| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:58933402-58933826 | Common:3; Rare:171 | ||||
| chr15:58988068-58988178 | Common:1; Rare:35 | ||||
| chr15:59104762-59105239 | Common:2; Rare:149 | ||||
| chr15:59372541-59372694 | Common:1; Rare:38 | ||||
| chr15:59372815-59373048 | Common:2; Rare:75 | ||||
| chr15:59437916-59438240 | Common:1; Rare:104 | ||||
| chr15:59657407-59657642 | Common:2; Rare:97 | ||||
| chr15:59689135-59689575 | Common:9; Rare:195 | ||||
| chr15:60397927-60398103 | Common:2; Rare:40 | ||||
| chr15:60479026-60479266 | Common:3; Rare:108 | ||||
| chr15:62060358-62060522 | Rare:62 | ||||
| chr15:62165269-62165429 | Common:1; Rare:43 | ||||
| chr15:62390435-62390633 | Common:1; Rare:95 | ||||
| chr15:62835389-62835669 | Common:2; Rare:64 | ||||
| chr15:63042505-63042943 | Common:4; Rare:135; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 |