| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58408430-58408686 | Common:4; Rare:80 | ||||
| chr19:58440134-58440482 | Common:6; Rare:93 | ||||
| chr19:58466871-58467115 | Common:1; Rare:78 | ||||
| chr19:58476023-58476184 | Rare:59 | ||||
| chr19:58499188-58499549 | Common:3; Rare:119; Clinvar:5; Clinvar (benign):2 | ||||
| chr19:58519767-58520017 | Rare:65 | ||||
| chr19:58554195-58554523 | Rare:90 | ||||
| chr19:58554939-58555183 | Common:1; Rare:81 | ||||
| chr19:58558897-58559126 | Common:1; Rare:72 | ||||
| chr19:58573033-58573209 | Rare:55 | ||||
| chr19:58573271-58573601 | Common:1; Rare:82 | ||||
| chr2:264021-264128 | Common:1; Rare:38 | ||||
| chr2:289013-289190 | Rare:25 | ||||
| chr2:677364-677557 | Common:1; Rare:80 | ||||
| chr2:3377791-3378021 | Common:1; Rare:65 |