-45378770 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):8 | ||||
| chr15:45402166-45402433 | Common:6; Rare:88; Clinvar:1 | ||||
| chr15:45522680-45523130 | Common:1; Rare:138 | ||||
| chr15:45587041-45587446 | Common:2; Rare:101; Clinvar:6; Clinvar (benign):1 | ||||
| chr15:47183801-47184306 | Common:6; Rare:264 | ||||
| chr15:47184311-47184922 | Common:11; Rare:240 | ||||
| chr15:48177430-48178170 | Rare:182 | ||||
| chr15:48331307-48331474 | Common:3; Rare:57 | ||||
| chr15:48331871-48332178 | Common:5; Rare:79 | ||||
| chr15:48644646-48645564 | Common:2; Rare:416; Clinvar:8; Clinvar (benign):12 | ||||
| chr15:48645643-48646038 | Common:2; Rare:119; Clinvar (benign):1 |