| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74841840-74842594 | Common:1; Rare:306 | ||||
| chr15:74842600-74843031 | Rare:161 | ||||
| chr15:74843044-74843418 | Common:5; Rare:265 | ||||
| chr15:74872930-74873188 | Common:3; Rare:113 | ||||
| chr15:74873269-74873518 | Common:11; Rare:128 | ||||
| chr15:74890011-74890141 | Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74906373-74906710 | Common:1; Rare:138 | ||||
| chr15:74906698-74906971 | Common:3; Rare:216 | ||||
| chr15:74937529-74938315 | Common:11; Rare:485 | ||||
| chr15:74956701-74956984 | Common:3; Rare:256 | ||||
| chr15:74957001-74957300 | Common:2; Rare:136 | ||||
| chr15:74995290-74995730 | Common:15; Rare:239 | ||||
| chr15:75023548-75023751 | Common:1; Rare:59 | ||||
| chr15:75201656-75202018 | Common:3; Rare:245 | ||||
| chr15:75202074-75202234 | Rare:37 |