| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025303-240025503 | Common:1; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:240560759-240560836 | Rare:33 | ||||
| chr2:240561031-240561313 | Common:4; Rare:127 | ||||
| chr2:241149456-241149613 | Common:1; Rare:50 | ||||
| chr2:241315184-241315277 | Rare:33 | ||||
| chr2:241315656-241315981 | Common:5; Rare:128 | ||||
| chr2:241637555-241637704 | Common:1; Rare:80 | ||||
| chr20:381219-381391 | Common:2; Rare:44 | ||||
| chr20:1118465-1118670 | Common:3; Rare:65 | ||||
| chr20:1894385-1894522 | Common:1; Rare:28 | ||||
| chr20:1894740-1895027 | Common:1; Rare:101 | ||||
| chr20:2652430-2652642 | Common:6; Rare:70 | ||||
| chr20:3889162-3889396 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4686402-4686684 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5119913-5120172 | Common:1; Rare:88 |