| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74792861-74793261 | Common:1; Rare:74 | ||||
| chr15:74815523-74815900 | Common:2; Rare:60 | ||||
| chr15:74857190-74857730 | Common:1; Rare:80 | ||||
| chr15:74858098-74858498 | Common:2; Rare:77 | ||||
| chr15:74859480-74859880 | Common:2; Rare:99 | ||||
| chr15:74870014-74870378 | Common:4; Rare:90 | ||||
| chr15:74870753-74871410 | Common:2; Rare:107 | ||||
| chr15:74896051-74896557 | Common:4; Rare:173; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr15:74946626-74947026 | Common:2; Rare:91 | ||||
| chr15:74956063-74956463 | Rare:169 | ||||
| chr15:74958580-74958900 | Common:1; Rare:57 | ||||
| chr15:75008980-75009330 | Common:1; Rare:52 | ||||
| chr15:75029648-75030092 | Common:9; Rare:191 | ||||
| chr15:75031880-75032260 | Rare:65 | ||||
| chr15:75044411-75045415 | Common:4; Rare:252 |