| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47335032-47335323 | Rare:62 | ||||
| chr2:47691256-47691546 | Common:4; Rare:55 | ||||
| chr2:47785854-47786040 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr2:47795668-47796048 | Common:4; Rare:97; Clinvar:21; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr2:47798476-47798690 | Common:2; Rare:80; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr2:47803223-47803489 | Common:1; Rare:101; Clinvar:21; Clinvar (benign):14 | ||||
| chr2:47806078-47806324 | Common:1; Rare:107; Clinvar:30; Clinvar (benign):16; Clinvar (pathogenic):7 | ||||
| chr2:47810399-47810470 | Common:1; Rare:24 | ||||
| chr2:47812470-47812743 | Common:2; Rare:82 | ||||
| chr2:47813240-47813571 | Common:4; Rare:70 | ||||
| chr2:47906426-47906818 | Common:2; Rare:151 | ||||
| chr2:54290258-54290336 | Common:1; Rare:16 | ||||
| chr2:54560438-54560554 | Common:2; Rare:34 | ||||
| chr2:54564133-54564158 | Rare:4 | ||||
| chr2:54618157-54618239 | Common:1; Rare:26 |