| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20525331-20525570 | Common:1; Rare:51 | ||||
| chr2:20576801-20576882 | Rare:11 | ||||
| chr2:20578877-20579074 | Common:2; Rare:34 | ||||
| chr2:20595590-20595772 | Common:1; Rare:42 | ||||
| chr2:20596052-20596191 | Common:1; Rare:22 | ||||
| chr2:23379218-23379553 | Common:13; Rare:56 | ||||
| chr2:23925588-23925861 | Common:1; Rare:58 | ||||
| chr2:23926031-23926530 | Common:1; Rare:110 | ||||
| chr2:24342528-24342702 | Rare:22 | ||||
| chr2:24365148-24365268 | Rare:17 | ||||
| chr2:24490752-24491354 | Common:3; Rare:203 | ||||
| chr2:24887174-24887265 | Common:1; Rare:27 | ||||
| chr2:24920522-24920800 | Common:3; Rare:72 | ||||
| chr2:24927061-24927157 | Common:2; Rare:25 | ||||
| chr2:25161558-25161753 | Common:4; Rare:108; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 |