| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44589304-44589523 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:44613429-44613722 | Rare:65; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr15:44726773-44727073 | Common:1; Rare:41 | ||||
| chr15:44784328-44784448 | Rare:16 | ||||
| chr15:45094111-45094512 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):1 | ||||
| chr15:45095177-45095550 | Common:3; Rare:90; Clinvar (pathogenic):1 | ||||
| chr15:45095553-45095723 | Common:1; Rare:52; Clinvar:1 | ||||
| chr15:45096977-45097052 | Rare:19 | ||||
| chr15:45097145-45097697 | Rare:170; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr15:45106298-45106432 | Common:2; Rare:28; Clinvar (benign):1 | ||||
| chr15:45107307-45107757 | Common:2; Rare:98; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:45110648-45110773 | Common:3; Rare:56; Clinvar (benign):1 | ||||
| chr15:45135177-45135554 | Common:4; Rare:139 | ||||
| chr15:45144805-45144943 | Rare:37 | ||||
| chr15:45145887-45145981 | Common:2; Rare:18 |