| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037912-48038117 | Common:5; Rare:64 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 | ||||
| chr13:48303656-48303907 | Rare:84; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48476356-48476552 | Rare:25 | ||||
| chr13:48533038-48533110 | Common:2; Rare:23 | ||||
| chr13:48975774-48975952 | Common:1; Rare:62 | ||||
| chr13:48976156-48976246 | Rare:25 | ||||
| chr13:48976533-48976828 | Common:1; Rare:86 | ||||
| chr13:49110228-49110397 | Common:2; Rare:47 | ||||
| chr13:49247790-49247999 | Rare:60 | ||||
| chr13:49443996-49444522 | Common:2; Rare:163 | ||||
| chr13:49495567-49495750 | Rare:36 | ||||
| chr13:49495867-49496335 | Common:4; Rare:114 | ||||
| chr13:49585471-49585660 | Common:1; Rare:68 | ||||
| chr13:49628414-49628571 | Rare:40 |