| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58440134-58440469 | Common:6; Rare:88 | ||||
| chr19:58466879-58467079 | Common:1; Rare:61 | ||||
| chr19:58499212-58499545 | Common:2; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:58554933-58555172 | Common:1; Rare:79 | ||||
| chr19:58573274-58573677 | Common:2; Rare:101 | ||||
| chr2:677362-677557 | Common:1; Rare:82 | ||||
| chr2:2324933-2325159 | Common:1; Rare:45 | ||||
| chr2:2331216-2331528 | Common:3; Rare:63 | ||||
| chr2:3377774-3377953 | Rare:52 | ||||
| chr2:3379608-3379785 | Common:2; Rare:74 | ||||
| chr2:3558269-3558565 | Common:6; Rare:108 | ||||
| chr2:3575080-3575345 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:9423410-9423700 | Rare:90 | ||||
| chr2:9474522-9474630 | Common:6; Rare:50 | ||||
| chr2:9555621-9555926 | Common:2; Rare:99 |