| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23969796-23969987 | Common:11; Rare:128 | ||||
| chr14:24051700-24052180 | Common:11; Rare:336 | ||||
| chr14:24052410-24052810 | Common:6; Rare:137 | ||||
| chr14:24081460-24081830 | Common:6; Rare:308; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:24093815-24094514 | Common:14; Rare:410; Clinvar (benign):2 | ||||
| chr14:24094573-24094691 | Rare:30 | ||||
| chr14:24094620-24095132 | Common:4; Rare:194 | ||||
| chr14:24095280-24095790 | Common:3; Rare:125 | ||||
| chr14:24113971-24115428 | Common:11; Rare:789 | ||||
| chr14:24132291-24132519 | Rare:82 | ||||
| chr14:24135922-24136310 | Common:3; Rare:323 | ||||
| chr14:24141360-24141973 | Common:7; Rare:402 | ||||
| chr14:24146526-24147010 | Common:5; Rare:354 | ||||
| chr14:24147087-24147601 | Common:10; Rare:320 | ||||
| chr14:24147700-24148594 | Common:5; Rare:377 |